Lungs from donation after cardiac death for transplantation.

We read with interest the publication by Zych et al .[ 1] regarding lung transplantation from donation after cardiac death (DCD) donors. Concern that DCD lungs might be inferior to lungs from brain-dead donors appears to be significant barriers to widespread adoption. Our prior studies [2, 3], which also represent that a large portion of the national DCD lung transplantation experience, have been very favourable, and we advocate its utilization as a means of overcoming the donor shortage. We have approached selection, procurement and implantation of DCD organs in a fashion analogous to that for brain-dead donors with essentially no modification of our standardized protocols. There have been concerns about the timing and dosage of heparin for DCD lung harvest. Delayed heparin administration after cardiac death does not seem to affect thrombus formation in an animal model of lung procurement after cardiac death, and concerns about thrombosis appear unfounded [4]. We noted that the authors did not administer heparin prior to cardiac arrest. However, at this juncture, we routinely administer full-dose heparin prior to a withdrawal of support and hope to expand the pool to include donors in whom heparin is not permitted. We noticed that the authors had a higher primary graft dysfunction (PGD) 3 score on arrival to the intensive care unit in the DCD group, whereas in our series 91% of patients had PGD scores of 0 at T0, T24, T48 and T72 h. The survival in our series was 97% at 30 days, 91% at 1 and 2 years, respectively, and 71% at 3 and 4 years, and our growing experience suggests that recipient survival and early graft function using DCD lungs are excellent. Concerns about diminished organ quality are unwarranted, and the use of DCD lungs should be expanded. We whole-heartedly agree with the authors that DCD lungs are a valuable and excellent source of good quality organs for transplantation.

[1]  L. Bertolaccini,et al.  Correlation sometimes implies causation: possible roles of correlation analysis between 18 fluorine-fluorodeoxyglucose positron emission tomography/computed tomography and thymic epithelial neoplasms. , 2013, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[2]  S. Murthy,et al.  Timing of Heparin and Thrombus Formation in Donor Lungs after Cardiac Death , 2012, Thoracic and Cardiovascular Surgeon.

[3]  K. Matsuo,et al.  The utility of [18F]-fluorodeoxyglucose positron emission tomography-computed tomography in thymic epithelial tumours. , 2012, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[4]  M. Amrani,et al.  Lungs from donation after circulatory death donors: an alternative source to brain-dead donors? Midterm results at a single institution. , 2012, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[5]  S. Murthy,et al.  Growing single-center experience with lung transplantation using donation after cardiac death. , 2012, The Annals of thoracic surgery.

[6]  T. Go,et al.  Usefulness of [18F]fluoro-2-deoxy-D-glucose positron emission tomography for predicting the World Health Organization malignancy grade of thymic epithelial tumors. , 2011, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[7]  Yukiko Nakamura,et al.  Utility of 18FDG-PET for differentiating the grade of malignancy in thymic epithelial tumors. , 2008, Lung cancer.

[8]  A. Mehta,et al.  Early experience with lung transplantation using donors after cardiac death. , 2008, The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation.

[9]  J. Choi,et al.  18F-FDG PET/CT of thymic epithelial tumors: usefulness for distinguishing and staging tumor subgroups. , 2006, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.