Department of Cardiology, Rigshospitalet, University of Copenhagen, Blegdamsvej 9, Copenhagen 2100, Denmark.
Department of Endocrinology, Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark.
Europace. 2023 Feb 16;25(2):291-299. doi: 10.1093/europace/euac217.
Thyroid dysfunction is considered the most frequent complication to amiodarone treatment, but data on its occurrence outside clinical trials are sparse. The present study aimed to examine the incidence of thyroid dysfunction following initiation of amiodarone treatment in a nationwide cohort of patients with and without heart failure (HF).
In Danish registries, we identified all patients with first-time amiodarone treatment during the period 2000-18, without prior thyroid disease or medication. The primary outcome was a composite of thyroid diagnoses and initiation of thyroid drugs. Outcomes were assessed at 1-year follow-up, and for patients free of events in the first year, in a landmark analysis for the subsequent 5 years. We included 43 724 patients with first-time amiodarone treatment, of whom 16 939 (38%) had HF. At 1-year follow-up, the cumulative incidence and adjusted hazard ratio (HR) of the primary outcome were 5.3% and 1.37 (95% confidence interval 1.25-1.50) in patients with a history of HF and 4.2% in those without HF (reference). In the 1-year landmark analysis, the subsequent 5-year cumulative incidences and adjusted HRs of the primary outcome were 5.3% (reference) in patients with 1-year accumulated dose <27.38 g [corresponding to average daily dose (ADD <75 mg)], 14.0% and HR 2.74 (2.46-3.05) for 27.38-45.63 g (ADD 75-125 mg), 20.0% and HR 4.16 (3.77-4.59) for 45.64-63.88 g (ADD 126-175 mg), and 24.5% and HR 5.30 (4.82-5.90) for >63.88 g (ADD >175 mg).
Among patients who initiated amiodarone treatment, around 5% had thyroid dysfunction at 1-year follow-up, with a slightly higher incidence in those with HF. A dose-response relationship was observed between the 1-year accumulated amiodarone dose and the subsequent 5-year cumulative incidence of thyroid dysfunction.
甲状腺功能障碍被认为是胺碘酮治疗最常见的并发症,但临床试验以外的数据对此类并发症的发生情况则较为匮乏。本研究旨在调查在丹麦全国范围内接受胺碘酮治疗的伴有或不伴有心力衰竭(HF)的患者队列中,甲状腺功能障碍的发生情况。
我们在丹麦的登记处确定了所有在 2000-18 年期间首次接受胺碘酮治疗且无既往甲状腺疾病或药物治疗的患者。主要结局是甲状腺诊断和甲状腺药物治疗的综合指标。在 1 年随访时评估结局,并对第 1 年无事件发生的患者进行了后续 5 年的里程碑分析。我们纳入了 43724 名首次接受胺碘酮治疗的患者,其中 16939 名(38%)患有 HF。在 1 年随访时,有 HF 病史患者的主要结局累积发生率和调整后的风险比(HR)为 5.3%和 1.37(95%置信区间 1.25-1.50),无 HF 病史患者为 4.2%(参考)。在 1 年的里程碑分析中,主要结局的后续 5 年累积发生率和调整后的 HR 分别为:1 年累积剂量 <27.38 g(相当于平均日剂量(ADD <75 mg)的患者为 5.3%(参考),27.38-45.63 g(ADD 75-125 mg)的患者为 14.0%和 HR 2.74(2.46-3.05),45.64-63.88 g(ADD 126-175 mg)的患者为 20.0%和 HR 4.16(3.77-4.59),>63.88 g(ADD >175 mg)的患者为 24.5%和 HR 5.30(4.82-5.90)。
在接受胺碘酮治疗的患者中,约有 5%在 1 年随访时出现甲状腺功能障碍,伴有 HF 的患者发生率略高。胺碘酮 1 年累积剂量与随后 5 年甲状腺功能障碍累积发生率之间存在剂量-反应关系。