The Safety of an Adenosine A1-Receptor Antagonist, Rolofylline, in Patients with Acute Heart Failure and Renal Impairment
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  • 作者:Professor John R. Teerlink (1)
    Vicente J. Iragui (2)
    Jay P. Mohr (3)
    Peter E. Carson (4)
    Paul J. Hauptman (5)
    David H. Lovett (1)
    Alan B. Miller (6)
    Ileana L. Pi?a (7)
    Scott Thomson (8)
    Paul D. Varosy (9)
    Michael R. Zile (10)
    John G. F. Cleland (11)
    Michael M. Givertz (12)
    Marco Metra (13)
    Piotr Ponikowski (14)
    Adriaan A. Voors (15)
    Beth A. Davison (16)
    Gad Cotter (16)
    Denise Wolko (17)
    Paul DeLucca (17)
    Christina M. Salerno (18)
    George A. Mansoor (19)
    Howard Dittrich (20)
    Christopher M. O’Connor (1)
    Barry M. Massie
  • 刊名:Drug Safety
  • 出版年:2012
  • 出版时间:March 2012
  • 年:2012
  • 卷:35
  • 期:3
  • 页码:233-244
  • 全文大小:191KB
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    15. Givertz MM, Massie BM, Fields TK, et al. The effects of KW-3902, an adenosine A1-receptor antagonist,on diuresis and renal function in patients with acute decompensated heart failure and renal impairment or diuretic resistance. J Am Coll Cardiol 2007 Oct 16; 50 (16): 1551-0 CrossRef
    16. Dittrich HC, Gupta DK, Hack TC, et al. The effect of KW-3902, an adenosine A1 receptor antagonist, on renal function and renal plasma flow in ambulatory patients with heart failure and renal impairment. J Card Fail 2007 Oct; 13 (8): 609-7 CrossRef
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  • 作者单位:Professor John R. Teerlink (1)
    Vicente J. Iragui (2)
    Jay P. Mohr (3)
    Peter E. Carson (4)
    Paul J. Hauptman (5)
    David H. Lovett (1)
    Alan B. Miller (6)
    Ileana L. Pi?a (7)
    Scott Thomson (8)
    Paul D. Varosy (9)
    Michael R. Zile (10)
    John G. F. Cleland (11)
    Michael M. Givertz (12)
    Marco Metra (13)
    Piotr Ponikowski (14)
    Adriaan A. Voors (15)
    Beth A. Davison (16)
    Gad Cotter (16)
    Denise Wolko (17)
    Paul DeLucca (17)
    Christina M. Salerno (18)
    George A. Mansoor (19)
    Howard Dittrich (20)
    Christopher M. O’Connor (1)
    Barry M. Massie

    1. San Francisco Veterans Affairs Medical Center and University of California, San Francisco, San Francisco, CA, USA
    2. University of California, San Diego, San Diego, CA, USA
    3. Columbia University College of Physicians and Surgeons, New York, NY, USA
    4. Washington DC Veterans Affairs Medical Center and Georgetown University, Washington, DC, USA
    5. St Louis University School of Medicine, St Louis, MO, USA
    6. University of Florida Health Science Center, Jacksonville, Jacksonville, FL, USA
    7. Cleveland Veterans Affairs Medical Center and Case Western Reserve University, Cleveland, OH, USA
    8. San Diego Veterans Affairs Medical Center University of California, San Diego, San Diego, CA, USA
    9. Veterans Affairs Eastern Colorado Health Care System and University of Colorado Denver, Denver, CO, USA
    10. RHJ Department of Veterans Affairs Medical Center and Medical University of South Carolina, Charleston, SC, USA
    11. University of Hull, Kingston Upon Hull, UK
    12. Brigham and Women’s Hospital, Boston, MA, USA
    13. University of Brescia, Brescia, Italy
    14. Medical University, Clinical Military Hospital, Wroclaw, Poland
    15. University Medical Center Groningen, Groningen, the Netherlands
    16. Momentum Research, Inc., Durham, NC, USA
    17. Merck Research Laboratories, North Wales, PA, USA
    18. Merck Research Laboratories, Rahway, NJ, USA
    19. NovaCardia, Inc., San Diego, CA, USA
    20. Duke University Medical Center, Durham, NC, USA
  • ISSN:1179-1942
文摘
Background: Adenosine exerts actions in multiple organ systems, and adenosine receptors are a therapeutic target in many development programmes. Objective: The aim of this analysis was to evaluate the safety of rolofylline, an adenosine A1-receptor antagonist, in patients with acute heart failure. Methods: The effect of rolofylline was investigated in patients hospitalized for acute heart failure with impaired renal function. Intravenous rolofylline 30 mg or placebo was infused over 4 hours daily for up to 3 days. Adverse events (AEs) and serious AEs (SAEs) were recorded from baseline through 7 and 14 days, respectively, and clinical events were adjudicated through 60 days. Results: Of 2033 patients enrolled, 2002 received study drug randomized 2 : 1 to rolofylline or placebo. Rolofylline and placebo were associated with a similar risk of pre-specified groups of AEs or SAEs, other than selected neurological events. Investigator-reported seizures occurred in 11 (0.8%) rolofylline-treated patients and zero patients receiving placebo (p = 0.02). Stroke occurred in 21 (1.6%) patients assigned to rolofylline compared with 3 (0.5%) placebo-treated patients through 60 days with a greater risk for stroke in the rolofylline group (hazard ratio 3.49; 95% CI 1.04, 11.71; p = 0.043). There was no temporal relation to rolofylline administration and no specific stroke subtype or clinical characteristics that predicted stroke in the rolofylline group. Conclusions: Rolofylline treatment was associated with an increased seizure rate, an anticipated complication of A1-receptor antagonists. An unanticipated, disproportionate increase in strokes in the rolofylline-treated patients emerged, although no clear temporal relation, aetiology, stroke subtype or interacting factor suggestive of a causal mechanism was identified. Further research into stroke as a potential complication of adenosine-modulating therapies is required. Additionally, this study underscores the value of longer follow-up durations for AEs, even for agents with short treatment periods, such as in acute heart failure. Trial Registration: ClinicalTrials.gov identifiers NCT00328692 and NCT00354458.

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