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拉贝洛尔与肼屈嗪治疗妊娠合并重度高血压急症的对比试验。

A comparative trial of labetalol and hydralazine in the acute management of severe hypertension complicating pregnancy.

作者信息

Mabie W C, Gonzalez A R, Sibai B M, Amon E

出版信息

Obstet Gynecol. 1987 Sep;70(3 Pt 1):328-33.

PMID:3306494
Abstract

Sixty peripartum patients with diastolic blood pressures (BP) 110 mmHg or higher were randomized in a 2:1 ratio to receive repeated intravenous injections of either labetalol (20-80 mg) or hydralazine (5 mg) until the diastolic BP was below 100 mmHg. There were four treatment failures in the labetalol group (N = 40) and none in the hydralazine group (N = 20). Hydralazine lowered mean arterial pressure (MAP) more than did labetalol (33.3 +/- 13.2 versus 25.5 +/- 11.2 mmHg; mean +/- SD), but labetalol had a more rapid effect. There was considerable interpatient variability in the dose of labetalol required to control BP, which could not be predicted by any clinical characteristic before therapy. The duration of action also varied in the labetalol group, with the shortest duration occurring in those patients who required the highest dosage for BP control. No significant fetal or neonatal problems ascribable to drug treatment were noted in the 13 instances in which labetalol was given before delivery. However, fetal distress occurred in two of the six cases involving antenatal hydralazine. We conclude that labetalol appears to be a safe and effective alternative to hydralazine for treating hypertension in the peripartum period, but serious rare side effects have not yet been quantified.

摘要

60名舒张压(BP)达到或高于110mmHg的围产期患者按2:1的比例随机分组,分别接受重复静脉注射拉贝洛尔(20 - 80mg)或肼屈嗪(5mg),直至舒张压低于100mmHg。拉贝洛尔组(N = 40)有4例治疗失败,肼屈嗪组(N = 20)无治疗失败病例。肼屈嗪降低平均动脉压(MAP)的幅度大于拉贝洛尔(分别为33.3±13.2mmHg和25.5±11.2mmHg;均值±标准差),但拉贝洛尔起效更快。控制血压所需的拉贝洛尔剂量在患者之间存在很大差异,治疗前的任何临床特征都无法预测该剂量。拉贝洛尔组的作用持续时间也有所不同,血压控制所需剂量最高的患者作用持续时间最短。在分娩前使用拉贝洛尔的13例病例中,未发现与药物治疗相关的明显胎儿或新生儿问题。然而,在6例产前使用肼屈嗪的病例中,有2例出现胎儿窘迫。我们得出结论,在围产期治疗高血压方面,拉贝洛尔似乎是肼屈嗪的一种安全有效的替代药物,但严重罕见的副作用尚未量化。

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