Maintenance infusion rate of oxytocin after initial 1-IU bolus for elective Cesarean delivery: a dose-finding study.

IF 3.4 3区 医学 Q1 ANESTHESIOLOGY
Linda Boonstra, Jose C A Carvalho, William Turner, Kristi Downey, Xiang Y Ye, Jackie Thomas, Mrinalini Balki
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引用次数: 0

Abstract

Purpose: The purpose of our study was to determine the minimum effective dose of oxytocin maintenance infusion required to maintain adequate uterine tone in 90% of patients (ED90) after administration of the initial bolus at elective Cesarean delivery (CD) under spinal anesthesia.

Methods: We conducted a prospective, double-blind dose-finding study with biased coin up-down design. Immediately after delivery, a 1-IU oxytocin bolus was administered, followed by a maintenance infusion. The obstetrician assessed the uterine tone by palpation as satisfactory or unsatisfactory. In case of unsatisfactory response, the dose for the next patient was increased by 2 IU·hr-1. For satisfactory response, the dose for the next patient was either decreased by 2 IU·hr-1 with a probability of 1/9, or remained unchanged. The primary outcome was a satisfactory uterine tone from five minutes after delivery until discharge from postanesthesia care unit. The secondary outcomes were blood loss, need for additional uterotonics, and side effects.

Results: We analyzed data for 40 patients. The ED90 of oxytocin maintenance infusion was 4.5 IU·hr-1 (95% confidence interval, 3.3 to 5.5) based on the isotonic regression estimator. The median [interquartile range] blood loss was 861 [553-1,181] mL; 18% received additional uterotonics, and 38% developed hypotension post delivery.

Conclusion: Based on the results of this dose-finding study, we recommend a maintenance infusion rate of 4.5 IU·hr-1 following an oxytocin bolus of 1 IU for adequate uterine tone in pregnant patients undergoing elective CDs. This infusion rate is four-fold lower than that required without an initial bolus.

Study registration: ClinicalTrials.gov ( NCT04946006 ); first submitted 25 June 2021.

择期剖宫产术中首次注射 1-IU 催产素后的维持输注率:一项剂量摸底研究。
目的:我们的研究目的是确定在脊髓麻醉下择期剖宫产(CD)时,在给予初始栓剂后维持 90% 患者足够子宫张力(ED90)所需的催产素维持输注最小有效剂量:我们进行了一项前瞻性双盲剂量调查研究,采用了偏向硬币上下的设计。分娩后立即注射 1-IU 催产素,然后进行维持输注。产科医生通过触诊评估子宫张力是否满意。如果反应不满意,下一位患者的剂量增加 2 IU-hr-1。如果反应令人满意,下一位患者的剂量要么减少 2 IU-hr-1(概率为 1/9),要么保持不变。主要结果是,从分娩后 5 分钟到从麻醉后护理病房出院,子宫张力令人满意。次要结果是失血量、是否需要额外使用子宫收缩剂以及副作用:我们分析了 40 名患者的数据。根据等张回归估算,催产素维持输注的 ED90 为 4.5 IU-hr-1(95% 置信区间,3.3 至 5.5)。失血量的中位数[四分位间范围]为 861 [553-1,181] mL;18%的产妇接受了额外的子宫收缩剂,38%的产妇在分娩后出现低血压:根据这项剂量摸底研究的结果,我们建议在注射 1 IU 催产素后,以 4.5 IU-hr-1 的输注速度维持足够的子宫张力。该输注率比不注射催产素的情况下所需的输注率低四倍:研究注册:ClinicalTrials.gov(NCT04946006);2021 年 6 月 25 日首次提交。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.50
自引率
7.10%
发文量
161
审稿时长
6-12 weeks
期刊介绍: The Canadian Journal of Anesthesia (the Journal) is owned by the Canadian Anesthesiologists’ Society and is published by Springer Science + Business Media, LLM (New York). From the first year of publication in 1954, the international exposure of the Journal has broadened considerably, with articles now received from over 50 countries. The Journal is published monthly, and has an impact Factor (mean journal citation frequency) of 2.127 (in 2012). Article types consist of invited editorials, reports of original investigations (clinical and basic sciences articles), case reports/case series, review articles, systematic reviews, accredited continuing professional development (CPD) modules, and Letters to the Editor. The editorial content, according to the mission statement, spans the fields of anesthesia, acute and chronic pain, perioperative medicine and critical care. In addition, the Journal publishes practice guidelines and standards articles relevant to clinicians. Articles are published either in English or in French, according to the language of submission.
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