Syllabus updates
The AOD syllabus is constantly evolving with the literature. When new material is added to the syllabus, push notifications will alert you to visit this page.
Updates
Recent literature Updates
Added April 26
Emergency front-of-neck access in pediatric anesthesia: A narrative review
Abstract
Background and objectives: Children undergoing airway management during general anesthesia may experience airway complications resulting in a rare but life-threatening situation known as "Can't Intubate, Can't Oxygenate". This situation requires immediate recognition, advanced airway management, and ultimately emergency front-of-neck access. The absence of standardized procedures, lack of readily available equipment, inadequate knowledge, and training often lead to failed emergency front-of-neck access, resulting in catastrophic outcomes. In this narrative review, we examined the latest evidence on emergency front-of-neck access in children.
Methods: A comprehensive literature was performed the use of emergency front-of-neck access (eFONA) in infants and children.
Results: Eighty-six papers were deemed relevant by abstract. Finally, eight studies regarding the eFONA technique and simulations in animal models were included. For all articles, their primary and secondary outcomes, their specific animal model, the experimental design, the target participants, and the equipment were reported.
Conclusion: Based on the available evidence, we propose a general approach to the eFONA technique and a guide for implementing local protocols and training. Additionally, we introduce the application of innovative tools such as 3D models, ultrasound, and artificial intelligence, which can improve the precision, safety, and training of this rare but critical procedure.
added March 25, 2024
Mediastinal Masses, Anesthetic Interventions and Airway Compression in Adults: A Prospective Observational Study
Philip M. Hartigan, M.D., Sergey Karamnov, M.D., et al Anesthesiology 2022; 136:104–14
NOTE by William Rosenblatt, MD
This observational study is an example of how it has taken more than 30 years for evidence to catch up with practice. This study contradicts a long held belief in the management of the patient with a mediastinal mass, though most clinicians working with these patients knew that there was a "myth" around the dogma that all of these patients were at particular risk.
ABSTRACT
Background: Central airway occlusion is a feared complication of general
anesthesia in patients with mediastinal masses. Maintenance of spontaneous
ventilation and avoiding neuromuscular blockade are recommended to reduce
this risk. Physiologic arguments supporting these recommendations are controversial
and direct evidence is lacking. The authors hypothesized that, in
adult patients with moderate to severe mediastinal mass–mediated tracheobronchial
compression, anesthetic interventions including positive pressure
ventilation and neuromuscular blockade could be instituted without compromising
central airway patency.
Methods: Seventeen adult patients with large mediastinal masses requiring
general anesthesia underwent awake intubation followed by continuous video
bronchoscopy recordings of the compromised portion of the airway during
staged induction. Assessments of changes in anterior–posterior airway diameter
relative to baseline (awake, spontaneous ventilation) were performed using
the following patency scores: unchanged = 0; 25 to 50% larger = +1; more
than 50% larger = +2; 25 to 50% smaller = −1; more than 50% smaller = −2.
Assessments were made by seven experienced bronchoscopists in side-by-side
blinded and scrambled comparisons between (1) baseline awake, spontaneous
breathing; (2) anesthetized with spontaneous ventilation; (3) anesthetized with
positive pressure ventilation; and (4) anesthetized with positive pressure ventilation
and neuromuscular blockade. Tidal volumes, respiratory rate, and inspiratory/
expiratory ratio were similar between phases.
Results: No significant change from baseline was observed in the mean
airway patency scores after the induction of general anesthesia (0 [95% CI, 0
to 0]; P = 0.953). The mean airway patency score increased with the addition
of positive pressure ventilation (0 [95% CI, 0 to 1]; P = 0.024) and neuromuscular
blockade (1 [95% CI, 0 to 1]; P < 0.001). No patient suffered airway
collapse or difficult ventilation during any anesthetic phase.
Conclusions: These observations suggest a need to reassess prevailing
assumptions regarding positive pressure ventilation and/or paralysis and
mediastinal mass–mediated airway collapse, but do not prove that conventional
(nonstaged) inductions are safe for such patients.
(ANESTHESIOLOGY 2022; 136:104–14)
March 19
Video Laryngoscopy vs Direct Laryngoscopy for Endotracheal Intubation in the Operating RoomK A Cluster Randomized Clinical Trial
Kurt Ruetzler, MD; Sergio Bustamante, MD; Marc T. Schmidt; Federico Almonacid-Cardenas, MD;
Andra Duncan, MD; Andrew Bauer, MD; Alparslan Turan, MD; Nikolaos J. Skubas, MD; Daniel I. Sessler, MD;
for the Collaborative VLS Trial Group
JAMA. doi:10.1001/jama.2024.0762 Published online March 18, 2024.
IMPORTANCE Endotracheal tubes are typically inserted in the operating room using direct
laryngoscopy. Video laryngoscopy has been reported to improve airway visualization;
however, whether improved visualization reduces intubation attempts in surgical patients
is unclear.
OBJECTIVE To determine whether the number of intubation attempts per surgical procedure is
lower when initial laryngoscopy is performed using video laryngoscopy or direct laryngoscopy.
DESIGN, SETTING, AND PARTICIPANTS Cluster randomized multiple crossover clinical trial
conducted at a single US academic hospital. Patients were adults aged 18 years or older
having elective or emergent cardiac, thoracic, or vascular surgical procedures who required
single-lumen endotracheal intubation for general anesthesia. Patients were enrolled from
March 30, 2021, to December 31, 2022. Data analysis was based on intention to treat.
INTERVENTIONS Two sets of 11 operating roomswere randomized on a 1-week basis to perform
hyperangulated video laryngoscopy or direct laryngoscopy for the initial intubation attempt.
MAIN OUTCOMES AND MEASURES The primary outcomewas the number of operating room
intubation attempts per surgical procedure. Secondary outcomes were intubation failure,
defined as the responsible clinician switching to an alternative laryngoscopy device for any
reason at any time, or by more than 3 intubation attempts, and a composite of airway and
dental injuries.
RESULTS Among 8429 surgical procedures in 7736 patients, the median patient age was 66
(IQR, 56-73) years, 35%(2950) were women, and 85%(7135) had elective surgical
procedures. More than 1 intubation attempt was required in 77 of 4413 surgical procedures
(1.7%) randomized to receive video laryngoscopy vs 306 of 4016 surgical procedures (7.6%)
randomized to receive direct laryngoscopy, with an estimated proportional odds ratio for the
number of intubation attempts of 0.20 (95%CI, 0.14-0.28; P < .001). Intubation failure
occurred in 12 of 4413 surgical procedures (0.27%) using video laryngoscopy vs 161 of 4016
surgical procedures (4.0%) using direct laryngoscopy (relative risk, 0.06; 95%CI, 0.03-0.14;
P < .001) with an unadjusted absolute risk difference of −3.7%(95%CI, −4.4%to −3.2%).
Airway and dental injuries did not differ significantly between video laryngoscopy (41 injuries
[0.93%]) vs direct laryngoscopy (42 injuries [1.1%]).
CONCLUSION AND RELEVANCE In this study among adults having surgical procedures who
required single-lumen endotracheal intubation for general anesthesia, hyperangulated video
laryngoscopy decreased the number of attempts needed to achieve endotracheal intubation
compared with direct laryngoscopy at a single academic medical center in the US. Results
suggest that video laryngoscopymay be a preferable approach for intubating patients
undergoing surgical procedures.
Updated Sept 6
Video versus Direct Laryngoscopy for Tracheal Intubation of
Critically Ill Adults
Matthew E. Prekker, M.D., M.P.H., Brian E. Driver, M.D., et al
BACKGROUND Whether video laryngoscopy as compared with direct laryngoscopy increases the
likelihood of successful tracheal intubation on the !rst attempt among critically ill adults is uncertain.
In a multicenter, randomized trial conducted at 17 emergency departments and intensive care units
(ICUs), we randomly assigned critically ill adults undergoing tracheal intubation to the videolaryngoscope
group or the direct-laryngoscope group. The primary outcome was successful intubation
on the !rst attempt. The secondary outcome was the occurrence of severe complications during
intubation; severe complications were de!ned as severe hypoxemia, severe hypotension, new or
increased vasopressor use, cardiac arrest, or death.
The trial was stopped for e$cacy at the time of the single preplanned interim analysis.
Among 1417 patients who were included in the !nal analysis (91.5% of whom underwent intubation that
was performed by an emergency medicine resident or a critical care fellow), successful intubation on the
!rst attempt occurred in 600 of the 705 patients (85.1%) in the video-laryngoscope group and in 504 of
the 712 patients (70.8%) in the direct-laryngoscope group (absolute risk di,erence, 14.3 percentage
points; 95% con!dence interval [CI], 9.9 to 18.7; P<0.001). A total of 151 patients (21.4%) in the videolaryngoscope
group and 149 patients (20.9%) in the direct-laryngoscope group had a severe
complication during intubation (absolute risk di,erence, 0.5 percentage points; 95% CI, −3.9 to 4.9).
Safety outcomes, including esophageal intubation, injury to the teeth, and aspiration, were similar in
the two groups.
Among critically ill adults undergoing tracheal intubation in an emergency department
or ICU, the use of a video laryngoscope resulted in a higher incidence of successful intubation on the
!rst attempt than the use of a direct laryngoscope. (Funded by the U.S. Department of Defense; DEVICE
ClinicalTrials.gov number, NCT05239195.)
RESULTS
CONCLUSIONS
likelihood of successful tracheal intubation on the !rst attempt among critically ill adults is uncertain.
In a multicenter, randomized trial conducted at 17 emergency departments and intensive care units
(ICUs), we randomly assigned critically ill adults undergoing tracheal intubation to the videolaryngoscope
group or the direct-laryngoscope group. The primary outcome was successful intubation
on the !rst attempt. The secondary outcome was the occurrence of severe complications during
intubation; severe complications were de!ned as severe hypoxemia, severe hypotension, new or
increased vasopressor use, cardiac arrest, or death.
The trial was stopped for e$cacy at the time of the single preplanned interim analysis.
Among 1417 patients who were included in the !nal analysis (91.5% of whom underwent intubation that
was performed by an emergency medicine resident or a critical care fellow), successful intubation on the
!rst attempt occurred in 600 of the 705 patients (85.1%) in the video-laryngoscope group and in 504 of
the 712 patients (70.8%) in the direct-laryngoscope group (absolute risk di,erence, 14.3 percentage
points; 95% con!dence interval [CI], 9.9 to 18.7; P<0.001). A total of 151 patients (21.4%) in the videolaryngoscope
group and 149 patients (20.9%) in the direct-laryngoscope group had a severe
complication during intubation (absolute risk di,erence, 0.5 percentage points; 95% CI, −3.9 to 4.9).
Safety outcomes, including esophageal intubation, injury to the teeth, and aspiration, were similar in
the two groups.
Among critically ill adults undergoing tracheal intubation in an emergency department
or ICU, the use of a video laryngoscope resulted in a higher incidence of successful intubation on the
!rst attempt than the use of a direct laryngoscope. (Funded by the U.S. Department of Defense; DEVICE
ClinicalTrials.gov number, NCT05239195.)
Updated Sept 6
Transnasal Videoendoscopy for Preoperative AirwayRisk Stratification: Development and Validation of a Multivariable Risk Prediction Model
Alexander!Barclay-Steuart, MD, MBA,* Hanna L.!Großhennig,* Phillip!Sasu, MD,*
Viktor A.!Wünsch, MD,* Rupert!Stadlhofer, MD,† Joanna!Berger, MD,† Maria!Stark, MSc‡
Susanne!Sehner, MSc,‡ Christian!Zöllner, MD,* and Martin!Petzoldt, MD*
(Anesth Analg 2023;136:1164–73)
BACKGROUND: Transnasal "exible videoendoscopy (TVE) of the larynx is a standard of care
for the detection and staging of pharyngolaryngeal lesions in otorhinolaryngology. Patients frequently
present with existing TVE examinations before anesthesia. Although these patients
are considered high risk, the diagnostic value of TVE for airway risk strati#cation is currently
unknown. How can captured images or videos be used for anesthesia planning, and which
lesions are most concerning? This study aimed to develop and validate a multivariable risk prediction
model for dif#cult airway management based on TVE #ndings and to determine whether
the discrimination of the Mallampati score can be improved by adding this new TVE model.
METHODS: This retrospective single-center development and validation study assessed 4021
patients who underwent 4524 otorhinolaryngologic surgeries at the University Medical Centre
Hamburg-Eppendorf between January 1, 2011, and April 30, 2018, with electronically stored
TVE videos and included 1099 patients who underwent 1231 surgeries. TVE videos and anesthesia
charts were systematically reviewed in a blinded fashion. The Least Absolute Shrinkage
and Selection Operator (LASSO) regression analysis was used for variable selection, model
development, and cross validation.
RESULTS: The prevalence of dif#cult airway management was 24.7% (304/1231). Lesions at
the vocal cords, epiglottis, or hypopharynx were not selected by the LASSO regression, while
lesions at the vestibular folds (ß-coef#cient 0.123), supraglottic region (ß-coef#cient 0.161),
arytenoids (ß-coef#cient 0.063), and viewing restrictions on the rima glottidis that cover $50%
of the glottis area (ß-coef#cient 0.485) and pharyngeal secretion retention (ß-coef#cient 0.372)
were relevant risk factors for dif#cult airway management. The model was adjusted for sex, age,
and body mass index. The area under the receiver operating characteristic curve (95% con#-
dence interval) of the Mallampati score was 0.61 (0.57–0.65) and 0.74 (0.71–0.78) of the TVE
model combined with Mallampati (P < .001).
CONCLUSIONS: Stored images and videos from TVE examinations can be reused for the purpose
of predicting risk associated with airway management. Vestibular fold, supraglottic, and
arytenoid lesions are most concerning, especially if they are accompanied by secretion retention
or restrict the glottic view. Our data indicate that the TVE model improves discrimination of
the Mallampati score and might, therefore, be a useful addition to traditional bedside airway risk
examinations.
Updated Sept 6
Oxygenation during the apnoeic phase preceding intubation in adults in prehospital, emergency department, intensive care and operating theatre environments (Review)
White LD, Vlok RA, Thang CY, Tian DH, Melhuish TM. Oxygenation during the apnoeic phase preceding intubation in adults in prehospital, emergency department, intensive care and operating theatre environments. Cochrane Database Syst Rev. 2023;8(8):CD013558.
A B S T R A C T
Background
Apnoeic oxygenation is the delivery of oxygen during the apnoeic phase preceding intubation. It is used to prevent respiratory
complications of endotracheal intubation that have the potential to lead to significant adverse events including dysrhythmia,
haemodynamic decompensation, hypoxic brain injury and death. Oxygen delivered by nasal cannulae during the apnoeic phase
of intubation (apnoeic oxygenation) may serve as a non-invasive adjunct to endotracheal intubation to decrease the incidence of
hypoxaemia, morbidity and mortality.
Objectives
To evaluate the benefits and harms of apnoeic oxygenation before intubation in adults in the prehospital, emergency department, intensive
care unit and operating theatre environments compared to no apnoeic oxygenation during intubation.
Search methods
We used standard, extensive Cochrane search methods. The latest search date was 4 November 2022.
Selection criteria
We included randomized controlled trials (RCTs) and quasi-RCTs that compared the use of any form of apnoeic oxygenation including
high flow and low flow nasal cannulae versus no apnoeic oxygenation during intubation. We defined quasi-randomization as participant
allocation to each arm by means that were not truly random, such as alternation, case record number or date of birth. We excluded
comparative prospective cohort and comparative retrospective cohort studies, physiological modelling studies and case reports.
Data collection and analysis
We used standard Cochrane methods. Our primary outcomes were 1. hospital stay and 2. incidence of severe hypoxaemia. Our secondary
outcomes were 3. incidence of hypoxaemia, 4. lowest recorded saturation of pulse oximetry (SpO2), 5. intensive care unit (ICU) stay, 6. first
pass success rate, 7. adverse events and 8. mortality. We used GRADE to assess certainty of evidence.
Oxygenation during the apnoeic phase preceding intubation in adults in prehospital, emergency department, intensive care and
operating theatre environments (Review)
Main results
We included 23 RCTs (2264 participants) in our analyses. Eight studies (729 participants) investigated the use of low-flow (15 L/minute
or less), and 15 studies (1535 participants) investigated the use of high-flow (greater than 15 L/minute) oxygen. Settings were varied and
included the emergency department (2 studies, 327 participants), ICU (7 studies, 913 participants) and operating theatre (14 studies, 1024
participants). We considered two studies to be at low risk of bias across all domains.
None of the studies reported on hospital length of stay. In predominately critically ill people, there may be little to no diGerence in the
incidence of severe hypoxaemia (SpO2 less than 80%) when using apnoeic oxygenation at any flow rate from the start of apnoea until
successful intubation (risk ratio (RR) 0.86, 95% confidence interval (CI) 0.66 to 1.11; P = 0.25, IN = 0%; 15 studies, 1802 participants; lowcertainty
evidence).
There was insuGicient evidence of any eGect on the incidence of hypoxaemia (SpO2 less than 93%) (RR 0.58, 95% CI 0.23 to 1.46; P = 0.25, IN
= 36%; 3 studies, 489 participants; low-certainty evidence). There may be an improvement in the lowest recorded oxygen saturation, with
a mean increase of 1.9% (95% CI 0.75% to 3.05%; P < 0.001, IN = 86%; 15 studies, 1525 participants; low-certainty evidence). There may be
a reduction in the duration of ICU stay with the use of apnoeic oxygenation during intubation (mean diGerence (MD) O1.13 days, 95% CI
O1.51 to O0.74; P < 0.0001, IN = 46%; 5 studies, 815 participants; low-certainty evidence). There may be little to no diGerence in first pass
success rate (RR 1.00, 95% CI 0.93 to 1.08; P = 0.79, IN = 0%; 8 studies, 826 participants; moderate-certainty evidence). There may be little
to no diGerence in incidence of adverse events including oral trauma, arrhythmia, aspiration, hypotension, pneumonia and cardiac arrest
when apnoeic oxygenation is used. There was insuGicient evidence about any eGect on mortality (RR 0.84, 95% CI 0.70 to 1.00; P = 0.06,
IN = 0%; 6 studies, 1015 participants; low-certainty evidence).
Authors' conclusions
There was some evidence that oxygenation during the apnoeic phase of intubation may improve the lowest recorded oxygen saturation.
However, the diGerences in oxygen saturation were unlikely to be clinically significant. This did not translate into any measurable eGect on
the incidence of hypoxaemia or severe hypoxaemia in a group of predominately critically ill people. We were unable to assess the influence
on hospital length of stay; however, there was a reduction in ICU stay in the apnoeic oxygenation group. The mechanism for this is unclear
as there was little to no diGerence in first pass success or adverse event rates.
Updated June 17
Clinical tests for confirming tracheal intubation or excluding oesophageal intubation: a diagnostic test accuracy systematic review and meta-analysis
Unrecognised oesophageal intubation causes preventable serious harm to patients undergoing tracheal intubation. When capnography is unavailable or doubted, clinicians still use clinical findings to confirm tracheal intubation, or exclude oesophageal intubation, and false reassurance from clinical examination is a recurring theme in fatal cases of unrecognised oesophageal intubation. We conducted a systematic review and meta-analysis of the diagnostic accuracy of five clinical examination tests and the oesophageal detector device when used to confirm tracheal intubation. We searched four databases for studies reporting index clinical tests against a reference standard, from inception to 28 February 2023. We included 49 studies involving 10,654 participants. Methodological quality was overall moderate to high. We looked at misting (three studies, 115 participants); lung auscultation (three studies, 217 participants); combined lung and epigastric auscultation (four studies, 506 participants); the oesophageal detector device (25 studies, 3024 participants); 'hang-up' (two non-human studies); and chest rise (one non-human study). The reference standards used were capnography (22 studies); direct vision (10 studies); and bronchoscopy (three studies). When used to confirm tracheal intubation, misting has a false positive rate (95%CI) of 0.69 (0.43-0.87); lung auscultation 0.14 (0.08-0.23); five-point auscultation 0.18 (0.08-0.36); and the oesophageal detector device 0.05 (0.02-0.09). Tests to exclude events that invariably lead to severe damage or death must have a negligible false positive rate. Misting or auscultation have too high a false positive rate to reliably exclude oesophageal intubation and there is insufficient evidence to support the use of 'hang-up' or chest rise. The oesophageal detector device may be considered where other more reliable means are not available, though waveform capnography remains the reference standard for confirmation of tracheal intubation.
Updated June 16
Efficacy of a hybrid technique of simultaneous videolaryngoscopy with flexible bronchoscopy in children with difficult direct laryngoscopy in the Pediatric Difficult Intubation Registry
- PMID: 37322572
- DOI: 10.1111/anae.16049
Abstract
Children with difficult tracheal intubation are at increased risk of severe complications, including hypoxaemia and cardiac arrest. Increasing experience with the simultaneous use of videolaryngoscopy and flexible bronchoscopy (hybrid) in adults led us to hypothesise that this hybrid technique could be used safely and effectively in children under general anaesthesia. We reviewed observational data from the international Pediatric Difficult Intubation Registry from 2017 to 2021 to assess the safety and efficacy of hybrid tracheal intubation approaches in paediatric patients. In total, 140 patients who underwent 180 attempts at tracheal intubation with the hybrid technique were propensity score-matched 4:1 with 560 patients who underwent 800 attempts with a flexible bronchoscope. In the hybrid group, first attempt success was 70% (98/140) compared with 63% (352/560) in the flexible bronchoscope group (odds ratio (95%CI) 1.4 (0.9-2.1), p = 0.1). Eventual success rates in the matched groups were 90% (126/140) for hybrid vs. 89% (499/560) for flexible bronchoscope (1.1 (0.6-2.1), p = 0.8). Complication rates were similar in both groups (15% (28 complications in 182 attempts) hybrid; 13% (102 complications in 800 attempts) flexible bronchoscope, p = 0.3). The hybrid technique was more likely than flexible bronchoscopy to be used as a rescue technique following the failure of another technique (39% (55/140) vs. 25% (138/560), 2.1 (1.4-3.2) p < 0.001). While technically challenging, the hybrid technique has success rates similar to other advanced airway techniques, few complications and may be considered an alternative technique when developing an airway plan for paediatric patients whose tracheas are difficult to intubate under general anaesthesia.
Updated May 29
Nasendoscopy to Predict Difficult Videolaryngoscopy: A Multivariable Model Development Study
Background: Transnasal videoendoscopy (TVE) is the standard of care when staging pharyngolaryngeal lesions. This prospective study determined if preoperative TVE improves the prediction of difficult videolaryngoscopic intubation in adults with expected difficult airway management in addition to the Simplified Airway Risk Index (SARI).
Methods: 374 anesthetics were included (252 with preoperative TVE). The primary outcome was a difficult airway alert issued by the anesthetist after Macintosh videolaryngoscopy. SARI, clinical factors (dysphagia, dysphonia, cough, stridor, sex, age and height) and TVE findings were used to fit three multivariable mixed logistic regression models; least absolute shrinkage and selection operator (LASSO) regression was used to select co-variables.
Results: SARI predicted the primary outcome (odds ratio [OR] 1.33; 95% confidence interval [CI] 1.13-1.58). The Akaike information criterion for SARI (327.1) improved when TVE parameters were added (311.0). The Likelihood ratio test for SARI plus TVE parameters was better than for SARI plus clinical factors (p < 0.001). Vestibular fold lesions (OR 1.82; 95% CI 0.40-8.29), epiglottic lesions (OR 3.37; 0.73-15.54), pharyngeal secretion retention (OR 3.01; 1.05-8.63), restricted view on rima glottidis <50% (OR 2.13; 0.51-8.89) and ≥50% (OR 2.52; 0.44-14.56) were concerning.
Conclusion: TVE improved prediction of difficult videolaryngoscopy in addition to traditional bedside airway examinations.
Updated May 20
Pre-Extubation Cuffed Tube Leak Test and Subsequent Post-Extubation Laryngeal Edema: Prospective, Single-Center Evaluation of PICU Patients
Abstract
Objectives: We performed our standard air leak, leak percentage, and cuff leak percentage tests in pediatric patients intubated with microcuff pediatric tracheal tubes (MPTTs) just before extubation. We examined the association between test findings and the subsequent occurrence of post-extubation laryngeal edema (PLE).
Design: Prospective, single-center, observational study.
Setting: PICU (June 1, 2020 to May 31, 2021).
Patients: Pediatric patients intubated and scheduled for extubation during the day shift in the PICU.
Interventions: Multiple pre-extubation leak tests were performed on each patient immediately before extubation. In our center, the standard leak test is positive if a leak is audible at 30 cm H2O applied pressure with the MPTT cuff deflated. Two other tests were calculated in the pressure control-assist control ventilator mode using the following formulas: leak percentage with deflated cuff = (inspiratory tidal volume [Vt]-expiratory Vt) × 100/inspiratory Vt; cuff leak percentage = (expiratory Vt with inflated cuff-expiratory Vt with deflated cuff) × 100/expiratory Vt with inflated cuff.
Measurements and main results: The diagnostic criteria for PLE was made by at least two healthcare professionals and included upper airway stricture with stridor-requiring nebulized epinephrine. Eighty-five pediatric patients (< 15 yr) who had been intubated for at least 12 hours using the MPTT were included. Positive rates for the standard leak, leak percentage (cutoff 10%), and cuff leak percentage (cutoff 10%) tests were 0.27, 0.20, and 0.64, respectively. The standard leak, leak percentage, and cuff leak tests showed sensitivities of 0.36, 0.27, and 0.55, respectively; and specificities of 0.74, 0.81, and 0.35, respectively. PLE occurred in 11 of 85 patients (13%), and there were no instances of needing reintubation.
Conclusions: The pre-extubation leak tests in current practice for intubated pediatric patients in the PICU all lack diagnostic accuracy for PLE.
A randomized controlled trial comparing three supraglottic airway devices used as a conduit to facilitate tracheal intubation with flexible bronchoscopy
Can J Anaesth April 13, 2023
Purpose: Once difficult ventilation and intubation are declared, guidelines suggest the use of a supraglottic airway (SGA) as a rescue device to ventilate and, if oxygenation is restored, subsequently as an intubation conduit. Nevertheless, few trials have formally studied recent SGA devices in patients. Our objective was to compare the efficacy of three second-generation SGA devices as conduits for bronchoscopy-guided endotracheal intubation.
Methods: In this prospective, single-blinded three-arm randomized controlled trial, patients with an American Society of Anesthesiologists Physical Status of I-III undergoing general anesthesia were randomized to bronchoscopy-guided endotracheal intubation using AuraGain™, Air-Q® Blocker, or i-gel® devices. We excluded patients with contraindications to an SGA or drugs and who were pregnant or had a neck, spine, or respiratory anomaly. The primary outcome was intubation time, measured from SGA circuit disconnection to CO2 measurement. Secondary outcomes included ease, time, and success of SGA insertion; success of intubation on first attempt; overall intubation success; number of attempts to intubate; ease of intubation; and ease of SGA removals.
Results: One hundred and fifty patients were enrolled from March 2017 to January 2018. Median intubation times were similar across the three groups (Air-Q Blocker, 44 sec; AuraGain, 45 sec; i-gel, 36 sec; P = 0.08). The i-gel was faster to insert (i-gel: 10 sec; Air-Q Blocker, 16 sec; AuraGain, 16 sec; P < 0.001) and easier to insert (Air-Q Blocker vs i-gel, P = 0.001; AuraGain vs i-gel, P = 0.002). Success of SGA insertion, success of intubation, and number of attempts were similar. The Air-Q Blocker was easier to remove than the i-gel (P < 0.001).
Conclusion: All three second-generation SGA devices performed similarly regarding intubation. Despite minor benefits of the i-gel, clinicians should select their SGA based on clinical experience.
Updated May 15
2023 Anaesthesia May 5.
Videolaryngoscopy vs. flexible fibrescopy for tracheal intubation in patients with cervical spine immobilisation: a randomised controlled trial
In patients with cervical spine immobilisation, tracheal intubation devices other than a direct laryngoscope are frequently used to facilitate tracheal intubation and avoid related complications. In this randomised controlled trial, we compared videolaryngoscopic and fibrescopic tracheal intubation in patients with a cervical collar. Tracheal intubation was performed using either a videolaryngoscope with a non-channelled Macintosh blade (n = 166) or a flexible fibrescope (n = 164) in patients having elective cervical spine surgery whose neck was immobilised with a cervical collar to simulate a difficult airway. The primary outcome was the first attempt success rate of tracheal intubation. Secondary outcomes were the overall success rate of tracheal intubation; time to tracheal intubation; use of additional airway manoeuvres; and incidence and severity of tracheal intubation-related airway complications. First attempt success rate was higher in the videolaryngoscope group than in the fibrescope group (164/166 (98.8%) vs. 149/164 (90.9%), p = 0.003). Tracheal intubation was successful within three attempts in all patients. Median (IQR [range]) time to tracheal intubation was shorter (50.0 (41.0-72.0 [25.0-170.0]) s vs. 81.0 (65.0-107.0 [24.0-178.0]) s, p < 0.001) and additional airway manoeuvres were less frequent (30/166 (18.1%) vs. 91/164 (55.5%), p < 0.001) in the videolaryngoscope group compared with the fibrescope group. The incidence and severity of intubation-related airway complications were not different between the two groups. When performing tracheal intubation in patients with a cervical collar, videolaryngoscopy with a non-channelled Macintosh blade was superior to flexible fibrescopy.
Updated May 15
Videolaryngoscopy versus direct laryngoscopy for tracheal intubation in neonates
Background: Establishment of a secure airway is a critical part of neonatal resuscitation in the delivery room and the neonatal intensive care unit. Videolaryngoscopy has the potential to facilitate successful endotracheal intubation, and decrease adverse consequences of a delay in airway stabilization. Videolaryngoscopy may enhance visualization of the glottis and intubation success in neonates. This is an update of a review first published in 2015, and updated in 2018.
