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The role of prescription drugs in female overactive bladder syndrome—A population‐wide cohort study

PURPOSE: Overactive bladder (OAB) syndrome has severe effects on quality of life. Certain drugs are known risk factors for OAB but have not been investigated in a population‐wide cohort. The objective of this study was to investigate the role of prescription drugs in the etiology of the OAB. METHODS...

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Autores principales: Umek, Wolfgang, Gleiss, Andreas, Bodner‐Adler, Barbara, Reichardt, Berthold, Rinner, Christoph, Heinze, Georg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027558/
https://www.ncbi.nlm.nih.gov/pubmed/31808271
http://dx.doi.org/10.1002/pds.4920
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author Umek, Wolfgang
Gleiss, Andreas
Bodner‐Adler, Barbara
Reichardt, Berthold
Rinner, Christoph
Heinze, Georg
author_facet Umek, Wolfgang
Gleiss, Andreas
Bodner‐Adler, Barbara
Reichardt, Berthold
Rinner, Christoph
Heinze, Georg
author_sort Umek, Wolfgang
collection PubMed
description PURPOSE: Overactive bladder (OAB) syndrome has severe effects on quality of life. Certain drugs are known risk factors for OAB but have not been investigated in a population‐wide cohort. The objective of this study was to investigate the role of prescription drugs in the etiology of the OAB. METHODS: Retrospective cohort study using a population‐wide database of 4 185 098 OAB‐naïve women followed Strengthening the Reporting of Observational Studies in Epidemiology guidelines. We investigated the subscription use of anticholinergic medication and 188 chemical substances, which are suspected triggers for OAB (trigger medications [TMs]). We hypothesized a relationship between the prescription for one or more TM and the prescription for anticholinergic medication against OAB (marker medication [MM]). RESULTS: The use of MM in Austria increased from 2009 to 2012 on average by 0.025 percentage points per year (95% confidence interval [CI]: 0.015‐0.036). In December 2012, 1 in 123 women filled a prescription for any MM, equaling an average utilization of 0.84%. The relative risk of filling a prescription for a MM 6 months after filling a prescription for a TM was 2.70 (95% CI: 2.64‐2.77). All investigated medication classes showed a higher risk for the prescription for MM. Medication from classes “genitourinary system and sex hormones” and “systemic anti‐infectives” caused the highest increase in risk (109% and 89%, respectively). Prescriptions for class “cardiovascular system” caused the lowest increase in the risk (15%). CONCLUSION: Certain prescription medications are a significant risk factor for the need to take anticholinergic medication as a consequence.
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spelling pubmed-70275582020-02-24 The role of prescription drugs in female overactive bladder syndrome—A population‐wide cohort study Umek, Wolfgang Gleiss, Andreas Bodner‐Adler, Barbara Reichardt, Berthold Rinner, Christoph Heinze, Georg Pharmacoepidemiol Drug Saf Original Reports PURPOSE: Overactive bladder (OAB) syndrome has severe effects on quality of life. Certain drugs are known risk factors for OAB but have not been investigated in a population‐wide cohort. The objective of this study was to investigate the role of prescription drugs in the etiology of the OAB. METHODS: Retrospective cohort study using a population‐wide database of 4 185 098 OAB‐naïve women followed Strengthening the Reporting of Observational Studies in Epidemiology guidelines. We investigated the subscription use of anticholinergic medication and 188 chemical substances, which are suspected triggers for OAB (trigger medications [TMs]). We hypothesized a relationship between the prescription for one or more TM and the prescription for anticholinergic medication against OAB (marker medication [MM]). RESULTS: The use of MM in Austria increased from 2009 to 2012 on average by 0.025 percentage points per year (95% confidence interval [CI]: 0.015‐0.036). In December 2012, 1 in 123 women filled a prescription for any MM, equaling an average utilization of 0.84%. The relative risk of filling a prescription for a MM 6 months after filling a prescription for a TM was 2.70 (95% CI: 2.64‐2.77). All investigated medication classes showed a higher risk for the prescription for MM. Medication from classes “genitourinary system and sex hormones” and “systemic anti‐infectives” caused the highest increase in risk (109% and 89%, respectively). Prescriptions for class “cardiovascular system” caused the lowest increase in the risk (15%). CONCLUSION: Certain prescription medications are a significant risk factor for the need to take anticholinergic medication as a consequence. John Wiley and Sons Inc. 2019-12-05 2020-02 /pmc/articles/PMC7027558/ /pubmed/31808271 http://dx.doi.org/10.1002/pds.4920 Text en © 2019 The Authors. Pharmacoepidemiology & Drug Safety Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Reports
Umek, Wolfgang
Gleiss, Andreas
Bodner‐Adler, Barbara
Reichardt, Berthold
Rinner, Christoph
Heinze, Georg
The role of prescription drugs in female overactive bladder syndrome—A population‐wide cohort study
title The role of prescription drugs in female overactive bladder syndrome—A population‐wide cohort study
title_full The role of prescription drugs in female overactive bladder syndrome—A population‐wide cohort study
title_fullStr The role of prescription drugs in female overactive bladder syndrome—A population‐wide cohort study
title_full_unstemmed The role of prescription drugs in female overactive bladder syndrome—A population‐wide cohort study
title_short The role of prescription drugs in female overactive bladder syndrome—A population‐wide cohort study
title_sort role of prescription drugs in female overactive bladder syndrome—a population‐wide cohort study
topic Original Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027558/
https://www.ncbi.nlm.nih.gov/pubmed/31808271
http://dx.doi.org/10.1002/pds.4920
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