Pharmacological therapy of benign prostatic hyperplasia/lower urinary tract symptoms: an overview for the practising clinician

被引:75
作者
Chapple, CR [1 ]
机构
[1] Royal Hallamshire Hosp, Sheffield Teaching Hosp NHS Trust, Dept Urol, Sheffield S10 2JF, S Yorkshire, England
关键词
D O I
10.1111/j.1464-410X.2004.05022.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Less than 10 years ago surgery and watchful-waiting were the only widely accepted management options for lower urinary tract symptoms (LUTS) suggestive of benign prostatic hyperplasia (BPH) and benign prostatic obstruction (BPO). There has been an enormous decline in the popularity of surgery and it is now apparent that medication is the most frequently used treatment for BPH/LUTS; this has arguably therefore been the most major change in urological clinical practice in the last decade. Currently alpha(1)-adrenoceptor antagonists are the commonest medical therapy, and are thought to act by relaxing prostatic smooth muscle, the neural or so-called 'dynamic' component of BPO. 5alpha-reductase inhibitors (finasteride, dutasteride) are another option for BPH/LUTS, which reduce prostatic mass and therefore the mechanical or 'static' component of BPO. In the last 10 years there have been four direct comparative studies between alpha(1)-adrenoceptor antagonists and finasteride, including their combination, the results of which, and their implications for therapy, are discussed. Another group of agents are the phytotherapeutic extracts, which act via various mechanisms, many as yet poorly defined. This review critically assesses existing publications relating to the medical management of BPH/LUTS.
引用
收藏
页码:738 / 744
页数:7
相关论文
共 41 条
[11]   Finasteride: A long-term follow-up in the treatment of recurrent hematuria associated with benign prostatic hyperplasia [J].
Delakas, D ;
Lianos, E ;
Karyotis, I ;
Cranidis, A .
UROLOGIA INTERNATIONALIS, 2001, 67 (01) :69-72
[12]  
Furberg CD, 2000, JAMA-J AM MED ASSOC, V283, P1967
[13]   HIGH PREVALENCE OF BENIGN PROSTATIC HYPERTROPHY IN THE COMMUNITY [J].
GARRAWAY, WM ;
COLLINS, GN ;
LEE, RJ .
LANCET, 1991, 338 (8765) :469-471
[14]   EFFECT OF FINASTERIDE, A 5-ALPHA-REDUCTASE INHIBITOR ON PROSTATE TISSUE ANDROGENS AND PROSTATE-SPECIFIC ANTIGEN [J].
GELLER, J .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1990, 71 (06) :1552-1555
[15]   THE EFFECT OF FINASTERIDE IN MEN WITH BENIGN PROSTATIC HYPERPLASIA [J].
GORMLEY, GJ ;
STONER, E ;
BRUSKEWITZ, RC ;
IMPERATOMCGINLEY, J ;
WALSH, PC ;
MCCONNELL, JD ;
ANDRIOLE, GL ;
GELLER, J ;
BRACKEN, BR ;
TENOVER, JS ;
VAUGHAN, ED ;
PAPPAS, F ;
TAYLOR, A ;
BINKOWITZ, B ;
NG, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (17) :1185-1191
[16]  
ISAACS JT, 1990, PROSTATE, P1
[17]   Natural history of prostatism: Longitudinal changes in voiding symptoms in community dwelling men [J].
Jacobsen, SJ ;
Girman, CJ ;
Guess, HA ;
Rhodes, T ;
Oesterling, JE ;
Lieber, MM .
JOURNAL OF UROLOGY, 1996, 155 (02) :595-600
[18]   Tolerability of α-blockade with doxazosin as a therapeutic option for symptomatic benign prostatic hyperplasia in the elderly patient:: A pooled analysis of seven double-blind, placebo-controlled studies [J].
Kaplan, SA ;
D'Alisera, PM .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 1998, 53 (03) :M201-M206
[19]  
Kirby Roger, 1999, Journal of Urology, V161, P266
[20]   Efficacy and tolerability of doxazosin and finasteride, alone or in combination, in treatment of symptomatic benign prostatic hyperplasia: The Prospective European Doxazosin and Combination Therapy (PREDICT) trial [J].
Kirby, RS ;
Roehrborn, C ;
Boyle, P ;
Bartsch, G ;
Jardin, A ;
Cary, MM ;
Sweeney, M ;
Grossman, EB .
UROLOGY, 2003, 61 (01) :119-126