TY - JOUR
T1 - The use of hepatitis B core antibody-positive donor livers does not appear to have a deleterious effect on graft survival in liver transplantation for hepatitis C
AU - Rayhill, S.
AU - Schwartz, J.
AU - Ham, J.
AU - Carithers, R.
AU - Lei, Y.
AU - Bhattacharya, R.
AU - Liou, I.
AU - Landis, C.
AU - Lamaye, A.
AU - Rakita, R.
AU - Dick, A.
AU - Healey, P.
AU - Halldorson, J.
AU - Bhakthavatsalam, R.
AU - Perkins, J.
AU - Reyes, J.
PY - 2010/12
Y1 - 2010/12
N2 - Introduction The use of hepatitis B core antibody-positive donor livers (HBcAb +) has steadily increased. According to a recent multivariate analysis of United Network for Organ Sharing (UNOS) data, there was no significant increase in the risk of using these donors. The increased risk among the hepatitis C virus (HCV)-positive subgroup noted in a univariate model disappeared upon multivariate analysis. However, deeper scrutiny may show that HCV-positive recipients may be at increased risk with HBcAb + donor livers, as they require simultaneous treatment with two antiviral regimens there may be deleterious interactions between the two viruses. Thus, the issue of HBcAb + donors for HCV-positive recipients merits more detailed analysis. Methods Using UNOS registry data of all liver transplantations performed during the Model for End-Stage Liver Disease era from February 2002 through November 2007, we analyzed graft survival using Kaplan-Meier and Cox regression analyses. Results Of the 12,543 HCV-positive recipients, 2,543 received HBcAb - livers and 853 received HBcAb + livers. While Kaplan- Meier analysis showed significantly lower graft survival among HCV-negative recipients of HBcAb + livers (P = .0001), there was no significant effect on graft survival among the HCV-positive population (P = .2). To detect an early effect in HCV-positive recipients, we examined 1-year graft survival, observing no significant difference (P = .3). To exclude a possible late effect, we examined graft survival in the HCV-positive population conditional upon surviving at least 1 year after transplantation; no significant difference was observed (P = .6). The elimination of potentially confounding codiagnoses, such as hepatitis B virus, alcoholism, acute graft failure, and hepatocellular cancer did not alter the findings. On univariate analysis, the lack of a significant effect persisted among the HCV population. However, the significant effect observed in the univariate model for the HCV-negative population became insignificant when combined with other risk factors in the multivariate model. Conclusion The use of HBcAb + livers in recipients with HCV did not appear to have a significant impact on grat survival.
AB - Introduction The use of hepatitis B core antibody-positive donor livers (HBcAb +) has steadily increased. According to a recent multivariate analysis of United Network for Organ Sharing (UNOS) data, there was no significant increase in the risk of using these donors. The increased risk among the hepatitis C virus (HCV)-positive subgroup noted in a univariate model disappeared upon multivariate analysis. However, deeper scrutiny may show that HCV-positive recipients may be at increased risk with HBcAb + donor livers, as they require simultaneous treatment with two antiviral regimens there may be deleterious interactions between the two viruses. Thus, the issue of HBcAb + donors for HCV-positive recipients merits more detailed analysis. Methods Using UNOS registry data of all liver transplantations performed during the Model for End-Stage Liver Disease era from February 2002 through November 2007, we analyzed graft survival using Kaplan-Meier and Cox regression analyses. Results Of the 12,543 HCV-positive recipients, 2,543 received HBcAb - livers and 853 received HBcAb + livers. While Kaplan- Meier analysis showed significantly lower graft survival among HCV-negative recipients of HBcAb + livers (P = .0001), there was no significant effect on graft survival among the HCV-positive population (P = .2). To detect an early effect in HCV-positive recipients, we examined 1-year graft survival, observing no significant difference (P = .3). To exclude a possible late effect, we examined graft survival in the HCV-positive population conditional upon surviving at least 1 year after transplantation; no significant difference was observed (P = .6). The elimination of potentially confounding codiagnoses, such as hepatitis B virus, alcoholism, acute graft failure, and hepatocellular cancer did not alter the findings. On univariate analysis, the lack of a significant effect persisted among the HCV population. However, the significant effect observed in the univariate model for the HCV-negative population became insignificant when combined with other risk factors in the multivariate model. Conclusion The use of HBcAb + livers in recipients with HCV did not appear to have a significant impact on grat survival.
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U2 - 10.1016/j.transproceed.2010.09.023
DO - 10.1016/j.transproceed.2010.09.023
M3 - Article
C2 - 21168646
AN - SCOPUS:78650440268
SN - 0041-1345
VL - 42
SP - 4141
EP - 4144
JO - Transplantation proceedings
JF - Transplantation proceedings
IS - 10
ER -