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Treatment of severe immune thrombocytopenia associated with systemic lupus erythematosus: 59 cases.

机译:重度系统性红斑狼疮伴发的免疫性血小板减少症59例治疗。

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OBJECTIVE: To evaluate the response to treatment in a large cohort of patients with systemic lupus erythematosus (SLE) associated with autoimmune thrombocytopenia. METHODS: Response to treatment was assessed retrospectively in 59 patients with SLE, either definite (n = 44) or incomplete (n = 15), associated with frank autoimmune thrombocytopenia (defined as platelet count < 50 x 10(9)/l). Response to treatment was classified as complete (CR: platelet count > 150 x 10(9)/l), partial (PR: platelet count > 50 x 10/l), or failure (FR) in the other cases. RESULTS: Oral prednisone alone was used in 50 of the 59 patients (mean initial dose 1 mg/kg body weight/day). A response was obtained in 80% of cases (CR in 28. PR in 12) but only 11 (22%) had a sustained response (CR, n = 7; PR, n = 4). In contrast, combined treatment with prednisone and either danazol (n = 18) or hydroxychloroquine (n = 11) resulted in 50% (7 CR, 2 PR) and 64% (4 CR, 3 PR) longterm responses, respectively, allowing prednisone to be withdrawn or the dose tapered below 0.2 mg/kg body weight/day. High dose methylprednisolone pulses (n = 10) and intravenous immunoglobulin (IVIG) (n = 31) resulted in positive responses in 60% (4 CR, 2 PR) and 65% (12 CR, 8 PR) of cases, respectively, but the response was transient in each case. Splenectomy (n = 17) resulted in 65% longterm responses (10 CR, 1 PR). Only 2 longterm partial responses were obtained with the 22 immunosuppressant-containing regimens administered to 14 patients. At the end of the study. a response was observed in 52 (88%) patients [CR: 36 (61%), PR: 16 (27%)], mainly as a result of splenectomy or combined treatment with prednisone and either danazol or hydroxychloroquine. CONCLUSION: Longterm remission was obtained in the majority of patients. The major treatments inducing remission were splenectomy and prednisone combined with danazol or hydroxychloroquine.
机译:目的:评估系统性红斑狼疮(SLE)伴自身免疫性血小板减少症的一大批患者对治疗的反应。方法:回顾性评估59例SLE患者的治疗反应,无论是明确的(n = 44)还是不完全的(n = 15),与坦率的自身免疫性血小板减少症(定义为血小板计数<50 x 10(9)/ l)有关。在其他情况下,对治疗的反应分为完全(CR:血小板计数> 150 x 10(9)/ l),部分(PR:血小板计数> 50 x 10 / l)或衰竭(FR)。结果:59例患者中有50例仅使用口服泼尼松治疗(平均初始剂量为1 mg / kg体重/天)。在80%的病例中有反应(CR在28例中,PR在12例中),但只有11例(22%)有持续反应(CR,n = 7; PR,n = 4)。相比之下,泼尼松和达那唑(n = 18)或羟氯喹(n = 11)的联合治疗分别产生50%(7 CR,2 PR)和64%(4 CR,3 PR)的长期反应,允许泼尼松停用或剂量逐渐降低至0.2 mg / kg体重/天以下。高剂量甲基强的松龙脉冲(n = 10)和静脉内免疫球蛋白(IVIG)(n = 31)分别在60%(4 CR,2 PR)和65%(12 CR,8 PR)的病例中产生阳性反应,但是在每种情况下,响应都是短暂的。脾切除术(n = 17)导致65%的长期反应(10 CR,1 PR)。给予14例患者的22种含免疫抑制剂的方案仅获得2种长期部分反应。在研究结束时。 52例患者(88%)观察到有反应[CR:36(61%),PR:16(27%)],主要是由于脾切除术或泼尼松和达那唑或羟氯喹联合治疗的结果。结论:大多数患者均可获得长期缓解。引起缓解的主要方法是脾切除术和泼尼松联合达那唑或羟氯喹。

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