Objectives: To determine the effectiveness and safety of videolaryngoscopy compared to direct laryngoscopy in decreasing the time and attempts required for endotracheal intubation and increasing the success rate on first intubation attempt in neonates (0 to 28 days of age).
Search methods: In November 2022, we updated the search for trials evaluating videolaryngoscopy for neonatal endotracheal intubation in CENTRAL, MEDLINE, Embase, CINAHL, and BIOSIS. We also searched abstracts of the Pediatric Academic Societies, clinical trials registries (www.
Clinicaltrials: gov; www.controlled-trials.com), and reference lists of relevant studies.
Selection criteria: Randomized controlled trials (RCTs), quasi-RCTs, cluster-RCTs, or cross-over trials, in neonates (0 to 28 days of age), evaluating videolaryngoscopy with any device used for endotracheal intubation compared with direct laryngoscopy.
Data collection and analysis: Three review authors performed data collection and analysis, as recommended by Cochrane Neonatal. Two review authors independently assessed studies identified by the search strategy for inclusion. We used the GRADE approach to assess the certainty of the evidence.
Main results: The updated search yielded 7786 references, from which we identified five additional RCTs for inclusion, seven ongoing trials, and five studies awaiting classification. Three studies were included in the previous version of the review. For this update, we included eight studies, which provided data on 759 intubation attempts in neonates. We included neonates of either sex, who were undergoing endotracheal intubation in international hospitals. Different videolaryngoscopy devices (including C-MAC, Airtraq, and Glidescope) were used in the studies. For the primary outcomes; videolaryngoscopy may not reduce the time required for successful intubation when compared with direct laryngoscopy (mean difference [MD] 0.74, 95% confidence interval [CI] -0.19 to 1.67; 5 studies; 505 intubations; low-certainty evidence). Videolaryngoscopy may result in fewer intubation attempts (MD -0.08, 95% CI -0.15 to 0.00; 6 studies; 659 intubations; low-certainty evidence). Videolaryngoscopy may increase the success of intubation at the first attempt (risk ratio [RR] 1.24, 95% CI 1.13 to 1.37; risk difference [RD] 0.14, 95% CI 0.08 to 0.20; number needed to treat for an additional beneficial outcome [NNTB] 7, 95% CI 5 to 13; 8 studies; 759 intubation attempts; low-certainty evidence). For the secondary outcomes; the evidence is very uncertain about the effect of videolaryngoscopy on desaturation or bradycardia episodes, or both, during intubation (RR 0.94, 95% CI 0.38 to 2.30; 3 studies; 343 intubations; very-low certainty evidence). Videolaryngoscopy may result in little to no difference in the lowest oxygen saturations during intubation compared with direct laryngoscopy (MD -0.76, 95% CI -5.74 to 4.23; 2 studies; 359 intubations; low-certainty evidence). Videolaryngoscopy likely results in a slight reduction in the incidence of airway trauma during intubation attempts compared with direct laryngoscopy (RR 0.21, 95% CI 0.05 to 0.79; RD -0.04, 95% CI -0.07 to -0.01; NNTB 25, 95% CI 14 to 100; 5 studies; 467 intubations; moderate-certainty evidence). There were no data available on other adverse effects of videolaryngoscopy. We found a high risk of bias in areas of allocation concealment and performance bias in the included studies.
Authors' conclusions: Videolaryngoscopy may increase the success of intubation on the first attempt and may result in fewer intubation attempts, but may not reduce the time required for successful intubation (low-certainty evidence). Videolaryngoscopy likely results in a reduced incidence of airway-related adverse effects (moderate-certainty evidence). These results suggest that videolaryngoscopy may be more effective and potentially reduce harm when compared to direct laryngoscopy for endotracheal intubation in neonates. Well-designed, adequately powered RCTS are necessary to confirm the efficacy and safety of videolaryngoscopy in neonatal intubation.
Updated March 25, 2023
The incidence of awake tracheal intubation in anesthetic practice is decreasing: a historical cohort study of the years 2014–2020 at a single tertiary care institution
J. Adam Law, MD, FRCPC . Apiraami Thana, MD . Andrew D. Milne, MD
Abstract Purpose Awake tracheal intubation (ATI) is recommended in airway management guidelines when significant difficulty is predicted with airway management. Use of the technique may be declining, which may have implications for patient safety or for skills acquisition and maintenance. This historical cohort database study sought to determine if the use of ATI was decreasing in our adult tertiary care center. Methods With institutional research ethics board approval, we queried our anesthesia information management system for cases with ATI descriptors for each year from 2014 to 2020. Records of the retrieved cases were independently reviewed by all three authors to verify they met inclusion criteria for the ATI cohort prior to analysis for the primary outcome. Secondary outcome measures included airway device and route used for ATI, first attempt and ultimate success rates, and reported adverse issues recorded in cases of failed ATI or those requiring more than one attempt. Results A total of 692 cases of ATI were identified between 2014 and 2020. There was a statistically significant decrease in yearly ATIs over the seven-year study period (Chi square goodness of fit, P\0.001), with ATI use decreasing by about 50%. First attempt success was significantly greater with use of flexible bronchoscopy vs video laryngoscopy to facilitate ATI (84% vs 60%; P\ 0.001), while there was no difference in first attempt success with the oral vs nasal route (82% vs 82%; P = 1.0). Conclusion In this single-center historical cohort study, the use of ATI decreased significantly from 2014 to 2020. Whether this decrease will result in morbidity or mortality related to airway management is currently unclear. Regardless, it has implications for training opportunities and maintenance of competence in performing the procedure.
Updated March 6
Updated Feb 27
Success and Time to Oxygen Delivery for Scalpel-Finger-
Cannula and Scalpel-Finger-Bougie Front-of-Neck Access: A Randomized Crossover Study With a Simulated “Can’t Intubate, Can’t Oxygenate” Scenario in a Manikin Model With Impalpable Neck Anatomy
Jinbin Zhang, et al
August 2022 • Volume 135 • Number 2
BACKGROUND: Emergency front-of-neck access (FONA) is particularly challenging with impal- pable neck anatomy. We compared 2 techniques that are based on a vertical midline neck incision, followed by finger dissection and then either a cannula or scalpel puncture to the cricothyroid membrane.
METHODS: A manikin simulation scenario of impalpable neck anatomy and bleeding was cre- ated. Sixty-five anesthesiologists undergoing cricothyrotomy training performed scalpel-finger- cannula (SFC) and scalpel-finger-bougie (SFB) cricothyrotomy in random order. Primary outcomes were time to oxygen delivery and first-attempt success; data were analyzed using multilevel mixed-effects models.
RESULTS: SFC was associated with a shorter time to oxygen delivery on univariate (median time difference, −61.5 s; 95% confidence interval [CI], −84.7 to −38.3; P < .001) and mul- tivariable (mean time difference, −62.1 s; 95% CI, −83.2 to −41.0; P < .001) analyses. Higher first-attempt success was reported with SFC than SFB (47 of 65 [72.3%] vs 18 of 65 [27.7%]). Participants also had higher odds at achieving first-attempt success with SFC than SFB (odds ratio [OR], 10.7; 95% CI, 3.3–35.0; P < .001). Successful delivery of oxy- gen after the “can’t intubate, can’t oxygenate” (CICO) declaration within 3 attempts and 180 seconds was higher (84.6% vs 63.1%) and more likely with SFC (OR, 5.59; 95% CI, 1.7–18.9; P = .006). Analyzing successful cases only, SFC achieved a shorter time to oxygen delivery (mean time difference, −24.9 s; 95% CI, −37.8 to −12.0; P < .001), but a longer time to cuffed tube insertion (mean time difference, +56.0 s; 95% CI, 39.0–73.0; P < .001). After simulation training, most participants preferred SFC in patients with impalpable neck anatomy (75.3% vs 24.6%).
CONCLUSIONS: In a manikin simulation of impalpable neck anatomy and bleeding, the SFC approach demonstrated superior performance in oxygen delivery and was also the preferred technique of the majority of study participants. Our study findings support the use of a cannula- based FONA technique for achieving oxygenation in a CICO situation, with the prerequisite that appropriate training and equipment are available. (Anesth Analg 2022;135:376–84)
Updated Jan 2, 2023
Video-Assisted Laryngoscopy for Pediatric Tracheal Intubation in the Emergency Department: A Multicenter Study of Clinical Outcomes
Kelsey A. Miller, MD, EdM*; Andzelika Dechnik, MD; Andrew F. Miller, MD; et al
Study objective: To explore the association between video-assisted laryngoscopy (use of a videolaryngoscope regardless of where
laryngoscopists direct their gaze), first-attempt success, and adverse airway outcomes.
Methods: We conducted an observational study using data from 2 airway consortiums that perform prospective surveillance: the
National Emergency Airway Registry for Children (NEAR4KIDS) and a pediatric emergency medicine airway education
collaborative. Data collected included patient and procedural characteristics and procedural outcomes. We performed
multivariable analyses of the association of video-assisted laryngoscopy with individual patient outcomes and evaluated the
association between site-level video-assisted laryngoscopy use and tracheal intubation outcomes.
Results: The study cohort included 1,412 tracheal intubation encounters performed from January 2017 to March 2021 across 11
participating sites. Overall, the first-attempt success was 70.0%. Video-assisted laryngoscopy was associated with increased odds
of first-attempt success (odds ratio [OR] 2.01; 95% confidence interval [CI], 1.48 to 2.73) and decreased odds of severe adverse
airway outcomes (OR 0.70; 95% CI, 0.58 to 0.85) including decreased severe hypoxia (OR 0.69; 95% CI, 0.55 to 0.87). Sites
varied substantially in the use of video-assisted laryngoscopy (range from 12.9% to 97.8%), and sites with high use of videoassisted
laryngoscopy (> 80%) experienced increased first-attempt success even after adjusting for individual patient
laryngoscope use (OR 2.30; 95% CI, 1.79 to 2.95).
Conclusion: Video-assisted laryngoscopy is associated with increased first-attempt success and fewer adverse airway outcomes
for patients intubated in the pediatric emergency department. There is wide variability in the use of video-assisted laryngoscopy,
and the high use is associated with increased odds of first-attempt success. [Ann Emerg Med. 2022;-:1-10.]
Updated December 27, 2022
Emergency Department Intubations in Patients With Angioedema: A Report from the National Emergency Airway Registry
Benjamin J. Sandefur MD, Xiao-Wei Liu MD, Amy H. Kaji MD, PHD, Ronna L. Campbell MD, PhD, Brian E. Driver MD, Ron M. Walls MD, Jestin N.
Carlson MD, MSC and Calvin A. Brown MD
Journal of Emergency Medicine, 2021-11-01, Volume 61, Issue 5, Pages 481-488,
Abstract
Background
Angioedema, a localized swelling of subcutaneous and submucosal tissues, may involve the upper airway. A subset of patients
presenting for emergent evaluation of angioedema will require intubation. Little is known about airway management practices in
patients with angioedema requiring intubation in the emergency department (ED).
Objective
To describe airway management practices in patients intubated for angioedema in the ED.
Methods
We analyzed data from the National Emergency Airway Registry. All patients with an intubation attempt for angioedema between
January 1, 2016 and December 31, 2018 were included. We report univariate descriptive data as proportions with cluster-adjusted
95% confidence intervals.
Results
Of 19,071 patient encounters, intubation was performed for angioedema in 98 (0.5%). First-attempt success was achieved in 81%,
with emergency physicians performing the procedure in 94% of encounters. The most common device used was a flexible endoscope
(49%), and 42% of attempts were via a nasal route. Pharmacologic methods included sedation with paralysis (61%), topical
anesthesia with or without sedation (13% and 13%, respectively), and sedation only (10%). Among 19 (19%) patients requiring
additional attempts, intubation was achieved on second attempt in 10 (53%). The most common adverse events were hypotension
(13%) and hypoxemia (12%). Cricothyrotomy occurred in 2 patients (2%). No deaths were observed.
Conclusions
Angioedema was a rare indication for intubation in the ED setting. Emergency physicians achieved first-attempt success in 81% of
encounters and used a broad range of intubation devices and methods, including flexible endoscopic techniques. Cricothyrotomy was
rare, and no ED deaths were reported. © 2021 Elsevier Inc.
Updated Nov 22, 2022
The impact of head and neck radiation on airway management: a retrospective data review
CORRESPONDENCE
Ila Sharma, MD . Wenli Dong, MS . Catherine N. Vu, MD . Gang Zheng, MD
Can J Anesth/J Can Anesth (2022) 69:1562–1564 https://doi.org/10.1007/s12630-022-02331-z
Updated Nov 2, 2022
Airway management in patients with suspected or confirmed traumatic spinal cord injury: a narrative review of current evidence
M. D. Wiles
Anaesthesia 2022, 77, 1120-1128
Around 1 million people sustain a spinal cord injury each year, which can have significant psychosocial, physical
and socio-economic consequences for patients, their families and society. The aim of this review is to provide
clinicians with a summary of recent studies of direct relevance to the airway management of patients with
confirmed or suspected traumatic spinal cord injury to promote best clinical practice. All airway interventions
are associated with some degree of movement of the cervical spine; in general, these are very small and
whether these are clinically significant in terms of impingement of the spinal cord is unclear. Manual in-line
stabilisation does not effectively immobilise the cervical spine and increases the likelihood of difficult and failed
tracheal intubation. There is no clear evidence of benefit of awake tracheal intubation techniques in terms of
prevention of secondary spinal cord injury. Videolaryngoscopy appears to cause a similar degree of cervical
spine displacement as flexible bronchoscope-guided tracheal intubation and is an appropriate alternative
approach. Direct laryngoscopy does cause a slightly greater degree of cervical spinal movement during
tracheal intubation than videolaryngoscopy, but this does not appear to increase the risk of spinal cord
compression. The risk of spinal cord injury during tracheal intubation appears to be minimal even in the
presence of gross cervical spine instability. Depending on the clinical situation, practitioners should choose the
tracheal intubation technique with which they are most proficient and that is most likely to minimise cervical
spine movement.
Updated Oct 5, 2022
Has the time really come for universal videolaryngoscopy?
Tim M. Cook1,2,* and Michael F. Aziz3
This editorial accompanies: Videolaryngoscopy versus direct laryngoscopy for adults undergoing tracheal intubation: a Cochrane systematic
review and meta-analysis update by Hansel et al., Br J Anaesth 2022:129:612e623, doi: 10.1016/j.bja.2022.05.027
and
Videolaryngoscopy as a first-intention technique for tracheal intubation in unselected surgical patients: a before and after observational
study by De Jong et al., Br J Anaesth 2022:129:624e634, doi: 10.1016/j.bja.2022.05.030
Summary
Recent evidence, highlighted in this editorial, creates a strong argument for universal use of videolaryngoscopy in
anaesthesia to improve efficiency and safety of tracheal intubation. In a recent study published in the British Journal of
Anaesthesia, the authors implemented widespread (66%) use of videolaryngoscopy as first choice in one hospital and
compared this with a control hospital, in which this was not implemented. Increased videolaryngoscopy use was
associated with a significant fall in the rate of difficult airways, use of airway rescue techniques, and operator-reported
difficulty, whilst in the control hospitals no such changes were seen. Locations outside the operating theatre might also
benefit from universal laryngoscopy, but the evidence base is less robust, most notably in pre-hospital emergency
medicine. The extent to which variation in results in different locations is attributable to different patient factors or
organisational and operator factors is considered.
British Journal of Anaesthesia, 129 (4): 474e477 (2022)
Updated Oct 2, 2022
Airway management in patients with suspected or confirmed traumatic spinal cord injury: a narrative review of current evidence
M.D. Wiles
Anaesthesia 2022 77 1120-8
Around 1 million people sustain a spinal cord injury each year, which can have significant psychosocial, physical
and socio-economic consequences for patients, their families and society. The aim of this review is to provide
clinicians with a summary of recent studies of direct relevance to the airway management of patients with
confirmed or suspected traumatic spinal cord injury to promote best clinical practice. All airway interventions
are associated with some degree of movement of the cervical spine; in general, these are very small and
whether these are clinically significant in terms of impingement of the spinal cord is unclear. Manual in-line
stabilisation does not effectively immobilise the cervical spine and increases the likelihood of difficult and failed
tracheal intubation. There is no clear evidence of benefit of awake tracheal intubation techniques in terms of
prevention of secondary spinal cord injury. Videolaryngoscopy appears to cause a similar degree of cervical
spine displacement as flexible bronchoscope-guided tracheal intubation and is an appropriate alternative
approach. Direct laryngoscopy does cause a slightly greater degree of cervical spinal movement during
tracheal intubation than videolaryngoscopy, but this does not appear to increase the risk of spinal cord
compression. The risk of spinal cord injury during tracheal intubation appears to be minimal even in the
presence of gross cervical spine instability. Depending on the clinical situation, practitioners should choose the
tracheal intubation technique with which they are most proficient and that is most likely to minimise cervical
spine movement.
Updated 8-15-22
Preventing unrecognised oesophageal intubation: a consensus guideline
Anaesthesia 2022, Chrimes, N and the PUMA working group
Summary
Across multiple disciplines undertaking airway management globally, preventable episodes of unrecognised
oesophageal intubation result in profound hypoxaemia, brain injury and death. These events occur in the
hands of both inexperienced and experienced practitioners. Current evidence shows that unrecognised
oesophageal intubation occurs sufficiently frequently to be a major concern and to merit a co-ordinated
approach to address it. Harm from unrecognised oesophageal intubation is avoidable through reducing the
rate of oesophageal intubation, combined with prompt detection and immediate action when it occurs. The
detection of `sustained exhaled carbon dioxide´ using waveform capnography is the mainstay for excluding
oesophageal placement of an intended tracheal tube. Tube removal should be the default response when
sustained exhaled carbon dioxide cannot be detected. If default tube removal is considered dangerous,
urgent exclusion of oesophageal intubation using valid alternative techniques is indicated, in parallel with
evaluation of other causes of inability to detect carbon dioxide. The tube should be removed if timely
restoration of sustained exhaled carbon dioxide cannot be achieved. In addition to technical interventions,
strategies are required to address cognitive biases and the deterioration of individual and team performance
in stressful situations, to which all practitioners are vulnerable. These guidelines provide recommendations for
preventing unrecognised oesophageal intubation that are relevant to all airway practitioners independent of
geography, clinical location, discipline or patient type.
Updated 7-14-22
Videolaryngoscopes versus direct laryngoscopes in children: Ranking systematic review with network meta-analysesof randomized clinical trials
Clístenes C. de Carvalho et al
Pediatric Anesthesia. 2022;00:1–15.
AbstractBackground: Videolaryngoscopes improve tracheal intubation in adult patients, but we currently do not know whether they are similarly beneficial for children. We de-signed this ranking systematic review to compare individual video and direct laryngo-scopes for efficacy and safety of orotracheal intubation in children.Methods: We searched PubMed and five other databases on January 27, 2021. We in-cluded randomized clinical trials with patients aged ≤18 years, comparing different la-ryngoscopes for the outcomes: failed first intubation attempt; failed intubation within two attempts; failed intubation; glottic view; time for intubation; complications. In addition, we assessed the quality of evidence according to GRADE recommendations.Results: We included 46 studies in the meta-analyses. Videolaryngoscopy reduced the risk of failed first intubation attempt (RR = 0.43; 95% CI: 0.31–0.61; p= .001) and failed intubation within two attempts (RR = 0.33; 95% CI: 0.33–0.33; p< .001) in chil-dren aged <1 year. Videolaryngoscopy also reduced the risk of major complications in both children aged <1 year (RR = 0.33; 95% CI: 0.12–0.96; p= .046) and children aged 0–18 years (RR = 0.40; 95% CI: 0.25–0.65; p= .002). We did not find significant difference between videolaryngoscopy and direct laryngoscopy for time to intuba-tion in children aged <1 year (MD = −0.95 s; 95% CI: −5.45 to 3.57 s; p= .681), and children aged 0–18 years (MD = 1.65 s; 95% CI: −1.00 to 4.30 s; p= .222). Different videolaryngoscopes were associated with different performance metrics within this meta-analysis. The overall quality of the evidence ranged from low to very low.Conclusion: Videolaryngoscopes reduce the risk of failed first intubation attempts and major complications in children compared to direct laryngoscopes. However, not all videolaryngoscopes have the same performance metrics, and more data is needed to clarify which device may be better in different clinical scenarios. Additionally, care must be taken while interpreting our results and rankings due to the available evi-dence's low or very low quality.
Updated 7-8-22
Review of Commercially Available Supraglottic Airway Devices for Prehospital Combat Casualty Care
Background: Airway obstruction is the second leading cause of potentially survivable death on the battlefield. The Committee on Tactical Combat Casualty Care lists airway optimization among the top 5 battlefield research and development priorities; however, studies show that combat medics lack access to the recommended supraglottic airway (SGA) devices. SGA devices are an alternative airway management technique to endotracheal tube intubation. Reports have shown SGA devices are easier to use and take fewer attempts to provide patent airflow to the patient when compared to endotracheal tube intubation. Military settings require a higher degree of skill to perform airway management on patients due to the environment, limited availability of equipment, and potential chaos of the battlefield. Finding the optimal SGA device for the military setting is an unmet need. The International Organization for Standardization describes basic functional requirements for SGA devices, as well as patient configurations and size limitations. Beyond that, no SGA device manufacturer states that their devices are intended for military settings.
Materials and methods: We conducted a market review of 25 SGA devices that may meet inclusion into the medics' aid bag. The company's official "Instructions for Use" document, Google Scholar, and FDA reports were reviewed to obtain information for each SGA device.
Results: Twenty-five commercially available SGA devices are explored from manufacturer online sources. A commercially available device list is shown later in this paper, which provides the device's features, indications, and contraindications based on the manufacturer's product information documentation.
Conclusions: There are a variety of devices that require further testing to determine whether they should be included in sets, kits, and outfits.
Updated 6-16-22
E D I T O R I A L COMMENT The role of Scalpel-bougie cricothyroidotomy in managing emergency Front of Neck Airway access. A review and technical update for ENT surgeons
In October 2016, an editorial was published jointly in Clinical Otolaryngology and the British Journal of Anaesthesia concerning the
appropriate management of the difficult airway in a situation of “Can’t Intubate Can’t Oxygenate” (CICO).1 It highlighted the importance of joint working between surgeons and anaesthetists and also made a case for the wider use of the scalpel-bougie cricothyroidotomy technique in securing a Front of Neck Airway (FONA), especially in an emergency. Almost all cases of an unexpectedly difficult airway are encountered by anaesthetists without the presence of an ENT surgeon.2,3 The Difficult Airway Society (DAS) has developed guidelines for the management of such situations (Figure 1) based on research that suggests that scalpel-bougie cricothyroidotomy is the safest way of securing an airway in emergency situations.4 Custom and practice in ENT surgery dictate that a surgical tracheostomy is the appropriate immediate technique for securing an airway when intubation is impossible. However, surgical tracheostomy should be seen as just one technique available to ENT surgeons in this situation. Firstly, the scalpel-bougie cricothyroidotomy technique is recommended by DAS as the first line management in the CICO situation and is the primary intervention expected of those attending with surgical expertise. Secondly, the number of open surgical tracheostomies performed both by trainees and substantive ENT staff is declining such that confidence in performing an emergency tracheostomy in a timely manner cannot be guaranteed by all ENT surgeons undertaking on-call duties. Approximately twothirds of tracheostomies performed in the United Kingdom at present are performed percutaneously (mostly by non-surgeons) and there may be a relative reduction in complications using this technique in appropriate patients.5,6 With regards to open tracheostomies, the 2014 UK NCEPOD report found 41% of the procedures were carried out by senior trainees, and the most senior surgeon was a consultant in 47% (although trainees were present for 84% of these).6 This reduction in exposure to performing these procedures means that confidence and competence to perform them in a high-pressure situation is likely to be adversely affected. The joint editorial notes that the DAS algorithms are guidelines. Ultimately, the decision as to the type of surgical airway performed is at the discretion of the surgeon which should be based on their own experience and skill set.
Clinical Otolaryngology. 2018;43:791–794.
6-3-22
Upper airway pressure distribution during nasal high-flow therapy
Abstract
Two working mechanisms of Nasal High-Flow Therapy (NHFT) are washout of anatomical dead space and provision of positive end-expiratory pressure (PEEP). The extent of both mechanisms depends on the respiration aerodynamics and the corresponding pressure distribution: at end-expiration the onset of uniform pressure indicates the jet penetration length, and the level of the uniform pressure is the PEEP. The clinical problem is that adequate measurements in patients are presently impossible. In this study, the respiratory pressure distribution is therefore measured in 3D-printed anatomically correct upper-airway models of an adult and an infant. Assuming that elastic fluctuations in airway anatomy are sufficiently small, the aerodynamics in these rigid models will be very similar to the aerodynamics in patients. It appears that, at end-expiration, the jet penetrates into or slightly beyond the nasal cavity, hardly depending on cannula size or NHFT flow rate. PEEP is approximately proportional to the square of the flow rate: it can be doubled by increasing the flow rate by 40%. In the adult model, PEEP is accurately predicted by the dynamic pressure at the prong-exits, but in the infant model this method fails. During respiration, large pressure fluctuations occur when the cannula is relatively large compared to the nostrils.
5-11-22
Tube Cuff Location and Perhaps a Call to Reconsider the Use of Uncuffed Tracheal Tubes
Malaak Isa, MD,* Josef Holzki, MD, PhD,† Anna Hagemeier, MSc,‡ Markus A. Rothschild, MD, PhD,*
and Charles J. Coté, MD§ (Anesth Analg XXX;XXX:00–00)2021
BACKGROUND: Some in vivo studies question the traditional “funnel-shaped” infant larynx; further
anatomic examinations were warranted. Examination of fixative free fresh autopsy laryngeal
and upper tracheal specimens and multiple measurements was needed to determine consistency
between current tracheal tube designs and anatomic observations.
METHODS: Larynges from 19 males and 11 females (Caucasian term newborn to 126 months)
were examined by the same forensic pathologist. Measurements included anterior/posterior
(A/P) and transverse (T) diameters of the cricoid outlet (CO), interarytenoid diameter (IAD), cricothyroid
membrane (CTM), distance from the vocal cords (VC) to CO (VC-CO), and calibration of
the larynx lumen with uncuffed tracheal tubes as measuring rods. Assessment of “safe tracheal
tube placement” was assessed using manufacturer recommended cuffed Microcuff (Kimberly-
Clark, Koblenz, Germany) tubes.
RESULTS: In 77% (95% confidence interval [CI], 58-90) of specimens, the proximal end of the
cuff was within the CO and in 23% even with or close to the CO. The VC-CO varied from 9.1
to 13.17 mm in infants, 11.55 to 15.17 mm in toddlers, and 13.19 to 18.34 mm in children.
The AP/T ratio of the CO was nearly 0.99 in most larynges; the IAD was greater than CO in all
specimens. The CTM could be minimally distended in all specimens.
CONCLUSIONS: First, despite being marketed as a safer tracheal tube design, the proximal
end of the Microcuff cuff rested within or close to the cricoid cartilage theoretically increasing
potential cuff-induced injury when using the VC markings for positioning. Our data suggest that
the optimal cuff free distance (VC-CO) would be ~13.5 mm for a Microcuff internal diameter (ID)
size 3.0, ~15 mm for size 3.5, and ~16 to 19 mm for greater sizes.
Second, the CO was virtually circular in all specimens, suggesting that appropriately sized
uncuffed tubes should provide an adequate seal in most neonates and toddlers, thus avoiding
the potential for cuff-related necrosis injury.
Third, the IAD was always greater than CO confirming that the narrowest point of the infant larynx
is the nondistensible cricoid cartilage and not the easily distended glottis.
Fourth, appropriately sized Microcuff tubes with the cuff deflated completely filled the lumen of
the CO and proximal trachea in all specimens. Our data suggest the need for all manufacturers
to further evaluate tracheal tube cuff locations and lengths in relation to the VC safe insertion
markings, particularly for neonates and toddlers.
Fifth, the CTM is minimally distensible, thus having important implications for emergency surgical
airway access with most currently available emergency airway devices.
5-1-22
Extubation of the potentially difficult airway in the intensive care unit
Joffe A, Barnes CR. Extubation of the potentially difficult airway in the intensive care unit. Curr Opin Anaesthesiol. 2022;35(2):122-129.
Purpose of review
Extubation in the intensive care unit (ICU) is associated with a failure rate requiring reintubation in 10– 20% patients further associated with significant morbidity and mortality. This review serves to highlight recent advancements and guidance on approaching extubation for patients at risk for difficult or failed extubation (DFE).
Recent findings
Recent literature including closed claim analysis, meta-analyses, and national society guidelines demonstrate that extubation in the ICU remains an at-risk time for patients. Identifiable strategies aimed at optimizing respiratory mechanics, patient comorbidities, and airway protection, as well as preparing an extubation strategy have been described as potential methods to decrease occurrence of DFE.
Summary
Extubation in the ICU remains an elective decision and patients found to be at risk should be further optimized and planning undertaken prior to proceeding. Extubation for the at-risk patient should be operationalized utilizing easily reproducible strategies, with airway experts present to guide decision making and assist in reintubation if needed.
4/27/22
Videolaryngoscopy vs. direct Macintosh laryngoscopy in tracheal intubation in adults: a ranking systematic review and network meta-analysis
C. C. de Carvalho,1 D. M. da Silva,2 V. M. Lemos,3 T. G. B. dos Santos,4 I. C. Agra,5
G. M. Pinto,6 I. B. Ramos,7 Y. S. C. Costa8 and J. M. Santos Neto9
Summary
Videolaryngoscopes are thought to improve glottic view and facilitate tracheal intubation compared with the
Macintosh direct laryngoscope. However, we currently do not know which one would be the best choice in most
patients undergoing anaesthesia. We designed this systematic review with network meta-analyses to rank the
different videolaryngoscopes and the Macintosh direct laryngoscope.We conducted searches in PubMed and a
further five databases on 11 January 2021.We included randomised clinical trials with patients aged ≥16 years,
comparing different videolaryngoscopes, or videolaryngoscopes with the Macintosh direct laryngoscope for the
outcomes: failed intubation; failed first intubation attempt; failed intubation within two attempts; difficult
intubation; percentage of glottic opening seen; difficult laryngoscopy; and time needed for intubation. We
assessed the quality of evidence according to GRADE recommendations and included 179 studies in the metaanalyses.
