首页> 外文期刊>European Journal of Haematology >Risk of placenta-mediated pregnancy complications or pregnancy-related VTE in VTE-asymptomatic families of probands with VTE and heterozygosity for factor V Leiden or G20210 prothrombin mutation
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Risk of placenta-mediated pregnancy complications or pregnancy-related VTE in VTE-asymptomatic families of probands with VTE and heterozygosity for factor V Leiden or G20210 prothrombin mutation

机译:VTE先天性无症状先兆者的胎盘介导的妊娠并发症或与妊娠有关的VTE的风险,这些先兆者是VTE莱顿或G20210凝血酶原突变的先兆者

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Background: Few studies have evaluated the risk of pregnancy-related adverse events in asymptomatic relatives of probands for VTE and factor V Leiden or the G20210A variant. The antepartum management of this population ranges from antepartum anticoagulation therapy to clinical surveillance. Objective: To evaluate the risk of placenta-mediated pregnancy complications and pregnancy-related VTE in VTE-asymptomatic families of probands with VTE and who are heterozygous carriers of either factor V Leiden or PT-G20210A mutation. Methods: One hundred and fifty-eight relatives, who had 415 pregnancies, were retrospectively evaluated. Odds ratios and 95% confidence intervals were calculated to compare pregnancy outcomes between women with and without thrombophilia. Results: In the factor V Leiden group, 22 placenta-mediated pregnancy events of 152 pregnancies (14.4%) were reported, compared with 25 adverse events of 172 pregnancies in the G20210A prothrombin group (14.5%) and 13 adverse events of 91 pregnancies in the non-carrier group (14.2%). Carriers of factor V Leiden or G20210A prothrombin were not associated with a higher risk of pregnancy-adverse outcomes compared with non-carriers: OR 1.02 (95% CI, 0.40-2.25) and 1.25 (95% CI, 0.48-3.24), respectively. Four episodes of pregnancy-associated VTE of 415 pregnancies (0.96%) were recorded. Two episodes of VTE in the G20210A group, one in the factor V Leiden group, and one episode in the non-carrier group were noted. Conclusions: In VTE-asymptomatic relatives of probands with VTE, the presence of factor V Leiden or the G20210A prothrombin mutation in heterozygosis should not lead to a decision to instigate antepartum prophylaxis.
机译:背景:很少有研究评估无症状先证者VTE和V因子Leiden或G20210A变体的无症状亲属的妊娠相关不良事件的风险。该人群的产前管理范围从产前抗凝治疗到临床监测。目的:评估在VTE无症状先兆者中有胎盘介导的妊娠并发症和与妊娠有关的VTE的风险,这些先兆者是VTE莱顿或PT-G20210A突变的杂合子。方法:回顾性分析158例有415例妊娠的亲属。计算几率和95%置信区间以比较有和没有血栓形成倾向的妇女的妊娠结局。结果:在V Leiden因子组中,报告了22例胎盘介导的妊娠事件,共152例妊娠(占14.4%),而G20210A凝血酶原组的25例不良事件,即172例妊娠(占14.5%),13例91例妊娠的不良事件。非运营商组(14.2%)。与非携带者相比,携带因子V Leiden或G20210A凝血酶原的携带者与更高的妊娠不良结局风险无关:OR 1.02(95%CI,0.40-2.25)和1.25(95%CI,0.48-3.24) 。记录了四次415例妊娠相关的VTE(0.96%)。在G20210A组中发生了2次VTE发作,在因子V Leiden组中发生了1次发作,在非携带者组中发生了1次发作。结论:在具有先兆静脉血栓的先证者的无静脉血栓栓塞的亲属中,杂合症中存在因子V Leiden或G20210A凝血酶原突变不应导致进行预防产前预防的决定。

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