Evidence map›Paper›PMID 35229273›Full record

ArticleHepatology international2022

Low platelets: a new and simple prognostic marker for patients with hepatitis E virus-related acute liver failure.

Xiuying Mu, Jun Zou, Jing Chen, Jingjing Tong, Lian Ma, Peng Ning, Huajie Li, Zhiqian Feng, Tao Yang, Kai Liu and 11 more

Abstract read
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Article in Hepatology international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
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  11. Platelets as a Gauge of Liver Disease Kinetics?International journal of molecular sciences · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

Xiuying Mu *Peking University 302 Clinical Medical School, Beijing, China.
Jun Zou *The Fourth People's Hospital of Nanning, Guangxi, China.
Jing ChenSenior Department of Liver Diseases, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Jingjing TongSenior Department of Liver Diseases, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Lian MaThe Fourth People's Hospital of Nanning, Guangxi, China.
Peng NingSenior Department of Liver Diseases, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Huajie LiPeking University 302 Clinical Medical School, Beijing, China.
Zhiqian FengThe Second School of Clinical Medicine, Southern Medical University, Guangzhou, China.
Tao YangSenior Department of Infectious Diseases, Fifth Medical Center of Chinese, PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Xisihuan Road, Fengtai District, Beijing, 100039, China.
Kai LiuSenior Department of Infectious Diseases, Fifth Medical Center of Chinese, PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Xisihuan Road, Fengtai District, Beijing, 100039, China.
Wen-Jing CaoSenior Department of Infectious Diseases, Fifth Medical Center of Chinese, PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Xisihuan Road, Fengtai District, Beijing, 100039, China.
Ming-Ju ZhouSenior Department of Infectious Diseases, Fifth Medical Center of Chinese, PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Xisihuan Road, Fengtai District, Beijing, 100039, China.
Chao ZhangSenior Department of Infectious Diseases, Fifth Medical Center of Chinese, PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Xisihuan Road, Fengtai District, Beijing, 100039, China.
Ji-Yuan ZhangSenior Department of Infectious Diseases, Fifth Medical Center of Chinese, PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Xisihuan Road, Fengtai District, Beijing, 100039, China.
Yan-Mei JiaoSenior Department of Infectious Diseases, Fifth Medical Center of Chinese, PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Xisihuan Road, Fengtai District, Beijing, 100039, China.
Jin-Wen SongSenior Department of Infectious Diseases, Fifth Medical Center of Chinese, PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Xisihuan Road, Fengtai District, Beijing, 100039, China.
Xing FanSenior Department of Infectious Diseases, Fifth Medical Center of Chinese, PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Xisihuan Road, Fengtai District, Beijing, 100039, China.
Ming ShiSenior Department of Infectious Diseases, Fifth Medical Center of Chinese, PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Xisihuan Road, Fengtai District, Beijing, 100039, China.
Jinhua HuSenior Department of Liver Diseases, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Ruonan XuSenior Department of Infectious Diseases, Fifth Medical Center of Chinese, PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Xisihuan Road, Fengtai District, Beijing, 100039, China. xuruonan2004@aliyun.com.
Fu-Sheng WangPeking University 302 Clinical Medical School, Beijing, China. fswang302@163.com.

Funding

Key R&D projects in Nanning 20193008-1The National Natural Innovation Fund Project 81721002
6 · The paper itself

Abstract

BACKGROUND AND

aimsHepatitis E virus-related acute liver failure (HEV-ALF) rapidly worsens and has a high mortality. However, no simple and specific parameters for predicting short-term mortality are available.

methodsA derivation cohort including 97 patients with HEV-ALF and another validation cohort were enrolled. Laboratory and clinical parameters were recorded. Platelet count, model for end-stage liver disease (MELD), and King's College criteria (KCC) were separately used for predicting mortality, and the levels of cytokines associated with systemic inflammation, platelet production, and platelet activation were measured.

resultsPlatelet counts were significantly lower in patients with HEV-ALF, and nonsurvivors had lower platelet counts than survivors (p < 0.001). Platelet count was an independent risk factor for predicting 28- and 90-day mortality in patients with HEV-ALF. The AUROC of the baseline platelet count (cutoff, 131 × 10

conclusionsDecreased platelet count is a simple and reliable indicator for predicting 28- and 90-day mortality in patients with HEV-ALF. Overactivation of platelets is an important risk for platelet counts decrease, and treatment aiming at platelet count recovery may be considered.

Indexed as

End Stage Liver DiseaseHepatitis E virusLiver Failure, AcuteHumansPlatelet Factor 4PrognosisP-SelectinSeverity of Illness IndexThrombopoietinPlatelet Factor 4P-SelectinThrombopoietinAcute hepatitisAcute liver failureHepatitis E virusKing’s College criteriaModel for end-stage liver diseaseMortalityOutcomePlatelet countPrognosisSystemic inflammation

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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.