Division of Drug Informatics, School of Pharmacy, Kindai University, 3-4-1 Kowakae, Higashiosaka City, Osaka 577-8502, Japan.
Int J Med Sci. 2021 Aug 27;18(15):3574-3580. doi: 10.7150/ijms.61412. eCollection 2021.
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. 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). 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). Polypharmacy was suggested as an independent risk factor for AIH. Careful assessment of the appropriateness of prescription is warranted.
胺碘酮富含碘,因此在临床实践中,胺碘酮引起的甲状腺功能减退症(AIH)是一个主要的副作用。这种药物用于心律失常患者,特别是心房颤动,最常见的持续性心律失常。超过 70%的心房颤动患者同时服用多种药物,这可能导致复杂的药物相互作用。因此,多药治疗可能与 AIH 的表达有关。在这项研究中,我们研究了多药治疗与 AIH 之间的关系。我们使用 2006 年 1 月至 2020 年 5 月期间从日本医学信息研究所(日本东京)构建的大型处方组织数据库中收集的数据进行了回顾性研究。为了研究与胺碘酮相关的处方药物数量与 AIH 之间的关系,我们将患者分为两组:多药治疗(≥5 种处方药物)和非多药治疗(<5 种处方药物)。然后,我们对两组进行了序列对称分析:在发生胺碘酮之后发生的甲状腺素事件和在发生胺碘酮之前发生的甲状腺素事件。最后,我们在另外两组中进行了病例对照研究:那些在发生胺碘酮之后开甲状腺素的患者(AIH 组;n=555)和那些在发生胺碘酮之后没有开甲状腺素的患者(非-AIH 组;n=6192)。序列对称分析显示,在多药治疗组和非多药治疗组中,胺碘酮与甲状腺素之间均存在显著关联。两组调整后的序列比值范围分别为 12.0-16.7 和 7.3-9.0。病例对照研究表明,在首次开胺碘酮处方时同时服用≥5 种药物显著增加 AIH 的可能性(比值比:1.48,95%置信区间:1.18-1.84)。多药治疗被认为是 AIH 的一个独立危险因素。有必要对处方的适当性进行仔细评估。