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机构地区:[1]郑州大学护理学院临床教研室,河南郑州450052 [2]郑州大学第一附属医院皮肤性病科,河南郑州450052
出 处:《临床皮肤科杂志》2012年第7期440-442,共3页Journal of Clinical Dermatology
摘 要:目的:探讨咪唑斯汀长疗程递减疗法治疗慢性荨麻疹的疗效和安全性。方法:将患者随机分为试验组和对照组,每组各50例。前者采用长疗程递减疗法(10mg,1日1次×4周→10mg,2日1次×4周→10 mg,3日1次×4周),后者采用长疗程连续疗法,即咪唑斯汀10mg,每日1次,连续12周。并检测患者治疗前后血浆组胺水平的变化。结果:试验组和对照组的有效率分别为85.11%、89.36%,二者差异无统计学意义(x^2=0.382,P=0.536);治疗后试验组和对照组的血浆组胺水平分别为(2.54±0.91)nmol/L、(2.38±1.04)nmol/L,差异也无统计学意义(t=0.795,P=0.429)。结论:咪唑斯汀长疗程递减疗法治疗慢性荨麻疹安全、有效,且方便,值得临床推广应用。Objective: To observe the efficacy and safety of long-term decrement mizolastine therapy in the treatment of chronic urticaria. Methods: One hundred patients with chronic urticaria were randomly divided into two groups, the experi- mental group and control group. The experimental group was treated with long-term decrement mizolastine therapy (10 mg ev- ery day in the first four weeks, 10 mg every other day in the next 4 weeks, 10 mg per three days in the last 4 weeks),and the control group with long-term mizolastine therapy (10 mg every day for 12 weeks). In addition, EIA was used to detect the plasma level of histamine in both groups before and after treatment. Results: The total effective rate of the experimental group was 85.11%, and 89.36% in the control group respectively. There was no significant difference between the two groups' total effective rate ( X2 = 0.382, P= 0.536). After treatment, The plasma level of histamine was (2.54±0.91)nmol/L in the experimental group, compared to (2.38±1.04)nmol/L in the control group (t = 0.795, P= 0.429). Conclusions: It is effective, safe and convenient for long-term decrement mizolastine therapy in the treatment of chronic urticaria.
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