Matthieu Jabaudon , Pierre Boucher , Etienne Imhoff , Russell Chabanne , Jean-Sébastien Faure , Laurence Roszyk , Sandrine Thibault , Raiko Blondonnet , Gael Clairefond , Renaud Guérin , and Sébastien Perbet Sophie Cayot , Thomas Godet , Bruno Pereira , Vincent Sapin , Jean-Etienne Bazin , Emmanuel Futier , and Jean-Michel Constantin Am. J. Resp. Crit. Care Med. Mar 15, 2017, vol. 195, no. 6: 792-800
Rationale: Sevoflurane improves gas exchange, and reduces alveolar edema and inflammation in preclinical studies of lung injury, but its therapeutic effects have never been investigated in acute respiratory distress syndrome (ARDS).
Objectives: To assess whether sevoflurane would improve gas exchange and inflammation in ARDS.
Methods: We did a parallel, open-label single-center randomized controlled trial at three intensive care units from a French university hospital between April 2014 and February 2016. Adult patients were randomized within 24 hours of moderate-to-severe ARDS onset to receive either intravenous midazolam or inhaled sevoflurane for 48 hours. The primary outcome was the PaO2/FiO2 ratio on Day 2. Secondary endpoints included alveolar and plasma levels of cytokines and soluble form of the receptor for advanced glycation end-products, and safety. Investigators who did the analyses were masked to group allocation. Analysis was by intention to treat.
Measurements and Main Results: Twenty-five patients were assigned to the sevoflurane group and 25 to the midazolam group. On Day 2, PaO2/FiO2 ratio was higher in the sevoflurane group than in the midazolam group (mean ± SD, 205 ± 56 vs. 166 ± 59, respectively; P = 0.04). There was a significant reduction over time in cytokines and soluble form of the receptor for advanced glycation end-products levels in the sevoflurane group, compared with the midazolam group, and no serious adverse event was observed with sevoflurane.
Conclusions: In patients with ARDS, use of inhaled sevoflurane improved oxygenation and decreased levels of a marker of epithelial injury and of some inflammatory markers, compared with midazolam.