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首页> 外文期刊>BJU international >A randomized, double-blind crossover study of tamsulosin and controlled-release doxazosin in patients with benign prostatic hyperplasia.
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A randomized, double-blind crossover study of tamsulosin and controlled-release doxazosin in patients with benign prostatic hyperplasia.

机译:坦索罗辛和控释多沙唑嗪在前列腺增生患者中的随机,双盲交叉研究。

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摘要

OBJECTIVE: To compare the effects of the doxazosin gastrointestinal therapeutic system, extended-release (doxazosin-GITS) formulation, and tamsulosin, another alpha1-antagonist, on total International Prostate Symptom Score (IPSS) and maximum urinary flow rate (Qmax) in treating patients with benign prostatic hyperplasia (BPH). PATIENTS AND METHODS: Data were analysed from a prospective, randomized, double-blind, crossover study of men aged 50-80 years with concomitant BPH and hypertension as inclusion criteria. Fifty-two men were treated in four phases: phase I, placebo run-in for 2 weeks; phase II, first study drug doxazosin-GITS or tamsulosin for 8 weeks; phase III, washout with placebo for 2 weeks; and phase IV, second study drug tamsulosin or doxazosin-GITS for 8 weeks. Doxazosin-GITS was started at 4 mg/day and tamsulosin at 0.4 mg/day, and then titrated to 8 mg/day and 0.8 mg/day, respectively, after 4 weeks of therapy if the increase in Qmax was < 3 mL/s or the reduction in total IPSS was < 30%. Efficacy assessments included the IPSS and Qmax. Changes in blood pressure were not analysed, as most patients were actually not hypertensive. Endpoint efficacy data were analysed using an analysis of covariance model, with terms for sequence, phase, patients and sequence within patients, in addition to the baseline as covariate. Forty-seven men were treated in both efficacy arms of the study and were evaluable for analysis. RESULTS: Doxazosin-GITS and tamsulosin significantly relieved lower urinary tract symptoms and significantly increased Qmax from baseline (P = 0.001). Doxazosin-GITS produced significantly greater improvements than tamsulosin in total IPSS (P = 0.019) and obstructive subscores (P = 0.004) at the last treatment visit. The difference between doxazosin-GITS and tamsulosin in improving Qmax approached significance in favour of the former (mean change from baseline 2.6 vs 1.7 mL/s, respectively; between-group difference P = 0.089). Both treatments were well tolerated. CONCLUSIONS: Treatment with doxazosin-GITS was significantly more effective than tamsulosin in relieving lower urinary tract symptoms.
机译:目的:比较多沙唑嗪胃肠道治疗系统,缓释(doxazosin-GITS)配方和坦索罗辛(另一种α1拮抗剂)对国际前列腺总症状评分(IPSS)和最大尿流率(Qmax)的影响前列腺增生(BPH)患者。患者与方法:数据来自于前瞻性,随机,双盲,交叉研究,研究对象为年龄在50-80岁的男性,同时伴有BPH和高血压。 52名男子分四个阶段接受治疗:第一阶段,安慰剂磨合2周;第二阶段,首先研究药物多沙唑嗪-GITS或坦索罗辛持续8周;第三阶段,用安慰剂冲洗2周;第四阶段,第二项研究药物坦索罗辛或多沙唑嗪-GITS治疗8周。如果Qmax的增加<3 mL / s,则在治疗4周后,Doxazosin-GITS开始于4 mg /天,坦洛新为0.4 mg /天,然后分别滴定至8 mg /天和0.8 mg /天。或IPSS总数减少了<30%。功效评估包括IPSS和Qmax。由于大多数患者实际上并非高血压,因此未分析血压变化。使用协方差分析模型对终点功效数据进行了分析,除基线为协变量外,还对序列,阶段,患者和患者体内的序列进行了分析。本研究的两个功效组均治疗了47名男性,可以评估其分析能力。结果:Doxazosin-GITS和坦索罗辛显着缓解了下尿路症状,并显着提高了从基线开始的Qmax(P = 0.001)。在上次治疗就诊时,Doxazosin-GITS的总IPSS(P = 0.019)和阻塞性亚评分(P = 0.004)的改善明显大于坦索罗辛。多沙唑嗪-GITS和坦洛新之间在改善Qmax上的差异接近显着性,以前者为佳(分别从基线2.6和1.7 mL / s的平均值变化;组间差异P = 0.089)。两种治疗均耐受良好。结论:多沙唑嗪-GITS治疗在缓解下尿路症状方面比坦索罗辛显着更有效。

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