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Treatment of chronic viral hepatitis C in children and adolescents: UK experience
  1. M Abdel-Hady1,
  2. S Bansal2,
  3. S M Davison3,
  4. M Brown1,
  5. S A Tizzard2,
  6. S Mulla3,
  7. E Barnes4,
  8. P Davies5,
  9. G Mieli-Vergani2,
  10. D A Kelly1
  1. 1Liver Unit, Birmingham Children's Hospital, Birmingham, UK
  2. 2Children's Liver Centre, King's College Hospital, London, UK
  3. 3Liver Unit, Leeds Teaching Hospitals, Leeds, UK
  4. 4Peter Medawar Building for Pathogen Research and Oxford NIHR BRC, Oxford University, Oxford, UK
  5. 5Institute of Child's Health, Birmingham Children's Hospital, Birmingham, UK
  1. Correspondence to Dr M Abdel-Hady, Liver Unit, Birmingham Children's Hospital, Steelhouse Lane, Birmingham B4 6NH, UK; mona.abdelhady{at}bch.nhs.uk

Abstract

Aim To review the efficacy and tolerability of pegylated interferon-α and ribavirin for treatment of chronic hepatitis C (CHC) in children in the UK.

Methods Retrospective review of children treated for CHC in 3 UK paediatric specialist liver centres between 2005 and 2010. Data on viral response to treatment, demographic and clinical details were collected. Treatment outcome was assessed by the absence of detectable viral RNA in blood 24 weeks after treatment—sustained viral response (SVR).

Results 75 children were included; 34 genotype 1; 39 genotypes 2 and 3; 2 genotype 4. Overall SVR was achieved in 54/71 (76%); 65% genotype 1; 89% genotypes 2 and 3; 100% genotype 4. Early response at 12 weeks was achieved in 53 and sustained in 47 (89%). Data on rapid response after 4 weeks of treatment were available in 25; 17/25 (68%) responded and 16 of these (94%) achieved SVR. IL28 T/T genotype was associated with higher SVR. There were no significant changes in weight and height z scores from baseline compared with 24 weeks post-treatment follow-up. No child discontinued treatment due to side effects, although 43 required dose modification. Treatment affected quality of life (QoL) in the initial 12 weeks of treatment, which improved by the end of treatment.

Conclusions Children respond well to therapy for CHC. Treatment was tolerated with minimal impact on QoL and no significant effect on growth. Knowledge of viral and IL28 genotypes and early viral response is useful to plan treatment in children and provide appropriate counselling.

  • Hepatology
  • Infectious Diseases

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