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Marco Lanfranconi
Giuseppe Bruschi
Tiziano Colombo
Claudio Russo
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Ann Thorac Surg 2003;75:1200-1204
© 2003 The Society of Thoracic Surgeons


Original article: cardiovascular

Successful experience in bridging patients to heart transplantation with the MicroMed Debakey ventricular assist device

Ettore Vitali, MDa*, Marco Lanfranconi, MDa, Elena Ribera, MDa, Giuseppe Bruschi, MDa, Tiziano Colombo, MDa, Maria Frigerio, MDb, Claudio Russo, MDa

a Department of Cardiac Surgery, Milan, Italy
b Department of Cardiology "A. De Gasperis," Niguarda Ca’ Granda Hospital, Milan, Italy

Accepted for publication October 17, 2002.

* Address reprint requests to Dr Vitali, Department of Cardiac Surgery "A. De Gasperis," Niguarda Ca’ Granda Hospital, Piazza Ospedale Maggiore, 3, 20162 Milan, Italy.
e-mail: evitali{at}ospedale-niguarda.it

BACKGROUND: Pulsatile left ventricular assist devices are used with increasing frequency to bridge patients with end-stage heart failure to heart transplantation (HTx). Implantation of pulsatile devices is a cumbersome surgical procedure that is associated with major complications, such as bleeding, thromboembolism, and infection. Recently, a continuous axial flow left ventricular assist device (DeBakey ventricular assist device) has been introduced with the goal of reducing the incidence of major complications.

METHODS: We reviewed our experience with 11 patients who received a DeBakey ventricular assist device axial flow pump for bridge to HTx from April 2000 through November 2001.

RESULTS: Two patients (18.2%) died of multiple-organ failure while on left ventricular assist device support. Bleeding requiring thoracotomy occurred in 2 patients (18.2%). One patient had a minor neurologic event, and one patient developed left ventricular assist device thrombosis, which was successfully treated without pump exchange. Renal failure developed in 1 patient and hepatic dysfunction in 2 patients. There were no instances of right heart failure. No device, pocket, or drive-line infections occurred. Nine patients (9 of 11, 81.8%) had HTx within 51 ± 49 days (range, 11 to 141 days) after left ventricular assist device implant. One patient died 29 days after HTx because of acute rejection.

CONCLUSIONS: The continuous axial flow DeBakey ventricular assist device had reliable features, including a high rate of bridge to HTx. This device had low complication and system failure rates. We consider the DeBakey ventricular assist device a favorable alternative to pulsatile heart assist devices as a bridge to HTx.




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