The C-MAC and C-MAC D-Blade were top ranked for avoiding failed intubation, but we did not find
statistically significant differences between any two distinct videolaryngoscopes for this outcome. Further, the CMAC
D-Blade performed significantly better than the C-MAC Macintosh blade for difficult laryngoscopy. We
found statistically significant differences between the laryngoscopes for time to intubation, but these differences
were not considered clinically relevant. The evidence was judged as of low or very low quality overall. In
conclusion, different videolaryngoscopes have differential intubation performance and some may be currently
preferred among the available devices. Furthermore, videolaryngoscopes and the Macintosh direct
laryngoscope may be considered clinically equivalent for the time taken for tracheal intubation. However,
despite the rankings from our analyses, the current available evidence is not sufficient to ensure significant
superiority of one device or a small set of them over the others for our intubation-related outcomes.
4/11/22
Extubation of the potentially difficult airway in the intensive care unit
Aaron Joffea,b and Christopher R. Barnesa
Current Opinion Volume 35 ! Number 2 ! April 2022
Purpose of review
Extubation in the intensive care unit (ICU) is associated with a failure rate requiring reintubation in 10–
20% patients further associated with significant morbidity and mortality. This review serves to highlight
recent advancements and guidance on approaching extubation for patients at risk for difficult or failed
extubation (DFE).
Recent findings
Recent literature including closed claim analysis, meta-analyses, and national society guidelines
demonstrate that extubation in the ICU remains an at-risk time for patients. Identifiable strategies aimed at
optimizing respiratory mechanics, patient comorbidities, and airway protection, as well as preparing an
extubation strategy have been described as potential methods to decrease occurrence of DFE.
Summary
Extubation in the ICU remains an elective decision and patients found to be at risk should be further
optimized and planning undertaken prior to proceeding. Extubation for the at-risk patient should be
operationalized utilizing easily reproducible strategies, with airway experts present to guide decision
making and assist in reintubation if needed.
Keywords
difficult extubation, failed extubation, high flow nasal cannula, noninvasive ventilation
4/2/22
Tracheal intubation using intubating laryngeal tube iLTS-D™ and LMA Fastrach™ in 99 adult patients: A prospective multicentric randomised non-inferiority study
M. Zuercher, MD a,*, G. Casso, MD b, V. Krugel, MD c, A. Poti!e, MD a, M.P. Barry, PhD a, P. Schoettker, PhD
JCA 2022 78, 110671
Laryngeal Tube Suction-Disposable (iLTS-D™, VBM, Sulz a. N., Germany) compared to the Laryngeal Mask Airway (LMA) Fastrach™ (Teleflex, Athlone, Ireland). We hypothesised that the iLTS-D™ would be non-inferior to the LMA Fastrach™ for tracheal intubation and ventilation. Design Multicentric, non-inferiority, randomised controlled study. Setting Operating rooms from two tertiary and one secondary centre in Switzerland from January 2017 to July 2019. The investigators were trained anaesthetists with extensive experience with laryngeal masks but limited to laryngeal tubes. The study was discontinued after the planned interim analysis. atients Ninety-nine adult patients were included after randomisation. The inclusion criteria were American Society of Anesthesiologists physical status 1 to 3 in patients scheduled for elective surgery requiring tracheal intubation. Patients with a history of difficult intubation were excluded. Interventions After anaesthesia induction and once neuromuscular blockade was obtained, ventilation was initiated, and tracheal intubation was performed through the randomised device with the flexible endoscope tip placed proximally to the tip of the tracheal tube (visualised blind intubation). easurements The primary outcome was the intubation success rate after two attempts. The secondary outcomes were time to intubation, successful ventilation rate, time to achieve ventilation, and gastric access success rate. ain results The overall intubation success rate was significantly higher in the Fastrach™ group than in the iLTS-D ™ group (91.8% vs 70.0%, p ! 0.00). No difference was found in the ventilation success rate (9% for iLTS-D ™ and 100% for LMA Fastrach™ p ! 0.829). The time to achieve ventilation and intubation were similar between the groups. No maor airway complications were noted. Conclusions Although both supraglottic devices provided the same effective ventilation rate, the LMA Fastrach™ was superior to the iLTS-D™ as a conduit for intubation in 99 adult patients without a known difficult intubation. These preliminary results need to be confirmed in studies that include a larger population. Trial registration Clinicaltrials.gov, 21.09.201, Identification Number NCT029229.
3/21/22
Patient and surgery factors associated with the incidence of
failed and difficult intubation
R. Schnittker,1 S.D. Marshall2 and J. Berecki-Gisolf3
Anaesthesia 2020, 75, 756–766
Summary
Estimates of the rate and risk-factors for difficult airway rarely include a denominator for the number of
anaesthetics. Approaches such as self-reporting and crowd-sourcing of airway incidents may help identify
specific lessons from clinical episodes, but the lack of denominator data, biased reporting and under-reporting
does not allow a comprehensive population-based assessment. We used an established state-wide dataset to
determine the incidence of failed and difficult intubations between 2015 and 2017 in the state of Victoria in
Australia, along with associated patient and surgical risk-factors. A total of 861,533 general anaesthesia
episodes were analysed. Of these, 4092 patients with difficult or failed intubation were identified; incidence
rates of 0.52% (2015–2016) and 0.43% (2016–2017), respectively. Difficult/failed intubations were most
common in patients aged 45–75 and decreased for older age groups, with risk being lower for patients
aged >85 than patients aged 35–44. The risk for failed/difficult intubation increased significantly for: patients
undergoing emergency surgery (OR 1.80); obese patients (OR 2.48); increased ASA physical status; and
increased Charlson Comorbidity Index. Across all age groups, procedures on the nervous system (OR 1.92) and
endocrine system (OR 2.03) had the highest risk of failed/difficult intubation. The relative reduced risk for failed/
difficult intubations in the elderly population is a novel finding that contrasts with previous research and may
suggest a ‘compression of morbidity’ effect as a moderator. Administrative databases have the potential to
improve understanding of peri-operative risk of rare events at a population level.
Updated 3/11/22
Review Article:Apnoeic oxygenation in paediatric anaesthesia: a narrative review
C. Lyons and M. Callaghan
Anaesthesia 2021, 76, 118–127
Summary
Apnoeic oxygenation refers to oxygenation in the absence of any patient or ventilator effort to move the lungs.
This phenomenon was first described in humans in the mid-20th century but has seen renewed interest in the
last decade following the demonstration of apnoeic oxygenation with low-flow, and subsequently high-flow,
nasal oxygen. This narrative review summarises our understanding of apnoeic oxygenation in the paediatric
population. We examine the evidence supporting oxygenation via tracheal tube, modified laryngoscopes and
nasal cannulae. The evidence for prolongation of safe apnoea time at induction of anaesthesia is also appraised.
We explore the capacity for carbon dioxide clearance, flow rate selection with high-flow nasal oxygen and
complications associated with the technique. It remains uncertain whether apnoeic oxygenation in paediatric
patients results in a meaningful clinical benefit compared with standard care for outcomes such as the number
of tracheal intubation attempts or the incidence of hypoxaemia. In particular, the role of apnoeic oxygenation in
paediatric difficult airway management is unclear as this has not been the targeted focus of any published
research to date.
Updated 2/27/22
Frequency and Risk Factors for Difficult Intubation in Women Undergoing General Anesthesia for Cesarean Delivery: A Multicenter Retrospective Cohort Analysis
Reale SC, Bauer ME, Klumpner TT, et al. Frequency and Risk Factors for Difficult Intubation in Women Undergoing General Anesthesia for Cesarean Delivery: A Multicenter Retrospective Cohort Analysis. Anesthesiology. 2022.
Estimates for the incidence of difficult intubation in the obstetric population vary widely, though prior studies reporting rates of difficult intubation in obstetrics are older and limited by smaller samples. The goals of this study were to provide a contemporary estimate of the frequency of difficult and failed intubation in women undergoing general anesthesia for cesarean delivery and to elucidate risk factors for difficult intubation in women undergoing general anesthesia for cesarean delivery.
This is a multicenter, retrospective cohort study utilizing the Multicenter Perioperative Outcomes Group database. The study population included women aged 15-44 undergoing general anesthesia for cesarean delivery between 2004 and 2019 at one of 45 medical centers. Co-primary outcomes included the frequencies of difficult and failed intubation. Difficult intubation was defined as Cormack-Lehane view ≥3, intubation attempts ≥3, rescue fiberoptic intubation, rescue supraglottic airway, or surgical airway. Failed intubation was defined as any attempt at intubation without successful endotracheal tube placement. Rates of difficult and failed intubation were assessed. Several patient demographic, anatomical, and obstetric factors were evaluated for potential associations with difficult intubation.
We identified 14,748 cases of cesarean delivery performed under general anesthesia. There were 295 cases of difficult intubation, with a frequency of 1:49 (95% CI: 1:55, 1:44) (n=14,531). There were 18 cases of failed intubation, with a frequency of 1:808 (95% CI: 1:1,276, 1:511) (n=14,537). Factors with the highest point estimates for the odds of difficult intubation included increased body mass index, Mallampati score III or IV, small hyoid to mentum distance, limited jaw protrusion, limited mouth opening, and cervical spine limitations.
In this large, multi-center, contemporary study of over 14,000 general anesthetics for cesarean delivery, we observed an overall risk of difficult intubation of 1:49 and a risk of failed intubation of 1:808. Most risk factors for difficult intubation were non-obstetric in nature. These data demonstrate that difficult intubation in obstetrics remains an ongoing concern.
Updated 2/16/22
Patient and surgery factors associated with the incidence of failed and difficult intubation
Abstract
Estimates of the rate and risk-factors for difficult airway rarely include a denominator for the number of anaesthetics. Approaches such as self-reporting and crowd-sourcing of airway incidents may help identify specific lessons from clinical episodes, but the lack of denominator data, biased reporting and under-reporting does not allow a comprehensive population-based assessment. We used an established state-wide dataset to determine the incidence of failed and difficult intubations between 2015 and 2017 in the state of Victoria in Australia, along with associated patient and surgical risk-factors. A total of 861,533 general anaesthesia episodes were analysed. Of these, 4092 patients with difficult or failed intubation were identified; incidence rates of 0.52% (2015-2016) and 0.43% (2016-2017), respectively. Difficult/failed intubations were most common in patients aged 45-75 and decreased for older age groups, with risk being lower for patients aged >85 than patients aged 35-44. The risk for failed/difficult intubation increased significantly for: patients undergoing emergency surgery (OR 1.80); obese patients (OR 2.48); increased ASA physical status; and increased Charlson Comorbidity Index. Across all age groups, procedures on the nervous system (OR 1.92) and endocrine system (OR 2.03) had the highest risk of failed/difficult intubation. The relative reduced risk for failed/difficult intubations in the elderly population is a novel finding that contrasts with previous research and may suggest a 'compression of morbidity' effect as a moderator. Administrative databases have the potential to improve understanding of peri-operative risk of rare events at a population level.
doi: 10.1111/anae.14997. Epub 2020 Mar 31.
Updated 2/10/22
EDITORIAL New evidence to inform decisions and guidelines in difficult airway management
Alistair F. McNarry1,* and Takashi Asai2
1Department of Anaesthesia, NHS Lothian, Edinburgh, UK and 2Department of Anesthesiology, Dokkyo Medical
University Saitama Medical Centre, Koshigaya, Japan
British Journal of Anaesthesia,
doi: 10.1016/j.bja.2021.03.003
Advance Access Publication
Update 2/1/22
Endotracheal Tube Cuff Leaks: Causes, Consequences, and Management
Mohammad El-Orbany, MD* and M. Ramez Salem, MD†
The consequences of endotracheal tube (ETT) cuff leak may range from a bubbling noise to a
life-threatening ventilatory failure. Although the definitive solution is ETT replacement, this is
often neither needed nor safe to perform. Frequently, the leak is not caused by a structural
defect in the ETT. Cuff underinflation, cephalad migration of the ETT (partial tracheal extubation),
misplaced orogastric or nasogastric tubes, wide discrepancy between ETT and tracheal
diameters, or increased peak airway pressure can cause leaks around intact cuffs. Correction
of these problems will stop the leak without ETT replacement. Alternatively, ETT cuff, pilot balloon,
and inflation system damage due to inadvertent trauma or manufacturing defects may
be responsible. Conservative management ideas (management without ETT replacement) were
previously published to solve the problem. However, when a large structural defect is identified
or conservative measures fail, ETT replacement becomes necessary. This can be performed
with direct laryngoscopy if laryngeal visualization is adequate. A difficult exchange with possible
airway loss should be anticipated, and prepared for, when there are signs and/or history
of difficult intubation. A risk/benefit analysis of each individual situation is warranted before
decisions are made on how best to proceed. Alternative back-up ventilation plans should be
preformulated and the necessary equipment ready before the exchange. In this review, various
management concerns and plans are discussed, and a simple algorithm to manage leaky ETT
cuff situations is presented. (Anesth Analg 2013;117:428–34)
Update 1/13/22
(this is a high level review of facemark ventilation.- WHR)
Facemask ventilation
W.P.L. Bradley1,2 and C. Lyons3,4
BJA Education, 22(1): 5e11 (2022)
! Facemask ventilation is a core airway management
skill that functions as both a primary
technique and a rescue technique of oxygenation.
! The prevalence of difficult mask ventilation is
approximately 1% and of impossible mask ventilation
is approximately 0.05%.
! A two-handed grip and optimisation of the patient’s
and anaesthetist’s positioning can
improve facemask ventilation.
! Facemask ventilation can be improved by using
neuromuscular blocking drugs.
! Complications of facemask ventilation are rare.
Update 1/4/21
Font-of-neck airway rescue with impalpable anatomy during a simulated cannot intubate caFrFnnot oxygenate scenario: scalpelefingerecannula versus scalpelefingerebougie in a sheep model
Andrew Heard et al
Background: Front-of-neck airway rescue in a cannot intubate cannot oxygenate (CICO) scenario with impalpable
anatomy is particularly challenging. Several techniques have been described based on a midline vertical neck incision
with subsequent finger dissection, followed by either a cannula or scalpel puncture of the now palpated airway. We
explored whether the speed of rescue oxygenation differs between these techniques.
Methods: In a high-fidelity simulation of a CICO scenario in anaesthetised Merino sheep with impalpable front-of-neck
anatomy, 35 consecutive eligible participants undergoing airway training performed scalpelefingerecannula and scalpelefingerebougie
in a random order. The primary outcome was time from airway palpation to first oxygen delivery.
Data, were analysed with Cox proportional hazards.
Results: Scalpelefingerecannulawas associated with shorter time to first oxygen delivery on univariate (hazard ratio [HR].
11.37; 95% confidence interval [CI], 5.14e25.13; P<0.001) andmultivariate (HR.8.87; 95% CI, 4.31e18.18; P<0.001) analyses. In
themultivariablemodel, consultant grade was also associated with quicker first oxygen delivery compared with registrar
grade (HR.3.28; 95% CI, 1.36e7.95; P.0.008).With scalpelefingerecannula, successful oxygen delivery within 3min of CICO
declaration and 2 attempts wasmore frequent; 97% vs 63%, P<0.001. In analyses of successful cases only, scalpelefingerecannula
resulted in earlier improvement in arterial oxygen saturations (e25 s; 95% CI, e35 to e15; P<0.001), but a
longer time to first capnography reading (.89 s; 95% CI, 69 to 110; P<0.001). Nomajor complications occurred in either arm.
Conclusions: The scalpelefingerecannula technique was associated with superior oxygen delivery performance during a
simulated CICO scenario in sheep with impalpable front-of-neck anatomy.
British Journal of Anaesthesia, 2020 doi: 10.1016/j.bja.2020.04.067
Updated 12/27/21
Front of neck access to the airway: A narrative review
X. Onrubiaa, G. Frovab, M. Sorbelloc, ∗
The concept of Front of Neck Access (FONA) covers a large amount of techniques, principles, problems and
debates. The aim of this review is to discuss the issue of FONA with special regard to the sole cricothyrotomy,
including all technical issues starting from landmark identification to different approaches, either surgical or
percutaneous.
Other open questions remain, such as choice of inner diameter, presence of a cuff, potential advantages of
Seldinger based techniques, including bougie assisted ones, timing and decision making. Despite being a simple
maneuver, cricothyrotomy remains a very complex concept, which should be a core skill of any physician
approaching the airway and as simple as it is, it can make the difference between life and death.
https://doi.org/10.1016/j.tacc.2018.06.001
2210-8440/ ˝ 2018.
Updated 12/15/21
2022 American Society of Anesthesiologists Practice Guidelines for Management of the Difficult Airway*
Updated 11/29/21
Management of haematoma after thyroid surgery: systematic review and multidisciplinary consensus guidelines from the Difficult Airway Society, the British Association of Endocrine and Thyroid Surgeons and the British Association of Otorhinolaryngology, Head and Neck Surgery
H. A. Iliff,K. El-Boghdadly, I. Ahmad, et al
Anaesthesia 2021
Summary
Haematoma after thyroid surgery can lead to airway obstruction and death. We therefore developed guidelines
to improve the safety of peri-operative care of patients undergoing thyroid surgery. We conducted a systematic
review to inform recommendations, with expert consensus used in the absence of high-quality evidence, and a
Delphi study was used to ratify recommendations. We highlight the importance of multidisciplinary team
management and make recommendations in key areas including: monitoring; recognition; post-thyroid
surgery emergency box; management of suspected haematoma following thyroid surgery; cognitive aids; posthaematoma
evacuation care; day-case thyroid surgery; training; consent and pre-operative communication;
postoperative communication; and institutional policies. The guidelines support a multidisciplinary approach
to the management of suspected haematoma following thyroid surgery through oxygenation and evaluation;
haematoma evacuation; and tracheal intubation. They have been produced with materials to support
implementation. While these guidelines are specific to thyroid surgery, the principles may apply to other forms
of neck surgery. These guidelines and recommendations provided are the first in this area and it is hoped they
will support multidisciplinary team working, improving care and outcomes for patients having thyroid surgery.
Updated 11/14/21
A Predictor of Difficult Airway: The Tasli Classification in Transnasal Flexible Laryngoscopy
*Hamdi Tasli, *Nesibe Esra Karaman, †Dilber Isler, and *Bugra Subasi, *yK€utahya, Turkey
Journal of Voice, July 2021
Abstract: Introduction. Dif!cult airway is de!ned as dif!culty or failure in one or more steps in upper airway
management. Evaluation of the upper airway with physical examination methods and endoscopic devices is crucial
in predicting dif!cult airway. The aim of this study was to evaluate bedside tests, Cormack Lehane (CL) and
Tasli Classi!cation (TC) scores of the patients and it was aimed to reveal the role of TC which will be performed
preoperatively as a predictor of dif!cult tracheal intubation (DTI).
Methods. The study included a total of 98 patients who underwent surgical treatment under general anesthesia.
Demographic data, including age, gender, and body mass index (BMI), and bedside tests consisting Modi!ed
Mallampati Classi!cation (MMC), thyromental (TD) and sternomental (SD) distances, neck circumference
(NC), interincisor distance (IID), CL and TC were recorded.
Results. Evaluation was made of 64 (65.3%) male and 34 (34.7%) female patients ranging in age from 18 to
84 years (mean age: 50.35 § 0.47 years). The successfully intubated patients (SIP) group comprised 68 (69.4%)
patients, and the dif!cult intubation patients (DIP) group, 30 (30.6%). According to CL, the numbers of SIP and
DIP constituting grade 1 was 29 (42.6%) and one (3.3%); grade 2a was 29 (42.6%) and one (3.3%); grade 2b was
eight (11.8%) and three (10%); grade 3a was one (1.5%) and six (20%); grade 3b was one (1.5%) and 14 (46.7%)
respectively. Grade 4 was only detected in the DIP group in 5 (16.7%) patients. According to TC, the numbers of
SIP and DIP constituting grade 1 was 20 (29.4%) and 1 (3.3%); grade 2a was 37 (54.4%) and seven (23.3%); grade
2b was 10 (14.7%) and 18 (60%); grade 3 was one (1.5%) and two (6.7%) respectively. Grade 4 was only detected
in the DIP group in two (6.7%) patients.
Conclusion. The TC, CL, NC and BMI scores were higher in the DIP group and higher TC scores (grade 2b, 3,
and 4) can be a predictor of dif!cult airway. However, it may be more bene!cial to use TC as a complementary
diagnostic tool with bedside tests such as NC, SM, TM and MMC, rather than used alone.
Key words: Diff{cult Airway—The Cormack-Lehane Classi!cation—Transnasal Flexible Laryngoscopy—Bedside
Tests—The Tasli Classi!cation.
Updated 11/13/21
Error traps in pediatric difficult airway management
Difficult airway management in children is associated with significant morbidity. This narrative review on error traps in airway management aims to highlight the common pitfalls and proposes solutions to optimize best practices for pediatric difficult airway management. We have categorized common errors of pediatric difficult airway management into three main error traps: preparation, performance, and proficiency, and present potential strategies to improve patient safety and successful tracheal intubation in infants and children with difficult airways.
Updated 10-31-21
A comparison of patient and provider perceptions of awake tracheal intubations
Colin Archer, MD . John Veall, MD, FRCPC . Laura V. Duggan, MD, FRCPC .
Andrew Downey, MBBS, Hons, FANZCA . Peter Rose, MD, FRCPC
Can J Anesth/J Can Anesth, Oct 2021
Updated 10-29-21
An international survey about rapid sequence intubation of
10,003 anaesthetists and 16 airway experts
M. Zdravkovic,1,2 J. Berger-Estilita,3 M. Sorbello,4 C. A. Hagberg5
Anaesthesia. 2020;75(3):313-322.
Summary
Pulmonary aspiration of gastric content is a significant cause of anaesthesia-related morbidity and mortality.
High-quality prospective randomised evidence to support prevention strategies, such as rapid sequence
intubation, is difficult to generate due to well-described practical, ethical and methodological barriers. We
aimed to generate an understanding of worldwide practice through surveying clinically practicing anaesthetists
and airway experts. Our survey was designed to assess the influence of: departmental standards; patient
factors; socio-economic factors; training; and supervision.Wesurveyed 10,003 anaesthetists who responded to
an invitation to participate on LinkedIn. We then surveyed 16 international airway experts on the same content.
When asked about a hypothetical patient with intestinal obstruction, respondents expressed preferences for
[OR (95%CI)]: the head-up or -down position 4.26 (3.98–4.55), p < 0.001; nasogastric tube insertion 29.5 (26.9–
32.3), p < 0.001; and the use of cricoid force 2.80 (2.62–3.00), p < 0.001, as compared with a hypothetical
patient without intestinal obstruction also requiring rapid sequence intubation. Respondents from lower
income countries were more likely to prefer [OR (95%CI]: the supine position 2.33 (2.00–2.63), p < 0.001;
nasogastric tube insertion 1.29 (1.09–1.51), p = 0.002; and cricoid force application 2.54 (2.09–3.09), p < 0.001
as compared with respondents from higher income countries for a hypothetical patient with intestinal
obstruction. This survey, which we believe is the largest of its kind, demonstrates that preferences for
positioning, nasogastric tube use and cricoid force application during rapid sequence intubation vary
substantially. Achieving agreed consensus may yield better training in the principles of rapid sequence
intubation.
Updated 10-23-21
EDITORIAL New evidence to inform decisions and guidelines in difficult airway management
Alistair F. McNarry, Takashi Asai
Updated 9-18-21
Comparison of videolaryngoscopy and direct laryngoscopy for tracheal intubation in obstetrics: a mixed-methods systematic review and meta-analysis
Ryan Howle, MBChB, FRCA . Desire Onwochei, MBBS, FRCA . Siew-Ling Harrison, MBBS, FRCA . Neel Desai, MBChB, FRCA
Abstract
Purpose The incidence of difficult and failed intubation is higher in obstetrical patients than in the general population because of anatomic and physiologic changes in pregnancy. Videolaryngoscopy improves the success rate of intubation and reduces complications when compared with direct laryngoscopy in adults; however, it is not known whether this extends to obstetrical surgery. The aim of this study was to examine the efficacy, efficiency, and safety of videolaryngoscopy compared with direct laryngoscopy in obstetrics.
Source Central, CINAHL, Embase, MEDLINE and Web of Science databases were searched from inception to 27 May 2020 with no restrictions. Inclusion criteria included randomized-controlled trials (RCTs), observational studies, case series, and case reports that reported the application of videolaryngoscopy to intubate the trachea in pregnant patients having general anesthesia.
Department of Anaesthesia, Guy’s and St Thomas’ NHS Foundation Trust, London, UK
Principal findings Overall, four RCTs with 428 participants, nine observational studies, and 35 case reports/series with 100 participants were included. On meta-analysis of three trials, the co-primary outcomes of first-attempt success rate (risk ratio, 1.02; 95% confidence intervals [CI], 0.98 to 1.06; P = 0.29; I2 = 0%) and time to tracheal intubation (mean difference, 1.20 sec; 95% CI, - 6.63 to 9.04; P = 0.76; I2 = 95%) demonstrated no difference between videolaryngoscopy and direct laryngoscopy in parturients without difficult airways. Observational studies and case reports underline the role of videolaryngoscopy as a primary choice when difficulty with tracheal intubation is expected or as a rescue modality in difficult or failed intubations.
Conclusions Evidence for the utility of videolaryngoscopy continues to evolve but supports its increased adoption in obstetrics where videolaryngoscopes should be immediately available for use as a first-line device.
Can J Anesth/J Can Anesth https://doi.org/10.1007/s12630-020-01908-w
Updated 9-3-21
Carbon dioxide monitoring in children-A narrative review of physiology, value, and pitfalls in clinical practice
Abstract
Continuous capnography has been recognised as an essential monitoring device in all anesthetized patients, despite which airway device is in use, regardless of their location, as a measure to improve patient safety. Capnography is the non-invasive measurement of a sample of the exhaled carbon dioxide which has multiple clinical uses including as a method to confirm placement of a tracheal tube and/or to assess ventilation, perfusion and metabolism. Notably, capnography is used during routine paediatric anesthesia to assess ventilation and as a surrogate measure for arterial carbon dioxide pressure. The inaccuracies associated with these surrogate measures need to be considered to inform improved ventilation management of infants and children. This review highlights some major principles to understand the carbon dioxide elimination, the physiology of paediatric capnography, the clinical application and the limitations of capnography during anesthesia for neonates, infants and small children.
Paediatric Anaesthesia 2021 Aug;31(8):839-845.
PMID: 34008907 DOI: 10.1111/pan.14208
Updated 8-20-21
Evaluation of super-obesity and super-super-obesity as risk factors for difficult intubation in patients undergoing bariatric surgery
Mohamed Mahmoud, M.D., et al
Background: Super-obesity is a serious disorder which requires bariatric surgery. The association of
super-obesity and difficult intubation was not adequately established.
Objectives: To determine if super-obesity and super-super-obesity are associated with difficult intubation or not.
Setting: University Hospital.
Methods: A cohort of obese patients scheduled for bariatric surgery was prospectively recruited.
Super-obesity and super-super-obesity were defined as body mass index !50 kg/m2 and 60 kg/m2,
respectively. Intubation difficulty was assessed by 2 methods: (1) intubation difficulty scale; (2) number
of intubation attempts. Risk factors for difficult intubation were recorded. Univariate and multivariate
analysis for risk factors for difficult intubation and difficult mask ventilation were performed.
Results: A total of 658 patients were enrolled in the study including 205 (31%) super-obese and 52
(8%) super-super-obese patients. Ninety-nine (15%) patients required more than 1 intubation
attempt, while 215 (33%) patients had intubation difficulty scale !5. Ninety-four (14.4%) patients
had mask ventilation of moderate difficulty, while only 2 (.3%) patients needed 2-person ventilation.
The independent risk factors for difficult intubation using the two stated definitions were STOP-Bang
and Mallampati score values. The independent risk factors for mask ventilation of moderate difficulty
were STOP-Bang score, Mallampati score, and limited neck extension.
Conclusion: Within obese patients, neither super-obesity nor super-super-obesity was associated
with difficult intubation or difficult mask ventilation. High STOP-Bang and Mallampati score are
the independent factors for difficult intubation. (Surg Obes Relat Dis 2021;-:1–7.)
Updated 7-23-21
Comparison between ultrasound-guided and digital palpation techniques for identification of the cricothyroid membrane: a meta- analysis
Kuo-Chuan Hung1, I-Wen Chen1, Chien-Ming Lin1 and Cheuk-Kwan Sun2,3,* 1Department of Anesthesiology, Chi Mei Medical Center, Tainan, Taiwan, 2Department of Emergency Medicine, E-Da
Hospital, Kaohsiung, Taiwan and 3College of Medicine, I-Shou University, Kaohsiung, Taiwan
Updated 7-15-21
Emergency department evaluation of patients with angiotensinconverting enzyme inhibitor associated angioedema
Philip A. Mudd, MD, PhDa, et al
American Journal of Emergency Medicine 38 (2020) 2596–2601
Introduction: Angiotensin converting enzyme inhibitor (ACEi) associated angioedema is frequently encountered
in the emergency department. Airwaymanagement is the primary treatment, but published evidence supporting
the decision to intubate patients with this condition is extremely limited.
Method: We performed a retrospective study of all cases of ACEi associated angioedema encountered in a large,
urban, tertiary referral emergency department. We classi!ed demographics, duration of symptoms before presentation,
physical exam !ndings and nasopharyngoscopy !ndings in patients that did and did not require intubation.
