Evidence map›Paper›PMID 33544904›Full record

ArticleHepatology (Baltimore, Md.)2021

The Impact of Direct-Acting Antiviral Therapy on End-Stage Liver Disease Among Individuals with Chronic Hepatitis C and Substance Use Disorders.

Haesuk Park, Xinyi Jiang, Hyun Jin Song, Vincent Lo Re, Lindsey M Childs-Kean, Wei-Hsuan Lo-Ciganic, Robert L Cook, David R Nelson

Abstract readComparative Study
In one paragraph

Article in Hepatology (Baltimore, Md.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Haesuk ParkPharmaceutical Outcomes and PolicyCollege of PharmacyUniversity of FloridaGainesvilleFL.ORCID 0000-0003-3299-8111
Xinyi JiangPharmaceutical Outcomes and PolicyCollege of PharmacyUniversity of FloridaGainesvilleFL.ORCID 0000-0002-9097-2641
Hyun Jin SongPharmaceutical Outcomes and PolicyCollege of PharmacyUniversity of FloridaGainesvilleFL.ORCID 0000-0003-4779-6555
Vincent Lo ReDivision of Infectious DiseasesDepartment of Medicine and Center for Clinical Epidemiology and BiostatisticsDepartment of Biostatistics, Epidemiology, and InformaticsPerelman School of MedicineUniversity of PennsylvaniaPhiladelphiaPA.
Lindsey M Childs-KeanPharmacotherapy and Translational ResearchCollege of PharmacyUniversity of FloridaGainesvilleFL.ORCID 0000-0002-5985-7979
Wei-Hsuan Lo-CiganicPharmaceutical Outcomes and PolicyCollege of PharmacyUniversity of FloridaGainesvilleFL.ORCID 0000-0001-6590-4770
Robert L CookDepartment of MedicineUniversity of FloridaGainesvilleFL.ORCID 0000-0002-7770-3754
David R NelsonDepartment of MedicineUniversity of FloridaGainesvilleFL.ORCID 0000-0001-6344-8548

Funding

Using social networks to map and evaluate team science across CTSA hubsUL1TR001427 · NCATS · UNIVERSITY OF FLORIDA · PI MITCHELL, DUANE A. · 2015 to 2024
$37.2M
Southern HIV and Alcohol Research Consortium Administrative and Research Support CoreU24AA022002 · NIAAA · UNIVERSITY OF FLORIDA · PI COOK, ROBERT L · 2012 to 2022
$5.5M
Medicaid Prior Authorization Policies for Chronic Hepatitis C Treatment in Vulnerable PopulationsK01DA045618 · NIDA · UNIVERSITY OF FLORIDA · PI PARK, HAESUK · 2018 to 2022
$648k
NCATS NIH HHS UL1 TR001427NIAAA NIH HHS U24 AA022002NIDA NIH HHS K01 DA045618
6 · The paper itself

Abstract

BACKGROUND AND

aimsOur aim was to evaluate the impact of direct-acting antivirals (DAAs) on decompensated cirrhosis (DCC) and HCC in patients with chronic HCV and substance use disorder (SUD) compared with those without an SUD. APPROACH AND

resultsThis retrospective cohort study used the MarketScan database (2013-2018) to identify 29,228 patients with chronic HCV, where 22% (n = 6,385) had ≥1 SUD diagnosis. The inverse probability of treatment weighted multivariable Cox proportional hazard models were used to compare the risk of developing DCC and HCC. Among the those who were noncirrhotic, treatment reduced the DCC risk among SUD (adjusted hazard ratio [aHR] 0.13; 95% CI, 0.06-0.30) and non-SUD (aHR 0.11; 95% CI, 0.07-0.18), whereas the risk for HCC was not reduced for the SUD group (aHR 0.91; 95% CI, 0.33-2.48). For those with cirrhosis, compared with patients who were untreated, treatment reduced the HCC risk among SUD (aHR, 0.33; 95% CI, 0.13-0.88) and non-SUD (aHR, 0.40; 95% CI, 0.25-0.65), whereas the risk for DCC was not reduced for the SUD group (aHR, 0.64; 95% CI, 0.37-1.13). Among patients with cirrhosis who were untreated, the SUD group had a higher risk of DCC (aHR, 1.52; 95% CI, 1.03-2.24) and HCC (aHR, 1.69; 95% CI, 1.05-2.72) compared with non-SUD group.

conclusionsAmong the HCV SUD group, DAA treatment reduced the risk of DCC but not HCC for those who were noncirrhotic, whereas DAA treatment reduced the risk of HCC but not DCC for those with cirrhosis. Among the nontreated, patients with an SUD had a significantly higher risk of DCC and HCC compared with those without an SUD. Thus, DAA treatment should be considered for all patients with HCV and an SUD while also addressing the SUD.

Indexed as

Administrative Claims, HealthcareAdolescentAdultAgedAntiviral AgentsCarcinoma, HepatocellularDatabases, FactualEnd Stage Liver DiseaseFemaleHepatitis C, ChronicHumansIncidenceLiver CirrhosisLiver NeoplasmsMaleMiddle AgedAntiviral Agents

Identifiers

PMID33544904
PMCPMC8339171

What OpenQuestion holds

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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.