Fruci Stefano, Salvi Silvia, Moresi Sascia, Gallini Francesca, Dell'Aquila Marco, Arena Vincenzo, Di Stasio Enrico, Ferrazzani Sergio, De Carolis Sara, Lanzone Antonio
UOC di Patologia Ostetrica, Dipartimento Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Fondazione Policlinico Universitario A. Gemelli IRCCS, Largo Agostino Gemelli 8, 00168 Rome, Italy.
UOC di Patologia Ostetrica, Dipartimento Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Fondazione Policlinico Universitario A. Gemelli IRCCS, Largo Agostino Gemelli 8, 00168 Rome, Italy.
Eur J Obstet Gynecol Reprod Biol. 2023 Apr;283:37-42. doi: 10.1016/j.ejogrb.2023.01.036. Epub 2023 Feb 1.
Preeclampsia (PE) is the major cause of maternal morbidity and mortality and the leading cause of premature delivery worldwide. As well as intrauterine growth restriction (IUGR), PE is associated with pathogenic evidence of placental malperfusion and ischemia. Recent literature has highlighted the potential of pravastatin in the prevention and treatment of these conditions. Aim of this study is to describe perinatal outcomes and placental histopathological findings in a small series of pregnant women with severe PE and IUGR treated with pravastatin on compassionate grounds. Two-year follow up of these babies is provided.
Between October 2017 and October 2019 in Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy, women with singleton pregnancy between 19.6 and 27.6 gestational weeks, who presented with severe PE and IUGR were counselled for a compassionate treatment with Pravastatin 40 mg a day. Treated women were compared with controls identified with similar data in terms of gestational age at diagnosis, clinical maternal data, Doppler severity findings. Neonates were followed up for two years.
The median time from diagnosis to delivery was 39 days (IQR 20) for women in the pravastatin group and 20 days (IQR 20.5) for controls. Looking to maternal blood exams, in the group of women treated with pravastatin, maximum transaminase, creatinine levels were lower than in controls, where the minimum platelet count was higher. Placenta examination did not reveal any significant differences in placental histopathological findings. No significant differences were observed in the investigated perinatal data, as well as in infant follow-up, although an increased prenatal weight gain was found in treated pregnancies in comparison to controls.
Our data did not allow us to find significant differences in pregnancy outcome and infant follow-up, as well as in placental histological picture in preeclamptic patients when pravastatin is administered in the late second trimester. However, we suggest its possible role in stabilizing the disease, increasing the prenatal weight gain and prolonging the duration of pregnancy, thus preventing the progression to a more severe maternal disease.
子痫前期(PE)是全球孕产妇发病和死亡的主要原因,也是早产的主要原因。与胎儿生长受限(IUGR)一样,PE与胎盘灌注不良和缺血的病理证据有关。最近的文献强调了普伐他汀在预防和治疗这些疾病方面的潜力。本研究的目的是描述一小系列因同情而接受普伐他汀治疗的重度PE和IUGR孕妇的围产期结局和胎盘组织病理学发现。并对这些婴儿进行了两年的随访。
2017年10月至2019年10月期间,在意大利罗马圣心天主教大学综合医院的圣心基金会,对妊娠19.6至27.6周的单胎妊娠妇女进行了咨询,这些妇女患有重度PE和IUGR,接受同情治疗,每天服用40毫克普伐他汀。将接受治疗的妇女与在诊断时的孕周、临床产妇数据、多普勒严重程度检查结果等方面具有相似数据的对照组进行比较。对新生儿进行了两年的随访。
普伐他汀组妇女从诊断到分娩的中位时间为39天(四分位间距20),对照组为20天(四分位间距20.5)。在产妇血液检查方面,接受普伐他汀治疗的妇女组中,最高转氨酶、肌酐水平低于对照组,而最低血小板计数较高。胎盘检查未发现胎盘组织病理学发现有任何显著差异。在所研究的围产期数据以及婴儿随访中未观察到显著差异,尽管与对照组相比,接受治疗的妊娠中产前体重增加有所增加。
我们的数据不允许我们在妊娠中期晚期给予普伐他汀时,在子痫前期患者的妊娠结局、婴儿随访以及胎盘组织学情况方面发现显著差异。然而,我们建议其在稳定疾病、增加产前体重增加和延长妊娠期方面可能发挥作用,从而防止进展为更严重的母体疾病。