妊娠期抗凝血剂

Peter W. Howie
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引用次数: 0

摘要

血栓栓塞性疾病仍然是妊娠期的一个严重问题,抗凝剂在治疗和预防方面都发挥着重要作用。华法林是最方便的药物,但可能导致产妇和胎儿出血问题,特别是在妊娠晚期和分娩期间。妊娠早期使用华法林也有很小的胚胎病风险,但这些风险可能被夸大了。肝素不能穿过胎盘屏障,但仍可能导致妊娠期出血问题。全静脉肝素仅适合短期使用,而皮下肝素已被引入长期治疗。这个方案是有用的进步,但长期使用仍然有挫伤和产妇骨脱矿的问题。妊娠期急性血栓栓塞事件的标准治疗是持续静脉注射肝素,然后皮下注射肝素或华法林,后者在妊娠36周时改变。在预防血栓栓塞方面,趋势是采取更有选择性的方法,在怀孕期间给予高危人群抗凝血,在分娩和产褥期给予所有有血栓栓塞史的人抗凝血。使用人工心脏瓣膜的患者在妊娠期间必须使用抗凝剂,由于皮下肝素不足,应使用华法林至36周,然后持续静脉注射肝素直至分娩。妊娠期抗凝治疗没有一种方法是完全没有风险的,所有的管理政策必须基于对个体患者的风险-收益比的估计。
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Anticoagulants in Pregnancy

Thromboembolic disorders are still a serious problem in pregnancy and anticoagulants have an important part to play in both treatment and prevention.

Warfarin is the most convenient drug to give but can cause maternal and fetal bleeding problems, especially during late pregnancy and delivery. There are also small risks of embryopathy from warfarin in early pregnancy but these may have been overstated. Heparin, which has to be given parenterally, does not cross the placental barrier but can still cause bleeding problems in pregnancy. Full intravenous heparin is only suitable for short-term use, and subcutaneous heparin has been introduced for long-term therapy. This regimen is a useful advance but long-term use still has problems of bruising and maternal bone demineralization.

The standard treatment of acute thromboembolic events in pregnancy is continuous intravenous heparin followed by either subcutaneous heparin or warfarin, the latter being changed at 36 weeks gestation. In the prophylaxis of thromboembolism, the trend istowards a more selective approach, anticoagulants being given during pregnancy to those at highest risk and during labour and the puerperium to all with a previous history of thromboembolism. Anticoagulants during pregnancy are necessary in patients with artificial heart valves and, because subcutaneous heparin is not sufficient, warfarin should be used until 36 weeks followed by continuous intravenous heparin until delivery.

No method of anticoagulation during pregnancy is entirely free of risk and all management policies must be based on an estimate of risk-benefit ratio in individual patients.

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