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Impact of Admission White Blood Cell Count on Short- and Long-term Mortality in Patients With Type A Acute Aortic Dissection: An Observational Study

Studies have shown inflammation is involved in the development of acute aortic dissection (AAD). The hypothesis that white blood cell count (WBCc) on admission may have an impact on the short- and long-term outcomes of type A AAD was tested in a large-scale, prospective observational cohort study. F...

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Autores principales: Fan, Xiaohan, Huang, Bi, Lu, Haisong, Zhao, Zhenhua, Lu, Zhinan, Yang, Yanmin, Zhang, Shu, Hui, Rutai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620771/
https://www.ncbi.nlm.nih.gov/pubmed/26496299
http://dx.doi.org/10.1097/MD.0000000000001761
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author Fan, Xiaohan
Huang, Bi
Lu, Haisong
Zhao, Zhenhua
Lu, Zhinan
Yang, Yanmin
Zhang, Shu
Hui, Rutai
author_facet Fan, Xiaohan
Huang, Bi
Lu, Haisong
Zhao, Zhenhua
Lu, Zhinan
Yang, Yanmin
Zhang, Shu
Hui, Rutai
author_sort Fan, Xiaohan
collection PubMed
description Studies have shown inflammation is involved in the development of acute aortic dissection (AAD). The hypothesis that white blood cell count (WBCc) on admission may have an impact on the short- and long-term outcomes of type A AAD was tested in a large-scale, prospective observational cohort study. From 2008 to 2010, a total of 570 consecutive patients with type A AAD in Fuwai hospital were enrolled and were followed up. Baseline characteristics and WBCc on admission were collected. The primary outcomes were 30-day and long-term all-cause mortality. During a median of 1.89 years of follow-up, the 30-day and long-term all-cause mortality were 10.7% and 6.5%, respectively. Univariate Cox regression analysis identified admission WBCc as an independent predictor of 30-day mortality when considered as a continuous variable or as a categorical variable using the cutoff of 11.0  × 10(9) cells/L (all P < 0.05). After adjustment for age, sex, C-reactive protein, d-dimer, and surgical intervention, elevated admission WBCc (>11.0 × 10(9) cells/L) remained an independent predictor of 30-day mortality of AAD (hazard ratio = 3.31, 95% confidence interval 1.38–7.93, P = 0.007). No impact of admission WBCc was observed on the long-term all-cause mortality. In conclusion, elevated admission WBCc may be valuable as a predictor of 30-day mortality, and may be useful in the risk stratification of type A AAD during hospitalization.
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spelling pubmed-46207712015-10-27 Impact of Admission White Blood Cell Count on Short- and Long-term Mortality in Patients With Type A Acute Aortic Dissection: An Observational Study Fan, Xiaohan Huang, Bi Lu, Haisong Zhao, Zhenhua Lu, Zhinan Yang, Yanmin Zhang, Shu Hui, Rutai Medicine (Baltimore) 3400 Studies have shown inflammation is involved in the development of acute aortic dissection (AAD). The hypothesis that white blood cell count (WBCc) on admission may have an impact on the short- and long-term outcomes of type A AAD was tested in a large-scale, prospective observational cohort study. From 2008 to 2010, a total of 570 consecutive patients with type A AAD in Fuwai hospital were enrolled and were followed up. Baseline characteristics and WBCc on admission were collected. The primary outcomes were 30-day and long-term all-cause mortality. During a median of 1.89 years of follow-up, the 30-day and long-term all-cause mortality were 10.7% and 6.5%, respectively. Univariate Cox regression analysis identified admission WBCc as an independent predictor of 30-day mortality when considered as a continuous variable or as a categorical variable using the cutoff of 11.0  × 10(9) cells/L (all P < 0.05). After adjustment for age, sex, C-reactive protein, d-dimer, and surgical intervention, elevated admission WBCc (>11.0 × 10(9) cells/L) remained an independent predictor of 30-day mortality of AAD (hazard ratio = 3.31, 95% confidence interval 1.38–7.93, P = 0.007). No impact of admission WBCc was observed on the long-term all-cause mortality. In conclusion, elevated admission WBCc may be valuable as a predictor of 30-day mortality, and may be useful in the risk stratification of type A AAD during hospitalization. Wolters Kluwer Health 2015-10-23 /pmc/articles/PMC4620771/ /pubmed/26496299 http://dx.doi.org/10.1097/MD.0000000000001761 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 3400
Fan, Xiaohan
Huang, Bi
Lu, Haisong
Zhao, Zhenhua
Lu, Zhinan
Yang, Yanmin
Zhang, Shu
Hui, Rutai
Impact of Admission White Blood Cell Count on Short- and Long-term Mortality in Patients With Type A Acute Aortic Dissection: An Observational Study
title Impact of Admission White Blood Cell Count on Short- and Long-term Mortality in Patients With Type A Acute Aortic Dissection: An Observational Study
title_full Impact of Admission White Blood Cell Count on Short- and Long-term Mortality in Patients With Type A Acute Aortic Dissection: An Observational Study
title_fullStr Impact of Admission White Blood Cell Count on Short- and Long-term Mortality in Patients With Type A Acute Aortic Dissection: An Observational Study
title_full_unstemmed Impact of Admission White Blood Cell Count on Short- and Long-term Mortality in Patients With Type A Acute Aortic Dissection: An Observational Study
title_short Impact of Admission White Blood Cell Count on Short- and Long-term Mortality in Patients With Type A Acute Aortic Dissection: An Observational Study
title_sort impact of admission white blood cell count on short- and long-term mortality in patients with type a acute aortic dissection: an observational study
topic 3400
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620771/
https://www.ncbi.nlm.nih.gov/pubmed/26496299
http://dx.doi.org/10.1097/MD.0000000000001761
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