慢性血小板减少性紫癜的预后。

S Kuriya, T Nomura
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引用次数: 0

摘要

由日本卫生和福利部造血器官特发性疾病研究委员会开展的一项治疗慢性特发性血小板减少性紫癜(ITP)的多中心前瞻性研究目前正在进行中。在这项研究中,我们分析了256例慢性ITP患者的临床记录,以确定预后因素。截至1988年11月,中位观察期为34个月,256例患者中有174例(68%)存活,11例(4%)死亡,71例(28%)随访失败。只有一名患者的直接死因是出血。最后观察时基于血小板计数的患者状态评估显示,48%的患者处于缓解状态,21%的患者表现出改善,31%的患者保持不变或恶化。单因素分析确定了与预后良好相关的4个参数:血小板计数小于2 × 10(4)/微升,随访1年后血小板计数大于10 × 10(4)/微升,初始剂量皮质类固醇和脾切除术期间最大血小板计数大于10 × 10(4)/微升。
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Prognosis of chronic thrombocytopenic purpura.

A multicenter prospective study on the treatment of chronic idiopathic thrombocytopenic purpura (ITP), conducted by the Idiopathic Disorders of Hematopoietic Organ Research Committee, the Ministry of Health and Welfare of Japan, is currently in progress. In this study we analyzed the clinical records of 256 patients with chronic ITP in order to define the prognostic factors. As of November, 1988 after a median observation period of 34 months, 174 of the 256 patients (68%) were alive, 11 (4%) dead and 71 (28%) lost to follow-up. Bleeding was a direct cause of death in only one patient. Assessment of the status of patients based on platelet count at the final observation revealed that 48% of patients were in remission, 21% showed improvement, and 31% remained unchanged or worsened. Univariate analyses identified 4 parameters associated with favorable prognosis: presenting platelet count less than 2 x 10(4)/microliters, platelet count greater than 10 X 10(4)/microliters after one-year follow-up, maximal platelet count greater than 10 X 10(4)/microliters during administration of the initial dose of corticosteroids and splenectomy.

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