Results: We identi!ed a total of 190 separate encounters from 183 unique patients who presented during the 3-
year period of the study. Eighteen (9.5%) of these patients required intubation. Patients requiring intubationwere
more likely to presentwithin 6 h of the onset of angioedema symptoms. Anterior tongue swelling, vocal changes,
drooling, and dyspnea were signi!cantly more common in patients requiring intubation. Isolated lip swelling
was present in 54% of all patients and was the only !nding signi!cantly more common in the group that did
not require intubation.
Conclusions: Rapid progression of symptoms within the !rst 6 h of angioedema onset, anterior tongue swelling,
vocal changes, drooling and dyspnea are associated with intubation for ACEi associated angioedema. Isolated lip
swelling is signi!cantly more common in patients that do not require intubation. Our data provide risk strati!cation
guidance for providers treating patients with suspected ACEi associated angioedema in the emergency
department.
Updated 7-2-21
Evaluation of super-obesity and super-super-obesity as risk factors for difficult intubation in patients undergoing bariatric surgery
Mohamed Mahmoud, M.D., Ahmed M. Hasanin, M.D., D.E.S.A.*, Maha Mostafa, M.D.,
Fatema Alhamade, M.Sc., Bassant Abdelhamid, M.D., Mona Elsherbeeny, M.D.
Department of Anesthesia and Critical Care Medicine, Cairo University, Cairo, Egypt
Received 20 October 2020; accepted 31 March 2021
Abstract Background: Super-obesity is a serious disorder which requires bariatric surgery. The association of
super-obesity and difficult intubation was not adequately established.
Objectives: To determine if super-obesity and super-super-obesity are associated with difficult intubation
or not.
Setting: University Hospital.
Methods: A cohort of obese patients scheduled for bariatric surgery was prospectively recruited.
Super-obesity and super-super-obesity were defined as body mass index !50 kg/m2 and 60 kg/m2,
respectively. Intubation difficulty was assessed by 2 methods: (1) intubation difficulty scale; (2) number
of intubation attempts. Risk factors for difficult intubation were recorded. Univariate and multivariate
analysis for risk factors for difficult intubation and difficult mask ventilation were performed.
Results: A total of 658 patients were enrolled in the study including 205 (31%) super-obese and 52
(8%) super-super-obese patients. Ninety-nine (15%) patients required more than 1 intubation
attempt, while 215 (33%) patients had intubation difficulty scale !5. Ninety-four (14.4%) patients
had mask ventilation of moderate difficulty, while only 2 (.3%) patients needed 2-person ventilation.
The independent risk factors for difficult intubation using the two stated definitions were STOP-Bang
and Mallampati score values. The independent risk factors for mask ventilation of moderate difficulty
were STOP-Bang score, Mallampati score, and limited neck extension.
Conclusion: Within obese patients, neither super-obesity nor super-super-obesity was associated
with difficult intubation or difficult mask ventilation. High STOP-Bang and Mallampati score are
the independent factors for difficult intubation. (Surg Obes Relat Dis 2021;-:1–7.) ! 2021 American
Society for Bariatric Surgery. Published by Elsevier Inc. All rights reserved.
Updated 6/23/21
Airway events in obese vs. non-obese elective surgical patients: a cross-sectional observational study
Anaesthesia. 2021 Jun 22 PMID: 3415671 DOI: 10.1111/anae.15513
Abstract
Obesity is an increasingly prevalent comorbidity within the UK population. The aim of this study was to determine the proportion of obese patients in an elective surgical population. The second aim was to determine the choice of airway equipment and incidence of airway events in obese vs. non-obese patients. We conducted a cross-sectional observational study over two 24-h periods in March 2018 across 39 hospitals in the greater London area. Data were collected regarding 1874 patients. The incidence of obesity was 32% in the study population compared with 26% in the general UK population (p < 0.0001). Minor airway events were defined as: desaturation to Sp O2 < 90%; failed mask ventilation; supraglottic airway device problem; aspiration; airway trauma and difficult intubation; or recognised oesophageal intubation. Major airway events were defined as: unrecognised oesophageal intubation; a 'cannot intubate cannot oxygenate' emergency; the need for unplanned front-of-neck airway; cardiac arrest; or unplanned intensive care unit admission due to an airway event. In total, 89 minor and two major airway events were recorded. Obese patients were more likely to experience a minor airway event (RR 2.39, 95%CI 1.60-3.57), the most common being desaturation (Sp O2 < 90%). The use of a supraglottic airway device in obese vs. non-obese patients was associated with increased airway events (RR 3.46 [1.88-6.40]). Tracheal intubation vs. supraglottic airway device use increased with obesity class but was not associated with a decrease in airway events (RR 0.90 [0.53-1.55]). Our data suggest that obesity is more common in the elective surgical vs. general population and minor airway events are more common in obese vs. non-obese elective patients.
Updated 6/16/21
Manual in-line stabilisation during tracheal intubation:
effective protection or harmful dogma?
M. D. Wiles
Consultant, Department of Anaesthesia, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK
Anaesthesia 2021, 76, 850–853
This month’s ‘Contemporary Classic’ focuses on a landmark
paper from the 1990s. The study by Nolan and Wilson
examined tracheal intubation in patients with a suspected
cervical spine injury [1], a topic which still remains a clinical
concern for anaesthetists today. Cervical spine injury occurs
in 3%–4% of trauma patients, with around 25% of these
patients having a cervical spinal cord injury [2]. Cervical cord
injury is more common in patients who have a reduced
Glasgow Coma Scale (GCS), and around 25% will have
injuries to other body systems [2]. As a result, these patients
are likely to require airway intervention, either to protect/
secure their airway or to facilitate treatment or investigation
of their injuries. Clinicians are often worried about the
possibility that tracheal intubation may either worsen an
existing neurological deficit or cause a new spinal cord
injury. This is despite there being little published evidence
showing an association between tracheal intubation and
either primary or secondary cervical cord damage [3, 4].
Updated 6/9/21
Airway Management in Surgical Patients WithObstructive Sleep Apnea
Edwin Seet, MBBS, MMed, FAMS,* Mahesh Nagappa, MD,† and David T. Wong, MD, FRCPC‡
Obstructive sleep apnea (OSA) is the most common sleep-related breathing disorder, and the
difficult airway is perhaps the anesthesiologists’ quintessential concern. OSA and the difficult
airway share certain similar anatomical, morphological, and physiological features. Individual
studies and systematic reviews of retrospective, case-control, and large database studies have
shown a likely association between patients with OSA and the difficult airway; OSA patients
have a 3- to 4-fold higher risk of difficult intubation, difficult mask ventilation, or a combination
of both. The presence of OSA should initiate proactive perioperative management in anticipation
of a difficult airway. Prudent intraoperative management comprises the use of regional
anesthesia where possible and considering an awake intubation technique where there is the
presence of notable difficult airway predictors and risk of rapid desaturation following induction
of general anesthesia. Familiarity with difficult airway algorithms, cautious extubation, and
appropriate postoperative monitoring of patients with OSA are necessary to mitigate perioperative
risks. (Anesth Analg 2021;132:1321–7)
Updated 5-25-21
Carbon dioxide monitoring in children – a narrative review of physiology, value and pitfalls in clinical practice
Susan Humphreys, Andreas Schibler, Britta S von Ungern-Sternberg
Introduction
Continuous capnography has been recognised as an essential monitoring device in all
anaesthetised patients, despite which airway device is in use, regardless of their location, as a
measure to improve patient safety 1. Capnography is the non-invasive measurement of a sample
of the exhaled carbon dioxide (CO2) which has multiple clinical uses including as a method to
confirm placement of a tracheal tube and/or to assess ventilation, perfusion and metabolism.
Notably, capnography is used during routine paediatric anaesthesia to assess ventilation and as a
surrogate measure for arterial carbon dioxide pressure (PaCO2). The inaccuracies associated with
these surrogate measures need to be considered to inform improved ventilation management of
infants and children. This review highlights some major principles to understand the CO2
elimination, the physiology of paediatric capnography, the clinical application and the limitations
of capnography during anaesthesia for neonates, infants and small children.
Paediatr Anaesth, 2021, epub before print
Updated 5-20-21
Evaluation of super-obesity and super-super-obesity as risk factors for difficult intubation in patients undergoing bariatric surgery
Mohamed Mahmoud, M.D., Ahmed M. Hasanin, M.D., D.E.S.A.*, Maha Mostafa, M.D.,
Fatema Alhamade, M.Sc., Bassant Abdelhamid, M.D., Mona Elsherbeeny, M.D.
Background: Super-obesity is a serious disorder which requires bariatric surgery. The association of
super-obesity and difficult intubation was not adequately established.
Objectives: To determine if super-obesity and super-super-obesity are associated with difficult intubation
or not.
Setting: University Hospital.
Methods: A cohort of obese patients scheduled for bariatric surgery was prospectively recruited.
Super-obesity and super-super-obesity were defined as body mass index !50 kg/m2 and 60 kg/m2,
respectively. Intubation difficulty was assessed by 2 methods: (1) intubation difficulty scale; (2) number
of intubation attempts. Risk factors for difficult intubation were recorded. Univariate and multivariate
analysis for risk factors for difficult intubation and difficult mask ventilation were performed.
Results: A total of 658 patients were enrolled in the study including 205 (31%) super-obese and 52
(8%) super-super-obese patients. Ninety-nine (15%) patients required more than 1 intubation
attempt, while 215 (33%) patients had intubation difficulty scale !5. Ninety-four (14.4%) patients
had mask ventilation of moderate difficulty, while only 2 (.3%) patients needed 2-person ventilation.
The independent risk factors for difficult intubation using the two stated definitions were STOP-Bang
and Mallampati score values. The independent risk factors for mask ventilation of moderate difficulty
were STOP-Bang score, Mallampati score, and limited neck extension.
Conclusion: Within obese patients, neither super-obesity nor super-super-obesity was associated
with difficult intubation or difficult mask ventilation. High STOP-Bang and Mallampati score are
the independent factors for difficult intubation. (Surg Obes Relat Dis 2021;-:1–7.) ! 2021 American
Society for Bariatric Surgery.
Updated 4-29-21
Economic analysis of the use of video laryngoscopy versus direct laryngoscopy in the surgical setting
Aim: Compared with direct laryngoscopy (DL), video laryngoscopy (VL) offers clinical benefits in routine and difficult airways. The health economic benefit of VL versus DL for routine tracheal intubation remains unknown. Materials & methods: This analysis compared VL and DL health economic outcomes, including total inpatient costs, length of hospital stay (LOS), postoperative intensive care unit (ICU) admission and incidence of procedurally associated complications. Results: Patients with VL had decreased inpatient cost (US$1144-5891 across eight major diagnostic categories [MDC]); >1-day LOS reduction in five MDC; reduced odds for postoperative ICU admission (0.04-0.68) and reduced odds of respiratory complications in three MDC (0.43-0.90). Conclusion: Video laryngoscopy may lower total costs, reduce LOS and decrease the likelihood of postoperative ICU admission.
- PMID: 33904779
- DOI: 10.2217/cer-2021-0068
Updated 4-21-21
Ultrasound identification of the cricothyroid membrane: the newstandard in preparing for front-of-neck airway access
Michael S. Kristensen1,* and Wendy H. Teoh2
Conclusions
The meta-analysis by Hung and colleagues4 unequivocally documents the superiority of ultrasound for guiding identification and marking of the cricothyroid membrane, and the
limitations of palpation methods, especially in the obese and in those with pathology of the neck. The clinical consequences should be that, in cases where pre-induction visual inspection
or palpation methods do not with certainty identify the cricothyroid membrane and the midline of the airway, the cricothyroid membrane should be identified with ultrasonography
and marked with the patient in extended-neck position. Subsequently, the patient can be placed in the desired position for airway management and induction. In case that the initial
airway management fails and front-of-neck airway access is needed, the patient can be returned to the extended-neck position, and the marking of the centre of the cricothyroid
membrane will again be correct.
Updated 4-13-21
Success and Complications of the Ketamine-Only Intubation Method in the Emergency Department
Abstract
Background: Rapid sequence intubation (RSI), defined as near-simultaneous administration of a sedative and neuromuscular blocking agent, is the most common and successful method of tracheal intubation in the emergency department. However, RSI is sometimes avoided when the physician believes there is a risk of a can't intubate/can't oxygenate scenario or critical hypoxemia because of distorted anatomy or apnea intolerance. Traditionally, topical anesthesia alone or in combination with low-dose sedation are used when physicians deem RSI too risky. Recently, a ketamine-only strategy has been suggested as an alternative approach.
Objective: We compared first attempt success and complications between ketamine-only, topical anesthesia alone or with low-dose sedation, and RSI approaches.
Methods: We analyzed registry data from the National Emergency Airway Registry, comprising emergency department intubation data from 25 centers from January 2016 to December 2018. We excluded pediatric patients (<14 years of age), those in cardiac and respiratory arrest, or those with an alternate pharmacologic approach (i.e., neuromuscular blocking agent only or nonketamine sedative alone). We analyzed first attempt intubation success and adverse events across the 3 intubation approaches. We calculated differences in outcomes between the ketamine-only and topical anesthesia groups.
Results: During the study period, 12,511 of 19,071 intubation encounters met inclusion criteria, including 102 (0.8%) intubated with ketamine alone, 80 (0.6%) who had intubation facilitated by topical anesthesia, and 12,329 (98.5%) who underwent RSI. Unadjusted first attempt success was 61%, 85%, and 90% for the 3 groups, respectively. Hypoxemia (defined as oxygen saturation <90%) occurred in 16%, 13%, and 8% of patients during the first attempt, respectively. At least 1 adverse event occurred in 32%, 19%, and 14% of the courses of intubation for the 3 groups, respectively. In comparing the ketamine-only and topical anesthesia groups, the difference in first pass success was -24% (95% confidence interval -37% to -12%), and the difference in number of cases with ≥1 adverse event was 13% (95% confidence interval 0-25%), both favoring the topical anesthesia group.
Conclusion: Although sometimes advocated, the ketamine-only intubation approach is uncommon and is associated with lower success and higher complications compared with topical anesthesia and RSI approaches.
Updated 4-7-21
Quantification of the effect of body mass index on cricothyroid membrane depth: a cross-sectional analysis of clinical CT images
Ghaffar, S. et al
Abstract
OBJECTIVES: The recommended front of neck access procedure in can't intubate, can't oxygenate scenarios relies on palpation of the cricothyroid membrane (CTM), or dissection of the neck down to the larynx if CTM is impalpable. CTM palpation is particularly challenging in obese patients, most likely due to an increased distance between the skin and the CTM (CTM depth). The aims of this study were to measure the CTM depth in a representative clinical sample, and to quantify the relationship between body mass index (BMI) and CTM depth. METHODS: This is a retrospective analysis of 355 clinical CT scans performed at a teaching hospital over an 8-month period. CTM depth was measured by two radiologists, and mean CTM depth calculated. Age, gender, height and weight were recorded, and BMI calculated. Linear relationships between patient characteristics and CTM depth were assessed in order to derive a predictive equation for calculating CTM depth. The variables included for this model were those with a strong association with CTM depth, that is, a p value of 0.10 or less. RESULTS: Mean CTM depth was 8.12 mm (IQR 6.36-11.70). There was no association between CTM depth and sex (beta -0.33, 95% CI -1.33 to 0.68, p=0.53), height (cm) (beta 0.01, 95% CI -0.05 to 0.06, p=0.79) or age (years) (beta -0.01, 95% CI 0.10 to 0.15, p=0.62). Increasing weight (kg) (beta 0.12, 95% CI 0.10 to 0.15, p<0.001) and BMI (kg/m(3)) (beta 0.52, 95% CI 0.44 to 0.60, p<0.001) were strongly associated with CTM depth. Predicted CTM depth increased from 6.4 mm (95% CI 4.9 to 8.1) at a BMI of 20 kg/m(2) to 16.8 (95% CI 13.7 to 20.1) at BMI 40 kg/m(2). CONCLUSION: CTM depth was strongly associated with BMI in a retrospective analysis of patients having clinical CT scans.
Emerg Med J Feb 2021
Updated 3-26-21
Evaluation and Management of the Physiologically Difficult Airway: Consensus Recommendations From Society for Airway Management
Rebecca L. Kornas, MD,* Clark G. Owyang, MD,† John C. Sakles, MD,‡ Lorraine J. Foley, MD, MBA
Multiple international airway societies have created guidelines for the management of the difficult
airway. In critically ill patients, there are physiologic derangements beyond inadequate
airway protection or hypoxemia. These risk factors contribute to the “physiologically difficult
airway” and are associated with complications including cardiac arrest and death. Importantly,
they are largely absent from international guidelines. Thus, we created management recommendations
for the physiologically difficult airway to provide practical guidance for intubation
in the critically ill. Through multiple rounds of in-person and telephone conferences, a multidisciplinary
working group of 12 airway specialists (Society for Airway Management’s Special
Projects Committee) over a time period of 3 years (2016–2019) reviewed airway physiology
topics in a modified Delphi fashion. Consensus agreement with the following recommendations
among working group members was generally high with 80% of statements showing agreement
within a 10% range on a sliding scale from 0% to 100%. We limited the scope of this analysis to
reflect the resources and systems of care available to out-of-operating room adult airway providers.
These recommendations reflect the practical application of physiologic principles to airway
management available during the analysis time period. (Anesth Analg 2021;132:395–405)
Added 3/5/21
Barry N. Singleton1,*, Fiachra K. Morris2, Barbaros Yet3, Donal J. Buggy4 and Zane B. Perkins5
Effectiveness of intubation devices in patients with cervical spine immobilisation: a systematic review and network meta-analysis
Background: Cervical spine immobilisation increases the difficulty of tracheal intubation. Many intubation devices have
been evaluated in this setting, but their relative performance remains uncertain.
Methods: MEDLINE, EMBASE, and the Cochrane Library were searched to identify randomised trials comparing two or
more intubation devices in adults with cervical spine immobilisation. After critical appraisal, a random-effects network
meta-analysis was used to pool and compare device performance. The primary outcome was the probability of firstattempt
intubation success (first-pass success). For relative performance, the Macintosh direct laryngoscopy blade was
chosen as the reference device.
Conclusions: For intubation performed with cervical immobilisation, seven devices had a better probability of first-pass
success compared with the Macintosh. However, more studies using MILS (rather than a cervical collar or other alternative)
are needed, which more accurately represent clinical practice.
British Journal of Anaesthesia, xxx (xxx): xxx (xxxx)
doi: 10.1016/j.bja.2020.12.041
Advance Access Publication Date:
Added 1/30/21
Comparison between ultrasound-guided and digital palpation techniques for identification of the cricothyroid membrane: a meta-analysis.
Hung KC, Chen IW, Lin CM, Sun CK. Br J Anaesth. 2021;126(1):e9-e11.
Surgical cricothyrotomy is a potentially life-saving procedure in the ‘cannot intubate/cannot oxygenate’ scenario. As this procedure is not performed frequently, the conventional use of digital palpation to identify the cricothyroid membrane carries the risk of misidentification and failed cricothyrotomy. The recent introduction of ultrasound-guided identification of the cricothyroid membrane could be a potential solution. A few published RCTs have shown the effectiveness of this ultrasound approach for improving the success rate of cricothyroid membrane identification compared with the conventional palpation technique. However, most of these trials were small scale and conducted in different settings (e.g. emergency room or anaesthesia care unit), and a number of studies failed to show significant differences in the accuracy of cricothyroid membrane identification between the two techniques. Furthermore, there are concerns that the use of ultrasound technique may prolong the procedure time, which can be life threatening in an emergency situation. We conducted this meta-analysis to analyse whether the ultrasound-guided approach is superior to the palpation technique
Added 1/20/21
Airway management in the critically ill
Sheila Nainan Myatra
Despite advances in the management of critically ill patients, tracheal intubation in these patients remains a
high-risk procedure associated with increased morbidity and mortality. Recent interventions to enhance patient
safety and improve first pass success in tracheal intubation emphasize reducing repeated attempts at tracheal
intubation, oxygen desaturation and cardiovascular collapse during airway management by optimizing
patient physiology to mitigate risks and avoid complications. These include various strategies to improve periintubation
oxygenation like use of noninvasive ventilation, high flow nasal cannula oxygen and gentle mask
ventilation between induction of anesthesia and laryngoscopy; use of a videolaryngoscope and a bougie;
careful selection of drugs including neuromuscular blocking agent; improved strategies to avoid
haemodynamic collapse; rescue oxygenation strategies and human factor considerations.
Summary
Recognizing the challenges and using the appropriate interventions to improve first pass tracheal intubation
success, while maintaining patient safety are essential during tracheal intubation in critically ill patients. This
review will provide recommendations based on the current evidence, various guidelines and expert opinion in
the field. Further research will help us better understand the best strategies to improve patient outcomes.
Current Opinion in Critical Care
2020, published ahead of print
Added 10/15/21
An international survey about rapid sequence intubation of 10,003 anaesthetists and 16 airway experts
Added 9/3/20
Use of the intubating laryngeal mask airway in the emergency
department: A ten-year retrospective review
Brian E. Driver, Marc Martel , Tarissa Lai , Tracy A.Markob, Robert F. Reardon
American Journal of Emergency Medicine 38 (2020) 1367–1372
Background: Extraglottic devices, such as the intubating laryngeal mask airway (ILMA), facilitate ventilation and oxygenation and are useful for emergency airway management, especially as rescue devices. In the operating room setting the ILMA has been highly successful. However, its performance in the ED has not been described. We sought to describe the indications for and success of the ILMA when used in the ED. Methods: We performed retrospective, observational study of patients who had an LMA® Fastrach™ (hereafter termed ILMA) placed in a single ED between 2007 and 2017. Patients were identified by keyword search of ED notes in the electronic medical record. Trained abstractors reviewed charts and videos to determine patient characteristics, indication for ILMA placement, success of oxygenation and ventilation, intubation methods and success, and complications related to the device. Results: During the study period 218 patients had an ILMA placed in the ED. The ILMA was used as a primary device in 118 patients (54%), and as a rescue device in 100 patients (46%). The median number of ILMA uses per faculty physician during the study period was 3. The ILMA oxygenated and ventilated successfully in 212 instances (98%), including 96 times (96%) when used as a rescue airway. Failure of oxygenation was due to tracheal injury (2), abnormal laryngeal inlet anatomy (2), or poor operator technique (1). Intubation through the ILMA was successful in 159 of 192 patients (83%), including a success rate of 81% (112 of 139 patients) with blind intubation. Conclusion: The ILMAwas highly successful in oxygenation, with reasonable intubation success, even when used infrequently by emergency physicians. The ILMA should be considered a valuable primary and rescue intubation device in the ED.
Added 11/18/19
Difficult Airway Society guidelines for awake tracheal intubation (ATI) in adults.
Abstract
Awake tracheal intubation has a high success rate and a favourable safety profile but is underused in cases of anticipated difficult airwaymanagement. These guidelines are a comprehensive document to support decision making, preparation and practical performance of awake tracheal intubation. We performed a systematic review of the literature seeking all of the available evidence for each element of awake tracheal intubation in order to make recommendations. In the absence of high-quality evidence, expert consensus and a Delphi study were used to formulate recommendations. We highlight key areas of awake tracheal intubation in which specific recommendations were made, which included: indications; procedural setup; checklists; oxygenation; airway topicalisation; sedation; verification of tracheal tube position; complications; management of unsuccessful awake tracheal intubation; post-tracheal intubation management; consent; and training. We recognise that there are a range of techniques and regimens that may be effective and one such example technique is included. Breaking down the key practical elements of awake tracheal intubation into sedation, topicalisation, oxygenation and performance might help practitioners to plan, perform and address complications. These guidelines aim to support clinical practice and help lower the threshold for performing awake tracheal intubation when indicated.
Added 11/10/19
The midline approach for endotracheal intubation using GlideScope video laryngoscopy could provide better glottis exposure in adults: a randomized controlled trial.
BACKGROUND:
Previous studies have demonstrated that the common laryngoscopic approach (right-sided) and midline approach are both used for endotracheal intubation by direct laryngoscopy. Although the midline approach is commonly recommended for video laryngoscopy (VL) in the clinic, there is a lack of published evidences to support this practice. This study aimed to evaluate the effects of different video laryngoscopic approaches on intubation.
METHODS:
Two hundred sixty-two patients aged 18 years who underwent elective surgery under general anaesthesia and required endotracheal intubation were included in the present prospective, randomized, controlled study. The participants were randomly and equally allocated to the right approach (Group R) or midline approach (Group M). All the intubations were conducted by experienced anaesthetists using GlideScope video laryngoscopy. The primary outcomes were Cormack-Lehane laryngoscopic views (CLVs) and first-pass success (FPS) rates. The secondary outcomes were the time to glottis exposure, time to tracheal intubation, haemodynamic responses and other adverse events. Comparative analysis was performed between the groups.
RESULTS:
Finally, 262 patients completed the study, and all the tracheas were successfully intubated. No significant differences were observed in the patient characteristics and airway assessments (P > 0.05). Compared with Group R, Group M had a better CLV (χ2 = 14.706, P = 0.001) and shorter times to glottis exposure (8.82 ± 2.04 vs 12.38 ± 1.81; t = 14.94; P < 0.001) and tracheal intubation (37.19 ± 5.01 vs 45.23 ± 4.81; t = 13.25; P < 0.001), but no difference was found in the FPS rate (70.2% vs 71.8%; χ2 = 0.074; P = 0.446) and intubation procedure time (29.86 ± 2.56 vs 30.46 ± 2.97, t = 1.75, P = 0.081). Between the groups, the rates of hoarseness or sore throat, minor injury, hypoxemia and changes in SBP and HR showed no significant difference (P > 0.05).
CONCLUSION:
Although the FPS rate did not differ based on the laryngoscopic approach, the midline approach could provide better glottis exposure and shorter times to glottis exposure and intubation. The midline approach should be recommended for teaching in VL-assisted endotracheal intubation.
Added 10/24/19
High-Flow Nasal Oxygen Improves Safe Apnea Time in Morbidly Obese Patients Undergoing General Anesthesia: A Randomized Controlled Trial.
BACKGROUND:
Morbidly obese patients undergoing general anesthesia are at risk of hypoxemia during anesthesia induction. High-flow nasal oxygenation use during anesthesia induction prolongs safe apnea time in nonobese surgical patients. The primary objective of our study was to compare safe apnea time, between patients given high-flow nasal oxygenation or conventional facemask oxygenation during anesthesia induction, in morbidly obese surgical patients.
METHODS:
Research ethics board approval was obtained. Elective surgical patients ≥18 years with body mass index ≥40 kg·m were included. Patients with severe comorbidity, gastric reflux disease, known difficult airway, or nasal obstruction were excluded. After obtaining informed consent patients were randomized. In the intervention (high-flow nasal oxygenation) group, preoxygenation was provided by 100% nasal oxygen for 3 minutes at 40 L·minute; in the control group, preoxygenation was delivered using a facemask with 100% oxygen, targeting end-tidal O2 >85%. Anesthesia was induced with propofol, remifentanil, and rocuronium. Bag-mask ventilation was not performed. At 2 minutes after rocuronium, videolaryngoscopy was performed. If the laryngoscopy grade was I or II, laryngoscope was left in place and the study was continued; if grade III or IV was observed, the patient was excluded from the study. During the apnea period, high-flow nasal oxygenation patients received nasal oxygen at 60 L·minute; control group patients received no supplemental oxygen. The primary outcome, safe apnea time, was reached when oxygen saturation measured by pulse oximetry (SpO2) fell to 95% or maximum 6 minutes of apnea. The patient was then intubated. T tests and χ analyses were used to compare groups. P < .05 was considered significant.
RESULTS:
Forty patients completed the study. Baseline parameters were comparable between groups. Safe apnea time was significantly longer (261.4 ± 77.7 vs 185.5 ± 52.9 seconds; mean difference [95% CI], 75.9 [33.3-118.5]; P = .001) and the minimum peri-intubation SpO2 was higher (91.0 ± 3.5 vs 88.0 ± 4.8; mean difference [95% CI], 3.1 [0.4-5.7]; P = .026) in the high-flow nasal oxygenation group compared to the control group.
CONCLUSIONS:
High-flow nasal oxygenation, compared to conventional oxygenation, provided a longer safe apnea time by 76 seconds (40%) and higher minimum SpO2 in morbidly obese patients during anesthesia induction. High-flow oxygenation use should be considered in morbidly obese surgical patients.
Added 10/16/19
A Narrative Review of Oxygenation During Pediatric Intubation and Airway Procedures.
Abstract
Hypoxemia is a common complication in the pediatric operating room during endotracheal intubation and airway procedures and is a precursor to serious adverse events. Small children and infants are at greater risk of hypoxemia due to their high metabolic requirements and propensity to alveolar collapse during general anesthesia. To improve the care and safety of this vulnerable population, continued efforts must be directed to mitigate hypoxemia and the risk of subsequent serious adverse events. Apneic oxygenation has been shown to significantly prolong the safe apnea time until desaturation in infants, children, and adults and may reduce the incidence of desaturation during emergency intubation of critically ill patients. Successful apneic oxygenation depends on adequate preoxygenation, patent upper and lower airways, and a source of continuous oxygen delivery. Humidified, high-flow nasal oxygenation systems have been shown to provide excellent conditions for effective apneic oxygenation in adults and children and have the added benefit of providing some carbon dioxide clearance in adults; although, this latter benefit has not been shown in children. Humidified, high-flow nasal oxygenation systems may also be useful during spontaneous ventilation for airway procedures in children by minimizing room air entrainment and maintaining adequate oxygenation allowing for a deeper anesthetic. The use of apneic oxygenation and humidified, high-flow nasal oxygenation systems in the pediatric operating room reduces the incidence of hypoxemia and may be effective in decreasing related complications.
Added 9/26/19
Supraglottic airway devices in difficult airway management: a retrospective cohort study of 658,104 general anaesthetics registered in the Danish Anaesthesia Database.
