4.7 Article

Nucleic Acid Testing for Diagnosis of Perinatally Acquired Hepatitis C Virus Infection in Early Infancy

Journal

CLINICAL INFECTIOUS DISEASES
Volume 73, Issue 9, Pages E3340-E3346

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciaa949

Keywords

hepatitis C virus; vertical transmission; perinatal infection; nucleic acid amplification test

Funding

  1. National Institutes of Health [R01-AI096882, UL1TR002733]
  2. National Center for Advancing Translational Sciences
  3. Abigail Wexner Research Institute at Nationwide Children's Hospital

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This study aimed to investigate the sensitivity of modern HCV-RNA RT-PCR platforms for early diagnosis of perinatally acquired infection. The results showed that early HCV-RNA screening demonstrated 100% sensitivity and 100% specificity in detecting infected infants, highlighting its potential for aiding HCV surveillance and diagnosis in this population.
Background. Most US children with perinatal hepatitis C virus (HCV) exposure fail to receive the recommended anti-HCV antibody test at age >= 18 months. Earlier testing for viral RNA might facilitate increased screening, but sensitivity of this approach has not been established. We hypothesized that modern HCV-RNA RT-PCR platforms would adequately detect infected infants. Methods. Nationwide Children's Hospital electronic health records from 1/1/2008 to 30/6/2018 were reviewed to identify perinatally exposed infants tested by HCV-RNA RT-PCR at age 2-6 months. Diagnostic performance was determined using a composite case definition: (1) infected children had positive repeat HCV-RNA testing or positive anti-HCV at age >= 24 months; (2) uninfected children lacked these criteria and had negative anti-HCV at age >= 18 months. Results. 770 perinatally exposed infants underwent HCV-RNA testing at age 2-6 months. Of these, 28 (3.6%) tested positive; viremia was confirmed in all who underwent repeat testing (n = 27). Among 742 infants with negative HCV-RNA results, 226 received follow-up anti-HCV testing at age =18 months, of whom 223 tested negative. Three children had low-positive anti-HCV results at age 18-24 months that were negative upon retesting after age 24 months, possibly indicating waning maternal antibodies. Using the composite case definitions, early HCV-RNA screening demonstrated sensitivity of 100% (87.5-100%, Wilson-Brown 95% CI) and specificity of 100% (98.3-100%). Conclusions. Modern HCV-RNA RT-PCR assays have excellent sensitivity for early diagnosis of perinatally acquired infection and could aid HCV surveillance given the substantial loss to follow-up at >= 18 months of age.

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