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Assessment of Potential Drug–Drug Interactions in Hospitalized Cardiac Patients of a Secondary Care Hospital in the United Arab Emirates

OBJECTIVE: To identify the types, severity, and documentation grades of potential drug–drug interactions (pDDIs) and to identify the predictors of pDDIs among hospitalized cardiac patients. METHODS: This was a cross-sectional study. All the patients who were admitted for >24 h in a cardiology war...

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Autores principales: Khan, Muhammad Zeeshan, Sridhar, Sathvik Belagodu, Gupta, Pradeep Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400031/
https://www.ncbi.nlm.nih.gov/pubmed/30911559
http://dx.doi.org/10.4103/jrpp.JRPP_18_46
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author Khan, Muhammad Zeeshan
Sridhar, Sathvik Belagodu
Gupta, Pradeep Kumar
author_facet Khan, Muhammad Zeeshan
Sridhar, Sathvik Belagodu
Gupta, Pradeep Kumar
author_sort Khan, Muhammad Zeeshan
collection PubMed
description OBJECTIVE: To identify the types, severity, and documentation grades of potential drug–drug interactions (pDDIs) and to identify the predictors of pDDIs among hospitalized cardiac patients. METHODS: This was a cross-sectional study. All the patients who were admitted for >24 h in a cardiology ward of a general hospital of the United Arab Emirates and prescribed with cardiac medications were included. The occurrence of any pDDI between cardiac medications and other coprescribed medications was identified using Micromedex database 2.0(®) and graded and documented based on the severity and documentation. FINDINGS: A total of 842 pDDIs were identified in 155 patients. The overall relevant frequency for the occurrence of pDDIs was found to be 87.74%. A total of 79 pairs of pDDIs were identified. Among identified pDDIs, 41.33% and 56.65% were major and moderate severity type, respectively, whereas 12.32% were excellent and 36.81% were good documentation grade. The majority of pDDIs were between aspirin-bisoprolol (11.64%). Patients taking more than seven drugs (odds ratio [OR] = 9.90; 95% confidence interval [CI]: 2.28–42.99), polypharmacy (OR = 3.86; 95% CI: 0.93–16.08), and number of medical conditions (OR 0.25; 95% CI: 0.09–0.68) were significant predictors of pDDIs. CONCLUSION: The study fosters the importance of regular and close monitoring for pDDIs among cardiac patients. Thus, multicenter interventional studies are required to determine the exact nature and types of pDDIs in the local population.
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spelling pubmed-64000312019-03-25 Assessment of Potential Drug–Drug Interactions in Hospitalized Cardiac Patients of a Secondary Care Hospital in the United Arab Emirates Khan, Muhammad Zeeshan Sridhar, Sathvik Belagodu Gupta, Pradeep Kumar J Res Pharm Pract Brief Communication OBJECTIVE: To identify the types, severity, and documentation grades of potential drug–drug interactions (pDDIs) and to identify the predictors of pDDIs among hospitalized cardiac patients. METHODS: This was a cross-sectional study. All the patients who were admitted for >24 h in a cardiology ward of a general hospital of the United Arab Emirates and prescribed with cardiac medications were included. The occurrence of any pDDI between cardiac medications and other coprescribed medications was identified using Micromedex database 2.0(®) and graded and documented based on the severity and documentation. FINDINGS: A total of 842 pDDIs were identified in 155 patients. The overall relevant frequency for the occurrence of pDDIs was found to be 87.74%. A total of 79 pairs of pDDIs were identified. Among identified pDDIs, 41.33% and 56.65% were major and moderate severity type, respectively, whereas 12.32% were excellent and 36.81% were good documentation grade. The majority of pDDIs were between aspirin-bisoprolol (11.64%). Patients taking more than seven drugs (odds ratio [OR] = 9.90; 95% confidence interval [CI]: 2.28–42.99), polypharmacy (OR = 3.86; 95% CI: 0.93–16.08), and number of medical conditions (OR 0.25; 95% CI: 0.09–0.68) were significant predictors of pDDIs. CONCLUSION: The study fosters the importance of regular and close monitoring for pDDIs among cardiac patients. Thus, multicenter interventional studies are required to determine the exact nature and types of pDDIs in the local population. Medknow Publications & Media Pvt Ltd 2019 /pmc/articles/PMC6400031/ /pubmed/30911559 http://dx.doi.org/10.4103/jrpp.JRPP_18_46 Text en Copyright: © 2019 Journal of Research in Pharmacy Practice http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Brief Communication
Khan, Muhammad Zeeshan
Sridhar, Sathvik Belagodu
Gupta, Pradeep Kumar
Assessment of Potential Drug–Drug Interactions in Hospitalized Cardiac Patients of a Secondary Care Hospital in the United Arab Emirates
title Assessment of Potential Drug–Drug Interactions in Hospitalized Cardiac Patients of a Secondary Care Hospital in the United Arab Emirates
title_full Assessment of Potential Drug–Drug Interactions in Hospitalized Cardiac Patients of a Secondary Care Hospital in the United Arab Emirates
title_fullStr Assessment of Potential Drug–Drug Interactions in Hospitalized Cardiac Patients of a Secondary Care Hospital in the United Arab Emirates
title_full_unstemmed Assessment of Potential Drug–Drug Interactions in Hospitalized Cardiac Patients of a Secondary Care Hospital in the United Arab Emirates
title_short Assessment of Potential Drug–Drug Interactions in Hospitalized Cardiac Patients of a Secondary Care Hospital in the United Arab Emirates
title_sort assessment of potential drug–drug interactions in hospitalized cardiac patients of a secondary care hospital in the united arab emirates
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400031/
https://www.ncbi.nlm.nih.gov/pubmed/30911559
http://dx.doi.org/10.4103/jrpp.JRPP_18_46
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