Evidence map›Paper›PMID 30483552›Full record

ArticleJGH open : an open access journal of gastroenterology and hepatology2017

Asunaprevir and daclatasvir in hemodialysis patients with chronic hepatitis C virus genotype 1b infection.

Taiga Otsuka, Yasunori Kawaguchi, Toshihiko Mizuta, Yasushi Ide, Futa Koga, Takanori Kumagai, Wataru Yoshioka, Kenichiro Murayama, Osamu Rikitake, Yuji Ikeda and 1 more

Abstract read
In one paragraph

Article in JGH open : an open access journal of gastroenterology and hepatology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

  1. Pooled it
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  3. 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

11 authors.

Taiga OtsukaDepartment of Internal Medicine, Division of Hepatology Saga University Hospital Saga Japan.
Yasunori KawaguchiHepato-Biliary and Pancreatology Division Saga Medical Center Koseikan Saga Japan.
Toshihiko MizutaDepartment of Internal Medicine Imari-Arita Kyoritsu Hospital Saga Japan.
Yasushi IdeDepartment of Internal Medicine Karatsu Red Cross Hospital Saga Japan.
Futa KogaDepartment of Internal Medicine, Division of Hepatology Saga University Hospital Saga Japan.
Takanori KumagaiDepartment of Internal Medicine Taku City Hospital Saga Japan.
Wataru YoshiokaDepartment of Internal Medicine, Division of Hepatology Saga University Hospital Saga Japan.
Kenichiro MurayamaDepartment of Internal Medicine, Division of Hepatology Saga University Hospital Saga Japan.
Osamu RikitakeDepartment of Internal Medicine Rikitake Clinic Saga Japan.
Yuji IkedaDepartment of Internal Medicine, Division of Nephrology Saga University Hospital Saga Japan.
Iwata OzakiDepartment of Internal Medicine, Division of Hepatology Saga University Hospital Saga Japan.ORCID 0000-0001-8542-1434

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimPatients requiring hemodialysis show high morbidity with hepatitis C virus (HCV) infection, but there are difficulties associated with interferon-based therapies. Asunaprevir and daclatasvir could help patients with HCV genotype 1b because the drugs have a nonrenal metabolism and show good viral eradication. We evaluated the efficacy and safety of combined asunaprevir and daclatasvir therapy.

methodsThis was a multicenter prospective trial of patients with chronic hepatitis or compensated cirrhosis from HCV genotype 1b who had end-stage renal disease requiring chronic hemodialysis. Asunaprevir and daclatasvir were administered orally (100 mg twice daily and 60 mg once daily, respectively) for 24 weeks. The primary end-point was the proportion of patients achieving sustained virological response 12, defined as HCV RNA <15 IU/mL undetectable at 12 weeks after completion of asunaprevir and daclatasvir treatment.

resultsBetween December 2014 and December 2015, 23 dialysis patients were enrolled, and 22 patients completed the protocol therapy. Sustained virological response 12 rates were 91.3% (95% confidence interval: 72.0-98.9) in the intention-to-treat and 95.5% (95% confidence interval: 77.2-99.9) in the per-protocol populations. Serum aminotransferase significantly decreased after initiation of asunaprevir and daclatasvir (

conclusionsAsunaprevir and daclatasvir could help patients with chronic hepatitis C receiving hemodialysis. Close collaboration with dialysis physicians is important when treating these patients because hemodialysis carries life-threatening risks.

Indexed as

asunaprevirdaclatasvirdirect‐acting antiviralshemodialysishepatitis C virus

Identifiers

PMID30483552
PMCPMC6207006

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