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蒲地蓝消炎口服液治疗寻常型痤疮的临床疗效观察 被引量:4

The clinical observation of treatment in the acne vulgaris with Pudilanxiaoyan oral liquid
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摘要 目的:观察蒲地蓝消炎口服液治疗寻常型痤疮的疗效并进行分析。方法:将本院收治的126例寻常型痤疮患者按随机数字表法分成治疗组和对照组,治疗组64例给予蒲地蓝消炎口服液,对照组62例给予丹参酮胶囊口服,治疗周期为6周。所有患者在治疗3周、6周时观察临床疗效,比较痤疮分级的变化。结果:治疗3周后治疗组和对照组有效率分别为75.0%和75.8%,2组之间比较差异无统计学意义(!2=0.50,P>0.05);治疗6周后2组有效率分别为93.8%和85.5%,2组之间差异有统计学意义(!2=8.50,P<0.05);治疗组和对照组治疗结束后总皮损、炎症性皮损和非炎症性皮损比较差异有统计学意义(P<0.05);治疗后2组分级差异有统计学意义(!2=16.8,P<0.05)。结论:蒲地蓝消炎口服液治疗寻常型痤疮疗效好,值得临床推广。 Objective To observe the clinical curative effect Pudilanxiaoyan oral liquid for the treatment of acne vulgaris. Methods : 126 acne patients were randomly divided into the treatment group and the control group. The 64 cases in the treatment group were treated with Pudilanxiaoyan oral liquid and the 62 cases in the control group were treated with Salvia ketone capsule. The treatment cycle was 6 weeks. The clinical effects 3 weeks and 6 weeks after the treatment were evaluated, the alteration of the classification of acne improved levels were compared. Rusuhs The effective rate in treatment group and the control group 3 weeks after the treatment were 75.0% and 75.8% respectively, the difference was not significant (x^2 =0.50 ,P 〉 0.05 ) ; The total effective rates in treatment group was 93.8% , significantly higher than the control group ( 85.5% ) , the difference was significant ( x^2 = 8.50, P 〈 0. 05 ). The inflammatory lesions, non- inflammatory lesions and the total lesions were significant different between the treatment group and control group before and after the treatment ( P 〈 0. 05 ) ; There were significant differences in classification of the two groups after the treatment, the difference was statistically significant ( x^2= 16. 8, P 〈 0. 05 ). Conlusion The Pudilanxiaoyan oral liquid was effective in the treatment of the ache vulgaris, worthy of spreading therapeutic schedule.
出处 《中国中医基础医学杂志》 CAS CSCD 北大核心 2014年第5期697-699,共3页 JOURNAL OF BASIC CHINESE MEDICINE
关键词 寻常型痤疮 治疗 分级 蒲地蓝消炎口服液 Ache Treatment Classification
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