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A period of immobility after remifentanil administration protects from nausea: an experimental randomized cross-over study

机译:瑞芬太尼给药后的一段静止状态可防止恶心:一项实验性随机交叉研究

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Background The opioid remifentanil induces a decrease of vestibulo-ocular reflex function, which has been associated with nausea and vomiting when the subjects are moved. The study investigates in healthy female volunteers if immobility after remifentanil administration protects from nausea and vomiting. Methods In volunteers, a standardized movement intervention (a manually applied head-trunk movement forward, backward and sideward) was started 5?min (session A), 35?min (session B) or 60?min (session C) after cessation of a remifentanil infusion (0.15?μg?·?kg?1?·?min?1). In a cross-over design, 16 participants were randomized to the early (sessions A and B) or the late intervention group (sessions A and C). Nausea was assessed using a 11-point numerical rating scale before and after each movement intervention. Differences within and between groups were assessed with non-parametric tests for paired and unpaired data. Results Comparing sessions A, B and C, intensity of nausea was time-dependent after cessation of remifentanil administration ( p =?0.015). In the early intervention group, nausea decreased from median 5.0 [IQR 1.5;6.0] in session A to 2.0 [1.0;3.0] in session B ( p =?0.094); in the late intervention group nausea decreased from 3.5 [2.0;5.0] in session A to 0.5 [0.0;2.0] in session C ( p =?0.031). Conclusions In summary, in young healthy women, immobility after remifentanil administration protects from nausea and vomiting in a time-dependent manner. In analogy to motion sickness, opioid-induced nausea and vomiting in female volunteers can be triggered by movement. Trial registration German Clinical Trials Register DRKS00010667 . The trial was registered retrospectively on June, 20th 2016.
机译:背景阿片类药物瑞芬太尼引起前庭眼反射功能的降低,这与受试者移动时的恶心和呕吐有关。这项研究在健康的女性志愿者中进行了研究,研究表明服用瑞芬太尼后的运动能力可以防止恶心和呕吐。方法在志愿者中,停止运动后5分钟(A节),35分钟(B节)或60分钟(C节)开始进行标准化的运动干预(手动向前移动头,向后和向侧面移动)。瑞芬太尼输液(0.15?g?·?kg ?1 ?·?min ?1 )。在交叉设计中,将16名参与者随机分为早期(A和B节)或晚期干预组(A和C节)。在每次运动干预之前和之后,使用11点数字评分表评估恶心。组内和组之间的差异通过非参数检验评估配对和非配对数据。结果与A,B和C疗程相比,瑞芬太尼停药后恶心程度与时间有关(p =?0.015)。在早期干预组中,恶心程度从A节的中位数5.0 [IQR 1.5; 6.0]降至B节的2.0 [1.0; 3.0](p =?0.094)。晚期干预组中的恶心程度从A节的3.5 [2.0; 5.0]降至C节的0.5 [0.0; 2.0](p =?0.031)。结论总而言之,在年轻健康的女性中,服用瑞芬太尼后的运动不依赖于时间,可以防止恶心和呕吐。与晕车类似,运动可能会触发阿片类药物引起的女性恶心和呕吐。试验注册德国临床试验注册DRKS00010667。该试验已于2016年6月20日进行回顾性注册。

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