Govindasamy Vaisnavy, Kamel Mohammed Amer, Volucke Gabriele, Javed Aashir, Palchaudhuri Upayan, Kazi Sayed Irfan, Albanna Ahmad, Akileh Mays, Mukherjee Rohit, Nusrat Rabia, Qaiser Tayyaba, Elzain Hassan Eman Ibrahim, Azhar Muhammad Muneeb, Hashmi Tallal Mushtaq, Ahmed Mushood, Hasan Ali, Ahmed Raheel
Department of Medicine, James Cook University Hospital, Middlesbrough TS4 3BW, UK.
Department of Medicine, Al-Quds University, East Jerusalem 20002, Palestine.
Med Sci (Basel). 2025 Jul 13;13(3):91. doi: 10.3390/medsci13030091.
Severe maternal hypertension is linked to adverse perinatal outcomes. Both nifedipine and hydralazine are commonly used antihypertensive agents in this setting. A comprehensive literature search was conducted in PubMed, Cochrane Library, and EMBASE from inception to April 2024 to identify randomized controlled trials comparing oral or sublingual nifedipine with intravenous hydralazine for the management of severe hypertension, with or without preeclampsia/eclampsia. A random-effects meta-analysis was performed using RevMan. Seven randomized controlled trials were included. The pooled analysis demonstrated no significant difference between the two agents regarding time to achieve optimal blood pressure control (MD = -1.08 min, 95% CI = -6.66 to 4.49), caesarean delivery (OR = 0.62, 95% CI = 0.38 to 1.03), neonatal birth weight (MD = 57.65 g, 95% CI = -209.09 to -324.40), NICU admissions (OR = 0.90, 95% CI = 0.41 to 1.98), and 5-min APGAR scores (MD = 0.1, 95% CI = -0.20 to 0.39). However, patients receiving nifedipine had significantly lower odds of experiencing medication-related adverse events (OR = 0.62, 95% CI = 0.40 to 0.97). Nifedipine and intravenous hydralazine showed comparable efficacy in achieving optimal blood pressure control and similar maternal and neonatal outcomes. However, nifedipine was associated with significantly fewer maternal adverse effects, indicating superior tolerability.
重度孕产妇高血压与不良围产期结局相关。硝苯地平和肼屈嗪都是这种情况下常用的抗高血压药物。从数据库建立至2024年4月,在PubMed、Cochrane图书馆和EMBASE中进行了全面的文献检索,以确定比较口服或舌下含服硝苯地平与静脉注射肼屈嗪治疗重度高血压(无论有无子痫前期/子痫)的随机对照试验。使用RevMan进行随机效应荟萃分析。纳入了七项随机对照试验。汇总分析表明,在实现最佳血压控制的时间(MD=-1.08分钟,95%CI=-6.66至4.49)、剖宫产(OR=0.62,95%CI=0.38至1.03)、新生儿出生体重(MD=57.65克,95%CI=-209.09至324.40)、新生儿重症监护病房(NICU)入院率(OR=0.90,95%CI=0.41至1.98)和5分钟阿氏评分(MD=0.1,95%CI=-0.20至0.39)方面,两种药物之间无显著差异。然而,接受硝苯地平治疗的患者发生药物相关不良事件的几率显著较低(OR=0.62,95%CI=0.40至0.97)。硝苯地平和静脉注射肼屈嗪在实现最佳血压控制方面显示出相当的疗效,母婴结局相似。然而,硝苯地平导致的孕产妇不良反应明显较少,表明其耐受性更好。