Dan K, Gomi S, Kuramoto A, Maekawa T, Nomura T
Third Department of Internal Medicine, Nippon Medical School, Tokyo, Japan.
Int J Hematol. 1992 Jun;55(3):287-92.
A multicenter prospective study on the treatment of chronic idiopathic thrombocytopenic purpura (ITP) was conducted by the Idiopathic Disorders of Hematopoietic Organs Research Committee (IDHORC), the Ministry of Health and Welfare of Japan. The aim of the study was to establish an improved therapeutic guide for chronic ITP. Of the 247 eligible patients 175 have been followed up to the present time, 16 patients have died, and 56 have been lost to follow-up. The median follow-up time was 55 months (range: 1 to 91 months). Of the 206 patients treated with corticosteroids, 13.1% achieved sustained complete remission. Splenectomy produced remissions in 52.5% of 72 patients evaluated 12 months after operation. Eighty-five patients were treated with immunosuppressive agents, but the response rates were low and the effect was transient in most cases. In the patients followed up without any specific treatment, the mean platelet counts showed slight improvement. Of the 16 patients who died during the observation period, only one died of bleeding; the remaining 15 died of causes unrelated to thrombocytopenia. It is noteworthy that five patients who were treated with corticosteroids or immunosuppressive agents died of infection.
日本厚生省造血器官特发性疾病研究委员会(IDHORC)开展了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。该研究的目的是建立一套改进的慢性ITP治疗指南。在247例符合条件的患者中,175例患者随访至今,16例患者死亡,56例患者失访。中位随访时间为55个月(范围:1至91个月)。在206例接受皮质类固醇治疗的患者中,13.1%实现了持续完全缓解。脾切除术使72例术后12个月接受评估的患者中有52.5%获得缓解。85例患者接受了免疫抑制剂治疗,但反应率较低,且在大多数情况下效果是短暂的。在未接受任何特异性治疗而接受随访的患者中,平均血小板计数略有改善。在观察期内死亡的16例患者中,仅1例死于出血;其余15例死于与血小板减少无关的原因。值得注意的是,5例接受皮质类固醇或免疫抑制剂治疗的患者死于感染。