Optimal timing of hepatitis C treatment among HIV/HCV coinfected ESRD patients: Pre- vs posttransplant.


Journal

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
ISSN: 1600-6143
Titre abrégé: Am J Transplant
Pays: United States
ID NLM: 100968638

Informations de publication

Date de publication:
06 2019
Historique:
received: 14 09 2018
revised: 28 11 2018
accepted: 13 12 2018
pubmed: 28 12 2018
medline: 15 7 2020
entrez: 28 12 2018
Statut: ppublish

Résumé

Patients with end-stage renal disease (ESRD) who are coinfected with hepatitis C virus (HCV) and human immunodeficiency virus (HIV) have access to effective treatment options for HCV infection. However, they also have access to HCV-infected kidneys, which historically afford shorter times to transplantation. Given the high waitlist mortality and rapid progression of liver fibrosis among coinfected kidney-only transplant candidates, identification of the optimal treatment strategy is paramount. Two strategies, treatment pre- and posttransplant, were compared using Monte Carlo microsimulation of 1 000 000 candidates. The microsimulation was stratified by liver fibrosis stage at waitlist addition and wait-time over a lifetime time horizon. Treatment posttransplant was consistently cost-saving as compared to treatment pretransplant due to the high cost of dialysis. Among patients with low fibrosis disease (F0-F1), treatment posttransplant also yielded higher life months (LM) and quality-adjusted life months (QALM), except among F1 candidates with wait times ≥ 18 months. For candidates with advanced liver disease (F2-F4), treatment pretransplant afforded more LM and QALM unless wait time was <18 months. Moreover, treatment pretransplant was cost-effective for F2 candidates with wait times >71 months and F3 candidates with wait times >18 months. Thus, optimal timing of HCV treatment differs based on liver disease severity and wait time, favoring pretransplant treatment when cirrhosis development prior to transplant seems likely.

Identifiants

pubmed: 30589503
doi: 10.1111/ajt.15239
pmc: PMC6538449
mid: NIHMS1003931
pii: S1600-6135(22)09125-0
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1806-1819

Subventions

Organisme : NIAID NIH HHS
ID : P30 AI042853
Pays : United States
Organisme : NIDA NIH HHS
ID : P30 DA040500
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA031059
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK117675
Pays : United States

Informations de copyright

© 2018 The American Society of Transplantation and the American Society of Transplant Surgeons.

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Auteurs

Brittany A Shelton (BA)

University of Alabama at Birmingham Comprehensive Transplant Institute, Birmingham, Alabama.

Gideon Berdahl (G)

University of Alabama at Birmingham Comprehensive Transplant Institute, Birmingham, Alabama.

Deirdre Sawinski (D)

University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.

Benjamin P Linas (BP)

Boston University School of Medicine, Boston, Massachusetts.

Peter P Reese (PP)

University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.

Margaux N Mustian (MN)

University of Alabama at Birmingham Comprehensive Transplant Institute, Birmingham, Alabama.

Rhiannon D Reed (RD)

University of Alabama at Birmingham Comprehensive Transplant Institute, Birmingham, Alabama.

Paul A MacLennan (PA)

University of Alabama at Birmingham Comprehensive Transplant Institute, Birmingham, Alabama.

Jayme E Locke (JE)

University of Alabama at Birmingham Comprehensive Transplant Institute, Birmingham, Alabama.

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