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肼屈嗪大剂量注射与持续滴注治疗妊娠高血压急症的比较研究

Management of hypertensive emergencies of pregnancy by hydralazine bolus injection vs continuous drip--a comparative study.

作者信息

Begum Mosammat Rashida, Quadir Ehsan, Begum Anowara, Akhter Sayeba, Rahman Khalilur

机构信息

Dhaka Medical College, Dhaka, Bangladesh.

出版信息

Medscape Womens Health. 2002 Sep-Oct;7(5):1.

Abstract

This prospective study was conducted at Dhaka Medical College and Hospital, Bangladesh. The objective was to identify the time required to control high blood pressure levels in obstetric patients by injection of hydralazine in a bolus intravenous dose vs continuous drip. Seventy-seven patients with eclampsia and hypertensive emergencies comprised the target population. Patients were managed either by hydralazine drip in normal saline (existing official protocol, n = 33) or hydralazine bolus injection (as experiment, n = 44) until diastolic blood pressure fell to 90-95 mmHg. Results were compared. Student's t-test was done for statistical significance, and a P value of <.05 was considered as significant. The groups were similar with respect to maternal age and their mean systolic and diastolic blood pressure at the time of enrollment. Patients who received bolus injection required less time to achieve the therapeutic goal (65.23 +/- 23.38 minutes) than continuous drip (186.36 +/- 79.77 minutes; P <.001). The experimental group also required significantly lower doses (6.68 +/- 1.66 mg) in comparison to that required by control group (20.07 +/- 11.38 mg; P <.001). There was no overshoot hypotension in either group. The data suggest that hydralazine bolus dose is equally safe and more effective than continuous drip in the management of hypertensive emergencies in pregnancy.

摘要

这项前瞻性研究在孟加拉国达卡医学院及医院开展。目的是确定静脉推注与持续滴注肼屈嗪控制产科患者高血压水平所需的时间。77例子痫和高血压急症患者构成目标人群。患者分别采用生理盐水持续滴注肼屈嗪(现行官方方案,n = 33)或肼屈嗪推注(作为实验,n = 44)进行治疗,直至舒张压降至90 - 95 mmHg。对结果进行比较。采用学生t检验进行统计学显著性分析,P值<0.05被视为具有显著性。两组在产妇年龄以及入组时的平均收缩压和舒张压方面相似。接受推注的患者达到治疗目标所需时间(65.23±23.38分钟)比持续滴注组(186.36±79.77分钟;P<0.001)少。与对照组所需剂量(20.07±11.38 mg;P<0.001)相比,实验组所需剂量也显著更低(6.68±1.66 mg)。两组均未出现过度低血压。数据表明,在妊娠高血压急症的治疗中,肼屈嗪推注剂量同样安全且比持续滴注更有效。

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