妊娠期原发性免疫性血小板减少症的管理

J. Bussel, M. Hou, D. Cines
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摘要

(N Engl J Med. 2023;389:540-548) 免疫性血小板减少症(ITP)是一种自身免疫性疾病,其特点是免疫球蛋白 G 抗血小板抗体导致血小板生成减少和血小板清除增加。在美国,每 10,000 人中就有三分之一的人患有此病。ITP在育龄妇女中更为常见,在怀孕期间,血小板计数可能会下降,需要特别的医疗护理。免疫球蛋白 G 抗血小板抗体也会影响胎儿。ITP 的临床变异性使诊断和治疗变得更加复杂,管理的许多方面仍存在不确定性。本文重点介绍有关原发性 ITP 风险评估和管理的最新研究。
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Management of Primary Immune Thrombocytopenia in Pregnancy
(N Engl J Med. 2023;389:540–548) Immune thrombocytopenia (ITP) is an autoimmune disorder characterized by immunoglobulin G antiplatelet antibodies that lead to reduced platelet production and increased platelet clearance. It affects 1 in 3 people per 10,000 in the United States. ITP is more common in women of childbearing age, and during pregnancy, platelet counts may decrease, requiring special medical attention. Immunoglobulin G antiplatelet antibodies can also affect the fetus. The clinical variability of ITP complicates diagnosis and treatment, and uncertainty remains for many aspects of management. This article focuses on recent research on the risk assessment and management of primary ITP.
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