Indications for using supraglottic airway devices have widened over time and they now hold a prominent role in guidelines for difficult airway management. We aimed to describe the use of supraglottic airway devices in difficult airway management. We included adult patients undergoing general anaesthesia registered in the Danish Anaesthesia Database from 2008 to 2012 whose airway management had been recorded as difficult, defined as: ≥ 3 tracheal intubation attempts; failed tracheal intubation; or difficult facemask ventilation. In the Danish Anaesthesia Database, a separate difficult airway management module requires the technique used in each successive airway management attempt to be recorded. The primary aim of the study was to describe the use of supraglottic airway devices in cases of difficult airway management. Secondary aims were to examine success rates of supraglottic airway devices in difficult airway management cases, and specifically in the cases of 'cannot intubate, cannot facemask ventilate'. Difficult airway management occurred in 4898 (0.74% (95%CI 0.72-0.76%)) of 658,104 records of general anaesthesia. Supraglottic airway devices were used or use was attempted in 607 cases of difficult airway management (12.4% (95%CI 11.5-13.3%)), and were successful in 395 (65.1% (95%CI 61.2-68.8%)) cases. In 'cannot intubate, cannot facemask ventilate' situations, supraglottic airway devices were used in 86 (18.9% (95%CI 15.6-22.8%)) of 455 records and were successful in 54 (62.8% (95%CI 52.2-72.3%)) cases. We found that supraglottic airway devices are not widely used in the management of the difficult airway despite their prominent role in difficult airway management guidelines
Added 9/19/19
A Narrative Review of Oxygenation During Pediatric Intubation and Airway Procedures
Added 9/3/19
The Clinical Use of Cricoid Pressure
First, Do No Harm
Added 8/15/19
BACKGROUND:
Prior to the anticipated difficult airway, the emergency physician commonly palpates the neck to identify the presumed location of the cricothyroid membrane (CTM). In the event of a "cannot-intubate, cannot‑oxygenate" airway, precise CTM localization is vital to the success of a cricothyrotomy and hence, the patient's survival.
OBJECTIVE:
This narrative review will summarize the prospective studies evaluating CTM identification. It will demonstrate the inaccuracy of the classically used landmark palpation technique. It will then describe the use of ultrasound (US) as a superior tool for CTM identification, illustrate the technique itself, and propose its implementation in the pre-intubation checklist for the anticipated difficult airway.
DISCUSSION:
Evidence demonstrates that physicians are not sufficiently accurate in palpating the CTM in both cadavers and volunteers in a stable non-emergent setting. In preparing for a real-time intubation, this fine motor task would be more difficult to achieve. Moreover, this particular patient group may often exhibit difficult airway features. US has been demonstrated to be superior for locating the CTM than landmark palpation across body habitus, gender, and failed airway simulations. This technique carries a short learning curve even without prior airway US experience, along with a high retention rate. An illustrative tutorial is provided.
CONCLUSION:
Emergency physicians may apply this US technique for CTM localization in preparation for an anticipated difficult airway. However, since this technique takes longer than landmark palpation, using US is not recommended once already in the midst of a failed airway situation.
Copyright © 2018 Elsevier Inc. All rights reserved.
Added 8/2/19
Airway changes following labor and delivery in preeclamptic parturients: a prospective case control study.
BACKGROUND:
Preeclampsia is associated with greater narrowing of the airway than normal pregnancy, but it is not known if these changes worsen during labor and delivery. The aim of the study was to evaluate the airway during and after labor in women with or without preeclampsia.
METHODS:
Twenty-five normal and 25 severely preeclamptic pregnant women in early labor were recruited in this single-center, prospective, case-control study. Airway assessment was performed (a) before active labor (b) within one hour of delivery and (c) 24-48 h postpartum. The Mallampati grade was the primary outcome. Sonographic measurements of tongue thickness, anterior neck soft tissue at the level of the hyoid bone and the vocal cords, thyromental distance, and neck circumference, were secondary outcomes.
RESULTS:
The Mallampati score increased from the pre-labor to the post-labor period in both preeclamptic and normotensive patients (P=0.001 and P=0.002 respectively). A significant difference in tissue thickness at the hyoid level was observed between preeclamptic and normotensive patients pre-labor (P=0.035), post-labor (P=0.05) and postpartum (P=0.05). There was no significant difference in thyromental distance or neck circumference between groups at any time. The total duration of labor and a Mallampati change by one grade correlated (Spearman correlation coefficient 0.473).
CONCLUSION:
Airway sonography may provide useful bedside anatomical information for prediction of difficult laryngoscopy. The change in airway dimensions and the Mallampati score during labor may persist for 48 h postpartum in both groups. Those with prolonged labor are more susceptible to changes in airway dimensions.
Added 7/17/19
Supraglottic airway devices in difficult airway management: a retrospective cohort study of 658,104 general anaesthetics registered in the Danish Anaesthesia Database. Anaesthesia. 2019 Feb;74(2):151-157. doi: 10.1111/anae.14443. Epub 2018 Oct 4.
Indications for using supraglottic airway devices have widened over time and they now hold a prominent role in guidelines for difficult airway management. We aimed to describe the use of supraglottic airway devices in difficult airway management. We included adult patients undergoing general anaesthesia registered in the Danish Anaesthesia Database from 2008 to 2012 whose airway management had been recorded as difficult, defined as: ≥ 3 tracheal intubation attempts; failed tracheal intubation; or difficult facemask ventilation. In the Danish Anaesthesia Database, a separate difficult airway management module requires the technique used in each successive airway management attempt to be recorded. The primary aim of the study was to describe the use of supraglottic airway devices in cases of difficult airway management. Secondary aims were to examine success rates of supraglottic airway devices in difficult airway management cases, and specifically in the cases of 'cannot intubate, cannot facemask ventilate'. Difficult airway management occurred in 4898 (0.74% (95%CI 0.72-0.76%)) of 658,104 records of general anaesthesia. Supraglottic airway devices were used or use was attempted in 607 cases of difficult airway management (12.4% (95%CI 11.5-13.3%)), and were successful in 395 (65.1% (95%CI 61.2-68.8%)) cases. In 'cannot intubate, cannot facemask ventilate' situations, supraglottic airway devices were used in 86 (18.9% (95%CI 15.6-22.8%)) of 455 records and were successful in 54 (62.8% (95%CI 52.2-72.3%)) cases. We found that supraglottic airway devices are not widely used in the management of the difficult airway despite their prominent role in difficult airway management guideline
Added 6/27/19
Endotracheal Intubation with the King Laryngeal Tube™ In Situ Using Video Laryngoscopy and a Bougie: A Retrospective Case Series and Cadaveric Crossover Study.
J Emerg Med. 2017 Apr;52(4):403-408
Removal of a functioning King laryngeal tube (LT) prior to establishing a definitive airway increases the risk of a "can't intubate, can't oxygenate" scenario. We previously described a technique utilizing video laryngoscopy (VL) and a bougie to intubate around a well-seated King LT with the balloons deflated; if necessary, the balloons can be rapidly re-inflated and ventilation resumed.
OBJECTIVE:
Our objective is to provide preliminary validation of this technique.
METHODS:
Emergency physicians performed all orotracheal intubations in this two-part study. Part 1 consisted of a historical analysis of VL recordings from emergency department (ED) patients intubated with the King LT in place over a two-year period at our institution. In Part 2, we analyzed VL recordings from paired attempts at intubating a cadaver, first with a King LT in place and then with the device removed, with each physician serving as his or her own control. The primary outcome for all analyses was first-pass success.
RESULTS:
There were 11 VL recordings of ED patients intubated with the King LT in place (Part 1) and 11 pairs of cadaveric VL recordings (Part 2). The first-pass success rate was 100% in both parts. In Part 1, the median time to intubation was 43 s (interquartile range [IQR] 36-60 s). In Part 2, the median time to intubation was 23 s (IQR 18-35 s) with the King LT in place and 17 s (IQR 14-18 s) with the King LT removed.
CONCLUSIONS:
Emergency physicians successfully intubated on the first attempt with the King LT in situ. The technique described in this proof-of-concept study seems promising and merits further validation.
Added 6/13/19
Pre-operative voice evaluation as a hypothetical predictor of difficult laryngoscopy.
Anaesthesia. 2019 Jun 11.
We examined the potential for voice sounds to predict a difficult airway as compared with prediction by the modified Mallampati test. A total of 453 patients scheduled for elective surgery under general anaesthesia with tracheal intubation were studied. Five phonemes were recorded and their formants analysed. Difficult laryngoscopy was defined as the Cormack-Lehane grade 3 or 4. Univariate and multivariate logistic regression were used to examine the association between some variables (mouth opening, sternomental distance, modified Mallampati and formants) and difficult laryngoscopy. Difficult laryngoscopy was reported in 29/453 (6.4%) patients. Among five regression models evaluated, the model achieving better performance to predict difficult laryngoscopy, after a variable selection criteria (stepwise, multivariate) and included a modified Mallampati classification (OR 2.920; 95%CI 1.992-4.279; p < 0.001), first formant of /i/(iF1) (OR 1.003; 95%CI 1.002-1.04; p < 0.001), and second formant of /i/(iF2) (OR 0.998; 95%CI 0.997-0.998; p < 0.001). The receiver operating curve for a regression model that included both formants and Mallampati showed an area under curve of 0.918, higher than formants alone (area under curve 0.761) and modified Mallampati alone (area under curve 0.874). Voice presented a significant association with difficult laryngoscopy during general anaesthesia showing a 76.1% probability of correctly classifying a randomly selected patient.
Added 6/3/19
The DIFFMASK score for predicting difficult facemask ventilation: a cohort study of 46,804 patients.
Abstract
Facemask ventilation is an essential part of airway management. Correctly predicting difficulties in facemask ventilation may reduce the risk of morbidity and mortality among patients at risk. We aimed to develop and evaluate a weighted risk score for predicting difficult facemask ventilation during anaesthesia. We analysed a cohort of 46,804 adult patients who were assessed pre-operatively airway for 13 predictors of difficult airway management and subsequently underwent facemask ventilation during general anaesthesia. We developed the Difficult Facemask (DIFFMASK) score in two consecutive steps: first, a multivariate regression analysis was performed; and second, the regression coefficients of the adjusted regression model were converted into a clinically applicable weighted point score. The predictive accuracy of the DIFFMASK score was evaluated by assessment of receiver operating characteristic curves. The prevalence of difficult facemask ventilation was 1.06% (95%CI 0.97-1.16). Following conversion of regression coefficients into 0, 1, 2 or 3 points, the cumulated DIFFMASK score ranged from 0 to 18 points and the area under the receiver operating characteristic curve was 0.82. The Youden index indicated a sum score ≥ 5 as an optimal cut-off value for prediction of difficult facemask ventilation giving a sensitivity of 85% and specificity of 59%. The DIFFMASK score indicated that a score of 6-10 points represents a population of patients who may require heightened attention when facemask ventilation is planned, compared with those patients who are obviously at a high- or low risk of difficulties. The DIFFMASK score may be useful in a clinical context but external, prospective validation is needed.
© 2019 Association of Anaesthetists.
Added 5/24/19
The inaccuracy of using landmark techniques for cricothyroid membrane identification: a comparison of three techniques.
OBJECTIVES:
Successful cricothyrotomy is predicated on accurate identification of the cricothyroid membrane (CTM) by palpation of superficial anatomy. However, recent research has indicated that accuracy of the identification of the CTM can be as low as 30%, even in the hands of skilled providers. To date, there are very little data to suggest how to best identify this critical landmark. The objective was to compare three different methods of identifying the CTM.
METHODS:
A convenience sample of patients and physician volunteers who met inclusion criteria was consented. The patients were assessed by physician volunteers who were randomized to one of three methods for identifying the CTM (general palpation of landmarks vs. an approximation based on four finger widths vs. an estimation based on overlying skin creases of the neck). Volunteers would then mark the skin with an invisible but florescent pen. A single expert evaluator used ultrasound to identify the superior and inferior borders of the CTM. The variably colored florescent marks were then visualized with ultraviolet light and the accuracy of the various methods was recorded as the primary outcome. Additionally, the time it took to perform each technique was measured. Descriptive statistics and report 95% confidence intervals (CIs) are reported.
RESULTS:
Fifty adult patients were enrolled, 52% were female, and mean body mass index was 28 kg/m(2) (95% CI = 26 to 29 kg/m(2) ). The general palpation method was successful 62% of the time (95% CI = 48% to 76%) and took an average of 14 seconds to perform (range = 5 to 45 seconds). In contrast, the four-finger technique was successful 46% of the time (95% CI = 32% to 60%) and took an average of 12 seconds to perform (range = 6 to 40 seconds). Finally, the neck crease method was successful 50% of the time (95% CI = 36% to 64%) and took an average of 11 seconds to perform (range = 5 to 15 seconds).
CONCLUSIONS:
All three methods performed poorly overall. All three techniques might potentially be even less accurate in instances where the superficial anatomy is not palpable due to body habitus. These findings should alert clinicians to the significant risk of a misplaced cricothyrotomy and highlight the critical need for future research.
Added 5/16/19
The inaccuracy of using landmark techniques for cricothyroid membrane identification: a comparison of three techniques.
OBJECTIVES:
Successful cricothyrotomy is predicated on accurate identification of the cricothyroid membrane (CTM) by palpation of superficial anatomy. However, recent research has indicated that accuracy of the identification of the CTM can be as low as 30%, even in the hands of skilled providers. To date, there are very little data to suggest how to best identify this critical landmark. The objective was to compare three different methods of identifying the CTM.
METHODS:
A convenience sample of patients and physician volunteers who met inclusion criteria was consented. The patients were assessed by physician volunteers who were randomized to one of three methods for identifying the CTM (general palpation of landmarks vs. an approximation based on four finger widths vs. an estimation based on overlying skin creases of the neck). Volunteers would then mark the skin with an invisible but florescent pen. A single expert evaluator used ultrasound to identify the superior and inferior borders of the CTM. The variably colored florescent marks were then visualized with ultraviolet light and the accuracy of the various methods was recorded as the primary outcome. Additionally, the time it took to perform each technique was measured. Descriptive statistics and report 95% confidence intervals (CIs) are reported.
RESULTS:
Fifty adult patients were enrolled, 52% were female, and mean body mass index was 28 kg/m(2) (95% CI = 26 to 29 kg/m(2) ). The general palpation method was successful 62% of the time (95% CI = 48% to 76%) and took an average of 14 seconds to perform (range = 5 to 45 seconds). In contrast, the four-finger technique was successful 46% of the time (95% CI = 32% to 60%) and took an average of 12 seconds to perform (range = 6 to 40 seconds). Finally, the neck crease method was successful 50% of the time (95% CI = 36% to 64%) and took an average of 11 seconds to perform (range = 5 to 15 seconds).
CONCLUSIONS:
All three methods performed poorly overall. All three techniques might potentially be even less accurate in instances where the superficial anatomy is not palpable due to body habitus. These findings should alert clinicians to the significant risk of a misplaced cricothyrotomy and highlight the critical need for future research.
Added 5/3/19
Added 4/3/19
Added 3/28/19
Emergency surgical cricothyroidotomy: 24 successful cases leading to a simple ‘scalpel–finger–tube’ method
Emergency Medicine Australia, Volume24,2012
Added 2/20/19
Current practice for awake fiberoptic intubation- some unanswered questions
Editorial T Murphy and B Howes
Anesthesia 2017, 72, 678-9
Mask ventilation.
Effective mask ventilation is an essential skill for any practitioner engaged in airway management. Recent methods to objectively describe mask ventilation using waveform capnography help practitioners to monitor and communicate the effectiveness of maskventilation. Gentle mask ventilation is now considered acceptable during rapid sequence induction/intubation after loss of consciousness, hence reducing the incidence of hypoxia prior to tracheal intubation. Mask ventilation can be enhanced with muscle relaxation, a double C-E grip, and jaw thrust. This is particularly relevant for patients with reduced apnoea time. An awareness of the complications associated with mask ventilation may help reduce the morbidity associated with this technique. Effective ventilationtechnique and optimum device selection are important aspects for resuscitation of the newborn. Teaching correct establishment and maintenance of mask ventilation is essential for safe patient care. This review will examine some of the latest developments concerning mask ventilation for adult and paediatric patients.
Added 12/28/18
Note from Will Rosenblatt, MD The following article from EMS services lends evidence to what we have believed for many years, and was in-part confirmed in 2004 from the landmark paper from Tom Mort, that there is a point of diminishing returns when it comes to repeated attempts at airway management. Validation is a wonderful thing - both validation of our opinions and of prior research. I encourage you to read the full article.
Defining the plateau point: When are further attempts futile in out-ofhospital
advanced airway management?☆
Jeffrey L. Jarvisa,b,⁎, Dustin Bartonc, Henry Wangd
A B S T R A C T
Background: We sought to characterize the number of attempts required to achieve advanced airway management (AAM) success.
Methods: Using 4 years of data from a national EMS electronic health record system, we examined the following subsets of attempted AAM: 1) cardiac arrest intubation (CA-ETI), 2) non-arrest medical intubation (MED-ETI), 3) non-arrest trauma intubation (TRA-ETI), 4) rapid-sequence intubation (RSI), 5) sedation-assisted ETI (SAI), and 6) supraglottic airway (SGA). We determined the first pass and overall success rates, as well as the point of additional attempt futility (“plateau point”).
Results: Among 57,209 patients there were 64,291 AAM. CA-ETI performance was: first-pass success (FPS) 71.4% (95% CI: 70.9–71.9%), 4 attempts to reach 91.5% (91.2–91.9%) success plateau. MED-ETI performance was: FPS 66.0% (95% CI: 65.1–67.0%), 3 attempts to reach 79.2% (78.4–80.0%) success plateau. TRA-ETI performance was: FPS 61.6% (95% CI: 59.3–63.9%), 3 attempts to reach 75.8% (73.7–77.8%) success plateau. RSI performance was: FPS 76.1% (95% CI: 75.1–77.1%), 5 attempts to reach 95.8% (95.3–96.2%) success plateau. SAI performance was: FPS 66.9% (95% CI: 65.1–68.6%), 3 attempts to 85.3% (83.9–86.6%) success plateau. SGA performance was: FPS 88.7% (95% CI: 88.0–89.3%), 5 attempts to reach 92.8% (92.3–93.4%) success plateau.
Conclusion: Multiple attempts are often needed to accomplish successful AAM. The number of attempts needed to accomplish AAM varies with AAM technique. These results may guide AAM practices
Added 11/24/18
Obstructing pathology of the upper airway in a post-NAP4 world: time to wake up to its optimal management
Law JA, Morris IR, Malpas G Canadian Journal of Anesthesia/Journal canadien d'anesthésie
Editorial: No Abstract
Added 11/13/18
Added 10/5/18
Predictive risk factors of failed laryngeal mask airway insertion at first attempt.
Abstract
Objectives A failed first attempt at laryngeal mask airway (LMA) insertion could increase the risk of laryngospasm, hypoxemia, and postoperative sore throat. This study was performed to investigate the risk factors for failed first-attempt LMA placement. Methods In total, 461 patients who underwent general anesthesia with a Supreme LMA (Teleflex Medical, Shanghai, China) and who had an American Society of Anesthesiologists (ASA) physical status of I to III were prospectively enrolled. The LMA was inserted after anesthetic induction. We recorded the insertion conditions and each patient's age, ASA status, body weight, body mass index (BMI), duration of anesthesia, size of LMA, and cuff pressure; the years of work experience of the anesthesiologists; and the use or nonuse of lidocaine gel as a lubricant. Results Successful first-attempt placement of the Supreme LMA was achieved in 438 (95.10%) patients, while first-attempt placement failed in 23 (4.99%). Significant risk factors for failure of first-attempt LMA insertion included high age, high body weight, BMI of <20 kg/m2, and insertion without using lidocaine gel. Conclusions A patient age of >61 years, high body weight, BMI of <20 kg/m2, and insertion without lidocaine gel could significantly increase the risk of failed first-attempt Supreme LMA insertion.
Added 9/28/18
Effect of a Strategy of Initial Laryngeal Tube Insertion vs Endotracheal Intubation on 72-Hour Survival in Adults With Out-of-Hospital Cardiac Arrest: A Randomized Clinical Trial.
JAMA. 2018 Aug 28;320(8):769-778
IMPORTANCE:
Emergency medical services (EMS) commonly perform endotracheal intubation (ETI) or insertion of supraglottic airways, such as the laryngeal tube (LT), on patients with out-of-hospital cardiac arrest (OHCA). The optimal method for OHCA advanced airway management is unknown.
OBJECTIVE:
To compare the effectiveness of a strategy of initial LT insertion vs initial ETI in adults with OHCA.
DESIGN, SETTING, AND PARTICIPANTS:
Multicenter pragmatic cluster-crossover clinical trial involving EMS agencies from the Resuscitation Outcomes Consortium. The trial included 3004 adults with OHCA and anticipated need for advanced airway management who were enrolled from December 1, 2015, to November 4, 2017. The final date of follow-up was November 10, 2017.
INTERVENTIONS:
Twenty-seven EMS agencies were randomized in 13 clusters to initial airway management strategy with LT (n = 1505 patients) or ETI (n = 1499 patients), with crossover to the alternate strategy at 3- to 5-month intervals.
MAIN OUTCOMES AND MEASURES:
The primary outcome was 72-hour survival. Secondary outcomes included return of spontaneous circulation, survival to hospital discharge, favorable neurological status at hospital discharge (Modified Rankin Scale score ≤3), and key adverse events.
RESULTS:
Among 3004 enrolled patients (median [interquartile range] age, 64 [53-76] years, 1829 [60.9%] men), 3000 were included in the primary analysis. Rates of initial airway success were 90.3% with LT and 51.6% with ETI. Seventy-two hour survival was 18.3% in the LT group vs 15.4% in the ETI group (adjusted difference, 2.9% [95% CI, 0.2%-5.6%]; P = .04). Secondary outcomes in the LT group vs ETI group were return of spontaneous circulation (27.9% vs 24.3%; adjusted difference, 3.6% [95% CI, 0.3%-6.8%]; P = .03); hospital survival (10.8% vs 8.1%; adjusted difference, 2.7% [95% CI, 0.6%-4.8%]; P = .01); and favorable neurological status at discharge (7.1% vs 5.0%; adjusted difference, 2.1% [95% CI, 0.3%-3.8%]; P = .02). There were no significant differences in oropharyngeal or hypopharyngeal injury (0.2% vs 0.3%), airway swelling (1.1% vs 1.0%), or pneumonia or pneumonitis (26.1% vs 22.3%).
CONCLUSIONS AND RELEVANCE:
Among adults with OHCA, a strategy of initial LT insertion was associated with significantly greater 72-hour survival compared with a strategy of initial ETI. These findings suggest that LT insertion may be considered as an initial airway management strategy in patients with OHCA, but limitations of the pragmatic design, practice setting, and ETI performance characteristics suggest that further research is warranted.
TRIAL REGISTRATION:
ClinicalTrials.gov Identifier: NCT02419573.
Added September 24, 2018
Crit Care. 2018 Sep 23;22(1):236. doi: 10.1186/s13054-018-2150-6.
Risk factors and outcomes for airway failure versus non-airway failure in the intensive care unit: a multicenter observational study of 1514 extubation procedures.
Patients liberated from invasive mechanical ventilation are at risk of extubation failure, including inability to breathe without a tracheal tube (airway failure) or without mechanical ventilation (non-airway failure). We sought to identify respective risk factors for airway failure and non-airway failure following extubation.
METHODS:
The primary endpoint of this prospective, observational, multicenter study in 26 intensive care units was extubation failure, defined as need for reintubation within 48 h following extubation. A multinomial logistic regression model was used to identify risk factors for airway failure and non-airway failure.
RESULTS:
Between 1 December 2013 and 1 May 2015, 1514 patients undergoing extubation were enrolled. The extubation-failure rate was 10.4% (157/1514), including 70/157 (45%) airway failures, 78/157 (50%) non-airway failures, and 9/157 (5%) mixed airway and non-airway failures. By multivariable analysis, risk factors for extubation failure were either common to airway failure and non-airway failure: intubation for coma (OR 4.979 (2.797-8.864), P < 0.0001 and OR 2.067 (1.217-3.510), P = 0.003, respectively, intubation for acute respiratory failure (OR 3.395 (1.877-6.138), P < 0.0001 and OR 2.067 (1.217-3.510), P = 0.007, respectively, absence of strong cough (OR 1.876 (1.047-3.362), P = 0.03 and OR 3.240 (1.786-5.879), P = 0.0001, respectively, or specific to each specific mechanism: female gender (OR 2.024 (1.187-3.450), P = 0.01), length of ventilation > 8 days (OR 1.956 (1.087-3.518), P = 0.025), copious secretions (OR 4.066 (2.268-7.292), P < 0.0001) were specific to airway failure, whereas non-obese status (OR 2.153 (1.052-4.408), P = 0.036) and sequential organ failure assessment (SOFA) score ≥ 8 (OR 1.848 (1.100-3.105), P = 0.02) were specific to non-airway failure. Both airway failure and non-airway failure were associated with ICU mortality (20% and 22%, respectively, as compared to 6% in patients with extubation success, P < 0.0001).
CONCLUSIONS:
Specific risk factors have been identified, allowing us to distinguish between risk of airway failure and non-airway failure. The two conditions will be managed differently, both for prevention and curative strategies.
Added September 7, 2018
Gastric emptying is not prolonged in obese patients.
BACKGROUND:
Obesity is associated with a poor anesthetic risk, in part because of the greater aspiration rates. A greater gastric residue and lower stomach pH have been implicated. The relationship of obesity to gastric emptying is ill-defined. with contradicting reports stating shorter, similar, and longer times compared with nonobese subjects. The aim of the present study was to compare gastric emptying in obese and nonobese subjects at a university hospital.
METHODS:
A total of 19 obese (body mass index [BMI] >40 kg/m(2)) and 20 nonobese (BMI <30 kg/m(2)) subjects underwent a standardized scintigraphic gastric emptying study. The participants consumed a standard semisolid, technetium-99m-labeled meal. Images were acquired immediately and 1, 2, and 4 hours after meal completion. The interval to evacuate one half of the counts measured at meal completion) and retention (the percentage of counts in stomach at each measurement point) were recorded.
RESULTS:
The mean age and BMI was 35 years and 45 kg/m(2) in the obese and 44 years and 26 kg/m(2) in the nonobese group, respectively. No differences were found between the 2 groups regarding gastric emptying. Regression analysis showed no statistical association between the BMI and gastric emptying, including multivariate analysis, considering BMI, age, and gender.
CONCLUSION:
A scintigraphy test of a labeled meal was used to evaluate gastric emptying in obese and nonobese subjects. In accordance with other published data, no significant difference was found between the 2 groups. The anesthetic risks in the obese should be attributed to factors other than delayed gastric emptying (i.e., anatomic variation, increased rates of hiatal hernia and reflux).
Added Aug 29, 2018
Obesity and GERD.
Abstract
Epidemiologic data have demonstrated that obesity is an important risk factor for the development of gastroesophageal reflux disease (GERD). There is also accumulating data that obesity is associated with complications related to longstanding reflux such as erosive esophagitis, Barrett esophagus, and esophageal adenocarcinoma. Central obesity, rather than body mass index, appears to be more closely associated with these complications. Surgical data are confounded by the concomitant repair of prevalent hiatal hernias in many patients.
Added Aug 1, 2018
Videolaryngoscope versus Macintosh laryngoscope for tracheal intubation in adults with obesity: A systematic review and meta-analysis.
Hoshijima H, Denawa Y, Tominaga A, Nakamura C, Shiga T, Nagasaka H. J Clin Anesth. 2018 Feb;44:69-75.Author information
Abstract
STUDY OBJECTIVE:
Videolaryngoscopy has become more common since the 2000s. Despite several anecdotal reports in the literature, it remains unclear whether videolaryngoscopy is superior to direct Macintosh laryngoscopy for tracheal intubation in adults with obesity. This systematic review and meta-analysis focused on prospective randomised trials comparing videolaryngoscopes with the Macintosh laryngoscope for tracheal intubation in adults with obesity.
DESIGN:
Systematic review, Meta-analysis SETTING: Operating room, Obesity patients MEASUREMENTS: Data on success rate, intubation time, and glottic visualisation during tracheal intubation were extracted from the identified studies. In a subgroup analysis, we also compared the parameters for videolaryngoscopes with a tracheal tube guide channel and those without a tracheal tube guide channel. Data from individual trials were combined, and the DerSimonian and Laird random-effect model was used to calculate either the pooled relative risk (RR) or the weighted mean difference (WMD) as well as the corresponding 95% confidence intervals (CI).
MAIN RESULTS:
Eleven articles describing 13 trials met the inclusion criteria. The performance of videolaryngoscopes was superior to that of the Macintosh laryngoscope for all outcomes. (Success rate; RR=1.11, 95% CI 1.04 to 1.18, p=0.001, I2=63%, Intubation time; WMD=-16.1, 95% CI -31.1 to -1.10, p=0.04, I2=97%, Glottic visualisation; RR=1.19, 95% CI 1.09 to 1.30, p<0.0001, I2=76%) In the subgroup analysis, the performance of both types of videolaryngoscopes (with and without a tracheal tube guide channel) was superior to that of the Macintosh laryngoscope, except for intubation time with the videolaryngoscopes without a tracheal tube guide channel.
CONCLUSIONS:
Videolaryngoscopes were superior to the Macintosh laryngoscope for tracheal intubation in adults with obesity. (GRADE score: low or very low.).
The following list includes citations that have been incorporated into the AOD lectures.
Added July 16, 2018
Work of breathing for cuffed and uncuffed pediatric endotracheal tubes in an in vitro lung model setting.
Thomas J, Weiss M, Cannizzaro, Both CP, Schmidt AR, Paediatr Anaesth. 2018 Jul 13.
Abstract
BACKGROUND:
Over the last decade, cuffed endotracheal tubes are increasingly used in pediatric anesthesia and also in pediatric intensive care. However, the smaller inner diameter of cuffed endotracheal tubes and, implicitly, the increased endotracheal tube resistance is still a matter of debate.
