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Percutaneous coronary intervention for left main stem disease: Impact of diabetes mellitus on mortality
OBJECTIVES: We assessed the impact of diabetes mellitus (DM) on mortality after percutaneous coronary intervention (PCI) for left main stem (LMS) disease. Second, we compared mortality outcomes between non‐insulin treated (NITDM) and insulin treated diabetes (ITDM) in different clinical settings. BA...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687181/ https://www.ncbi.nlm.nih.gov/pubmed/32134178 http://dx.doi.org/10.1002/ccd.28818 |
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author | Bawamia, Bilal R. Egred, Mohaned Jackson, Matthew Purcell, Ian Austin, David Zaman, Azfar G. |
author_facet | Bawamia, Bilal R. Egred, Mohaned Jackson, Matthew Purcell, Ian Austin, David Zaman, Azfar G. |
author_sort | Bawamia, Bilal R. |
collection | PubMed |
description | OBJECTIVES: We assessed the impact of diabetes mellitus (DM) on mortality after percutaneous coronary intervention (PCI) for left main stem (LMS) disease. Second, we compared mortality outcomes between non‐insulin treated (NITDM) and insulin treated diabetes (ITDM) in different clinical settings. BACKGROUND: There is a paucity of “real world” outcomes data in diabetic patients undergoing LMS PCI. METHODS: We undertook a retrospective analysis of consecutive patients undergoing unprotected LMS PCI at 2 high volume tertiary centers. Diabetic status and clinical setting for PCI were recorded. The primary outcome measure was all‐cause 30‐day and long‐term mortality (up to 36 months) post index PCI. RESULTS: Between 2003 and 2017, 2,675 patients undergoing index LMS PCI were analyzed. Of those, 77.1% were non‐DM, 15.8% NITDM, and 7.1% ITDM. Overall, DM status was not associated with higher 30‐day mortality (OR 1.39, 95% CI 0.89–2.16, p = .15). During a median follow‐up of 36 months, there was a borderline statistical association of DM with long‐term mortality in all PCI settings (HR 1.31, 95% CI 1.00–1.71, p = .05). Compared to non‐DM, ITDM but not NITDM was associated with short‐ and long‐term mortality in all clinical presentations. CONCLUSIONS: Overall, DM did not impact on 30‐day mortality and had only a borderline statistical association with long‐term mortality. It did not have an influence on mortality in non‐emergency LMS PCI. The impact of DM on mortality outcomes following LMS PCI was only significant in the insulin treated patients. |
format | Online Article Text |
id | pubmed-7687181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76871812020-12-05 Percutaneous coronary intervention for left main stem disease: Impact of diabetes mellitus on mortality Bawamia, Bilal R. Egred, Mohaned Jackson, Matthew Purcell, Ian Austin, David Zaman, Azfar G. Catheter Cardiovasc Interv CORONARY ARTERY DISEASE OBJECTIVES: We assessed the impact of diabetes mellitus (DM) on mortality after percutaneous coronary intervention (PCI) for left main stem (LMS) disease. Second, we compared mortality outcomes between non‐insulin treated (NITDM) and insulin treated diabetes (ITDM) in different clinical settings. BACKGROUND: There is a paucity of “real world” outcomes data in diabetic patients undergoing LMS PCI. METHODS: We undertook a retrospective analysis of consecutive patients undergoing unprotected LMS PCI at 2 high volume tertiary centers. Diabetic status and clinical setting for PCI were recorded. The primary outcome measure was all‐cause 30‐day and long‐term mortality (up to 36 months) post index PCI. RESULTS: Between 2003 and 2017, 2,675 patients undergoing index LMS PCI were analyzed. Of those, 77.1% were non‐DM, 15.8% NITDM, and 7.1% ITDM. Overall, DM status was not associated with higher 30‐day mortality (OR 1.39, 95% CI 0.89–2.16, p = .15). During a median follow‐up of 36 months, there was a borderline statistical association of DM with long‐term mortality in all PCI settings (HR 1.31, 95% CI 1.00–1.71, p = .05). Compared to non‐DM, ITDM but not NITDM was associated with short‐ and long‐term mortality in all clinical presentations. CONCLUSIONS: Overall, DM did not impact on 30‐day mortality and had only a borderline statistical association with long‐term mortality. It did not have an influence on mortality in non‐emergency LMS PCI. The impact of DM on mortality outcomes following LMS PCI was only significant in the insulin treated patients. John Wiley & Sons, Inc. 2020-03-05 2020-10-01 /pmc/articles/PMC7687181/ /pubmed/32134178 http://dx.doi.org/10.1002/ccd.28818 Text en © 2020 The Authors. Catheterization and Cardiovascular Interventions published by Wiley Periodicals, Inc. 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 | CORONARY ARTERY DISEASE Bawamia, Bilal R. Egred, Mohaned Jackson, Matthew Purcell, Ian Austin, David Zaman, Azfar G. Percutaneous coronary intervention for left main stem disease: Impact of diabetes mellitus on mortality |
title | Percutaneous coronary intervention for left main stem disease: Impact of diabetes mellitus on mortality |
title_full | Percutaneous coronary intervention for left main stem disease: Impact of diabetes mellitus on mortality |
title_fullStr | Percutaneous coronary intervention for left main stem disease: Impact of diabetes mellitus on mortality |
title_full_unstemmed | Percutaneous coronary intervention for left main stem disease: Impact of diabetes mellitus on mortality |
title_short | Percutaneous coronary intervention for left main stem disease: Impact of diabetes mellitus on mortality |
title_sort | percutaneous coronary intervention for left main stem disease: impact of diabetes mellitus on mortality |
topic | CORONARY ARTERY DISEASE |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687181/ https://www.ncbi.nlm.nih.gov/pubmed/32134178 http://dx.doi.org/10.1002/ccd.28818 |
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