Key result
A ≥30% decrease in BNP at day 5 in patients with severe acutely decompensated heart failure was associated with a 67% short-term and 47% long-term risk reduction in all-cause mortality (p≤0.001).
Why the study?
BNP level is a prognostic marker for all-cause mortality in ADHF, but whether early BNP changes help predict outcome in patients requiring inotropes for severe ADHF is not known.
Observational (n=1,038)
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“the SURVIVE trial demonstrated no survival difference between levosimendan and dobutamine during long-term follow-up despite evidence for an early reduction of plasma B-type natriuretic peptide level for levosimendan. These findings may be related to the short duration of treatment in the trial, a selective effect of levosimendan in specific subgroups, or the lack of a true difference between the 2 drugs. Further studies are needed to distinguish between these possibilities”
May link greater BNP reduction to survival in acute HF; hypothesis-generating, needs prospective confirmation before guiding therapy.
OBJECTIVES: The purpose of this analysis was to examine whether decreases in B-type natriuretic peptide (BNP) levels during the first few days of hospitalization were associated with greater survival in patients with severe acutely decompensated heart failure (ADHF). BACKGROUND: BNP level is a prognostic marker for all-cause mortality (ACM) in ADHF; whether early BNP changes can also help predict outcome in patients who need inotropes for treatment of severe ADHF is not known. METHODS: We retrospectively assessed the association between changes in BNP levels and ACM in patients from the SURVIVE (Survival of Patients with Acute Heart Failure in Need of Intravenous Inotropic Support) trial--a randomized, controlled trial comparing levosimendan to dobutamine treatment in patients hospitalized with ADHF. BNP levels were measured at baseline and at days 1, 3, and 5. A patient was classified as a "responder" if the follow-up BNP level was >or=30% lower than baseline BNP. The relationship between early BNP response and subsequent ACM over short- (31-day) and long-term (180-day) intervals was evaluated. RESULTS: Of 1,327 SURVIVE patients, this analysis included 1,038 who had BNP samples at both baseline and day 5. Responders at days 1, 3, and 5 had lower ACM than did nonresponders (p <or= 0.001), with day-5 levels showing superior discriminating value. Short-term ACM (31-day) risk reduction was 67% in day-5 BNP responders compared with nonresponders, whereas long-term (180-day) ACM risk reduction was 47%. CONCLUSIONS: Patients with lowered BNP on treatment for ADHF had reduced mortality risks (31- and 180-day) compared to those with little or no BNP decrease. These results suggest that early lowering of BNP predicts both short- and long-term mortality risks. BNP reduction may therefore serve as a suitable prognostic marker of ACM.
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Cohen‐Solal et al. (2009) conducted an observational in Severe acutely decompensated heart failure (ADHF) (n=1,038). BNP decrease ≥30% from baseline at day 5 vs. Nonresponders (little or no BNP decrease) was evaluated on All-cause mortality (ACM) over short- (31-day) and long-term (180-day) intervals (67% risk reduction (31-day); 47% risk reduction (180-day), p=≤0.001). A ≥30% decrease in BNP at day 5 in patients with severe acutely decompensated heart failure was associated with a 67% short-term and 47% long-term risk reduction in all-cause mortality (p≤0.001).
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