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确定布比卡因 0.0625%与芬太尼 2μg/ml 以 40 分钟固定间隔给药的最佳程控间断硬膜外推注容量:偏倚硬币上下序贯分配试验。

Determination of the optimal programmed intermittent epidural bolus volume of bupivacaine 0.0625% with fentanyl 2 μg.ml at a fixed interval of forty minutes: a biased coin up-and-down sequential allocation trial.

机构信息

Department of Anesthesia and Pain Management, Micare Research Centre, Mount Sinai Hospital, University of Toronto, Toronto, Canada.

Department of Pediatrics, Micare Research Centre, Mount Sinai Hospital, University of Toronto, Toronto, Canada.

出版信息

Anaesthesia. 2018 Apr;73(4):459-465. doi: 10.1111/anae.14159. Epub 2017 Dec 2.

DOI:10.1111/anae.14159
PMID:29197080
Abstract

The optimum time interval for 10 ml boluses of bupivacaine 0.0625% + fentanyl 2 μg.ml as part of a programmed intermittent epidural bolus regimen has been found to be 40 min. This regimen was shown to be effective without the use of supplementary patient-controlled epidural analgesia boluses in 90% of women during the first stage of labour, although with a rate of sensory block to ice above T6 in 34% of women. We aimed to determine the optimum programmed intermittent epidural bolus volume at a 40 min interval to provide effective analgesia in 90% of women (EV ) during the first stage of labour, without the use of patient-controlled epidural analgesia. We performed a prospective double-blind dose-finding study using the biased coin up-and-down sequential allocation method in 40 women. The estimated EV was 11.0 (95%CI 10.0-11.7) ml with the isotonic regression method and 10.7 (95%CI 10.3-11.0) ml with the truncated Dixon and Mood method. Overall, 18 women had a sensory block above T6, and 37 women exhibited no motor block. No women required treatment for hypotension. In conclusion, it is not possible to reduce the programmed intermittent epidural bolus volume from 10 ml, used in our current regimen, without compromising the quality of analgesia. Using this regimen, a high proportion of women will develop a sensory block above T6.

摘要

研究发现,在布比卡因 0.0625%+芬太尼 2μg/ml 的 10ml 推注剂量方案中,最佳推注间隔时间为 40 分钟。该方案在分娩第一阶段,90%的女性无需使用额外的患者自控硬膜外镇痛推注即可有效,尽管 34%的女性感觉阻滞程度超过 T6。我们旨在确定最佳的 40 分钟间隔程控间歇性硬膜外推注容量,以在分娩第一阶段 90%的女性(EV)中提供有效镇痛,而无需使用患者自控硬膜外镇痛。我们在 40 名女性中进行了一项前瞻性、双盲、剂量发现研究,采用偏置硬币上下序贯分配方法。用等渗回归法估计 EV 为 11.0(95%CI 10.0-11.7)ml,用截断的 Dixon 和 Mood 法估计 EV 为 10.7(95%CI 10.3-11.0)ml。总的来说,18 名女性感觉阻滞超过 T6,37 名女性无运动阻滞。没有女性因低血压需要治疗。总之,在不影响镇痛质量的情况下,无法将我们目前方案中使用的程控间歇性硬膜外推注量从 10ml 减少。使用这种方案,很大比例的女性会出现 T6 以上的感觉阻滞。

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