首页> 外文期刊>Chest: The Journal of Circulation, Respiration and Related Systems >Venous thromboembolism, thrombophilia, antithrombotic therapy, and pregnancy: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (8th Edition).
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Venous thromboembolism, thrombophilia, antithrombotic therapy, and pregnancy: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (8th Edition).

机译:静脉血栓栓塞,血栓形成,抗血栓治疗和妊娠:美国胸科医师学院循证临床实践指南(第8版)。

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This article discusses the management of venous thromboembolism (VTE) and thrombophilia, as well as the use of antithrombotic agents, during pregnancy and is part of the American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (8th Edition). Grade 1 recommendations are strong and indicate that benefits do, or do not, outweigh risks, burden, and costs. Grade 2 recommendations are weaker and imply that the magnitude of the benefits and risks, burden, and costs are less certain. Support for recommendations may come from high-quality, moderate-quality or low-quality studies; labeled, respectively, A, B, and C. Among the key recommendations in this chapter are the following: for pregnant women, in general, we recommend that vitamin K antagonists should be substituted with unfractionated heparin (UFH) or low-molecular-weight heparin (LMWH) [Grade 1A], except perhaps in women with mechanical heart valves. For pregnant patients, we suggest LMWH over UFH for the prevention and treatment of VTE (Grade 2C). For pregnant women with acute VTE, we recommend that subcutaneous LMWH or UFH should be continued throughout pregnancy (Grade 1B) and suggest that anticoagulants should be continued for at least 6 weeks postpartum (for a total minimum duration of therapy of 6 months) [Grade 2C]. For pregnant patients with a single prior episode of VTE associated with a transient risk factor that is no longer present and no thrombophilia, we recommend clinical surveillance antepartum and anticoagulant prophylaxis postpartum (Grade 1C). For other pregnant women with a history of a single prior episode of VTE who are not receiving long-term anticoagulant therapy, we recommend one of the following, rather than routine care or full-dose anticoagulation: antepartum prophylactic LMWH/UFH or intermediate-dose LMWH/UFH or clinical surveillance throughout pregnancy plus postpartum anticoagulants (Grade 1C). For such patients with a higher risk thrombophilia, in addition to postpartum prophylaxis, we suggest antepartum prophylactic or intermediate-dose LMWH or prophylactic or intermediate-dose UFH, rather than clinical surveillance (Grade 2C). We suggest that pregnant women with multiple episodes of VTE who are not receiving long-term anticoagulants receive antepartum prophylactic, intermediate-dose, or adjusted-dose LMWH or intermediate or adjusted-dose UFH, followed by postpartum anticoagulants (Grade 2C). For those pregnant women with prior VTE who are receiving long-term anticoagulants, we recommend LMWH or UFH throughout pregnancy (either adjusted-dose LMWH or UFH, 75% of adjusted-dose LMWH, or intermediate-dose LMWH) followed by resumption of long-term anticoagulants postpartum (Grade 1C). We suggest both antepartum and postpartum prophylaxis for pregnant women with no prior history of VTE but antithrombin deficiency (Grade 2C). For all other pregnant women with thrombophilia but no prior VTE, we suggest antepartum clinical surveillance or prophylactic LMWH or UFH, plus postpartum anticoagulants, rather than routine care (Grade 2C). For women with recurrent early pregnancy loss or unexplained late pregnancy loss, we recommend screening for antiphospholipid antibodies (APLAs) [Grade 1A]. For women with these pregnancy complications who test positive for APLAs and have no history of venous or arterial thrombosis, we recommend antepartum administration of prophylactic or intermediate-dose UFH or prophylactic LMWH combined with aspirin (Grade 1B). We recommend that the decision about anticoagulant management during pregnancy for pregnant women with mechanical heart valves include an assessment of additional risk factors for thromboembolism including valve type, position, and history of thromboembolism (Grade 1C). While patient values and preferences are important for all decisions regarding antithrombotic therapy in pregnancy, this is particularly so for women with mechanical heart valves. For these women, we recommend either adjusted-d
机译:本文讨论了妊娠期间静脉血栓栓塞(VTE)和血栓形成的管理,以及抗血栓形成药物的使用,并且是《美国胸科医师学院循证临床实践指南》(第8版)的一部分。等级1的建议很强,并且表明收益确实超过了风险,负担和成本。 2级建议较弱,暗示收益和风险,负担和成本的大小不确定。对建议的支持可能来自高质量,中等质量或低质量的研究;本章的主要建议包括以下内容:对于孕妇,一般而言,我们建议应使用普通肝素(UFH)或低分子量的维生素K拮抗剂代替维生素K拮抗剂。肝素(LMWH)[1A级],也许在有机械心脏瓣膜的女性中除外。对于孕妇,我们建议LMWH优于UFH来预防和治疗VTE(2C级)。对于患有急性VTE的孕妇,我们建议在整个妊娠期间应继续皮下LMWH或UFH(1B级),并建议抗凝剂应在产后至少持续6周(总最小治疗时间为6个月)[等级2C]。对于先前仅发生VTE且不再存在短暂危险因素且没有血栓形成倾向的孕妇,我们建议进行产前临床监测和产后抗凝预防(1C级)。对于其他以前曾接受过VTE且没有长期抗凝治疗的孕妇,我们建议采用以下一种治疗方法,而不是常规护理或全剂量抗凝治疗:产前预防性LMWH / UFH或中等剂量LMWH / UFH或整个妊娠期间的临床监测以及产后抗凝药(1C级)。对于这类具有较高血栓形成风险的患者,除了预防产后,我们建议产前预防或中等剂量的LMWH或预防或中等剂量的UFH,而不是临床监测(2C级)。我们建议未接受长期抗凝剂治疗的多发性VTE孕妇应接受产前预防,中剂量或调整剂量的LMWH或中剂量或调整剂量的UFH,然后再接受产后抗凝剂(2C级)。对于那些接受长期抗凝治疗且先前接受过VTE的孕妇,我们建议在整个怀孕期间服用LMWH或UFH(调整剂量的LMWH或UFH,调整剂量的LMWH的75%,或中等剂量的LMWH),然后再长期服用产后长期抗凝剂(1C级)。我们建议对既往没有VTE病史但抗凝血酶缺乏症的孕妇进行产前和产后预防(2C级)。对于所有其他有血栓形成但无静脉血栓栓塞的孕妇,我们建议产前临床监测或预防性LMWH或UFH,加上产后抗凝剂,而不是常规护理(2C级)。对于反复发作的早期妊娠丢失或无法解释的晚期妊娠丢失的妇女,我们建议筛查抗磷脂抗体(1LA级)。对于患有这些妊娠并发症的妇女,其APLA呈阳性且无静脉或动脉血栓形成史,我们建议在产前服用预防性或中剂量UFH或预防性LMWH联合阿司匹林(1B级)。我们建议,对于有机械心脏瓣膜的孕妇,在妊娠期进行抗凝治疗的决定应包括对血栓栓塞的其他危险因素进行评估,包括瓣膜类型,位置和血栓栓塞的病史(1C级)。尽管患者的价值观和偏好对于怀孕期间有关抗血栓治疗的所有决定都很重要,但对于有机械心脏瓣膜的女性而言尤其如此。对于这些女性,我们建议您选择调整后的

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