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Peripartum cardiomyopathy: disease or syndrome?
Peripartum cardiomyopathy (PPCM) is a rare form of pregnancy-associated heart failure and is considered to be a diagnosis of exclusion. There are many hypotheses on the aetiology of PPCM; however, the exact pathophysiological mechanism remains unknown. It shows many resemblances to other conditions,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613742/ https://www.ncbi.nlm.nih.gov/pubmed/31693481 http://dx.doi.org/10.1136/heartjnl-2018-314252 |
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author | Baris, Lucia Cornette, Jérôme Johnson, Mark R Sliwa, Karen Roos-Hesselink, Jolien W |
author_facet | Baris, Lucia Cornette, Jérôme Johnson, Mark R Sliwa, Karen Roos-Hesselink, Jolien W |
author_sort | Baris, Lucia |
collection | PubMed |
description | Peripartum cardiomyopathy (PPCM) is a rare form of pregnancy-associated heart failure and is considered to be a diagnosis of exclusion. There are many hypotheses on the aetiology of PPCM; however, the exact pathophysiological mechanism remains unknown. It shows many resemblances to other conditions, such as familial dilated cardiomyopathy or myocarditis, and therefore it can be hard to make a definite diagnosis. We describe four cases of peripartum-onset heart failure in women who were suspected of having PPCM. We discuss the differential diagnosis, pathophysiological mechanisms and various diagnostic modalities. |
format | Online Article Text |
id | pubmed-6613742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-66137422019-07-23 Peripartum cardiomyopathy: disease or syndrome? Baris, Lucia Cornette, Jérôme Johnson, Mark R Sliwa, Karen Roos-Hesselink, Jolien W Heart Review Peripartum cardiomyopathy (PPCM) is a rare form of pregnancy-associated heart failure and is considered to be a diagnosis of exclusion. There are many hypotheses on the aetiology of PPCM; however, the exact pathophysiological mechanism remains unknown. It shows many resemblances to other conditions, such as familial dilated cardiomyopathy or myocarditis, and therefore it can be hard to make a definite diagnosis. We describe four cases of peripartum-onset heart failure in women who were suspected of having PPCM. We discuss the differential diagnosis, pathophysiological mechanisms and various diagnostic modalities. BMJ Publishing Group 2019-03 2019-02-12 /pmc/articles/PMC6613742/ /pubmed/31693481 http://dx.doi.org/10.1136/heartjnl-2018-314252 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Baris, Lucia Cornette, Jérôme Johnson, Mark R Sliwa, Karen Roos-Hesselink, Jolien W Peripartum cardiomyopathy: disease or syndrome? |
title | Peripartum cardiomyopathy: disease or syndrome? |
title_full | Peripartum cardiomyopathy: disease or syndrome? |
title_fullStr | Peripartum cardiomyopathy: disease or syndrome? |
title_full_unstemmed | Peripartum cardiomyopathy: disease or syndrome? |
title_short | Peripartum cardiomyopathy: disease or syndrome? |
title_sort | peripartum cardiomyopathy: disease or syndrome? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613742/ https://www.ncbi.nlm.nih.gov/pubmed/31693481 http://dx.doi.org/10.1136/heartjnl-2018-314252 |
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