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卡贝缩宫素与缩宫素预防剖宫产术后产后出血的不良反应:一项随机对照试验

Adverse Effects of Carbetocin versus Oxytocin in the Prevention of Postpartum Haemorrhage after Caesarean Section: A Randomized Controlled Trial.

作者信息

Mannaerts D, Van der Veeken L, Coppejans H, Jacquemyn Y

机构信息

Department of Obstetrics and Gynaecology, Antwerp University Hospital (UZA), Edegem, Belgium.

Research Group ASTARC (Antwerp Surgical Training, Anatomy and Research Centre), University of Antwerp (UA), Antwerp, Belgium.

出版信息

J Pregnancy. 2018 Jan 2;2018:1374150. doi: 10.1155/2018/1374150. eCollection 2018.

DOI:10.1155/2018/1374150
PMID:29484209
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5816867/
Abstract

PURPOSE

To compare the incidence of nausea, vomiting, and arterial hypotension between carbetocin and oxytocin to prevent haemorrhage after caesarean section (CS).

METHODS

A randomized controlled trial in term pregnant women undergoing planned CS. Groups were randomized to carbetocin or oxytocin. Blood pressure (BP), heart rate, presence of nausea/vomitus, and need for vasopressors were evaluated throughout surgery. Preoperative and postoperative haemoglobin and haematocrit levels were compared.

RESULTS

Fifty-eight women were randomized (carbetocin = 32; oxytocin = 26). Both medications had hypotensive effect, difference in BP for carbetocin versus oxytocin: systolic (14.4 ± 2.4 mmHg versus 8.5 ± 1.8 mmHg); diastolic (7.8 ± 1.6 mmHg versus 8.9 ± 3.0 mmHg) without significant difference between the drugs ( = 0.1 and = 0.7). Both groups had similar needs for vasopressors. The presence of nausea was not rare, but the difference was not statistically significant ( = 0.4). Average blood loss was slightly lower in the carbetocin group but not statistically significant ( = 0.8).

CONCLUSION

In planned CS, a possible clinical significant lower incidence of nausea after carbetocin was noted but this was not statistically significant. There were no differences regarding BP, heart rate, the need for vasopressor, and blood loss. The study was registered in the International Journal of Clinical Trials (ISRCTN 95504420, 2/2017).

摘要

目的

比较卡贝缩宫素和缩宫素预防剖宫产术后出血时恶心、呕吐和动脉低血压的发生率。

方法

对计划行剖宫产术的足月孕妇进行一项随机对照试验。将研究对象随机分为卡贝缩宫素组或缩宫素组。在整个手术过程中评估血压(BP)、心率、恶心/呕吐情况以及血管升压药的使用需求。比较术前和术后血红蛋白及血细胞比容水平。

结果

58名女性被随机分组(卡贝缩宫素组 = 32例;缩宫素组 = 26例)。两种药物均有降压作用,卡贝缩宫素与缩宫素的血压差异:收缩压(14.4±2.4mmHg对8.5±1.8mmHg);舒张压(7.8±1.6mmHg对8.9±3.0mmHg),两组药物间无显著差异(P = 0.1和P = 0.7)。两组对血管升压药的需求相似。恶心的发生率并不罕见,但差异无统计学意义(P = 0.4)。卡贝缩宫素组的平均失血量略低,但无统计学意义(P = 0.8)。

结论

在计划剖宫产术中,卡贝缩宫素后恶心发生率可能有临床意义的降低,但无统计学意义。在血压、心率、血管升压药需求和失血量方面无差异。该研究已在《国际临床试验杂志》注册(ISRCTN 95504420,2017年2月)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9734/5816867/056195f1e656/JP2018-1374150.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9734/5816867/6d9049fab1ee/JP2018-1374150.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9734/5816867/471a7337b66c/JP2018-1374150.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9734/5816867/056195f1e656/JP2018-1374150.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9734/5816867/6d9049fab1ee/JP2018-1374150.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9734/5816867/471a7337b66c/JP2018-1374150.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9734/5816867/056195f1e656/JP2018-1374150.003.jpg

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