Thorac Cardiovasc Surg 1998; 46(2): 93-96
DOI: 10.1055/s-2007-1010197
Original Thoracic

© Georg Thieme Verlag Stuttgart · New York

Effect of Lung Allograft Ischaemia Duration on Postreperfusion Graft Function and Postoperative Course

M. Bund1 , M. Strüber2 , J. Heine1 , K. Jaeger1 , T. Wahlers2 , A. Haverich2 , S. Piepenbrock1
  • 1Department of Anaesthesiology
  • 2Department of Thoracic and Cardiovascular Surgery
  • Hannover Medical School, Hannover, Cermany
Further Information

Publication History

1997

Publication Date:
19 March 2008 (online)

Abstract

Lung transplantation is limited by the effects of ischaemia. Previous clinical studies related graft ischaemia duration to postoperative pulmonary function in the ICU, morbidity, and overall survival. This report describes the intraoperative pulmonary allograft function immediately after reperfusion. 23 lung transplantations (15 bilateral, 8 Single) were analysed. Donor selection and organ procurement were identical. After pulmonary vasodilation with prostacyclin, allografts were flush-perfused with cold modified Euro-Collins Solution. Mean duration of lung ischaemia was 255.1 ± 35.1 min (190-314 min). Ischaemia times did not differ with respect to the recipient's disease or the use of extracorporeal circulation. After reperfusion, oxygenation indices deteriorated in 73.9% of patients compared with the native lungs (313.4 ± 163.5 vs427.2 ± 96.1, p = 0.006). Linear regression ana lysis and subgroup analysis both revealed a significant influence of the duration of allograft ischaemia on early transplant function. Ischaemia of more than 4 hours resulted in an acceptable but significantly lower PaO2 (254.9 ± 143.3 mmHg vs 463.0 ± 149.2 mmHg, p = 0.011). However, mean time until extubation and time spent in the ICU were not affected. It is concluded that flush-perfusion of the lung with modified Euro-Collins Solution provides reliable preservation of lung function up to four hours. Longer ischaemia, up to six hours, is followed by an acceptable but progressively reduced early transplant function.