4.5 Article

A comparison of the efficacy and tolerability of tamsulosin and finasteride in patients with lower urinary tract symptoms suggestive of benign prostatic hyperplasia

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PROSTATE CANCER AND PROSTATIC DISEASES
卷 6, 期 4, 页码 315-323

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NATURE PUBLISHING GROUP
DOI: 10.1038/sj.pcan.4500680

关键词

prostatic hyperplasia; adrenergic alpha-antagonists; tamsulosin; finasteride; randomised controlled trial

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In this multicentre, double-blind study, patients with LUTS/BPH were randomised to 26 weeks with finasteride 5 mg once daily (n - 204) or tamsulosin 0.4 mg once daily (n = 199). Double-blind treatment was continued for another 26 weeks (total treatment duration: 1y). The primary efficacy parameter was the difference in mean change in total Symptom Problem Index (SPI) from baseline to end point at week-26 in the intention-to-treat (ITT) and per protocol (PP) populations. Tamsulosin induced a greater improvement in total SPI (-5.2 points or -37%) compared to finasteride (-4.5 points or -31%) at week-26 (P = 0.055 in ITT and P = 0.032 in PP). Tamsulosin improved urinary symptoms (particularly the more bothersome storage symptoms) and flow more quickly than finasteride. The difference was statistically significant for the SPI from week-1 (reduction, respectively, -2.5 vs -1.8 points, P = 0.043) to week-18 and for Q(max) from week-1 (increase, respectively, 2.3 vs 0.7 ml/s, P = 0.0007) to week-12. Both treatments were well tolerated with a comparable incidence of adverse events, including urinary retention.

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