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遗传性易栓症在妊娠期的治疗意义。

Therapeutic Implications of Inherited Thrombophilia in Pregnancy.

机构信息

University of Medicine and Pharmacy Carol Davila, Bucharest, Romania.

Victor Babes Clinic Hospital, Bucharest, Romania.

出版信息

Am J Ther. 2019 May/Jun;26(3):e364-e374. doi: 10.1097/MJT.0000000000000985.

Abstract

BACKGROUND

Inherited (hereditary) thrombophilia is a genetic disorder that affects coagulation, being responsible for more than 60% of idiopathic (spontaneous or unprovoked) thromboembolic events. Association of inherited thrombophilia with pregnancy increases the risk of thromboembolic disease, and it may be related to many complications, such as preeclampsia, recurrent miscarriage intrauterine growth restriction, early detachment of placenta, and prematurity.

AREAS OF UNCERTAINTY

Interpretation of a positive test for thrombophilia in pregnant women is difficult because they have many natural changes in the coagulation system. Genetic diagnosis of thrombophilia, after a thrombotic event or during a pregnancy complication, has a major importance, not only to define its etiology but also to determine the duration of anticoagulant treatment and risk stratification for prophylaxis treatment.

DATA SOURCES

Literature search was performed using electronic database (PubMed) between April 1981 and November 2018. We used different keywords and MeSH terms to generate the most relevant results related to the inherited thrombophilia and its impact on pregnancy.

RESULTS

Screening for inherited thrombophilia in young women is recommended in case of personal history of venous thromboembolism, first-degree relatives with a history of high-risk thrombophilia, or personal history of second-trimester miscarriage. Decision to recommend thromboprophylaxis with anticoagulant treatment in pregnant women with inherited thrombophilia is determined by history of venous thromboembolism, type and associated risk of inherited thrombophilia, and presence of additional risk factors. Low-molecular-weight heparins are the preferred agents for prophylaxis in pregnancy, while the doses vary depending on thrombophilia type, personal history, and associated risk factors.

CONCLUSIONS

Association between 2 procoagulant conditions, inherited thrombophilia and pregnancy, has an important impact for the mother and fetus. This review will summarize the impact of each inherited prothrombotic factor on cardiovascular and pregnancy outcomes and will discuss the role of anticoagulation treatment for women diagnosed with inherited thrombophilia.

摘要

背景

遗传性(遗传性)血栓形成倾向是一种影响凝血的遗传疾病,占特发性(自发性或自发性)血栓栓塞事件的 60%以上。遗传性血栓形成倾向与妊娠的关联增加了血栓栓塞疾病的风险,并且可能与许多并发症有关,例如子痫前期、复发性流产、宫内生长受限、早期胎盘脱离和早产。

不确定性领域

在孕妇中解释血栓形成倾向的阳性测试很困难,因为她们的凝血系统有许多自然变化。遗传性血栓形成倾向的基因诊断,无论是在血栓形成事件后还是在妊娠并发症期间,都具有重要意义,不仅可以确定其病因,还可以确定抗凝治疗的持续时间和预防治疗的风险分层。

数据来源

文献检索是使用电子数据库(PubMed)在 1981 年 4 月至 2018 年 11 月之间进行的。我们使用了不同的关键词和 MeSH 术语来生成与遗传性血栓形成倾向及其对妊娠的影响最相关的结果。

结果

如果有静脉血栓栓塞史、有高危血栓形成倾向的一级亲属史或有妊娠中期流产史,建议对年轻女性进行遗传性血栓形成倾向筛查。建议在有遗传性血栓形成倾向的孕妇中预防性使用抗凝药物治疗,取决于静脉血栓栓塞史、遗传性血栓形成的类型和相关风险、以及是否存在其他危险因素。低分子量肝素是妊娠预防性治疗的首选药物,而剂量取决于血栓形成倾向的类型、个人病史和相关危险因素。

结论

2 种促凝状态,遗传性血栓形成倾向和妊娠之间的关联对母亲和胎儿有重要影响。本综述将总结每种遗传性促血栓形成因素对心血管和妊娠结局的影响,并讨论诊断为遗传性血栓形成倾向的妇女抗凝治疗的作用。

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