Evidence map›Paper›PMID 35426781›Full record

Trial reportHealth technology assessment (Winchester, England)2022

Supraglottic airway device versus tracheal intubation in the initial airway management of out-of-hospital cardiac arrest: the AIRWAYS-2 cluster RCT.

Jonathan R Benger, Kim Kirby, Sarah Black, Stephen J Brett, Madeleine Clout, Michelle J Lazaroo, Jerry P Nolan, Barnaby C Reeves, Maria Robinson, Lauren J Scott and 8 more

Open access · diamondAbstract readMulticenter StudyRandomized Controlled TrialPragmatic Clinical Trial
In one paragraph

Trial report in Health technology assessment (Winchester, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 7 institutions in 1 country.

Jonathan R BengerFaculty of Health and Applied Sciences, University of the West of England, Bristol, UK.ORCID 0000-0001-6131-0916
Kim KirbyFaculty of Health and Applied Sciences, University of the West of England, Bristol, UK.ORCID 0000-0002-8092-7978
Sarah BlackResearch, Audit and Improvement Department, South Western Ambulance Service NHS Foundation Trust, Exeter, UK.ORCID 0000-0001-6678-7502
Stephen J BrettDepartment of Surgery and Cancer, Imperial College Healthcare NHS Trust, London, UK.ORCID 0000-0003-4545-8413
Madeleine CloutClinical Trials and Evaluation Unit, Bristol Trials Centre, University of Bristol, Bristol, UK.ORCID 0000-0001-7645-1199
Michelle J LazarooClinical Trials and Evaluation Unit, Bristol Trials Centre, University of Bristol, Bristol, UK.ORCID 0000-0002-8893-0522
Jerry P NolanBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0003-3141-3812
Barnaby C ReevesClinical Trials and Evaluation Unit, Bristol Trials Centre, University of Bristol, Bristol, UK.ORCID 0000-0002-5101-9487
Maria RobinsonResearch, Audit and Improvement Department, South Western Ambulance Service NHS Foundation Trust, Exeter, UK.ORCID 0000-0002-6978-8575
Lauren J ScottClinical Trials and Evaluation Unit, Bristol Trials Centre, University of Bristol, Bristol, UK.ORCID 0000-0003-3129-5123
Helena SmarttClinical Trials and Evaluation Unit, Bristol Trials Centre, University of Bristol, Bristol, UK.ORCID 0000-0001-5285-2262
Adrian SouthResearch, Audit and Improvement Department, South Western Ambulance Service NHS Foundation Trust, Exeter, UK.ORCID 0000-0003-2121-8829
Elizabeth A StokesHealth Economic Research Centre, Nuffield Department of Population Health, University of Oxford, Oxford, UK.ORCID 0000-0002-4179-1369
Jodi TaylorClinical Trials and Evaluation Unit, Bristol Trials Centre, University of Bristol, Bristol, UK.ORCID 0000-0001-7171-8923
Matthew ThomasIntensive Care Unit, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.ORCID 0000-0002-3299-3495
Sarah VossFaculty of Health and Applied Sciences, University of the West of England, Bristol, UK.ORCID 0000-0001-5044-5145
Sarah WordsworthHealth Economic Research Centre, Nuffield Department of Population Health, University of Oxford, Oxford, UK.ORCID 0000-0002-2361-3040
Chris A RogersClinical Trials and Evaluation Unit, Bristol Trials Centre, University of Bristol, Bristol, UK.ORCID 0000-0002-9624-2615
University of Bristol · GBNational Institute for Health Research · GBSouth Western Ambulance Service NHS Foundation Trust · GBUniversity of the West of England · GBImperial College Healthcare NHS Trust · GBRoyal United Hospital · GBUniversity Hospitals Bristol NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhen a cardiac arrest occurs, cardiopulmonary resuscitation should be started immediately. However, there is limited evidence about the best approach to airway management during cardiac arrest.

objectiveThe objective was to determine whether or not the i-gel

designThis was a pragmatic, open, parallel, two-group, multicentre, cluster randomised controlled trial. A cost-effectiveness analysis accompanied the trial.

settingThe setting was four ambulance services in England.

participantsPatients aged ≥ 18 years who had a non-traumatic out-of-hospital cardiac arrest and were attended by a participating paramedic were enrolled automatically under a waiver of consent between June 2015 and August 2017. Follow-up ended in February 2018.

