Transplantation Proceedings
Volume 36, Issue 3 , Pages 620-622, April 2004

Mechanical circulatory support in severe heart failure: single-center experience

  • E Vitali

      Affiliations

    • Department of Cardiac Surgery “Angelo De Gasperis,” Niguarda Cà Granda Hospital, Milan, Italy
    • Corresponding Author InformationAddress reprint requests to Dr Ettore Vitali, Department of Cardiac Surgery “Angelo De Gasperis,” Niguarda Hospital, Piazza Ospedale Maggiore, 3, 20162 Milano, Italy
  • ,
  • M Lanfranconi

      Affiliations

    • Department of Cardiac Surgery “Angelo De Gasperis,” Niguarda Cà Granda Hospital, Milan, Italy
  • ,
  • G Bruschi

      Affiliations

    • Department of Cardiac Surgery “Angelo De Gasperis,” Niguarda Cà Granda Hospital, Milan, Italy
  • ,
  • E Ribera

      Affiliations

    • Department of Cardiac Surgery “Angelo De Gasperis,” Niguarda Cà Granda Hospital, Milan, Italy
  • ,
  • A Garatti

      Affiliations

    • Department of Cardiac Surgery “Angelo De Gasperis,” Niguarda Cà Granda Hospital, Milan, Italy
  • ,
  • T Colombo

      Affiliations

    • Department of Cardiac Surgery “Angelo De Gasperis,” Niguarda Cà Granda Hospital, Milan, Italy
  • ,
  • C.F Russo

      Affiliations

    • Department of Cardiac Surgery “Angelo De Gasperis,” Niguarda Cà Granda Hospital, Milan, Italy

Abstract 

Ventricular assist devices (VADs) have become important therapeutic tools to treat patients with end-stage cardiac failure. VADs are an essential component of transplantation programs as they successfully bridge individuals who would otherwise die. Recently left ventricular VAD (LVAD) therapy has been proposed as alternative to heart transplantation (HTx) for patients who are not transplant candidates. Other indications have now expanded into areas such as postcardiotomy failure, acute myocarditis, and acute massive myocardial infarction. From 1988 to May 2003, 80 patients received left or biventricular mechanical circulatory support including 78 as a bridge to and two as an alternative to HT. All patients survived the operation. Mean duration of VAD support was 77 ± 150 days. Fifty-one points (63.8%) underwent heart transplantation; 3 (3.8%) recovered and were weaned from VADs. Major bleeding episodes occurred in 11 patients (13.8%) and major neurologic events occurred in 8 (10%). Sixteen patients (20%) were discharged home while waiting for HTx. Twenty-two patients (27.5%) died on VAD. In conclusion, VAD therapy proved effective in bridging patients with end-stage heart failure to HTx. While on LVAD support patients who were assisted with implantable wearable devices could be discharged at home, improving their 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.
 

PII: S0041-1345(04)00194-0

doi:10.1016/j.transproceed.2004.02.050

Transplantation Proceedings
Volume 36, Issue 3 , Pages 620-622, April 2004