(Circulation. 2005;111:1487-1491.)
© 2005 American Heart Association, Inc.
Heart Failure |
From the Clinical Scholars Program, Division of Cardiology, North Shore University Hospital, Manhasset, NY (J.D.S.-B., H.A.S.), and Division of Cardiovascular Medicine, University of Michigan, Ann Arbor (K.D.A.).
Correspondence to Jonathan D. Sackner-Bernstein, MD, FACC, Clinical Scholars Program, Division of Cardiology, Cohen 1, North Shore University Hospital, 300 Community Dr, Manhasset, NY 11030. E-mail jonathansb{at}yahoo.com
Received August 13, 2004; revision received November 26, 2004; accepted January 11, 2005.
Background Renal function is an important prognostic factor for patients with acutely decompensated heart failure (ADHF). We investigated the renal effects of nesiritide as treatment for ADHF.
Methods and Results Randomized clinical trials comparing nesiritide with either placebo or active control for ADHF were identified by electronic and manual searches and thorough review of US Food and Drug Administration files available via the website. Worsening renal function was defined as an increase in serum creatinine >0.5 mg/dL. Relative risk across all studies was determined by meta-analysis with Mantel-Haenszel fixed-effects models (RRMH). Risk of dialysis and medical intervention for worsening renal function were compared between therapies. Frequency of worsening renal function was determined from 5 randomized studies that included 1269 patients. Use of Food and Drug Administrationapproved doses of nesiritide (
0.03 µg · kg1 · min1) significantly increased the risk of worsening renal function compared with noninotrope-based control (RRMH, 1.52; 95% CI, 1.16 to 2.00; P=0.003) or any control therapy, including noninotrope- and inotrope-based therapies (RRMH, 1.54; 95% CI, 1.19 to 1.98; P=0.001). Even low-dose nesiritide (
0.015 µg · kg1 · min1) significantly increased risk (P=0.012 and P=0.006 compared with noninotrope- and inotrope-based controls, respectively), as did nesiritide administered at any dose up to 0.06 µg · kg1 · min1 (P=0.002 and P=0.001, respectively). There was no difference in the need for dialysis between therapies.
Conclusions Nesiritide significantly increases the risk of worsening renal function in patients with ADHF. Whether worsening renal function reflects hemodynamic effect or renal injury is unknown, but the prognostic importance of worsening renal function suggests the need for further investigation in appropriately powered clinical trials.
Key Words: heart failure kidney meta-analysis natriuretic peptides pharmacology
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Does Nesiritide Increase Risks for Renal Failure and Death? Journal Watch Cardiology, May 6, 2005; 2005(506): 2 - 2. [Full Text] |
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D. Spurgeon Drug for heart failure increases mortality BMJ, April 30, 2005; 330(7498): 981 - 981. [Full Text] [PDF] |
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J. D. Sackner-Bernstein, M. Kowalski, M. Fox, and K. Aaronson Short-term Risk of Death After Treatment With Nesiritide for Decompensated Heart Failure: A Pooled Analysis of Randomized Controlled Trials JAMA, April 20, 2005; 293(15): 1900 - 1905. [Abstract] [Full Text] [PDF] |
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U. Elkayam, D. J. Wang, T. C. Dowling, D. Meadows, T. Ayala, J. Marshall, S. Minshall, N. Greenberg, E. Thattassery, M. L. Fisher, et al. Letter Regarding Article by Wang et al, "Nesiritide Does Not Improve Renal Function in Patients With Chronic Heart Failure and Worsening Serum Creatinine" * Response Circulation, April 12, 2005; 111(14): e182 - e183. [Full Text] [PDF] |
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J. R. Teerlink and B. M. Massie Nesiritide and Worsening of Renal Function: The Emperor's New Clothes? Circulation, March 29, 2005; 111(12): 1459 - 1461. [Full Text] [PDF] |
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