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Predicting value of white cell count and total bilirubin on clinical outcomes in patients with ST-elevation myocardial infarction following percutaneous coronary intervention: a cohort study

OBJECTIVES: A combined equation based on white cell count (WCC) and total bilirubin (TB) was assessed for its ability to predict adverse clinical outcomes in patients with acute ST-segment elevation myocardial infarction (STEMI) with primary percutaneous coronary intervention (PCI). DESIGN: A single...

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Autores principales: Tuxun, Munire, Zhao, Qian, Xiang, Yang, Liu, Fen, Shan, Chun-Fang, Zhou, Xin-Rong, Song, Ning, Waisiding, Ajiguli, Zhang, Xue-He, Aihemaiti, Gulandanmu, Yang, Yi-Ning, Li, Xiao-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044918/
https://www.ncbi.nlm.nih.gov/pubmed/32075822
http://dx.doi.org/10.1136/bmjopen-2019-031227
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author Tuxun, Munire
Zhao, Qian
Xiang, Yang
Liu, Fen
Shan, Chun-Fang
Zhou, Xin-Rong
Song, Ning
Waisiding, Ajiguli
Zhang, Xue-He
Aihemaiti, Gulandanmu
Yang, Yi-Ning
Li, Xiao-Mei
author_facet Tuxun, Munire
Zhao, Qian
Xiang, Yang
Liu, Fen
Shan, Chun-Fang
Zhou, Xin-Rong
Song, Ning
Waisiding, Ajiguli
Zhang, Xue-He
Aihemaiti, Gulandanmu
Yang, Yi-Ning
Li, Xiao-Mei
author_sort Tuxun, Munire
collection PubMed
description OBJECTIVES: A combined equation based on white cell count (WCC) and total bilirubin (TB) was assessed for its ability to predict adverse clinical outcomes in patients with acute ST-segment elevation myocardial infarction (STEMI) with primary percutaneous coronary intervention (PCI). DESIGN: A single-centre, prospective cohort study. SETTING: The First Affiliated Hospital of Xinjiang Medical University. METHOD: A total of 615 patients with STEMI postprimary PCI were enrolled. WCC and TB were collected at admission. Logistic regression was used to determine the combined equation. The primary endpoints were in-hospital mortality and major adverse cardiovascular events (MACE), which composed of cardiac death, cardiac shock, malignant arrhythmia (ventricular tachycardia, ventricular fibrillation), severe cardiac insufficiency, non-fatal myocardial infarction, angina pectoris readmission, severe cardiac insufficiency (cardiac III–IV level), stent restenosis and target vessels revascularisation during the hospitalisation and 36 months follow-up period. RESULT: 77 patients occurred in MACE during the hospitalisation (17 in-hospital mortality). WCC and TB were taken as an independent variables to make a category of logistic regression analysis of in-hospital MACE, the logistic regression model was: logit (P)=−8.00+0.265 WCC+0.077 TB, the combination of WCC and TB was more valuable on evaluating the in-hospital mortality (area under the curve 0.804, 95% CI 0.678 to 0.929, p<0.001). Multivariate logistic regression analysis showed that combined detection was an independent risk factor for in-hospital MACE (OR 5.85, 95% CI 3.425 to 9.990, p=0.032). During the follow-up period, 172 patients (29.5%) developed MACE. But the combined detection did not predict the long-term clinical outcome. CONCLUSION: The combination of WCC and TB is an independent predictor for in-hospital outcomes in patients with STEMI than single detection.
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spelling pubmed-70449182020-03-09 Predicting value of white cell count and total bilirubin on clinical outcomes in patients with ST-elevation myocardial infarction following percutaneous coronary intervention: a cohort study Tuxun, Munire Zhao, Qian Xiang, Yang Liu, Fen Shan, Chun-Fang Zhou, Xin-Rong Song, Ning Waisiding, Ajiguli Zhang, Xue-He Aihemaiti, Gulandanmu Yang, Yi-Ning Li, Xiao-Mei BMJ Open Cardiovascular Medicine OBJECTIVES: A combined equation based on white cell count (WCC) and total bilirubin (TB) was assessed for its ability to predict adverse clinical outcomes in patients with acute ST-segment elevation myocardial infarction (STEMI) with primary percutaneous coronary intervention (PCI). DESIGN: A single-centre, prospective cohort study. SETTING: The First Affiliated Hospital of Xinjiang Medical University. METHOD: A total of 615 patients with STEMI postprimary PCI were enrolled. WCC and TB were collected at admission. Logistic regression was used to determine the combined equation. The primary endpoints were in-hospital mortality and major adverse cardiovascular events (MACE), which composed of cardiac death, cardiac shock, malignant arrhythmia (ventricular tachycardia, ventricular fibrillation), severe cardiac insufficiency, non-fatal myocardial infarction, angina pectoris readmission, severe cardiac insufficiency (cardiac III–IV level), stent restenosis and target vessels revascularisation during the hospitalisation and 36 months follow-up period. RESULT: 77 patients occurred in MACE during the hospitalisation (17 in-hospital mortality). WCC and TB were taken as an independent variables to make a category of logistic regression analysis of in-hospital MACE, the logistic regression model was: logit (P)=−8.00+0.265 WCC+0.077 TB, the combination of WCC and TB was more valuable on evaluating the in-hospital mortality (area under the curve 0.804, 95% CI 0.678 to 0.929, p<0.001). Multivariate logistic regression analysis showed that combined detection was an independent risk factor for in-hospital MACE (OR 5.85, 95% CI 3.425 to 9.990, p=0.032). During the follow-up period, 172 patients (29.5%) developed MACE. But the combined detection did not predict the long-term clinical outcome. CONCLUSION: The combination of WCC and TB is an independent predictor for in-hospital outcomes in patients with STEMI than single detection. BMJ Publishing Group 2020-02-18 /pmc/articles/PMC7044918/ /pubmed/32075822 http://dx.doi.org/10.1136/bmjopen-2019-031227 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Cardiovascular Medicine
Tuxun, Munire
Zhao, Qian
Xiang, Yang
Liu, Fen
Shan, Chun-Fang
Zhou, Xin-Rong
Song, Ning
Waisiding, Ajiguli
Zhang, Xue-He
Aihemaiti, Gulandanmu
Yang, Yi-Ning
Li, Xiao-Mei
Predicting value of white cell count and total bilirubin on clinical outcomes in patients with ST-elevation myocardial infarction following percutaneous coronary intervention: a cohort study
title Predicting value of white cell count and total bilirubin on clinical outcomes in patients with ST-elevation myocardial infarction following percutaneous coronary intervention: a cohort study
title_full Predicting value of white cell count and total bilirubin on clinical outcomes in patients with ST-elevation myocardial infarction following percutaneous coronary intervention: a cohort study
title_fullStr Predicting value of white cell count and total bilirubin on clinical outcomes in patients with ST-elevation myocardial infarction following percutaneous coronary intervention: a cohort study
title_full_unstemmed Predicting value of white cell count and total bilirubin on clinical outcomes in patients with ST-elevation myocardial infarction following percutaneous coronary intervention: a cohort study
title_short Predicting value of white cell count and total bilirubin on clinical outcomes in patients with ST-elevation myocardial infarction following percutaneous coronary intervention: a cohort study
title_sort predicting value of white cell count and total bilirubin on clinical outcomes in patients with st-elevation myocardial infarction following percutaneous coronary intervention: a cohort study
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044918/
https://www.ncbi.nlm.nih.gov/pubmed/32075822
http://dx.doi.org/10.1136/bmjopen-2019-031227
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