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Screening Rheumatic Heart Disease in 1530 New Caledonian Adolescents
BACKGROUND: In New Caledonia, a South Pacific archipelago whose inhabitants comprise Melanesians, Europeans/whites, Wallisians, Futunans, Polynesians, and Asians, the prevalence of rheumatic heart disease (RHD) is 0.9% to 1% at ages 9 and 10. It could be higher at the age of 16, but this remains to...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428581/ https://www.ncbi.nlm.nih.gov/pubmed/32336214 http://dx.doi.org/10.1161/JAHA.119.015017 |
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author | Chatard, Jean‐Claude Dubois, Thomas Espinosa, Florian Kamblock, Joël Ledos, Pierre‐Henri Tarpinian, Emmanuel Da Costa, Antoine |
author_facet | Chatard, Jean‐Claude Dubois, Thomas Espinosa, Florian Kamblock, Joël Ledos, Pierre‐Henri Tarpinian, Emmanuel Da Costa, Antoine |
author_sort | Chatard, Jean‐Claude |
collection | PubMed |
description | BACKGROUND: In New Caledonia, a South Pacific archipelago whose inhabitants comprise Melanesians, Europeans/whites, Wallisians, Futunans, Polynesians, and Asians, the prevalence of rheumatic heart disease (RHD) is 0.9% to 1% at ages 9 and 10. It could be higher at the age of 16, but this remains to be verified. METHODS AND RESULTS: A total of 1530 Melanesian, Métis, white, Wallisian, Futunan, Polynesian, and Asian adolescents benefited from a transthoracic echocardiogram. Definite or borderline RHD, nonrheumatic valve lesions, congenital heart defects, family and personal history of acute rheumatic fever, and socioeconomic factors were collected. The prevalence of cardiac abnormalities was 8.1%, made up of 4.1% RHD including 2.4% definite and 1.7% borderline RHD, 1.7% nonrheumatic valve lesions, and 2.3% congenital anomalies. In whites and Asians, there were no cases of RHD. RHD was higher in the Wallisian, Futunan, and Polynesian group (7.6%) when compared with Melanesians (5.3%) and Métis (2.9%). The number of nonrheumatic valve lesions was not statistically different in the different ethnicities. The prevalence of RHD was higher in adolescents with a personal history of acute rheumatic fever, in those living in overcrowded conditions, and in those whose parents were unemployed or had low‐income occupations, such as the farmers or manual workers. CONCLUSIONS: RHD was 4 times higher in adolescents at age 16 than at ages 9 and 10 (4.1% versus 0.9%–1%). No cases of RHD were observed in whites and Asians. The determining factors were history of acute rheumatic fever and socioeconomic factors. |
format | Online Article Text |
id | pubmed-7428581 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74285812020-08-17 Screening Rheumatic Heart Disease in 1530 New Caledonian Adolescents Chatard, Jean‐Claude Dubois, Thomas Espinosa, Florian Kamblock, Joël Ledos, Pierre‐Henri Tarpinian, Emmanuel Da Costa, Antoine J Am Heart Assoc Original Research BACKGROUND: In New Caledonia, a South Pacific archipelago whose inhabitants comprise Melanesians, Europeans/whites, Wallisians, Futunans, Polynesians, and Asians, the prevalence of rheumatic heart disease (RHD) is 0.9% to 1% at ages 9 and 10. It could be higher at the age of 16, but this remains to be verified. METHODS AND RESULTS: A total of 1530 Melanesian, Métis, white, Wallisian, Futunan, Polynesian, and Asian adolescents benefited from a transthoracic echocardiogram. Definite or borderline RHD, nonrheumatic valve lesions, congenital heart defects, family and personal history of acute rheumatic fever, and socioeconomic factors were collected. The prevalence of cardiac abnormalities was 8.1%, made up of 4.1% RHD including 2.4% definite and 1.7% borderline RHD, 1.7% nonrheumatic valve lesions, and 2.3% congenital anomalies. In whites and Asians, there were no cases of RHD. RHD was higher in the Wallisian, Futunan, and Polynesian group (7.6%) when compared with Melanesians (5.3%) and Métis (2.9%). The number of nonrheumatic valve lesions was not statistically different in the different ethnicities. The prevalence of RHD was higher in adolescents with a personal history of acute rheumatic fever, in those living in overcrowded conditions, and in those whose parents were unemployed or had low‐income occupations, such as the farmers or manual workers. CONCLUSIONS: RHD was 4 times higher in adolescents at age 16 than at ages 9 and 10 (4.1% versus 0.9%–1%). No cases of RHD were observed in whites and Asians. The determining factors were history of acute rheumatic fever and socioeconomic factors. John Wiley and Sons Inc. 2020-04-26 /pmc/articles/PMC7428581/ /pubmed/32336214 http://dx.doi.org/10.1161/JAHA.119.015017 Text en © 2020 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Chatard, Jean‐Claude Dubois, Thomas Espinosa, Florian Kamblock, Joël Ledos, Pierre‐Henri Tarpinian, Emmanuel Da Costa, Antoine Screening Rheumatic Heart Disease in 1530 New Caledonian Adolescents |
title | Screening Rheumatic Heart Disease in 1530 New Caledonian Adolescents |
title_full | Screening Rheumatic Heart Disease in 1530 New Caledonian Adolescents |
title_fullStr | Screening Rheumatic Heart Disease in 1530 New Caledonian Adolescents |
title_full_unstemmed | Screening Rheumatic Heart Disease in 1530 New Caledonian Adolescents |
title_short | Screening Rheumatic Heart Disease in 1530 New Caledonian Adolescents |
title_sort | screening rheumatic heart disease in 1530 new caledonian adolescents |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428581/ https://www.ncbi.nlm.nih.gov/pubmed/32336214 http://dx.doi.org/10.1161/JAHA.119.015017 |
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