Objectives: To assess whether patients breathing spontaneously under standard oxygen could be recognized early as acute respiratory distress syndrome patients according to the current Berlin definition. Design: A post hoc analysis from two prospective studies. Setting: Twenty-three French ICUs. Patients: All patients admitted for acute hypoxemic respiratory failure and treated with noninvasive ventilation were analyzed. Patients with cardiogenic pulmonary edema, acute exacerbation of chronic obstructive pulmonary disease, or hypercapnia were excluded. Interventions: None. Measurements and Main results: The PaO2/FIO2 ratio was estimated at admission under standard oxygen and then under noninvasive ventilation 1 hour after initiation and within the first 24 hours. Among the 219 patients treated with noninvasive ventilation for acute hypoxemic respiratory failure, 180 (82%) had bilateral infiltrates including 161 patients with PaO2/FIO2 less than or equal to 300 mm Hg under standard oxygen. Among them, 127 were treated with positive end-expiratory pressure of at least 5 cm H2O, and 120 (94%) fulfilled criteria for acute respiratory distress syndrome within the first 24 hours. The mortality rate of patients with bilateral infiltrates and PaO2/FIO2 less than or equal to 300 mm Hg under standard oxygen was 29%, a rate very close to that of intubated patients with acute respiratory distress syndrome in the Berlin definition. Conclusions: Almost all patients with pulmonary bilateral infiltrates and a PaO2/FIO2 less than or equal to 300 mm Hg under standard oxygen fulfilled the acute respiratory distress syndrome criteria under noninvasive ventilation within the first 24 hours. Their mortality rate was similar to that reported in the Berlin definition of acute respiratory distress syndrome. Therefore, spontaneous breathing patients with the acute respiratory distress syndrome criteria could be identified early without positive pressure ventilation. This work was performed at the Medical ICU of CHU de Poitiers, France. Supplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal’s website (http://ift.tt/29S62lw). Dr. Frat’s institution disclosed that financial support was provided by the following organizations for the original study: The French Ministry of Health supported the study through the grant “Projet Hospitalier de Recherche Clinique Interrégional” grant of year 2010; the French society of intensive care (Société de Réanimation de Langue Française, SRLF) and of pneumology (Société de Pneumologie de Langue Française, SPLF) through the grant “Bourse de recherche SRLF-SPLF” grant of year 2010; the firm “La Mutuelle de Poitiers; and the firm “AADAIRC.” Dr. Frat disclosed that Fisher & Paykel HeathCare provided the equipment for all the participating centers and he received fees from lectures and he received funding from SOS oxygene. The remaining authors have disclosed that they do not have any potential conflicts of interest. For information regarding this article, E-mail: r.coudroy@yahoo.fr Copyright © by 2017 by the Society of Critical Care Medicine and Wolters Kluwer Health, Inc. All Rights Reserved.
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