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Outcomes and Quality of Life Issues in the Pharmacological Management of Benign Prostatic Hyperplasia (BPH)

Overview
Publisher Dove Medical Press
Date 2008 Mar 25
PMID 18360626
Citations 4
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Abstract

Background: Benign prostatic hyperplasia (BPH) is a common disease of the aging male population. BPH treatment includes a variety of pharmacological and surgical interventions. The goal of this paper is to review the natural history of BPH, outcomes of pharmacological management, effects on quality of life (QoL), future pharmacotherapies, and associated patient-focused perspectives.

Materials And Methods: Medline searches for the keywords benign prostatic hyperplasia, BPH, alpha blockers, 5 alpha-reductase, and quality of life were performed. Relevant literature was reviewed and analyzed.

Results: Alpha blockers, 5 alpha-reductase inhibitors, and phytotherapy are the three categories of pharmaceutical interventions currently available for BPH. Various clinical trials have shown that alpha blockers and 5 alpha-reductase inhibitors are safe, efficacious, and improve QoL in patients with BPH. The evidence for phytotherapeutics is not as convincing. The current armamentarium of pharmaceutical interventions are encompassed in these three classes of medications. New pharmacotherapies based on novel mechanisms are on the horizon.

Conclusion: There are a variety of safe and efficacious medical therapies available for the management of BPH and it is important for the practicing physician to have an understanding of these pharmacotherapies and their potential impact on the patient. There is not enough evidence to make a recommendation regarding phytotherapy use. New classes of drugs for BPH will likely find their way into routine use.

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Leoci R, Aiudi G, Silvestre F, Lissner E, Lacalandra G Prostate. 2014; 74(11):1132-41.

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Superselective α-adrenergic blockers versus transurethral resection of the prostate: a prospective comparison of health-related quality of life outcome after treating patients with benign prostatic hyperplasia.

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References
1.
Schulman C, Lock T, Buzelin J, Boeminghaus F, Stephenson T, Talja M . Long-term use of tamsulosin to treat lower urinary tract symptoms/benign prostatic hyperplasia. J Urol. 2001; 166(4):1358-63. View

2.
Roberts R, Lieber M, Jacobson D, Girman C, Jacobsen S . Limitations of using outcomes in the placebo arm of a clinical trial of benign prostatic hyperplasia to quantify those in the community. Mayo Clin Proc. 2005; 80(6):759-64. DOI: 10.1016/S0025-6196(11)61530-9. View

3.
Andersson K, Chapple C, Hofner K . Future drugs for the treatment of benign prostatic hyperplasia. World J Urol. 2002; 19(6):436-42. DOI: 10.1007/s00345-002-0253-8. View

4.
Fong Y, Milani S, Djavan B . Role of phytotherapy in men with lower urinary tract symptoms. Curr Opin Urol. 2004; 15(1):45-8. DOI: 10.1097/00042307-200501000-00011. View

5.
Stachon A, Schluter T, Junker K, Knopf H, Neuser R, Krieg M . The secretion of endothelin-1 by microvascular endothelial cells from human benign prostatic hyperplasia is inhibited by vascular endothelial growth factor. Growth Factors. 2004; 22(4):281-9. DOI: 10.1080/08977190400004835. View