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Safety and Efficacy of Remimazolam Compared With Placebo and Midazolam for?Moderate Sedation During Bronchoscopy

机译:雷米唑仑与安慰剂和咪达唑仑相比在支气管镜检查中适度镇静的安全性和有效性

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Background While the complexity of flexible bronchoscopy has increased, standard options for moderate sedation medications have not changed in three decades. There is a need to improve moderate sedation while maintaining safety. Remimazolam was developed to address shortcomings of current sedation strategies. Methods A prospective, double-blind, randomized, multicenter, parallel group trial was performed at 30 US sites. The efficacy and safety of remimazolam for sedation during flexible bronchoscopy were compared with placebo and open-label midazolam. Results The success rates were 80.6%?in the remimazolam arm, 4.8%?in the placebo arm (P P P?= .0001) and midazolam (12.0 min; 95%?CI, 5.0-15.0). Remimazolam registered superior restoration of neuropsychiatric function compared with placebo and midazolam. Safety was comparable among all three arms, and 5.6%?of the patients in the remimazolam group had serious treatment-emergent adverse events as compared with 6.8%?in the placebo group. Conclusions Remimazolam administered under the supervision of a pulmonologist was effective and safe for moderate sedation during flexible bronchoscopy. In an exploratory analysis, it demonstrated a shorter onset of action and faster neuropsychiatric recovery than midazolam.
机译:背景技术尽管柔性支气管镜的复杂性有所增加,但中度镇静药物的标准选择在过去的三十年中没有改变。需要在保持安全性的同时改善中度镇静作用。 Remimazolam是为解决当前镇静策略的缺点而开发的。方法在美国30个地点进行了一项前瞻性,双盲,随机,多中心,平行组试验。比较了瑞美马唑仑在柔性支气管镜检查中的镇静效果和安全性,并与安慰剂和开标签咪达唑仑进行了比较。结果雷马咪唑组的成功率为80.6%,安慰剂组(P P P = .0001)和咪达唑仑的成功率为4.8%(12.0 min; 95%CI,5.0-15.0)。与安慰剂和咪达唑仑相比,雷米唑仑具有更好的神经精神功能恢复。三组的安全性相当,雷马唑仑组有5.6%的患者出现严重的治疗紧急事件,而安慰剂组为6.8%。结论在肺科医师的监督下给予雷马马唑仑在柔性支气管镜检查中进行中度镇静是有效和安全的。在一项探索性分析中,与咪达唑仑相比,它表现出了更快的起效和更快的神经精神恢复。

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