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The Journal of Thoracic and Cardiovascular Surgery, Vol 104, 139-150, Copyright © 1992 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
MA Breda, DC Drinkwater, H Laks, S Bhuta, B Ho, E Kaczer, JL Sebastian and P Chang
Current methods of myocardial preservation for transplantation are
suboptimal. A newly developed intracellular cardioplegic and storage
solution (modified University of Wisconsin solution, group 1) was compared
in a randomized, blinded fashion with our present clinical protocol,
Stanford cardioplegic solution and saline storage (group 2) in an isolated
neonatal pig model. After arrest and storage for 12 hours at 4 degrees C,
biopsy specimens were taken from six group 1 hearts and five group 2 hearts
for examination under an electron microscope and assessment of high-energy
phosphate levels and water content. The remainder (group 1, n = 7; group 2,
n = 6) were reperfused with blood for 50 minutes, after which function
curves were obtained at left ventricular end-diastolic pressures of 3 to 12
mm Hg and biopsy tissue was taken. Eight control hearts (group 3) were
cannulated in situ and perfused on the circuit without arrest or
intervening ischemia. Stroke and minute work index curves were
approximately threefold and fivefold higher for group 1 (modified
University of Wisconsin solution) than for group 2 (Stanford), respectively
(p less than 0.01). The hearts preserved with University of Wisconsin
solution did not differ in function from unpreserved control hearts (group
3). High-energy phosphate levels were better maintained in group 1 than
group 2 (p less than 0.05), and water content was lower (p less than 0.01).
Semiquantitative grading of electron micrographs paralleled the functional
and biochemical results. Conclusion: Modified University of Wisconsin
intracellular solution provides markedly better heart preservation than
conventionally used cardioplegic and storage solutions.
ARTICLES
Successful long-term preservation of the neonatal heart with a modified intracellular solution
Division of Cardiothoracic Surgery, University of California, Los Angeles School of Medicine 90024-1741.
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