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Cardiac resynchronization therapy in patients with chronic Chagas cardiomyopathy: long-term follow up
INTRODUCTION: Chagas disease is a major cause of cardiomyopathy and sudden death in our country. It has a high mortality when their patients develop New York Heart Association (NYHA) class IV. OBJECTIVE: The objective of this study is to analyze the clinical outcome of patients with Chagas' car...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Cirurgia Cardiovascular
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389487/ https://www.ncbi.nlm.nih.gov/pubmed/24896160 http://dx.doi.org/10.5935/1678-9741.20140008 |
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author | de Araújo, Edgard Ferreira Chamlian, Eduardo Gregório Peroni, Alexey Pomares Pereira, Wilson Lopes Gandra, Sylvio Matheus de Aquino Rivetti, Luiz Antonio |
author_facet | de Araújo, Edgard Ferreira Chamlian, Eduardo Gregório Peroni, Alexey Pomares Pereira, Wilson Lopes Gandra, Sylvio Matheus de Aquino Rivetti, Luiz Antonio |
author_sort | de Araújo, Edgard Ferreira |
collection | PubMed |
description | INTRODUCTION: Chagas disease is a major cause of cardiomyopathy and sudden death in our country. It has a high mortality when their patients develop New York Heart Association (NYHA) class IV. OBJECTIVE: The objective of this study is to analyze the clinical outcome of patients with Chagas' cardiomyopathy with congestive heart failure with optimized pharmacological therapy, undergoing cardiac resynchronization therapy. METHODS: Between January 2004 and February 2009, 72 patients with Chagas' cardiomyopathy in NYHA class III and IV underwent cardiac resynchronization therapy and were monitored to assess their clinical evolution. We used the t test or the Wilcoxon test to compare the same variable in two different times. A P value < 0.05 was established as statistically significant. RESULTS: The average clinical follow-up was 46.6 months (range 4-79 months). At the end of the evaluation, 87.4% of patients were in NYHA class I or II (P<0.001). There was response to therapy in 65.3% of patients (P<0.001), with an overall mortality of 34.7%. CONCLUSION: In patients with chronic Chagas cardiomyopathy undergoing cardiac resynchronization therapy, we found the following statistically significant changes: improvement in NYHA class and increase of left ventricle ejection fraction, a decrease of the systolic final diameter and systolic final left ventricle volume and improvement of patient survival. |
format | Online Article Text |
id | pubmed-4389487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Sociedade Brasileira de Cirurgia Cardiovascular |
record_format | MEDLINE/PubMed |
spelling | pubmed-43894872015-04-14 Cardiac resynchronization therapy in patients with chronic Chagas cardiomyopathy: long-term follow up de Araújo, Edgard Ferreira Chamlian, Eduardo Gregório Peroni, Alexey Pomares Pereira, Wilson Lopes Gandra, Sylvio Matheus de Aquino Rivetti, Luiz Antonio Rev Bras Cir Cardiovasc Original Articles INTRODUCTION: Chagas disease is a major cause of cardiomyopathy and sudden death in our country. It has a high mortality when their patients develop New York Heart Association (NYHA) class IV. OBJECTIVE: The objective of this study is to analyze the clinical outcome of patients with Chagas' cardiomyopathy with congestive heart failure with optimized pharmacological therapy, undergoing cardiac resynchronization therapy. METHODS: Between January 2004 and February 2009, 72 patients with Chagas' cardiomyopathy in NYHA class III and IV underwent cardiac resynchronization therapy and were monitored to assess their clinical evolution. We used the t test or the Wilcoxon test to compare the same variable in two different times. A P value < 0.05 was established as statistically significant. RESULTS: The average clinical follow-up was 46.6 months (range 4-79 months). At the end of the evaluation, 87.4% of patients were in NYHA class I or II (P<0.001). There was response to therapy in 65.3% of patients (P<0.001), with an overall mortality of 34.7%. CONCLUSION: In patients with chronic Chagas cardiomyopathy undergoing cardiac resynchronization therapy, we found the following statistically significant changes: improvement in NYHA class and increase of left ventricle ejection fraction, a decrease of the systolic final diameter and systolic final left ventricle volume and improvement of patient survival. Sociedade Brasileira de Cirurgia Cardiovascular 2014 /pmc/articles/PMC4389487/ /pubmed/24896160 http://dx.doi.org/10.5935/1678-9741.20140008 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles de Araújo, Edgard Ferreira Chamlian, Eduardo Gregório Peroni, Alexey Pomares Pereira, Wilson Lopes Gandra, Sylvio Matheus de Aquino Rivetti, Luiz Antonio Cardiac resynchronization therapy in patients with chronic Chagas cardiomyopathy: long-term follow up |
title | Cardiac resynchronization therapy in patients with chronic Chagas
cardiomyopathy: long-term follow up |
title_full | Cardiac resynchronization therapy in patients with chronic Chagas
cardiomyopathy: long-term follow up |
title_fullStr | Cardiac resynchronization therapy in patients with chronic Chagas
cardiomyopathy: long-term follow up |
title_full_unstemmed | Cardiac resynchronization therapy in patients with chronic Chagas
cardiomyopathy: long-term follow up |
title_short | Cardiac resynchronization therapy in patients with chronic Chagas
cardiomyopathy: long-term follow up |
title_sort | cardiac resynchronization therapy in patients with chronic chagas
cardiomyopathy: long-term follow up |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389487/ https://www.ncbi.nlm.nih.gov/pubmed/24896160 http://dx.doi.org/10.5935/1678-9741.20140008 |
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