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
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
269-279Subventions
Organisme : NIA NIH HHS
ID : F32 AG067642
Pays : United States
Informations de copyright
© 2022 The Author(s).
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