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术中心肌保护:含血与无血心脏停搏液的比较

Intraoperative myocardial protection: a comparison of blood and asanguineous cardioplegia.

作者信息

Codd J E, Barner H B, Pennington D G, Merjavy J P, Kaiser G C, Devine J E, Willman V L

出版信息

Ann Thorac Surg. 1985 Feb;39(2):125-33. doi: 10.1016/s0003-4975(10)62551-9.

Abstract

Cardiac arrest was achieved in 84 patients using asanguineous cardioplegia and in 97 patients using cold blood potassium cardioplegia. The patient groups were similar in age, sex ratio, and preoperative risk factors. Other than the cardioplegic solution used, the conduct of each operation was identical. There were no differences in mean total pump time (118 minutes for the asanguineous cardioplegia group versus 117 minutes for the cold blood cardioplegia group) or cross-clamp time (73.5 versus 70 minutes, respectively). However, the blood cardioplegia group had a greater number of distal anastomoses per patient (3.9 versus 3.7; p less than 0.05). Myocardial protection was assessed clinically and by serial electrocardiograms. Cellular integrity was determined by release of the myocardial isoenzyme of serum creatine kinase (CK-MB). Cellular morphology was studied in 6 randomly selected patients in each group by electron microscopic examination of left ventricular myocardial samples obtained before and after bypass. Three patients given blood cardioplegia and 5 given asanguineous cardioplegia required intraaortic balloon counterpulsation at termination of bypass. There were no ultrastructural changes in either group. Electrocardiographic changes (Minnesota code) occurred in 12 of 84 patients receiving asanguineous cardioplegia versus 12 of 97 patients receiving cold blood potassium cardioplegia. To maintain a satisfactory cardiac index (greater than 2.0 L/min/m2), 38 of 84 patients given asanguineous cardioplegia versus 25 of 97 patients given blood cardioplegia required inotropic support up to 24 hours postoperatively (p less than 0.05). Infarct size determined from CK-MB release was significantly greater (p less than 0.05) in patients given asanguineous cardioplegia (36.27 gm-equivalents) than in those given blood cardioplegia (26.7 gm-equivalents).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

84例患者使用无血心脏停搏液实现心脏停搏,97例患者使用冷血钾心脏停搏液。两组患者在年龄、性别比例和术前危险因素方面相似。除了所使用的心脏停搏液外,每次手术的操作过程相同。平均总灌注时间(无血心脏停搏液组为118分钟,冷血心脏停搏液组为117分钟)或主动脉阻断时间(分别为73.5分钟和70分钟)没有差异。然而,冷血心脏停搏液组每名患者的远端吻合口数量更多(3.9个对3.7个;p<0.05)。通过临床评估和系列心电图评估心肌保护情况。通过血清肌酸激酶心肌同工酶(CK-MB)的释放来确定细胞完整性。通过对每组6例随机选择的患者在体外循环前后获取的左心室心肌样本进行电子显微镜检查,研究细胞形态。3例接受冷血心脏停搏液的患者和5例接受无血心脏停搏液的患者在体外循环结束时需要主动脉内球囊反搏。两组均未出现超微结构变化。84例接受无血心脏停搏液的患者中有12例出现心电图变化(明尼苏达编码),97例接受冷血钾心脏停搏液的患者中有12例出现心电图变化。为维持满意的心指数(大于2.0L/min/m²),84例接受无血心脏停搏液的患者中有38例与97例接受冷血心脏停搏液的患者中有25例术后需要长达24小时的正性肌力支持(p<0.05)。根据CK-MB释放确定的梗死面积,接受无血心脏停搏液的患者(36.27克当量)显著大于接受冷血心脏停搏液的患者(26.7克当量)(p<0.05)。(摘要截断于250字)

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