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作 者:廖敦[1] 温淑华[1] 李轩[1] LIAO Dun;WEN Shuhua;LI Xuan(Andrology Department,People's Hospital of Dongguan,Guangdong Province,Dongguan 523000,China))
机构地区:[1]东莞市人民医院中医男科,广东东莞523000
出 处:《光明中医》2020年第13期1954-1956,共3页GUANGMING JOURNAL OF CHINESE MEDICINE
摘 要:目的观察火郁汤加减治疗慢性非细菌性前列腺炎的疗效,探讨慢性前列腺炎发病的机制。方法将符合观察标准的112例慢性非细菌性前列腺炎患者随机分为火郁汤组(试验组)与前列倍喜胶囊组(对照组),每组56例,8周为一个疗程,对治疗前后2组NIH-CPSI评分进行对比分析,评价2组临床疗效。结果2组治疗后NIH-CPSI总积分均较治疗前降低,治疗后试验组NIH-CPSI积分下降及症状改善情况优于对照组(P<0.05)。试验组与对照组总有效率分别为89.29%、73.21%,差异有统计学意义(P<0.05)。结论火郁汤加减治疗慢性前列腺炎疗效显著,湿郁在慢性前列腺炎的发病中占重要地位,针对湿郁病机治疗慢性非细菌性前列腺炎为本病的治疗提供了新的思路。Objective To observe the clinical efficacy of Huoyu decoration(HYD)in the treatment of chronic non-bacterial prostatitis.Methods 112 patients with chronic non-bacterial prostatitis were randomly divided into two groups.The treatment group of 56 cases was given HYD,and the control group of 56 cases was given Qianlie Beixi capsule(QLBXC).After 8 weeks of treatment,the changes of NIH-CPSI scores were observed and the clinical efficacy of the two groups was compared.Results The total NIH-CPSI scores of the experimental group and the control group before treatment were(28.61±8.66)and(27.87±7.63)respectively(P>0.05).After treatment,the total NIH-CPSI scores of the two groups were respectively(9.08±6.19)and(15.31±12.42)respectively.Compared with that before treatment,the improvement of symptoms and the decline of scores in the experimental group were better than that in the control group(P<0.05).The total effective rate of the treatment group was 89.29%,and that of the control group was 73.21%.The comparison difference between the two groups was statistically significant(P<0.05).Conclusion It is efficacy and safety of the HYD in treatment of chronic non-bacterial prostatitis.It is a new method for the treatment of chronic non-bacterial prostatitis from the treatment of dampness and stagnation.
关 键 词:热淋 火郁汤 湿郁 慢性非细菌性前列腺炎 前列倍喜胶囊
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