目的:评价沙利度胺治疗幼年特发性关节炎(juvenile idiopathic arthritis,JIA)的临床疗效和安全性。方法:12例传统治疗方案治疗病情无缓解的JIA患儿,应用沙利度胺治疗(每日2 mg/kg),记录治疗前后患儿的症状、体征、实验室指标及沙利度胺治疗的不良反应。结果:沙利度胺治疗6个月后,患儿泼尼松用量由每日1.92±0.16 mg/kg 降至0.49±0.42 mg/kg (P<0.01),并有4例能停用泼尼松治疗。12例患儿外周血白细胞计数、ESR、CRP、血清铁蛋白(SF)较治疗前均明显下降(P<0.01); 8例患儿血红蛋白明显升高(P<0.01)。多关节型JIA患儿平均受累关节数由5个以上降至0~2个(P<0.01),附着点炎症型患儿双“4”字征转阴,Schober′s征转阴。治疗过程中未出现严重不良反应。结论:沙利度胺对JIA有显著的临床疗效,可以作为传统治疗方案无效后的治疗措施。
Abstract
OBJECTIVE: To evaluate the efficacy of thalidomide in the treatment of juvenile idiopathic arthritis (JIA). METHODS: Twelve children with JIA who did not respond to conventional treatment were administered with thalidomide (2 mg/kg daily). The symptoms, signs, and laboratory test results were compared before and after treatment. The thalidomide-related side effects were observed. RESULTS: The average dosage of prednisone was reduced from 1.92±0.16 mg/kg?d to 0.49±0.42 mg/kg?d in the 12 patients 6 months after thalidomide treatment (P<0.01). Four patients did not need prednisone treatment any more. White blood cell count, erythrocyte sedimentation rate (ESR), C reactive protein (CRP) and serum ferritin (SF) significantly decreased after treatment in all of 12 patients (P<0.01). Hemoglobin level increased to normal in 8 patients after treatment (P<0.01). The number of affected joints decreased from 5 before treatment to zero to 2 after treatment in patients with polyarticular JIA (P<0.01). Signs of hip involvement and Schober′s sign turned negative in enthesitis-related cases. No thalidomide-related side effects were observed. CONCLUSIONS: Thalidomide is effective in the treatment of JIA in children who do not respond to conventional treatment.
关键词
幼年特发性关节炎 /
沙利度胺 /
儿童
Key words
Juvenile idiopathic arthritis /
Thalidomide /
Child
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