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Eur J Cardiothorac Surg 2003;23:748-755
© 2003 Elsevier Science NL
Department of Cardiovascular Surgery, Albert-Ludwigs University Freiburg, Hugstetterstrasse 55, 79106 Freiburg, Germany
Received 26 September 2002; received in revised form 22 January 2003; accepted 23 January 2003.
* Corresponding author. Tel.: +49-761-270-6138; fax: +49-761-270-2550
e-mail: siegenth{at}ch11.ukl.uni-freiburg.de
Objectives: Device-related infections remain a considerable problem of left-ventricular support. We compared the device-related-infections between the HeartMate left ventricular assist device (LVAD) and the Jarvik 2000 permanent LVAD, a device with a novel retroauricular power-supply. Methods: Between December 2000 and September 2002 we implanted the HeartMate-vented, electrical-system in 11 patients and the permanent Jarvik 2000 in six patients. Total support time was 1626 patient-days (HeartMate, 26271 days) versus 1246 patient-days (Jarvik 2000, 8411 days). As potential risk factors for infection we analyzed age, preoperative hospital-days, total protein, cardiac index, maximal oxygen uptake, use of inotropes, LVAD risk-score-index and Aaronson-Mancini-score, intubation time, and intensive care unit stay. We used the Center of Disease Control definitions for surgical site infections. Results: HeartMate-patients were younger than Jarvik 2000 patients (46±13 versus 58±6 years, P=0.056), there were no other differences in the risk factors. Four HeartMate-patients needed late (
48 h) surgical revisions for bleeding/hematomas versus no revisions in the Jarvik 2000 patients. In the HeartMate-patients, there were seven (64%) driveline-infections, five (45%) device-pocket infections, and three (27%) bloodstream-infections, or 0.43 device-related infections/100 patient-days. Infections occurred early (34±31 days). Three patients required urgent transplantation due to bloodstream infection. There were no adverse outcomes in the HeartMate-group due to infection. In the Jarvik 2000 patients, there was one driveline-infection (16%) after 270 days of support (0.08 device-related infections/100 patient-days), significantly less than in the HeartMate-group (P=0.044). Driveline infections resolved with antibiotics and local wound care in the Jarvik 2000 patient, but only in one of seven HeartMate-patients. Conclusions: Implantation of the Jarvik 2000 is associated with less device-related infections than the HeartMate-LVAD. The power-supply of the permanent Jarvik 2000 is suitable for long-term mechanical support.
Key Words: Heart failure Left ventricular assist device TCI Heartmate Jarvik 2000 Infection
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