Trends and three-year outcomes of hepatitis C virus-viremic donor heart transplant for hepatitis C virus-seronegative recipients.

D+, HCV-viremic donor DAAs, direct-acting antivirals DCD, donation after circulatory death D–, HCV-seronegative donor ECMO, extracorporeal membranous oxygenation HCV, hepatitis C virus HT, heart transplant IABP, intra-aortic balloon pump IQR, interquartile range LVAD, left ventricular assist device MCS, mechanical circulatory support R–, HCV-seronegative recipient SRTR, Scientific Registry of Transplant Recipients aHR, adjusted hazard ratio aOR, adjusted odds ratio donor pool heart transplant hepatitis C outcomes

Journal

JTCVS open
ISSN: 2666-2736
Titre abrégé: JTCVS Open
Pays: Netherlands
ID NLM: 101768541

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 21 07 2021
revised: 17 10 2022
accepted: 24 10 2022
entrez: 2 1 2023
pubmed: 3 1 2023
medline: 3 1 2023
Statut: epublish

Résumé

Heart transplants (HTs) from hepatitis C virus (HCV)-viremic donors to HCV-seronegative recipients (HCV D+/R-) have good 6-month outcomes, but practice uptake and long-term outcomes overall and among candidates on mechanical circulatory support (MCS) have yet to be established. Using the Scientific Registry of Transplant Recipients, we identified US adult HCV-seronegative HT recipients (R-) from 2015 to 2021. We classified donors as HCV-seronegative (D-) or HCV-viremic (D+). We used multivariable regression to compare post-HT extracorporeal membranous oxygenation, dialysis, pacemaker, acute rejection, and risk of post-HT mortality between HCV D+/R- and HCV D-/R-. Models were adjusted for donor, recipient, and transplant characteristics and center HT volume. We performed subgroup analyses of recipients bridged with MCS. From 2015 to 2021, the number of HCV D+/R- HT increased from 1 to 181 and the number of centers performing HCV D+/R- HT increased from 1 to 60. Compared with HCV D-/R- recipients, HCV D+/R- versus D-/R- recipients overall and among patients bridged with MCS had similar odds of post-HT extracorporeal membranous oxygenation, dialysis, pacemaker, and acute rejection; and mortality risk at 30 days, 1 year, and 3 years (all HCV D+/R- and D-/R- HT have similar outcomes at 3 years' posttransplant. These results underscore the opportunity provided by HCV D+/R- HT, including among the growing population bridged with MCS, and the potential benefit of further expanding use of HCV+ allografts.

Identifiants

pubmed: 36590744
doi: 10.1016/j.xjon.2022.10.007
pii: S2666-2736(22)00372-2
pmc: PMC9801334
doi:

Types de publication

Journal Article

Langues

eng

Pagination

269-279

Subventions

Organisme : NIA NIH HHS
ID : F32 AG067642
Pays : United States

Informations de copyright

© 2022 The Author(s).

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Auteurs

Jessica M Ruck (JM)

Division of Cardiac Surgery, Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Md.

Alice L Zhou (AL)

Division of Cardiac Surgery, Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Md.

Laura B Zeiser (LB)

Division of Cardiac Surgery, Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Md.

Diane Alejo (D)

Division of Cardiac Surgery, Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Md.

Christine M Durand (CM)

Division of Infection Disease, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Md.

Allan B Massie (AB)

Division of Transplant Surgery, Department of Surgery, NYU Langone Health, New York, NY.

Dorry L Segev (DL)

Division of Transplant Surgery, Department of Surgery, NYU Langone Health, New York, NY.
Scientific Registry of Transplant Recipients, Minneapolis, Minn.

Errol L Bush (EL)

Division of Cardiac Surgery, Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Md.

Ahmet Kilic (A)

Division of Cardiac Surgery, Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Md.

Classifications MeSH