Evidence map›Paper›PMID 39060786›Full record

ArticleJournal of general internal medicine2025

Identifying and Linking Patients At Risk for MASLD with Advanced Fibrosis to Care in Primary Care.

Ted G Xiao, Lauren Witek, Richa A Bundy, Adam Moses, Corey S Obermiller, Andrew D Schreiner, Ajay Dharod, Mark W Russo, Sean R Rudnick

Abstract read
In one paragraph

Article in Journal of general internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

9 authors.

Ted G XiaoDepartment of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.ORCID 0000-0001-5869-5878
Lauren WitekInformatics and Analytics, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Richa A BundyInformatics and Analytics, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Adam MosesInformatics and Analytics, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Corey S ObermillerInformatics and Analytics, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Andrew D SchreinerDepartment of Medicine, Medical University of South Carolina, Charleston, SC, USA.
Ajay DharodDepartment of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Mark W RussoDivision of Liver Diseases and Transplant, Atrium Health Carolina Medical Center, Charlotte, NC, USA.
Sean R RudnickSection of Gastroenterology and Hepatology, Wake Forest School of Medicine, Winston-Salem, NC, USA. srudnick@wakehealth.edu.

Funding

Wake Forest School of Medicine Clinical Scholar in InformaticsWake Forest School of Medicine Intramural
6 · The paper itself

Abstract

BACKGROUND AND

aimsSeverity of fibrosis is the driver of liver-related outcomes in metabolic dysfunction-associated steatotic liver disease (MASLD), and non-invasive testing such as fibrosis-4 (FIB-4) score is utilized for risk stratification. We aimed to determine if primary care patients at risk for MASLD and advanced fibrosis were evaluated with subsequent testing. A secondary aim was to determine if at-risk patients with normal aminotransferases had advanced fibrosis.

methodsPrimary care patients at increased risk for MASLD with advanced fibrosis (n = 91,914) were identified using previously established criteria. Patients with known alternative/concomitant etiology of liver disease or cirrhosis were excluded. The study cohort included patients with calculated FIB-4 score in 2020 (n = 52,006), and stratified into low, indeterminate, and high likelihood of advanced fibrosis. Among those at indeterminate/high risk, rates of subsequent testing were measured.

resultsRisk stratification with FIB-4 characterized 77% (n = 40,026) as low risk, 17% (n = 8847) as indeterminate, and 6% (n = 3133) as high risk. Among indeterminate/high-risk patients (n = 11,980), 78.7% (n = 9433) had aminotransferases within normal limits, 0.95% (n = 114) had elastography, and 8.2% (n = 984) were referred for subspecialty evaluation.

conclusionIn this cohort of primary care patients at risk for MASLD with fibrosis, the FIB-4 score identified a substantial proportion of indeterminate/high-risk patients, the majority of which had normal aminotransferase levels. Low rates of subsequent testing were observed. These data suggest that a majority of patients at increased risk for liver-related outcomes remain unrecognized and highlight opportunities to facilitate their identification.

Indexed as

Fatty LiverLiver CirrhosisAdultAgedCohort StudiesFemaleHumansMaleMiddle AgedPrimary Health CareRisk AssessmentRisk FactorsSeverity of Illness Indexadvanced fibrosisfibrosis-4 scoreMASLDnon-invasive testingscreening

Identifiers

PMID39060786
PMCPMC11861828

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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.