Derivation and validation of a simple clinical risk-model in heart failure based on 6 minute walk test performance and NT-proBNP status - Do we need specificity for sex and beta-blockers?

被引:16
作者
Frankenstein, L. [1 ]
Goode, K. [3 ]
Ingle, L. [2 ]
Remppis, A. [1 ]
Schellberg, D. [1 ]
Nelles, M. [1 ]
Katus, H. A. [1 ]
Clark, A. L. [3 ]
Cleland, J. G. F. [3 ]
Zugck, C. [1 ]
机构
[1] Univ Klinikum Heidelberg, Heidelberg, Germany
[2] Leeds Metropolitan Univ, Carnegie Mellon Res Inst, Leeds LS1 3HE, W Yorkshire, England
[3] Univ Hull, Dept Acad Cardiol, Kingston Upon Hull, Yorks, England
关键词
Chronic heart failure; Risk prediction; Beta-blockers; Sex; BRAIN NATRIURETIC PEPTIDE; PROGNOSTIC VALUE; PREDICT; SURVIVAL; GENDER; STRATIFICATION; POPULATION; CARVEDILOL; METOPROLOL; EXERCISE;
D O I
10.1016/j.ijcard.2009.08.005
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background: It is unclear whether risk prediction strategies in chronic heart failure (CHF) need to be specific for sex or beta-blockers. We examined this problem and developed and validated the consequent risk models based on 6-minute-walk-test and NT-proBNP. Methods: The derivation cohort comprised 636 German patients with systolic dysfunction. They were validated against 676 British patients with similar aetiology. ROC-curves for 1-year mortality identified cutoff values separately for specificity (none, sex, beta-blocker, both). Patients were grouped according to number of cut-offs met (group I/II/III - 0/1/2 cut-offs). Results: Widest separation between groups was achieved with sex-and beta-blocker-specific cut offs. In the derivation population, 1-year mortality was 0%, 8%, 31% for group I, II and III, respectively. In the validation population, 1-year rates in the three risk groups were 2%, 7%, 14%, respectively, after application of the same cut-offs. Conclusion: Risk stratification for CHF should perhaps take sex and beta-blocker usage into account. We derived and independently validated relevant risk models based on 6-minute-walk-tests and NT-proBNP. Specifying sex and use of beta-blockers identified three distinct sub-groups with widely differing prognosis. In clinical practice, it may be appropriate to tailor the intensity of follow-up and/or the treatment strategy according to the risk-group. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:74 / 78
页数:5
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