Factors associated with hepatitis C antibody seroconversion after transplantation of kidneys from hepatitis C infected donors to hepatitis C naïve recipients.


Journal

Renal failure
ISSN: 1525-6049
Titre abrégé: Ren Fail
Pays: England
ID NLM: 8701128

Informations de publication

Date de publication:
Nov 2020
Historique:
entrez: 31 7 2020
pubmed: 31 7 2020
medline: 15 5 2021
Statut: ppublish

Résumé

We aimed to assess the probability and factors associated with the presence of hepatitis C virus (HCV) antibody among HCV seronegative kidney transplant recipients receiving HCV-infected (nucleic acid testing positive) donor kidneys. This is a retrospective review examining HCV antibody seroconversion of all kidney transplant recipients receiving an organ from an HCV-infected donor between 1 March 2018 and 2 December 2019 at a high-volume kidney transplant center in the southeast United States. Of 97 patients receiving HCV-infected kidneys, the final cohort consisted of 85 recipients with 5 (5.9%) recipients noted to have HCV antibody seroconversion in the setting of HCV viremia. The HCV RNA level at closest time of antibody measurement was higher in the seroconverted patients versus the ones who never converted [median and (interquartile range): 1,091,500 (345,000-8,360,000) vs 71,500 (73-313,000), HCV antibody should not be considered routine screening for presence of infection in previously HCV naïve kidney transplant recipients receiving kidneys from HCV-infected donors, as only a modest percentage have antibody despite active viremia. The assessment of HCV viral load should be routine in all transplant recipients receiving organs from public health service increased risk donors.

Sections du résumé

BACKGROUND BACKGROUND
We aimed to assess the probability and factors associated with the presence of hepatitis C virus (HCV) antibody among HCV seronegative kidney transplant recipients receiving HCV-infected (nucleic acid testing positive) donor kidneys.
METHODS METHODS
This is a retrospective review examining HCV antibody seroconversion of all kidney transplant recipients receiving an organ from an HCV-infected donor between 1 March 2018 and 2 December 2019 at a high-volume kidney transplant center in the southeast United States.
RESULTS RESULTS
Of 97 patients receiving HCV-infected kidneys, the final cohort consisted of 85 recipients with 5 (5.9%) recipients noted to have HCV antibody seroconversion in the setting of HCV viremia. The HCV RNA level at closest time of antibody measurement was higher in the seroconverted patients versus the ones who never converted [median and (interquartile range): 1,091,500 (345,000-8,360,000) vs 71,500 (73-313,000),
CONCLUSIONS CONCLUSIONS
HCV antibody should not be considered routine screening for presence of infection in previously HCV naïve kidney transplant recipients receiving kidneys from HCV-infected donors, as only a modest percentage have antibody despite active viremia. The assessment of HCV viral load should be routine in all transplant recipients receiving organs from public health service increased risk donors.

Identifiants

pubmed: 32729359
doi: 10.1080/0886022X.2020.1798784
pmc: PMC7472509
doi:

Substances chimiques

Hepatitis C Antibodies 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

767-775

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Auteurs

Uchenna Agbim (U)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.

Orsolya Cseprekal (O)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Department of Surgery, University of Tennessee Health Science Center, Memphis, TN, USA.
Department of Transplantation and Surgery, Semmelweis University, Budapest, Hungary.

Masahiko Yazawa (M)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Department of Surgery, University of Tennessee Health Science Center, Memphis, TN, USA.
Division of Nephrology and Hypertension, St. Marianna University School of Medicine, Tokyo, Japan.

Manish Talwar (M)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Department of Surgery, University of Tennessee Health Science Center, Memphis, TN, USA.

Vasanthi Balaraman (V)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Department of Surgery, University of Tennessee Health Science Center, Memphis, TN, USA.

Anshul Bhalla (A)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Department of Surgery, University of Tennessee Health Science Center, Memphis, TN, USA.

Pradeep S B Podila (PSB)

Faith and Health Division, Methodist Le Bonheur Healthcare, Memphis, TN, USA.
Division of Health Systems Management and Policy, School of Public Health, The University of Memphis, Memphis, TN, USA.

Benedict Maliakkal (B)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Department of Surgery, University of Tennessee Health Science Center, Memphis, TN, USA.

Satheesh Nair (S)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Department of Surgery, University of Tennessee Health Science Center, Memphis, TN, USA.

James D Eason (JD)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Department of Surgery, University of Tennessee Health Science Center, Memphis, TN, USA.

Miklos Z Molnar (MZ)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Department of Surgery, University of Tennessee Health Science Center, Memphis, TN, USA.
Department of Transplantation and Surgery, Semmelweis University, Budapest, Hungary.

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