Pancreas transplantation from hepatitis C viremic donors to uninfected recipients
Despite utilization of hepatitis C viremic organs for hepatitis C naïve recipients (HCV D+/R‐) in other solid organ transplants, HCV viremic pancreata remain an unexplored source of donor organs. This study reports the first series of HCV D+/R‐ pancreas transplants. HCV D+/R‐ had shorter waitlist ti...
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Published in: | American journal of transplantation Vol. 21; no. 5; pp. 1931 - 1936 |
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Abstract | Despite utilization of hepatitis C viremic organs for hepatitis C naïve recipients (HCV D+/R‐) in other solid organ transplants, HCV viremic pancreata remain an unexplored source of donor organs. This study reports the first series of HCV D+/R‐ pancreas transplants. HCV D+/R‐ had shorter waitlist times compared to HCV D‐/R‐, waiting a mean of 16 days from listing for HCV‐positive organs. HCV D+/R‐ had a lower match allocation sequence than HCV D‐/R‐, and this correlated with receipt of organs with a lower Pancreas Donor Risk Index (PDRI) score. All HCV D+/R‐ had excellent graft function with a mean follow‐up of 438 days and had undetectable HCV RNA levels by a mean of 23 days after initiation of HCV‐directed therapy. The rates of infectious complications, reoperation, readmission, rejection, and length of stay were not impacted by donor HCV status. A national review of potential ideal pancreas donors found that 37% of ideal HCV‐negative pancreas allografts were transplanted, compared to only 5% of ideal HCV‐positive pancreas allografts. The results of the current study demonstrate the safety of accepting HCV‐positive pancreata for HCV‐naïve recipients and advocates for increased utilization of ideal HCV‐positive pancreas allografts.
Transplantation of hepatitis C viremic pancreata into hepatitis C naïve recipients yield excellent outcomes. |
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AbstractList | Despite utilization of hepatitis C viremic organs for hepatitis C naïve recipients (HCV D+/R-) in other solid organ transplants, HCV viremic pancreata remain an unexplored source of donor organs. This study reports the first series of HCV D+/R- pancreas transplants. HCV D+/R- had shorter waitlist times compared to HCV D-/R-, waiting a mean of 16 days from listing for HCV-positive organs. HCV D+/R- had a lower match allocation sequence than HCV D-/R-, and this correlated with receipt of organs with a lower Pancreas Donor Risk Index (PDRI) score. All HCV D+/R- had excellent graft function with a mean follow-up of 438 days and had undetectable HCV RNA levels by a mean of 23 days after initiation of HCV-directed therapy. The rates of infectious complications, reoperation, readmission, rejection, and length of stay were not impacted by donor HCV status. A national review of potential ideal pancreas donors found that 37% of ideal HCV-negative pancreas allografts were transplanted, compared to only 5% of ideal HCV-positive pancreas allografts. The results of the current study demonstrate the safety of accepting HCV-positive pancreata for HCV-naïve recipients and advocates for increased utilization of ideal HCV-positive pancreas allografts. Despite utilization of hepatitis C viremic organs for hepatitis C naïve recipients (HCV D+/R‐) in other solid organ transplants, HCV viremic pancreata remain an unexplored source of donor organs. This study reports the first series of HCV D+/R‐ pancreas transplants. HCV D+/R‐ had shorter waitlist times compared to HCV D‐/R‐, waiting a mean of 16 days from listing for HCV‐positive organs. HCV D+/R‐ had a lower match allocation sequence than HCV D‐/R‐, and this correlated with receipt of organs with a lower Pancreas Donor Risk Index (PDRI) score. All HCV D+/R‐ had excellent graft function with a mean follow‐up of 438 days and had undetectable HCV RNA levels by a mean of 23 days after initiation of HCV‐directed therapy. The rates of infectious complications, reoperation, readmission, rejection, and length of stay were not impacted by donor HCV status. A national review of potential ideal pancreas donors found that 37% of ideal HCV‐negative pancreas allografts were transplanted, compared to only 5% of ideal HCV‐positive pancreas allografts. The results of the current study demonstrate the safety of accepting HCV‐positive pancreata for HCV‐naïve recipients and advocates for increased utilization of ideal HCV‐positive pancreas allografts. Transplantation of hepatitis C viremic pancreata into hepatitis C naïve recipients yield excellent outcomes. Despite utilization of hepatitis C viremic organs for hepatitis C naïve recipients (HCV D+/R‐) in other solid organ transplants, HCV viremic pancreata remain an unexplored source of donor organs. This study reports the first series of HCV D+/R‐ pancreas transplants. HCV D+/R‐ had shorter