The minimal informative monitoring interval of N-terminal pro-B-type natriuretic peptide in patients with stable heart failure

被引:3
|
作者
Dai, Zhehao [1 ,2 ]
Asano, Taku [1 ]
Takahashi, Osamu [2 ]
Komiyama, Nobuyuki [1 ]
Ohde, Sachiko [2 ]
机构
[1] St Lukes Int Hosp, Dept Cardiol, Chuo Ku, 9-1 Akashi Cho, Tokyo 1040045, Japan
[2] St Lukes Int Univ, Grad Sch Publ Hlth, Chuo Ku, 3-6-2 Tsukiji, Tokyo 1040045, Japan
关键词
N-terminal pro-B-type natriuretic peptide (NT-proBNP); Heart failure; Minimal informative monitoring interval; Signal-to-noise ratio; GUIDED THERAPY; INTRAINDIVIDUAL VARIATION; EJECTION FRACTION; BNP; ASSOCIATION; MANAGEMENT; MORTALITY; SURVIVAL; SOCIETY; TRIAL;
D O I
10.1186/s12872-020-01537-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background N-terminal pro-B-type natriuretic peptide (NT-proBNP) is a potential biomarker for monitoring the status of heart failure. However, the optimal monitoring interval of NT-proBNP is unknown. This study sought to investigate the minimal informative monitoring interval of NT-proBNP in patients with stable chronic heart failure. Methods This retrospective cohort study included patients who were admitted due to heart failure and subsequently followed with serial NT-proBNP measurements in a tertiary hospital. We analyzed NT-proBNP measured between six months after discharge and the earliest timepoint of: an alteration of medication regimen, readmission due to worsening of heart failure, or all-cause death. To distinguish progression of the disease from biological variability and measurement error, the signal-to-noise ratio method was applied with a random-effects model. Results In the 368 patients included, NT-proBNP was measured for a median 6 times. In the random-effects model, signal (progression of disease) exceeded noise (biological variability and measurement error) at 7.9 months (95% confidence interval [CI]: 5.1-9.6), while noise corresponded to a 61% increase from baseline. In stratified analysis using the AHEAD risk score, the minimal informative monitoring interval shortened as the risk score increased (0-1 point: 12.2 months [95%CI: 10.3-14.4]; 2-3 points: 8.0 months [95%CI: 6.8-9.7]; 4-5 points: 3.3 months [95%CI: 3.0-3.8]). Conclusions In patients with stable chronic heart failure, the minimal informative monitoring interval of NT-proBNP measurement was 7.9 months in the current population, which varied with underlying risks. The optimal monitoring interval could be lengthened for patients at lower risks.
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页数:9
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