Evidence map›Paper›PMID 30147941›Full record

ArticleBMJ open gastroenterology2018

Systematic review and meta-analysis: real-world effectiveness of direct-acting antiviral therapies in chronic hepatitis C genotype 3 in Asia.

Bin Wei, Fanpu Ji, Yee Hui Yeo, Eiichi Ogawa, Christopher D Stave, Shuangsuo Dang, Zongfang Li, Norihiro Furusyo, Ramsey C Cheung, Mindie H Nguyen

Abstract read
In one paragraph

Article in BMJ open gastroenterology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. "Sell an Ox" - The Price of Cure for Hepatitis C in Two Countries.International journal of health policy and management · 2020
    Article
  5. Article
  6. Article
  7. 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

10 authors.

Bin Wei *Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, USA.
Fanpu JiDivision of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, USA.
Yee Hui YeoDivision of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, USA.
Eiichi OgawaDivision of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, USA.
Christopher D StaveLane Library, School of Medicine, Stanford University, Stanford, California, USA.
Shuangsuo DangDepartment of Infectious Diseases, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, People's Republic of China.
Zongfang LiShaanxi Provincial Clinical Research Center for Hepatic & Splenic Diseases, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, People's Republic of China.
Norihiro FurusyoDepartment of General Internal Medicine, Kyushu University Hospital, Fukuoka, Japan.
Ramsey C CheungDivision of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, USA.
Mindie H NguyenDivision of Gastroenterology and Hepatology, Veterans Affairs Palo Alto Health Care System, Palo Alto, California, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenotype 3 (GT3) is a common chronic hepatitis C (CHC) genotype in Asia. Direct-acting antiviral (DAA) regimens have high cure rates, but real-world results are limited for Asia.

aimTo determine the real-world effectiveness of DAAs for patients with CHC GT3 in Asia.

methodsA systematic search was performed in PubMed (including MEDLINE), Embase, and selected international meeting abstract repositories. Eligible studies were postmarketing observational studies from Asia with the primary outcome of sustained virological response 12 weeks after completion of treatment (SVR12).

resultsA total of 15 studies with 4230 patients yielded a pooled SVR12 of 92.7%. High heterogeneity (

conclusionSofosbuvir+ribavirin for 24 weeks is the most widely used and generally well-tolerated DAA therapy in Asia. However, its effectiveness is not optimal in GT3 patients with cirrhosis.

Indexed as

adverse drug reactionsgenotypehepatitis Cliver cirrhosis

Identifiers

PMID30147941
PMCPMC6104766

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.