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Polypharmacy Is Associated With Amiodarone-Induced Hypothyroidism

Background: Amiodarone is rich in iodine, so in clinical practice amiodarone-induced hypothyroidism (AIH) is a major side effect. This drug is used in patients with arrhythmias, especially atrial fibrillation, the most common sustained arrhythmia. Polypharmacy, which can result in complex drug-drug...

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Autores principales: Yokoyama, Satoshi, Tanaka, Yuki, Hosomi, Kouichi, Takada, Mitsutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8436091/
https://www.ncbi.nlm.nih.gov/pubmed/34522184
http://dx.doi.org/10.7150/ijms.61412
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author Yokoyama, Satoshi
Tanaka, Yuki
Hosomi, Kouichi
Takada, Mitsutaka
author_facet Yokoyama, Satoshi
Tanaka, Yuki
Hosomi, Kouichi
Takada, Mitsutaka
author_sort Yokoyama, Satoshi
collection PubMed
description Background: Amiodarone is rich in iodine, so in clinical practice amiodarone-induced hypothyroidism (AIH) is a major side effect. This drug is used in patients with arrhythmias, especially atrial fibrillation, the most common sustained arrhythmia. Polypharmacy, which can result in complex drug-drug interactions, occurs in more than 70% of the patients with atrial fibrillation. Therefore, polypharmacy may be involved in the expression of AIH. In this study, we investigated the association between polypharmacy and AIH. Methods: We conducted a retrospective study using data from January 2006 to May 2020 collected from a large, organized database of prescriptions constructed by the Japan Medical Information Research Institute, Inc. (Tokyo, Japan). To investigate the association between number of prescribed drugs with amiodarone and AIH, we divided patients into two groups: polypharmacy (≥ 5 prescribed drugs) and non-polypharmacy (< 5 prescribed drugs). We then performed a sequence symmetry analysis on the two groups: incident thyroxine after incident amiodarone and incident thyroxine before incident amiodarone. Finally, we conducted a case-control study on two further groups: those prescribed thyroxine after incident amiodarone (AIH group; n=555) and those not prescribed thyroxine after incident amiodarone (non-AIH group; n=6,192). Results: Sequence symmetry analysis revealed a significant association between amiodarone and thyroxine in both the polypharmacy and non-polypharmacy groups. The ranges for the adjusted sequence ratio in the two groups were 12.0-16.7 and 7.3-9.0, respectively. The case-control study showed that ≥5 prescribed drugs at the first prescription of amiodarone were found to significantly increase the odds of AIH (odds ratio: 1.48, 95% confidence interval: 1.18-1.84). Conclusion: Polypharmacy was suggested as an independent risk factor for AIH. Careful assessment of the appropriateness of prescription is warranted.
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spelling pubmed-84360912021-09-13 Polypharmacy Is Associated With Amiodarone-Induced Hypothyroidism Yokoyama, Satoshi Tanaka, Yuki Hosomi, Kouichi Takada, Mitsutaka Int J Med Sci Research Paper Background: Amiodarone is rich in iodine, so in clinical practice amiodarone-induced hypothyroidism (AIH) is a major side effect. This drug is used in patients with arrhythmias, especially atrial fibrillation, the most common sustained arrhythmia. Polypharmacy, which can result in complex drug-drug interactions, occurs in more than 70% of the patients with atrial fibrillation. Therefore, polypharmacy may be involved in the expression of AIH. In this study, we investigated the association between polypharmacy and AIH. Methods: We conducted a retrospective study using data from January 2006 to May 2020 collected from a large, organized database of prescriptions constructed by the Japan Medical Information Research Institute, Inc. (Tokyo, Japan). To investigate the association between number of prescribed drugs with amiodarone and AIH, we divided patients into two groups: polypharmacy (≥ 5 prescribed drugs) and non-polypharmacy (< 5 prescribed drugs). We then performed a sequence symmetry analysis on the two groups: incident thyroxine after incident amiodarone and incident thyroxine before incident amiodarone. Finally, we conducted a case-control study on two further groups: those prescribed thyroxine after incident amiodarone (AIH group; n=555) and those not prescribed thyroxine after incident amiodarone (non-AIH group; n=6,192). Results: Sequence symmetry analysis revealed a significant association between amiodarone and thyroxine in both the polypharmacy and non-polypharmacy groups. The ranges for the adjusted sequence ratio in the two groups were 12.0-16.7 and 7.3-9.0, respectively. The case-control study showed that ≥5 prescribed drugs at the first prescription of amiodarone were found to significantly increase the odds of AIH (odds ratio: 1.48, 95% confidence interval: 1.18-1.84). Conclusion: Polypharmacy was suggested as an independent risk factor for AIH. Careful assessment of the appropriateness of prescription is warranted. Ivyspring International Publisher 2021-08-27 /pmc/articles/PMC8436091/ /pubmed/34522184 http://dx.doi.org/10.7150/ijms.61412 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Yokoyama, Satoshi
Tanaka, Yuki
Hosomi, Kouichi
Takada, Mitsutaka
Polypharmacy Is Associated With Amiodarone-Induced Hypothyroidism
title Polypharmacy Is Associated With Amiodarone-Induced Hypothyroidism
title_full Polypharmacy Is Associated With Amiodarone-Induced Hypothyroidism
title_fullStr Polypharmacy Is Associated With Amiodarone-Induced Hypothyroidism
title_full_unstemmed Polypharmacy Is Associated With Amiodarone-Induced Hypothyroidism
title_short Polypharmacy Is Associated With Amiodarone-Induced Hypothyroidism
title_sort polypharmacy is associated with amiodarone-induced hypothyroidism
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8436091/
https://www.ncbi.nlm.nih.gov/pubmed/34522184
http://dx.doi.org/10.7150/ijms.61412
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