AIMS:
This in vitro study investigated work of breathing and inspiratory airway pressures in cuffed and uncuffed endotracheal tubes and the impact of pressure support ventilation and automatic tube compensation.
METHODS:
In 5 simulated neonatal and pediatric lung models, the Active Servo Lung 5000 and an intensive care ventilator were used to quantify the differences in work of breathing under spontaneous breathing (with and without pressure support ventilation and automatic tube compensation) between cuffed and uncuffed endotracheal tubes. Additionally, differences in inspiratory airway pressures, measured either proximal or distal of the endotracheal tube, between cuffed and uncuffed endotracheal tubes under mechanical ventilation were investigated.
RESULTS:
Work of breathing was overall 10.27% [95% confidence interval 9.01-11.94] higher with cuffed than with uncuffed endotracheal tubes and was dramatically reduced by 34.19% [95% confidence interval 31.61-35.25] with the application of pressure support. Automatic tube compensation almost diminished work of breathing differences between the 2 endotracheal tube types in nearly all pediatric lung models. Peak inspiratory and mean airway pressures measured at the proximal endotracheal tube end revealed significantly higher values in cuffed than in uncuffed endotracheal tubes. However, these differences measured at the distal end of the endotracheal tube became minimal.
CONCLUSION:
This in vitro study confirmed significant differences in work of breathing and inspiratory pressures between cuffed and uncuffed endotracheal tubes. Work of breathing, however, is almost neutralized by pressure support ventilation with automatic tube compensation and distal inspiratory airway pressures that, from a clinical perspective, are not significantly increased.
© 2018 John Wiley & Sons Ltd.
KEYWORDS:
cuffed vs uncuffed endotracheal tubes; inspiratory airway pressure; work of breathing
Added July 10, 2018
Cricoid Pressure During Induction for Tracheal Intubation in Critically Ill Children: A Report From National Emergency Airway Registry for Children.
Kojima T1, Harwayne-Gidansky I2, Shenoi AN3, Owen EB4, Napolitano N5, Rehder KJ6, Adu-Darko MA7, Nett ST8, Spear D9, Meyer K10, Giuliano JS Jr11, Tarquinio KM12, Sanders RC Jr13, Lee JH14, Simon DW15, Vanderford PA16, Lee AY17, Brown CA 3rd18, Skippen PW19, Breuer RK20, Toedt-Pingel I21, Parsons SJ22, Gradidge EA23, Glater LB24, Culver K2, Nadkarni VM25, Nishisaki A25; National Emergency Airway Registry for Children (NEAR4KIDS) and Pediatric Acute Lung Injury and Sepsis Investigators (PALISI).
Pediatr Crit Care Med. 2018 Jun;19(6):528-537
Abstract
OBJECTIVES:
Cricoid pressure is often used to prevent regurgitation during induction and mask ventilation prior to high-risk tracheal intubation in critically ill children. Clinical data in children showing benefit are limited. Our objective was to evaluate the association between cricoid pressure use and the occurrence of regurgitation during tracheal intubation for critically ill children in PICU.
DESIGN:
A retrospective cohort study of a multicenter pediatric airway quality improvement registry.
SETTINGS:
Thirty-five PICUs within general and children's hospitals (29 in the United States, three in Canada, one in Japan, one in Singapore, and one in New Zealand).
PATIENTS:
Children (< 18 yr) with initial tracheal intubation using direct laryngoscopy in PICUs between July 2010 and December 2015.
INTERVENTIONS:
None.
MEASUREMENTS AND MAIN RESULTS:
Multivariable logistic regression analysis was used to evaluate the association between cricoid pressure use and the occurrence of regurgitation while adjusting for underlying differences in patient and clinical care factors. Of 7,825 events, cricoid pressure was used in 1,819 (23%). Regurgitation was reported in 106 of 7,825 (1.4%) and clinical aspiration in 51 of 7,825 (0.7%). Regurgitation was reported in 35 of 1,819 (1.9%) with cricoid pressure, and 71 of 6,006 (1.2%) without cricoid pressure (unadjusted odds ratio, 1.64; 95% CI, 1.09-2.47; p = 0.018). On multivariable analysis, cricoid pressure was not associated with the occurrence of regurgitation after adjusting for patient, practice, and known regurgitation risk factors (adjusted odds ratio, 1.57; 95% CI, 0.99-2.47; p = 0.054). A sensitivity analysis in propensity score-matched cohorts showed cricoid pressure was associated with a higher regurgitation rate (adjusted odds ratio, 1.01; 95% CI, 1.00-1.02; p = 0.036).
CONCLUSIONS:
Cricoid pressure during induction and mask ventilation before tracheal intubation in the current ICU practice was not associated with a lower regurgitation rate after adjusting for previously reported confounders. Further studies are needed to determine whether cricoid pressure for specific indication with proper maneuver would be effective in reducing regurgitation events.
Added July 6
Roth D1, Pace NL, Lee A, Hovhannisyan K, Warenits AM, Arrich J, Herkner H.
Cochrane Database Syst Rev. 2018 May 15
Abstract
BACKGROUND:
The unanticipated difficult airway is a potentially life-threatening event during anaesthesia or acute conditions. An unsuccessfully managed upper airway is associated with serious morbidity and mortality. Several bedside screening tests are used in clinical practice to identify those at high risk of difficult airway. Their accuracy and benefit however, remains unclear.
OBJECTIVES:
The objective of this review was to characterize and compare the diagnostic accuracy of the Mallampati classification and other commonly used airway examination tests for assessing the physical status of the airway in adult patients with no apparent anatomical airway abnormalities. We performed this individually for each of the four descriptors of the difficult airway: difficult face mask ventilation, difficult laryngoscopy, difficult tracheal intubation, and failed intubation.
SEARCH METHODS:
We searched major electronic databases including CENTRAL, MEDLINE, Embase, ISI Web of Science, CINAHL, as well as regional, subject specific, and dissertation and theses databases from inception to 16 December 2016, without language restrictions. In addition, we searched the Science Citation Index and checked the references of all the relevant studies. We also handsearched selected journals, conference proceedings, and relevant guidelines. We updated this search in March 2018, but we have not yet incorporated these results.
SELECTION CRITERIA:
We considered full-text diagnostic test accuracy studies of any individual index test, or a combination of tests, against a reference standard. Participants were adults without obvious airway abnormalities, who were having laryngoscopy performed with a standard laryngoscope and the trachea intubated with a standard tracheal tube. Index tests included the Mallampati test, modified Mallampati test, Wilson risk score, thyromental distance, sternomental distance, mouth opening test, upper lip bite test, or any combination of these. The target condition was difficult airway, with one of the following reference standards: difficult face mask ventilation, difficult laryngoscopy, difficult tracheal intubation, and failed intubation.
DATA COLLECTION AND ANALYSIS:
We performed screening and selection of the studies, data extraction and assessment of methodological quality (using QUADAS-2) independently and in duplicate. We designed a Microsoft Access database for data collection and used Review Manager 5 and R for data analysis. For each index test and each reference standard, we assessed sensitivity and specificity. We produced forest plots and summary receiver operating characteristic (ROC) plots to summarize the data. Where possible, we performed meta-analyses to calculate pooled estimates and compare test accuracy indirectly using bivariate models. We investigated heterogeneity and performed sensitivity analyses.
MAIN RESULTS:
We included 133 (127 cohort type and 6 case-control) studies involving 844,206 participants. We evaluated a total of seven different prespecified index tests in the 133 studies, as well as 69 non-prespecified, and 32 combinations. For the prespecified index tests, we found six studies for the Mallampati test, 105 for the modified Mallampati test, six for the Wilson risk score, 52 for thyromental distance, 18 for sternomental distance, 34 for the mouth opening test, and 30 for the upper lip bite test. Difficult face mask ventilation was the reference standard in seven studies, difficult laryngoscopy in 92 studies, difficult tracheal intubation in 50 studies, and failed intubation in two studies. Across all studies, we judged the risk of bias to be variable for the different domains; we mostly observed low risk of bias for patient selection, flow and timing, and unclear risk of bias for reference standard and index test. Applicability concerns were generally low for all domains. For difficult laryngoscopy, the summary sensitivity ranged from 0.22 (95% confidence interval (CI) 0.13 to 0.33; mouth opening test) to 0.67 (95% CI 0.45 to 0.83; upper lip bite test) and the summary specificity ranged from 0.80 (95% CI 0.74 to 0.85; modified Mallampati test) to 0.95 (95% CI 0.88 to 0.98; Wilson risk score). The upper lip bite test for diagnosing difficult laryngoscopy provided the highest sensitivity compared to the other tests (P < 0.001). For difficult tracheal intubation, summary sensitivity ranged from 0.24 (95% CI 0.12 to 0.43; thyromental distance) to 0.51 (95% CI 0.40 to 0.61; modified Mallampati test) and the summary specificity ranged from 0.87 (95% CI 0.82 to 0.91; modified Mallampati test) to 0.93 (0.87 to 0.96; mouth opening test). The modified Mallampati test had the highest sensitivity for diagnosing difficult tracheal intubation compared to the other tests (P < 0.001). For difficult face mask ventilation, we could only estimate summary sensitivity (0.17, 95% CI 0.06 to 0.39) and specificity (0.90, 95% CI 0.81 to 0.95) for the modified Mallampati test.
AUTHORS' CONCLUSIONS:
Bedside airway examination tests, for assessing the physical status of the airway in adults with no apparent anatomical airway abnormalities, are designed as screening tests. Screening tests are expected to have high sensitivities. We found that all investigated index tests had relatively low sensitivities with high variability. In contrast, specificities were consistently and markedly higher than sensitivities across all tests. The standard bedside airway examination tests should be interpreted with caution, as they do not appear to be good screening tests. Among the tests we examined, the upper lip bite test showed the most favourable diagnostic test accuracy properties. Given the paucity of available data, future research is needed to develop tests with high sensitivities to make them useful, and to consider their use for screening difficult face mask ventilation and failed intubation. The 27 studies in 'Studies awaiting classification' may alter the conclusions of the review, once we have assessed them.
Added June 6, 2018
Cochrane Database Syst Rev. 2018 Jun 4;6
Videolaryngoscopy versus direct laryngoscopy for tracheal intubation in neonates.
Lingappan K, Arnold JL, Fernandes CJ, Pammi M.
Abstract
BACKGROUND:
Establishment of a secure airway is a critical part of neonatal resuscitation in the delivery room and the neonatal unit. Videolaryngoscopy has the potential to facilitate successful endotracheal intubation and decrease adverse consequences of delay in airway stabilization. Videolaryngoscopy may enhance visualization of the glottis and intubation success in neonates.
OBJECTIVES:
To determine the efficacy and safety of videolaryngoscopy compared to direct laryngoscopy in decreasing the time and attempts required for endotracheal intubation and increasing the success rate at first intubation in neonates.
SEARCH METHODS:
We used the search strategy of Cochrane Neonatal. In May 2017, we searched for randomized controlled trials (RCT) evaluating videolaryngoscopy for neonatal endotracheal intubation in Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, Embase, CINAHL, abstracts of the Pediatric Academic Societies, websites for registered trials at www.clinicaltrials.gov and www.controlled-trials.com, and reference lists of relevant studies.
SELECTION CRITERIA:
RCTs or quasi-RCTs in neonates evaluating videolaryngoscopy for endotracheal intubation compared with direct laryngoscopy.
DATA COLLECTION AND ANALYSIS:
Review authors performed data collection and analysis as recommended by Cochrane Neonatal. Two review authors independently assessed studies identified by the search strategy for inclusion.We used the GRADE approach to assess the quality of evidence.
MAIN RESULTS:
The search yielded 7057 references of which we identified three RCTs for inclusion, four ongoing trials and one study awaiting classification. All three included RCTs compared videolaryngoscopy with direct laryngoscopy during intubation attempts by trainees.Time to intubation was similar between videolaryngoscopy and direct laryngoscopy (mean difference (MD) -0.62, 95% confidence interval (CI) -6.50 to 5.26; 2 studies; 311 intubations) (very low quality evidence). Videolaryngoscopy did not decrease the number of intubation attempts (MD -0.05, 95% CI -0.18 to 0.07; 2 studies; 427 intubations) (very low quality evidence). Moderate quality evidence suggested that videolaryngoscopy increased the success of intubation at first attempt (typical risk ratio (RR) 1.44, 95% CI 1.20 to 1.73; typical risk difference (RD) 0.19, 95% CI 0.10 to 0.28; number needed to treat for an additional beneficial outcome (NNTB) 5, 95% CI 4 to 10; 3 studies; 467 intubation attempts).Desaturation episodes during intubation attempts were similar between videolaryngoscopy and direct laryngoscopy (MD -0.76, 95% CI -5.74 to 4.23; 2 studies; 359 intubations) (low quality evidence). There was no difference in the incidence of airway trauma due to intubation attempts (RR 0.10, 95% CI 0.01 to 1.80; RD -0.04, 95% CI -0.09 to -0.00; 1 study; 213 intubations) (low quality evidence).There were no data available on other adverse effects of videolaryngoscopy.
AUTHORS' CONCLUSIONS:
Moderate to very low quality evidence suggests that videolaryngoscopy increases the success of intubation in the first attempt but does not decrease the time to intubation or the number of attempts for intubation. However, these studies were conducted with trainees performing the intubations and these results highlight the potential usefulness of the videolaryngoscopy as a teaching tool. Well-designed, adequately powered RCTs are necessary to confirm efficacy and address safety and cost-effectiveness of videolaryngoscopy for endotracheal intubation in neonates by trainees and those proficient in direct laryngoscopy.
Added 5/31/18
Importance The tracheal tube introducer, known as the bougie, is typically used to aid tracheal intubation in poor laryngoscopic views or after intubation attempts fail. The effect of routine bougie use on first-attempt intubation success is unclear.
Added 5/15/18
Rahmani F, Parsian Z, Shahsavarinia K, Pouraghaei M, Negargar S, Mehdizadeh Esfanjani R, Soleimanpour H.
Anesth Pain Med. 2017 Nov 12;7(6):e58350.
BACKGROUND:
Intubation and maintaining airway are crucial in the management of critically ill patients in the emergency department. Correct tracheal intubation should be confirmed by the physician, otherwise oesophageal intubation could lead to hypoxia with detrimental consequences and even death. Sonography can be used to determine proper placement of the tracheal tube.
METHODS:
In this study, 75 patients, with an indication of intubation and age older than 18 years entered the study. An emergency medicine performed real-time sonography of the trachea to evaluate the correct placement of endotracheal tube. Tube passage (snowstorm) and vocal cord angel widening (bullet sign) were evaluated, and then both lungs sliding and diaphragm movement were evaluated to confirm correct tube placement and ventilation.
RESULTS:
In this study, 75 patients entered the study. The mean age of the patients was 61.12; 47 patients (62.7%) were male and 28 (37.3%) were female. The reason of intubation was the decreased level of consciousness in 22 cases (29.3%), cardiopulmonary arrest in 22 patients (29.3%), respiratory distress in 9 patients (12%), shock in 10 patients (13.3%), and seizure in 1 case. Snowstorm sign was seen in 72 patients (96%). Bullet sign was objected in 24 cases (32%). Lung sliding was seen bilaterally in 63 patients (84%) and unilaterally in 7 patients (9.3 %), but it was not noticed in 6.7% of the patients (5 patients).
CONCLUSIONS:
Transverse tracheal and lung sonography in the emergency department can be a fast measure to confirm correct endotracheal intubation.
Added 5/1/18
Nasal highflow eliminates CO2 from lower airways.
Bräunlich J, Goldner F, Wirtz H. Respir Physiol Neurobiol. 2017 Aug;242:86-88.
INTRODUCTION:
Nasal highflow (NHF) has a growing evidence in treatment of hypoxemic respiratory failure. There are preliminary data available about use in acute and chronic type-II-respiratory failure. Unfortunately underlying mechanisms of NHF are not well understood. Increase in airway pressure seems too small to explain the observed reduction in hypercapnia. Most interesting effects are wash-out of upper airways and reduction of functional dead space. There are no data available about a wash-out of lower airways.
METHODS:
We established a sheep lung model to evaluate CO2-wash-out in lower airways. Therefore we placed measuring and insufflation catheter in maximal expanded lung. The lung was not ventilated in order to minimize influence of CO2 rebreathing and increase in airway pressure. Airway pressure and CO2 values were measured in lower airways and in tracheal space.
RESULTS:
CO2 was decreased by NHF in lower airways and in tracheal space. Changes in CO2 were flow dependent. There was also an increase in airway pressure in these settings.
CONCLUSIONS:
NHF is able to decrease CO2 in lower airways in a flow-dependent manner. This effect is independent of an increase in airway pressure and CO2-rebreathing. So wash-out is an important reason for efficiency of NHF in decreasing hypercapnia.
Added 3/1/18
The Utility of the C-MAC as a Direct Laryngoscope for Intubation in the Emergency Department.
Sakles JC, Mosier JM, Patanwala AE, Arcaris B, Dicken JM. J Emerg Med. 2016 Oct;51(4):349-357
Abstract
BACKGROUND:
Although the C-MAC (Karl Storz, Tuttlingen, Germany) is a video laryngoscope (VL), it can also be used as a direct laryngoscope (DL).
OBJECTIVE:
The goal of this study was to evaluate the utility of the C-MAC as a DL for intubations in the emergency department (ED).
METHODS:
This was an analysis of prospectively collected continuous quality-improvement data during the 6-year period from February 1, 2009 to January 31, 2015, when both the C-MAC and Macintosh DL (Mac DL) were clinically available in our ED. This analysis included adult patients who underwent rapid sequence intubation by an emergency medicine resident in the ED with a C-MAC initially used as a DL or a Mac DL. The primary outcome measure was the first pass success (FPS).
RESULTS:
When the C-MAC was used as a DL, the initial DL attempt was successful in 199 of 346 (57.6%) cases. When the attempt could not be completed using the C-MAC as a DL, the operator utilized the video monitor and successfully completed the intubation using VL in 104 of 134 (77.6%) cases, thus achieving an overall FPS of 303 of 346 (87.6%). When the Mac DL was used, the FPS was 505 of 671 (75.3%).
CONCLUSIONS:
The C-MAC is a useful device for DL because in the event of a failed DL attempt, operators have the option of switching to the video monitor to successfully complete the intubation using VL without having to make a second attempt.
Capnography versus standard monitoring for emergency department procedural sedation and analgesia.
Wall BF, Magee K, Campbell SG, Zed PJ.Cochrane Database Syst Rev. 2017 Mar 23;3:CD010698. dAuthor information
BACKGROUND:
Procedural sedation and analgesia (PSA) is used frequently in the emergency department (ED) to facilitate painful procedures and interventions. Capnography, a monitoring modality widely used in operating room and endoscopy suite settings, is being used more frequently in the ED setting with the goal of reducing cardiopulmonary adverse events. As opposed to settings outside the ED, there is currently no consensus on whether the addition of capnography to standard monitoring modalities reduces adverse events in the ED setting.
OBJECTIVES:
To assess whether capnography in addition to standard monitoring (pulse oximetry, blood pressure and cardiac monitoring) is more effective than standard monitoring alone to prevent cardiorespiratory adverse events (e.g. oxygen desaturation, hypotension, emesis, and pulmonary aspiration) in ED patients undergoing PSA.
SEARCH METHODS:
We searched the Cochrane Central Register of Controlled Trials (2016, Issue 8), and MEDLINE, Embase, and CINAHL to 9 August 2016 for randomized controlled trials (RCTs) and quasi-randomized trials of ED patients requiring PSA with no language restrictions. We searched meta-registries (www.controlled-trials.com, www.clinicalstudyresults.org, and clinicaltrials.gov) for ongoing trials (February 2016). We contacted the primary authors of included studies as well as scientific advisors of capnographydevice manufacturers to identify unpublished studies (February 2016). We handsearched conference abstracts of four organizations from 2010 to 2015.
SELECTION CRITERIA:
We included any RCT or quasi-randomized trial comparing capnography and standard monitoring to standardmonitoring alone for ED patients requiring PSA.
DATA COLLECTION AND ANALYSIS:
Two authors independently performed study selection, data extraction, and assessment of methodological quality for the 'Risk of bias' tables. An independent researcher extracted data for any included studies that our authors were involved in. We contacted authors of included studies for incomplete data when applicable. We used Review Manager 5 to combine data and calculate risk ratios (RR) and 95% confidence intervals (CI) using both random-effects and fixed-effect models.
MAIN RESULTS:
We identified three trials (κ = 1.00) involving 1272 participants. Comparing the capnography group to the standardmonitoring group, there were no differences in the rates of oxygen desaturation (RR 0.89, 95% CI 0.48 to 1.63; n = 1272, 3 trials; moderate quality evidence) and hypotension (RR 2.36, 95% CI 0.98 to 5.69; n = 986, 1 trial; moderate quality evidence). There was only one episode of emesis recorded without significant difference between the groups (RR 3.10, 95% CI 0.13 to 75.88, n = 986, 1 trial; moderate quality evidence). The quality of evidence for the primary outcomes was moderate with downgrades primarily due to heterogeneity and reporting bias.There were no differences in the rate of airway interventions performed (RR 1.26, 95% CI 0.94 to 1.69; n = 1272, 3 trials; moderate quality evidence). In the subgroup analysis, we found a higher rate of airway interventions for adults in the capnography group (RR 1.44, 95% CI 1.16 to 1.79; n = 1118, 2 trials; moderate quality evidence) with a number needed to treat for an additional harmful outcome of 12. Although statistical heterogeneity was reduced, there was moderate quality of evidence due to outcome definition heterogeneity and limited reporting bias. None of the studies reported recovery time.
AUTHORS' CONCLUSIONS:
There is a lack of convincing evidence that the addition of capnography to standard monitoring in ED PSA reduces the rate of clinically significant adverse events. Evidence was deemed to be of moderate quality due to population and outcome definition heterogeneity and limited reporting bias. Our review was limited by the small number of clinical trials in this setting.
Added 2/5/18
Comparison Between Direct and Video-assisted Laryngoscopy for Intubations in a Pediatric Emergency Department.
Eisenberg MA, Green-Hopkins I, Werner H, Nagler J
Acad Emerg Med. 2016 Aug;23(8):870-7.
OBJECTIVES:
The objective was to compare video-assisted laryngoscopy (VAL) to direct laryngoscopy (DL) on success rate and complication rate of intubations performed in a pediatric emergency department (ED).
METHODS:
This is a retrospective cohort study of attempted intubations of children aged 0-18 years in a pediatric ED between 2004 and 2014 with first attempt by an ED provider. In VAL, the laryngoscopist attempts direct visualization of the glottis with a C-MAC video laryngoscope while the video monitor is used for real-time guidance by a supervisor, back-up visualization for the laryngoscopist should the direct view be inadequate, and confirmation of endotracheal tube passage through the vocal cords. We performed univariate comparisons of intubations using DL to intubations using VAL on rates of first-pass success, complications, and whether the patient was successfully intubated by an ED provider. We then created a logistic regression model to adjust for provider experience level, difficult airway characteristics, and indications for intubation to compare intubations using DL to intubations using VAL for each outcome.
RESULTS:
We identified 452 endotracheal intubations of 422 unique patients, of which 445 intubations had a first attempt by an ED provider. Six intubations were excluded due to insufficient information available in the record. Of the included intubations, 240 (55%) were attempted with DL and 199 (45%) with VAL. The overall first-pass success rate was 71% in the DL group and 72% in the VAL group. After adjustment for covariates, the first-pass success rate was similar between laryngoscopy approaches (adjusted odds ratio = 1.23, 95% confidence interval = 0.78 to 1.94).
CONCLUSIONS:
We found no difference between DL and VAL with regard to first-pass intubation success rate, complication rate, or rate of successful intubation by ED providers for children undergoing intubation in a pediatric ED.
Added 1/11/18
Effect of video laryngoscopy on trauma patient survival: a randomized controlled trial.
Yeatts DJ, Dutton RP, Hu PF, Chang YW, Brown CH, Chen H, Grissom TE, Kufera JA, Scalea TM.
Many resuscitation scenarios include the use of emergency intubation to support injured patients. New video-guided airway management technology is available, which may minimize the risk to patients from this procedure.
METHODS:
This was a controlled clinical trial conducted in the trauma receiving unit in a university-affiliated urban hospital in which 623 consecutive adult patients requiring emergency airway management were prospectively randomized to intubation with either the direct laryngoscope (DL) or the GlideScope video laryngoscope (GVL) device.
RESULTS:
The primary outcome was survival to hospital discharge. There was no significant difference in mortality between the GVL group (28 [9%] of 303) and the DL group (24 [8%] of 320) (p = 0.43) for all patients. Within a smaller cohort identified retrospectively, there was a higher mortality rate seen in the subgroup of patients with severe head injuries (head Abbreviated Injury Scale [AIS] score > 3) who were randomized to intubation with GVL (22 [30%] of 73) versus DL (16 [14%] of 112) (p = 0.047). Among all patients, median intubation duration in seconds was significantly higher for the GVL group (median, 56; interquartile range, 40-81) than for the DL group (median, 40; interquartile range, 24-68) (p < 0.001). Among those with severe head injuries, median intubation duration in seconds was also significantly higher for the GVL group (median, 74) than for the DL group (median, 65) (p < 0.003). Correspondingly, this group also experienced a greater incidence of low oxygen saturations of 80% or less (27 [50%] of 54 for the GVL group and 15 [24%] of 63 for the DL group; p = 0.004). There were no significant differences between the two groups in first-pass success (80% for GVL and 81% for DL, p = 0.46).
CONCLUSION:
Use of the GlideScope did not influence survival to hospital discharge among all patients and was associated with longer intubation times than direct laryngoscopy. Among the video laryngoscope cohort, a smaller subgroup of severe head injury trauma patients identified retrospectively seemed to be associated with a greater incidence of hypoxia of 80% or less and mortality.
Added 1/5/18
Effect of video laryngoscopy on trauma patient survival: a randomized controlled trial.
Yeatts DJ1, Dutton RP, Hu PF, Chang YW, Brown CH, Chen H, Grissom TE, Kufera JA, Scalea TM.
J Trauma Acute Care Surg. 2013 Aug;75(2):212-9. doi: 10.1097/TA.0b013e318293103d.
BACKGROUND:
Many resuscitation scenarios include the use of emergency intubation to support injured patients. New video-guided airway management technology is available, which may minimize the risk to patients from this procedure.
METHODS:
This was a controlled clinical trial conducted in the trauma receiving unit in a university-affiliated urban hospital in which 623 consecutive adult patients requiring emergency airway management were prospectively randomized to intubation with either the direct laryngoscope (DL) or the GlideScope video laryngoscope (GVL) device.
RESULTS:
The primary outcome was survival to hospital discharge. There was no significant difference in mortality between the GVL group (28 [9%] of 303) and the DL group (24 [8%] of 320) (p = 0.43) for all patients. Within a smaller cohort identified retrospectively, there was a higher mortality rate seen in the subgroup of patients with severe head injuries (head Abbreviated Injury Scale [AIS] score > 3) who were randomized to intubation with GVL (22 [30%] of 73) versus DL (16 [14%] of 112) (p = 0.047). Among all patients, median intubation duration in seconds was significantly higher for the GVL group (median, 56; interquartile range, 40-81) than for the DL group (median, 40; interquartile range, 24-68) (p < 0.001). Among those with severe head injuries, median intubation duration in seconds was also significantly higher for the GVL group (median, 74) than for the DL group (median, 65) (p < 0.003). Correspondingly, this group also experienced a greater incidence of low oxygen saturations of 80% or less (27 [50%] of 54 for the GVL group and 15 [24%] of 63 for the DL group; p = 0.004). There were no significant differences between the two groups in first-pass success (80% for GVL and 81% for DL, p = 0.46).
CONCLUSION:
Use of the GlideScope did not influence survival to hospital discharge among all patients and was associated with longer intubation times than direct laryngoscopy. Among the video laryngoscope cohort, a smaller subgroup of severe head injury trauma patients identified retrospectively seemed to be associated with a greater incidence of hypoxia of 80% or less and mortality.
Added 12/13/17
Morbidity and mortality in children undergoing bronchoscopy for foreign body removal.
Roberts CA, Carr MM. Laryngoscope. 2017 Aug 17.
Abstract
OBJECTIVES/HYPOTHESIS:
Analyze morbidity and mortality among children undergoing bronchoscopy for foreign body removal.
STUDY DESIGN:
Multicenter retrospective review using the American College of Surgeons Pediatric National Surgical Quality Improvement Program from 2014 and 2015.
METHODS:
Patients were identified using Current Procedural Terminology code 31635. Demographics, time to surgery, operative times, hospitalization time, and complications were collected. Multivariate logistic regression was used to identify predictive factors for major adverse events.
RESULTS:
Three hundred thirty-four patients were included (mean age 3.7 years, 59.0% male). Preoperative sepsis syndrome was present in 5.7% of patients and 8.1% had asthma. Of the patients, 5.1% percent of patients had a tracheostomy. Bronchoscopy was performed by an otolaryngologist (65.4%) or a pediatric surgeon (33.1%). Mean operative time was 27.4 minutes, whereas mean total operating room time was 54.6 minutes. Airway foreign bodies were located in 269 patients (80.5%), with 62.5% being located in the mainstem bronchus. Operative time was longer when foreign bodies were in the mainstem bronchus or distal to it. Mean time to surgery from admission was 0 days, and mean duration of hospitalization was 1 day. One patient (0.3%) required reoperation for respiratory reasons, and three (0.9%) required readmission for related reasons. No patients remained hospitalized at 30 days. Two (0.6%) had a postoperative pneumonia, and two (0.6%) required reintubation. One patient death (0.3%) occurred within 2 weeks of bronchoscopy. No significant differences were identified in operative time, time to surgery, or hospitalization time based on age, gender, presence of a tracheostomy, or surgical specialty.
