首页> 外文期刊>Circulation: An Official Journal of the American Heart Association >Thrombolytic therapy for the treatment of prosthetic heart valve thrombosis in pregnancy with low-dose, slow infusion of tissue-type plasminogen activator
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Thrombolytic therapy for the treatment of prosthetic heart valve thrombosis in pregnancy with low-dose, slow infusion of tissue-type plasminogen activator

机译:低剂量,缓慢输注组织型纤溶酶原激活剂的孕妇溶栓性人工瓣膜血栓形成治疗

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BACKGROUND - : Prosthetic valve thrombosis during pregnancy is life-threatening for mother and fetus, and the treatment of this complication is unclear. Cardiac surgery in pregnancy is associated with very high maternal and fetal mortality and morbidity. Thrombolytic therapy has rarely been used in these patients. The aim of this study is to evaluate the safety and efficacy of low-dose (25 mg), slow infusion (6 hours) of tissue-type plasminogen activator for the treatment of prosthetic valve thrombosis in pregnant women. METHODS AND RESULTS - : Between 2004 and 2012, tissue-type plasminogen activator was administered to 24 consecutive women in 25 pregnancies with 28 prosthetic valve thrombosis episodes (obstructive, n=15; nonobstructive, n=13). Mean age of the patients was 29±6 years. Thrombolytic therapy sessions were performed under transesophageal echocardiography guidance. The mean dose of tissue-type plasminogen activator used was 48.7±29.5 mg (range, 25-100mg). All episodes resulted in complete thrombus lysis after thrombolytic therapy. One patient had placental hemorrhage with preterm live birth at the 30th week, and 1 patient had minor bleeding. CONCLUSIONS - : Low-dose, slow infusion of tissue-type plasminogen activator with repeated doses as needed is an effective therapy with an excellent thrombolytic success rate for the treatment of prosthetic valve thrombosis in pregnant women. This protocol also seems to be safer than cardiac surgery or any alternative medical strategies published to date. Thrombolytic therapy should be considered first-line therapy in pregnant patients with prosthetic valve thrombosis.
机译:背景-怀孕期间的人工瓣膜血栓形成危及母亲和胎儿的生命,目前尚不清楚该并发症的治疗方法。妊娠期心脏手术与极高的母婴死亡率和发病率有关。这些患者很少使用溶栓治疗。这项研究的目的是评估低剂量(25 mg),缓慢输注(6小时)组织型纤溶酶原激活剂治疗孕妇人工瓣膜血栓形成的安全性和有效性。方法和结果-:在2004年至2012年之间,对25例妊娠中连续24例女性进行了组织型纤溶酶原激活剂治疗,其中28例发生了人工瓣膜血栓形成(阻塞性,n = 15;非阻塞性,n = 13)。患者的平均年龄为29±6岁。在经食道超声心动图指导下进行溶栓治疗。使用的组织型纤溶酶原激活剂的平均剂量为48.7±29.5 mg(范围为25-100mg)。所有这些事件导致溶栓治疗后血栓完全溶解。 1名患者在第30周发生胎盘出血并早产,1名患者出现轻微出血。结论-:低剂量,缓慢输注组织型纤溶酶原激活剂并根据需要重复给药是一种有效的疗法,具有优异的溶栓成功率,可用于治疗孕妇的人工瓣膜血栓。该协议似乎也比心脏手术或迄今为止发布的任何其他医学策略更安全。对于人工瓣膜血栓形成的孕妇,应考虑溶栓治疗的一线治疗。

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