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Benign prostatic hyperplasia as a progressive disease: a guide to the risk factors and options for medical management
Benign prostatic hyperplasia (BPH) is a complex disease that is progressive in many men. BPH is commonly associated with bothersome lower urinary tract symptoms; progressive disease can also result in complications such as acute urinary retention (AUR) and BPH-related surgery. It is therefore import...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Blackwell Publishing Ltd
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2440415/ https://www.ncbi.nlm.nih.gov/pubmed/18479366 http://dx.doi.org/10.1111/j.1742-1241.2008.01785.x |
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author | Emberton, M Cornel, E B Bassi, P F Fourcade, R O Gómez, J M F Castro, R |
author_facet | Emberton, M Cornel, E B Bassi, P F Fourcade, R O Gómez, J M F Castro, R |
author_sort | Emberton, M |
collection | PubMed |
description | Benign prostatic hyperplasia (BPH) is a complex disease that is progressive in many men. BPH is commonly associated with bothersome lower urinary tract symptoms; progressive disease can also result in complications such as acute urinary retention (AUR) and BPH-related surgery. It is therefore important to identify men at increased risk of BPH progression to optimise therapy. Several factors are associated with progression, including age and prostate volume (PV). Serum prostate-specific antigen level is closely correlated with PV, making it useful for determining the risk of BPH progression. Medical therapy is the most frequently used treatment for BPH. 5-alpha-reductase inhibitors impact the underlying disease and decrease PV; this results in improved symptoms, urinary flow and quality of life, and a reduced risk of AUR and BPH-related surgery. Alpha-blockers achieve rapid symptom relief but do not reduce the overall risk of AUR or BPH-related surgery, presumably because they have no effect on PV. Combination therapy provides greater and more durable benefits than either monotherapy and is a recommended option in treatment guidelines. The Combination of Avodart® and Tamsulosin (CombAT) study is currently evaluating the combination of dutasteride with tamsulosin over 4 years in a population of men at increased risk of BPH progression. A preplanned 2-year analysis has shown sustained symptom improvement with combination therapy, significantly greater than with either monotherapy. CombAT is also the first study to show benefit in improving BPH symptoms for combination therapy over the alpha-blocker, tamsulosin, from 9 months of treatment. |
format | Text |
id | pubmed-2440415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-24404152008-07-25 Benign prostatic hyperplasia as a progressive disease: a guide to the risk factors and options for medical management Emberton, M Cornel, E B Bassi, P F Fourcade, R O Gómez, J M F Castro, R Int J Clin Pract Review Articles Benign prostatic hyperplasia (BPH) is a complex disease that is progressive in many men. BPH is commonly associated with bothersome lower urinary tract symptoms; progressive disease can also result in complications such as acute urinary retention (AUR) and BPH-related surgery. It is therefore important to identify men at increased risk of BPH progression to optimise therapy. Several factors are associated with progression, including age and prostate volume (PV). Serum prostate-specific antigen level is closely correlated with PV, making it useful for determining the risk of BPH progression. Medical therapy is the most frequently used treatment for BPH. 5-alpha-reductase inhibitors impact the underlying disease and decrease PV; this results in improved symptoms, urinary flow and quality of life, and a reduced risk of AUR and BPH-related surgery. Alpha-blockers achieve rapid symptom relief but do not reduce the overall risk of AUR or BPH-related surgery, presumably because they have no effect on PV. Combination therapy provides greater and more durable benefits than either monotherapy and is a recommended option in treatment guidelines. The Combination of Avodart® and Tamsulosin (CombAT) study is currently evaluating the combination of dutasteride with tamsulosin over 4 years in a population of men at increased risk of BPH progression. A preplanned 2-year analysis has shown sustained symptom improvement with combination therapy, significantly greater than with either monotherapy. CombAT is also the first study to show benefit in improving BPH symptoms for combination therapy over the alpha-blocker, tamsulosin, from 9 months of treatment. Blackwell Publishing Ltd 2008-07 /pmc/articles/PMC2440415/ /pubmed/18479366 http://dx.doi.org/10.1111/j.1742-1241.2008.01785.x Text en © 2008 The Authors. Journal compilation © 2008 Blackwell Publishing Ltd |
spellingShingle | Review Articles Emberton, M Cornel, E B Bassi, P F Fourcade, R O Gómez, J M F Castro, R Benign prostatic hyperplasia as a progressive disease: a guide to the risk factors and options for medical management |
title | Benign prostatic hyperplasia as a progressive disease: a guide to the risk factors and options for medical management |
title_full | Benign prostatic hyperplasia as a progressive disease: a guide to the risk factors and options for medical management |
title_fullStr | Benign prostatic hyperplasia as a progressive disease: a guide to the risk factors and options for medical management |
title_full_unstemmed | Benign prostatic hyperplasia as a progressive disease: a guide to the risk factors and options for medical management |
title_short | Benign prostatic hyperplasia as a progressive disease: a guide to the risk factors and options for medical management |
title_sort | benign prostatic hyperplasia as a progressive disease: a guide to the risk factors and options for medical management |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2440415/ https://www.ncbi.nlm.nih.gov/pubmed/18479366 http://dx.doi.org/10.1111/j.1742-1241.2008.01785.x |
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