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Clinically relevant drug–drug interactions among elderly people with dementia

PURPOSE: Increased numbers of drugs and changes in pharmacokinetic and pharmacodynamic parameters among elderly people contribute to increased prevalence of adverse drug reactions. Drug–drug interactions (DDIs) are an important reason for admission to hospital and elderly people with dementia are pa...

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Autores principales: Sönnerstam, Eva, Sjölander, Maria, Lövheim, Hugo, Gustafsson, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132551/
https://www.ncbi.nlm.nih.gov/pubmed/29967921
http://dx.doi.org/10.1007/s00228-018-2514-5
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author Sönnerstam, Eva
Sjölander, Maria
Lövheim, Hugo
Gustafsson, Maria
author_facet Sönnerstam, Eva
Sjölander, Maria
Lövheim, Hugo
Gustafsson, Maria
author_sort Sönnerstam, Eva
collection PubMed
description PURPOSE: Increased numbers of drugs and changes in pharmacokinetic and pharmacodynamic parameters among elderly people contribute to increased prevalence of adverse drug reactions. Drug–drug interactions (DDIs) are an important reason for admission to hospital and elderly people with dementia are particularly vulnerable. The aims of the present study were to assess the occurrence and characteristics of clinically relevant DDIs and to investigate potential risk factors associated with DDIs among elderly people with dementia. METHODS: People ≥ 65 years with dementia, admitted to two hospitals in Northern Sweden, were included. The medical records of 458 patients were reviewed. Clinically relevant DDIs were identified using the Janusmed interactions database. Pharmacological classification was conducted using Stockley’s classification system. RESULTS: A total of 401 DDIs were identified among 43.2% of the study population, of which 98.5% had interactions that may require dose adjustment and 7.6% had drug combinations that should be avoided. Pharmacodynamic interactions were most common, of which furosemide–citalopram (n = 35) were most frequently observed. Omeprazol–citalopram (n = 25) was the most common drug combination among pharmacokinetic interactions. Citalopram and warfarin were the most commonly involved drug substances. An association was found between a higher number of medications being prescribed and having at least one DDI. CONCLUSION: Clinically relevant drug–drug interactions are prevalent among elderly people with dementia living in Northern Sweden. Drug–drug interactions should be identified in order to manage and prevent adverse outcomes. This is particularly important among this group of people especially when multiple medications are being prescribed.
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spelling pubmed-61325512018-09-14 Clinically relevant drug–drug interactions among elderly people with dementia Sönnerstam, Eva Sjölander, Maria Lövheim, Hugo Gustafsson, Maria Eur J Clin Pharmacol Pharmacoepidemiology and Prescription PURPOSE: Increased numbers of drugs and changes in pharmacokinetic and pharmacodynamic parameters among elderly people contribute to increased prevalence of adverse drug reactions. Drug–drug interactions (DDIs) are an important reason for admission to hospital and elderly people with dementia are particularly vulnerable. The aims of the present study were to assess the occurrence and characteristics of clinically relevant DDIs and to investigate potential risk factors associated with DDIs among elderly people with dementia. METHODS: People ≥ 65 years with dementia, admitted to two hospitals in Northern Sweden, were included. The medical records of 458 patients were reviewed. Clinically relevant DDIs were identified using the Janusmed interactions database. Pharmacological classification was conducted using Stockley’s classification system. RESULTS: A total of 401 DDIs were identified among 43.2% of the study population, of which 98.5% had interactions that may require dose adjustment and 7.6% had drug combinations that should be avoided. Pharmacodynamic interactions were most common, of which furosemide–citalopram (n = 35) were most frequently observed. Omeprazol–citalopram (n = 25) was the most common drug combination among pharmacokinetic interactions. Citalopram and warfarin were the most commonly involved drug substances. An association was found between a higher number of medications being prescribed and having at least one DDI. CONCLUSION: Clinically relevant drug–drug interactions are prevalent among elderly people with dementia living in Northern Sweden. Drug–drug interactions should be identified in order to manage and prevent adverse outcomes. This is particularly important among this group of people especially when multiple medications are being prescribed. Springer Berlin Heidelberg 2018-07-02 2018 /pmc/articles/PMC6132551/ /pubmed/29967921 http://dx.doi.org/10.1007/s00228-018-2514-5 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Pharmacoepidemiology and Prescription
Sönnerstam, Eva
Sjölander, Maria
Lövheim, Hugo
Gustafsson, Maria
Clinically relevant drug–drug interactions among elderly people with dementia
title Clinically relevant drug–drug interactions among elderly people with dementia
title_full Clinically relevant drug–drug interactions among elderly people with dementia
title_fullStr Clinically relevant drug–drug interactions among elderly people with dementia
title_full_unstemmed Clinically relevant drug–drug interactions among elderly people with dementia
title_short Clinically relevant drug–drug interactions among elderly people with dementia
title_sort clinically relevant drug–drug interactions among elderly people with dementia
topic Pharmacoepidemiology and Prescription
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132551/
https://www.ncbi.nlm.nih.gov/pubmed/29967921
http://dx.doi.org/10.1007/s00228-018-2514-5
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