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69例血栓性血小板减少性紫癜患者的临床特征与预后

[Clinical characteristics and outcome of 69 patients with thrombotic thrombocytopenic purpura].

作者信息

Zhang J L, Xing H Z, Wang F, Wan D M, Jiang Z X, Wang M

机构信息

Department of Hematology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.

出版信息

Zhonghua Nei Ke Za Zhi. 2022 Jul 1;61(7):797-800. doi: 10.3760/cma.j.cn112138-20210810-00541.

Abstract

To analyze the clinical characteristics, diagnosis, treatment and outcome of patients with thrombotic thrombocytopenic purpura (TTP). The clinical data of 69 adult patients with TTP were retrospectively analyzed. There were 19 males and 50 females with a median age of 42 (18-79) years. PLASMIC score 6-7 was recognized in 82.8% (53/64) patients. The activity of von Willebrand factor-cleaving protease (ADAMTS13), which was detected in 21 patients before treatment, was less than 5% in 17 patients and 5%-10% in 3 patients. All 69 patients were treated with plasma exchange (PEX) and/or fresh frozen plasma infusion (PI), 43 of whom were also given glucocorticoid. In addition to PEX/PI and glucocorticoid, rituximab and/or immunosuppressants were administrated in 20 patients. The median follow-up time was 12 (1-57) months. The remission rate was 69.6%, while the relapse rate was 11.6%. The 2-year overall survival (OS) rate was 69.6%±5.5%. The univariate and multivariate analysis showed that relapsed/refractory disease was an independent risk factor for OS. The 2-year OS rate of relapsed/refractory patients was significantly lower than that of the rest patients (41.5%±9.8% vs. 83.7%±5.6%, <0.001). Regarding the unfavorable prognosis in relapsed/refractory patients, rituximab and/or immunosuppressants are strongly recommended for sake of improving the overall survival.

摘要

分析血栓性血小板减少性紫癜(TTP)患者的临床特征、诊断、治疗及预后。回顾性分析69例成年TTP患者的临床资料。其中男性19例,女性50例,中位年龄42(18 - 79)岁。82.8%(53/64)的患者PLASMIC评分为6 - 7分。21例患者治疗前检测血管性血友病因子裂解蛋白酶(ADAMTS13)活性,17例患者活性小于5%,3例患者活性为5% - 10%。69例患者均接受了血浆置换(PEX)和/或新鲜冰冻血浆输注(PI)治疗,其中43例还给予了糖皮质激素。除PEX/PI和糖皮质激素外,20例患者使用了利妥昔单抗和/或免疫抑制剂。中位随访时间为12(1 - 57)个月。缓解率为69.6%,复发率为11.6%。2年总生存率(OS)为69.6%±5.5%。单因素和多因素分析显示,复发/难治性疾病是OS的独立危险因素。复发/难治性患者的2年OS率显著低于其余患者(41.5%±9.8% vs. 83.7%±5.6%,<0.001)。鉴于复发/难治性患者预后不良,强烈推荐使用利妥昔单抗和/或免疫抑制剂以提高总生存率。

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