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成人原发免疫性血小板减少症中医诊治专家共识 被引量:18

Traditional Chinese medicine expert consensus on the diagnosis and management of adult primary immune thrombocytopenia
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摘要 本专家共识就成人原发免疫性血小板减少症的中医病名、主要病机、病机的主要特点和主要临床表现进行了标化和凝练,并就中医和中西医结合治疗本病提出了指导意见。本病分为出血证候和(或)虚损证候,治疗遵循分层次、个体化原则,对血小板计数≥20×10^(9)/L或无明显出血表现者,采用中医药为主治疗;对血小板计数<20×10^(9)/L或存在明显出血表现者,采用中西医结合治疗。不推荐使用大剂量地塞米松或标准剂量泼尼松治疗本病,以避免治疗性伤害。对症治疗能够有效提高患者生活质量,进而有助于提升血小板计数,必须予以充分重视。 This expert consensus has standardized and summarized the traditional Chinese medicine(TCM)disease name,main pathogenesis,main characteristics and main clinical manifestations of adult primary immune thrombocytopenia(ITP),and put forward the guidance of TCM and integrated traditional Chinese and Western medicine treatments of ITP.ITP associates with haematologic syndromes and(or)deficiency syndromes.Treatment should be applied by following stratification and individualization principle.For those patients with platelet count≥20×10^(9)/L or without obvious bleeding manifestations,TCM is the main treatment.The patients with platelet count<20×10^(9)/L or obvious bleeding manifestations could be treated with integrated traditional Chinese and Western medicine.The use of high-dose dexamethasone or standard-dose-prednisone are not recommended for the treatment of ITP to avoid therapeutic injury.Symptomatic treatment can effectively improve patients’life quality,and thus contribute to the increase of platelet count,which must be fully paid attention to.
作者 中华中医药学会血液病分会 朱文伟 陈信义 周永明 Chinese Society of Hematology,China Association of Chinese Medicine;ZHU Wen-wei;CHEN Xin-yi;ZHOU Yong-ming(不详;Yueyang Hospital of Integrated Traditional Chinese and Western Medicine,Shanghai University of Traditional Chinese Medicine,Shanghai 200437,China;Dongzhimen Hospital,Beijing University of Chinese Medicine,Beijing 100700,China)
出处 《中华中医药杂志》 CAS CSCD 北大核心 2022年第4期2129-2133,共5页 China Journal of Traditional Chinese Medicine and Pharmacy
基金 国家自然科学基金项目(No.81973798,No.81774258) 上海市临床重点专科(中医专业)建设项目(No.shslczdzk05201)。
关键词 原发免疫性血小板减少症 紫癜病 专家共识 Primary immune thrombocytopenia Purpura disease Expert consensus
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