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Remimazolam Versus Midazolam for Sedation in Mechanically Ventilated Patients with Severe Pneumonia: A Randomized Controlled Trial

Hao-Bo Kong, Jing-Jing Pan, Min Liang, Shufeng Yu, Xuehui Fang Xuehui

Journal of Intensive Care Medicine, 2026

68 participants

Abstract

PurposePatients with severe pneumonia in the intensive care unit often require mechanical ventilation and sedation. Midazolam, a common sedative, is limited by prolonged sedation and accumulation. Remimazolam besylate, a novel ultra-short-acting benzodiazepine, offers efficacy and safety. This study compared remimazolam and midazolam for sedation in mechanically ventilated patients with severe pneumonia.MethodsThis single-center, prospective, randomized controlled trial enrolled 68 adults with severe pneumonia requiring invasive mechanical ventilation, targeting a Richmond Agitation-Sedation Scale (RASS) score of -3 to 0. Patients were randomized 1:1 to receive either remimazolam (initial dose 0.2 mg/kg/h) or midazolam (initial dose 0.02 mg/kg/h), all receiving remifentanil for analgesia. The primary outcome was the proportion of time spent within the target RASS range without rescue sedation during the first 72 h after randomization. Secondary outcomes included hemodynamic parameters, oxygen saturation, duration of mechanical ventilation, ventilator-free days at day 28 +(VFD-28), and 28-day mortality.ResultsBaseline characteristics were comparable, and the median percentage of time within the target RASS range was 100% (p = 0.989) for both groups. Rescue sedation was required in 11.8% of the remimazolam group and 17.6% of the midazolam group (p = 0.734). No significant differences were observed in mean arterial pressure, heart rate, oxygen saturation, duration of mechanical…

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Evidence Hub reads this as a randomized trial, done in people. Its evidence level is 2 of 5 (High · randomized trial). Randomized trials of a reasonable size are the strongest single-study design. Reported size: 68 participants or records.

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