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1 d for 1 hour with a hyperkalemic, cold blood cardioplegic solution.
2 erfusion followed by isolated perfusion with cardioplegic solution.
3 rmacological agents in order to offer better cardioplegic solutions.
5 rest and rewarming, incubated in crystalloid cardioplegic solution (24 mEq/L K+, 4 degrees C) for 2 h
6 olerance to ischemia, adenosine-supplemented cardioplegic solution also may reduce bleeding after car
9 for 7 hours) or placebo (both also added to cardioplegic solutions) beginning just before anesthesia
10 n (n=60); or PCO/cardioplegia, incubation in cardioplegic solution containing 100 micromol/L of the P
11 monary artery were occluded with snares, and cardioplegic solution containing histamine was injected
14 dilution of blood in 4:1 (blood:crystalloid) cardioplegic solutions may nullify these advantages and
15 maged following isolation and perfusion with cardioplegic solution (n = 6), imaged in vivo (n = 6), o
16 tion for 2 hours in hypothermic hyperkalemic cardioplegic solution (n=60); or PCO/cardioplegia, incub
17 the 1970 s, the development of hyperkalaemic cardioplegic solutions revolutionised cardiac surgery by
18 ed after the infusion of St Thomas' Hospital cardioplegic solution, stored at 4 degrees C for 4 hours
22 assium channels were activated by augmenting cardioplegic solutions with adenosine (200 mumol/L) or t
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