Women's Helath, Epsom and St Helier University Hospitals NHS Trust, Carshalton, Sutton, UK
Women's Health, Kingston Hospital NHS Foundation Trust, Kingston upon Thames, London, UK.
BMJ Open. 2022 Jul 13;12(7):e059519. doi: 10.1136/bmjopen-2021-059519.
There are numerous studies reporting a disproportionally high prevalence of thrombophilia in women with a history of recurrent miscarriage (RM), which has led to overdiagnosis and treatment without an improvement in clinical outcomes. The objective of our study was to assess the prevalence of inherited and acquired thrombophilia in a large cohort of women with a history of early RM using internationally agreed diagnostic criteria and inclusion parameters and compare it to the meta-analysis results of existing literature.
DESIGN: Retrospective cohort study and systematic review of literature.
This is a retrospective cohort study set-up in two dedicated tertiary centres for women with RM in Southwest London and Surrey. We reviewed all the available literature related to causes of RMs. We ascertained the prevalence of thrombophilia in the study population and compared it with historical and published prevalence in the general population.
1155 women between 2012 and 2017. All patients had three or more first trimester miscarriages and a full thrombophilia screen.
The overall prevalence of thrombophilia in our study population is 9.2% (106/1155) with 8.1% (94/1155) of cases positive for inherited thrombophilia, which is similar to the general population; Factor V Leiden (4.9%; 57/1155) and prothrombin gene mutation (2.9%; 34/1155) were the most common inherited thrombophilias, while only 1% (12/1155) tested positive for acquired thrombophilia. Persistent positive lupus anticoagulant (LA) was found in 0.5% (6/1155) and persistent positive anticardiolipin (ACL) antibodies with a value ≥40 U/mL was found in 0.5% (6/1155) of patients. Tests for LA/ACL were performed a minimum of 12 weeks apart thus meeting the revised Sapporo criteria for a diagnosis of antiphospholipid syndrome.
The findings of our study demonstrate that the prevalence of inherited thrombophilia is similar in women with RM to that in the general population. Similarly, the prevalence of acquired thrombophilia, using the revised Sapporo criteria, in the cohort of RMs is similar to that in the general population. Therefore, we do not recommend investigation or treatment of inherited or acquired thrombophilia in women with RM.
CRD42020223554.
有大量研究报告称,反复性流产(RM)病史的女性中存在极高比例的血栓形成倾向,这导致过度诊断和治疗,但并未改善临床结局。本研究的目的是使用国际公认的诊断标准和纳入参数,评估大量早期 RM 病史女性中遗传性和获得性血栓形成倾向的流行率,并将其与现有文献的荟萃分析结果进行比较。
设计:回顾性队列研究和文献系统评价。
这是一项在伦敦西南部和萨里的两家专门的 RM 女性治疗中心设立的回顾性队列研究。我们回顾了所有与 RM 病因相关的可用文献。我们确定了研究人群中的血栓形成倾向患病率,并将其与历史和已发表的普通人群患病率进行了比较。
2012 年至 2017 年期间的 1155 名女性。所有患者均有三次或更多的早期妊娠流产,且进行了全面的血栓形成筛查。
本研究人群的总体血栓形成倾向患病率为 9.2%(106/1155),其中 8.1%(94/1155)的病例为遗传性血栓形成倾向阳性,这与普通人群相似;因子 V 莱顿(4.9%;57/1155)和凝血酶原基因突变(2.9%;34/1155)是最常见的遗传性血栓形成倾向,而仅 1%(12/1155)的病例检测出获得性血栓形成倾向阳性。持续阳性狼疮抗凝物(LA)占 0.5%(6/1155),持续阳性抗心磷脂抗体(ACL)抗体且值≥40 U/mL 占 0.5%(6/1155)。LA/ACL 检测至少相隔 12 周进行,因此符合抗磷脂综合征的修订撒尔普斯堡标准。
本研究结果表明,RM 病史女性的遗传性血栓形成倾向患病率与普通人群相似。同样,使用修订撒尔普斯堡标准,RM 队列中的获得性血栓形成倾向患病率与普通人群相似。因此,我们不建议对 RM 病史的女性进行遗传性或获得性血栓形成倾向的检查或治疗。
PROSPERO 注册号:CRD42020223554。