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Thrombocytopenia in pregnancy

机译:孕妇血小板减少

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摘要

Thrombocytopenia develops in 5% to 10% of women during pregnancy or in the immediate postpartum period. A low platelet count is often an incidental feature, but it might also provide a biomarker of a coexisting systemic or gestational disorder and a potential reason for a maternal intervention or treatment that might pose harm to the fetus. This chapter reflects our approach to these issues with an emphasis on advances made over the past 5 to 10 years in understanding and managing the more common causes of thrombocytopenia in pregnancy. Recent trends in the management of immune thrombocytopenia translate into more women contemplating pregnancy while on treatment with thrombopoietin receptor agonists, rituximab, or mycophenylate, which pose known or unknown risks to the fetus. New criteria to diagnose preeclampsia, judicious reliance on measurement of ADAMTS13 to make management decisions in suspected thrombotic thrombocytopenic purpura, new evidence supporting the efficacy and safety of anticomplement therapy for atypical hemolytic uremic syndrome during pregnancy, and implications of thrombotic microangiopathies for subsequent pregnancies are evolving rapidly. The goals of the chapter are to help the hematology consultant work through the differential diagnosis of thrombocytopenia in pregnancy based on trimester of presentation, severity of thrombocytopenia, and coincident clinical and laboratory manifestations, and to provide guidance for dealing with some of the more common and difficult diagnostic and management decisions.
机译:孕妇或产后即刻,血小板减少症的发生率在5%至10%之间。血小板计数低通常是偶然的特征,但它也可能提供系统性或妊娠性疾病共存的生物标志物,以及可能对胎儿造成伤害的母亲干预或治疗的潜在原因。本章反映了我们对这些问题的处理方法,重点介绍了过去5到10年在了解和管理孕妇血小板减少的常见原因方面取得的进展。免疫性血小板减少症管理的最新趋势表明,越来越多的妇女在接受血小板生成素受体激动剂,利妥昔单抗或霉酚酸酯治疗时怀孕,这会对胎儿造成已知或未知风险。诊断子痫前期的新标准,明智地依靠ADAMTS13的测定来做出可疑的血栓性血小板减少性紫癜的管理决策,支持非互补溶血尿毒症综合征期间抗补体疗法的有效性和安全性的新证据,以及血栓性微血管病对随后妊娠的影响正在发展迅速。本章的目的是帮助血液学顾问根据孕晚期,血小板减少症的严重程度以及临床和实验室表现的一致性对孕妇的血小板减少症进行鉴别诊断,并为处理一些较常见的和困难的诊断和管理决策。

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