Dexamethasone treatment for the acute respiratory distress syndrome: a multicentre, randomised controlled trial.

Autor:	Villar J; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain; Multidisciplinary Organ Dysfunction Evaluation Research Network, Research Unit, Hospital Universitario Dr Negrín, Las Palmas de Gran Canaria, Spain; Keenan Research Center for Biomedical Science at the Li Ka Shing Knowledge Institute, St Michael's Hospital, Toronto, ON, Canada. Electronic address: jesus.villar54@gmail.com., Ferrando C; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain; Department of Anesthesiology & Critical Care, Hospital Clinic, Barcelona, Spain; Department of Anesthesiology, Hospital Clínico Universitario de Valencia, Valencia, Spain., Martínez D; Intensive Care Unit, Hospital Virgen de la Arrixaca, Murcia, Spain., Ambrós A; Intensive Care Unit, Hospital General de Ciudad Real, Ciudad Real, Spain., Muñoz T; Intensive Care Unit, Hospital Universitario de Cruces, Barakaldo, Spain., Soler JA; Intensive Care Unit, Hospital Virgen de la Arrixaca, Murcia, Spain., Aguilar G; Department of Anesthesiology, Hospital Clínico Universitario de Valencia, Valencia, Spain., Alba F; Intensive Care Unit, Hospital Nuestra Señora del Prado, Toledo, Spain., González-Higueras E; Intensive Care Unit, Hospital Virgen de La Luz, Cuenca, Spain., Conesa LA; Intensive Care Unit, Hospital Virgen de la Arrixaca, Murcia, Spain., Martín-Rodríguez C; Intensive Care Unit, Hospital General de Ciudad Real, Ciudad Real, Spain., Díaz-Domínguez FJ; Intensive Care Unit, Complejo Universitario Asistencial de León, León, Spain., Serna-Grande P; Intensive Care Unit, Hospital Universitario de Cruces, Barakaldo, Spain., Rivas R; Intensive Care Unit, Hospital Galdakao-Usansolo, Usansolo, Spain., Ferreres J; Intensive Care Unit, Hospital Clínico Universitario, Valencia, Spain., Belda J; Department of Anesthesiology, Hospital Clínico Universitario de Valencia, Valencia, Spain., Capilla L; Intensive Care Medicine, Hospital Universitario Morales Meseguer, Murcia, Spain; Intensive Care Unit, Hospital General Universitario Rafael Méndez, Lorca, Murcia, Spain., Tallet A; Intensive Care Unit, Hospital General de Segovia, Segovia, Spain., Añón JM; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain; Intensive Care Unit, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain., Fernández RL; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain; Multidisciplinary Organ Dysfunction Evaluation Research Network, Research Unit, Hospital Universitario Dr Negrín, Las Palmas de Gran Canaria, Spain., González-Martín JM; Biostatistics Research Unit, Hospital Universitario Dr Negrín, Las Palmas de Gran Canaria, Spain.
Jazyk:	angličtina
Zdroj:	The Lancet. Respiratory medicine [Lancet Respir Med] 2020 Mar; Vol. 8 (3), pp. 267-276. Date of Electronic Publication: 2020 Feb 07.
DOI:	10.1016/S2213-2600(19)30417-5
Abstrakt:	Background: There is no proven specific pharmacological treatment for patients with the acute respiratory distress syndrome (ARDS). The efficacy of corticosteroids in ARDS remains controversial. We aimed to assess the effects of dexamethasone in ARDS, which might change pulmonary and systemic inflammation and result in a decrease in duration of mechanical ventilation and mortality. Methods: We did a multicentre, randomised controlled trial in a network of 17 intensive care units (ICUs) in teaching hospitals across Spain in patients with established moderate-to-severe ARDS (defined by a ratio of partial pressure of arterial oxygen to the fraction of inspired oxygen of 200 mm Hg or less assessed with a positive end-expiratory pressure of 10 cm H 2 O or more and FiO 2 of 0·5 or more at 24 h after ARDS onset). Patients with brain death, terminal-stage disease, or receiving corticosteroids or immunosuppressive drugs were excluded. Eligible patients were randomly assigned based on balanced treatment assignments with a computerised randomisation allocation sequence using blocks of 10 opaque, sealed envelopes to receive immediate treatment with dexamethasone or continued routine intensive care (control group). Patients in the dexamethasone group received an intravenous dose of 20 mg once daily from day 1 to day 5, which was reduced to 10 mg once daily from day 6 to day 10. Patients in both groups were ventilated with lung-protective mechanical ventilation. Allocation concealment was maintained at all sites during the trial. Primary outcome was the number of ventilator-free days at 28 days, defined as the number of days alive and free from mechanical ventilation from day of randomisation to day 28. Secondary outcome was all-cause mortality 60 days after randomisation. All analyses were done according to the intention-to-treat principle. This study is registered with ClinicalTrials.gov, NCT01731795. Findings: Between March 28, 2013, and Dec 31, 2018, we enrolled 277 patients and randomly assigned 139 patients to the dexamethasone group and 138 to the control group. The trial was stopped by the data safety monitoring board due to low enrolment rate after enrolling more than 88% (277/314) of the planned sample size. The mean number of ventilator-free days was higher in the dexamethasone group than in the control group (between-group difference 4·8 days [95% CI 2·57 to 7·03]; p<0·0001). At 60 days, 29 (21%) patients in the dexamethasone group and 50 (36%) patients in the control group had died (between-group difference -15·3% [-25·9 to -4·9]; p=0·0047). The proportion of adverse events did not differ significantly between the dexamethasone group and control group. The most common adverse events were hyperglycaemia in the ICU (105 [76%] patients in the dexamethasone group vs 97 [70%] patients in the control group), new infections in the ICU (eg, pneumonia or sepsis; 33 [24%] vs 35 [25%]), and barotrauma (14 [10%] vs 10 [7%]). Interpretation: Early administration of dexamethasone could reduce duration of mechanical ventilation and overall mortality in patients with established moderate-to-severe ARDS. Funding: Fundación Mutua Madrileña, Instituto de Salud Carlos III, The European Regional Development's Funds, Asociación Científica Pulmón y Ventilación Mecánica. (Copyright © 2020 Elsevier Ltd. All rights reserved.)
Databáze:	MEDLINE
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