CONCLUSIONS:
Bronchoscopy for identification and removal of airway foreign bodies had minimal morbidity in this group.
Added 12/4/17
The Impact of a Soiled Airway on Intubation Success in the Emergency Department When Using the GlideScope or the Direct Laryngoscope.
Sakles JC, Corn GJ, Hollinger P, Arcaris B, Patanwala AE, Mosier JM1. Acad Emerg Med. 2017 May;24(5):628-636. doi: 10.1111/acem.13160. Epub 2017 Mar 17.
BACKGROUND:
The objective was to determine the impact of a soiled airway on firstpass success when using the GlideScope video laryngoscope or the direct laryngoscope for intubation in the emergency department (ED).
METHODS:
Data were prospectively collected on all patients intubated in an academic ED from July 1, 2007, to June 30, 2016. Patients ≥ 18 years of age, who underwent rapid sequence intubation by an emergency medicine resident with the GlideScope or the direct laryngoscope, were included in the analysis. Data were stratified by device used (GlideScope or direct laryngoscope). The primary outcome was firstpass success. Patients were categorized as those without blood or vomitus (CLEAN) and those with blood or vomitus (SOILED) in their airway. Multivariate regression models were developed to control for confounders.
RESULTS:
When using the GlideScope, the firstpass success was lower in the SOILED group (249/306; 81.4%) than the in CLEAN group (586/644, 91.0%; difference = 9.6%; 95% confidence interval [CI] = 4.7%-14.5%). Similarly, when using the direct laryngoscope, the firstpass success was lower in the SOILED group (186/284, 65.5%) than in the CLEAN group (569/751, 75.8%; difference = 10.3%; 95% CI = 4.0%-16.6%). The SOILED airway was associated with a decreased firstpass success in both the GlideScope cohort (adjusted odds ratio [aOR] = 0.4; 95% CI = 0.3-0.7) and the direct laryngoscope cohort (aOR = 0.6; 95% CI = 0.5-0.8).
CONCLUSION:
Soiling of the airway was associated with a reduced firstpass success during emergency intubation, and this reduction occurred to a similar degree whether using either the GlideScope or the direct laryngoscope
Predictors of complicated airway foreign body extraction.
Sjogren PP, Mills TJ, Pollak AD, Muntz HR, Meier JD1, Grimmer JF.
Laryngoscope. 2017 Aug 16. doi: 10.1002/lary.26814. [Epub ahead of print]
OBJECTIVES:
To evaluate outcomes of foreign body aspiration (FBA) and to investigate surgeon and hospital volume as risk factors for a complicated course.
METHODS:
Children with FBA in a multihospital network were identified from January 2005 to September 2015. Demographic information, surgeon, and hospital location were reviewed. Mean operative time and hospital length of stay were recorded. Cases requiring intensive care unit admission, hospital stay greater than 24 hours, need for more than one bronchoscopy, operative time greater than 1 hour, or death were considered "complicated."
RESULTS:
A total of 450 cases of airway foreign body extraction were performed. Patient ages ranged from 0.6 to 18.8 years, with a median age of 1.9 years. Bronchoscopy with foreign body extraction was performed by 55 different surgeons at 11 different facilities. There were one to 24 surgeons for each facility, with an average number of 5.4 surgeons per facility. A total of 88 (19.6%) cases were considered complicated, including five (1.1%) deaths. Increased rates of complications were seen with unwitnessed aspiration (P = 0.008) and hyperlucency (P < 0.001) or infiltrates (P = 0.001) on chest radiographs. No significant association was found between surgeon type or facility as related to a complicated case.
CONCLUSIONS:
Unwitnessed aspiration events and abnormalities on chest radiograph may be associated with a more complicatedcourse in children with FBA. This multihospital study identified a low number of procedures by many surgeons; however, surgeon and hospital volume did not significantly correlate with higher complication rates.
Added 11/15/17
The Impact of a Soiled Airway on Intubation Success in the Emergency Department When Using the GlideScope or the Direct Laryngoscope.
Sakles JC1, Corn GJ, Hollinger P, Arcaris B, Patanwala AE, Mosier JM1. Acad Emerg Med. 2017 May;24(5):628-636.
BACKGROUND:
The objective was to determine the impact of a soiled airway on firstpass success when using the GlideScope video laryngoscope or the direct laryngoscope for intubation in the emergency department (ED).
METHODS:
Data were prospectively collected on all patients intubated in an academic ED from July 1, 2007, to June 30, 2016. Patients ≥ 18 years of age, who underwent rapid sequence intubation by an emergency medicine resident with the GlideScope or the direct laryngoscope, were included in the analysis. Data were stratified by device used (GlideScope or direct laryngoscope). The primary outcome was firstpass success. Patients were categorized as those without blood or vomitus (CLEAN) and those with blood or vomitus (SOILED) in their airway. Multivariate regression models were developed to control for confounders.
RESULTS:
When using the GlideScope, the firstpass success was lower in the SOILED group (249/306; 81.4%) than the in CLEAN group (586/644, 91.0%; difference = 9.6%; 95% confidence interval [CI] = 4.7%-14.5%). Similarly, when using the direct laryngoscope, the firstpass success was lower in the SOILED group (186/284, 65.5%) than in the CLEAN group (569/751, 75.8%; difference = 10.3%; 95% CI = 4.0%-16.6%). The SOILED airway was associated with a decreased firstpass success in both the GlideScope cohort (adjusted odds ratio [aOR] = 0.4; 95% CI = 0.3-0.7) and the direct laryngoscope cohort (aOR = 0.6; 95% CI = 0.5-0.8).
CONCLUSION:
Soiling of the airway was associated with a reduced firstpass success during emergency intubation, and this reduction occurred to a similar degree whether using either the GlideScope or the direct laryngoscope.
Added 11/5/17
Difficult Airway Characteristics Associated with First-Attempt Failure at Intubation Using Video Laryngoscopy in the Intensive Care Unit.
Joshi R, Hypes CD, Greenberg J, Snyder L, Malo J, Bloom JW, Chopra H, Sakles JC, Mosier JM.
Ann Am Thorac Soc. 2017 Mar;14(3):368-375. doi: 10.1513/AnnalsATS.201606-472OC.
Video laryngoscopy has overcome the need to align the anatomic axes to obtain a view of the glottic opening to place a tracheal tube. However, despite this advantage, a large number of attempts are unsuccessful. There are no existing data on anatomic characteristics in critically ill patients associated with a failed first attempt at laryngoscopy when using video laryngoscopy.
OBJECTIVES:
To identify characteristics associated with first-attempt failure at intubation when using video laryngoscopy in the intensive care unit (ICU).
METHODS:
This is an observational study of 906 consecutive patients intubated in the ICU with a video laryngoscope between January 2012 and January 2016 in a single-center academic medical ICU. After each intubation, the operator completed a data collection form, which included information on difficult airway characteristics, device used, and outcome of each attempt. Multivariable regression models were constructed to determine the difficult airway characteristics associated with a failed first attempt at intubation.
MEASUREMENTS AND MAIN RESULTS:
There were no significant differences in sex, age, reason for intubation, or device used between first-attempt failures and first-attempt successes. First-attempt successes more commonly reported no difficult airway characteristics were present (23.9%; 95% confidence interval [CI], 20.7-27.0% vs. 13.3%; 95% CI, 8.0-18.8%). In logistic regression analysis of the entire 906-patient database, blood in the airway (odds ratio [OR], 2.63; 95% CI, 1.64-4.20), airway edema (OR, 2.85; 95% CI, 1.48-5.45), and obesity (OR, 1.59; 95% CI, 1.08-2.32) were significantly associated with first-attempt failure. Data collection on limited mouth opening and secretions began after the first 133 intubations, and we fit a second logistic model to examine cases in which these additional difficult airway characteristics were collected. In this subset (n = 773), the presence of blood (OR, 2.73; 95% CI, 1.60-4.64), cervical immobility (OR, 3.34; 95% CI, 1.28-8.72), and airway edema (OR, 3.10; 95% CI, 1.42-6.70) were associated with first-attempt failure.
CONCLUSIONS:
In this single-center study, presence of blood in the airway, airway edema, cervical immobility, and obesity are associated with higher odds of first-attempt failure, when intubation was performed with video laryngoscopy in an ICU.
Added 10/14/17
Management of Patients with Predicted Difficult Airways in an Academic Emergency Department.
Sakles JC, Douglas MJK, Hypes CD, Patanwala AE, Mosier JM. J Emerg Med. 2017 Aug;53(2):163-171
Abstract
BACKGROUND:
Patients with difficult airways are sometimes encountered in the emergency department (ED), however, there is a little data available regarding their management.
OBJECTIVES:
To determine the incidence, management, and outcomes of patients with predicted difficult airways in the ED.
METHODS:
Over the 1-year period from July 1, 2015 to June 30, 2016, data were prospectively collected on all patients intubated in an academic ED. After each intubation, the operator completed an airway management data form. Operators performed a pre-intubation difficult airway assessment and classified patients into routine, challenging, or difficult airways. All non-arrest patients were included in the study.
RESULTS:
There were 456 patients that met inclusion criteria. Fifty (11%) had predicted difficult airways. In these 50 patients, neuromuscular blocking agents (NMBAs) were used in 40 (80%), an awake intubation technique with light sedation was used in 7 (14%), and no medications were used in 3 (6%). In the 40 difficult airway patients who underwent NMBA facilitated intubation, a video laryngoscope (GlideScope 21, Verathon, Bothell, WA and C-MAC 19, Karl Storz, Tuttlingen, Germany) was used in each of these, with a first-pass success of 90%. In the 7 patients who underwent awake intubation, a video laryngoscope was used in 5, and a flexible fiberoptic scope was used in 2. Ketamine was used in 6 of the awake intubations. None of these difficult airway patients required rescue with a surgical airway.
CONCLUSIONS:
Difficult airways were predicted in 11% of non-arrest patients requiring intubation in the ED, the majority of which were managed using an NMBA and a video laryngoscope with a high first-pass success.
Added 9/30/17
Comparison Between Direct and Video-assisted Laryngoscopy for Intubations in a PediatricEmergency Department.
Eisenberg MA, Green-Hopkins I, Werner H, Nagler J. Acad Emerg Med. 2016 Aug;23(8):870-7.
Abstract
OBJECTIVES:
The objective was to compare video-assisted laryngoscopy (VAL) to direct laryngoscopy (DL) on success rate and complication rate of intubations performed in a pediatric emergency department (ED).
METHODS:
This is a retrospective cohort study of attempted intubations of children aged 0-18 years in a pediatric ED between 2004 and 2014 with first attempt by an ED provider. In VAL, the laryngoscopist attempts direct visualization of the glottis with a C-MAC video laryngoscope while the video monitor is used for real-time guidance by a supervisor, back-up visualization for the laryngoscopist should the direct view be inadequate, and confirmation of endotracheal tube passage through the vocal cords. We performed univariate comparisons of intubations using DL to intubations using VAL on rates of first-pass success, complications, and whether the patient was successfully intubated by an ED provider. We then created a logistic regression model to adjust for provider experience level, difficult airway characteristics, and indications for intubation to compare intubations using DL to intubations using VAL for each outcome.
RESULTS:
We identified 452 endotracheal intubations of 422 unique patients, of which 445 intubations had a first attempt by an ED provider. Six intubations were excluded due to insufficient information available in the record. Of the included intubations, 240 (55%) were attempted with DL and 199 (45%) with VAL. The overall first-pass success rate was 71% in the DL group and 72% in the VAL group. After adjustment for covariates, the first-pass success rate was similar between laryngoscopy approaches (adjusted odds ratio = 1.23, 95% confidence interval = 0.78 to 1.94).
CONCLUSIONS:
We found no difference between DL and VAL with regard to first-pass intubation success rate, complication rate, or rate of successful intubation by ED providers for children undergoing intubation in a pediatric ED.
Added 9/21/17
Apneic oxygenation is associated with a reduction in the incidence of hypoxemia during the RSI of patients with intracranial hemorrhage in the emergency department.
Abstract
Critically ill patients undergoing emergent intubation are at risk of oxygen desaturation during the management of their airway. Patients with intracranial hemorrhage (ICH) are particularly susceptible to the detrimental effects of hypoxemia. Apneic oxygenation (AP OX) may be able to reduce the occurrence of oxygen desaturation during the emergent intubation of these patients. We sought to assess the effect AP OX on oxygen desaturation during the rapid sequence intubation (RSI) of patients with ICH in the emergency department (ED). We prospectively collected data on all patients intubated in an urban academic ED over the 2-year period from July 1, 2013 to June 30, 2015. Following each intubation, the operator completed a standardized continuous quality improvement (CQI) data form, which included information on patient, operator and intubation characteristics. Operators recorded data on the use of AP OX, the oxygen flow rate used for AP OX, and the starting and lowest saturations during intubation. Adult patients with ICH who underwent RSI by emergency medicine (EM) residents were included in the analyses. The primary outcome variable was any oxygen saturation <90 % during the intubation. We performed a backward stepwise multivariate logistic regression analysis to identify variables associated with oxygen desaturation. The primary independent variable of interest was the use of AP OX during the intubation. Inclusion criteria for the study was met by 127 patients. AP OX was used in 72 patients (AP OX group) and was not used in 55 patients (NO AP OX group). The incidence of desaturation was 5/72 (7 %) in the AP OX group and was 16/55 (29 %) in the NO AP OX group. In the multivariate logistic regression analysis the use of AP OX was associated with a reduced odds of desaturation (aOR 0.13; 95 % CI 0.03-0.53). Patients with ICH who received AP OX during RSI in the ED were seven times less likely to have an oxygen saturation of <90 % during the intubation compared to patients who did not receive AP OX. AP OX is a simple intervention that may minimize the risk of oxygen desaturation during the RSI of patients with ICH.
Added 8/23/27
Management of Patients with Predicted Difficult Airways in an Academic Emergency Department.
Sakles JC, Douglas MJK, Hypes CD, Patanwala AE, Mosier JM
J Emerg Med. 2017 Aug;53(2):163-171. doi: 10.1016/j.jemermed.2017.04.003. Epub 2017 Jun 9.
Abstract
BACKGROUND:
Patients with difficult airways are sometimes encountered in the emergency department (ED), however, there is a little data available regarding their management.
OBJECTIVES:
To determine the incidence, management, and outcomes of patients with predicted difficult airways in the ED.
METHODS:
Over the 1-year period from July 1, 2015 to June 30, 2016, data were prospectively collected on all patients intubated in an academic ED. After each intubation, the operator completed an airway management data form. Operators performed a pre-intubation difficult airway assessment and classified patients into routine, challenging, or difficult airways. All non-arrest patients were included in the study.
RESULTS:
There were 456 patients that met inclusion criteria. Fifty (11%) had predicted difficult airways. In these 50 patients, neuromuscular blocking agents (NMBAs) were used in 40 (80%), an awake intubation technique with light sedation was used in 7 (14%), and no medications were used in 3 (6%). In the 40 difficult airway patients who underwent NMBA facilitated intubation, a video laryngoscope (GlideScope 21, Verathon, Bothell, WA and C-MAC 19, Karl Storz, Tuttlingen, Germany) was used in each of these, with a first-pass success of 90%. In the 7 patients who underwent awake intubation, a video laryngoscope was used in 5, and a flexible fiberoptic scope was used in 2. Ketamine was used in 6 of the awake intubations. None of these difficult airway patients required rescue with a surgical airway.
CONCLUSIONS:
Difficult airways were predicted in 11% of non-arrest patients requiring intubation in the ED, the majority of which were managed using an NMBA and a video laryngoscope with a high first-pass success.
Added 8/4/17
Surgical Management of Supraglottic Stenosis Using Intubationless Optiflow.
Tam K, Jeffery C, Sung CK.
Ann Otol Rhinol Laryngol. 2017 Aug 1
Abstract
OBJECTIVE:
Airway management during endoscopic surgical treatment of supraglottic and pharyngeal stenosis is often challenging and can be accomplished by various means, including tracheostomy, jet ventilation, or direct laryngoscopy. We describe CO2 laser excision of supraglottic-pharyngeal stenosis using intubationless Optiflow high-flow nasal cannula (HFNC).
METHODS:
A 55-year-old male presented with dyspnea and dysphagia secondary to severe supraglottic-pharyngeal stenosis in the setting of previous chemoradiation for a T0N2aM0 squamous cell carcinoma. Laryngoscopy revealed severe supraglottic-pharyngeal stenosis with tethering of the epiglottis to the lateral pharyngeal walls. Optiflow HFNC was used to deliver 70 L/min of oxygen. After anesthetic induction, CO2 laser microlaryngoscopy was utilized to release scar tissue along the lateral epiglottic border, opening up the supraglottic airway sufficiently for endotracheal intubation and further laser resection.
RESULTS:
Airway management with Optiflow HFNC allowed initial endoscopic surgical access, partial stenotic release, and intubation. From anesthetic induction to intubation, the patient remained apneic for 26 minutes. The patient's stenosis was successfully addressed, and 10-month follow-up demonstrated stable patency of the airway.
CONCLUSION:
Optiflow is an important new tool in the management of severe supraglottic stenosis. It provides sufficient oxygenation to perform extended apneic surgery and improves endoscopic surgical access in a limited airway.
KEYWORDS:
high flow nasal cannula; laryngeal stenosis; laryngology; laryngotracheal stenosis; miscellaneous; optiflow; otolaryngology; pre-oxygenation; supraglottic stenosis
Added 7/21/17
The use of Transnasal Humidified Rapid-Insufflation Ventilatory Exchange (THRIVE) in 17 cases of subglottic stenosis.
To K, Harding F, Scott M, Milligan P, Nixon IJ, Adamson R, McNarry AF
Clin Otolaryngol. 2017 Jun 21
Shared airway management in patients with subglottic stenosis (SGS) is challenging for both the anaesthetist and surgeon. Various methods of airway management have been described but currently no gold standard exists. Jet ventilation has been described as the preferred technique despite a UK National Survey highlighting potential complications including pneumothorax, pneumomediastinum, surgical emphysema, hypoxia and death. This article is protected by copyright.
Added 5/16/17
Safety and Efficacy of Dexmedetomidine as a Sedative Agent for Performing Awake Intubation: A Meta-analysis.
Zhou LJ1, Fang XZ, Gao J, Zhangm Y, Tao LJ Am J Ther. 2016 Nov/Dec;23(6):e1788-e1800.
Abstract
To compare the efficacy and safety of dexmedetomidine with other alternative sedative agents used for performing awake intubation. We conducted a meta-analysis of randomized controlled trials (RCTs) that compared the effects of dexmedetomidine with other alternative sedative agents used during awake intubation. The biomedical databases PubMed, Science Direct, and the Cochrane Library were searched for relevant RCTs with no restriction on the language of publication. The efficacy (level of sedation, success rate for intubation at the first attempt, intubation time, intubation conditions, and patient satisfaction) and safety (incidence of hypertension, hypotension, tachycardia, bradycardia, hypoxia, postsurgical memory, hoarseness, and sore throat) were assessed. Thirteen RCTs with a combined subject population of 591 patients came within the purview of this meta-analysis. Use of dexmedetomidine was associated with a higher Ramsay sedation scale score [mean difference (MD): 1.02, 95% confidence interval (CI), 0.77-1.28, P < 0.00001], vocal cord movement score (MD = 0.72, 95% CI, 0.20-1.24, P = 0.007), coughing scores (MD = 0.66, 95% CI, 0.10-1.22, P = 0.02), limb movement scores (MD = 0.69, 95% CI, 0.47-0.91, P < 0.00001); increased risk of bradycardia [relative risk (RR): 3.03, 95% CI, 1.38-6.68, P = 0.006] and hypotension (RR: 2.87, 95% CI, 1.44-5.75, P = 0.003); and lower risk of hypoxia (RR: 0.32, 95% CI, 0.15-0.70; P = 0.004) and postsurgical memory (RR: 0.50, 95% CI, 0.35-0.72, P = 0.0002). As indicated by our results, dexmedetomidine appears to be an effective and well-tolerated agent for performing awake intubation. Its use was associated with better intubation conditions, preservation of airway patency, and reduced recall of intubation, as compared with the traditional sedative agents. The risk of bradycardia and hypotension was significantly higher with dexmedetomidine as compared with that with other sedatives. However, these were easily managed with atropine and vasoactive agents.
Added 5/9/17
Incidence and risk factors for early postoperative reintubations
Tillquist MN, Gabriel RA, Dutton RP, Urman RD. J Clin Anesth. 2016 Jun;31:80-9
STUDY OBJECTIVE:
Reintubations are associated with significantly increased morbidity and mortality, increased hospital length of stay, and increased cost. Our aim was to assess the national incidence and associated risk factors for unanticipated early postoperative reintubations.
DESIGN:
Using the National Anesthesia Clinical Outcomes Registry (NACOR) from 2010 to 2014, multivariate logistic regression was fitted to determine if various patient, surgical, intraoperative, or provider data were associated with unanticipated early postoperative reintubations.
SETTING:
NACOR from 2010 to 2014.
PATIENTS:
A total of 2,970,904 cases were included. Multivariate analysis controlled for patient age, sex, and American Society of Anesthesiologists (ASA) Physical Status.
INTERVENTIONS:
None.
MEASUREMENTS:
We report odds ratios (ORs) and 95% confidence intervals (CIs) for the relative odds of an association of predictor variable with reintubations.
MAIN RESULTS:
The incidence of unanticipated early postoperative reintubations from the NACOR database was 0.061%. Overall, reintubations were more likely in the extremes of age (age under 1 year had OR = 3.46, 95% confidence interval [CI] = 2.64-4.52 and age 80+ has OR = 1.80, 95% CI = 1.50-2.15 when compared with age 19-49 years), patients with ASA Physical Status 3 and 4 (OR = 4.06, 95% CI = 3.38-4.86 and OR = 8.65, 95% CI = 7.11-10.52, respectively, when compared with ASA 1), longer case duration (180-360 minutes OR = 13.87, 95% CI = 10.7-17.98 when compared with cases less than 60 minute duration), and cases that had a resident trainee present (OR = 1.22, 95% CI = 1.03-1.44 when compared with no resident present). Thoracic and vascular surgical procedures had the highest rates of reintubation when compared with general surgery (OR = 3.47, 95% CI = 2.81-4.28 and OR = 1.51, 95% CI = 1.24-1.82, respectively).
CONCLUSIONS:
A number of risk factors correlate with an increased risk of unanticipated early postoperative reintubations, including extremes of age, patients with greater medical comorbidities, longer operations, and patients undergoing thoracic procedures.
Added 5/3/17
Preoxygenation: Physiologic Basis, Benefits, and Potential Risks.
Nimmagadda U1, Salem MR, Crystal GJ.
Anesth Analg. 2017 Feb;124(2):507-517.
Added 4/26/17
Angioedema in the emergency department: a practical guide to differential diagnosis and management.
Bernstein JA, Cremonesi P, Hoffmann TK, Hollingsworth J, Int J Emerg Med. 2017 Dec;10(1):15
Angioedema is a common presentation in the emergency department (ED). Airway angioedema can be fatal; therefore, prompt diagnosis and correct treatment are vital.
OBJECTIVE OF THE REVIEW:
Based on the findings of two expert panels attended by international experts in angioedema and emergency medicine, this review aims to provide practical guidance on the diagnosis, differentiation, and management of histamine- and bradykinin-mediated angioedema in the ED.
REVIEW:
The most common pathophysiology underlying angioedema is mediated by histamine; however, ED staff must be alert for the less common bradykinin-mediated forms of angioedema. Crucially, bradykinin-mediated angioedema does not respond to the same treatment as histamine-mediated angioedema. Bradykinin-mediated angioedema can result from many causes, including hereditary defects in C1 esterase inhibitor (C1-INH), side effects of angiotensin-converting enzyme inhibitors (ACEis), or acquired deficiency in C1-INH. The increased use of ACEis in recent decades has resulted in more frequent encounters with ACEi-induced angioedema in the ED; however, surveys have shown that many ED staff may not know how to recognize or manage bradykinin-mediated angioedema, and hospitals may not have specific medications or protocols in place.
CONCLUSION:
ED physicians must be aware of the different pathophysiologic pathways that lead to angioedema in order to efficiently and effectively manage these potentially fatal conditions.
Added 4/18/17
Perioperative Complications in Obstructive Sleep Apnea Patients Undergoing Surgery: A Review of the Legal Literature.
Fouladpour N1, Jesudoss R, Bolden N, Shaman Z, Auckley D. Anesth Analg. 2016 Jan;122(1):145-51.
Abstract
BACKGROUND:
Obstructive sleep apnea (OSA) is common in patients undergoing surgery. OSA, known or suspected, has been associated with significant perioperative adverse events, including severe neurologic injury and death. This study was undertaken to assess the legal consequences associated with poor outcomes related to OSA in the perioperative setting.
METHODS:
A retrospective review of the legal literature was performed by searching 3 primary legal databases between the years 1991 and 2010 for cases involving adults with known or suspected OSA who underwent a surgical procedure associated with an adverse perioperative outcome. OSA had to be directly implicated in the outcome, and surgical mishaps (i.e., uncontrolled bleeding) were excluded. The adverse perioperative outcome had to result in a lawsuit that was then adjudicated in a court of law with a final decision rendered. Data were abstracted from each case regarding patient demographics, type of surgery, type and location of adverse event, associated anesthetic and opioid use, and legal outcome.
RESULTS:
Twenty-four cases met the inclusion criteria. The majority (83%) occurred in or after 2007. Patients were young (average age, 41.7 years), male (63%), and had a known diagnosis of OSA (96%). Ninety-two percent of cases were elective with 33.3% considered general procedures, 37.5% were ears, nose and throat procedures for the treatment of OSA, and 29.1% were considered miscellaneous interventions. Complications occurred intraoperatively (21%), in the postanesthesia care unit (33%), and on the surgical floors (46%). The most common complications were respiratory arrest in an unmonitored setting and difficulty in airway management. Immediate adverse outcomes included death (45.6%), anoxic brain injury (45.6%), and upper airway complications (8%). Overall, 71% of the patients died, with 6 of the 11 who suffered anoxic brain injury dying at an average of 113 days later. The use of opioids and general anesthetics was believed to play a role in 38% and 58% of cases, respectively. Verdicts favored the plaintiffs in 58% of cases and the defendants in 42%. In cases favoring the plaintiff, the average financial penalty was $2.5 million (±$2.3 million; range, $650,000--$7.7 million).
CONCLUSIONS:
Perioperative complications related to OSA are increasingly being reported as the central contention of malpractice suits. These cases can be associated with severe financial penalties. These data likely underestimate the actual medicolegal burden, given that most such cases are settled out of court and are not accounted for in the legal literature.
Added 4/13/17
Videolaryngoscopy versus direct laryngoscopy for adult patients requiring tracheal intubation.
Lewis SR1, Butler AR, Parker J, Cook TM, Smith AF. Cochrane Database Syst Rev. 2016 Nov 15;11:CD011136.
BACKGROUND:
Successful tracheal intubation during general anaesthesia traditionally requires a line of sight to the larynx attained by positioning the head and neck and using a laryngoscope to retract the tongue and soft tissues of the floor of the mouth. Difficulties with intubation commonly arise, and alternative laryngoscopes that use digital and/or fibreoptic technology have been designed to improve visibility when airway difficulty is predicted or encountered. Among these devices, a rigid videolaryngoscope (VLS) uses a blade to retract the soft tissues and transmits a lighted video image to a screen.
OBJECTIVES:
Our primary objective was to assess whether use of videolaryngoscopy for tracheal intubation in adults requiring general anaesthesia reduces risks of complications and failure compared with direct laryngoscopy. Our secondary aim was to assess the benefits and risks of these devices in selected population groups, such as adults with obesity and those with a known or predicted difficult airway.
SEARCH METHODS:
We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE and Embase on 10 February 2015. Our search terms were relevant to the review question and were not limited by outcomes. We carried out clinical trials register searches and forward and backward citation tracking. We reran the search on 12 January 2016; we added potential new studies of interest from the 2016 search to a list of 'Studies awaiting classification', and we will incorporate these studies into the formal review during the review update.
SELECTION CRITERIA:
We considered all randomized controlled trials and quasi-randomized studies with adult patients undergoing laryngoscopy performed with a VLS or a Macintosh laryngoscope in a clinical, emergency or out-of-hospital setting. We included parallel and cross-over study designs.
DATA COLLECTION AND ANALYSIS:
Two review authors independently assessed trial quality and extracted data, consulting a third review author to resolve disagreements. We used standard Cochrane methodological procedures, including assessment of risk of bias.
