Kidney transplant from hepatitis C viremic donors into aviremic recipients and risk for post-transplant BK and cytomegalovirus infection.


Journal

Transplant infectious disease : an official journal of the Transplantation Society
ISSN: 1399-3062
Titre abrégé: Transpl Infect Dis
Pays: Denmark
ID NLM: 100883688

Informations de publication

Date de publication:
Aug 2022
Historique:
revised: 06 04 2022
received: 02 03 2022
accepted: 16 04 2022
pubmed: 27 6 2022
medline: 13 8 2022
entrez: 26 6 2022
Statut: ppublish

Résumé

kidney transplantation from Hepatitis C virus (HCV) viremic donors to uninfected recipients is associated with excellent short-term outcomes. However, HCV viremia might be associated with an increased risk for post-transplant viral complications. We designed a retrospective study of HCV-negative kidney-only transplant recipients between 2018 and 2020. Recipients were grouped into group 1; HCV-negative donors, and group 2; HCV-viremic donors. Patients were matched 1:1 using propensity score. The primary objectives were to compare the incidence of cytomegalovirus (CMV) viremia ≥ 200 ml/IU, and BK viremia ≥1000 copies/ml between the groups. Secondary outcomes included group comparison of CMV disease, BK viremia ≥10 000 copies/ml, and 1-year patient and allograft survival. The study included 634 patients in group 1, and 71 patients in group 2. Sixty-five pairs of patients were matched. Incidence of CMV viremia (33.3% vs. 40.0%, p = .4675), and BK viremia (15.9% vs. 27.7%, p = .1353) did not differ significantly between groups in the matched cohort. Incidence of CMV disease (81.0% vs. 76.9%, p = 1.000), and BK viremia ≥10 000 copies/ml (9.5% vs. 16.9%, p = .2987) were comparable between groups. There was no difference in the 1-year patient or allograft survival between groups. kidney transplant from HCV-viremic donors is not associated with increased risk for BK or CMV viremia.

Sections du résumé

BACKGROUND BACKGROUND
kidney transplantation from Hepatitis C virus (HCV) viremic donors to uninfected recipients is associated with excellent short-term outcomes. However, HCV viremia might be associated with an increased risk for post-transplant viral complications.
METHODS METHODS
We designed a retrospective study of HCV-negative kidney-only transplant recipients between 2018 and 2020. Recipients were grouped into group 1; HCV-negative donors, and group 2; HCV-viremic donors. Patients were matched 1:1 using propensity score. The primary objectives were to compare the incidence of cytomegalovirus (CMV) viremia ≥ 200 ml/IU, and BK viremia ≥1000 copies/ml between the groups. Secondary outcomes included group comparison of CMV disease, BK viremia ≥10 000 copies/ml, and 1-year patient and allograft survival.
RESULTS RESULTS
The study included 634 patients in group 1, and 71 patients in group 2. Sixty-five pairs of patients were matched. Incidence of CMV viremia (33.3% vs. 40.0%, p = .4675), and BK viremia (15.9% vs. 27.7%, p = .1353) did not differ significantly between groups in the matched cohort. Incidence of CMV disease (81.0% vs. 76.9%, p = 1.000), and BK viremia ≥10 000 copies/ml (9.5% vs. 16.9%, p = .2987) were comparable between groups. There was no difference in the 1-year patient or allograft survival between groups.
CONCLUSION CONCLUSIONS
kidney transplant from HCV-viremic donors is not associated with increased risk for BK or CMV viremia.

Identifiants

pubmed: 35752929
doi: 10.1111/tid.13887
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13887

Informations de copyright

© 2022 Wiley Periodicals LLC.

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Auteurs

Reem Daloul (R)

Division of Nephrology, Kidney and Pancreas Transplant Program, Allegheny General Hospital, Pittsburgh, Pennsylvania, USA.

Kendra Schnelle (K)

Department of Internal Medicine, Division of Pharmacy, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.

Lauren Von Stein (L)

Department of Internal Medicine, Division of Pharmacy, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.

April Logan (A)

Department of Surgery, Division of Transplantation, The Ohio State University College of Medicine, Columbus, Ohio, USA.

Priyamvada Singh (P)

Department of Internal Medicine, Division of Nephrology, The Ohio State University College of Medicine, Columbus, Ohio, USA.

Priya Yenebere (P)

Department of Internal Medicine, Division of Nephrology, The Ohio State University College of Medicine, Columbus, Ohio, USA.

Todd Pesavento (T)

Department of Internal Medicine, Division of Nephrology, The Ohio State University College of Medicine, Columbus, Ohio, USA.

Kenneth Washburn (K)

Department of Surgery, Division of Transplantation, The Ohio State University College of Medicine, Columbus, Ohio, USA.

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