Evidence map›Paper›PMID 28973363›Full record

Trial reportJAMA2017

Effect of Lung Recruitment and Titrated Positive End-Expiratory Pressure (PEEP) vs Low PEEP on Mortality in Patients With Acute Respiratory Distress Syndrome: A Randomized Clinical Trial.

Writing Group for the Alveolar Recruitment for Acute Respiratory Distress Syndrome Trial (ART) Investigators, Alexandre Biasi Cavalcanti, Érica Aranha Suzumura, Ligia Nasi Laranjeira, Denise de Moraes Paisani, Lucas Petri Damiani, Helio Penna Guimarães, Edson Renato Romano, Marisa de Moraes Regenga, Luzia Noriko Takahashi Taniguchi and 22 more

10 registry-linked trialsAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 10 registered trials, which are not on this map. Cited by 458 papers, 13 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
458citing papers in PubMed, 13 pooled it
–field-weighted citation impact
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.

NCT01374022 nacompletednot on this map

Randomized Controlled Trial of Maximum Alveolar Recruitment Maneuver Plus Titrated PEEP Versus ARDSNet Strategy for ARDS

TypeinterventionalSponsorHospital do CoracaoRan2011 to 2017Enrolled1,013ConditionsRespiratory Distress Syndrome, AdultArmsART Strategy, ARDSNet Strategy
NCT03569774 nawithdrawnnot on this mapstarted 2018, after this paper: background citation

The Effect of Individualized PEEP Compared to Low PEEP on Tissue Oxygenation During One Lung Ventilation in Obese Patients Undergoing Thoracic Surgery

TypeinterventionalSponsorDionne PeacherRan2018 to 2021Enrolled0ConditionsOne-Lung Ventilation, Obesity, Lung DiseasesArmsOne-lung ventilation with individualized PEEP, One-lung ventilation with low PEEP
NCT04387669 unknown statusnot on this mapstarted 2020, after this paper: background citation

Maneuver for Evaluating the Potential Recruitability of the Pulmonary Parenchyme in Patients With ARDS

Typeobservational_patient_registrySponsorUniversity Hospital, CaenRan2020 to 2021Enrolled42ConditionsAcute Respiratory Distress Syndrome
NCT04998253 early_phase1completednot on this mapstarted 2020, after this paper: background citation

A Randomized Pilot Clinical Trial of the Effects in Oxygenation and Hypoxic Pulmonary Vasoconstriction of Sevoflurane in Patient's Whit ARDS Secondary to Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV2)

TypeinterventionalSponsorUnidad Temporal COVID-19 en Centro CitibanamexRan2020 to 2021Enrolled24ConditionsHypoxic Pulmonary Vasoconstriction, Hypoxemia, Acute Respiratory Distress Syndrome, SARS-CoV-2 Acute Respiratory DiseaseArmsEffects in oxygenation and hypoxic pulmonary vasoconstriction
NCT05386901 nacompletednot on this mapstarted 2022, after this paper: background citation

The Effects of Individualized Lung-protective Ventilation With Lung Dynamic Compliance-guided Positive End-expiratory Pressure(PEEP) Titration on Postoperative Pulmonary Complications of Pediatric Video-assisted Thoracoscopic Surgery

TypeinterventionalSponsorJiaxiang ChenRan2022 to 2024Enrolled63ConditionsAnesthesia, SurgeryArmsConventional positive end-expiratory pressure(PEEP), Lung dynamic compliance guided positive end-expiratory pressure(PEEP)
NCT05702411 naunknown statusnot on this mapstarted 2021, after this paper: background citation

Air Stacking Technique For Pulmonary Reexpansion In The Ventilator After Expiratory Pause During Aspiration In Closed System

TypeinterventionalSponsorHospital Nossa Senhora da ConceicaoRan2021 to 2023Enrolled39ConditionsCritical CareArmsAir Stacking Technique, No Air Stacking Technique
NCT06698913 naactive not recruitingnot on this mapstarted 2021, after this paper: background citation

Feasibility and Efficacy of Automated Lateral Decubitus Therapy in Hypoxemic Respiratory Failure

