Sakamoto T, Yamashita C, Okada M
Department of Surgery, Division II, Kobe University School of Medicine, 7-5-2 Kusunoki-cho, Chuo-ku, Kobe 650-0017.
Ann Thorac Cardiovasc Surg. 1999 Feb;5(1):21-6.
In lung transplantation, the safety period of the ischemic time of the graft is within 6 hours. Because of the problem of donor shortage, it is essential to extend the safety period of the preservation time of the donor lung. However, the longer the preservation time is, the more severe is the resulting ischemia-reperfusion injury. This study was designed to evaluate the efficacy of initial controlled perfusion pressure in the reduction of ischemia-reperfusion injury in a 24-hour preserved lung. Japanese white rabbit lungs were flushed with a low-potassium dextran solution (4C, 500 ml) after injection of prostaglandin E1 (20 microgram, bolus via PA) and submersed in the same solution for 24 hours at 4C. After preservation, the left lung was reperfused using an extracorporeal lung perfusion model which comprised of a closed circuit combined with a membrane deoxygenator. Assessment of lung function included gas analysis of influent and effluent blood and mean pulmonary artery perfusion pressure. Then the lung wet/dry weight ratio was calculated. In group I of the control group (n=6), the left lung was reperfused immediately following flushing (without preservation) at a flow rate of 50 ml/min for 60 minutes. In groups II and III, grafts were stored for 24 hours. In group II, grafts (n=6) were reperfused at a flow rate of 50 ml/min for 60 minutes. In group III (n =6), the flow rate was controlled by maintaining the perfusion pressure below 30 mmHg during the initial 5 minutes and was increased to 50 ml/min for the subsequent 60 minutes. In group II, the mean pulmonary artery pressure during perfusion increased rapidly, and oxygenation deteriorated. All grafts developed pulmonary edema within 12 minutes after reperfusion. Examination of the specimen revealed that the peripheral lung was not perfused. In group III, the mean pulmonary artery perfusion pressure was maintained below 30 mmHg, and oxygenation was preserved sufficiently throughout the experiment (delta PO2 > 100 mmHg) with no significant difference from control values. In conclusion, ischemia-reperfusion injury of the 24-hour preserved lung was attenuated prominently by controlling initial perfusion pressure for 5 minutes.
在肺移植中,移植物缺血时间的安全期在6小时以内。由于供体短缺问题,延长供体肺保存时间的安全期至关重要。然而,保存时间越长,由此产生的缺血-再灌注损伤就越严重。本研究旨在评估初始控制性灌注压力在减轻保存24小时的肺的缺血-再灌注损伤中的效果。在注射前列腺素E1(20微克,经肺动脉推注)后,用低钾右旋糖酐溶液(4℃,500毫升)冲洗日本白兔的肺,并在4℃下将其浸泡在相同溶液中24小时。保存后,使用由闭合回路与膜式氧合器组成的体外肺灌注模型对左肺进行再灌注。肺功能评估包括流入和流出血液的气体分析以及平均肺动脉灌注压力。然后计算肺湿/干重比。对照组I组(n = 6)在冲洗后(未保存)立即以50毫升/分钟的流速再灌注左肺60分钟。II组和III组的移植物保存24小时。II组(n = 6)的移植物以50毫升/分钟的流速再灌注60分钟。III组(n = 6)在最初5分钟内通过将灌注压力维持在30毫米汞柱以下来控制流速,并在随后的60分钟内将流速增加到50毫升/分钟。II组在灌注期间平均肺动脉压力迅速升高,氧合恶化。所有移植物在再灌注后12分钟内均出现肺水肿。标本检查显示外周肺未灌注。III组平均肺动脉灌注压力维持在30毫米汞柱以下,并且在整个实验过程中氧合充分保持(ΔPO2>100毫米汞柱),与对照值无显著差异。总之,通过控制初始灌注压力5分钟,可显著减轻保存24小时的肺的缺血-再灌注损伤。