Volume 139, Issue 1 , Pages 75-79, 18 February 2010
Plasma B-type natriuretic peptide reduction predicts long-term response to levosimendan therapy in acutely decompensated chronic heart failure
Abstract
Objective
We sought to identify predictors of long-term response to levosimendan therapy among patients' baseline features and treatment-induced changes in acutely decompensated chronic heart failure (ADHF).
Methods
Ninety-eight consecutive patients [aged 64
±
10 years, New York Heart Association (NYHA) classes III–IV, left ventricular ejection fraction <
35%], 69 treated with levosimendan and 29 with standard therapy, underwent a clinical, echocardiographic and biochemical assessment before and after treatment. All patients were subsequently followed for 6 months for death or rehospitalization for ADHF.
Results
Compared to standard therapy, levosimendan induced a significant improvement in NYHA class (F
=
37.529, p
<
0.001), B-type natriuretic peptide (BNP, F
=
22.917, p
<
0.001), left ventricular ejection fraction (F
=
23.561, p
<
0.001), transmitral E deceleration time (DT, F
=
6.499, p
=
0.013) and E/e ratio (F
=
10.812, p
=
0.003). During follow-up, 88 of 98 patients (90%) experienced an event. Event-free survival (days alive and out of hospital) at 6 months was similar in two groups (median, 48 days, log-rank test p
=
0.6760). In the levosimendan group, treatment-induced percent BNP change was the best predictor of events (OR
=
0.970, 95% CI
=
0.954–0.986, p
<
0.001). A cut-off for BNP change of 58% predicted events with 87% sensitivity and 83% specificity. Event-free survival was longer in patients with a BNP reduction ≥
58% (median, 135 versus 43 days, p
=
0.0001).
Conclusion
Treatment-induced BNP reduction is an independent predictor of 6-month outcome following levosimendan therapy in ADHF.
Keywords: Levosimendan, Heart failure, Survival, Prognosis, Natriuretic peptides
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PII: S0167-5273(08)01053-X
doi:10.1016/j.ijcard.2008.10.003
© 2008 Elsevier Ireland Ltd. All rights reserved.
Volume 139, Issue 1 , Pages 75-79, 18 February 2010
