首页> 外文期刊>International journal of clinical practice >Comparative rapid onset of efficacy between doxazosin gastrointestinal therapeutic system and tamsulosin in patients with lower urinary tract symptoms from benign prostatic hyperplasia: a multicentre, prospective, randomised study.
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Comparative rapid onset of efficacy between doxazosin gastrointestinal therapeutic system and tamsulosin in patients with lower urinary tract symptoms from benign prostatic hyperplasia: a multicentre, prospective, randomised study.

机译:多沙唑嗪胃肠治疗系统和坦索罗辛在良性前列腺增生引起的下尿路症状患者中的快速起效比较:一项多中心,前瞻性,随机研究。

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摘要

AIMS: To compare the rapidity of improvement in lower urinary tract symptoms (LUTS) for the doxazosin gastrointestinal therapeutic system (GITS) and tamsulosin in benign prostatic hyperplasia (BPH) patients. METHODS: A total of 207 patients were randomised to one of two groups for a 12-week daily treatment with doxazosin-GITS 4 mg or tamsulosin 0.2 mg. The primary end-point was to compare the early onsets of efficacy between the two drugs. This was assessed by analysing the changes from baseline in the total International Prostate Symptom Score (IPSS) in the early period of treatment. Secondary aims were to compare improvements in obstructive/irritative subscore and quality of life (QoL) score between the two groups, and to evaluate the adverse events (AEs) with the drugs. RESULTS: After 12 weeks of treatment, both groups showed significant improvements in IPSS scores (total, obstructive and irritative subscores, QoL score) from baseline (p < 0.0001). However, the doxazosin-GITS group showed significantly greater improvements in total IPSS and obstructive subscore than the tamsulosin group in the early period (p < 0.05). Improvements in irritative subscore (within 4 weeks) and QoL score (during 12 weeks) were not significantly different between the groups. The incidences of AEs were similar between the groups. CONCLUSION: In this study, doxazosin-GITS showed significantly more rapid onset of efficacy and similar AEs compared with tamsulosin in BPH patients with LUTS. We believe this will probably improve patient compliance. Future studies with a larger number of patients and a longer follow-up period will be required to confirm this.
机译:目的:比较良性前列腺增生(BPH)患者中多沙唑嗪胃肠治疗系统(GITS)和坦索罗辛改善下尿路症状(LUTS)的速度。方法:将207例患者随机分为两组,分别接受多沙唑嗪-GITS 4 mg或坦索罗辛0.2 mg每日治疗12周。主要终点是比较两种药物之间的早期疗效。通过分析治疗初期国际前列腺症状总评分(IPSS)与基线相比的变化来评估这一点。次要目的是比较两组之间阻塞性/刺激性子评分和生活质量(QoL)得分的改善,并评估药物的不良事件(AE)。结果:治疗12周后,两组患者的IPSS评分(总,阻塞性和刺激性评分,QoL评分)均较基线水平有显着改善(p <0.0001)。然而,与坦索罗辛组相比,多沙唑嗪-GITS组在总IPSS和梗阻性亚评分方面的改善明显大于坦洛新组(p <0.05)。刺激性评分(4周内)和QoL评分(12周内)的改善在两组之间无显着差异。两组之间的AE发生率相似。结论:在本研究中,与坦索罗辛相比,多沙唑嗪-GITS在BTS合并LUTS的患者中起效更快,且与AE相比相似。我们相信这可能会改善患者的依从性。需要进一步的研究以更多的患者和更长的随访期来证实这一点。

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