MAIN RESULTS:
We included 64 studies identified during the 2015 search that enrolled 7044 adult participants and compared a VLS of one or more designs with a Macintosh laryngoscope. We identified 38 studies awaiting classification and seven ongoing studies. Of the 64 included studies, 61 included elective surgical patients, and three were conducted in an emergency setting. Among 48 studies that included participants without a predicted difficult airway, 15 used techniques to simulate a difficult airway. Seven recruited participants with a known or predicted difficult airway, and the remaining studies did not specify or included both predicted and not predicted difficult airways. Only two studies specifically recruited obese participants. It was not possible to blind the intubator to the device, and we noted a high level of inevitable heterogeneity, given the large number of studies.Statistically significantly fewer failed intubations were reported when a VLS was used (Mantel-Haenszel (M-H) odds ratio (OR), random-effects 0.35, 95% confidence Interval (CI) 0.19 to 0.65; 38 studies; 4127 participants), and fewer failed intubations occurred when a VLS was used in participants with an anticipated difficult airway (M-H OR, random-effects 0.28, 95% CI 0.15 to 0.55; six studies; 830 participants). We graded the quality of this evidence as moderate on the basis of the GRADE system. Failed intubations were fewer when a VLS was used in participants with a simulated difficult airway (M-H OR, random-effects 0.18, 95% CI 0.04 to 0.77; nine studies; 810 participants), but groups with no predicted difficult airway provided no significant results (M-H OR, random-effects 0.61, 95% CI 0.22 to 1.67; 19 studies; 1743 participants).Eight studies reported on hypoxia, and only three of these described any events; results showed no differences between devices for this outcome (M-H OR, random-effects 0.39, 95% CI 0.10 to 1.44; 1319 participants). Similarly, few studies reported on mortality, noting no differences between devices (M-H OR, fixed-effect 1.09, 95% CI 0.65 to 1.82; two studies; 663 participants), and only one study reporting on the occurrence of respiratory complications (78 participants); we graded these three outcomes as very low quality owing to lack of data. We found no statistically significant differences between devices in the proportion of successful first attempts (M-H OR, random-effects 1.27, 95% CI 0.77 to 2.09; 36 studies; 4731 participants) nor in those needing more than one attempt. We graded the quality of this evidence as moderate. Studies reported no statistically significant differences in the incidence of sore throat in the postanaesthesia care unit (PACU) (M-H OR, random-effects 1.00 (95% CI 0.73 to 1.38); 10 studies; 1548 participants) nor at 24 hours postoperatively (M-H OR random-effects 0.54, 95% CI 0.27 to 1.07; eight studies; 844 participants); we graded the quality of this evidence as moderate. Data combined to include studies of cross-over design revealed statistically significantly fewer laryngeal or airway traumas (M-H OR, random-effects 0.68, 95% CI 0.48 to 0.96; 29 studies; 3110 participants) and fewer incidences of postoperative hoarseness (M-H OR, fixed-effect 0.57, 95% CI 0.36 to 0.88; six studies; 527 participants) when a VLS was used. A greater number of laryngoscopies performed with a VLS achieved a view of most of the glottis (M-H OR, random-effects 6.77, 95% CI 4.17 to 10.98; 22 studies; 2240 participants), fewer laryngoscopies performed with a VLS achieved no view of the glottis (M-H OR, random-effects 0.18, 95% CI 0.13 to 0.27; 22 studies; 2240 participants) and the VLS was easier to use (M-H OR, random-effects 7.13, 95% CI 3.12 to 16.31; seven studies; 568 participants).Although a large number of studies reported time required for tracheal intubation (55 studies; 6249 participants), we did not present an effects estimate for this outcome owing to the extremely high level of statistical heterogeneity (I2 = 96%).
AUTHORS' CONCLUSIONS:
Videolaryngoscopes may reduce the number of failed intubations, particularly among patients presenting with a difficult airway. They improve the glottic view and may reduce laryngeal/airway trauma. Currently, no evidence indicates that use of a VLS reduces the number of intubation attempts or the incidence of hypoxia or respiratory complications, and no evidence indicates that use of a VLS affects time required for intubation.
Added 3/22/17
Effect of Boussignac continuous positive airway pressure ventilation on Pao2 and Pao2/Fio2 ratio immediately after extubation in morbidly obese patients undergoing bariatric surgery: a randomized controlled trial.
Guimarães J, Pinho D, Nunes CS, Cavaleiro CS, Machado HS.
J Clin Anesth. 2016 Nov;34:562-70
Abstract
STUDY OBJECTIVE:Pathophysiological changes after laparoscopic Roux-en-Y gastric bypass may increase the risk of pulmonary complications in morbidly obese patients. The purpose of the study was to assess the impact of immediate postextubation use of Boussignac continuous positive airway pressure (CPAP) on arterial oxygenation in morbidly obese patients undergoing laparoscopic Roux-en-Y gastric bypass. The hypothesis is that the use of CPAP may improve oxygenation in the postoperative period when compared to Venturi mask.
DESIGN: Randomized controlled study.
SETTING: A tertiary referral hospital.
PATIENTS: Recruited morbidly obese adult patients undergoing laparoscopic Roux-en-Y gastric bypass.
INTERVENTIONS: Boussignac CPAP or Venturi mask was randomly applied immediately after extubation in the operating room and was maintained during the first 2 hours in the recovery room.
MEASUREMENTS: Pao2 and Pao2/fraction of inspired oxygen (Fio2) ratio values were measured preoperatively and at 1 (T1), 2 (T2), and 24 hours (T24) after extubation, through arterial blood samples. Secondary outcomes (spirometric parameters) were measured at the same periods. For comparison between groups, Student t test, Mann-Whitney U nonparametric test, and χ(2) test were used. Statistical significance is at P < .05.
MAIN RESULTS: Twenty-four patients were included, 12 in each group. There were no differences in preoperative evaluation. There were significant differences between groups in Pao2 and Pao2/Fio2 mean values at T1, T2, and T24, being superior in the Boussignac group. During the 24 hours postextubation, 9% of patients in the Boussignac group and 50% in the Venturi group had a Pao2 less than 60 mm Hg in at least 1 of the evaluations. After extubation, a Pao2/Fio2 ratio value less than 300 was observed in all patients in the Venturi group and in 55% in Boussignac group in at least 1 of the evaluations. There were no differences in spirometric parameters between groups at T1, T2, and T24.
CONCLUSIONS: Application of Boussignac CPAP for 2 hours after extubation improved oxygenation but did not improve forced expiratory volume at 1 second and forced vital capacity.
Added 3/3/17
Preoxygenation: Physiologic Basis, Benefits, and Potential Risks.
Nimmagadda U1, Salem MR, Crystal GJ. Anesth Analg. 2017 Feb;124(2):507-517.
Abstract
Preoxygenation before anesthetic induction and tracheal intubation is a widely accepted maneuver, designed to increase the body oxygen stores and thereby delay the onset of arterial hemoglobin desaturation during apnea. Because difficulties with ventilation and intubation are unpredictable, the need for preoxygenation is desirable in all patients. During emergence from anesthesia, residual effects of anesthetics and inadequate reversal of neuromuscular blockade can lead to hypoventilation, hypoxemia, and loss of airway patency. In accordance, routine preoxygenation before the tracheal extubation has also been recommended. The objective of this article is to discuss the physiologic basis, clinical benefits, and potential concerns about the use of preoxygenation. The effectiveness of preoxygenation is assessed by its efficacy and efficiency. Indices of efficacy include increases in the fraction of alveolar oxygen, increases in arterial oxygen tension, and decreases in the fraction of alveolar nitrogen. End points of maximal preoxygenation (efficacy) are an end-tidal oxygen concentration of 90% or an end-tidal nitrogen concentration of 5%. Efficiency of preoxygenation is reflected in the rate of decline in oxyhemoglobin desaturation during apnea. All investigations have demonstrated that maximal preoxygenationmarkedly delays arterial hemoglobin desaturation during apnea. This advantage may be blunted in high-risk patients. Various maneuvers have been introduced to extend the effect of preoxygenation. These include elevation of the head, apneic diffusion oxygenation, continuous positive airway pressure (CPAP) and/or positive end-expiratory pressure (PEEP), bilevel positive airway pressure, and transnasal humidified rapid insufflation ventilatory exchange. The benefit of apneic diffusion oxygenation is dependent on achieving maximal preoxygenation, maintaining airway patency, and the existence of a high functional residual capacity to body weight ratio. Potential risks of preoxygenation include delayed detection of esophageal intubation, absorption atelectasis, production of reactive oxygen species, and undesirable hemodynamic effects. Because the duration of preoxygenation is short, the hemodynamic effects and the accumulation of reactive oxygen species are insufficient to negate its benefits. Absorption atelectasis is a consequence of preoxygenation. Two approaches have been proposed to reduce the absorption atelectasis during preoxygenation: a modest decrease in the fraction of inspired oxygen to 0.8, and the use of recruitment maneuvers, such as CPAP, PEEP, and/or a vital capacity maneuver (all of which are commonly performed during the administration of anesthesia). Although a slight decrease in the fraction of inspired oxygen reduces atelectasis, it does so at the expense of a reduction in the protection afforded during apnea.
Added 2/28/17
Safety and Efficacy of Dexmedetomidine as a Sedative Agent for Performing Awake Intubation: A Meta-analysis.
Am J Ther. 2016 Nov/Dec;23(6):e1788-e1800.
Abstract
To compare the efficacy and safety of dexmedetomidine with other alternative sedative agents used for performing awake intubation. We conducted a meta-analysis of randomized controlled trials (RCTs) that compared the effects of dexmedetomidine with other alternative sedative agents used during awake intubation. The biomedical databases PubMed, Science Direct, and the Cochrane Library were searched for relevant RCTs with no restriction on the language of publication. The efficacy (level of sedation, success rate for intubation at the first attempt, intubation time, intubation conditions, and patient satisfaction) and safety (incidence of hypertension, hypotension, tachycardia, bradycardia, hypoxia, postsurgical memory, hoarseness, and sore throat) were assessed. Thirteen RCTs with a combined subject population of 591 patients came within the purview of this meta-analysis. Use of dexmedetomidine was associated with a higher Ramsay sedation scale score [mean difference (MD): 1.02, 95% confidence interval (CI), 0.77-1.28, P < 0.00001], vocal cord movement score (MD = 0.72, 95% CI, 0.20-1.24, P = 0.007), coughing scores (MD = 0.66, 95% CI, 0.10-1.22, P = 0.02), limb movement scores (MD = 0.69, 95% CI, 0.47-0.91, P < 0.00001); increased risk of bradycardia [relative risk (RR): 3.03, 95% CI, 1.38-6.68, P = 0.006] and hypotension (RR: 2.87, 95% CI, 1.44-5.75, P = 0.003); and lower risk of hypoxia (RR: 0.32, 95% CI, 0.15-0.70; P = 0.004) and postsurgical memory (RR: 0.50, 95% CI, 0.35-0.72, P = 0.0002). As indicated by our results, dexmedetomidine appears to be an effective and well-tolerated agent for performing awake intubation. Its use was associated with better intubation conditions, preservation of airway patency, and reduced recall of intubation, as compared with the traditional sedative agents. The risk of bradycardia and hypotension was significantly higher with dexmedetomidine as compared with that with other sedatives. However, these were easily managed with atropine and vasoactive agents.
Added 2/16/17
A comparison of videolaryngoscopes for tracheal intubation in predicted difficult airway: a feasibility study.
Vargas M, Pastore A, Aloj F, Laffey JG, Servillo G
Videolaryngoscopy has become increasingly attractive for the routine management of the difficult airway. Glidescope® is well studied in the literature while imago V-Blade® is a recent videolaryngoscope. This is a feasibility study with 1:1 case-control sequential allocation comparing Imago V-Blade ® and Glidescope® in predicted difficult airway settings.
METHODS:
Two senior anesthesiologists with no clinical experience in video assisted intubation but previously trained in a simulated scenario, performed the endotracheal intubations with Imago V-Blade® and Glidescope®. A third experienced anesthesiologist supervised the procedures. Forty-two patients, 21 for each group, with the presence of predicted difficult airway according to the Italian guideline were included. The primary end point is the feasibility of intubation. The secondary end-points are the success to intubate in the first attempt, the intubation time, the Cormack and Lehane score view, the comparison of the intubation difficulty scale (IDS) score and the need for maneuvers to aid the endotracheal intubation comparing Imago V-Blade® and Glidescope®.
RESULTS:
The intubation was achieved in 100% of cases in both groups. No differences were found in the first-attempt success rate (p = 0.383), intubation time (p = 0.280), Cormack and Lehane score view (p = 0.799) and IDS score (p = 0.252). Statistical differences were found in external laryngeal pressure (p = 0.005), advancement of the blade (p = 0.024) and use of increasing lifting force (p = 0.048).
CONCLUSIONS:
This feasibility study showed that the intubation with the newly introduced Imago V-Blade® is feasible. Further randomized and/or non-inferiority trials are needed to evaluate the benefit of Imago V-Blade® in this procedure.
Added 1/24/17
Massive Subcutaneous Emphysema and Bilateral Tension Pneumothoraces After Supplemental Oxygen Delivery via an Airway Exchange Catheter: A Case Report.
Hulst AH, Avis HJ, Hollmann MW, Stevens MF. AA Case Rep. 2017 Jan 15;8(2):26-28
A patient suffered massive subcutaneous emphysema and bilateral tension pneumothoraces after receiving supplemental oxygen through an airway exchange catheter (AEC). Complications of AEC placement include misplacement, direct injury to the larynx, bronchi or lung, barotrauma related to oxygen supplementation, and a loss of airway. We review these complications and discuss the specific risks of supplementing oxygen using an AEC. We suggest measures to limit pressure from the oxygen source and warn against advancing an AEC too far into the tracheobronchial tree.
WHR: This reports reminds us that even the best prophylactic and rescue procedures must be pursued with care. All procedures will have their own complications if not done properly.
Added AOD 12/23/16
Airway management for cervical spine surgery
Ehab Farag, Best Practice & Research Clinical Anesthesiology. Volume 30, Issue 1, March 2016, Pages 13–25
Added AOD 12/23/16
Choice of anesthesia for category-1 caesarian section in women with anticipated difficult tracheal intubation: the use of decision analysis
A.J. Krom et al. Anaesthesia 2016 (Pre-publication)
Abstract
A predicted difficult airway is sometimes considered a contra-indication to rapid sequence induction of general anaesthesia, even in an urgent case such as a category-1 caesarean section for fetal distress. However, formally assessing the risk is difficult because of the rarity and urgency of such cases. We have used decision analysis to quantify the time taken to establish anaesthesia, and probability of failure, of three possible anaesthetic methods, based on a systematic review of the literature. We considered rapid sequence induction of general anaesthesia with videolaryngoscopy, awake fibreoptic intubation and rapid spinal anaesthesia. Our results show a shorter mean (95% CI) time to induction of 100 (87-114) s using rapid sequence induction compared with 9 (7-11) min for awake fibreoptic intubation (p < 0.0001) and 6.3 (5.4-7.2) min for spinal anaesthesia (p < 0.0001). We calculate the risk of ultimate failed airway control after rapid sequence induction to be 21 (0-53) per 100,000 cases, and postulate that some mothers may accept such a risk in order to reduce potential fetal harm from an extended time interval until delivery. Although rapid sequence induction may not be the anaesthetic technique of choice for all cases in the circumstance of a category-1 caesarean section for fetal distress with a predicted difficult airway, we suggest that it is an acceptable option.
Added AOD 11/21/16
A cadaver study comparing three fibreoptic-assisted techniques for converting a supraglottic airway to a cuffed tracheal tube.
Olesnicky BL, Rehak A, Bestic WB, Brock JT, Patterson L. Anaesthesia. 2016 Nov 11. doi: 10.1111/anae.13733. [Epub ahead of print]
Abstract
After rescuing an airway with a supraglottic airway device, a method to convert it to a cuffed tracheal tube is often needed. The best method to do this has never been directly studied. We compared three techniques for conversion of a standard LMA® Unique airway to a cuffed endotracheal tube using a fibrescope. The primary endpoint was time to intubation, with secondary endpoints of success rate, perceived difficulty and preferred technique. We also investigated the relationship between level of training and prior training and experience with the techniques on the primary outcome. The mean (95% CI) time to intubation using a direct tracheal tube technique of 37 (31-42) s was significantly shorter than either the Aintree intubation catheter technique at 70 (60-80) s, or a guidewire technique at 126 (110-141) s (p < 0.001). Most (13/24) participants rated the tracheal tube as their preferred technique, while 11/24 preferred the Aintree technique. In terms of perceived difficulty, 23/24, 21/24 and 9/24 participants rated the tracheal tube technique, Aintree technique and guidewire technique, respectively, as either very easy or easy. There was no relationship between prior training, prior experience or level of training on time to completion of any of the techniques. We conclude the tracheal tube and Aintree techniques both provide a rapid and easy method for conversion of a supraglottic airway device to a cuffed tracheal tube. The guidewire technique cannot be recommended.
Added AOD 11/8/16
Mask Ventilation during Induction of General Anesthesia: Influences of Obstructive Sleep Apnea.
Sato S1, Hasegawa M, Okuyama M, Okazaki J, Kitamura Y, Sato Y, Ishikawa T, Sato Y, Isono S. Anesthesiology. 2016 Nov 2. [Epub ahead of print]
Abstract
BACKGROUND:
Depending on upper airway patency during anesthesia induction, tidal volume achieved by mask ventilation may vary. In 80 adult patients undergoing general anesthesia, the authors tested a hypothesis that tidal volume during mask ventilation is smaller in patients with sleep-disordered breathing priorly defined as apnea hypopnea index greater than 5 per hour.
METHODS:
One-hand mask ventilation with a constant ventilator setting (pressure-controlled ventilation) was started 20 s after injection of rocuronium and maintained for 1 min during anesthesia induction. Mask ventilation efficiency was assessed by the breath number needed to initially exceed 5 ml/kg ideal body weight of expiratory tidal volume (primary outcome) and tidal volumes (secondary outcomes) during initial 15 breaths (UMIN000012494).
RESULTS:
Tidal volume progressively increased by more than 70% in 1 min and did not differ between sleep-disordered breathing (n = 42) and non-sleep-disordered breathing (n = 38) patients. In post hoc subgroup analyses, the primary outcome breath number (mean [95% CI], 5.7 [4.1 to 7.3] vs. 1.7 [0.2 to 3.2] breath; P = 0.001) and mean tidal volume (6.5 [4.6 to 8.3] vs. 9.6 [7.7 to 11.4] ml/kg ideal body weight; P = 0.032) were significantly smaller in 20 sleep-disordered breathing patients with higher apnea hypopnea index (median [25th to 75th percentile]: 21.7 [17.6 to 31] per hour) than in 20 non-sleep disordered breathing subjects with lower apnea hypopnea index (1.0 [0.3 to 1.5] per hour). Obesity and occurrence of expiratory flow limitation during one-hand mask ventilation independently explained the reduction of efficiency of mask ventilation, while the use of two hands effectively normalized inefficient mask ventilation during one-hand mask ventilation.
CONCLUSIONS:
One-hand mask ventilation is difficult in patients with obesity and severe sleep-disordered breathing particularly when expiratory flow limitation occurs during mask ventilation.
Added AOD 11/2/16
Emergency ventilation with the Ventrain® through an airway exchange catheter in a porcine model of complete upper airway obstruction.
de Wolf MW1, Gottschall R2, Preussler NP2, Paxian M2, Enk D3.
Author information
PURPOSE:
During difficult airway management, oxygen insufflation through airway-exchange and intubating catheters (AEC/IC) can lead to life-threatening hyperinflation. Ventrain® was originally designed to facilitate emergency ventilation using active expiration through short, small-bore cannulas. Herein, we studied its efficacy (oxygenation and ventilation) and safety (avoidance of hyperinflation) in a long, small-bore AEC.
METHODS:
In six anesthetized pigs, the upper airway was obstructed, except for a 100 cm long, 3 mm internal diameter AEC. After apneic desaturation to a peripheral oxygen saturation (SpO2) of < 70%, ventilation through the AEC was started with Ventrain at an oxygen flow of 15 L·min-1, a frequency of 30 breaths·min-1, and an inspiration/expiration ratio of approximately 1:1. It was continued for ten minutes.
RESULTS:
Within one minute, severe hypoxia was reversed from a median [interquartile range] arterial saturation (SaO2) of 48 [34-56] % before initiation of Ventrain ventilation to 100 [99-100] % afterward (median difference 54%; 95% confidence interval [CI] 44 to 67; P = 0.028). In addition, hypercarbia was reversed from PaCO2 of 59 [53-61] mmHg to 40 [38-42] mmHg (median difference of -18 mmHg; 95% CI -21 to -15; P = 0.028). After ten minutes of Ventrain use, peak inspiratory and end-expiratory pressures were lower than during baseline pressure-controlled ventilation (8 [7-9] mmHg vs 12 [10-14] mmHg and -2 [-3 to +1] mmHg vs 4 [2 to 4] mmHg, respectively; P = 0.027 for both). No hemodynamic deterioration occurred.
CONCLUSION:
Ventrain provides rapid reoxygenation and effective ventilation through a small-bore AEC in pigs with an obstructed airway. In clinical emergency situations of obstructed airways, this device may be able to overcome problems of unintentional hyperinflation and high intrapulmonary pressures when ventilating through long, small-bore catheters and could therefore minimize the risks of barotrauma and hemodynamic instability.
Direct Versus Video Laryngoscopy for Intubating Adult Patients with Gastrointestinal Bleeding.
Carlson JN1, Crofts J1, Walls RM2, Brown CA 3rd2. West J Emerg Med. 2015 Dec;16(7):1052-6. doi: 10.5811/westjem.2015.8.28045.
Comment by Dr. Rosenblatt: Ive long said that VL should supplant DL, except maybe in one situation - the blood airway (i.e., GI bleed). Just about ready to say "I was wrong!" Lots of success with VL in documented GI bleed here.
Abstract
INTRODUCTION:
Video laryngoscopy (VL) has been advocated for several aspects of emergency airway management; however, there are still concerns over its use in select patient populations such as those with large volume hematemesis secondary to gastrointestinal (GI) bleeds. Given the relatively infrequent nature of this disease process, we sought to compare intubation outcomes between VL and traditional direct laryngoscopy (DL) in patients intubated with GI bleeding, using the third iteration of the National Emergency Airway Registry (NEARIII).
METHODS:
We performed a retrospective analysis of a prospectively collected national database (NEARIII) of intubations performed in United States emergency departments (EDs) from July 1, 2002, through December 31, 2012. All cases where the indication for intubation was "GI bleed" were analyzed. We included patient, provider and intubation characteristics. We compared data between intubation attempts initiated as DL and VL using parametric and non-parametric tests when appropriate.
RESULTS:
We identified 325 intubations, 295 DL and 30 VL. DL and VL cases were similar in terms of age, sex, weight, difficult airway predictors, operator specialty (emergency medicine, anesthesia or other) and level of operator training (post-graduate year 1, 2, etc). Proportion of successful first attempts (DL 261/295 (88.5%) vs. VL 28/30 (93.3%) p=0.58) and Cormack-Lehane grade views (p=0.89) were similar between devices. The need for device change was similar between DL [2/295 (0.7%) and VL 1/30 (3.3%); p=0.15].
CONCLUSION:
In this national registry of intubations performed in the ED for patients with GI bleeds, both DL and VL had similar rates of success, glottic views and need to change devices.
ADDED AOD 10/7/16
Effect of Boussignac continuous positive airway pressure ventilation on PaO2 and PaO2/FIO2 ratio immediately after extubation in morbidly obese patients undergoing bariatric surgery:
Guimarães J, et al.
Journal of Clinical Anesthesia (2016) 34, 562–570
Abstract
Study Objective: Pathophysiological changes after laparoscopic Roux-en-Y gastric bypass may increase the risk of pulmonary complications in morbidly obese patients. The purpose of the study was to assess the impact of immediate postextubation use of Boussignac continuous positive airway pressure (CPAP) on arterial oxygenation in morbidly obese patients undergoing laparoscopic Roux-en Y gastric bypass. The hypothesis is that the use of CPAP may improve oxygenation in the postoperative period when compared to Venturi mask. Design: Randomized controlled study.
Journal of Clinical Anesthesia (2016) 34, 562–570
ADDED AOD 9/22/16
Tracheal Malplacement of the King LT Airway May Be an Important Cause of Prehospital Device Failure.
Driver BE, Plummer D, Heegaard W, Reardon RF.
J Emerg Med. 2016 Sep 17. pii: S0736-4679(16)30454-1
BACKGROUND:
The King LT airway (King Systems, Noblesville, IN) is a popular extraglottic device that is widely used in the prehospital setting. We report a case of tracheal malplacement of the King airway with a severe kink in the distal tube.
CASE REPORT:
A 51-year-old unhelmeted motorcyclist collided with a freeway median and was obtunded when paramedics arrived. After bag mask ventilation, a King airway was placed uneventfully and the patient was transported to the emergency department. Because of the concern for an unstable cervical spine injury, a lateral cervical spine radiograph was obtained on arrival. No cervical injury was seen, but the King airway was noted to be malplaced; the King airway passed through the laryngeal inlet and became lodged on the anterior trachea, creating an acute kink between the two balloons. After reviewing the radiograph, ventilations were reassessed and remained adequate. Both balloons were deflated, and the King airway was removed; the patient was orotracheally intubated without complication. WHY SHOULD AN EMERGENCY PHYSICIAN BE AWARE OF THIS?: The King airway is a valuable prehospital airway that can be placed quickly and blindly with high success rates by inexperienced providers; the King airway, however, is not without complication. Ventilation was not impaired in this patient, but tracheal malplacement may be an important cause of prehospital device failure. If a first placement attempt of a King airway device fails, it is reasonable to reattempt King airway placement with a new, unkinked device before abandoning King airway placement.
ADDED AOD 9/12/16
Canadian Journal of Anesthesia/Journal canadien d'anesthésie
, Volume 63, Issue 8, pp 928–937
Introduction
During video laryngoscopy (VL) with angulated or hyper-curved blades, it is sometimes difficult to complete tracheal intubation despite a full view of the larynx. When using indirect VL, it has been suggested that it may be preferable to obtain a deliberately restricted view of the larynx to facilitate passage of the endotracheal tube. We used the GlideScope® GVL video laryngoscope (GVL) to test whether deliberately obtaining a restricted view would result in faster and easier tracheal intubation than with a full view of the larynx.
Methods
We recruited 163 elective surgical patients and randomly allocated the participants to one of two groups: Group F, where a full view of the larynx was obtained and held during GVL-facilitated tracheal intubation, and Group R, with a restricted view of the larynx (< 50% of glottic opening visible). Study investigators experienced in indirect VL performed the intubations. The intubations were recorded and the video recordings were subsequently assessed for total time to intubation, ease of intubation using a visual analogue scale (VAS; where 0 = easy and 100 = difficult), first-attempt success rate, and oxygen saturation after intubation. Complications were also assessed.
Results
The median [interquartile range (IQR)] time to intubation was faster in Group R than in Group F (27 [22-36] sec vs 36 [27-48] sec, respectively; median difference, 9 sec; 95% confidence interval [CI], 5 to 13; P < 0.001). The median [IQR] VAS rating for ease of intubation was also better in Group R than in Group F (14 [6-42) mm vs 50 mm [17-65], respectively; median difference, 20 mm; 95% CI, 10 to 31; P < 0.001). There was no difference between groups regarding the first-attempt success rate, oxygen saturation immediately after intubation, or complications.
Conclusions
Using the GVL with a deliberately restricted view of the larynx resulted in faster and easier tracheal intubation than with a full view and with no additional complications. Our study suggests that obtaining a full or Cormack-Lehane grade 1 view may not be desirable when using the GVL. This trial was registered at ClinicalTrials.gov: NCT02144207.
ADDED AOD 9/5/16
Transtracheal jet ventilation in the 'can't intubate can't oxygenate' emergency: a systematic review.
Duggan LV1, Ballantyne Scott B2, Law JA3, Morris IR4, Murphy MF5, Greendale DE, Br J Anaesth. 2016 Sep;117 Suppl 1:i28-i38.
Our goal was to determine the complication rates of TTJV in the CICO emergency compared with the emergency setting where CICO is not described (non-CICO emergency) or elective surgical setting. Several databases of published and unpublished literature were searched systematically for studies describing TTJV in human subjects. Complications were categorized as device failure, barotrauma (including subcutaneous emphysema), and miscellaneous. Device failure was defined by the inability to place and/or use the TTJV device, not patient survival.
Forty-four studies (428 procedures) met the inclusion criteria. Four studies included both emergency and elective procedures. Thirty studies described 132 emergency TTJV procedures; 90 were CICO emergencies. Eighteen studies described 296 elective TTJV procedures. Device failure occurred in 42% of CICO emergency vs 0% of non-CICO emergency (P<0.001) and 0.3% of elective procedures (P<0.001). Barotrauma occurred in 32% of CICO emergency vs 7% of non-CICO emergency (P<0.001) and 8% of elective procedures (P<0.001). The total number of procedures with any complication was 51% of CICO emergency vs 7% of non-CICO emergency (P<0.001) and 8% of elective procedures (P<0.001). Several reports described TTJV-related subcutaneous emphysema hampering subsequent attempts at surgical airway or tracheal intubation.
TTJV is associated with a high risk of device failure and barotrauma in the CICO emergency. Guidelines and recommendations supporting the use of TTJV in CICO should be reconsidered.
ADDED AOD 8/29/16
A Retrospective Study of Success, Failure, and Time Needed to Perform Awake Intubation
Thomas T. Joseph, M.D., Ph.D., Jonathan S. Gal, M.D., Samuel DeMaria, Jr., M.D., Hung-Mo Lin, Ph.D., Adam I. Levine, M.D., Jaime B. Hyman, M.D.
ABSTRACT
Background: Awake intubation is the standard of care for management of the anticipated di cult airway. e performance of awake intubation may be perceived as complex and time-consuming, potentially leading clinicians to avoid this technique of airway management. is retrospective review of awake intubations at a large academic medical center was performed to determine the average time taken to perform awake intubation, its e ects on hemodynamics, and the incidence and charac- teristics of complications and failure.
Methods: Anesthetic records from 2007 to 2014 were queried for the performance of an awake intubation. Of the 1,085 awake intubations included for analysis, 1,055 involved the use of a exible bronchoscope. Each awake intubation case was propensity matched with two controls (1:2 ratio), with similar comorbidities and intubations performed after the induction of anesthesia (n = 2,170). e time from entry into the operating room until intubation was compared between groups. e anesthetic records of all patients undergoing awake intubation were also reviewed for failure and complications.
Results: e median time to intubation for patients intubated post induction was 16.0min (interquartile range: 13 to 22) from entrance into the operating room. e median time to intubation for awake patients was 24.0 min (interquartile range: 19 to 31). e complication rate was 1.6% (17 of 1,085 cases). e most frequent complications observed were mucous plug, endotracheal tube cu leak, and inadvertent extubation. e failure rate for attempted awake intubation was 1% (n = 10). Conclusions: Awake intubations have a high rate of success and low rate of serious complications and failure. Awake intuba- tions can be performed safely and rapidly. (Anesthesiology 2016; 125:105-14)
heading 3 title 5 all else