病理性妊娠中的血栓形成

J. Angelovski
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摘要

摘要介绍。怀孕期间的许多情况都会产生血栓,据信血栓有保护功能,这是激素影响的结果,主要是孕激素的影响。这是一种生理状况,有助于胚胎成功着床和防止出血。附加的、遗传的或获得性的血栓形成原因破坏了自然平衡,为静脉血栓栓塞和妊娠后果创造了条件,如流产、宫内胎儿死亡、宫内生长迟缓、子痫和胎盘早剥。方法。该研究设计为一项回顾性流行病学横断面研究,于2016年6月至10月在斯科普里输血医学研究所进行。该研究包括目前病理性妊娠的患者。对所有患者进行止血、d -二聚体、抗凝血酶III、蛋白C、蛋白S、抗磷脂抗体、狼疮抗凝剂、MTHFR、Leiden因子V和凝血酶原突变等实验室分析。结果。该研究包括41例患者,其中3例因病史不充分而被排除,3例因接受皮质类固醇治疗而被排除,2例因实验室分析不完整而被排除,1例被证实患有系统性狼疮。数据分析显示,25%的患者有血栓形成家族史。最常见的MTHFR突变记录在26例(82%)患者中,其次是18例(55%)患者中出现的因子V突变。仅1例患者(2%)检测到AT III缺乏症。在12例(35%)患者中,DD与APTT明显缩短或DD水平不适当低的比例失调,这是低纤溶的间接指标。结论。病理性妊娠通常与血栓形成有关。高龄患者,血栓形成的家庭和个人病史表明妊娠并发症的高风险。由于目前与胎盘循环问题相关的高危妊娠频率增加,因此需要在妊娠期间更频繁地进行止血检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thrombophilia in Pathological Pregnancies
Abstract Introduction. Many situations in pregnancy create a thrombophilia, which is believed to have a protective function, which is the result of the hormone influence, primarily by gestagenic hormones. This is a physiological condition and it helps in successful implantation of the embryo and prevention of bleeding. The presence of additional, hereditary or acquired cause of thrombophilia disrupts the natural balance and creates conditions for venous thromboembolism and consequences for pregnancy, such as miscarriage, intrauterine fetal death, delayed intrauterine growth, eclampsia and abruption of the placenta. Methods. The study was designed as a retrospective epidemiological cross-sectional study and was conducted at the Institute of Transfusion Medicine in Skopje in the period from June to October 2016. The study included patients with current pathological pregnancies. The following laboratory analyses were conducted in all patients: hemostasis, D-dimer, antithrombin III, protein C, protein S, antiphospholipid antibodies, lupus anticoagulant, MTHFR, factor V Leiden and prothrombin mutation. Results. The study included 41 patients, of whom 3 were excluded due to an insufficient medical history, 3 who were receiving corticosteroid therapy, 2 due to incomplete laboratory analyses and one patient with proven systemic lupus. Data analysis showed that family history of thrombophilia was present in 25%. The most common MTHFR mutation was recorded in 26 (82%) patients, followed by the factor V mutation present in 18 (55%) of the examined patients. AT III deficiency was detected in only one patient (2%). In 12 patients (35%) a disturbed ratio of DD vs. markedly shortened APTT or inappropriately low levels of DD was registered, which is an indirect indicatorof hypofibrinolysis. Conclusion. Pathologic pregnancy is a condition that is often associated with thrombophilia. Advanced age of a patient, family and personal history of thrombotic conditions indicate a high risk of complications in pregnancy. Due to the current increased frequency of high risk pregnancies associated with circulation problems with the placenta, there is a need for more frequent hemostatic examinations in pregnancy.
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