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Patterns of Use of Adjunctive Therapies in Patients With Early Moderate to Severe ARDS: Insights From the LUNG SAFE Study

  • the LUNG SAFE Investigators and the ESICM Trials Group
  • Case Western Reserve University
  • University of Galway
  • University of Milano-Bicocca
  • Keenan Research Centre for Biomedical Science
  • Galway University Hospital
  • Assistance Publique-HÔpitaux de Paris, Université Paris Sud
  • Mt Sinai Hospital
  • Fondazione IRCCS San Gerardo dei Tintori
  • Sunnybrook Health Sciences Centre
  • University of Milan
  • Case Western Reserve University
  • University of Toronto
  • Regenerative Medicine Institute (REMEDI) at CÚRAM SFI Research Centre for Medical Devices
  • Biomedical Sciences Building working group(Internal)
  • National University of Ireland, Galway
  • Nephrology Services
  • Galway University Hospitals
  • University of Toronto and Program in Trauma
  • Dipartimento di Anestesia
  • Department of Anaesthesia and Intensive Care Medicine

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

50 Citations (Scopus)

Abstract

Background: Adjunctive strategies are an important part of the management of ARDS. However, their application in clinical practice remains inconsistent. Research Question: We wished to determine the frequency and patterns of use of adjunctive strategies in patients with moderate to severe ARDS (PaO2/FIO2 [P/F ratio] < 150) enrolled into the Large observational study to UNderstand the Global impact of Severe Acute respiratory FailurE (LUNG SAFE) study. Study Design and Methods: The LUNG SAFE study was an international, multicenter, prospective cohort study of patients with severe respiratory failure, conducted in 2014 in 459 ICUs from 50 countries. The primary objective of this substudy was to determine the frequency of use of widely available (neuromuscular blockade, prone position) adjuncts vs adjuncts requiring specialized equipment (extracorporeal membrane oxygenation, inhaled vasodilators, high-frequency ventilation) in patients in the first 48 h of moderate to severe ARDS (P/F ratio < 150). Results: Of 1,146 patients on invasive ventilation with moderate to severe ARDS, 811 patients (71%) received no adjunct within 48 h of ARDS onset. Of 335 (29%) that received adjunctive strategies, 252 (75%) received a single strategy, and 83 (25%) receiving more than one adjunct. Of ARDS nonsurvivors, 67% did not receive any adjunctive strategy in the first 48 h. Most patients (67%) receiving specialized adjuncts did not receive prone positioning or neuromuscular blockade. Patients that received adjuncts were more likely to have their ARDS recognized, be younger and sicker, have pneumonia, be more difficult to ventilate, and be in a European high-income country than those that did not receive adjuncts. Interpretation: Three in 10 patients with moderate to severe ARDS, and only one-third of nonsurvivors, received adjunctive strategies over the first 48 h of ARDS. A more consistent and evidence-driven approach to adjunct use may reduce costs and improve outcomes in patients with moderate to severe ARDS. Trial Registry: ClinicalTrials.gov; No.: NCT02010073; URL: www.clinicaltrials.gov

Original languageEnglish
Pages (from-to)1497-1505
Number of pages9
JournalChest
Volume157
Issue number6
DOIs
Publication statusPublished - Jun 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • extracorporeal membrane oxygenation
  • high-frequency oscillation ventilation
  • neuromuscular blockade
  • nitric oxide
  • prone positioning
  • Aged
  • Extracorporeal Membrane Oxygenation/methods
  • Female
  • Humans
  • Male
  • Middle Aged
  • Neuromuscular Blockade/methods
  • Positive-Pressure Respiration/methods
  • Prospective Studies
  • Respiratory Distress Syndrome/diagnosis
  • Severity of Illness Index
  • Treatment Outcome

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