妊娠早期内皮病变孕妇子痫前期预防的特点

D.G. Konkov, S.I. Zhuk, V.V. Rud, V.V. Buran
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The patients of the main group were divided into clinical subgroups: 31 pregnant women with GE in subgroup A received acetylsalicylic acid (ASA) at a dose of 75 mg per or per day; 33 patients with preclinical GE from subgroup B received L-arginine at a dose of 4-4.2 g per or per day; 52 pregnant women with preclinical GE who refused prophylactic treatment were included in the subgroup C. The control group involved 58 pregnant women with a physiological gestation and without GE.The clinical effectiveness of the therapy was assessed by comparing the number of cases of perinatal pathology in the I, II and III trimesters.Results. The use of L-arginine as an alternative preventive therapy for the development of preeclampsia and other perinatal pathology made possible to reduce the rate of preeclampsia significantly (RR 0.19, 95% CI: 0.05-0.77; p=0.02) and placental hyperplasia/hypoplasia (RR 0.17, 95% CI: 0.04-0.68; p=0.01), compared to patients who did not receive any preventive treatment. In pregnant women with early-onset gestational endotheliopathy who received L-arginine, placental dysfunction was not diagnosed in the II and III trimesters of pregnancy and there were no cases of fetal growth retardation. The use of L-arginine was not associated with side effects and/or adverse reactions in the proposed dose and frequency of administration and can be considered beneficial for the mother and the fetus.Conclusions. 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引用次数: 0

摘要

目的:评价l -精氨酸在预防临床前妊娠内皮病变(GE)患者子痫前期和降低其他围产期风险方面的临床效果。材料和方法。在Vinnytsya国立Pirogov纪念医科大学妇产科N. 1临床基地进行比较临床研究,116例经实验室和仪器研究(微量白蛋白尿和内皮依赖性血管舒张)诊断为临床前GE的孕妇(主要组)参加研究。主组患者分为临床亚组:A亚组31例GE孕妇接受乙酰水杨酸(ASA)治疗,剂量为75mg / d或/ d;来自B亚组的33例临床前GE患者接受l -精氨酸治疗,剂量为4-4.2 g /天或每天;将52例拒绝预防性治疗的临床前GE孕妇纳入c组。对照组为58例生理妊娠且未进行GE的孕妇。通过比较1、2、3个月围产儿病理例数,评价该疗法的临床疗效。使用l -精氨酸作为预防子痫前期和其他围产期病理发展的替代疗法,可以显著降低子痫前期的发生率(RR 0.19, 95% CI: 0.05-0.77;p=0.02)和胎盘增生/发育不全(RR 0.17, 95% CI: 0.04-0.68;P =0.01),与未接受任何预防治疗的患者相比。在接受l -精氨酸治疗的早发性妊娠内皮病变孕妇中,妊娠二、三期未诊断出胎盘功能障碍,无胎儿生长迟缓病例。在建议的剂量和给药频率下,l -精氨酸的使用与副作用和/或不良反应无关,可以认为对母亲和胎儿有益。对有中度围生期风险的孕妇(临床前GE)开具ASA和l -精氨酸药物,不仅可以延长妊娠期,而且可以防止严重围生期病理的发生。对于患有临床前型GE的孕妇,每次或每天服用l -精氨酸溶液(每日剂量- 4.0-4.2 g)的疗程处方更为显著的临床效果可能与药物的促内皮保护作用有关。妊娠期间使用l -精氨酸的适宜性仍有争议,需要进一步研究确定最佳剂量、初始使用时间和持续时间,以达到最佳的预防或治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The features of the prevention of preeclampsia in pregnant women with gestational endotheliopathy in the first trimester
The objective: to evaluate the clinical effectiveness of L-arginine in the prevention of preeclampsia and reduction of other perinatal risks in patients with preclinical gestational endotheliopathy (GE).Materials and methods. A comparative clinical study was performed at the clinical base of the Department of Obstetrics and Gynecology N. 1 of the Vinnytsya National Pirogov Memorial Medical University. 116 pregnant women with preclinical GE (main group), which was diagnosed by laboratory and instrumental research (microalbuminuria and endothelium-dependent vasodilatation), took part in the study. The patients of the main group were divided into clinical subgroups: 31 pregnant women with GE in subgroup A received acetylsalicylic acid (ASA) at a dose of 75 mg per or per day; 33 patients with preclinical GE from subgroup B received L-arginine at a dose of 4-4.2 g per or per day; 52 pregnant women with preclinical GE who refused prophylactic treatment were included in the subgroup C. The control group involved 58 pregnant women with a physiological gestation and without GE.The clinical effectiveness of the therapy was assessed by comparing the number of cases of perinatal pathology in the I, II and III trimesters.Results. The use of L-arginine as an alternative preventive therapy for the development of preeclampsia and other perinatal pathology made possible to reduce the rate of preeclampsia significantly (RR 0.19, 95% CI: 0.05-0.77; p=0.02) and placental hyperplasia/hypoplasia (RR 0.17, 95% CI: 0.04-0.68; p=0.01), compared to patients who did not receive any preventive treatment. In pregnant women with early-onset gestational endotheliopathy who received L-arginine, placental dysfunction was not diagnosed in the II and III trimesters of pregnancy and there were no cases of fetal growth retardation. The use of L-arginine was not associated with side effects and/or adverse reactions in the proposed dose and frequency of administration and can be considered beneficial for the mother and the fetus.Conclusions. Prescribing ASA and L-arginine drugs for pregnant women with a moderate degree of perinatal risk (preclinical GE) made possible not only to prolong pregnancy, but also to prevent the development of severe perinatal pathology. A more pronounced clinical effectiveness of the course prescription of solution of L-arginine per or (daily dose of L-arginine - 4.0-4.2 g) in pregnant women with preclinical form of GE may be associated with the endotheliotropic protective effect of the drug.The appropriateness of using L-arginine during pregnancy is still debated, and further researches are needed to determine the optimal dosage, initial period for using and duration for the best prophylactic or therapeutic effect.
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