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Multivessel Intervention in Myocardial Infarction with Cardiogenic Shock: CULPRIT-SHOCK Trial Outcomes in the PL-ACS Registry
Background: The aim of the study was a comparison of culprit-lesion-only (CL-PCI) with the multivessel percutaneous coronary intervention (MV-PCI) in terms of 30-day and 12-month mortality in a national registry. Methods: Patients from the PL-ACS registry with MI and CS were analyzed. Patients meeti...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122818/ https://www.ncbi.nlm.nih.gov/pubmed/33922373 http://dx.doi.org/10.3390/jcm10091832 |
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author | Gąsior, Mariusz Desperak, Piotr Dudek, Dariusz Witkowski, Adam Buszman, Paweł E. Trzeciak, Przemysław Hawranek, Michał Gierlotka, Marek Bartuś, Stanisław Grygier, Marek Zembala, Michał Stępińska, Janina Legutko, Jacek Wojakowski, Wojciech |
author_facet | Gąsior, Mariusz Desperak, Piotr Dudek, Dariusz Witkowski, Adam Buszman, Paweł E. Trzeciak, Przemysław Hawranek, Michał Gierlotka, Marek Bartuś, Stanisław Grygier, Marek Zembala, Michał Stępińska, Janina Legutko, Jacek Wojakowski, Wojciech |
author_sort | Gąsior, Mariusz |
collection | PubMed |
description | Background: The aim of the study was a comparison of culprit-lesion-only (CL-PCI) with the multivessel percutaneous coronary intervention (MV-PCI) in terms of 30-day and 12-month mortality in a national registry. Methods: Patients from the PL-ACS registry with MI and CS were analyzed. Patients meeting the criteria of the CULPRIT-SHOCK trial were divided into two groups: CL-PCI and MV-PCI groups. Results: Of the 3265 patients in the PL-ACS registry with MI complicated by CS, the criteria of the CULPRIT-SHOCK trial were met by 2084 patients (63.8%). The CL-PCI was performed in 883 patients, and MV-PCI was performed in 1045 patients. After the propensity score matching analysis, 617 well-matched pairs were obtained. In a 30-day follow-up, death from any cause occurred in 49.3% in the CL-PCI group and 57.0% in the MV-PCI group (RR 0.86, 95% CI 0.58–0.92, p = 0.0081). After 12 months, the rate of mortality was 62.5% in the CL-PCI group and 68.0% in the MV-PCI group (RR 0.92, 95% CI 0.84–1.01, p = 0.066). Conclusions: The results confirm the validity of CULPRIT-SHOCK findings in a national registry and current guideline-recommended strategy of revascularization limited to the infarct-related artery. |
format | Online Article Text |
id | pubmed-8122818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-81228182021-05-16 Multivessel Intervention in Myocardial Infarction with Cardiogenic Shock: CULPRIT-SHOCK Trial Outcomes in the PL-ACS Registry Gąsior, Mariusz Desperak, Piotr Dudek, Dariusz Witkowski, Adam Buszman, Paweł E. Trzeciak, Przemysław Hawranek, Michał Gierlotka, Marek Bartuś, Stanisław Grygier, Marek Zembala, Michał Stępińska, Janina Legutko, Jacek Wojakowski, Wojciech J Clin Med Article Background: The aim of the study was a comparison of culprit-lesion-only (CL-PCI) with the multivessel percutaneous coronary intervention (MV-PCI) in terms of 30-day and 12-month mortality in a national registry. Methods: Patients from the PL-ACS registry with MI and CS were analyzed. Patients meeting the criteria of the CULPRIT-SHOCK trial were divided into two groups: CL-PCI and MV-PCI groups. Results: Of the 3265 patients in the PL-ACS registry with MI complicated by CS, the criteria of the CULPRIT-SHOCK trial were met by 2084 patients (63.8%). The CL-PCI was performed in 883 patients, and MV-PCI was performed in 1045 patients. After the propensity score matching analysis, 617 well-matched pairs were obtained. In a 30-day follow-up, death from any cause occurred in 49.3% in the CL-PCI group and 57.0% in the MV-PCI group (RR 0.86, 95% CI 0.58–0.92, p = 0.0081). After 12 months, the rate of mortality was 62.5% in the CL-PCI group and 68.0% in the MV-PCI group (RR 0.92, 95% CI 0.84–1.01, p = 0.066). Conclusions: The results confirm the validity of CULPRIT-SHOCK findings in a national registry and current guideline-recommended strategy of revascularization limited to the infarct-related artery. MDPI 2021-04-22 /pmc/articles/PMC8122818/ /pubmed/33922373 http://dx.doi.org/10.3390/jcm10091832 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gąsior, Mariusz Desperak, Piotr Dudek, Dariusz Witkowski, Adam Buszman, Paweł E. Trzeciak, Przemysław Hawranek, Michał Gierlotka, Marek Bartuś, Stanisław Grygier, Marek Zembala, Michał Stępińska, Janina Legutko, Jacek Wojakowski, Wojciech Multivessel Intervention in Myocardial Infarction with Cardiogenic Shock: CULPRIT-SHOCK Trial Outcomes in the PL-ACS Registry |
title | Multivessel Intervention in Myocardial Infarction with Cardiogenic Shock: CULPRIT-SHOCK Trial Outcomes in the PL-ACS Registry |
title_full | Multivessel Intervention in Myocardial Infarction with Cardiogenic Shock: CULPRIT-SHOCK Trial Outcomes in the PL-ACS Registry |
title_fullStr | Multivessel Intervention in Myocardial Infarction with Cardiogenic Shock: CULPRIT-SHOCK Trial Outcomes in the PL-ACS Registry |
title_full_unstemmed | Multivessel Intervention in Myocardial Infarction with Cardiogenic Shock: CULPRIT-SHOCK Trial Outcomes in the PL-ACS Registry |
title_short | Multivessel Intervention in Myocardial Infarction with Cardiogenic Shock: CULPRIT-SHOCK Trial Outcomes in the PL-ACS Registry |
title_sort | multivessel intervention in myocardial infarction with cardiogenic shock: culprit-shock trial outcomes in the pl-acs registry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122818/ https://www.ncbi.nlm.nih.gov/pubmed/33922373 http://dx.doi.org/10.3390/jcm10091832 |
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