Firoz T, Magee L A, MacDonell K, Payne B A, Gordon R, Vidler M, von Dadelszen P
Department of Medicine, University of British Columbia, Vancouver, BC, Canada; Child and Family Research Institute, University of British Columbia, Vancouver, BC, Canada.
BJOG. 2014 Sep;121(10):1210-8; discussion 1220. doi: 10.1111/1471-0528.12737. Epub 2014 May 16.
Pregnant and postpartum women with severe hypertension are at increased risk of stroke and require blood pressure (BP) reduction. Parenteral antihypertensives have been most commonly studied, but oral agents would be ideal for use in busy and resource-constrained settings.
To review systematically, the effectiveness of oral antihypertensive agents for treatment of severe pregnancy/postpartum hypertension.
A systematic search of MEDLINE, EMBASE and the Cochrane Library was performed.
Randomised controlled trials in pregnancy and postpartum with at least one arm consisting of a single oral antihypertensive agent to treat systolic BP ≥ 160 mmHg and/or diastolic BP ≥ 110 mmHg.
Cochrane RevMan 5.1 was used to calculate relative risk (RR) and weighted mean difference by random effects.
We identified 15 randomised controlled trials (915 women) in pregnancy and one postpartum trial. Most trials in pregnancy compared oral/sublingual nifedipine capsules (8-10 mg) with another agent, usually parenteral hydralazine or labetalol. Nifedipine achieved treatment success in most women, similar to hydralazine (84% with nifedipine; relative risk [RR] 1.07, 95% confidence interval [95% CI] 0.98-1.17) or labetalol (100% with nifedipine; RR 1.02, 95% CI 0.95-1.09). Less than 2% of women treated with nifedipine experienced hypotension. There were no differences in adverse maternal or fetal outcomes. Target BP was achieved ~ 50% of the time with oral labetalol (100 mg) or methyldopa (250 mg) (47% labetelol versus 56% methyldopa; RR 0.85 95% CI 0.54-1.33).
Oral nifedipine, and possibly labetalol and methyldopa, are suitable options for treatment of severe hypertension in pregnancy/postpartum.
患有重度高血压的孕妇和产后女性中风风险增加,需要降低血压(BP)。肠外抗高血压药物是最常被研究的,但口服药物对于繁忙且资源有限的环境来说将是理想之选。
系统评价口服抗高血压药物治疗重度妊娠/产后高血压的有效性。
对MEDLINE、EMBASE和Cochrane图书馆进行了系统检索。
妊娠和产后的随机对照试验,至少有一组由单一口服抗高血压药物组成,用于治疗收缩压≥160mmHg和/或舒张压≥110mmHg。
使用Cochrane RevMan 5.1通过随机效应计算相对风险(RR)和加权平均差。
我们在妊娠中确定了15项随机对照试验(915名女性)和1项产后试验。妊娠中的大多数试验将口服/舌下硝苯地平胶囊(8-10mg)与另一种药物进行比较,通常是肠外肼屈嗪或拉贝洛尔。硝苯地平在大多数女性中取得了治疗成功,与肼屈嗪相似(硝苯地平组为84%;相对风险[RR]1.07,95%置信区间[95%CI]0.98-1.17)或拉贝洛尔(硝苯地平组为100%;RR 1.02,95%CI 0.95-1.09)。接受硝苯地平治疗的女性中不到2%出现低血压。母婴不良结局无差异。口服拉贝洛尔(100mg)或甲基多巴(250mg)约50%的时间能达到目标血压(拉贝洛尔为47%,甲基多巴为56%;RR 0.85,95%CI 0.54-1.33)。
口服硝苯地平,可能还有拉贝洛尔和甲基多巴,是治疗妊娠/产后重度高血压的合适选择。