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首页> 外文期刊>BJU international >Effect of dutasteride, tamsulosin and the combination on patient-reported quality of life and treatment satisfaction in men with moderate-to-severe benign prostatic hyperplasia: 2-year data from the CombAT trial.
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Effect of dutasteride, tamsulosin and the combination on patient-reported quality of life and treatment satisfaction in men with moderate-to-severe benign prostatic hyperplasia: 2-year data from the CombAT trial.

机译:度他雄胺,坦索罗辛及其组合对中至重度良性前列腺增生患者的患者报告的生活质量和治疗满意度的影响:CombAT试验的2年数据。

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摘要

OBJECTIVE: To investigate the effect of dutasteride and tamsulosin as combined therapy compared with each monotherapy for improving patient-reported health outcomes in men with moderate-to-severe urinary symptoms and prostate enlargement, reporting the pre-planned 2-year analyses from the CombAT trial. PATIENTS AND METHODS: The CombAT study is an ongoing, international, double-blind, randomized, parallel-group trial. Men aged >or=50 years with a clinical diagnosis of benign prostatic hyperplasia (BPH), an International Prostate Symptom Score (IPSS) of >or=12 units, a prostate volume of >or=30 mL, a total serum prostate-specific antigen level of 1.5-10 ng/mL and a peak urinary flow of >5 and or=125 mL, were randomized to receive 0.5 mg dutasteride, 0.4 mg tamsulosin or the combination once daily for 4 years. Symptoms were assessed every 3 months. The primary endpoint at 2 years was the change in IPSS from baseline. Secondary endpoints included various measures of health outcomes, which included the BPH Impact Index (BII), IPSS Question 8 (Q8), and the Patient Perception of Study Medication (PPSM) questionnaire. RESULTS: Combined therapy resulted in significantly greater improvements in BII and IPSS Q8 from baseline than did dutasteride from 3 months and compared with tamsulosin from 9 months (BII) or 12 months (IPSS Q8). Assessments using the PPSM questionnaire showed that a significantly higher proportion of patients were satisfied with and would request dutasteride and tamsulosin combined therapy than with each monotherapy at 24 months. CONCLUSIONS: Dutasteride and tamsulosin combined therapy provides significantly greater improvements in patient-reported quality of life and treatment satisfaction than both monotherapies at 2 years, following the trends for clinical improvements in symptom scores and peak urinary flow rates, in men with moderate-to-severe BPH symptoms.
机译:目的:探讨度他雄胺和坦索罗辛联合使用疗法与每种单一疗法相比对改善患者报告的中度至重度泌尿症状和前列腺肥大的男性的健康效果的作用,并从CombAT报告了2年期计划的分析试用。患者与方法:CombAT研究是一项正在进行的国际双盲,随机,平行分组试验。年龄≥50岁的男性,临床诊断为良性前列腺增生(BPH),国际前列腺症状评分(IPSS)≥12单位,前列腺体积≥30mL,总血清前列腺特异性抗原水平为1.5-10 ng / mL,峰值尿流量> 5和<或= 15 mL / s,最小排尿量为>或= 125 mL,随机接受0.5 mg度他雄胺,0.4 mg坦索罗辛或每天一次,持续4年。每3个月评估一次症状。 2年时的主要终点是IPSS与基线相比的变化。次要终点包括各种健康结局指标,包括BPH影响指数(BII),IPSS问题8(Q8)和患者对研究药物的认知度(PPSM)问卷。结果:相比于3个月的dutasteride,联合治疗导致BII和IPSS Q8的基线改善显着大于9个月(BII)或12个月(IPSS Q8)。使用PPSM问卷进行的评估显示,在24个月时,与每种单一疗法相比,对dutasteride和tamsulosin联合疗法的满意程度更高,并要求采用度他雄胺和坦索罗辛的疗法。结论:在中度至中等年龄的男性中,随着症状评分和尿液流速峰值的临床改善趋势,在两种情况下,度他雄胺和坦索罗辛联合治疗比两种单一疗法在患者报告的生活质量和治疗满意度方面的改善明显更大。严重的BPH症状。

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