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Comparison of Tamsulosin and Tadalafil effects in LUTS treatment considering patients' atherosclerosis risk level
INTRODUCTION: To date, no study evaluates the effect of atherosclerosis risk level on the efficacy of BPH drug therapies. Therefore, the present study aimed to assess the effect of atherosclerosis risk levels on the effectiveness of Tamsulosin and Tadalafil in LUTS treatment. METHODS: The present st...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283796/ https://www.ncbi.nlm.nih.gov/pubmed/35846856 http://dx.doi.org/10.1016/j.amsu.2022.104137 |
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author | Tavoosian, Ali Reis, Leonardo Oliveira Aluru, Pavan Khajavi, Alireza Aghamir, Seyed Mohammad Kazem |
author_facet | Tavoosian, Ali Reis, Leonardo Oliveira Aluru, Pavan Khajavi, Alireza Aghamir, Seyed Mohammad Kazem |
author_sort | Tavoosian, Ali |
collection | PubMed |
description | INTRODUCTION: To date, no study evaluates the effect of atherosclerosis risk level on the efficacy of BPH drug therapies. Therefore, the present study aimed to assess the effect of atherosclerosis risk levels on the effectiveness of Tamsulosin and Tadalafil in LUTS treatment. METHODS: The present study was a randomized clinical trial that assessed men with LUTS symptoms (at least six months). The inclusion criteria were being older than 50 years, international prostate symptom score (IPSS) ≥ 13, and maximum urinary flow rate (Qmax) between 4 and 15 ml/s. Framingham Risk Score was used to measure atherosclerosis risk. The patients were classified into four groups, including group 1: Patients with low risk and treated with Tamsulosin (0.4 mg/day), group 2: Patients with low risk and treated with Tadalafil (5 mg/day), group 3: Patients with high risk and treated with Tamsulosin (0.4 mg/day), group 4: Patients with high risk and treated with Tadalafil (5 mg/day). RESULTS: The study included 44 and 38 patients receiving Tamsulosin and Tadalafil, respectively. The means (SD) of the baseline age for the Tamsulosin and Tadalafil groups were equal to 60.6 (6.8) and 58.8 (6.7), respectively (p-value = 0.213). The models revealed no impact of the atherosclerosis risk level on the drugs' effects (p-values = 0.378, 0.975, 0.743 for IPSS, QMAX, and VOID, respectively). CONCLUSIONS: The present study's findings could not show the impact of atherosclerosis risk levels on the efficiency of Tamsolusin and Tadalafil in men with LUTS. |
format | Online Article Text |
id | pubmed-9283796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-92837962022-07-16 Comparison of Tamsulosin and Tadalafil effects in LUTS treatment considering patients' atherosclerosis risk level Tavoosian, Ali Reis, Leonardo Oliveira Aluru, Pavan Khajavi, Alireza Aghamir, Seyed Mohammad Kazem Ann Med Surg (Lond) Case-controlled Study INTRODUCTION: To date, no study evaluates the effect of atherosclerosis risk level on the efficacy of BPH drug therapies. Therefore, the present study aimed to assess the effect of atherosclerosis risk levels on the effectiveness of Tamsulosin and Tadalafil in LUTS treatment. METHODS: The present study was a randomized clinical trial that assessed men with LUTS symptoms (at least six months). The inclusion criteria were being older than 50 years, international prostate symptom score (IPSS) ≥ 13, and maximum urinary flow rate (Qmax) between 4 and 15 ml/s. Framingham Risk Score was used to measure atherosclerosis risk. The patients were classified into four groups, including group 1: Patients with low risk and treated with Tamsulosin (0.4 mg/day), group 2: Patients with low risk and treated with Tadalafil (5 mg/day), group 3: Patients with high risk and treated with Tamsulosin (0.4 mg/day), group 4: Patients with high risk and treated with Tadalafil (5 mg/day). RESULTS: The study included 44 and 38 patients receiving Tamsulosin and Tadalafil, respectively. The means (SD) of the baseline age for the Tamsulosin and Tadalafil groups were equal to 60.6 (6.8) and 58.8 (6.7), respectively (p-value = 0.213). The models revealed no impact of the atherosclerosis risk level on the drugs' effects (p-values = 0.378, 0.975, 0.743 for IPSS, QMAX, and VOID, respectively). CONCLUSIONS: The present study's findings could not show the impact of atherosclerosis risk levels on the efficiency of Tamsolusin and Tadalafil in men with LUTS. Elsevier 2022-07-09 /pmc/articles/PMC9283796/ /pubmed/35846856 http://dx.doi.org/10.1016/j.amsu.2022.104137 Text en © 2022 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case-controlled Study Tavoosian, Ali Reis, Leonardo Oliveira Aluru, Pavan Khajavi, Alireza Aghamir, Seyed Mohammad Kazem Comparison of Tamsulosin and Tadalafil effects in LUTS treatment considering patients' atherosclerosis risk level |
title | Comparison of Tamsulosin and Tadalafil effects in LUTS treatment considering patients' atherosclerosis risk level |
title_full | Comparison of Tamsulosin and Tadalafil effects in LUTS treatment considering patients' atherosclerosis risk level |
title_fullStr | Comparison of Tamsulosin and Tadalafil effects in LUTS treatment considering patients' atherosclerosis risk level |
title_full_unstemmed | Comparison of Tamsulosin and Tadalafil effects in LUTS treatment considering patients' atherosclerosis risk level |
title_short | Comparison of Tamsulosin and Tadalafil effects in LUTS treatment considering patients' atherosclerosis risk level |
title_sort | comparison of tamsulosin and tadalafil effects in luts treatment considering patients' atherosclerosis risk level |
topic | Case-controlled Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283796/ https://www.ncbi.nlm.nih.gov/pubmed/35846856 http://dx.doi.org/10.1016/j.amsu.2022.104137 |
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