Evidence map›Paper›PMID 40693211›Full record

ArticleCureus2025

Management and Outcomes of Chronic Hepatitis B in Pregnancy: A Retrospective Study from a Tertiary Center in Singapore.

Huanghuan Li, Sushmitha C, Rajneesh Kumar

Abstract read
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

3 authors.

Huanghuan LiGastroenterology and Hepatology, Sengkang General Hospital, Singapore, SGP.
Sushmitha CGastroenterology and Hepatology, Singapore General Hospital, Singapore, SGP.
Rajneesh KumarGastroenterology and Hepatology, Singapore General Hospital, Singapore, SGP.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction Hepatitis B virus (HBV) infection remains a leading cause of chronic viral hepatitis, particularly in Asia. Vertical transmission during pregnancy is a key contributor to chronic HBV prevalence, and maternal screening with HBV DNA quantification enables the identification of high-risk cases. Antiviral therapy is recommended for pregnant women with HBV DNA levels >200,000 IU/mL to reduce the risk of perinatal transmission. This study aimed to determine the prevalence of high maternal viral load in chronic HBV, assess the initiation of antiviral therapy, and evaluate hepatic flares following treatment cessation postpartum. Methods We conducted a retrospective audit of pregnant women with chronic HBV infection referred to a gastroenterology specialist clinic in Singapore from August 2015 to December 2022. Data were collected from electronic medical records. The audit was approved by the institutional board. Results Data from 112 patients were analysed. The mean age was 34.6 years (standard deviation (SD) ± 4.4). A total of 25.9% had HBV DNA levels >200,000 IU/mL, with a mean alanine aminotransferase (ALT) of 31.1 U/L, compared to 19.5 U/L in those with lower viral loads. Among high viral load patients, 89.7% (n=26) were started on antiviral therapy; 3 declined treatment. Two patients with a lower viral load but elevated ALT were also treated. Mean gestational age at delivery was 37.7 weeks (SD ± 2.3). Postpartum follow-up revealed 10 cases of hepatitis flare. Eight patients agreed to the re-initiation of treatment. No serious adverse events were reported. Conclusion A significant proportion of pregnant women with chronic HBV had high viral loads, necessitating treatment. Tenofovir disoproxil fumarate (TDF) was safe and well-tolerated. Postpartum monitoring is essential due to the risk of hepatic flares following treatment cessation.

Indexed as

chronic hepatitis b (chb)hepatitis in pregnancymaternal-fetal transmissiontenofovir alafenamide (taf)tenofovir disoproxil fumarate (tdf)

Identifiers

PMID40693211
PMCPMC12277853

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