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Platelet-leukocyte aggregate is associated with adverse events after surgical intervention for rheumatic heart disease

Platelet-leukocyte aggregate (PLA) is implicated in the etiology of both vascular lesions and cardiovascular events. This prospective cohort study aimed to examine the prognostic value of PLA for major adverse cardiac and cerebrovascular events (MACCE) and perioperative adverse events (AEs) in patie...

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Autores principales: Liu, Chaonan, Yang, Yang, Du, Lei, Chen, Si, Zhang, Jie, Zhang, Chongwei, Zhou, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737193/
https://www.ncbi.nlm.nih.gov/pubmed/31506454
http://dx.doi.org/10.1038/s41598-019-49253-3
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author Liu, Chaonan
Yang, Yang
Du, Lei
Chen, Si
Zhang, Jie
Zhang, Chongwei
Zhou, Jing
author_facet Liu, Chaonan
Yang, Yang
Du, Lei
Chen, Si
Zhang, Jie
Zhang, Chongwei
Zhou, Jing
author_sort Liu, Chaonan
collection PubMed
description Platelet-leukocyte aggregate (PLA) is implicated in the etiology of both vascular lesions and cardiovascular events. This prospective cohort study aimed to examine the prognostic value of PLA for major adverse cardiac and cerebrovascular events (MACCE) and perioperative adverse events (AEs) in patients with rheumatic heart disease undergoing surgical intervention by Cox proportional hazard regression and logistic regression. A total of 244 patients were included, of whom 7 were lost to follow-up. Among the analyzed 237 subjects who completed 3-year follow-up, 30 experienced MACCE and 38 experienced perioperative AEs. Preoperative PLA was higher in subjects who developed MACCE (13.32%) than in those who did not (8.69%, p = 0.040). In multivariate regression, elevated PLA was associated with increased MACCE (hazard ratio 1.51 for each quartile, 95% CI 1.07–2.13; p = 0.020), and perioperative AEs (odds ratio 1.61, 95% CI 1.14–2.26; p = 0.007). The optimal PLA cut-off for predicting MACCE was 6.8%. Subjects with PLA > 6.8% had a higher prevalence of MACCE (17.1% vs. 5.5%, p = 0.009) and perioperative AEs (19.9% vs. 8.6%, p = 0.018). Kaplan-Meier analysis showed shorter MACCE-free survival in patients with PLA > 6.8% (p = 0.007, log rank). Elevated preoperative PLA is associated with increased MACCE and perioperative AEs in patients with rheumatic valve disease undergoing surgical intervention.
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spelling pubmed-67371932019-09-22 Platelet-leukocyte aggregate is associated with adverse events after surgical intervention for rheumatic heart disease Liu, Chaonan Yang, Yang Du, Lei Chen, Si Zhang, Jie Zhang, Chongwei Zhou, Jing Sci Rep Article Platelet-leukocyte aggregate (PLA) is implicated in the etiology of both vascular lesions and cardiovascular events. This prospective cohort study aimed to examine the prognostic value of PLA for major adverse cardiac and cerebrovascular events (MACCE) and perioperative adverse events (AEs) in patients with rheumatic heart disease undergoing surgical intervention by Cox proportional hazard regression and logistic regression. A total of 244 patients were included, of whom 7 were lost to follow-up. Among the analyzed 237 subjects who completed 3-year follow-up, 30 experienced MACCE and 38 experienced perioperative AEs. Preoperative PLA was higher in subjects who developed MACCE (13.32%) than in those who did not (8.69%, p = 0.040). In multivariate regression, elevated PLA was associated with increased MACCE (hazard ratio 1.51 for each quartile, 95% CI 1.07–2.13; p = 0.020), and perioperative AEs (odds ratio 1.61, 95% CI 1.14–2.26; p = 0.007). The optimal PLA cut-off for predicting MACCE was 6.8%. Subjects with PLA > 6.8% had a higher prevalence of MACCE (17.1% vs. 5.5%, p = 0.009) and perioperative AEs (19.9% vs. 8.6%, p = 0.018). Kaplan-Meier analysis showed shorter MACCE-free survival in patients with PLA > 6.8% (p = 0.007, log rank). Elevated preoperative PLA is associated with increased MACCE and perioperative AEs in patients with rheumatic valve disease undergoing surgical intervention. Nature Publishing Group UK 2019-09-10 /pmc/articles/PMC6737193/ /pubmed/31506454 http://dx.doi.org/10.1038/s41598-019-49253-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liu, Chaonan
Yang, Yang
Du, Lei
Chen, Si
Zhang, Jie
Zhang, Chongwei
Zhou, Jing
Platelet-leukocyte aggregate is associated with adverse events after surgical intervention for rheumatic heart disease
title Platelet-leukocyte aggregate is associated with adverse events after surgical intervention for rheumatic heart disease
title_full Platelet-leukocyte aggregate is associated with adverse events after surgical intervention for rheumatic heart disease
title_fullStr Platelet-leukocyte aggregate is associated with adverse events after surgical intervention for rheumatic heart disease
title_full_unstemmed Platelet-leukocyte aggregate is associated with adverse events after surgical intervention for rheumatic heart disease
title_short Platelet-leukocyte aggregate is associated with adverse events after surgical intervention for rheumatic heart disease
title_sort platelet-leukocyte aggregate is associated with adverse events after surgical intervention for rheumatic heart disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737193/
https://www.ncbi.nlm.nih.gov/pubmed/31506454
http://dx.doi.org/10.1038/s41598-019-49253-3
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