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Ann Thorac Surg 2003;76:1993-1998
© 2003 The Society of Thoracic Surgeons


Original article: cardiovascular

Risk factor analysis of Swedish Left Ventricular Assist Device (LVAD) patients

Hans Granfeldt, MDa*, Bansi Koul, MD, PhDb, Lars Wiklund, MD, PhDc, Bengt Peterzén, MD, PhDa, Urban Lönn, MD, PhDd, Ankica Babic, PhDe, Henrik C. Ahn, MD, PhDa

a Departments of Cardiovascular Surgery and Anesthesia, University Hospital, Linköping, Sweden
e Institution for Medical Informatics, University Hospital, Linköping, Sweden
b University Hospital, Lund, Sweden
c University Hospital, Gothenburg, Sweden
d University Hospital, Uppsala, Sweden

Accepted for publication June 5, 2003.

* Address reprint requests to Dr Granfeldt, Departments of Cardiovascular Surgery and Anesthesia, University Hospital, S-58185 Linköping, Sweden.
e-mail: hans.granfeldt{at}lio.se

BACKGROUND: The use of left ventricular assist devices (LVADs) is established as a bridge to heart transplantation.

METHODS: All Swedish patients on the waiting list for heart transplantation, treated with LVAD since 1993 were retrospectively collected into a database and analyzed in regards to risk factors for mortality and morbidity.

RESULTS: Fifty-nine patients (46 men) with a median age of 49 years (range, 14 to 69 years), Higgins score median of 9 (range, 3 to 15), EuroScore median of 10 (range, 5 to 17) were investigated. Dominating diagnoses were dilated cardiomyopathy in 61% (n = 36) and ischemic cardiomyopathy in 18.6% (n = 11). The patients were supported with LVAD for a median time of 99.5 days (range, 1 to 873 days). Forty-five (76%) patients received transplants, and 3 (5.1%) patients were weaned from the device. Eleven patients (18.6%) died during LVAD treatment. Risk factor analysis for mortality before heart transplantation showed significance for a high total amount of autologous blood transfusions (p < 0.001), days on mechanical ventilation postoperatively (p < 0.001), prolonged postoperative intensive care unit stay (p = 0.007), and high central venous pressure 24 hours postoperatively and at the final measurement (p = 0.03 and 0.01, respectively). Mortality with LVAD treatment was 18.6% (n = 11). High C-reactive protein (p = 0.001), low mean arterial pressure (p = 0.03), and high cardiac index (p = 0.03) preoperatively were risk factors for development of right ventricular failure during LVAD treatment.

CONCLUSIONS: The Swedish experience with LVAD as a bridge to heart transplantation was retrospectively collected into a database. This included data from transplant and nontransplant centers. Figures of mortality and morbidity in the database were comparable to international experience. Specific risk factors were difficult to define retrospectively as a result of different protocols for follow-up among participating centers.




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