TY - JOUR
T1 - INOVASIA Study
T2 - A Multicenter Randomized Clinical Trial of Pravastatin to Prevent Preeclampsia in High-Risk Patients
AU - Akbar, Muhammad Ilham Aldika
AU - Azis, Muhammad Alamsyah
AU - Riu, Deviana Soraya
AU - Wawengkang, Ellen
AU - Ernawati, Ernawati
AU - Bachnas, Muhammad Adrianes
AU - Sulistyowati, Sri
AU - Dachlan, Erry Gumilar
AU - Mose, Johanes Cornelius
AU - Dekker, Gus
N1 - Publisher Copyright:
© 2022 Georg Thieme Verlag. All rights reserved.
PY - 2024/6/18
Y1 - 2024/6/18
N2 - Objective Our objective was to determine if treatment with pravastatin prevents preeclampsia in pregnant patients at risk of preeclampsia. Materials and Methods 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. Result 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%; p = 0.034; odds ratio [OR] = 0.034, 95% confidence interval [CI] = 0.202-0.905) and preterm birth (16.1 vs. 36%; p = 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, p = 0.048). Overall, the pravastatin group showed better perinatal outcomes. Neonates with low Apgar scores (<7) at 1 minute (5.7 vs. 25.6%, p = 0.000) and 5 minutes (2.3 vs. 25.6%, p = 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%; p = 0.069). Conclusion Pravastatin (20 mg bid) significantly reduces the risk of preterm preeclampsia and preterm birth in women at a high risk of developing preeclampsia. Key Points 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.
AB - Objective Our objective was to determine if treatment with pravastatin prevents preeclampsia in pregnant patients at risk of preeclampsia. Materials and Methods 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. Result 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%; p = 0.034; odds ratio [OR] = 0.034, 95% confidence interval [CI] = 0.202-0.905) and preterm birth (16.1 vs. 36%; p = 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, p = 0.048). Overall, the pravastatin group showed better perinatal outcomes. Neonates with low Apgar scores (<7) at 1 minute (5.7 vs. 25.6%, p = 0.000) and 5 minutes (2.3 vs. 25.6%, p = 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%; p = 0.069). Conclusion Pravastatin (20 mg bid) significantly reduces the risk of preterm preeclampsia and preterm birth in women at a high risk of developing preeclampsia. Key Points 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.
KW - maternal outcomes
KW - perinatal outcomes
KW - pravastatin
KW - preeclampsia
KW - short-term health
UR - http://www.scopus.com/inward/record.url?scp=85132022094&partnerID=8YFLogxK
U2 - 10.1055/a-1798-1925
DO - 10.1055/a-1798-1925
M3 - Article
C2 - 35292944
AN - SCOPUS:85132022094
SN - 0735-1631
VL - 41
SP - 1203
EP - 1211
JO - American Journal of Perinatology
JF - American Journal of Perinatology
IS - 9
ER -