Faculty of Medicine Universitas Airlangga, Department Obstetrics and Gynecology, Universitas Airlangga Hospital, Dr. Soetomo General Academic Hospital, Surabaya, Indonesia.
Faculty of Medicine Universitas Padjajaran, Department Obstetrics and Gynecology, Dr. Hasan Sadikin General Hospital, Bandung, Indonesia.
Am J Perinatol. 2024 Jul;41(9):1203-1211. doi: 10.1055/a-1798-1925. Epub 2022 Mar 15.
Our objective was to determine if treatment with pravastatin prevents preeclampsia in pregnant patients at risk of preeclampsia.
The study was performed in four major tertiary hospitals in Surabaya, Bandung, and Makassar between 2017 and 2021. Pregnant women at high risk of developing preeclampsia were recruited and randomized into an intervention group and control group. The control group received low-dose aspirin (80 mg) and calcium (1 g) daily, while the intervention group received additional pravastatin (20 mg twice daily) starting from 14 to 20 weeks' gestation until delivery. The pregnancy was followed until delivery, and the clinical data were collected. The primary outcome was the occurrence of preeclampsia.
A total of 173 people participated in this study, including 86 in the control group and 87 in the pravastatin group. The pravastatin group had a significantly lower rate of preterm preeclampsia (13.8 vs. 26.7%; = 0.034; odds ratio [OR] = 0.034, 95% confidence interval [CI] = 0.202-0.905) and preterm birth (16.1 vs. 36%; = 0.003; OR = 0.340, 95% CI = 0.165-0.7), mostly indicated preterm birth. Preeclampsia occurred later in the pravastatin group than in the control group (36.39 + 2.32 vs. 34.89 + 3.38 weeks, = 0.048). Overall, the pravastatin group showed better perinatal outcomes. Neonates with low Apgar scores (<7) at 1 minute (5.7 vs. 25.6%, = 0.000) and 5 minutes (2.3 vs. 25.6%, = 0.028) were significantly less common in the pravastatin group. Additionally, the rate of low birthweight babies (<2,500 g) was lower in the pravastatin group (27.6 vs. 40.7%; = 0.069).
Pravastatin (20 mg bid) significantly reduces the risk of preterm preeclampsia and preterm birth in women at a high risk of developing preeclampsia.
· This is an open-label multicenter RCT to evaluate pravastatin effect to prevent preeclampsia.. · Pravastatin significantly reduces the risk of preterm preeclampsia (PE) and preterm birth in high risk PE women.. · Pravastatin had a beneficial effect on perinatal outcomes, including Apgar scores and birth weight..
本研究旨在探讨普伐他汀治疗是否可预防子痫前期高危孕妇发生子痫前期。
本研究于 2017 年至 2021 年在泗水、万隆和望加锡的四家主要三级医院进行。招募子痫前期高危孕妇并随机分为干预组和对照组。对照组每天接受低剂量阿司匹林(80mg)和钙(1g)治疗,而干预组则从 14 至 20 周妊娠开始,每天接受两次普伐他汀(20mg)治疗,直至分娩。随访妊娠直至分娩,并收集临床数据。主要结局为子痫前期的发生。
共有 173 人参与了本研究,其中对照组 86 人,普伐他汀组 87 人。普伐他汀组早产子痫前期(13.8%比 26.7%; = 0.034;优势比 [OR] = 0.034,95%置信区间 [CI] = 0.202-0.905)和早产(16.1%比 36%; = 0.003;OR = 0.340,95%CI = 0.165-0.7)的发生率显著较低,且大多表现为早产。普伐他汀组子痫前期发生时间晚于对照组(36.39 + 2.32 比 34.89 + 3.38 周, = 0.048)。总体而言,普伐他汀组围产期结局较好。普伐他汀组新生儿 1 分钟(5.7%比 25.6%, = 0.000)和 5 分钟(2.3%比 25.6%, = 0.028)的低 Apgar 评分(<7)的发生率明显较低。此外,普伐他汀组低出生体重儿(<2500g)的发生率较低(27.6%比 40.7%; = 0.069)。
普伐他汀(20mg bid)可显著降低子痫前期高危孕妇发生早产子痫前期和早产的风险。
· 这是一项评估普伐他汀预防子痫前期的开放性、多中心 RCT。
· 普伐他汀可显著降低子痫前期高危孕妇发生早产子痫前期和早产的风险。
· 普伐他汀对围产期结局有有益影响,包括 Apgar 评分和出生体重。