Evidence map›Paper›PMID 31803945›Full record

Trial reportHepatology (Baltimore, Md.)2020

A Randomized Controlled Trial of an Integrated Alcohol Reduction Intervention in Patients With Hepatitis C Infection.

Rae Jean Proeschold-Bell, Donna M Evon, Jia Yao, Donna Niedzwiecki, Christina Makarushka, Kelly A Keefe, Ashwin A Patkar, Paolo Mannelli, James C Garbutt, John B Wong and 6 more

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Hepatology (Baltimore, Md.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 3 pooled it
2.8field-weighted citation impact, top 9% of its field
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

25 citing papers in PubMed, 3 syntheses or guidelines pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  4. Trial
  5. Trial
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Alcohol-related liver disease.Gastroenterology report · 2025
    Review
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  13. Article
  14. Review
  15. Article
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  17. Review
  18. Article
  19. Article
  20. Role of ALDH2 in Hepatic Disorders: Gene Polymorphism and Disease Pathogenesis.Journal of clinical and translational hepatology · 2021
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 1 country.

Rae Jean Proeschold-BellDuke Global Health Institute, Duke University, Durham, NC.ORCID 0000-0003-2008-3053
Donna M EvonDivision of Gastroenterology and Hepatology, Department of Medicine, University of North Carolina, Chapel Hill, NC.
Jia YaoDuke Center for Health Policy & Inequalities Research, Duke University, Durham, NC.
Donna NiedzwieckiDepartment of Biostatistics and Bioinformatics, Duke University, Durham, NC.
Christina MakarushkaDuke Center for Health Policy & Inequalities Research, Duke University, Durham, NC.
Kelly A KeefeDuke Center for Health Policy & Inequalities Research, Duke University, Durham, NC.
Ashwin A PatkarDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, Duke University, Durham, NC.
Paolo MannelliDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, Duke University, Durham, NC.
James C GarbuttBowles Center for Alcohol Studies, School of Medicine, University of North Carolina, Chapel Hill, NC.
John B WongDivision of Clinical Decision Making, Department of Medicine, Tufts Medical Center, Boston, MA.
Julius M WilderDivision of Gastroenterology, Department of Medicine, School of Medicine, Duke University, Durham, NC.
Santanu K DattaDepartment of Medicine, Duke University, Durham, NC.
Terra HodgeDivision of Gastroenterology, Department of Medicine, School of Medicine, Duke University, Durham, NC.
Susanna NaggieDuke Clinical Research Institute, Duke University, Durham, NC.ORCID 0000-0001-7721-6975
Michael W FriedDivision of Gastroenterology and Hepatology, Department of Medicine, University of North Carolina, Chapel Hill, NC.
Andrew J MuirDivision of Gastroenterology, Department of Medicine, School of Medicine, Duke University, Durham, NC.
Duke University · USUniversity of North Carolina at Chapel Hill · USDuke Medical Center · USTufts Medical Center · US

Funding

Social and Behavioral Sciences CoreP30AI064518 · NIAID · DUKE UNIVERSITY · PI Nwora Lance Okeke · 2005 to 2026
$50.5M
RCT of an Integrated Treatment of Persons with Co-Occurring HCV and Alcohol AbuseR01AA021133 · NIAAA · DUKE UNIVERSITY · PI MUIR, ANDREW J., PROESCHOLD-BELL, RAE JEAN ELIZABETH · 2013 to 2017
$3.5M
NIAAA NIH HHS R01 AA021133NIAAA NIH HHS R01AA021133-01A1NIAID NIH HHS 5P30 AI064518NIAID NIH HHS P30 AI064518
6 · The paper itself

Abstract

BACKGROUND AND

aimsHepatitis C virus (HCV) and alcohol use are patient risk factors for accelerated fibrosis progression, yet few randomized controlled trials have tested clinic-based alcohol interventions. APPROACH AND

resultsA total of 181 patients with HCV and qualifying alcohol screener scores at three liver center settings were randomly assigned to the following: (1) medical provider-delivered Screening, Brief Intervention, and Referral to Treatment (SBIRT), including motivational interviewing counseling and referral out for alcohol treatment (SBIRT-only), or (2) SBIRT plus 6 months of integrated colocated alcohol therapy (SBIRT + Alcohol Treatment). The timeline followback method was used to assess alcohol use at baseline and 3, 6, and 12 months. Coprimary outcomes were alcohol abstinence at 6 months and heavy drinking days between 6 and 12 months. Secondary outcomes included grams of alcohol consumed per week at 6 months. Mean therapy hours across 6 months were 8.8 for SBIRT-only and 10.1 for SBIRT + Alcohol Treatment participants. The proportion of participants exhibiting full alcohol abstinence increased from baseline to 3, 6, and 12 months in both treatment arms, but no significant differences were found between arms (baseline to 6 months, 7.1% to 20.5% for SBIRT-only; 4.2% to 23.3% for SBIRT + Alcohol Treatment; P = 0.70). Proportions of participants with any heavy drinking days decreased in both groups at 6 months but did not significantly differ between the SBIRT-only (87.5% to 26.7%) and SBIRT + Alcohol Treatment (85.7% to 42.1%) arms (P = 0.30). Although both arms reduced average grams of alcohol consumed per week from baseline to 6 and 12 months, between-treatment effects were not significant.

conclusionsPatients with current or prior HCV infection will engage in alcohol treatment when encouraged by liver medical providers. Liver clinics should consider implementing provider-delivered SBIRT and tailored alcohol treatment referrals as part of the standard of care.

Indexed as

Alcohol DrinkingAlcoholismHepatitis CLiver CirrhosisAlcohol AbstinenceAlcoholic BeveragesCounselingFemaleHumansMaleMass ScreeningMiddle AgedMotivational InterviewingReferral and ConsultationRisk AssessmentRisk Reduction Behavior

Identifiers

PMID31803945
PMCPMC7288780
OpenAlexW2992871672

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.