Noronha Neto C Carlos, Maia Sabina S B, Katz Leila, Coutinho Isabela C, Souza Alex R, Amorim Melania M
Post Graduate Program on Maternal and Child Health, Instituto de Medicina Integral Prof. Fernando Figueira, Recife, Pernambuco, Brazil.
PLoS One. 2017 Jan 26;12(1):e0168124. doi: 10.1371/journal.pone.0168124. eCollection 2017.
Changes during the puerperium are still unclear, particularly in women with hypertension. The choice of antihypertensives, both to control very high blood pressure episodes and to keep blood pressure stable, also requires further elucidation. Currently, there are no clear data to guide the decision for the choice of postpartum antihypertensives. Captopril plays an important role in the treatment of very high blood pressure episodes and may be used postpartum. Clonidine has been used as an alternative in pregnant or postpartum women with contraindications to captopril, with satisfactory effect. The objective of the present study was to evaluate the effectiveness and safety of clonidine compared to captopril for treating severe postpartum hypertension.
A randomized, drug-controlled, triple-blind clinical trial evaluating postpartum women receiving captopril or clonidine. Inclusion criteria consisted of: women with hypertensive disorders of pregnancy systolic blood pressure (SBP) ≥180 mmHg and/or diastolic blood pressure (DBP) ≥110 mmHg], requiring magnesium sulfate. Exclusion criteria were: heart disease, smoking, illicit drug use, contraindications to captopril, clonidine or oral medication, and having used captopril/clonidine previously. The primary outcome was the frequency of very high blood pressure episodes while in the obstetric intensive care unit. A total of 90 postpartum women met the study inclusion criteria, with 45 randomized to each group. There were fewer very high blood pressure episodes during hospitalization (2.1 ± 2.1 vs. 3.5 ± 4.7, p = 0.08), greater percentage reduction in SBP (14.0% ± 8.6% vs. 10.8% ± 8.8%, p = 0.08) and fewer women requiring sodium nitroprusside (2.3% vs. 13.3%; RR: 0.17; 95%CI: 0.02-1.39; p = 0.06) in the clonidine group compared to the captopril group; however, these differences were not significant. The groups were similar regarding daily mean SBP or DBP; however, on the third postpartum day, mean SBP was lower in the clonidine compared to the captopril group (151.9 ± 11.8 mmHg vs. 158.1 ± 13.6 mmHg, p = 0.02). Although not statistically significant, adverse reactions were more common in the captopril group (28.8%) compared to the clonidine group (18.6%).
Clonidine and captopril represent safe, effective treatments for severe postpartum hypertension.
clinicaltrials.gov: www.clinicaltrial.gov, NCT01761916.
产褥期的变化仍不明确,尤其是患有高血压的女性。在控制极高血压发作以及维持血压稳定方面,抗高血压药物的选择也需要进一步阐明。目前,尚无明确数据可指导产后抗高血压药物的选择决策。卡托普利在治疗极高血压发作中发挥着重要作用,可在产后使用。可乐定已被用作对卡托普利有禁忌证的孕妇或产后女性的替代药物,效果令人满意。本研究的目的是评估可乐定与卡托普利治疗重度产后高血压的有效性和安全性。
一项随机、药物对照、三盲临床试验,评估接受卡托普利或可乐定治疗的产后女性。纳入标准包括:患有妊娠高血压疾病(收缩压[SBP]≥180 mmHg和/或舒张压[DBP]≥110 mmHg)且需要硫酸镁治疗的女性。排除标准为:心脏病、吸烟、使用违禁药物、对卡托普利、可乐定或口服药物有禁忌证,以及既往使用过卡托普利/可乐定。主要结局是在产科重症监护病房期间极高血压发作的频率。共有90名产后女性符合研究纳入标准,每组随机分配45名。与卡托普利组相比,可乐定组住院期间极高血压发作次数更少(2.1±2.1次对3.5±4.7次,p = 0.08),收缩压降低百分比更高(14.0%±8.6%对10.8%±8.8%,p = 0.08),需要硝普钠治疗的女性更少(2.3%对13.3%;RR:0.17;95%CI:0.02 - 1.39;p = 0.06);然而,这些差异均无统计学意义。两组的每日平均收缩压或舒张压相似;但是,在产后第三天,可乐定组的平均收缩压低于卡托普利组(151.9±11.8 mmHg对158.1±13.6 mmHg,p = 0.02)。尽管无统计学意义,但卡托普利组的不良反应(28.8%)比可乐定组(18.6%)更常见。
可乐定和卡托普利是治疗重度产后高血压的安全、有效药物。
clinicaltrials.gov:www.clinicaltrial.gov,NCT01761916。