Journal of Cardiac Failure
Volume 16, Issue 11 , Pages 855-858, November 2010

NHLBI’s Program for VAD Therapy for Moderately Advanced Heart Failure: The REVIVE-IT Pilot Trial

  • J. Timothy Baldwin, PhD

      Affiliations

    • Division of Cardiovascular Sciences, National Heart, Lung, and Blood Institute, Bethesda, MD
    • Corresponding Author InformationReprint requests: J. Timothy Baldwin, PhD, Deputy Chief/Program Director, Advanced Technologies & Surgery Branch, Basic and Early Technology Research Program, Division of Cardiovascular Sciences, National Heart, Lung, and Blood Institute, Two Rockledge Centre, Room 8206, 6701 Rockledge Drive, Bethesda, MD 20892-7940. Tel: (301) 435-0513; Fax: (301) 480-1454.
  • ,
  • Douglas L. Mann, MD

      Affiliations

    • Cardiovascular Division, Washington University School of Medicine, St. Louis, MO

Received 5 April 2010; received in revised form 24 May 2010; accepted 15 June 2010. published online 20 July 2010.

Abstract 

Background

Ventricular assist devices (VADs) are used to bridge heart failure patients to transplantation, to allow their own hearts to recover, or as permanent (“destination”) therapy. To date, the use of VADs has been limited to late-stage heart failure patients because of the associated device risks. In 2008, a National Heart, Lung, and Blood Institute (NHLBI) working group met to evaluate the treatment of heart failure using VADs and to advise the institute on how therapy for heart failure may be best advanced by clinical trials involving the devices.

Methods and Results

Recognizing the improvements in VAD technology and in patient care and selection over the past decade, the working group recommended that a trial be performed to assess the use of chronic VAD therapy in patients who are less ill than those currently eligible for destination therapy. The hypothesis proposed for the trial is that VAD therapy may improve both survival and quality of life in moderately advanced heart failure patients who are neither inotrope-dependent nor exercise-intolerant and have not yet developed serious consequences such as malnourishment, end-organ damage, and immobility.

Conclusion

Based on the group’s recommendations, NHLBI issued an RFP in 2009 for the REVIVE-IT Pilot Trail, which will serve to test the hypothesis and inform the pivotal trial.

Key Words: Mechanical circulatory support, destination therapy, functional impairment, quality of life

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 See page 858 for disclosure information.

PII: S1071-9164(10)00712-8

doi:10.1016/j.cardfail.2010.06.414

Journal of Cardiac Failure
Volume 16, Issue 11 , Pages 855-858, November 2010