Assessment of a multimarker strategy for prediction of mortality in older heart failure patients: a cohort study

被引:19
作者
Bjurman, Christian [1 ]
Jensen, Juliana [1 ]
Petzold, Max [2 ]
Hammarsten, Ola [3 ]
Fu, Michael L. X. [1 ]
机构
[1] Univ Gothenburg, Dept Med, Sahlgrenska Univ Hosp, Ostra Hosp, Gothenburg, Sweden
[2] Univ Gothenburg, Ctr Appl Biostat, Dept Med, Gothenburg, Sweden
[3] Univ Gothenburg, Dept Clin Chem & Transfus Med, Inst Biomed, Sahlgrenska Acad, Gothenburg, Sweden
来源
BMJ OPEN | 2013年 / 3卷 / 03期
基金
瑞典研究理事会;
关键词
ELDERLY-PATIENTS; FOLLOW-UP; ASSOCIATION; MORBIDITY; SURVIVAL; DISEASE; STROKE; BNP;
D O I
10.1136/bmjopen-2012-002254
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Primarily to develop a multimarker score for prediction of 3-year mortality in older patients with decompensated heart failure (HF). Design: Prospective cohort study. Setting: Secondary care. Single centre. Patients and biomarkers: 131 patients, aged >= 65 years, with decompensated HF were included. Assessment of biomarkers was performed at discharge. Primary outcome measure: 3-year mortality. Results: Mean age was 73 +/- 11 years; mean left ventricular ejection fraction, 43 +/- 14%; 53% were male. The 3-year mortality was 53.4%. The following N-terminal brain natriuretic peptide (NTproBNP) levels could optimally stratify mortality: <2000 ng/l (n=39), 30.8% mortality; 2000-8000 ng/l (n=58), 51.7% mortality; and >8000 ng/l (n=34), 82.4% mortality. However, in the 2000-8000 ng/l range, NTproBNP levels had low-prognostic capacity, based on the area under the receiver operating characteristic curve (AUC=0.53; 95% CI 0.40 to 0.67). In this group, multivariate analysis identified age, cystatin C (CysC), and troponin T (TnT) levels as independent risk factors. A risk score based on these three risk factors separated a high-risk and low-risk groups within the NTproBNP range of 2000-8000 ng/l. The score exhibited a significantly higher AUC (0.75; 95% CI 0.62 to 0.86) than NTproBNP alone (p=0.03) in this NTproBNP group and had similar prognostic capacity as NTproBNP in patients below or above this NTproBNP range (p=0.57). Net reclassification improvement and integrated discriminatory improvement in the group with NTproBNP levels between 2000 and 8000 ng/l was 54% and 23%, respectively, and in the whole cohort 22% and 11%, respectively. Conclusions: Our results suggested that, to assess risk in HF, older patients required significantly higher levels of NTproBNP than younger patients. Furthermore, a risk score that included TnT and CysC at discharge, and age could improve risk stratification for mortality in older patients with HF in particular when NTproBNP was moderately elevated.
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收藏
页数:7
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