1. Neurally adjusted ventilatory assist in acute respiratory failure: a randomized controlled trial
- Author
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Rosa Lidia Fernández, Rosario Solano, Cesar Aldecoa, Jesús M González-Martín, Domingo Martínez, Jesús Villar, Carlos Ferrando, Ruth Corpas, Francisco Alba, José M. Añón, Isabel Murcia, Qin Sun, Anxela Vidal, Cristina Fernández, Elena González-Higueras, Raquel Montiel, Marina Soro, César E Pinedo, Dácil Parrilla, Jesús Rico-Feijoo, Songqiao Liu, David Pestaña, and Robert M. Kacmarek
- Subjects
medicine.medical_specialty ,Randomization ,Original ,medicine.medical_treatment ,Acute respiratory failure ,Ventilator-free days ,Critical Care and Intensive Care Medicine ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,Randomized controlled trial ,law ,Anesthesiology ,Neurally adjusted ventilatory assist ,Humans ,Medicine ,Intensive care unit ,Mortality ,Interactive Ventilatory Support ,Mechanical ventilation ,Respiratory Distress Syndrome ,Ventilators, Mechanical ,business.industry ,Lung-protective ventilation ,030208 emergency & critical care medicine ,Respiration, Artificial ,Confidence interval ,030228 respiratory system ,Anesthesia ,Etiology ,Respiratory Insufficiency ,business - Abstract
Purpose We hypothesized that neurally adjusted ventilatory assist (NAVA) compared to conventional lung-protective mechanical ventilation (MV) decreases duration of MV and mortality in patients with acute respiratory failure (ARF). Methods We carried out a multicenter, randomized, controlled trial in patients with ARF from several etiologies. Intubated patients ventilated for ≤ 5 days expected to require MV for ≥ 72 h and able to breathe spontaneously were eligible for enrollment. Eligible patients were randomly assigned based on balanced treatment assignments with a computerized randomization allocation sequence to two ventilatory strategies: (1) lung-protective MV (control group), and (2) lung-protective MV with NAVA (NAVA group). Allocation concealment was maintained at all sites during the trial. Primary outcome was the number of ventilator-free days (VFDs) at 28 days. Secondary outcome was all-cause hospital mortality. All analyses were done according to the intention-to-treat principle. Results Between March 2014 and October 2019, we enrolled 306 patients and randomly assigned 153 patients to the NAVA group and 153 to the control group. Median VFDs were higher in the NAVA than in the control group (22 vs. 18 days; between-group difference 4 days; 95% confidence interval [CI] 0 to 8 days; p = 0.016). At hospital discharge, 39 (25.5%) patients in the NAVA group and 47 (30.7%) patients in the control group had died (between-group difference − 5.2%, 95% CI − 15.2 to 4.8, p = 0.31). Other clinical, physiological or safety outcomes did not differ significantly between the trial groups. Conclusion NAVA decreased duration of MV although it did not improve survival in ventilated patients with ARF. Electronic supplementary material The online version of this article (10.1007/s00134-020-06181-5) contains supplementary material, which is available to authorized users.
- Published
- 2020
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