Multimarker strategy for the prediction of 31 days cardiac death in patients with acutely decompensated chronic heart failure

Abstract Background To investigate the combined prognostic value of admission serum levels of B-type natriuretic peptide (BNP), cardiac troponin I (cTnI) and high sensitivity C-reactive protein (hs-CRP), in patients hospitalized because of acutely decompensated severe (New York Heart Association cla...

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Published inInternational journal of cardiology Vol. 141; no. 3; pp. 284 - 290
Main Authors Zairis, Michael N, Tsiaousis, George Z, Georgilas, Anastassios Theodossis, Makrygiannis, Stamatis S, Adamopoulou, Evdokia N, Handanis, Stelios M, Batika, Pelagia C, Prekates, Athanasios A, Velissaris, Dimitris, Kouris, Nikolaos T, Mytas, Demetrios Z, Babalis, Demetrios K, Karidis, Kostas S, Foussas, Stefanos G
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Abstract Abstract Background To investigate the combined prognostic value of admission serum levels of B-type natriuretic peptide (BNP), cardiac troponin I (cTnI) and high sensitivity C-reactive protein (hs-CRP), in patients hospitalized because of acutely decompensated severe (New York Heart Association class III/IV) low-output chronic heart failure (CHF). Methods A total of 577 consecutive patients recruited in the 5 participating centers, were studied. Cardiac mortality by 31 days was the prespecified primary study end point. Results A total of 102 (17.7%) patients died by 31 days. When the study patients were divided according to the number of elevated study biomarkers, there was a significant gradual increased risk of 31-day cardiac death with increasing in the number of elevated biomarkers ( p < 0.001). The value of the discriminant C statistic for the Cox regression analysis, increased significantly when each of the study biomarkers was incorporated with the other risk predictors into a Cox regression model, with the highest C statistic value for the Cox regression model that included all the study biomarkers ( p < 0.001). By multivariate Cox regression analysis, elevated serum levels of BNP ( p = 0.002), cTnI ( p < 0.001) and hs-CRP ( p = 0.02) were independent predictors of the study end point. Conclusions In conclusion, in patients hospitalized for acute decompensation of severe (NYHA III/IV) low-output CHF, BNP, cTnI and hs-CRP upon admission offers enhanced early risk stratification. With increasing number of elevated biomarkers, the risk of 31-day cardiac death increases gradually that implies treatment intensification, and closer follow-up.
AbstractList BACKGROUNDTo investigate the combined prognostic value of admission serum levels of B-type natriuretic peptide (BNP), cardiac troponin I (cTnI) and high sensitivity C-reactive protein (hs-CRP), in patients hospitalized because of acutely decompensated severe (New York Heart Association class III/IV) low-output chronic heart failure (CHF).METHODSA total of 577 consecutive patients recruited in the 5 participating centers, were studied. Cardiac mortality by 31 days was the prespecified primary study end point.RESULTSA total of 102 (17.7%) patients died by 31 days. When the study patients were divided according to the number of elevated study biomarkers, there was a significant gradual increased risk of 31-day cardiac death with increasing in the number of elevated biomarkers (p<0.001). The value of the discriminant C statistic for the Cox regression analysis, increased significantly when each of the study biomarkers was incorporated with the other risk predictors into a Cox regression model, with the highest C statistic value for the Cox regression model that included all the study biomarkers (p<0.001). By multivariate Cox regression analysis, elevated serum levels of BNP (p=0.002), cTnI (p<0.001) and hs-CRP (p=0.02) were independent predictors of the study end point.CONCLUSIONSIn conclusion, in patients hospitalized for acute decompensation of severe (NYHA III/IV) low-output CHF, BNP, cTnI and hs-CRP upon admission offers enhanced early risk stratification. With increasing number of elevated biomarkers, the risk of 31-day cardiac death increases gradually that implies treatment intensification, and closer follow-up.
To investigate the combined prognostic value of admission serum levels of B-type natriuretic peptide (BNP), cardiac troponin I (cTnI) and high sensitivity C-reactive protein (hs-CRP), in patients hospitalized because of acutely decompensated severe (New York Heart Association class III/IV) low-output chronic heart failure (CHF). A total of 577 consecutive patients recruited in the 5 participating centers, were studied. Cardiac mortality by 31 days was the prespecified primary study end point. A total of 102 (17.7%) patients died by 31 days. When the study patients were divided according to the number of elevated study biomarkers, there was a significant gradual increased risk of 31-day cardiac death with increasing in the number of elevated biomarkers (p<0.001). The value of the discriminant C statistic for the Cox regression analysis, increased significantly when each of the study biomarkers was incorporated with the other risk predictors into a Cox regression model, with the highest C statistic value for the Cox regression model that included all the study biomarkers (p<0.001). By multivariate Cox regression analysis, elevated serum levels of BNP (p=0.002), cTnI (p<0.001) and hs-CRP (p=0.02) were independent predictors of the study end point. In conclusion, in patients hospitalized for acute decompensation of severe (NYHA III/IV) low-output CHF, BNP, cTnI and hs-CRP upon admission offers enhanced early risk stratification. With increasing number of elevated biomarkers, the risk of 31-day cardiac death increases gradually that implies treatment intensification, and closer follow-up.
