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The Journal of Thoracic and Cardiovascular Surgery, Vol 95, 103-111, Copyright © 1988 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
SJ Ledingham, MV Braimbridge and DJ Hearse
The effect of oxygenation (100% oxygen) of the St. Thomas' Hospital
cardioplegic solutions No. 1 (MacCarthy) and No.2 (Plegisol, Abbott
Laboratories, North Chicago, Ill.) was examined in the isolated working rat
heart subjected to long periods (3 hours for studies with solution No. 1
and 4 hours for studies with solution No. 2) of hypothermic (20 degrees C)
ischemic arrest with multidose (every 30 minutes) cardioplegic infusion. At
the aortic infusion point the oxygen tension of the oxygenated solutions
(measured at 20 degrees C) was in the range of 320 to 560 mm Hg whereas
that of the nonoxygenated solutions was less than 150 mm Hg. Twenty hearts
(10 oxygenated and 10 nonoxygenated) were studied for each solution. The
studies with solution No. 1 demonstrated that oxygenation led to a
significant (p less than 0.05) reduction in the incidence of persistent
ventricular fibrillation during postischemic reperfusion. Oxygenation of
the cardioplegic solution also improved postischemic functional recovery so
that the recovery of aortic flow was improved from 18.7% +/- 8.9% (of its
preischemic control level) in the nonoxygenated group to 54.6% +/- 6.6% in
the oxygenated group (p less than 0.025). Creatine kinase leakage was also
significantly reduced from 27.5 +/- 4.8 to 9.9 +/- 0.6 IU/15 min/gm dry
weight (p less than 0.005). Studies with solution No. 2 indicated that
protection was better than with solution No. 1, even in the absence of
oxygenation. A better degree of functional recovery was obtained after 4
hours of arrest with solution No. 2 than that obtained after only 3 hours
of arrest with solution No. 1, and persistent ventricular ventricular
fibrillation was never observed with solution No. 2. However, despite the
superior performance with solution No. 2, further improvements could be
obtained by oxygenation, with that time from the onset of reperfusion to
the return of regular sinus rhythm being reduced from 55 +/- 8 to 35 +/- 2
seconds (p less than 0.01), postischemic recovery of aortic flow increasing
from 59.8% +/- 7.4% to 85.7% +/- 2.5% (p less than 0.005), and creatine
kinase leakage being reduced from 38.1 +/- 7.3 to 16.2 +/- 1.5 IU/15 min/gm
dry weight (p less than 0.005). It is concluded that oxygenation of the St.
Thomas' Hospital cardioplegic solutions improves their ability to protect
the heart against long periods of ischemia and that this is manifested by
improved postischemic electrical stability, functional recovery, and
reduced creatine kinase leakage.
ARTICLES
Improved myocardial protection by oxygenation of St. Thomas' Hospital cardioplegic solutions. Studies in the rat
Cardiovascular Research, Rayne Institute, St. Thomas' Hospital, London, England.
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