Assessment of non-heart-beating donor (NHBD) kidneys for viability on machine perfusion

Citation
S. Balupuri et al., Assessment of non-heart-beating donor (NHBD) kidneys for viability on machine perfusion, CLIN CH L M, 38(11), 2000, pp. 1103-1106
Citations number
17
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
CLINICAL CHEMISTRY AND LABORATORY MEDICINE
ISSN journal
14346621 → ACNP
Volume
38
Issue
11
Year of publication
2000
Pages
1103 - 1106
Database
ISI
SICI code
1434-6621(200011)38:11<1103:AOND(K>2.0.ZU;2-Q
Abstract
The shortage of organs has resulted in renewed interest in organs from non- heart-beating donors (NHBD). Viability assessment of such organs may reduce the incidence of delayed graft function and primary nonfunction. In Phase III of the NHBD programme, introduction of machine perfusion enabled the as sessment of these marginal donors. Since then the graft survival has been 8 8.4% compared with the previous phase where machine perfusion or viability assessment was not done (45.5%). The parameters used were total glutathione S-transferase (GST) in the perfusate, the intrarenal vascular resistance ( IRVR) and flow characteristics over time. Methods: All NHBD kidneys were machine perfused through a locally developed perfusion system. The viability was assessed by serial measurements of the above-mentioned parameters. Results: Forty-two local NHBD kidneys were retrieved and one kidney was imp orted, of which 19 donors (i.e. 38 kidneys) were of the uncontrolled (categ ory II) donors. After viability assessment on machine perfusion; two kidney s were discarded due to positive tests for syphilis, four kidneys had high total GST levels, five kidneys due to high IRVR and poor flow characteristi cs and one did not flush on retrieval. Three kidneys were exported after vi ability tests. In 28 NHBD kidney recipients, immediate graft function was s een in two kidneys, 22 (84.6%) developed delayed graft function, One kidney had primary non-function, and two recipients lost their grafts, due to chr onic rejection and renal vein thrombosis. There were two deaths, unrelated to transplantation. Graft survival was achieved in 88.4% (23/26 graft survi val in phase III) of cases. Conclusion: Machine perfusion and assessment of NHBD kidneys has been succe ssfully introduced to the Newcastle NHBD programme. This approach, using re nal transplants from largely category II donors produced a success rate of 88.4% which was significantly better than the phase II period (45.5%) of th e program (p=0.023, Fisher 2 tail test).