Hendry P J, Labow R S, Keon W J
University of Ottawa Heart Institute, Ottawa Civic Hospital, Department of Surgery, Ontario, Canada.
J Thorac Cardiovasc Surg. 1993 Apr;105(4):667-73.
Numerous solutions have been advocated for the preservation of donor hearts, and there has been much interest in universal and intracellular preservation solutions. This study compared the effects of Euro-Collins, University of Wisconsin, and Bretschneider's solutions with the use of an in vitro human right atrial muscle preparation to assess recovery of function after a 24-hour period of simulated cardiac arrest. There were no statistically significant differences among groups in length, weight, cross-sectional area, initial developed force, or resting force of muscles, including those muscles that were contracted in Krebs-Henseleit solution and served as a control. After the 24-hour arrest period at either 4 degrees or 12 degrees C, the solution was changed back to Krebs-henseleit at 34 degrees C and recovery was assessed over 30 minutes. At 30 minutes, developed forces for muscles that were cooled to 4 degree C were 58.9%, 76.6%, and 60.7% of the control for Euro-Collins, University of Wisconsin, and Bretschneider's solutions, respectively (p = not significant). For those cooled to 12 degrees C, developed forces were 9.5%, 30.5%, and 95.6% of the control for Euro-Collins, University of Wisconsin, and Bretschneider's solutions (p = 0.0001). Bretscheider's solution resulted in greatly improved recovery compared with both Euro-Collins and University of Wisconsin solutions (p = 0.005), and University of Wisconsin solution was better than Euro-Collins solution (p = 0.02). Recovery of developed force was affected by temperature for Euro-Collins and University of Wisconsin solutions (p = 0.005 and p = 0.001, respectively) but not for Bretschneider's solution. Resting force was elevated in muscles that were cooled in both Euro-Collins and University of Wisconsin solutions at 12 degrees C compared with almost normal values for Bretschneider's solution at either temperature (p = 0.07). Bretschneider's solution has a very high buffering capacity, which may be beneficial for long-term preservation. In conclusion, Bretschneider's solution resulted in the best recovery of human atrial myocardial function after a 24-hour preservation period compared with Euro-Collins and University of Wisconsin solutions and should be considered for use in donor heart transportation. The variability in quality of preservation at different temperatures with either Euro-Collins or University of Wisconsin solution make them less desirable as preservation solutions because uniform temperatures are seldom obtained during donor heart transplantation.
人们已经提出了许多用于保存供体心脏的解决方案,并且对通用和细胞内保存溶液有很大兴趣。本研究使用体外人右心房肌制备物比较了欧林柯林斯溶液、威斯康星大学溶液和布雷施奈德溶液的效果,以评估在模拟心脏骤停24小时后的功能恢复情况。各组肌肉的长度、重量、横截面积、初始收缩力或静息力之间没有统计学上的显著差异,包括那些在克雷布斯-亨泽莱特溶液中收缩并作为对照的肌肉。在4℃或12℃下进行24小时的停搏期后,将溶液换回34℃的克雷布斯-亨泽莱特溶液,并在30分钟内评估恢复情况。在30分钟时,冷却至4℃的肌肉的收缩力分别为欧林柯林斯溶液、威斯康星大学溶液和布雷施奈德溶液对照组的58.9%、76.6%和60.7%(p值无显著性差异)。对于冷却至12℃的肌肉,收缩力分别为欧林柯林斯溶液、威斯康星大学溶液和布雷施奈德溶液对照组的9.5%、30.5%和95.6%(p = 0.0001)。与欧林柯林斯溶液和威斯康星大学溶液相比,布雷施奈德溶液导致的恢复情况有显著改善(p = 0.005),威斯康星大学溶液优于欧林柯林斯溶液(p = 0.02)。对于欧林柯林斯溶液和威斯康星大学溶液,收缩力的恢复受温度影响(分别为p = 0.005和p = 0.001),但布雷施奈德溶液不受影响。与布雷施奈德溶液在任何一个温度下几乎正常的值相比,在12℃下用欧林柯林斯溶液和威斯康星大学溶液冷却的肌肉中的静息力升高(p = 0.07)。布雷施奈德溶液具有非常高的缓冲能力,这可能有利于长期保存。总之,与欧林柯林斯溶液和威斯康星大学溶液相比,布雷施奈德溶液在24小时保存期后导致人心房心肌功能的最佳恢复,在供体心脏运输中应考虑使用。欧林柯林斯溶液或威斯康星大学溶液在不同温度下保存质量的变异性使得它们作为保存溶液不太理想,因为在供体心脏移植过程中很少能获得均匀的温度。