TypeinterventionalSponsorUniversity of Sao Paulo General HospitalRan2021 to 2025Enrolled80ConditionsRespiratory Insufficiency, ARDS, Post Cardiac Surgery Patients, Hypoxemic Respiratory FailureArmsRotational Therapy
NCT06840756 phase4recruitingnot on this mapstarted 2025, after this paper: background citation

Effects of Donor-recipient Sex-matched Versus Sex-mismatched Red Blood Cell Transfusion on Outcomes in Critically Ill Adult Patients

TypeinterventionalSponsorMichelle ZellerRan2025 to 2029Enrolled11,082ConditionsRed Blood Cell Transfusions, Sex Differences, Health Services, Critically Ill Intensive Care Unit PatientsArmsSex-mismatched red blood cell transfusions, Sex-matched red blood cell transfusions
NCT07251777 nacompletednot on this mapstarted 2023, after this paper: background citation

Prone vs Supine Position in Potential Organ Donors: PRODONAR Multicenter Clinical Trial

TypeinterventionalSponsorHospital de Alta Complejidad del Bicentenario Esteban EcheverríaRan2023 to 2025Enrolled254ConditionsProne Position, Donors, Lung Procurement, Tissue DonorsArmsProne position
NCT07511582 phase2recruitingnot on this mapstarted 2026, after this paper: background citation

Efficacy, Safety, and Tolerability of Methylprednisolone in Critically Ill Patients With the Hyperinflammatory Phenotype: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase II Trial

TypeinterventionalSponsorBin DuRan2026 to 2028Enrolled150ConditionsSepsis, Acute Respiratory Distress SyndromeArmsMethylprednisolone (MP), Placebo
3 · Its place in the literature

Who cites it

458 citing papers in PubMed, 13 syntheses or guidelines pooled it.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

32 authors.

