Development and validation of a risk model for in-hospital worsening heart failure from the Acute Decompensated Heart Failure National Registry (ADHERE)

被引:14
|
作者
DeVore, Adam D. [1 ,2 ]
Greiner, Melissa A. [1 ]
Sharma, Puza P. [3 ]
Qualls, Laura G. [1 ]
Schulte, Phillip J. [4 ]
Cooper, Lauren B. [1 ,2 ]
Mentz, Robert J. [1 ,2 ]
Pang, Peter S. [5 ]
Fonarow, Gregg C. [6 ]
Curtis, Lesley H. [1 ,2 ]
Hernandez, Adrian F. [1 ,2 ]
机构
[1] Duke Univ, Sch Med, Duke Clin Res Inst, Durham, NC USA
[2] Duke Univ, Sch Med, Dept Med, Durham, NC 27706 USA
[3] Novartis Pharmaceut, E Hanover, NJ USA
[4] Mayo Clin, Dept Hlth Sci Res, Rochester, MN USA
[5] Indiana Univ Sch Med, Indianapolis, IN 46202 USA
[6] Univ Calif Los Angeles, Ahmanson UCLA Cardiomyopathy Ctr, Los Angeles, CA USA
关键词
MORTALITY-RATES; OUTCOMES; DESIGN; TEZOSENTAN; RATIONALE; SYMPTOMS; RECEPTOR; PROTECT; AHF;
D O I
10.1016/j.ahj.2016.04.021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background A subset of patients hospitalized with acute heart failure experiences in-hospital worsening heart failure, defined as persistent or worsening signs or symptoms requiring an escalation of therapy. Methods We analyzed data from the Acute Decompensated Heart Failure National Registry (ADHERE) linked to Medicare claims to develop and validate a risk model for in-hospital worsening heart failure. Our definition of in-hospital worsening heart failure included events such as escalation of medical therapy (eg, inotropic medications) >12 hours after admission. We considered candidate risk prediction variables routinely assessed at admission, including age, medical history, biomarkers, and renal function. We used logistic regression with robust standard errors to generate a risk model in a 66% random derivation sample; we validated the model in the remaining 34%. We evaluated the calibration and discrimination of the model in both samples. Results We evaluated 23,696 patients hospitalized with acute heart failure. Baseline characteristics were well matched in the derivation and validation samples, and the occurrence of in-hospital worsening heart failure was similar in both samples (15.4% and 15.6%, respectively). In the multivariable model, the strongest predictors of in-hospital worsening heart failure were increased troponin and creatinine. The model was well calibrated and had good discrimination in the derivation sample (c statistic, 0.74) and validation sample (c statistic, 0.72). Conclusions The ADHERE worsening heart failure risk model is a clinical tool with good discrimination for use in patients hospitalized with acute heart failure to identify those at increased risk for in-hospital worsening heart failure. This tool may be useful to target treatment strategies for patients at high risk for in-hospital worsening heart failure.
引用
收藏
页码:198 / 205
页数:8
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