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Tadalafil vs. tamsulosin in the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia: a prospective, randomized study

INTRODUCTION: To compare the efiicacy of tadalafil 5 mg with tamsulosin 0.4 mg in the treatment of Lower urinary tract symptoms (LUTS) secondary to benign prostatic hyperplasia (BPH). MATERIAL AND METHODS: A randomized prospective study on patients diagnosed with LUTS secondary to BPH with 50 patien...

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Autores principales: Pogula, Vedamurthy Reddy, Kadiyala, Lalith Sagar, Gouru, Vijayabhaskar Reddy, Challa, Sivasankar Reddy, Byram, Ranadheer, Bodduluri, Sudeep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Polish Urological Association 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469005/
https://www.ncbi.nlm.nih.gov/pubmed/31011439
http://dx.doi.org/10.5173/ceju.2019.1570
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author Pogula, Vedamurthy Reddy
Kadiyala, Lalith Sagar
Gouru, Vijayabhaskar Reddy
Challa, Sivasankar Reddy
Byram, Ranadheer
Bodduluri, Sudeep
author_facet Pogula, Vedamurthy Reddy
Kadiyala, Lalith Sagar
Gouru, Vijayabhaskar Reddy
Challa, Sivasankar Reddy
Byram, Ranadheer
Bodduluri, Sudeep
author_sort Pogula, Vedamurthy Reddy
collection PubMed
description INTRODUCTION: To compare the efiicacy of tadalafil 5 mg with tamsulosin 0.4 mg in the treatment of Lower urinary tract symptoms (LUTS) secondary to benign prostatic hyperplasia (BPH). MATERIAL AND METHODS: A randomized prospective study on patients diagnosed with LUTS secondary to BPH with 50 patients in each group. Duration of the study is 12 weeks. Drug was given 30 min after dinner. Patients were assessed at baseline 1, 4 and 12 weeks with efficacy measures being Maximum flow rate (Qmax), Postvoid residual urine (PVR), International Prostate Symptom Score (IPSS), International Prostate Symptom Score Quality of life (IPSS QoL) and Sexual Health Inventory for Men (SHIM) scoring. Statistical analysis was done using paired sample t test and independent sample t test. RESULTS: In tadalafil group, 12 (24%) patients were having mild LUTS and 38 (76%) were having moderate LUTS. In tamsulosin group, 9 (18%) patients were having mild LUTS and 41 (82%) patients were having moderate LUTS. Seventeen patients in tadalafil group had associated ED (erectile dysfunction) and 13 patients had associated ED in tamsulosin group. CONCLUSIONS: When both groups were compared, tamsulosin showed better efficacy than tadalafil in treating LUTS secondary to BPH.
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spelling pubmed-64690052019-04-22 Tadalafil vs. tamsulosin in the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia: a prospective, randomized study Pogula, Vedamurthy Reddy Kadiyala, Lalith Sagar Gouru, Vijayabhaskar Reddy Challa, Sivasankar Reddy Byram, Ranadheer Bodduluri, Sudeep Cent European J Urol Original Paper INTRODUCTION: To compare the efiicacy of tadalafil 5 mg with tamsulosin 0.4 mg in the treatment of Lower urinary tract symptoms (LUTS) secondary to benign prostatic hyperplasia (BPH). MATERIAL AND METHODS: A randomized prospective study on patients diagnosed with LUTS secondary to BPH with 50 patients in each group. Duration of the study is 12 weeks. Drug was given 30 min after dinner. Patients were assessed at baseline 1, 4 and 12 weeks with efficacy measures being Maximum flow rate (Qmax), Postvoid residual urine (PVR), International Prostate Symptom Score (IPSS), International Prostate Symptom Score Quality of life (IPSS QoL) and Sexual Health Inventory for Men (SHIM) scoring. Statistical analysis was done using paired sample t test and independent sample t test. RESULTS: In tadalafil group, 12 (24%) patients were having mild LUTS and 38 (76%) were having moderate LUTS. In tamsulosin group, 9 (18%) patients were having mild LUTS and 41 (82%) patients were having moderate LUTS. Seventeen patients in tadalafil group had associated ED (erectile dysfunction) and 13 patients had associated ED in tamsulosin group. CONCLUSIONS: When both groups were compared, tamsulosin showed better efficacy than tadalafil in treating LUTS secondary to BPH. Polish Urological Association 2019-03-14 2019 /pmc/articles/PMC6469005/ /pubmed/31011439 http://dx.doi.org/10.5173/ceju.2019.1570 Text en Copyright by Polish Urological Association http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Pogula, Vedamurthy Reddy
Kadiyala, Lalith Sagar
Gouru, Vijayabhaskar Reddy
Challa, Sivasankar Reddy
Byram, Ranadheer
Bodduluri, Sudeep
Tadalafil vs. tamsulosin in the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia: a prospective, randomized study
title Tadalafil vs. tamsulosin in the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia: a prospective, randomized study
title_full Tadalafil vs. tamsulosin in the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia: a prospective, randomized study
title_fullStr Tadalafil vs. tamsulosin in the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia: a prospective, randomized study
title_full_unstemmed Tadalafil vs. tamsulosin in the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia: a prospective, randomized study
title_short Tadalafil vs. tamsulosin in the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia: a prospective, randomized study
title_sort tadalafil vs. tamsulosin in the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia: a prospective, randomized study
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469005/
https://www.ncbi.nlm.nih.gov/pubmed/31011439
http://dx.doi.org/10.5173/ceju.2019.1570
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