TY - JOUR
T1 - Predictors of mortality in adult patients with congestive heart failure receiving nesiritide - Retrospective analysis showing a potential adverse interaction between neseritide and acute renal dysfunction
AU - Iglesias, Jose I.
AU - DePalma, Laura
AU - Hom, Deborah
AU - Antoniotti, Maria
AU - Ayoub, Sammy
AU - Levine, Jerrold S.
N1 - Funding Information:
Acknowledgements. This work was supported by NIH grants DK59793 and by a Renal Innovations Program Award from Genzyme, Inc. Community Medical Center, Toms River, NJ, USA was the study institution.
Funding Information:
Conflict of interest statement. J.I.I has received speaker honoraria from Scios, Inc and Ortho Biotech, and J.S.L. has received research funding from Genzyme, inc.
PY - 2008/1
Y1 - 2008/1
N2 - Background. A recent meta-analysis has suggested that nesiritide (NES), a new agent for the treatment of congestive heart failure (CHF), is associated with an increased risk of short-term mortality. Methods. We retrospectively examined this issue among 1407 consecutive elderly CHF patients by Pearson's chi-squared test, and determined independent risk factors for 60-day mortality by multivariate analysis in a cohort of 682 patients for whom we had sufficient clinical and laboratory data. Results. Univariate analysis revealed that NES usage was associated with increased mortality (n = 1407, 10 vs 6%, P = 0.011; n = 682, 19 vs 12.5%, P = 0.046). However, by forward stepwise regression analysis, NES usage did not survive as an independent predictor of mortality. The following variables were independent predictors of mortality: development of acute renal failure (ARF) defined as an increase of serum creatinine (SCr) ≥0.5 mg/dl; lack of β-adrenergic blockade; increased admission blood urea nitrogen; digoxin use; and increased admission brain natriuretic peptide. When patients were stratified according to NES usage, ARF emerged as an independent risk factor for mortality only among patients who received NES. Strikingly, among CHF patients who developed ARF (n = 102), NES usage emerged as the only independent predictor of mortality (P = 0.006, OR = 3.73, 95% CI 1.45-9.56). Conclusion. We conclude that, while NES per se is not independently associated with an increased risk for mortality, the development of ARF in association with NES use may confer an increased risk of mortality.
AB - Background. A recent meta-analysis has suggested that nesiritide (NES), a new agent for the treatment of congestive heart failure (CHF), is associated with an increased risk of short-term mortality. Methods. We retrospectively examined this issue among 1407 consecutive elderly CHF patients by Pearson's chi-squared test, and determined independent risk factors for 60-day mortality by multivariate analysis in a cohort of 682 patients for whom we had sufficient clinical and laboratory data. Results. Univariate analysis revealed that NES usage was associated with increased mortality (n = 1407, 10 vs 6%, P = 0.011; n = 682, 19 vs 12.5%, P = 0.046). However, by forward stepwise regression analysis, NES usage did not survive as an independent predictor of mortality. The following variables were independent predictors of mortality: development of acute renal failure (ARF) defined as an increase of serum creatinine (SCr) ≥0.5 mg/dl; lack of β-adrenergic blockade; increased admission blood urea nitrogen; digoxin use; and increased admission brain natriuretic peptide. When patients were stratified according to NES usage, ARF emerged as an independent risk factor for mortality only among patients who received NES. Strikingly, among CHF patients who developed ARF (n = 102), NES usage emerged as the only independent predictor of mortality (P = 0.006, OR = 3.73, 95% CI 1.45-9.56). Conclusion. We conclude that, while NES per se is not independently associated with an increased risk for mortality, the development of ARF in association with NES use may confer an increased risk of mortality.
KW - Acute renal failure
KW - Brain natriuretic peptide
KW - Congestive heart failure
KW - Nesiritide
UR - http://www.scopus.com/inward/record.url?scp=44449152577&partnerID=8YFLogxK
U2 - 10.1093/ndt/gfm565
DO - 10.1093/ndt/gfm565
M3 - Article
C2 - 17804459
AN - SCOPUS:44449152577
VL - 23
SP - 144
EP - 153
JO - Nephrology Dialysis Transplantation
JF - Nephrology Dialysis Transplantation
SN - 0931-0509
IS - 1
ER -