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硝苯地平治疗重度子痫前期的临床疗效及围产期结局:荟萃分析

[Clinical efficacy and perinatal outcome of nifedipine for severe preeclampsia: meta-analysis].

作者信息

Liu Qian-qian, Yu Yan-hong, Gong Shi-peng, Huang Li-ping

机构信息

Department of Obstetrics and Gynecology, Southern Medical University, Guangzhou, China.

出版信息

Zhonghua Fu Chan Ke Za Zhi. 2012 Aug;47(8):592-7.

Abstract

OBJECTIVE

To assess the efficacy, side effects and perinatal outcome of nifedipine compared with other antihypertensives for treating severe preeclampsia in pregnant women.

METHODS

Randomized controlled trials (RCTs) that comparing nifedipine with other antihypertensives for severe preeclampsia were searched in PubMed, EMBase, Cochrane library, CNKI and VIP database etc(till January 2012). The quality of the included RCTs was evaluated, and Meta-analysis was performed with Rev Man 5.1 software.

RESULTS

Nine trials were included, involving 386 women in the nifedipine group, and 378 women in other antihypertensives group. Compared with other antihypertensives, nifidepine was associated with greater effective control of blood pressure (OR = 2.65, 95%CI: 1.65 - 4.25, P < 0.01). There was no clear difference in the time needed to control blood pressure (WMD = -3.64, 95%CI: -10.90 - 3.61, P = 0.32). Nifedipine could prolong gestation better than other antihypertensives (WMD = 5.14, 95%CI: 3.29 - 6.99, P < 0.01). There were no clear differences in maternal side effects headache (P = 0.28), palpitation (P = 0.06), and nausea vomiting (P = 0.28). No noticeable difference was found between the two groups in the Apgar score at five minutes (WMD = -0.21, 95%CI: -0.32 - 0.91, P = 0.72), neonatal respiratory distress syndrome (OR = 1.24, 95%CI: 0.57 - 2.67, P = 0.59), or perinatal deaths (OR = 0.49, 95%CI: 0.22 - 1.11, P = 0.09).

CONCLUSION

Nifedipine is associated with greater effective control of blood pressure and prolongation of gestation, with no additional neonatal respiratory distress syndrome or perinatal deaths, compared with other antihypertensives for women with severe preeclampsia.

摘要

目的

评估硝苯地平与其他抗高血压药物相比,治疗重度子痫前期孕妇的疗效、副作用及围产期结局。

方法

在PubMed、EMBase、Cochrane图书馆、中国知网和维普数据库等中检索(截至2012年1月)比较硝苯地平和其他抗高血压药物治疗重度子痫前期的随机对照试验(RCT)。对纳入的RCT质量进行评估,并用Rev Man 5.1软件进行Meta分析。

结果

纳入9项试验,硝苯地平组386例女性,其他抗高血压药物组378例女性。与其他抗高血压药物相比,硝苯地平能更有效地控制血压(OR = 2.65,95%CI:1.65 - 4.25,P < 0.01)。控制血压所需时间无明显差异(WMD = -3.64,95%CI:-10.90 - 3.61,P = 0.32)。硝苯地平比其他抗高血压药物能更好地延长孕周(WMD = 5.14,95%CI:3.29 - 6.99,P < 0.01)。母体副作用头痛(P = 0.28)、心悸(P = 0.06)和恶心呕吐(P = 0.28)无明显差异。两组在5分钟时的阿氏评分(WMD = -0.21,95%CI:-0.32 - 0.91,P = 0.72)、新生儿呼吸窘迫综合征(OR = 1.24,95%CI:0.57 - 2.67,P = 0.59)或围产期死亡(OR = 0.49,95%CI:0.22 - 1.11,P = 0.09)方面无显著差异。

结论

与其他抗高血压药物相比,硝苯地平能更有效地控制血压并延长孕周,对重度子痫前期女性不会增加新生儿呼吸窘迫综合征或围产期死亡的风险。

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