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Major adverse cardiovascular events in adult congenital heart disease: a population-based follow-up study from Taiwan

BACKGROUND: The aim of the present study was to identify the long-term major adverse cardiovascular events (MACE) in adult congenital heart disease (ConHD) patients in Taiwan. METHODS: From the National Health Insurance Research Database (1997-2010), adult patients (≥18 years) with ConHD were identi...

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Autores principales: Lin, Yu-Sheng, Liu, Pi-Hua, Wu, Lung-Sheng, Chen, Yu-Ming, Chang, Chee-Jen, Chu, Pao-Hsien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994523/
https://www.ncbi.nlm.nih.gov/pubmed/24655794
http://dx.doi.org/10.1186/1471-2261-14-38
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author Lin, Yu-Sheng
Liu, Pi-Hua
Wu, Lung-Sheng
Chen, Yu-Ming
Chang, Chee-Jen
Chu, Pao-Hsien
author_facet Lin, Yu-Sheng
Liu, Pi-Hua
Wu, Lung-Sheng
Chen, Yu-Ming
Chang, Chee-Jen
Chu, Pao-Hsien
author_sort Lin, Yu-Sheng
collection PubMed
description BACKGROUND: The aim of the present study was to identify the long-term major adverse cardiovascular events (MACE) in adult congenital heart disease (ConHD) patients in Taiwan. METHODS: From the National Health Insurance Research Database (1997-2010), adult patients (≥18 years) with ConHD were identified and compared to non-ConHD control patients. The primary end point was the incidence of MACE. Cox proportional hazards models were used to compute hazard ratios as estimates for multivariate adjusted relative risks with or without adjusting for age and sex. RESULTS: A total of 3,267 adult patients with ConHD were identified between 2000 and 2003 with a median follow-up of 11 years till December 31, 2010. The five most common types of ConHD were atrial septal defects, ventricular septal defects, patent ductus arteriosus, tetralogy of Fallot, and pulmonary stenosis. Overall, the incidence of MACE was 4.0-fold higher in the ConHD group compared with the controls. After adjustment for age and gender, the patients with ConHD had an increased risk of heart failure, malignant dysrhythmia, acute coronary syndrome, and stroke. The adult ConHD patients had a decreased life-long risk of MACE if they received surgical correction, especially in the patients with atrial septal defects. CONCLUSIONS: After a median of 11 years of follow-up, the Taiwanese patients with ConHD were at an increased risk of life-long cardiovascular MACE, including heart failure, stroke, acute coronary syndrome, and malignant dysrhythmia. Surgical correction may help to decrease long-term MACE in ConHD patients, especially those with ASD.
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spelling pubmed-39945232014-04-23 Major adverse cardiovascular events in adult congenital heart disease: a population-based follow-up study from Taiwan Lin, Yu-Sheng Liu, Pi-Hua Wu, Lung-Sheng Chen, Yu-Ming Chang, Chee-Jen Chu, Pao-Hsien BMC Cardiovasc Disord Research Article BACKGROUND: The aim of the present study was to identify the long-term major adverse cardiovascular events (MACE) in adult congenital heart disease (ConHD) patients in Taiwan. METHODS: From the National Health Insurance Research Database (1997-2010), adult patients (≥18 years) with ConHD were identified and compared to non-ConHD control patients. The primary end point was the incidence of MACE. Cox proportional hazards models were used to compute hazard ratios as estimates for multivariate adjusted relative risks with or without adjusting for age and sex. RESULTS: A total of 3,267 adult patients with ConHD were identified between 2000 and 2003 with a median follow-up of 11 years till December 31, 2010. The five most common types of ConHD were atrial septal defects, ventricular septal defects, patent ductus arteriosus, tetralogy of Fallot, and pulmonary stenosis. Overall, the incidence of MACE was 4.0-fold higher in the ConHD group compared with the controls. After adjustment for age and gender, the patients with ConHD had an increased risk of heart failure, malignant dysrhythmia, acute coronary syndrome, and stroke. The adult ConHD patients had a decreased life-long risk of MACE if they received surgical correction, especially in the patients with atrial septal defects. CONCLUSIONS: After a median of 11 years of follow-up, the Taiwanese patients with ConHD were at an increased risk of life-long cardiovascular MACE, including heart failure, stroke, acute coronary syndrome, and malignant dysrhythmia. Surgical correction may help to decrease long-term MACE in ConHD patients, especially those with ASD. BioMed Central 2014-03-21 /pmc/articles/PMC3994523/ /pubmed/24655794 http://dx.doi.org/10.1186/1471-2261-14-38 Text en Copyright © 2014 Lin et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Lin, Yu-Sheng
Liu, Pi-Hua
Wu, Lung-Sheng
Chen, Yu-Ming
Chang, Chee-Jen
Chu, Pao-Hsien
Major adverse cardiovascular events in adult congenital heart disease: a population-based follow-up study from Taiwan
title Major adverse cardiovascular events in adult congenital heart disease: a population-based follow-up study from Taiwan
title_full Major adverse cardiovascular events in adult congenital heart disease: a population-based follow-up study from Taiwan
title_fullStr Major adverse cardiovascular events in adult congenital heart disease: a population-based follow-up study from Taiwan
title_full_unstemmed Major adverse cardiovascular events in adult congenital heart disease: a population-based follow-up study from Taiwan
title_short Major adverse cardiovascular events in adult congenital heart disease: a population-based follow-up study from Taiwan
title_sort major adverse cardiovascular events in adult congenital heart disease: a population-based follow-up study from taiwan
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994523/
https://www.ncbi.nlm.nih.gov/pubmed/24655794
http://dx.doi.org/10.1186/1471-2261-14-38
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