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作 者:肖飞[1] 陈永华[1] 谷现恩[1] XIAO Fei;CHEN Yonghua;GU Xianen(Department of Urology,Beijing Chuiy- angliu Hospital Affiliated to Tsinghua University,Beijing100022,China)
机构地区:[1]清华大学附属北京市垂杨柳医院泌尿外科,北京100022
出 处:《中国性科学》2018年第5期13-15,共3页Chinese Journal of Human Sexuality
基 金:北京市朝阳区科技计划项目(CYSF162003)
摘 要:目的:评价复方玄驹胶囊联合前列舒通胶囊治疗ⅢB型前列腺炎患者的疗效和安全性。方法:100例ⅢB型前列腺炎患者分为观察组和对照组:50例为观察组,采用复方玄驹胶囊联合前列舒通胶囊治疗;50例为对照组,口服前列舒通胶囊治疗。结果:6周后随访时,观察组失访6例,对照组失访4例。两组患者治疗前入组时,一般情况比较差异无统计学意义(P>0.05),具有可比性。观察组总有效率为86.36%(38/44),高于对照组总有效率65.22%(30/46),差异具有统计学意义(P<0.01)。治疗6周后,观察组患者NIH-CPSI评分改善明显优于对照组,差异具有统计学意义(P<0.01)。治疗期间两组患者不良反应均轻微,无因此停药病例。结论:复方玄驹胶囊联合前列舒通胶囊治疗ⅢB型前列腺炎患者疗效可靠,副作用小,值得临床推广应用。Objective: To evaluate the efficacy and safety of Fufangxuanju capsule combined with Qianlieshutong capsule treatment on the patients with type ⅢB prostatitis. Methods: 100 patients withtype ⅢB prostatitis were divided into observation group( n = 50) and control group( n = 50). Observation group received treatment of Fufangxuanju capsule combined with Qianlieshutong capsule,while control group received Qianlieshutong capsule only. Results: In the 6-week follow-up survey,6 participants in observation group were lost,and 4 participants were lost in control group. The total effective rate of observation group was 86. 36%( 38/44),which was higher than that of control group( 65. 22%,30/46),with statistically significant difference( P〈0. 01). After treatment,NIH-CPSI of observation group was more significantly improved than that of control group( P〈0. 01). During the treatment,no obvious adverse reactions were observed among patients in the two groups. Conclusions: Treatment of Fufangxuanju capsule combined with Qianlieshutong capsule for patients with type ⅢB prostatitis is efficient and relatively safe,worthy of clinical application.
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