A comparison of intermittent and continuous arrest for prolonged hypothermic cardioplegia.
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Biomedical subjects
Publications and source records attributed to J H Rousou.
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We present a technique for administering cold cardioplegia that permits the pump technician to conveniently give the fluid. The method is comparable to that used in providing coronary perfusion for aortic valve procedures because it allows controlled volume flow and perfusion pressure. In addition, the technique is inherently safe from infusion of air bubbles.
A technique is described for venting the left ventricle during ischemic arrest without cannulation of the ventricle. This approach is ideally suited for coronary revascularization.
A case is presented of posterior left ventricular rupture occurring from resection of intramyocardial calcification during mitral valve replacement. The laceration was obvious on the operating table with discontinuation of cardiopulmonary bypass, but attempts at simple closure with buttressd sutures were unsuccessful. The ventricular defect was repaired by insertion of a low-porosity Dacron graft. A saphenous vein bypass graft was also placed between the aorta and circumflex coronary artery.
Myocardial high-energy phosphate and glucose-6-phosphate levels were determined in the in vivo pig heart model during ischemic arrest and reperfusion to determine the effectiveness of potassium cardioplegia in myocardial protection. Thirty-five pigs were divided into six experimental groups consisting of 2-hour normothermic arrest, 2-hour hypothemic arrest, 2-hour normothermic cardioplegic arrest, and 1-, 2-, and 3-hour hypothermic cardioplegic arrest. Myocardial biopsies from the left ventricle were obtained prior to arrest, every 30 minutes during the arrest interval, and at 30 and 60 minutes of reperfusion. The measurement of adenosine triphosphate and creatine phosphate showed that (1) cardioplegic arrest requires hypothermia to preserve high-energy phosphate levels in myocardial tissue; (2) hypothermia, while not completely protective alone, is more effective than potassium cardioplegia alone in providing myocardial preservation during 2-hour ischemic arrest; (3) the combination of potassium cardioplegia and hypothermia is additive in providing an effective means of maintaining myocardial high-energy phosphate stores during 1, 2, and 3 hours of ischemic arrest; (4) myocardial reperfusion does not allow a return to preischemic adenosine triphosphate (ATP) levels after 2 hours of arrest, except following hypothermic cardioplegia; and (5) extension of the duration of ischemic arrest to 3 hours using hypothermic cardioplegia prevents recovery of high-energy phosphate stores to preischemic levels during reperfusion. Optimal preservation can be achieved during 2 hours of ischemic arrest by using hypothermic potassium cardioplegia. The effects of myocardial reperfusion, however, prevent full ATP and creatine phosphate (CP) recovery following 3 hours of arrest. No other technique studied was as effective in providing myocardial preservation.
Controlled metabolic studies were used to gauge the relative efficacy of two cardioplegic solutions in 28 patients (14 in each group) undergoing multiple coronary artery bypass grafts. A solution containing magnesium-potassium (Plegisol) was compared to a standard potassium crystalloid cardioplegic solution. Measurements of coronary blood flow, coronary vascular resistance, coronary arteriovenous oxygen difference, myocardial oxygen consumption and extraction, and myocardial lactate and potassium extraction and release were all measured in the isolated, vented, paced, beating heart, before and for 15 minutes after a one hour arrest interval during which time revascularization was completed. During cardioplegic administration, the infusion flow rate, myocardial oxygen consumption and extraction, and lactate and potassium release and uptake were noted. The results indicate that during cardioplegic administration, the total oxygen consumed for both potassium and magnesium-potassium solutions did not significantly differ. The flow rate of the Mg-K solution was significantly higher than that of the potassium solution alone (510 vs. 398 ml/min). There was no lactate production during Mg-K administration, but 0.13 mEq/min of lactate was produced while potassium crystalloid cardioplegia was given. During myocardial reperfusion, oxygen extraction was maintained near prearrest levels in both groups. The only significant difference noted between the potassium and magnesium-potassium solutions were the higher coronary blood flow and oxygen consumption immediately upon reperfusion in the Mg-K group.(ABSTRACT TRUNCATED AT 250 WORDS)