Evidence map›Paper›PMID 35072713›Full record

Trial reportJAMA2022

Effect of Noninvasive Respiratory Strategies on Intubation or Mortality Among Patients With Acute Hypoxemic Respiratory Failure and COVID-19: The RECOVERY-RS Randomized Clinical Trial.

Gavin D Perkins, Chen Ji, Bronwen A Connolly, Keith Couper, Ranjit Lall, J Kenneth Baillie, Judy M Bradley, Paul Dark, Chirag Dave, Anthony De Soyza and 29 more

4 registry-linked trialsOpen access · bronzeAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 215 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
215citing papers in PubMed, 8 pooled it
59.0field-weighted citation impact, top 1% 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.

NCT05512585 nacompletednot on this map

A Physiological Study to Assess the Effects of Awake Prone Positioning in Healthy Volunteers Under Different Respiratory Support: A Randomized Crossover Study

TypeinterventionalSponsorRush University Medical CenterRan2022 to 2022Enrolled20ConditionsHealthyArmsawake prone positioning with advanced respiratory support (high-flow nasal cannula or continuous positive airway pressure)
NCT06189716 nacompletednot on this mapstarted 2024, after this paper: background citation

Evaluation of Gas Composition in the Oropharynx During High-flow Oxygen Therapy Through Nasal Cannula in Healthy Volunteers: a Physiological Study

TypeinterventionalSponsorI.M. Sechenov First Moscow State Medical UniversityRan2024 to 2024Enrolled20ConditionsHealthy VolunteersArmsHigh flow oxygen through nasal cannula
NCT06912360 narecruitingnot on this mapstarted 2025, after this paper: background citation

Use of (Continous Positive Airway Pressure) CPAP in the Management of Acute Hypoxemic Respiratory Failure

TypeinterventionalSponsorUniversité NAZI BONIRan2025 to 2026Enrolled240ConditionsAcute Respiratory FailureArmsCPAP
NCT07019701 nacompletednot on this mapstarted 2025, after this paper: background citation

Gas Composition in the Hypopharynx During High-flow Oxygen Therapy Through Nasal Cannula or Face Mask, or During Standard Oxygen Therapy Through a Non-Rebreather Face Mask in Healthy Volunteers

TypeinterventionalSponsorI.M. Sechenov First Moscow State Medical UniversityRan2025 to 2025Enrolled14ConditionsHealthy VolunteersArmsHigh flow oxygen through nasal cannula and face mask and standard oxygen therapy through non-rebreather face mask, and measurement of oxygen and carbon dioxide fraction in the hypopharynx
3 · Its place in the literature

Who cites it

215 citing papers in PubMed, 8 syntheses or guidelines pooled it, 402 citations in OpenAlex.

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155 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

39 authors at 15 institutions in 4 countries.

