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Drug-drug Interaction-related Uncontrolled Glycemia
CONTEXT: The literature of drug-drug interaction (DDI)-related uncontrolled causality, and preventability of DDI-induced UCG (HbA1c >7%) in outpatients glycemia (UCG) among outpatients with Type 2 diabetes mellitus is still limited. AIMS: The aim of this study is to identify the prevalence, mecha...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5810071/ https://www.ncbi.nlm.nih.gov/pubmed/29456372 http://dx.doi.org/10.4103/jpbs.JPBS_26_17 |
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author | Hammad, Mohamed Anwar Tangiisuran, Balamurugan Kharshid, Abeer Mohamed Abdul-Aziz, Noorizan Hassan, Yahaya Aziz, Nor Azizah Elsayed, Tarek Mohamed |
author_facet | Hammad, Mohamed Anwar Tangiisuran, Balamurugan Kharshid, Abeer Mohamed Abdul-Aziz, Noorizan Hassan, Yahaya Aziz, Nor Azizah Elsayed, Tarek Mohamed |
author_sort | Hammad, Mohamed Anwar |
collection | PubMed |
description | CONTEXT: The literature of drug-drug interaction (DDI)-related uncontrolled causality, and preventability of DDI-induced UCG (HbA1c >7%) in outpatients glycemia (UCG) among outpatients with Type 2 diabetes mellitus is still limited. AIMS: The aim of this study is to identify the prevalence, mechanism, severity, with Type 2 diabetes. SETTINGS AND DESIGN: A cross-sectional study was conducted in Penang General Hospital. METHODS: A computerized system for DDI checking was used to assess the severity and mechanism of DDIs. Drug interaction probability scale was used to evaluate the likelihood of DDIs. Preventability of DDIs has been determined by the instrument of Hallas. The UCG prevalence related to DDIs was further assessed. STATISTICAL ANALYSIS USED: SPSS 21.00 was used in this study. RESULTS: From 425 outpatients with HbA1c% test, their mean age was 58.7 ± 12.8 years. Only 225 (52.9%) cases had controlled glycemia while 200 (47.1%) cases with UCG. They had multiple comorbidities, with a mean number of 3.8 ± 2.2/patient and often prescribed with multiple medications, with a mean number of 6.33 ± 4.67/patient. It has been detected that 86 DDIs causing UCG in 46 patients (23%) with range of (1 – 4) DDIs per patient. Drugs with DDI-induced UCG were as follows: diuretics (79%), salbutamol (9.2%), cortisones (5.8%), and others (6%). The majority of these DDIs were categorized as possible (77.9%) and preventable (37%). CONCLUSION: Nearly one-quarter of UCG was induced by DDIs; most of these DDIs are possible, and more than one-third are preventable. It was concluded that thiazide diuretics have the highest prevalence of DDI-related UCG. |
format | Online Article Text |
id | pubmed-5810071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58100712018-02-16 Drug-drug Interaction-related Uncontrolled Glycemia Hammad, Mohamed Anwar Tangiisuran, Balamurugan Kharshid, Abeer Mohamed Abdul-Aziz, Noorizan Hassan, Yahaya Aziz, Nor Azizah Elsayed, Tarek Mohamed J Pharm Bioallied Sci Original Article CONTEXT: The literature of drug-drug interaction (DDI)-related uncontrolled causality, and preventability of DDI-induced UCG (HbA1c >7%) in outpatients glycemia (UCG) among outpatients with Type 2 diabetes mellitus is still limited. AIMS: The aim of this study is to identify the prevalence, mechanism, severity, with Type 2 diabetes. SETTINGS AND DESIGN: A cross-sectional study was conducted in Penang General Hospital. METHODS: A computerized system for DDI checking was used to assess the severity and mechanism of DDIs. Drug interaction probability scale was used to evaluate the likelihood of DDIs. Preventability of DDIs has been determined by the instrument of Hallas. The UCG prevalence related to DDIs was further assessed. STATISTICAL ANALYSIS USED: SPSS 21.00 was used in this study. RESULTS: From 425 outpatients with HbA1c% test, their mean age was 58.7 ± 12.8 years. Only 225 (52.9%) cases had controlled glycemia while 200 (47.1%) cases with UCG. They had multiple comorbidities, with a mean number of 3.8 ± 2.2/patient and often prescribed with multiple medications, with a mean number of 6.33 ± 4.67/patient. It has been detected that 86 DDIs causing UCG in 46 patients (23%) with range of (1 – 4) DDIs per patient. Drugs with DDI-induced UCG were as follows: diuretics (79%), salbutamol (9.2%), cortisones (5.8%), and others (6%). The majority of these DDIs were categorized as possible (77.9%) and preventable (37%). CONCLUSION: Nearly one-quarter of UCG was induced by DDIs; most of these DDIs are possible, and more than one-third are preventable. It was concluded that thiazide diuretics have the highest prevalence of DDI-related UCG. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5810071/ /pubmed/29456372 http://dx.doi.org/10.4103/jpbs.JPBS_26_17 Text en Copyright: © 2018 Journal of Pharmacy and Bioallied Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Hammad, Mohamed Anwar Tangiisuran, Balamurugan Kharshid, Abeer Mohamed Abdul-Aziz, Noorizan Hassan, Yahaya Aziz, Nor Azizah Elsayed, Tarek Mohamed Drug-drug Interaction-related Uncontrolled Glycemia |
title | Drug-drug Interaction-related Uncontrolled Glycemia |
title_full | Drug-drug Interaction-related Uncontrolled Glycemia |
title_fullStr | Drug-drug Interaction-related Uncontrolled Glycemia |
title_full_unstemmed | Drug-drug Interaction-related Uncontrolled Glycemia |
title_short | Drug-drug Interaction-related Uncontrolled Glycemia |
title_sort | drug-drug interaction-related uncontrolled glycemia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5810071/ https://www.ncbi.nlm.nih.gov/pubmed/29456372 http://dx.doi.org/10.4103/jpbs.JPBS_26_17 |
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