阿司匹林、低分子肝素或两者在预防复发性妊娠丢失和V Leiden因子突变妇女妊娠并发症中的作用

Cihan Karadağ, B. Akar, G. Gönenç, R. Aslancan, Nagihan Yılmaz, E. Çalışkan
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引用次数: 16

摘要

摘要目的:本研究旨在比较低分子肝素(LMWH)、低分子肝素联合低剂量阿司匹林或仅使用低剂量阿司匹林对复发性妊娠丢失(RPL)因子V Leiden突变(FVLM)患者妊娠结局的影响。材料与方法:对2764例RPL患者进行病因分析。测定了V - Leiden因子纯合子和杂合子的突变。随后,其中196名患者被诊断为FVLM并纳入研究;其中174人完成了研究。在妊娠第6周,参与者被随机分为三组。A组(n = 61)由每日口服100mg阿司匹林的患者组成,B组(n = 59)由每日口服40mg依诺肝素和100mg阿司匹林的患者组成,C组(n = 54)包括妊娠期间每日口服40mg依诺肝素的患者。结果:在完成研究的174例患者中,三组的活产率和流产率相似(p =。843和p =。694年,分别)。子痫、胎盘早剥、宫内胎儿生长受限、妊娠期糖尿病发生率组间比较差异无统计学意义。A组子痫前期患者数量明显高于B组和c组,A组早产水平明显高于B组和c组。结论:低剂量阿司匹林、低分子肝素加阿司匹林或单独使用低分子肝素对FVLM RPL患者的活产率相当。然而,低分子肝素降低了这组患者子痫前期的风险。因此低分子肝素可能对子痫前期有预防作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aspirin, low molecular weight heparin, or both in preventing pregnancy complications in women with recurrent pregnancy loss and factor V Leiden mutation
Abstract Objective: The aim of this study was to compare the effects of low molecular weight heparin (LMWH), LMWH plus low dose aspirin, or low dose aspirin only on pregnancy outcomes in recurrent pregnancy loss (RPL) patients with factor V Leiden mutation (FVLM). Materials and methods: A total of 2764 RPL patients were evaluated in for the etiology of RPL. Mutations in factor V Leiden homozygous and heterozygous were determined. Subsequently, 196 of these patients were diagnosed with FVLM and included in the study; of these 174 completed the study. At the sixth week of gestation of subsequent pregnancy participants were randomly distributed into three groups. Group A (n = 61) was composed of patients with an oral dose of 100 mg aspirin daily, Group B (n = 59) consisted of patients using 40 mg enoxaparin and 100 mg orally aspirin daily, and Group C (n = 54) included patients using 40 mg enoxaparin daily during pregnancy. Results: Among the 174 patients who completed the study, the live birth and miscarriage rates were similar for the three groups (p = .843 and p = .694, respectively). There was no significant difference among the groups in rates of eclampsia, placental abruption, intrauterine fetal growth restriction and gestational diabetes mellitus. The number of preeclamptic patients was significantly higher in Group A than Groups B and C. The levels of preterm birth was significantly higher in Group A than Groups B and C. Conclusion: Using low dose aspirin, LMWH plus aspirin, or LMWH alone yielded comparable live birth rates in RPL patients with FVLM. However, LMWH decreased the risk of preeclampsia in this group of patients. LMWH might therefore have a preventive role regarding preeclampsia.
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