Department of Urology, Gangnam Severance Hospital, Yonsei University Health System, Seoul, Korea.
Prostate Cancer Prostatic Dis. 2011 Dec;14(4):320-5. doi: 10.1038/pcan.2011.22. Epub 2011 Jul 26.
We aimed to evaluate the efficacy and safety of combination treatment using anticholinergics with α-blocker for initial treatment of both overactive bladder (OAB) and other lower urinary tract symptoms (LUTS), secondary to BPH. A 12-week, randomized, double-blind, placebo-controlled trial was conducted at four urology clinics in Korea, involving men, aged 50 years or older, with LUTS related to BPH and OAB. A total of 176 patients were randomly assigned to receive doxazosin (4 mg) plus placebo or doxazosin (4 mg) plus tolterodine SR (4 mg), once a day for 12 weeks. Changes from baseline in total International Prostate Symptom Score (IPSS), bladder diary variables, patient perception of bladder condition (PPBC), uroflowmetry, postvoid residual volume and IPSS subscores (voiding and storage) were analyzed. Of the 176 enrolled patients, 91 had doxazosin gastrointestinal therapeutic system (GITS) and placebo, and 85 had combined medication with doxazosin GITS and tolterodine SR. Compared with the doxazosin plus placebo group, the doxazosin plus tolterodine group showed significant reductions in IPSS storage subscore and improvement in the quality of life item, urgency episodes, as well as in micturition frequency at weeks 4 and 12. However, it failed to improve PPBC at week 4 as well as at week 12. Earlier intervention with anticholinergics plus α-blocker was tolerated well, including the questions about urinary retention (n=1) and dry mouth (n=2). Initial combination treatment of anticholinergics plus α-blocker showed positive results for men with LUTS related to BPH and OAB symptoms and did not increase the risk of urinary retention.
我们旨在评估抗胆碱能药物与 α 受体阻滞剂联合治疗对良性前列腺增生相关下尿路症状(LUTS)伴或不伴膀胱过度活动症(OAB)患者的疗效和安全性。这是一项为期 12 周的、在韩国 4 家泌尿科诊所进行的、随机、双盲、安慰剂对照的临床试验,共纳入年龄 50 岁及以上、因良性前列腺增生而伴有 LUTS 和 OAB 症状的男性患者。176 例患者被随机分为两组,分别接受多沙唑嗪(4mg)联合安慰剂或多沙唑嗪(4mg)联合托特罗定控释片(4mg)治疗,每天一次,疗程 12 周。分析从基线开始的总国际前列腺症状评分(IPSS)、膀胱日记变量、患者对膀胱状况的感知(PPBC)、尿流率、残余尿量和 IPSS 各分项评分(排尿和储尿)的变化。176 例入组患者中,91 例接受多沙唑嗪胃肠治疗系统(GITS)联合安慰剂治疗,85 例接受多沙唑嗪 GITS 联合托特罗定控释片治疗。与多沙唑嗪联合安慰剂组相比,多沙唑嗪联合托特罗定组在第 4 周和第 12 周时,IPSS 储尿分项评分显著降低,生活质量评分、尿急发作次数和排尿频率显著改善。但在第 4 周和第 12 周时,PPBC 均未得到改善。早期联合使用抗胆碱能药物和 α 受体阻滞剂的治疗方案耐受性良好,仅各有 1 例患者出现尿潴留相关问题(n=1)和口干相关问题(n=2)。对于因良性前列腺增生相关 LUTS 伴或不伴 OAB 症状的男性患者,抗胆碱能药物与 α 受体阻滞剂的初始联合治疗显示出积极的效果,并未增加尿潴留的风险。