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European Journal of Cardio-Thoracic Surgery, Vol 5, 458-464, Copyright © 1991 by European Association for Cardio-thoracic Surgery
J St. Louis, P Corcoran, S Rajan, J Conte, L Wolfinbarger, J Hu, PL Lange, YN Wang, SL Hilbert and A Analouei
The clinical use of cryopreserved allograft valves is rapidly increasing.
Viability of valve leaflet fibroblasts has been proposed to be critical to
durability. Harvesting of allograft valves involves variable warm ischemia
times, defined as the time from cessation of donor heart beat to initial
cooling for transport. This ischemic period has been implicated as one of
the more critical periods of injury to leaflet cell, even though adequate
characterization of this potentially injurious phase has never been
accomplished. The present study was undertaken to characterize the
metabolic response to warm ischemia in a porcine valve leaflet model. Valve
handling was similar to clinical valve harvest and transport protocols.
Injury was assessed by protein (1H) and phosphorus (31P) magnetic resonance
spectroscopy of 224 porcine semilunar valves. Leaflets were analyzed over
time for lactate accumulation and ATP degradation. A radiolabelled
incubation assay (48 valves) was used to measure proline accumulation by
fibroblasts. Electron microscopy was performed on 36 valves with varying
warm ischemia times. ATP stores were entirely depleted after 2 h hypoxia (p
less than 0.05). However, lactate continued to accumulate over 24 h.
Although aerobic metabolism ceased after 2 h warm ischemia, anaerobic
metabolism continued for up to 24 h, which may represent an extended window
for harvesting fresh tissue for allograft valve implantation.
ARTICLES
Effects of warm ischemia following harvesting of allograft cardiac valves
Department of Surgery, Georgetown University Medical Center, Washington, DC.
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