interventionParamedics were randomised 1 : 1 to use tracheal intubation (764 paramedics) or i-gel (759 paramedics) for their initial advanced airway management and were unblinded.

main outcome measuresThe primary outcome was modified Rankin Scale score at hospital discharge or 30 days after out-of-hospital cardiac arrest, whichever occurred earlier, collected by assessors blinded to allocation. The modified Rankin Scale, a measure of neurological disability, was dichotomised: a score of 0-3 (good outcome) or 4-6 (poor outcome/death). The primary outcome for the economic evaluation was quality-adjusted life-years, estimated using the EuroQol-5 Dimensions, five-level version.

resultsA total of 9296 patients (supraglottic airway group, 4886; tracheal intubation group, 4410) were enrolled [median age 73 years; 3373 (36.3%) women]; modified Rankin Scale score was known for 9289 patients. Characteristics were similar between groups. A total of 6.4% (311/4882) of patients in the supraglottic airway group and 6.8% (300/4407) of patients in the tracheal intubation group had a good outcome (adjusted difference in proportions of patients experiencing a good outcome: -0.6%, 95% confidence interval -1.6% to 0.4%). The supraglottic airway group had a higher initial ventilation success rate than the tracheal intubation group [87.4% (4255/4868) vs. 79.0% (3473/4397), respectively; adjusted difference in proportions of patients: 8.3%, 95% confidence interval 6.3% to 10.2%]; however, patients in the tracheal intubation group were less likely to receive advanced airway management than patients in the supraglottic airway group [77.6% (3419/4404) vs. 85.2% (4161/4883), respectively]. Regurgitation rate was similar between the groups [supraglottic airway group, 26.1% (1268/4865); tracheal intubation group, 24.5% (1072/4372); adjusted difference in proportions of patients: 1.4%, 95% confidence interval -0.6% to 3.4%], as was aspiration rate [supraglottic airway group, 15.1% (729/4824); tracheal intubation group, 14.9% (647/4337); adjusted difference in proportions of patients: 0.1%, 95% confidence interval -1.5% to 1.8%]. The longer-term outcomes were also similar between the groups (modified Rankin Scale: at 3 months, odds ratio 0.89, 95% confidence interval 0.69 to 1.14; at 6 months, odds ratio 0.91, 95% confidence interval 0.71 to 1.16). Sensitivity analyses did not alter the overall findings. There were no unexpected serious adverse events. Mean quality-adjusted life-years to 6 months were 0.03 in both groups (supraglottic airway group minus tracheal intubation group difference -0.0015, 95% confidence interval -0.0059 to 0.0028), and total costs were £157 (95% confidence interval -£270 to £583) lower in the tracheal intubation group. Although the point estimate of the incremental cost-effectiveness ratio suggested that tracheal intubation may be cost-effective, the huge uncertainty around this result indicates no evidence of a difference between groups. LIMITATIONS: Limitations included imbalance in the number of patients in each group, caused by unequal distribution of high-enrolling paramedics; crossover between groups; and the fact that participating paramedics, who were volunteers, might not be representative of all paramedics in the UK. Findings may not be applicable to other countries.

conclusionAmong patients with out-of-hospital cardiac arrest, randomisation to the supraglottic airway group compared with the tracheal intubation group did not result in a difference in outcome at 30 days. There were no notable differences in costs, outcomes and overall cost-effectiveness between the groups. FUTURE WORK: Future work could compare alternative supraglottic airway types with tracheal intubation; include a randomised trial of bag mask ventilation versus supraglottic airways; and involve other patient populations, including children, people with trauma and people in hospital.

trial registrationThis trial is registered as ISRCTN08256118.

fundingThis project was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme and supported by the NIHR Comprehensive Research Networks and will be published in full in

Indexed as

Cardiopulmonary ResuscitationOut-of-Hospital Cardiac ArrestAdultAgedAirway ManagementChildCost-Benefit AnalysisFemaleHumansIntubation, IntratrachealMaleQuality-Adjusted Life YearsQuality of LifeAIRWAY MANAGEMENTECONOMIC EVALUATIONOUT-OF-HOSPITAL CARDIAC ARRESTQUALITY OF LIFERANDOMISED CONTROLLED TRIAL

Identifiers

PMID35426781
PMCPMC9082259
OpenAlexW4224010141

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.