Evidence map›Paper›PMID 29333275›Full record

ArticleBMJ open gastroenterology2017

Barriers to care for chronic hepatitis C in the direct-acting antiviral era: a single-centre experience.

Peter Nguyen, Philip Vutien, Joseph Hoang, Sam Trinh, An Le, Lee Ann Yasukawa, Susan Weber, Linda Henry, Mindie H Nguyen

Open access · goldAbstract read
In one paragraph

Article in BMJ open gastroenterology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  8. Review
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  10. Telemedicine successfully engages marginalized rural hepatitis C patients in curative care.Journal of the Association of Medical Microbiology and Infectious Disease Canada = Journal officiel de l'Association pour la microbiologie medicale et l'infectiologie Canada · 2020
    Article
  11. 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 at 3 institutions in 1 country.

Peter NguyenDivision of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California, USA.
Philip VutienDivision of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California, USA.
Joseph HoangDivision of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California, USA.
Sam TrinhDivision of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California, USA.
An LeDivision of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California, USA.
Lee Ann YasukawaCenter for Clinical Informatics, Stanford School of Medicine, Palo Alto, California, USA.
Susan WeberCenter for Clinical Informatics, Stanford School of Medicine, Palo Alto, California, USA.
Linda HenryPharmaceutical Outcomes and of Policy, College of Pharmacy, University of Florida, Gainesville, Florida, USA.
Mindie H NguyenDivision of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California, USA.
Stanford Medicine · USStanford University · USUniversity of Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCure rates for chronic hepatitis C have improved dramatically with direct-acting antivirals (DAAs), but treatment barriers remain. We aimed to compare treatment initiation rates and barriers across both interferon-based and DAA-based eras.

methodsWe conducted a retrospective cohort study of all patients with chronic hepatitis C seen at an academic hepatology clinic from 1999 to 2016. Patients were identified to have chronic hepatitis C by the International Classification of Diseases, Ninth Revision codes, and the diagnosis was validated by chart review. Patients were excluded if they did not have at least one visit in hepatology clinic, were under 18 years old or had prior treatment with DAA therapy. Patients were placed in the DAA group if they were seen after 1 January 2014 and had not yet achieved virological cure with prior treatment. All others were considered in the interferon group.

results3202 patients were included (interferon era: n=2688; DAA era: n=514). Despite higher rates of decompensated cirrhosis and medical comorbidities in the DAA era, treatment and sustained virological response rates increased significantly when compared with the interferon era (76.7% vs 22.3%, P<0.001; 88.8% vs 55%, P<0.001, respectively). Lack of follow-up remained a significant reason for non-treatment in both groups (DAA era=24% and interferon era=45%). An additional 8% of patients in the DAA era were not treated due to insurance or issues with cost. In the DAA era, African-Americans, compared with Caucasians, had significantly lower odds of being treated (OR=0.37, P=0.02).

conclusionsDespite higher rates of medical comorbidities in the DAA era, considerable treatment challenges remain including cost, loss to follow-up and ethnic disparities.

Indexed as

chronic viral hepatitishealth service researchhepatitis c

Identifiers

PMID29333275
PMCPMC5759739
OpenAlexW2778632813

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.