Weaning from mechanical ventilation in intensive care units across 50 countries (WEAN SAFE): a multicentre, prospective, observational cohort study

WEAN SAFE Investigators, Tài Pham, Leo Heunks, Giacomo Bellani, Fabiana Madotto, Irene Aragao, Gaëtan Beduneau, Ewan Goligher, Giacomo Grasselli, Jon Henrik Laake, Jordi Mancebo, Oscar Peñuelas, Lise Piquilloud, Antonio Pesenti, Hannah Wunsch, Frank van Haren, Laurent Brochard, John G. Laffey*, Fekri Abrough, Subhash P. AcharyaPravin Amin, Yaseen Arabi, Philippe Bauer, Jeremy Beitler, Johan Berkius, Guillermo Bugedo, Luigi Camporota, Vladimir Cerny, Young Jae Cho, Kevin Clarkson, Elisa Estenssoro, Ewan Goligher, Alexey Gritsan, Seyed Mohammadreza Hashemian, Greet Hermans, Leo Heunks, Bojan Jovanovic, Kiyoyasu Kurahashi, Dimitrios Matamis, Onnen Moerer, Zsolt Molnar, Bernardo Panka, Alfred Papali, Óscar Peñuelas, Sébastien Perbet, Preveen Banwarie, Analía Garcia, Ning Liu, Navin Ramdhani, Tim Smith, Giovanni Vitale

*Corresponding author for this work

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Abstract

Background: Current management practices and outcomes in weaning from invasive mechanical ventilation are poorly understood. We aimed to describe the epidemiology, management, timings, risk for failure, and outcomes of weaning in patients requiring at least 2 days of invasive mechanical ventilation. Methods: WEAN SAFE was an international, multicentre, prospective, observational cohort study done in 481 intensive care units in 50 countries. Eligible participants were older than 16 years, admitted to a participating intensive care unit, and receiving mechanical ventilation for 2 calendar days or longer. We defined weaning initiation as the first attempt to separate a patient from the ventilator, successful weaning as no reintubation or death within 7 days of extubation, and weaning eligibility criteria based on positive end-expiratory pressure, fractional concentration of oxygen in inspired air, and vasopressors. The primary outcome was the proportion of patients successfully weaned at 90 days. Key secondary outcomes included weaning duration, timing of weaning events, factors associated with weaning delay and weaning failure, and hospital outcomes. This study is registered with ClinicalTrials.gov, NCT03255109. Findings: Between Oct 4, 2017, and June 25, 2018, 10 232 patients were screened for eligibility, of whom 5869 were enrolled. 4523 (77·1%) patients underwent at least one separation attempt and 3817 (65·0%) patients were successfully weaned from ventilation at day 90. 237 (4·0%) patients were transferred before any separation attempt, 153 (2·6%) were transferred after at least one separation attempt and not successfully weaned, and 1662 (28·3%) died while invasively ventilated. The median time from fulfilling weaning eligibility criteria to first separation attempt was 1 day (IQR 0–4), and 1013 (22·4%) patients had a delay in initiating first separation of 5 or more days. Of the 4523 (77·1%) patients with separation attempts, 2927 (64·7%) had a short wean (≤1 day), 457 (10·1%) had intermediate weaning (2–6 days), 433 (9·6%) required prolonged weaning (≥7 days), and 706 (15·6%) had weaning failure. Higher sedation scores were independently associated with delayed initiation of weaning. Delayed initiation of weaning and higher sedation scores were independently associated with weaning failure. 1742 (31·8%) of 5479 patients died in the intensive care unit and 2095 (38·3%) of 5465 patients died in hospital. Interpretation: In critically ill patients receiving at least 2 days of invasive mechanical ventilation, only 65% were weaned at 90 days. A better understanding of factors that delay the weaning process, such as delays in weaning initiation or excessive sedation levels, might improve weaning success rates. Funding: European Society of Intensive Care Medicine, European Respiratory Society.

Original languageEnglish
Pages (from-to)465-476
Number of pages12
JournalThe Lancet Respiratory Medicine
Volume11
Issue number5
Early online date21 Jan 2023
DOIs
Publication statusPublished - May 2023

Bibliographical note

Funding Information:
The WEAN SAFE study was initiated by the Acute Respiratory Failure Section of the European Society of Intensive Care Medicine (ESICM), and jointly financially supported and endorsed by ESICM and by the European Respiratory Society in the form of a clinical research collaboration. We thank the European Lung Foundation for input on the patient perspective. We gratefully acknowledge Guy Francois from ESICM for his assistance throughout this project from its inception. Thanks also to Jérôme Lambert (INSERM U1153 CRESS, Epidemiology and Clinical Statistics for Tumour, Respiratory, and Resuscitation Assessments [ECSTRRA] Team, Hôpital Saint Louis, Paris, France) for his valuable contribution on multistate models.

Funding Information:
The WEAN SAFE study was initiated by the Acute Respiratory Failure Section of the European Society of Intensive Care Medicine (ESICM), and jointly financially supported and endorsed by ESICM and by the European Respiratory Society in the form of a clinical research collaboration. We thank the European Lung Foundation for input on the patient perspective. We gratefully acknowledge Guy Francois from ESICM for his assistance throughout this project from its inception. Thanks also to Jérôme Lambert (INSERM U1153 CRESS, Epidemiology and Clinical Statistics for Tumour, Respiratory, and Resuscitation Assessments [ECSTRRA] Team, Hôpital Saint Louis, Paris, France) for his valuable contribution on multistate models.

Publisher Copyright:
© 2023 Elsevier Ltd

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