Evidence map›Paper›PMID 23703847›Full record

ArticleHepatology (Baltimore, Md.)2013

Evaluating progression of liver disease from repeat liver biopsies in children with chronic hepatitis C: a retrospective study.

Parvathi Mohan, Bruce A Barton, Michael R Narkewicz, Jean P Molleston, Regino P Gonzalez-Peralta, Philip Rosenthal, Karen F Murray, Barbara Haber, Kathleen B Schwarz, Zachary D Goodman

Abstract readMulticenter Study
In one paragraph

Article in Hepatology (Baltimore, Md.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 4 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Guideline
  2. Guideline
  3. KASL clinical practice guidelines: management of hepatitis C.Clinical and molecular hepatology · 2016
    Guideline
  4. KASL clinical practice guidelines: management of hepatitis C.Clinical and molecular hepatology · 2014
    Guideline
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. CDC Recommendations for Hepatitis C Testing Among Perinatally Exposed Infants and Children - United States, 2023.MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports · 2023
    Article
  11. Review
  12. Adolescent Hepatitis C: Prevalence, Impact, and Management Challenges.Adolescent health, medicine and therapeutics · 2021
    Review
  13. Review
  14. Article
  15. Article
  16. Observational
  17. Article
  18. Review
  19. [The guideline of prevention and treatment for hepatitis C: a 2015 update].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2015
    Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Parvathi MohanChildren's National Medical Center, The George Washington School of Medicine, Washington, DC.
Bruce A Barton
Michael R Narkewicz
Jean P Molleston
Regino P Gonzalez-Peralta
Philip Rosenthal
Karen F Murray
Barbara Haber
Kathleen B Schwarz
Zachary D Goodman

Funding

Pegylated Interferon +/- Ribavirin for Children with HCVU01DK067767 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI SCHWARZ, KATHLEEN · 2003 to 2008
$3.9M
NIDDK NIH HHS U01 DK067767
6 · The paper itself

Abstract

unlabelledClinical and histologic progression of liver disease in untreated children with chronic hepatitis C virus (HCV) infection is poorly documented. The aim of this retrospective study was to characterize changes in liver histology over time in a cohort of HCV-infected children who had more than one liver biopsy separated by over 1 year. Forty-four untreated children without concurrent liver diseases, who had repeat liver biopsies at eight U.S.-based medical centers, were included. Biopsies were scored by a single pathologist for inflammation, fibrosis, and steatosis and were correlated with demographic data including age at biopsy, time from infection to biopsies, and laboratory values such as serum alanine aminotransferase (ALT). Mode of transmission was vertical in 25 (57%) and from transfusions in 17 children (39%). Genotype 1 was present in 30/35 (84%) children. The mean age at first and final biopsy was 8.6 and 14.5 years, respectively, and the mean interval between biopsies was 5.8 ± 3.5 years. Duration of infection to biopsy was 7.7 and 13.5 years, respectively. Laboratory values did not change significantly between the biopsies. Inflammation was minimal in about 50% at both timepoints. Fibrosis was absent in 16% in both biopsies, limited to portal/periportal in 73% in the first biopsy, and 64% in the final biopsy. Between the two biopsies, the proportion of patients with bridging fibrosis/cirrhosis increased from 11% to 20% (P = 0.005).

conclusionAlthough in aggregate this cohort did not show significant histologic progression of liver disease over 5 years, 29.5% (n = 13) of children showed an increase in severity of fibrosis. These findings may have long-term implications for the timing of follow-up biopsies and treatment decisions.

Indexed as

AdolescentAlanine TransaminaseBiopsyChildChild, PreschoolDisease ProgressionFemaleHepatitis C, ChronicHumansInfantLiverLiver CirrhosisMaleRetrospective StudiesSeverity of Illness IndexAlanine Transaminase

Identifiers

PMID23703847
PMCPMC5493995

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.