Abstract

Abstract Introduction: Amiodarone (AMI), a class III anti-arrhythmic drug, is associated with a number of side effects, including thyroid dysfunction (both hypo- and hyperthyroidism), which is due to amiodarone's high iodine content and its direct toxic effect on the thyroid. Objective: To evaluate the incidence of Amiodarone induced thyrotoxicosis (AIT) (type, rate of occurrence) and to identify the risk factors involved in its occurrence. Material and method: We examined patients treated with amiodarone, between January 2002 and December 2011, who presented to our Department of Endocrinology Târgu Mures for thyroid dysfunctions. Results: The retrospective study included 87 patients with thyroid dysfunctions; 58 (66.7%) patients had AIT and 29 (33.3%) had Amiodarone induced hypothyroidism (AIH). In the AIT group: 35 were women (60.3%), 23 were men (39.7%); the average age was 61.60 ± 12.39 years. Risk factors identified for the AIT group were male gender (RR = OR = 3.8; Chi-squer = 5.7, p = 0.004) and pre-existing thyroid abnormalities (RR = 2.5, Chi-square = 4.1, p = 0.005). The thyroid dysfunction occurrence was heterogeneous (0.2-183 months). The patients with previous thyroid abnormalities developed earlier thyroid dysfunction compared to those with an apparently normal thyroid gland (22.25 ± 4.14 months versus 32.09 ± 7.69 months, p = 0.02, T test). Conclusion: In the context of the specific iodine geoclimatic intake and the area of origin, amiodarone - induced thyroid dysfunction spectrum is dominated by thyrotoxicosis. Screening and monitoring of thyroid function for patiens under chronic amiodarone treatment is necessary

Highlights

  • Amiodarone (AMI), a class III anti-arrhythmic drug, is associated with a number of side effects, including thyroid dysfunction, which is due to amiodarone's high iodine content and its direct toxic effect on the thyroid

  • Risk factors identified in the Amiodarone induced thyrotoxicosis (AIT) group were: male gender (RR = OR = 3.8; Chi-square = 5.7; p = 0.004) and pre-existing thyroid abnormalities (RR = 2.5; Chi-square = 4.1; p = 0.005)

  • Pre-existing thyroid abnormalities in our group were significant: 29 (76.31%) patients with type I AIT had a previous history of thyroid patology like diffuse goiter in 2 cases (6.9%), nodular goiter in 26 cases (89.7%) and Graves-Basedow disease in 1 case (3.4%)

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Summary

Introduction

Amiodarone (AMI), a class III anti-arrhythmic drug, is associated with a number of side effects, including thyroid dysfunction (both hypo- and hyperthyroidism), which is due to amiodarone's high iodine content and its direct toxic effect on the thyroid. Objective: To evaluate the incidence of Amiodarone induced thyrotoxicosis (AIT) (type, rate of occurrence) and to identify the risk factors involved in its occurrence. A 200 mg AMI tablet contains 75 mg of iodine, from which 6 mg are released per day, causing an overload 50–100 times greater than the WHO daily iodine recommendation (0.15–0.3 mg/day). This amount disturbs the complex physiology of the thyroid gland and has a direct toxic effect on thyrocytes [3,4,5]. Amiodarone induced thyrotoxicosis (AIT) has an incidence of 2–23%, with a higher frequency in iodine-deficient areas (2–13% in the U.S, 9.6% in Italy) [6,7,8].

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