Abstract Background To investigate the combined prognostic value of admission serum levels of B-type natriuretic peptide (BNP), cardiac troponin I (cTnI) and high sensitivity C-reactive protein (hs-CRP), in patients hospitalized because of acutely decompensated severe (New York Heart Association class III/IV) low-output chronic heart failure (CHF). Methods A total of 577 consecutive patients recruited in the 5 participating centers, were studied. Cardiac mortality by 31 days was the prespecified primary study end point. Results A total of 102 (17.7%) patients died by 31 days. When the study patients were divided according to the number of elevated study biomarkers, there was a significant gradual increased risk of 31-day cardiac death with increasing in the number of elevated biomarkers ( p < 0.001). The value of the discriminant C statistic for the Cox regression analysis, increased significantly when each of the study biomarkers was incorporated with the other risk predictors into a Cox regression model, with the highest C statistic value for the Cox regression model that included all the study biomarkers ( p < 0.001). By multivariate Cox regression analysis, elevated serum levels of BNP ( p = 0.002), cTnI ( p < 0.001) and hs-CRP ( p = 0.02) were independent predictors of the study end point. Conclusions In conclusion, in patients hospitalized for acute decompensation of severe (NYHA III/IV) low-output CHF, BNP, cTnI and hs-CRP upon admission offers enhanced early risk stratification. With increasing number of elevated biomarkers, the risk of 31-day cardiac death increases gradually that implies treatment intensification, and closer follow-up.
To investigate the combined prognostic value of admission serum levels of B-type natriuretic peptide (BNP), cardiac troponin I (cTnI) and high sensitivity C-reactive protein (hs-CRP), in patients hospitalized because of acutely decompensated severe (New York Heart Association class III/IV) low-output chronic heart failure (CHF). A total of 577 consecutive patients recruited in the 5 participating centers, were studied. Cardiac mortality by 31 days was the prespecified primary study end point. A total of 102 (17.7%) patients died by 31 days. When the study patients were divided according to the number of elevated study biomarkers, there was a significant gradual increased risk of 31-day cardiac death with increasing in the number of elevated biomarkers ( p < 0.001). The value of the discriminant C statistic for the Cox regression analysis, increased significantly when each of the study biomarkers was incorporated with the other risk predictors into a Cox regression model, with the highest C statistic value for the Cox regression model that included all the study biomarkers ( p < 0.001). By multivariate Cox regression analysis, elevated serum levels of BNP ( p = 0.002), cTnI ( p < 0.001) and hs-CRP ( p = 0.02) were independent predictors of the study end point. In conclusion, in patients hospitalized for acute decompensation of severe (NYHA III/IV) low-output CHF, BNP, cTnI and hs-CRP upon admission offers enhanced early risk stratification. With increasing number of elevated biomarkers, the risk of 31-day cardiac death increases gradually that implies treatment intensification, and closer follow-up.
Author Tsiaousis, George Z
Adamopoulou, Evdokia N
Makrygiannis, Stamatis S
Handanis, Stelios M
Velissaris, Dimitris
Mytas, Demetrios Z
Foussas, Stefanos G
Georgilas, Anastassios Theodossis
Zairis, Michael N
Batika, Pelagia C
Kouris, Nikolaos T
Karidis, Kostas S
Prekates, Athanasios A
Babalis, Demetrios K
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Issue 3
Keywords Acute decompensation
Chronic heart failure
Mortality
Multimarker strategy
Heart failure
Prognosis
Acute
Decompensation
Prediction
Cardiovascular disease
Chronic
Heart disease
Death
Strategy
Cardiology
Predictive factor
Day
Language English
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Snippet Abstract Background To investigate the combined prognostic value of admission serum levels of B-type natriuretic peptide (BNP), cardiac troponin I (cTnI) and...
To investigate the combined prognostic value of admission serum levels of B-type natriuretic peptide (BNP), cardiac troponin I (cTnI) and high sensitivity...
BACKGROUNDTo investigate the combined prognostic value of admission serum levels of B-type natriuretic peptide (BNP), cardiac troponin I (cTnI) and high...
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elsevier
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StartPage 284
SubjectTerms Acute decompensation
Acute Disease
Aged
Aged, 80 and over
Biological and medical sciences
Biomarkers - blood
C-Reactive Protein - metabolism
Cardiac Output
Cardiology. Vascular system
Cardiovascular
Chronic Disease
Chronic heart failure
Death, Sudden, Cardiac - epidemiology
Female
Follow-Up Studies
Heart
Heart Failure - blood
Heart Failure - diagnosis
Heart Failure - mortality
Heart failure, cardiogenic pulmonary edema, cardiac enlargement
Humans
Male
Medical sciences
Mortality
Multimarker strategy
Multivariate Analysis
Natriuretic Peptide, Brain - blood
Predictive Value of Tests
Prognosis
Proportional Hazards Models
Risk Factors
ROC Curve
Severity of Illness Index
Troponin I - blood
Title Multimarker strategy for the prediction of 31 days cardiac death in patients with acutely decompensated chronic heart failure
URI https://www.clinicalkey.es/playcontent/1-s2.0-S0167527308014228
https://dx.doi.org/10.1016/j.ijcard.2008.12.017
https://www.ncbi.nlm.nih.gov/pubmed/19157603
https://search.proquest.com/docview/733184135
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