TY - JOUR
T1 - Real-time monitoring of acute liver-allograft rejection using the banff schema
AU - Demetris, A. Juan
AU - Ruppert, K.
AU - Dvorchik, I.
AU - Jain, A.
AU - Minervini, M.
AU - Nalesnik, M. A.
AU - Randhawa, P.
AU - Wu, T.
AU - Zeevi, A.
AU - Abu-Elmagd, K.
AU - Eghtesad, B.
AU - Fontes, P.
AU - Cacciarelli, T.
AU - Marsh, W.
AU - Geller, D.
AU - Fung, J. J.
PY - 2002/11/15
Y1 - 2002/11/15
N2 - Background. The Banff schema is the internationally accepted standard for grading acute liver-allograft rejection, but it has not been prospectively tested. Methods. Complete Banff grading was prospectively applied to 2,038 liver-allograft biopsies from 901 adult tacrolimus-treated primary hepatic allograft recipients between August 1995 and September 2001. Histopathologic data was melded with demographic, clinical, and laboratory data into a database on an ongoing basis using locally developed software. Results. Acute rejection developed in 575 of 901 (64%) patients and the worst grade was mild in 422 of 575 (73%). At least one episode of moderate or severe acute rejection developed in 153 of 901 (17%) patients and most episodes, irrespective of severity, occurred within the first year after transplantation. Patients with moderate or severe acute rejection showed higher alanine aminotransferase (P=0.007) and aspartate aminotransferase (P=0.07) levels and were more likely to develop perivenular fibrosis on follow-up biopsies (P=0.001) and graft failure from acute or chronic rejection (P=0.004) than those with mild rejection. Regardless of severity, 80% of patients with acute rejection did not develop significant fibrosis in follow-up biopsies, and graft failure from acute or chronic rejection occurred in only 11 of 901 (1%) allografts. Conclusions. Most acute-rejection episodes are mild and do not lead to clinically significant architectural sequelae. When tested prospectively under real-life and -time conditions, the Banff schema can be used to identify those few patients who are potentially at risk for more significant problems. Creation, capture, and integration of non-free text, or "digital," pathology data can be used to prospectively conduct outcomes-based research in transplantation.
AB - Background. The Banff schema is the internationally accepted standard for grading acute liver-allograft rejection, but it has not been prospectively tested. Methods. Complete Banff grading was prospectively applied to 2,038 liver-allograft biopsies from 901 adult tacrolimus-treated primary hepatic allograft recipients between August 1995 and September 2001. Histopathologic data was melded with demographic, clinical, and laboratory data into a database on an ongoing basis using locally developed software. Results. Acute rejection developed in 575 of 901 (64%) patients and the worst grade was mild in 422 of 575 (73%). At least one episode of moderate or severe acute rejection developed in 153 of 901 (17%) patients and most episodes, irrespective of severity, occurred within the first year after transplantation. Patients with moderate or severe acute rejection showed higher alanine aminotransferase (P=0.007) and aspartate aminotransferase (P=0.07) levels and were more likely to develop perivenular fibrosis on follow-up biopsies (P=0.001) and graft failure from acute or chronic rejection (P=0.004) than those with mild rejection. Regardless of severity, 80% of patients with acute rejection did not develop significant fibrosis in follow-up biopsies, and graft failure from acute or chronic rejection occurred in only 11 of 901 (1%) allografts. Conclusions. Most acute-rejection episodes are mild and do not lead to clinically significant architectural sequelae. When tested prospectively under real-life and -time conditions, the Banff schema can be used to identify those few patients who are potentially at risk for more significant problems. Creation, capture, and integration of non-free text, or "digital," pathology data can be used to prospectively conduct outcomes-based research in transplantation.
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U2 - 10.1097/00007890-200211150-00016
DO - 10.1097/00007890-200211150-00016
M3 - Article
C2 - 12451268
AN - SCOPUS:0037112889
SN - 0041-1337
VL - 74
SP - 1290
EP - 1296
JO - Transplantation
JF - Transplantation
IS - 9
ER -