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The Journal of Thoracic and Cardiovascular Surgery, Vol 103, 194-198, Copyright © 1992 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
V Jeevanandam, ML Barr, JS Auteri, JA Sanchez, J Fong, FA Schenkel, CC Marboe, RE Michler, CR Smith and EA Rose
We have previously shown the safety and efficacy of University of Wisconsin
solution for hypothermic preservation of the human donor heart in a pilot
group of 16 transplant recipients. The present study is a randomized
clinical trial comparing University of Wisconsin solution to conventional
preservation using crystalloid cardioplegia and saline storage within a
4-hour limit of ischemia. Heart transplant recipients (n = 42) were
randomized into two groups: those receiving hearts preserved by University
of Wisconsin solution, the UWS group (n = 22), and those receiving hearts
preserved in the conventional manner, the CCS group (n = 20). Recipient
age, gender, heart disease, and preoperative inotropic support and donor
age, gender, and mean ischemic time in hours (UWS 2 hours 36 minutes, range
1 hour 36 minutes to 2 hours 53 minutes; CCS 2 hours 20 minutes, range 1
hour 20 minutes to 2 hours 44 minutes; p = not significant) were similar.
Significant differences observed between the two groups included (1) mean
time (minutes) from reperfusion to achieve a stable rhythm, (2) need for
intraoperative defibrillations, (3) need for transient cardiac pacing, and
(4) integrated postoperative creatinine kinase and aspartate
aminotransferase release over 48 hours. There was no difference in
postoperative electrocardiogram, endomyocardial biopsy, or hemodynamics.
One UWS patient died of sepsis and another of a ruptured cerebral aneurysm.
UWS is safe for donor organ arrest and preservation despite high viscosity
and potassium concentration. When compared with CCS hearts, hearts
preserved in UWS regained electrical activity more rapidly and had better
myocardial protection as demonstrated by enzymatic analysis. Further
investigation is required to determine the effects of UWS preservation on
long-term survival, to determine the prevalence of rejection and graft
atherosclerosis, and to test the ability of UWS to extend donor ischemic
time in human cardiac transplantation.
ARTICLES
University of Wisconsin solution versus crystalloid cardioplegia for human donor heart preservation. A randomized blinded prospective clinical trial
Department of Surgery, Columbia-Presbyterian Medical Center, New York, NY 10032.
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