Utilization of Organs From Donors According to Hepatitis C Antibody and Nucleic Acid Testing Status: Time for Change

被引:52
作者
Kling, C. E. [1 ]
Perkins, J. D. [1 ]
Landis, C. S. [2 ]
Limaye, A. P. [3 ]
Sibulesky, L. [1 ]
机构
[1] Univ Washington, Dept Surg, Div Transplant Surg, Seattle, WA 98195 USA
[2] Univ Washington, Dept Med, Div Gastroenterol & Hepatol, Seattle, WA USA
[3] Univ Washington, Dept Med, Div Allergy & Infect Dis, Seattle, WA USA
关键词
CELL-MEDIATED REJECTION; KIDNEY-TRANSPLANT BIOPSIES; RENAL-ALLOGRAFT PATHOLOGY; HLA ANTIBODIES; INTERNATIONAL VARIATION; WORKING CLASSIFICATION; HISTOLOGIC DIAGNOSIS; MICROARRAY DIAGNOSIS; MOLECULAR DIAGNOSIS; GRAFT LOSS;
D O I
10.1111/ajt.14386
中图分类号
R61 [外科手术学];
学科分类号
摘要
Previous studies have grouped all donors positive for hepatitis C virus (HCV) antibody (Ab). Only recently has donor HCV nucleic acid testing (NAT) become routine, and the impact of Ab and NAT status on organ utilization is unknown. Using the United Network for Organ Sharing database, we identified 9290 donors from 2015 to 2016 for whom both HCV Ab and NAT data were available and compared organ utilization by HCV status. Overall, 93.8% of donors were Ab negative and NAT negative (Ab-NAT-), 0.15% were Ab negative and NAT positive, 1.8% were Ab positive and NAT negative (Ab+NAT-), and 4.2% were both Ab and NAT positive (Ab+NAT+). Ab-NAT- donors donated at the highest rate for all organs except livers, of which Ab+NAT- donors donated at a higher rate (81.2% vs 73.2%, p = 0.03). Livers were discarded for reasons related to abnormal biopsies in Ab+NAT+ donors, whereas kidneys from Ab-or NAT- positive donors were discarded for reasons related to HCV status. Using a propensity score-matched model, we estimated that using Ab+NAT- donors at the same rate as Ab-NAT- donors could result in 48 more kidney donors, 37 more heart donors, and 15 more lung donors annually. We urge the use of HCV Ab+NAT- donors for appropriately selected and consenting recipients.
引用
收藏
页码:2863 / 2868
页数:6
相关论文
共 49 条
[1]  
[Anonymous], 2016, RPART PLOT PLOT RPAR
[2]  
[Anonymous], 2015, Package rpart
[3]   Pathologic Interpretation of Transbronchial Biopsy for Acute Rejection of Lung Allograft Is Highly Variable [J].
Arcasoy, S. M. ;
Berry, G. ;
Marboe, C. C. ;
Tazelaar, H. D. ;
Zamora, M. R. ;
Wolters, H. J. ;
Fang, K. C. ;
Keshavjee, S. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2011, 11 (02) :320-328
[4]   Tubular Lesions Predict Renal Outcome in Antineutrophil Cytoplasmic Antibody-Associated Glomerulonephritis after Rituximab Therapy [J].
Berden, Annelies E. ;
Jones, Rachel B. ;
Erasmus, Dianhdra D. ;
Walsh, Michael ;
Noel, Laure-Helene ;
Ferrario, Franco ;
Waldherr, Ruediger ;
Bruijn, Jan A. ;
Jayne, David R. ;
Bajema, Ingeborg M. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2012, 23 (02) :313-321
[5]  
Breiman F, 1984, OLSHEN STONE CLASSIF
[6]   Concordance Among Pathologists in the Second Cardiac Allograft Rejection Gene Expression Observational Study (CARGO II) [J].
Crespo-Leiro, Maria G. ;
Zuckermann, Andreas ;
Bara, Christoph ;
Mohacsi, Paul ;
Schulz, Uwe ;
Boyle, Andrew ;
Ross, Heather J. ;
Parameshwar, Jayan ;
Zakliczynski, Michael ;
Fiocchi, Roberto ;
Stypmann, Joerg ;
Hoefer, Daniel ;
Lehmkuhl, Hans ;
Deng, Mario C. ;
Leprince, Pascal ;
Berry, Gerald ;
Marboe, Charles C. ;
Stewart, Susan ;
Tazelaar, Henry D. ;
Baron, Helen M. ;
Coleman, Ian-Charles ;
Vanhaecke, Johan .
TRANSPLANTATION, 2012, 94 (11) :1172-1177
[7]   Early loss of renal transcripts in kidney allografts: Relationship to the development of histologic lesions and alloimmune effector mechanisms [J].
Einecke, G. ;
Broderick, G. ;
Sis, B. ;
Halloran, P. F. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2007, 7 (05) :1121-1130
[8]   Loss of Solute Carriers in T Cell-Mediated Rejection in Mouse and Human Kidneys: An Active Epithelial Injury-Repair Response [J].
Einecke, G. ;
Kayser, D. ;
Vanslambrouck, J. M. ;
Sis, B. ;
Reeve, J. ;
Mengel, M. ;
Famulski, K. S. ;
Bailey, C. G. ;
Rasko, J. E. J. ;
Halloran, P. F. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2010, 10 (10) :2241-2251
[9]   Antibody-Mediated Microcirculation Injury Is the Major Cause of Late Kidney Transplant Failure [J].
Einecke, G. ;
Sis, B. ;
Reeve, J. ;
Mengel, M. ;
Campbell, P. M. ;
Hidalgo, L. G. ;
Kaplan, B. ;
Halloran, P. F. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2009, 9 (11) :2520-2531
[10]  
Einecke G, 2016, AM J TRANSPLANT