Background
Differentiating heart failure (HF) induced renal dysfunction (RD) from intrinsic kidney disease is challenging. It has been demonstrated that biomarkers such as B-type natriuretic peptide (BNP) or the blood urea nitrogen to creatinine ratio (BUN/Creat) can identify high vs. low risk RD. Our objective was to determine if combination these biomarkers could further improve risk stratification and clinical phenotyping of patients with RD and HF.
Methods and Results
908 patients with a discharge diagnosis of HF were included. Median values were used to define elevated BNP (>1296 pg/ml) and BUN/Creat (>17). In the group without RD, survival was similar regardless of BNP and BUN/Creat (n=430, adjusted p=0.52). Similarly, in patients with both a low BNP and BUN/Creat, RD was not associated with mortality (n=250, adjusted HR=1.0, 95% CI 0.6-1.6, p=0.99). However, in patients with both an elevated BNP and BUN/Creat those with RD had a cardio-renal profile characterized by venous congestion, diuretic resistance, hypotension, hyponatremia, longer length of stay, greater inotrope use, and substantially worse survival compared to patients without RD (n=249, adjusted HR=1.8, 95% CI 1.2-2.7, p=0.008, p interaction=0.005).
Conclusions
In the setting of decompensated HF, the combined use of BNP and BUN/Creat stratifies patients with RD into groups with significantly different clinical phenotypes and prognosis.