waitlist times compared to HCV D‐/R‐, waiting a mean of 16 days from listing for HCV‐positive organs. HCV D+/R‐ had a lower match allocation sequence than HCV D‐/R‐, and this correlated with receipt of organs with a lower Pancreas Donor Risk Index (PDRI) score. All HCV D+/R‐ had excellent graft function with a mean follow‐up of 438 days and had undetectable HCV RNA levels by a mean of 23 days after initiation of HCV‐directed therapy. The rates of infectious complications, reoperation, readmission, rejection, and length of stay were not impacted by donor HCV status. A national review of potential ideal pancreas donors found that 37% of ideal HCV‐negative pancreas allografts were transplanted, compared to only 5% of ideal HCV‐positive pancreas allografts. The results of the current study demonstrate the safety of accepting HCV‐positive pancreata for HCV‐naïve recipients and advocates for increased utilization of ideal HCV‐positive pancreas allografts. |
Author | Soomro, Irfana Stewart, Zoe A. Mattoo, Aprajita Ali, Nicole M. Gelb, Bruce E. Lonze, Bonnie E. Tatapudi, Vashista S. Baptiste, Gillian Dagher, Nabil N. Montgomery, Robert A. |
Author_xml | – sequence: 1 givenname: Bonnie E. orcidid: 0000-0002-0973-1657 surname: Lonze fullname: Lonze, Bonnie E. organization: NYU Langone Health – sequence: 2 givenname: Gillian surname: Baptiste fullname: Baptiste, Gillian organization: NYU Langone Health – sequence: 3 givenname: Nicole M. surname: Ali fullname: Ali, Nicole M. organization: NYU Langone Health – sequence: 4 givenname: Nabil N. surname: Dagher fullname: Dagher, Nabil N. organization: NYU Langone Health – sequence: 5 givenname: Bruce E. surname: Gelb fullname: Gelb, Bruce E. organization: NYU Langone Health – sequence: 6 givenname: Aprajita surname: Mattoo fullname: Mattoo, Aprajita organization: NYU Langone Health – sequence: 7 givenname: Irfana surname: Soomro fullname: Soomro, Irfana organization: NYU Langone Health – sequence: 8 givenname: Vashista S. surname: Tatapudi fullname: Tatapudi, Vashista S. organization: NYU Langone Health – sequence: 9 givenname: Robert A. surname: Montgomery fullname: Montgomery, Robert A. organization: NYU Langone Health – sequence: 10 givenname: Zoe A. orcidid: 0000-0002-9074-5086 surname: Stewart fullname: Stewart, Zoe A. email: zoe.stewartlewis@nyulangone.org organization: NYU Langone Health |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33346951$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1056/NEJM199108153250702 10.1111/ctr.13989 10.5414/CN108858 10.1016/j.healun.2019.08.019 10.1111/j.1600-6143.2009.02996.x 10.7326/M17-2451 10.1111/ajt.15162 10.1016/S2468-1253(20)30081-9 10.1111/tid.13204 10.1097/TP.0000000000002949 10.1164/rccm.201712-2614LE 10.7326/M17-2871 10.1111/ajt.15673 10.1053/ajkd.2003.50057 10.1056/NEJMoa1812406 10.1002/hep.30540 10.1111/j.1600-6143.2009.02931.x 10.1111/ctr.13755 10.1111/ajt.14701 10.1097/TP.0000000000001673 10.1002/hep.29258 10.1900/RDS.2016.13.35 10.7326/M16-2575 10.1056/NEJMc1705221 10.1097/MD.0000000000007568 10.15585/mmwr.mm655051e1 10.1111/j.1399-0012.2009.01195.x |
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Copyright | 2020 The American Society of Transplantation and the American Society of Transplant Surgeons 2020 The American Society of Transplantation and the American Society of Transplant Surgeons. 2021 The American Society of Transplantation and the American Society of Transplant Surgeons |
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Keywords | pancreas / simultaneous pancreas-kidney transplantation infectious disease infection and infectious agents - viral: hepatitis C organ procurement and allocation donors and donation: deceased clinical research / practice organ allocation Scientific Registry for Transplant Recipients (SRTR) |
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Snippet | Despite utilization of hepatitis C viremic organs for hepatitis C naïve recipients (HCV D+/R‐) in other solid organ transplants, HCV viremic pancreata remain... Despite utilization of hepatitis C viremic organs for hepatitis C naïve recipients (HCV D+/R-) in other solid organ transplants, HCV viremic pancreata remain... |
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SubjectTerms | Allografts Blood & organ donations clinical research / practice Donors donors and donation: deceased Graft rejection Hepacivirus Hepatitis Hepatitis C Humans infection and infectious agents ‐ viral: hepatitis C infectious disease Kidney transplants organ allocation organ procurement and allocation Pancreas pancreas / simultaneous pancreas‐kidney transplantation Pancreas Transplantation Pancreas transplants Scientific Registry for Transplant Recipients (SRTR) Tissue Donors Transplants & implants Viremia Xenografts |
Title | Pancreas transplantation from hepatitis C viremic donors to uninfected recipients |
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