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Left ventricular remodelling after ST‐segment elevation myocardial infarction: sex differences and prognosis

AIMS: Left ventricular (LV) remodelling after ST‐segment elevation myocardial infarction (STEMI) worsens outcome. The effect of sex on LV post‐infarct remodelling is unknown. We therefore investigated the sex distribution and long‐term prognosis of LV post‐infarct remodelling after STEMI in the cont...

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Autores principales: van der Bijl, Pieter, Abou, Rachid, Goedemans, Laurien, Gersh, Bernard J., Holmes, David R., Ajmone Marsan, Nina, Delgado, Victoria, Bax, Jeroen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160476/
https://www.ncbi.nlm.nih.gov/pubmed/32059084
http://dx.doi.org/10.1002/ehf2.12618
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author van der Bijl, Pieter
Abou, Rachid
Goedemans, Laurien
Gersh, Bernard J.
Holmes, David R.
Ajmone Marsan, Nina
Delgado, Victoria
Bax, Jeroen J.
author_facet van der Bijl, Pieter
Abou, Rachid
Goedemans, Laurien
Gersh, Bernard J.
Holmes, David R.
Ajmone Marsan, Nina
Delgado, Victoria
Bax, Jeroen J.
author_sort van der Bijl, Pieter
collection PubMed
description AIMS: Left ventricular (LV) remodelling after ST‐segment elevation myocardial infarction (STEMI) worsens outcome. The effect of sex on LV post‐infarct remodelling is unknown. We therefore investigated the sex distribution and long‐term prognosis of LV post‐infarct remodelling after STEMI in the contemporary era of primary percutaneous coronary intervention (PCI) and optimal pharmacotherapy. METHODS AND RESULTS: Data were obtained from an ongoing primary PCI STEMI registry. LV remodelling was defined as ≥20% increase in LV end‐diastolic volume at either 3, 6, or 12 months post‐infarct, and LV remodelling impact on outcome was evaluated with a log‐rank test. A total population of 1995 STEMI patients were analysed (mean age 60 ± 12 years): 1527 (77%) men and 468 (23%) women. The mean age of male patients was 60±11 versus 63±13 years for women (P < 0.001). A total of 953 (48%) patients experienced LV remodelling in the first 12 months of follow‐up, and it was equally frequent amongst men (n = 729, 48%) and women (n = 224, 48%). After a median follow‐up of 94 (interquartile range 69–119) months, 225 patients died: 171 (11%) men and 54 (12%) women. No survival difference was seen between remodellers and non‐remodellers in the male (P = 0.113) and female (P = 0.920) groups. CONCLUSION: LV post‐infarct remodelling incidence, as well as long‐term survival of LV remodellers and non‐remodellers, was similar in men and women who were treated with primary PCI and optimal pharmacotherapy post‐STEMI.
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spelling pubmed-71604762020-04-20 Left ventricular remodelling after ST‐segment elevation myocardial infarction: sex differences and prognosis van der Bijl, Pieter Abou, Rachid Goedemans, Laurien Gersh, Bernard J. Holmes, David R. Ajmone Marsan, Nina Delgado, Victoria Bax, Jeroen J. ESC Heart Fail Original Research Articles AIMS: Left ventricular (LV) remodelling after ST‐segment elevation myocardial infarction (STEMI) worsens outcome. The effect of sex on LV post‐infarct remodelling is unknown. We therefore investigated the sex distribution and long‐term prognosis of LV post‐infarct remodelling after STEMI in the contemporary era of primary percutaneous coronary intervention (PCI) and optimal pharmacotherapy. METHODS AND RESULTS: Data were obtained from an ongoing primary PCI STEMI registry. LV remodelling was defined as ≥20% increase in LV end‐diastolic volume at either 3, 6, or 12 months post‐infarct, and LV remodelling impact on outcome was evaluated with a log‐rank test. A total population of 1995 STEMI patients were analysed (mean age 60 ± 12 years): 1527 (77%) men and 468 (23%) women. The mean age of male patients was 60±11 versus 63±13 years for women (P < 0.001). A total of 953 (48%) patients experienced LV remodelling in the first 12 months of follow‐up, and it was equally frequent amongst men (n = 729, 48%) and women (n = 224, 48%). After a median follow‐up of 94 (interquartile range 69–119) months, 225 patients died: 171 (11%) men and 54 (12%) women. No survival difference was seen between remodellers and non‐remodellers in the male (P = 0.113) and female (P = 0.920) groups. CONCLUSION: LV post‐infarct remodelling incidence, as well as long‐term survival of LV remodellers and non‐remodellers, was similar in men and women who were treated with primary PCI and optimal pharmacotherapy post‐STEMI. John Wiley and Sons Inc. 2020-02-14 /pmc/articles/PMC7160476/ /pubmed/32059084 http://dx.doi.org/10.1002/ehf2.12618 Text en © 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research Articles
van der Bijl, Pieter
Abou, Rachid
Goedemans, Laurien
Gersh, Bernard J.
Holmes, David R.
Ajmone Marsan, Nina
Delgado, Victoria
Bax, Jeroen J.
Left ventricular remodelling after ST‐segment elevation myocardial infarction: sex differences and prognosis
title Left ventricular remodelling after ST‐segment elevation myocardial infarction: sex differences and prognosis
title_full Left ventricular remodelling after ST‐segment elevation myocardial infarction: sex differences and prognosis
title_fullStr Left ventricular remodelling after ST‐segment elevation myocardial infarction: sex differences and prognosis
title_full_unstemmed Left ventricular remodelling after ST‐segment elevation myocardial infarction: sex differences and prognosis
title_short Left ventricular remodelling after ST‐segment elevation myocardial infarction: sex differences and prognosis
title_sort left ventricular remodelling after st‐segment elevation myocardial infarction: sex differences and prognosis
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160476/
https://www.ncbi.nlm.nih.gov/pubmed/32059084
http://dx.doi.org/10.1002/ehf2.12618
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