Kuriya S, Nomura T
Nihon Ketsueki Gakkai Zasshi. 1989 Dec;52(8):1379-85.
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.
由日本厚生省造血器官疾病研究委员会开展的一项关于慢性特发性血小板减少性紫癜(ITP)治疗的多中心前瞻性研究正在进行中。在本研究中,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,在中位观察期34个月后,256例患者中有174例(68%)存活,11例(4%)死亡,71例(28%)失访。出血仅为1例患者的直接死因。根据最后一次观察时的血小板计数对患者状况进行评估,结果显示48%的患者缓解,21%的患者病情改善,31%的患者病情无变化或恶化。单因素分析确定了4个与预后良好相关的参数:初始血小板计数低于2×10⁴/微升、随访一年后血小板计数高于10×10⁴/微升、初始剂量皮质类固醇给药期间最大血小板计数高于10×10⁴/微升以及脾切除术。