Writing Group for the Alveolar Recruitment for Acute Respiratory Distress Syndrome Trial (ART) Investigators
Alexandre Biasi CavalcantiHCor Research Institute, São Paulo, Brazil.
Érica Aranha SuzumuraHCor Research Institute, São Paulo, Brazil.
Ligia Nasi LaranjeiraHCor Research Institute, São Paulo, Brazil.
Denise de Moraes PaisaniHCor Research Institute, São Paulo, Brazil.
Lucas Petri DamianiHCor Research Institute, São Paulo, Brazil.
Helio Penna GuimarãesHCor Research Institute, São Paulo, Brazil.
Edson Renato RomanoHCor Research Institute, São Paulo, Brazil.
Marisa de Moraes RegengaHCor Research Institute, São Paulo, Brazil.
Luzia Noriko Takahashi TaniguchiHCor Research Institute, São Paulo, Brazil.
Cassiano TeixeiraHospital Moinhos de Vento, Porto Alegre, Brazil.
Roselaine Pinheiro de OliveiraIrmandade Santa Casa de Misericórdia de Porto Alegre, Porto Alegre, Brazil.
Flavia Ribeiro MachadoAnesthesiology, Pain, and Intensive Care Department, Federal University of São Paulo-UNIFESP, São Paulo, Brazil.
Fredi Alexander Diaz-QuijanoEpidemiology Department, School of Public Health, University of São Paulo, São Paulo, Brazil.
Meton Soares de Alencar FilhoHospital Maternidade São Vicente de Paulo, Barbalha, Brazil.
Israel Silva MaiaHospital Nereu Ramos, Florianópolis, Brazil.
Eliana Bernardete CaserHospital Unimed Vitória, Vitória, Brazil.
Wilson de Oliveira FilhoHospital e Pronto-Socorro 28 de Agosto, Manaus, Brazil.
Marcos de Carvalho BorgesUnidade de Emergência do Hospital das Clínicas da FMRP-USP, Ribeirão Preto, Brazil.
Priscilla de Aquino MartinsHospital Estadual Dr Jayme dos Santos Neves, Serra, Brazil.
Mirna MatsuiHospital Universitário da Universidade Federal da Grande Dourados, Dourados, Brazil.
Gustavo Adolfo Ospina-TascónDepartment of Intensive Care Medicine, Fundación Valle del Lili - Universidad ICESI, Cali, Colombia.
Thiago Simões GiancursiHospital Universitário do Oeste do Paraná, Cascavel, Brazil.
Nelson Dario Giraldo-RamirezHospital Pablo Tóbon Uribe, Medellín, Colombia.
Silvia Regina Rios VieiraHospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Maria da Graça Pasquotto de Lima AssefHospital Regional Hans Dieter Schmidt, Joinville, Brazil.
Mohd Shahnaz HasanUniversity Malaya Medical Centre, Kuala Lumpur, Malaysia.
Wojciech SzczeklikJagiellonian University Medical College; Department of Intensive Care and Perioperative Medicine, Krakow, Poland.
Fernando RiosHospital Nacional Alejandro Posadas, Moron, Argentina.
Marcelo Britto Passos AmatoCardio-Pulmonary Department, Pulmonary Division, Heart Institute (Incor), University of São Paulo, São Paulo, Brazil.
Otávio BerwangerHCor Research Institute, São Paulo, Brazil.
Carlos Roberto Ribeiro de CarvalhoCardio-Pulmonary Department, Pulmonary Division, Heart Institute (Incor), University of São Paulo, São Paulo, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: The effects of recruitment maneuvers and positive end-expiratory pressure (PEEP) titration on clinical outcomes in patients with acute respiratory distress syndrome (ARDS) remain uncertain. Objective: To determine if lung recruitment associated with PEEP titration according to the best respiratory-system compliance decreases 28-day mortality of patients with moderate to severe ARDS compared with a conventional low-PEEP strategy. Design, Setting, and Participants: Multicenter, randomized trial conducted at 120 intensive care units (ICUs) from 9 countries from November 17, 2011, through April 25, 2017, enrolling adults with moderate to severe ARDS. Interventions: An experimental strategy with a lung recruitment maneuver and PEEP titration according to the best respiratory-system compliance (n = 501; experimental group) or a control strategy of low PEEP (n = 509). All patients received volume-assist control mode until weaning. Main Outcomes and Measures: The primary outcome was all-cause mortality until 28 days. Secondary outcomes were length of ICU and hospital stay; ventilator-free days through day 28; pneumothorax requiring drainage within 7 days; barotrauma within 7 days; and ICU, in-hospital, and 6-month mortality. Results: A total of 1010 patients (37.5% female; mean [SD] age, 50.9 [17.4] years) were enrolled and followed up. At 28 days, 277 of 501 patients (55.3%) in the experimental group and 251 of 509 patients (49.3%) in the control group had died (hazard ratio [HR], 1.20; 95% CI, 1.01 to 1.42; P = .041). Compared with the control group, the experimental group strategy increased 6-month mortality (65.3% vs 59.9%; HR, 1.18; 95% CI, 1.01 to 1.38; P = .04), decreased the number of mean ventilator-free days (5.3 vs 6.4; difference, -1.1; 95% CI, -2.1 to -0.1; P = .03), increased the risk of pneumothorax requiring drainage (3.2% vs 1.2%; difference, 2.0%; 95% CI, 0.0% to 4.0%; P = .03), and the risk of barotrauma (5.6% vs 1.6%; difference, 4.0%; 95% CI, 1.5% to 6.5%; P = .001). There were no significant differences in the length of ICU stay, length of hospital stay, ICU mortality, and in-hospital mortality. Conclusions and Relevance: In patients with moderate to severe ARDS, a strategy with lung recruitment and titrated PEEP compared with low PEEP increased 28-day all-cause mortality. These findings do not support the routine use of lung recruitment maneuver and PEEP titration in these patients. Trial Registration: clinicaltrials.gov Identifier: NCT01374022.

Indexed as

AdultAgedFemaleHumansIntensive Care UnitsMaleMiddle AgedPneumothoraxPositive-Pressure RespirationRespiratory Distress SyndromeTidal VolumeTreatment Failure

Identifiers

PMID28973363
PMCPMC5710484

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.