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Risk Evaluation of Azithromycin-Induced QT Prolongation in Real-World Practice

BACKGROUND: Azithromycin exposure has been reported to increase the risk of QT prolongation and cardiovascular death. However, findings on the association between azithromycin and cardiovascular death are controversial, and azithromycin is still used in actual practice. Additionally, quantitative as...

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Autores principales: Choi, Young, Lim, Hong-Seok, Chung, Dahee, Choi, Jung-gu, Yoon, Dukyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204160/
https://www.ncbi.nlm.nih.gov/pubmed/30406128
http://dx.doi.org/10.1155/2018/1574806
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author Choi, Young
Lim, Hong-Seok
Chung, Dahee
Choi, Jung-gu
Yoon, Dukyong
author_facet Choi, Young
Lim, Hong-Seok
Chung, Dahee
Choi, Jung-gu
Yoon, Dukyong
author_sort Choi, Young
collection PubMed
description BACKGROUND: Azithromycin exposure has been reported to increase the risk of QT prolongation and cardiovascular death. However, findings on the association between azithromycin and cardiovascular death are controversial, and azithromycin is still used in actual practice. Additionally, quantitative assessments of risk have not been performed, including the risk of QT prolongation when patients are exposed to azithromycin in a real-world clinical setting. Therefore, in this study, we aimed to evaluate the risk of exposure to azithromycin on QT prolongation in a real-world clinical setting using a 21-year medical history database of a tertiary medical institution. METHODS: We analyzed the electrocardiogram results and relevant electronic health records of 402,607 subjects in a tertiary teaching hospital in Korea from 1996 to 2015. To evaluate the risk of QT prolongation of azithromycin, we conducted a case-control analysis using amoxicillin for comparison. Multiple logistic regression analysis was performed to correct for age, sex, accompanying drugs, and disease. RESULTS: The odds ratio (OR) for QT prolongation (QTc>450 ms in male and >460 ms in female) on azithromycin exposure was 1.40 (95% confidence interval [CI], 1.23-1.59), and the OR for severe QT prolongation (QTc>500 ms) was 1.43 (95% CI, 1.13-1.82). On the other hand, the ORs on exposure to amoxicillin were 1.06 (95% CI, 0.97-1.15) and 0.88 (95% CI, 0.70-1.09). In a subgroup analysis, the risk of QT prolongation in patients aged between 60 and 80 years was significantly higher when they are exposed to azithromycin. CONCLUSIONS: The risk of QT prolongation was increased when patients, particularly the elderly aged 60-79 years, were exposed to azithromycin. Therefore, clinicians should pay exercise caution using azithromycin or consider using other antibiotics, such as amoxicillin, instead of azithromycin.
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spelling pubmed-62041602018-11-07 Risk Evaluation of Azithromycin-Induced QT Prolongation in Real-World Practice Choi, Young Lim, Hong-Seok Chung, Dahee Choi, Jung-gu Yoon, Dukyong Biomed Res Int Research Article BACKGROUND: Azithromycin exposure has been reported to increase the risk of QT prolongation and cardiovascular death. However, findings on the association between azithromycin and cardiovascular death are controversial, and azithromycin is still used in actual practice. Additionally, quantitative assessments of risk have not been performed, including the risk of QT prolongation when patients are exposed to azithromycin in a real-world clinical setting. Therefore, in this study, we aimed to evaluate the risk of exposure to azithromycin on QT prolongation in a real-world clinical setting using a 21-year medical history database of a tertiary medical institution. METHODS: We analyzed the electrocardiogram results and relevant electronic health records of 402,607 subjects in a tertiary teaching hospital in Korea from 1996 to 2015. To evaluate the risk of QT prolongation of azithromycin, we conducted a case-control analysis using amoxicillin for comparison. Multiple logistic regression analysis was performed to correct for age, sex, accompanying drugs, and disease. RESULTS: The odds ratio (OR) for QT prolongation (QTc>450 ms in male and >460 ms in female) on azithromycin exposure was 1.40 (95% confidence interval [CI], 1.23-1.59), and the OR for severe QT prolongation (QTc>500 ms) was 1.43 (95% CI, 1.13-1.82). On the other hand, the ORs on exposure to amoxicillin were 1.06 (95% CI, 0.97-1.15) and 0.88 (95% CI, 0.70-1.09). In a subgroup analysis, the risk of QT prolongation in patients aged between 60 and 80 years was significantly higher when they are exposed to azithromycin. CONCLUSIONS: The risk of QT prolongation was increased when patients, particularly the elderly aged 60-79 years, were exposed to azithromycin. Therefore, clinicians should pay exercise caution using azithromycin or consider using other antibiotics, such as amoxicillin, instead of azithromycin. Hindawi 2018-10-14 /pmc/articles/PMC6204160/ /pubmed/30406128 http://dx.doi.org/10.1155/2018/1574806 Text en Copyright © 2018 Young Choi et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Choi, Young
Lim, Hong-Seok
Chung, Dahee
Choi, Jung-gu
Yoon, Dukyong
Risk Evaluation of Azithromycin-Induced QT Prolongation in Real-World Practice
title Risk Evaluation of Azithromycin-Induced QT Prolongation in Real-World Practice
title_full Risk Evaluation of Azithromycin-Induced QT Prolongation in Real-World Practice
title_fullStr Risk Evaluation of Azithromycin-Induced QT Prolongation in Real-World Practice
title_full_unstemmed Risk Evaluation of Azithromycin-Induced QT Prolongation in Real-World Practice
title_short Risk Evaluation of Azithromycin-Induced QT Prolongation in Real-World Practice
title_sort risk evaluation of azithromycin-induced qt prolongation in real-world practice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204160/
https://www.ncbi.nlm.nih.gov/pubmed/30406128
http://dx.doi.org/10.1155/2018/1574806
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