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Thyroid Dysfunction under Amiodarone in Patients with and without Congenital Heart Disease: Results of a Nationwide Analysis

Background: Amiodarone has a profound adverse toxicity profile. Large population-based analyses quantifying the risk of thyroid dysfunction (TD) in adults with and without congenital heart disease (ACHD) are lacking. Methods: All adults registered with a major German health insurer (≈9.2 million mem...

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Autores principales: Fischer, Alicia Jeanette, Enders, Dominic, Eckardt, Lars, Köbe, Julia, Wasmer, Kristina, Breithardt, Günter, De Torres Alba, Fernando, Kaleschke, Gerrit, Baumgartner, Helmut, Diller, Gerhard-Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8999848/
https://www.ncbi.nlm.nih.gov/pubmed/35407633
http://dx.doi.org/10.3390/jcm11072027
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author Fischer, Alicia Jeanette
Enders, Dominic
Eckardt, Lars
Köbe, Julia
Wasmer, Kristina
Breithardt, Günter
De Torres Alba, Fernando
Kaleschke, Gerrit
Baumgartner, Helmut
Diller, Gerhard-Paul
author_facet Fischer, Alicia Jeanette
Enders, Dominic
Eckardt, Lars
Köbe, Julia
Wasmer, Kristina
Breithardt, Günter
De Torres Alba, Fernando
Kaleschke, Gerrit
Baumgartner, Helmut
Diller, Gerhard-Paul
author_sort Fischer, Alicia Jeanette
collection PubMed
description Background: Amiodarone has a profound adverse toxicity profile. Large population-based analyses quantifying the risk of thyroid dysfunction (TD) in adults with and without congenital heart disease (ACHD) are lacking. Methods: All adults registered with a major German health insurer (≈9.2 million members) with amiodarone prescriptions were analyzed. Occurrence of amiodarone-associated TD was assessed. Results: Overall, 48,891 non-ACHD (37% female; median 73 years) and 886 ACHD (34% female; median 66 years) received amiodarone. Over 184,787 patient-years, 10,875 cases of TD occurred. The 10-year risk for TD was 38% in non-ACHD (35% ACHD). Within ACHD, compared to amiodarone-naïve patients, the hazard ratio (HR) for TD was 3.9 at 4 years after any amiodarone exposure. TD was associated with female gender (HR 1.42, p < 0.001) and younger age (HR 0.97 per 10 years, p = 0.009). Patients with congenital heart disease were not at increased risk (HR 0.98, p = 0.80). Diagnosis of complex congenital heart disease, however, was a predictor for TD (HR 1.56, p = 0.02). Amiodarone was continued in 47% of non-ACHD (38% ACHD), and 2.3% of non-ACHD (3.5% ACHD) underwent thyroid surgery/radiotherapy. Conclusions: Amiodarone-associated TD is common and comparable in non-ACHD and ACHD. While female gender and younger age are predictors for TD, congenital heart disease is not necessarily associated with an elevated risk.
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spelling pubmed-89998482022-04-12 Thyroid Dysfunction under Amiodarone in Patients with and without Congenital Heart Disease: Results of a Nationwide Analysis Fischer, Alicia Jeanette Enders, Dominic Eckardt, Lars Köbe, Julia Wasmer, Kristina Breithardt, Günter De Torres Alba, Fernando Kaleschke, Gerrit Baumgartner, Helmut Diller, Gerhard-Paul J Clin Med Article Background: Amiodarone has a profound adverse toxicity profile. Large population-based analyses quantifying the risk of thyroid dysfunction (TD) in adults with and without congenital heart disease (ACHD) are lacking. Methods: All adults registered with a major German health insurer (≈9.2 million members) with amiodarone prescriptions were analyzed. Occurrence of amiodarone-associated TD was assessed. Results: Overall, 48,891 non-ACHD (37% female; median 73 years) and 886 ACHD (34% female; median 66 years) received amiodarone. Over 184,787 patient-years, 10,875 cases of TD occurred. The 10-year risk for TD was 38% in non-ACHD (35% ACHD). Within ACHD, compared to amiodarone-naïve patients, the hazard ratio (HR) for TD was 3.9 at 4 years after any amiodarone exposure. TD was associated with female gender (HR 1.42, p < 0.001) and younger age (HR 0.97 per 10 years, p = 0.009). Patients with congenital heart disease were not at increased risk (HR 0.98, p = 0.80). Diagnosis of complex congenital heart disease, however, was a predictor for TD (HR 1.56, p = 0.02). Amiodarone was continued in 47% of non-ACHD (38% ACHD), and 2.3% of non-ACHD (3.5% ACHD) underwent thyroid surgery/radiotherapy. Conclusions: Amiodarone-associated TD is common and comparable in non-ACHD and ACHD. While female gender and younger age are predictors for TD, congenital heart disease is not necessarily associated with an elevated risk. MDPI 2022-04-05 /pmc/articles/PMC8999848/ /pubmed/35407633 http://dx.doi.org/10.3390/jcm11072027 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fischer, Alicia Jeanette
Enders, Dominic
Eckardt, Lars
Köbe, Julia
Wasmer, Kristina
Breithardt, Günter
De Torres Alba, Fernando
Kaleschke, Gerrit
Baumgartner, Helmut
Diller, Gerhard-Paul
Thyroid Dysfunction under Amiodarone in Patients with and without Congenital Heart Disease: Results of a Nationwide Analysis
title Thyroid Dysfunction under Amiodarone in Patients with and without Congenital Heart Disease: Results of a Nationwide Analysis
title_full Thyroid Dysfunction under Amiodarone in Patients with and without Congenital Heart Disease: Results of a Nationwide Analysis
title_fullStr Thyroid Dysfunction under Amiodarone in Patients with and without Congenital Heart Disease: Results of a Nationwide Analysis
title_full_unstemmed Thyroid Dysfunction under Amiodarone in Patients with and without Congenital Heart Disease: Results of a Nationwide Analysis
title_short Thyroid Dysfunction under Amiodarone in Patients with and without Congenital Heart Disease: Results of a Nationwide Analysis
title_sort thyroid dysfunction under amiodarone in patients with and without congenital heart disease: results of a nationwide analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8999848/
https://www.ncbi.nlm.nih.gov/pubmed/35407633
http://dx.doi.org/10.3390/jcm11072027
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