Evidence map›Paper›PMID 25233195›Full record

ReviewJournal of perinatology : official journal of the California Perinatal Association2014

Hepatitis B and C in pregnancy: a review and recommendations for care.

J C Dunkelberg, E M F Berkley, K W Thiel, K K Leslie

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of perinatology : official journal of the California Perinatal Association, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 3 pooled it
7.3field-weighted citation impact, top 2% of its field
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

32 citing papers in PubMed, 3 syntheses or guidelines pooled it, 112 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Therapeutic, preventive, and pathogenetic advances in viral hepatitis.Frontiers in cellular and infection microbiology · 2026
    Review
  5. Article
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  7. Review
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  12. Viral hepatitis and pregnancy.Nature reviews. Gastroenterology & hepatology · 2021
    Review
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  19. Review
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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

4 authors at 2 institutions in 1 country.

J C DunkelbergDepartment of Internal Medicine, University of Iowa Hospitals and Clinics, Iowa City, IA, USA.
E M F BerkleyDepartment of Obstetrics and Gynecology, Eastern Virginia Medical School, Norfolk, VA, USA.
K W ThielDepartment of Obstetrics and Gynecology, University of Iowa Hospitals and Clinics, Iowa City, IA, USA.
K K LeslieDepartment of Obstetrics and Gynecology, University of Iowa Hospitals and Clinics, Iowa City, IA, USA.
University of Iowa Hospitals and Clinics · USEastern Virginia Medical School · US

Funding

The Iowa Women's Reproductive Health Research Career Development CenterK12HD063117 · NICHD · UNIVERSITY OF IOWA · PI LESLIE, KIMBERLY K. · 2009 to 2013
$2.3M
NICHD NIH HHS K12 HD063117
6 · The paper itself

Abstract

Our objective was to provide a comprehensive review of the current knowledge regarding pregnancy and hepatitis B virus (HBV) or hepatitis C virus (HCV) infection as well as recent efforts to reduce the rate of mother-to-child transmission (MTCT). Maternal infection with either HBV or HCV has been linked to adverse pregnancy and birth outcomes, including MTCT. MTCT for HBV has been reduced to approximately 5% overall in countries including the US that have instituted postpartum neonatal HBV vaccination and immunoprophylaxis with hepatitis B immune globulin. However, the rate of transmission of HBV to newborns is nearly 30% when maternal HBV levels are greater than 200 000 IU ml(-1) (>6 log10 copies ml(-1)). For these patients, new guidelines from the European Association for the Study of the Liver (EASL) and the Asian Pacific Association for the Study of the Liver (APASL) indicate that, in addition to neonatal vaccination and immunoprophylaxis, treating with antiviral agents such as tenofovir disoproxil fumarate or telbivudine during pregnancy beginning at 32 weeks of gestation is safe and effective in preventing MTCT. In contrast to HBV, no therapeutic agents are yet available or recommended to further decrease the risk of MTCT of HCV, which remains 3 to 10%. HCV MTCT can be minimized by avoiding fetal scalp electrodes and birth trauma whenever possible. Young women with HCV should be referred for treatment post delivery, and neonates should be closely followed to rule out infection. New, better-tolerated treatment regimens for HCV are now available, which should improve outcomes for all infected individuals.

Indexed as

Infectious Disease Transmission, VerticalAntiviral AgentsBreast FeedingCesarean SectionContraindicationsDNA, ViralFemaleHepatitis B, ChronicHepatitis B virusHepatitis C, ChronicHumansLamivudineMass ScreeningPregnancyPregnancy Complications, InfectiousPregnancy OutcomeAntiviral AgentsDNA, ViralLamivudineTelbivudineThymidine

Identifiers

PMID25233195
PMCPMC4777346
OpenAlexW2027996973

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.