医学
指南
免疫性血小板减少症
埃尔特罗姆博帕格
血小板生成素受体
重症监护医学
疾病
人口
生活质量(医疗保健)
免疫系统
免疫学
自身免疫性疾病
介绍(产科)
疾病管理
儿科
罗米普洛斯蒂姆
血小板
内科学
初级保健
血液学
血小板输注
血小板生成素
护理标准
出处
期刊:PubMed
[National Institutes of Health]
日期:2025-12-14
卷期号:46 (12): 1105-1113
被引量:4
标识
DOI:10.3760/cma.j.cn121090-20251031-00494
摘要
Primary immune thrombocytopenia (ITP) is an acquired autoimmune disease characterized by impaired immune tolerance, leading to increased platelet destruction and decreased platelet production. In recent years, with population structure changes and disease management improvements in China, adult ITP exhibits a trend toward older age at presentation and increased incidence. Further, a proportion of patients are at risk of both bleeding and thrombosis. Based on its 2020 edition, this guideline integrates evidence-based medical evidence from domestic and international studies, updates the application of selected laboratory and auxiliary tests in diagnostic evaluation, refines strategies for emergency management and initial therapy, and systematically incorporates new treatment options, including thrombopoietin receptor agonists and small molecule kinase inhibitors. Moreover, it broadens combination regimens for subsequent treatment and places greater emphasis on balancing thrombotic risk and health-related quality of life in long-term management, thereby providing a reference for standardized and individualized care of adult ITP in China.
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