Gavin D PerkinsWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, England.
Chen JiWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, England.
Bronwen A ConnollyWellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Science, Queen's University Belfast, Belfast, Northern Ireland.
Keith CouperWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, England.
Ranjit LallWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, England.
J Kenneth BaillieRoslin Institute, University of Edinburgh, Midlothian, Scotland.
Judy M BradleyWellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Science, Queen's University Belfast, Belfast, Northern Ireland.
Paul DarkNIHR Manchester Biomedical Research Centre, University of Manchester, Manchester, England.
Chirag DaveUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, England.
Anthony De SoyzaPopulation and Health Science Institute, NIHR Biomedical Research Centre, Newcastle University, Newcastle upon Tyne, England.
Anna V DennisUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, England.
Anne DevrellWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, England.
Sara FairbairnGrange University Hospital, Aneurin Bevan University Health Board, Cwmbran, Wales.
Hakim GhaniWatford General Hospital, West Hertfordshire Hospitals NHS Trust, Watford, England.
Ellen A GormanWellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Science, Queen's University Belfast, Belfast, Northern Ireland.
Christopher A GreenUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, England.
Nicholas HartLane Fox Clinical Respiratory Physiology Research Centre, Guy's and St Thomas' NHS Foundation Trust, London, England.
Siew Wan HeeDivision of Health Sciences, Warwick Medical School, University of Warwick, Coventry, England.
Zoe KimbleyUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, England.
Shyam MadathilUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, England.
Nicola McGowanWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, England.
Benjamin MesserNewcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, England.
Jay NaisbittFairfield General Hospital, Pennine Acute Hospitals NHS Trust, Northern Care Alliance NHS Group, Bury, England.
Chloe NormanWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, England.
Dhruv ParekhUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, England.
Emma M ParkinFairfield General Hospital, Pennine Acute Hospitals NHS Trust, Northern Care Alliance NHS Group, Bury, England.
Jaimin PatelUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, England.
Scott E ReganWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, England.
Clare RossImperial College Healthcare NHS Trust, London, England.
Anthony J RostronSunderland Royal Hospital, South Tyneside and Sunderland NHS Foundation Trust, Sunderland, England.
Mohammad SaimUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, England.
Anita K SimondsRoyal Brompton and Harefield Hospital, Guy's and St Thomas' NHS Foundation Trust, London, England.
Emma SkiltonWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, England.
Nigel StallardDivision of Health Sciences, Warwick Medical School, University of Warwick, Coventry, England.
Michael SteinerInstitute for Lung Health, NIHR Leicester Biomedical Research Centre, Department of Respiratory Sciences, University of Leicester, Leicester, England.
Rama VancheeswaranWatford General Hospital, West Hertfordshire Hospitals NHS Trust, Watford, England.
Joyce YeungWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, England.
Daniel F McAuleyWellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Science, Queen's University Belfast, Belfast, Northern Ireland.
RECOVERY-RS Collaborators
The Recovery Center · USUniversity Hospitals Birmingham NHS Foundation Trust · GBUniversity of Warwick · GBNewcastle upon Tyne Hospitals NHS Foundation Trust · GBQueen's University Belfast · GBWest Hertfordshire Hospitals NHS Trust · GBAneurin Bevan University Health Board · GBClinical Research Institute · USGuy's and St Thomas' NHS Foundation Trust · GBImperial College Healthcare NHS Trust · GBPennine Acute Hospitals NHS Trust · GBUniversity of Leicester · GBUniversity of Manchester · GBKing's College London · GBRoslin Institute · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Continuous positive airway pressure (CPAP) and high-flow nasal oxygen (HFNO) have been recommended for acute hypoxemic respiratory failure in patients with COVID-19. Uncertainty exists regarding the effectiveness and safety of these noninvasive respiratory strategies. Objective: To determine whether either CPAP or HFNO, compared with conventional oxygen therapy, improves clinical outcomes in hospitalized patients with COVID-19-related acute hypoxemic respiratory failure. Design, Setting, and Participants: A parallel group, adaptive, randomized clinical trial of 1273 hospitalized adults with COVID-19-related acute hypoxemic respiratory failure. The trial was conducted between April 6, 2020, and May 3, 2021, across 48 acute care hospitals in the UK and Jersey. Final follow-up occurred on June 20, 2021. Interventions: Adult patients were randomized to receive CPAP (n = 380), HFNO (n = 418), or conventional oxygen therapy (n = 475). Main Outcomes and Measures: The primary outcome was a composite of tracheal intubation or mortality within 30 days. Results: The trial was stopped prematurely due to declining COVID-19 case numbers in the UK and the end of the funded recruitment period. Of the 1273 randomized patients (mean age, 57.4 [95% CI, 56.7 to 58.1] years; 66% male; 65% White race), primary outcome data were available for 1260. Crossover between interventions occurred in 17.1% of participants (15.3% in the CPAP group, 11.5% in the HFNO group, and 23.6% in the conventional oxygen therapy group). The requirement for tracheal intubation or mortality within 30 days was significantly lower with CPAP (36.3%; 137 of 377 participants) vs conventional oxygen therapy (44.4%; 158 of 356 participants) (absolute difference, -8% [95% CI, -15% to -1%], P = .03), but was not significantly different with HFNO (44.3%; 184 of 415 participants) vs conventional oxygen therapy (45.1%; 166 of 368 participants) (absolute difference, -1% [95% CI, -8% to 6%], P = .83). Adverse events occurred in 34.2% (130/380) of participants in the CPAP group, 20.6% (86/418) in the HFNO group, and 13.9% (66/475) in the conventional oxygen therapy group. Conclusions and Relevance: Among patients with acute hypoxemic respiratory failure due to COVID-19, an initial strategy of CPAP significantly reduced the risk of tracheal intubation or mortality compared with conventional oxygen therapy, but there was no significant difference between an initial strategy of HFNO compared with conventional oxygen therapy. The study may have been underpowered for the comparison of HFNO vs conventional oxygen therapy, and early study termination and crossover among the groups should be considered when interpreting the findings. Trial Registration: isrctn.org Identifier: ISRCTN16912075.

Indexed as

Continuous Positive Airway PressureIntubation, IntratrachealAdultCannulaCOVID-19FemaleHospital MortalityHumansLength of StayMaleMiddle AgedNoninvasive VentilationOxygen Inhalation TherapyRespiratory Insufficiency

Identifiers

PMID35072713
PMCPMC8787685
OpenAlexW4207047636

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.