Evidence map›Paper›PMID 41282013›Full record

ArticleFrontiers in medicine2025

Assessment of the risk of discontinuation of tenofovir disoproxil fumarate after delivery and the benefit of continued treatment in patients with immune tolerance.

Huan Liang, Hengkai Liang, Bobin Hu, Long Huang, Hongqian Liang, Minghua Su, Rongming Wang, Tumei Su, Qingmei Li, Yanfei Feng and 1 more

Abstract read
In one paragraph

Article in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

11 authors.

Huan Liang *Department of Infectious Diseases, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Hengkai Liang *Department of Infectious Diseases, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Bobin HuDepartment of Infectious Diseases, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Long HuangDepartment of Infectious Diseases, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Hongqian LiangDepartment of Infectious Diseases, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Minghua SuDepartment of Infectious Diseases, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Rongming WangDepartment of Infectious Diseases, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Tumei SuDepartment of Infectious Diseases, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Qingmei LiDepartment of Infectious Diseases, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Yanfei FengDepartment of Infectious Diseases, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Jianning JiangDepartment of Infectious Diseases, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Both domestic and foreign guidelines recommend that chronic hepatitis B virus (HBV) infection pregnant women in the immune tolerance phase (ITP) discontinue antiviral therapy after delivery, this study aimed to investigate the risk of postpartum drug withdrawal and the pros and cons of continuing treatment of tenofovir dipivoxil fumarate (TDF) in ITP pregnant women. Methods: The study group consisted of 116 naive pregnant women in ITP, the control group included 81 naive chronic hepatitis B (CHB) pregnant women with HBeAg-positive and high viral load. The study aimed to compare the risk of discontinue rebound within 48 weeks postpartum, the antiviral efficacy and bone and renal safety of continuing TDF treatment until 144 weeks postpartum between the two groups. Results: There was no significant difference in the reduction of HBV DNA levels between the ITP group and the CHB group prior to labor ( Conclusion: Postpartum discontinuation of TDF poses significant risks for immunotolerant pregnant women, whereas continuing TDF treatment for 144 weeks postpartum demonstrates favorable antiviral efficacy, bone and renal safety profiles.

Indexed as

benefitdiscontinuationimmune tolerance phaserisktenofovir disoproxil fumarate

Identifiers

PMID41282013
PMCPMC12634375

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.