Emergency department targeted screening for hepatitis C does not improve linkage to care

Inbal Houri1, Noya Horowitz1, Helena Katchman1

  • 1Department of Gastroenterology and Hepatology, Tel-Aviv Medical Center, Tel-Aviv 6423906, Israel.

Insights

Emergency department screening identified Hepatitis C virus (HCV) carriers among high-risk individuals, but did not increase antiviral treatment rates. New strategies are needed to improve care linkage for these patients.

Area of Science:

  • Hepatology
  • Infectious Diseases
  • Public Health

Background:

  • Hepatitis C virus (HCV) infection is a major cause of chronic liver disease globally.
  • New HCV treatments aim for viral elimination by 2030, necessitating effective screening strategies.
  • Emergency departments present an opportunity to identify asymptomatic HCV carriers.

Purpose of the Study:

  • To identify undiagnosed HCV carriers in high-risk emergency department attendees.
  • To link these identified carriers to antiviral treatment.

Main Methods:

  • A prospective, single-center study screened emergency department attendees using a risk factor questionnaire.
  • Screened risk factors included blood product exposure, high-prevalence country origin, drug use, HIV status, MSM, maternal HCV, incarceration history, and CKD.
  • HCV testing utilized serum antibody tests and/or an oral fluid test (OraQuick®).

Main Results:

  • Of 541 participants with risk factors, 3.1% tested positive for HCV, exceeding the local incidence (1.96%).
  • Positive cases were predominantly individuals who inject drugs (82%) or had a history of incarceration (64%).
  • Despite identification, 1-year follow-up showed no completed HCV-RNA testing, hepatology visits, or antiviral treatment initiation.

Conclusions:

  • Targeted HCV screening in emergency departments can identify undiagnosed carriers.
  • Current screening strategies in this setting do not effectively improve linkage to care and treatment rates.
  • Alternative approaches are required to enhance treatment access for high-risk populations.
Abstract

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