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Efficacy of Anticholinergics for Chronic Prostatitis/Chronic Pelvic Pain Syndrome in Young and Middle-Aged Patients: A Single-Blinded, Prospective, Multi-Center Study

机译:抗胆碱能器对年轻和中年患者慢性前列腺炎/慢性骨盆疼痛综合征的疗效:单一盲,前瞻性,多中心研究

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摘要

Purpose Chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) exhibits variable lower urinary tract symptoms (LUTS). The aim of this study was to evaluate the incidence of LUTS and the efficacy of an anticholinergic agent in young and middle-aged CP/CPPS patients. Methods Ninety-six men with CP/CPPS were randomly assigned in a single-blind fashion and received either ciprofloxacin (group 1, 49 patients) or ciprofloxacin and solifenacin (5 mg/day; group 2, 47 patients) for 8 weeks. The National Institutes of Health chronic prostatitis symptom index (NIH-CPSI), the International Prostate Symptom Score (IPSS), and the International Index of Erectile Function-5 (IIEF-5) were used to grade the patients' symptoms and the quality of life impact at the start of the study, and at 4 and 8 weeks from the initiation of the study. Results There was no significant difference between groups 1 and 2 with respect to age, duration of disease, or sub-domains of the IPSS, NIH-CPSI, or IIEF-5 at baseline. Of these patients, 67.4% had LUTS. Statistically significant differences were determined via the NIH-CPSI for total score and the pain and urinary domain scores. Statistically significant differences were determined via the IPSS for total score and the storage domain score. The total score of the IIEF-5 increased, but the change was not significant. There was no statistically significant difference in residual urine. Conclusions Many CP/CPPS patients had LUTS. Solifenacin in CP/CPPS demonstrated improvements in the NIH-CPSI and the IPSS total score and storage score. Storage factors significantly improved via the NIH-CPSI and IPSS assessments in the solifenacin treatment group.
机译:目的慢性前列腺炎/慢性盆腔疼痛综合征(CP / CPP)表现出可变的低尿路症状(LUT)。本研究的目的是评估嗜酸剂的发病和中年CP / CPP患者抗胆碱能药的疗效。方法采用含有CP / CPP的百分之九种男性以单一盲目的方式随机分配,并接受环丙沙星(第1族,49名患者)或环丙沙星和索尔锡(5毫克/天;第2次,47例,47名患者)8周。国家健康慢性前列腺症症状指数(NIH-CPSI),国际前列腺症状评分(IPS),以及国际勃起函数-5(IIEIIE-5)的国际指数用于分级患者的症状和质量生命影响在研究开始,并从研究开始时4和8周。结果基准,IPS,NIH-CPSI或IIEIIE-5在基线的年龄,疾病持续时间,患者或患者持续时间或2之间没有显着差异。在这些患者中,67.4%有LUT。通过NIH-CPSI确定统计学上的显着差异,以进行总分和疼痛和泌尿结构域分数。通过IPSS,通过IPS获得统计学上显着的差异,以获得总分和存储域分数。 IIET-5的总成绩增加,但变化并不重要。残留尿液没有统计学上显着的差异。结论许多CP / CPP患者有LUT。 CP / CPP中的Solifenacin在NIH-CPSI和IPS总分和储存分数中证明了改进。储存因子通过NIH-CPSI和Solifenacin治疗组的IPS评估显着改善。

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