Optimal timing of hepatitis C treatment among HIV/HCV coinfected ESRD patients: Pre- vs posttransplant.
Antiviral Agents
/ administration & dosage
Coinfection
/ complications
Computer Simulation
Cost Savings
Cost-Benefit Analysis
Disease Progression
Drug Administration Schedule
Female
HIV Infections
/ complications
Hepatitis C, Chronic
/ complications
Humans
Kidney Failure, Chronic
/ complications
Kidney Transplantation
Liver Cirrhosis
/ complications
Male
Middle Aged
Monte Carlo Method
Postoperative Period
Preoperative Period
Quality-Adjusted Life Years
Renal Dialysis
/ economics
Waiting Lists
health services and outcomes research
infection and infectious agents - viral: hepatitis C
infection and infectious agents - viral: human immunodeficiency virus (HIV)/acquired immunodeficiency syndrome (AIDS)
kidney transplantation/nephrology
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
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
1806-1819Subventions
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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