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Clinical profile of patients with advanced age and inflammatoric dilated cardiomyopathy on endomyocardial biopsy

BACKGROUND: Endomyocardial biopsy (EMB) is an important tool when patients with inflammatoric cardiomyopathy (DCMi) are evaluated. We aimed to assess the clinical profile of elderly patients with DCMi on EMB. METHODS: Retrospective study of all consecutive patients hospitalized from January 2007 to...

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Autores principales: Ohlow, Marc-Alexander, Chen, Ting-Hui, Schmidt, Andreas, Saenger, Joerg, Lauer, Bernward
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Science Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712365/
https://www.ncbi.nlm.nih.gov/pubmed/26788036
http://dx.doi.org/10.11909/j.issn.1671-5411.2015.06.007
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author Ohlow, Marc-Alexander
Chen, Ting-Hui
Schmidt, Andreas
Saenger, Joerg
Lauer, Bernward
author_facet Ohlow, Marc-Alexander
Chen, Ting-Hui
Schmidt, Andreas
Saenger, Joerg
Lauer, Bernward
author_sort Ohlow, Marc-Alexander
collection PubMed
description BACKGROUND: Endomyocardial biopsy (EMB) is an important tool when patients with inflammatoric cardiomyopathy (DCMi) are evaluated. We aimed to assess the clinical profile of elderly patients with DCMi on EMB. METHODS: Retrospective study of all consecutive patients hospitalized from January 2007 to December 2011 with clinical suspicion of DCMi undergoing EMB. Patients with evidence of DCMi on EMB (Group 1 ≥ 70 years, n = 85; Group 3 < 70 years; n = 418) were compared to patients of the same age group without evidence of DCMi on EMB (Group 2 ≥ 70 years, n = 45; Group 4 < 70 years; n = 147). RESULTS: Among 24,275 patients treated at our institution during the study period, 695 had clinical suspicion of DCMi and underwent EMB; 503 (2.1%) patients had DCMi on EMB. There were more male patients in Group 1, mean age was 74 ± 2.8 years, mean ejection fraction was 38% ± 14%. On presentation, signs of hemodynamic compromise (NYHA functional class III/IV, low cardiac output/index, and low cardiac power index) were more frequent in Group 1. EMB revealed viral genome in 78% of the patients, parvovirus B19 (PVB) was frequently encountered in both age groups (Group 1: 69.4% vs. Group 2: 59.6%); detection of more than one viral genome was more frequent in Group 1 (21.2% vs. 11.2%; P = 0.02) whereas the extent of immune response was significantly lower in individuals with advanced age. CONCLUSIONS: In patients ≥ 70 years with DCMi on EMB signs of hemodynamic compromise, detection of multiple viral genomes together with an overall lower extent of immune response were more frequently observed.
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spelling pubmed-47123652016-01-19 Clinical profile of patients with advanced age and inflammatoric dilated cardiomyopathy on endomyocardial biopsy Ohlow, Marc-Alexander Chen, Ting-Hui Schmidt, Andreas Saenger, Joerg Lauer, Bernward J Geriatr Cardiol Research Article BACKGROUND: Endomyocardial biopsy (EMB) is an important tool when patients with inflammatoric cardiomyopathy (DCMi) are evaluated. We aimed to assess the clinical profile of elderly patients with DCMi on EMB. METHODS: Retrospective study of all consecutive patients hospitalized from January 2007 to December 2011 with clinical suspicion of DCMi undergoing EMB. Patients with evidence of DCMi on EMB (Group 1 ≥ 70 years, n = 85; Group 3 < 70 years; n = 418) were compared to patients of the same age group without evidence of DCMi on EMB (Group 2 ≥ 70 years, n = 45; Group 4 < 70 years; n = 147). RESULTS: Among 24,275 patients treated at our institution during the study period, 695 had clinical suspicion of DCMi and underwent EMB; 503 (2.1%) patients had DCMi on EMB. There were more male patients in Group 1, mean age was 74 ± 2.8 years, mean ejection fraction was 38% ± 14%. On presentation, signs of hemodynamic compromise (NYHA functional class III/IV, low cardiac output/index, and low cardiac power index) were more frequent in Group 1. EMB revealed viral genome in 78% of the patients, parvovirus B19 (PVB) was frequently encountered in both age groups (Group 1: 69.4% vs. Group 2: 59.6%); detection of more than one viral genome was more frequent in Group 1 (21.2% vs. 11.2%; P = 0.02) whereas the extent of immune response was significantly lower in individuals with advanced age. CONCLUSIONS: In patients ≥ 70 years with DCMi on EMB signs of hemodynamic compromise, detection of multiple viral genomes together with an overall lower extent of immune response were more frequently observed. Science Press 2015-11 /pmc/articles/PMC4712365/ /pubmed/26788036 http://dx.doi.org/10.11909/j.issn.1671-5411.2015.06.007 Text en Institute of Geriatric Cardiology http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Research Article
Ohlow, Marc-Alexander
Chen, Ting-Hui
Schmidt, Andreas
Saenger, Joerg
Lauer, Bernward
Clinical profile of patients with advanced age and inflammatoric dilated cardiomyopathy on endomyocardial biopsy
title Clinical profile of patients with advanced age and inflammatoric dilated cardiomyopathy on endomyocardial biopsy
title_full Clinical profile of patients with advanced age and inflammatoric dilated cardiomyopathy on endomyocardial biopsy
title_fullStr Clinical profile of patients with advanced age and inflammatoric dilated cardiomyopathy on endomyocardial biopsy
title_full_unstemmed Clinical profile of patients with advanced age and inflammatoric dilated cardiomyopathy on endomyocardial biopsy
title_short Clinical profile of patients with advanced age and inflammatoric dilated cardiomyopathy on endomyocardial biopsy
title_sort clinical profile of patients with advanced age and inflammatoric dilated cardiomyopathy on endomyocardial biopsy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712365/
https://www.ncbi.nlm.nih.gov/pubmed/26788036
http://dx.doi.org/10.11909/j.issn.1671-5411.2015.06.007
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