Survey of Clinician Opinions on Kidney Transplantation from Hepatitis C Virus Positive Donors: Identifying and Overcoming Barriers.


Journal

Kidney360
ISSN: 2641-7650
Titre abrégé: Kidney360
Pays: United States
ID NLM: 101766381

Informations de publication

Date de publication:
Nov 2020
Historique:
entrez: 30 11 2020
pubmed: 1 12 2020
medline: 1 12 2020
Statut: ppublish

Résumé

Transplant practices related to use of organs from Hepatitis C virus infected donors (DHCV+) is evolving rapidly. We surveyed U.S. kidney transplant programs by email and professional society listserv postings between 7/19-1/20 to assess attitudes, management strategies, and barriers related to use of viremic (nucleic acid testing (NAT)+) donor organs in HCV uninfected recipients. Staff at 112 unique programs responded, representing 54% of U.S. adult kidney transplant programs and 69% of adult deceased donor kidney transplant volume in 2019. Most survey respondents were transplant nephrologists (46%) or surgeons (43%). Among responding programs, 67% currently transplant DHCV antibody+/NAT- organs under a clinical protocol or as standard of care. By comparison, only 58% offer DHCV NAT+ kidney transplant to HCV- recipients, including 35% under clinical protocols, 14% as standard of care, and 9% under research protocols. Following transplant of DHCV NAT+ organs to uninfected recipients, 53% start direct acting antiviral agent (DAA) therapy after discharge and documented viremia. Viral monitoring protocols after DHCV NAT+ to HCV uninfected recipient kidney transplantation varied substantially. 56% of programs performing these transplants report having an institutional plan to provide DAA treatment if declined by the recipient's insurance. Respondents felt a mean decrease in waiting time of ≥18 months (range 0-60) justifies the practice. Program concerns related to use of DHCV NAT+ kidneys include insurance coverage concerns (72%), cost (60%), and perceived risk of transmitting resistant infection (44%). Addressing knowledge about safety and logistical/financial barriers related to use of DHCV NAT+ kidney transplantation for HCV uninfected recipients may help reduced discards and expand the organ supply.

Sections du résumé

BACKGROUND BACKGROUND
Transplant practices related to use of organs from Hepatitis C virus infected donors (DHCV+) is evolving rapidly.
METHODS METHODS
We surveyed U.S. kidney transplant programs by email and professional society listserv postings between 7/19-1/20 to assess attitudes, management strategies, and barriers related to use of viremic (nucleic acid testing (NAT)+) donor organs in HCV uninfected recipients.
RESULTS RESULTS
Staff at 112 unique programs responded, representing 54% of U.S. adult kidney transplant programs and 69% of adult deceased donor kidney transplant volume in 2019. Most survey respondents were transplant nephrologists (46%) or surgeons (43%). Among responding programs, 67% currently transplant DHCV antibody+/NAT- organs under a clinical protocol or as standard of care. By comparison, only 58% offer DHCV NAT+ kidney transplant to HCV- recipients, including 35% under clinical protocols, 14% as standard of care, and 9% under research protocols. Following transplant of DHCV NAT+ organs to uninfected recipients, 53% start direct acting antiviral agent (DAA) therapy after discharge and documented viremia. Viral monitoring protocols after DHCV NAT+ to HCV uninfected recipient kidney transplantation varied substantially. 56% of programs performing these transplants report having an institutional plan to provide DAA treatment if declined by the recipient's insurance. Respondents felt a mean decrease in waiting time of ≥18 months (range 0-60) justifies the practice. Program concerns related to use of DHCV NAT+ kidneys include insurance coverage concerns (72%), cost (60%), and perceived risk of transmitting resistant infection (44%).
CONCLUSIONS CONCLUSIONS
Addressing knowledge about safety and logistical/financial barriers related to use of DHCV NAT+ kidney transplantation for HCV uninfected recipients may help reduced discards and expand the organ supply.

Identifiants

pubmed: 33251523
doi: 10.34067/KID.0004592020
pmc: PMC7695231
mid: NIHMS1629882
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Pagination

1291-1299

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK120518
Pays : United States

Déclaration de conflit d'intérêts

DISCLOSURES The authors of this manuscript have no conflicts of interest to disclose. KLL serves on the ASN Quality Committee and RMB serves on the ASN Policy Committee.

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Auteurs

Krista L Lentine (KL)

Saint Louis University Center for Abdominal Transplantation, St. Louis, MO.

John D Peipert (JD)

Northwestern University, Feinberg School of Medicine, Chicago, IL.
Northwestern University Transplant Outcomes Research Core, Chicago, IL.

Tarek Alhamad (T)

Washington University, Saint Louis, MO.

Yasar Caliskan (Y)

Saint Louis University Center for Abdominal Transplantation, St. Louis, MO.

Beatrice P Concepcion (BP)

Vanderbilt Transplant Center, Nashville, TN.

Rachel Forbes (R)

Vanderbilt Transplant Center, Nashville, TN.

Mark Schnitzler (M)

Saint Louis University Center for Abdominal Transplantation, St. Louis, MO.

Su-Hsin Chang (SH)

Washington University, Saint Louis, MO.

Matthew Cooper (M)

Medstar Georgetown Transplant Institute, Washington, DC.

Roy D Bloom (RD)

University of Pennsylvania, Philadelphia, PA.

Roslyn B Mannon (RB)

University of Nebraska, Omaha, NB.

David A Axelrod (DA)

University of Iowa, Iowa City, IA.

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Classifications MeSH