Prone Positioning in Severe Acute Respiratory Distress Syndrome

Claude Guérin(Inserm), Jean Reignier(La Roche College), Jean‐Christophe Richard(Centre de Recherche en Acquisition et Traitement de l'Image pour la Santé), Pascal Beuret, Arnaud Gacouin(Hôpital Pontchaillou), Thierry Boulain(Centre hospitalier universitaire d'Orléans), Emmanuelle Mercier(Centre Hospitalier Universitaire de Tours), Michel Badet(Centre Hospitalier Métropole Savoie), Alain Mercat(Université d'Angers), Olivier Baudin(Centre Hospitalier d'Angoulême), M. Clavel(Centre Hospitalier Universitaire de Limoges), Delphine Chatellier(Université de Poitiers), Samir Jaber(Inserm), Sylvène Rosselli(Hôpital Saint Joseph), Jordi Mancebo(Hospital de Sant Pau), Michel Sirodot(Centre Hospitalier Annecy Genevois), Gilles Hilbert(Université de Bordeaux), Christian Bengler(Université de Nîmes), Jack Richecoeur, Marc Gainnier(Hôpital de la Timone), Frédérique Bayle(Inserm), Gaël Bourdin(Centre de Recherche en Acquisition et Traitement de l'Image pour la Santé), Véronique Leray(Inserm), Raphaële Girard(Hospices Civils de Lyon), Loredana Baboi(Centre de Recherche en Acquisition et Traitement de l'Image pour la Santé), Louis Ayzac
New England Journal of Medicine
May 20, 2013
Cited by 4,053Open Access
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Abstract

BACKGROUND: Previous trials involving patients with the acute respiratory distress syndrome (ARDS) have failed to show a beneficial effect of prone positioning during mechanical ventilatory support on outcomes. We evaluated the effect of early application of prone positioning on outcomes in patients with severe ARDS. METHODS: In this multicenter, prospective, randomized, controlled trial, we randomly assigned 466 patients with severe ARDS to undergo prone-positioning sessions of at least 16 hours or to be left in the supine position. Severe ARDS was defined as a ratio of the partial pressure of arterial oxygen to the fraction of inspired oxygen (FiO2) of less than 150 mm Hg, with an FiO2 of at least 0.6, a positive end-expiratory pressure of at least 5 cm of water, and a tidal volume close to 6 ml per kilogram of predicted body weight. The primary outcome was the proportion of patients who died from any cause within 28 days after inclusion. RESULTS: A total of 237 patients were assigned to the prone group, and 229 patients were assigned to the supine group. The 28-day mortality was 16.0% in the prone group and 32.8% in the supine group (P<0.001). The hazard ratio for death with prone positioning was 0.39 (95% confidence interval [CI], 0.25 to 0.63). Unadjusted 90-day mortality was 23.6% in the prone group versus 41.0% in the supine group (P<0.001), with a hazard ratio of 0.44 (95% CI, 0.29 to 0.67). The incidence of complications did not differ significantly between the groups, except for the incidence of cardiac arrests, which was higher in the supine group. CONCLUSIONS: In patients with severe ARDS, early application of prolonged prone-positioning sessions significantly decreased 28-day and 90-day mortality. (Funded by the Programme Hospitalier de Recherche Clinique National 2006 and 2010 of the French Ministry of Health; PROSEVA ClinicalTrials.gov number, NCT00527813.).


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