Tm. Runge et al., ENHANCEMENT OF BRAIN PO(2) DURING CARDIOPULMONARY BYPASS USING A HYPEROSMOLAR OXYGEN-CARRYING SOLUTION, Artificial cells, blood substitutes, and immobilization biotechnology, 25(3), 1997, pp. 297-308
During the past decade a new syndrome has been recognized: cerebral hy
poxia secondary to cardiopulmonary bypass, resulting in impairment of
cognitive memory. The incidence of the syndrome appears to be no less
that 30% in patients over 65 years of age undergoing cardiac surgery.
There are several factors contributing to hypoxia produced by cardiopu
lmonary bypass. One of these factors is crystalloid pump prime and rep
lacement solutions devoid of (1) oxygen carrying capacity and (2) devo
id of protein and its colloid osmotic pressure. This shortcoming of ca
rdiopulmonary crystalloid solutions is partially responsible for two o
f the three major pathologic effects of cardiopulmonary bypass: (1) hy
poxia (2) interstitial fluid accumulation (anasarca, water-logging, ed
ema). This report describes an oxygen carrying hyperosmolar solution w
hich enhances brain pO(2) and diminishes interstitial fluid accumulati
on. This blood substitute consists of perfluorcarbons and saccharides,
but could consist of a hemoglobin variant plus hyperosmolar ingredien
ts other than saccharides. The advantage of perfluorochemical is its a
bility to access small channels and to be centrifuged off the patient
post-operatively with a cell saver. The advantage of saccharides is th
at they can be metabolized by the patient for energy, and they produce
a moderate diuresis coming off bypass.