Evidence map›Paper›PMID 27633520›Full record

ArticleScientific reports2016

A comprehensive validation of HBV-related acute-on-chronic liver failure models to assist decision-making in targeted therapeutics.

Yi Shen, Xulin Wang, Sheng Zhang, Gang Qin, Yanmei Liu, Yihua Lu, Feng Liang, Xun Zhuang

Abstract readValidation Study
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. [Research advances in diagnosis and treatment of liver failure in 2016].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2017
    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

8 authors.

Yi ShenDepartment of Epidemiology and Medical Statistics, Nantong University, Nantong, China.
Xulin WangDepartment of Epidemiology and Medical Statistics, Nantong University, Nantong, China.
Sheng ZhangDepartment of Epidemiology and Medical Statistics, Nantong University, Nantong, China.
Gang QinCenter for Liver Diseases, Nantong Third People's Hospital, Nantong University, Nantong, China.
Yanmei LiuDepartment of Epidemiology and Medical Statistics, Nantong University, Nantong, China.
Yihua LuDepartment of Epidemiology and Medical Statistics, Nantong University, Nantong, China.
Feng LiangQidong Third People's Hospital, Nantong, China.
Xun ZhuangDepartment of Epidemiology and Medical Statistics, Nantong University, Nantong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This research utilized an external longitudinal dataset of hepatitis B virus-related acute-on-chronic liver failure (HBV-ACLF) to compare and validate various predictive models that support the current recommendations to select the most effective predictive risk models to estimate short- and long-term mortality and facilitate decision-making about preferable therapeutics for HBV-ACLF patients. Twelve ACLF prognostic models were developed after a systematic literature search using the longitudinal data of 232 HBV-ACLF patients on the waiting list for liver transplantation (LT). Four statistical measures, the constant (A) and slope (B) of the fitted line, the area under the curve (C) and the net benefit (D), were calculated to assess and compare the calibration, discrimination and clinical usefulness of the 12 predictive models. According to the model calibration and discrimination, the logistic regression models (LRM2) and the United Kingdom model of end-stage liver disease(UKELD) were selected as the best predictive models for both 3-month and 5-year outcomes. The decision curve summarizes the benefits of intervention relative to the costs of unnecessary treatment. After the comprehensive validation and comparison of the currently used models, LRM2 was confirmed as a markedly effective prognostic model for LT-free HBV-ACLF patients for assisting targeted and standardized therapeutic decisions.

Indexed as

Clinical Decision-MakingMolecular Targeted TherapyAcute-On-Chronic Liver FailureCalibrationDiscriminant AnalysisHepatitis B virusHumansReproducibility of ResultsRisk Factors

Identifiers

PMID27633520
PMCPMC5025883

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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.