Cost-Effectiveness of Strategies for Treatment Timing for Perinatally Acquired Hepatitis C Virus

Megan Rose Curtis1,2,3,4,5,6, Rachel L Epstein5,6,7, Pamela Pei1

  • 1Medical Practice Evaluation Center, Massachusetts General Hospital, Boston.

JAMA Pediatrics
|March 11, 2024
PubMed

Insights

Early direct-acting antiviral (DAA) therapy for children with hepatitis C virus (HCV) infection at age 3 significantly reduces lifetime healthcare costs and increases life expectancy. Treating young children with HCV offers substantial clinical and economic benefits.

Area of Science:

  • Hepatology
  • Pediatric Infectious Diseases
  • Health Economics

Background:

  • Chronic hepatitis C virus (HCV) infection is increasing among pregnant individuals in the US, with vertical transmission occurring in 7-8% of births.
  • Direct-acting antiviral (DAA) therapy is now approved for children aged 3 years and older with HCV.
  • The comparative clinical and economic impact of early DAA therapy in young children with HCV remains largely unknown.

Purpose of the Study:

  • To develop a state-transition model to project clinical and economic outcomes for children with perinatally acquired HCV.
  • To investigate the cost-effectiveness of initiating DAA treatment at various ages in children with HCV.

Main Methods:

  • A state-transition model simulated the natural history and disease progression of perinatally acquired HCV in a cohort of 1000 US children from age 3 through death.
  • The model compared treatment strategies involving 8 weeks of DAA therapy initiated at ages 3, 6, 12, or 18 years, alongside a no-treatment comparator.
  • Key outcomes included projected life expectancy, average lifetime healthcare costs, and the incidence of cirrhosis, decompensated cirrhosis, and hepatocellular carcinoma (HCC).

Main Results:

  • Treating HCV at age 3 was associated with lower mean lifetime healthcare costs ($148,162) compared to deferring treatment until ages 6 ($164,292), 12 ($171,909), or 18 ($195,374).
  • Projected life expectancy was longest when treatment began at age 3 (78.36 life years), decreasing with delayed treatment initiation.
  • Early treatment at age 3 prevented an estimated 89 cases of cirrhosis, 27 cases of HCC, and 74 liver-related deaths per 1000 children compared to delaying treatment until age 6.

Conclusions:

  • DAA therapy initiated at age 3 for children with HCV is projected to reduce overall healthcare costs and improve survival compared to delaying treatment until age 6 or older.
  • Early intervention with DAA therapy offers significant clinical benefits, including reduced incidence of severe liver disease and mortality.
  • Enhancing access to DAA therapy for young children is crucial for realizing the full clinical and economic advantages of early HCV treatment.
Abstract