Key result
Elevated baseline BNP linked to ~2.9-fold higher mortality in advanced HF receiving CRT.
Why the study?
Does an elevated baseline BNP level predict all-cause mortality and heart failure hospitalization in patients with advanced heart failure receiving CRT-D?
Cohort (n=115)
No
Does an elevated baseline BNP level predict all-cause mortality and heart failure hospitalization in patients with advanced heart failure receiving CRT-D?
Hazard Ratio: 2.89 (95% CI 1.06–7.88)
Absolute Event Rate: 39% vs 14.9%
p-value: p=0.038
A single preimplantation BNP measurement >492 pg/mL can identify patients with advanced heart failure who remain at high risk for mortality and HF hospitalization despite receiving CRT-D therapy.
Elevated pre-CRT BNP may stratify mortality risk in advanced HF; extends prognostic observations but leaves practice change unproven.
BACKGROUND: Brain natriuretic peptide (BNP) level has emerged as a predictor of death and hospital readmission in patients with heart failure (HF). The value of baseline BNP assessment in advanced HF patients receiving cardiac resynchronization defibrillator therapy (CRT-D) has not been firmly established. HYPOTHESIS: We hypothesized that a baseline BNP level would predict all cause mortality and HF hospitalization in HF patients receiving cardiac resynchronization therapy. METHODS: A retrospective chart review of all patients having BNP assessment prior to implantation of a CRT-D for standard indications during 2004 and 2005 was conducted at the Veterans Affairs Pittsburgh Healthcare System. The primary endpoint was all-cause mortality and the secondary endpoint was HF-related hospitalization. We used findings from the receiver operating characteristic (ROC) curve to define low (<492 pg/mL) and high (> or =492 pg/mL) BNP groups. RESULTS: Out of 173 CRT-D recipients, 115 patients (mean age 67.0 +/- 10.7 years, New York Heart Association [NYHA] class 2.9 +/- 0.3, left ventricular ejection fraction [LVEF] 22.5% +/- 9.6%, QRS 148.3 +/- 30.4 ms) had preimplantation BNP measured (mean 559 +/- 761 pg/mL and median 315 pg/mL). During a mean follow-up time of 17.5 +/- 6.5 mo, 27 deaths (23.5%) and 31 HF hospitalizations (27.0%) were recorded. Compared to those with low BNP (n = 74), those of high BNP (n = 41) were older, had lower LVEF, higher creatinine levels, suffered more deaths, and HF hospitalizations. In multivariate regression models, higher BNP remained a significant predictor of both the primary endpoint (hazard ratio [HR]: 2.89, 95% confidence interval [CI] 1.06-7.88, p = 0.038) and secondary endpoint (HR: 4.23, 95% CI: 1.68-10.60, p = 0.002). CONCLUSIONS: Baseline BNP independently predicted mortality and HF hospitalization in a predominantly older white male population of advanced HF patients receiving CRT-D. Elevated BNP levels may identify a vulnerable HF population with a particularly poor prognosis despite CRT-D.
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El‐Saed et al. (2009) conducted a cohort in Advanced but stable heart failure receiving CRT-D (n=115). Elevated baseline Brain Natriuretic Peptide (BNP ≥ 492 pg/mL) vs. Low baseline Brain Natriuretic Peptide (BNP < 492 pg/mL) was evaluated on All-cause mortality (HR 2.89, 95% CI 1.06-7.88, p=0.038). Elevated baseline BNP levels (≥492 pg/mL) independently predicted an increased risk of all-cause mortality (HR 2.89) in advanced heart failure patients receiving cardiac resynchronization therapy.
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