Evidence map›Paper›PMID 24052911›Full record

ArticleHawai'i journal of medicine & public health : a journal of Asia Pacific Medicine & Public Health2013

New triple therapy for chronic hepatitis C: real life clinical experience in a community setting.

Matthew J Akiyama, Joy I Piotrowski, Marina M Roytman, Siu M A Chan, Leena K Hong, Leslie Huddleston, Ruby Trujillo, Naoky C S Tsai

Abstract read
In one paragraph

Article in Hawai'i journal of medicine & public health : a journal of Asia Pacific Medicine & Public Health, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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

3 citing papers in PubMed.

  1. Observational
  2. Observational
  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

8 authors.

Matthew J AkiyamaUniversity of Hawai'i Internal Medicine Residency Program, Honolulu, HI (M.J.A.).
Joy I Piotrowski
Marina M Roytman
Siu M A Chan
Leena K Hong
Leslie Huddleston
Ruby Trujillo
Naoky C S Tsai

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent advances in treatment of chronic hepatitis C virus have improved significantly due to the introduction of two new protease inhibitors-telaprevir and boceprevir. In combination with the previous standard of care, peginterferon and ribavirin, telaprevir and boceprevir have demonstrated improved sustained virologic response rates for HCV genotype 1 patients by approximately 30%. The purpose of this study was to assess the validity of large clinical trial data with respect to efficacy and side effects in a community setting in Honolulu, Hawai'i. This retrospective study was performed by reviewing the charts of 59 chronic HCV patients who were started on triple therapy from July 1, 2011 to July 7, 2012. Sustained virologic response was attained by 73% of patients treated with telaprevir and 46% of patients treated with boceprevir respectively. Our clinical experience with telaprevir demonstrates that SVR rates are compatible with published literature values. Rates of SVR in our cohort were also similar to those reported in cirrhotic patients - about 50%. Due to small number of patients treated with a boceprevir-based regimen, it is difficult to compare our experience with pivotal trial experience. The side effect profiles for the two protease inhibitors were similar to the literature values except for more rectal irritation and a higher incidence and severity of anemia on telaprevir therapy in the clinical setting. While not intended to be conclusive, our study demonstrates that clinical trial data are largely compatible with the outcomes obtained in our community setting.

Indexed as

Community Health ServicesAntiviral AgentsDrug Therapy, CombinationFemaleHepatitis C, ChronicHumansInterferon-alphaMaleMiddle AgedOligopeptidesPolyethylene GlycolsProlineRetrospective StudiesRibavirinViral LoadAntiviral AgentsInterferon-alphaN-(3-amino-1-(cyclobutylmethyl)-2,3-dioxopropyl)-3-(2-((((1,1-dimethylethyl)amino)carbonyl)amino)-3,3-dimethyl-1-oxobutyl)-6,6-dimethyl-3-azabicyclo(3.1.0)hexan-2-carboxamideOligopeptidesPolyethylene GlycolsProlineRibavirintelaprevirboceprevircommunity experienceHCVIncivekreal clinical settingtelaprevirtriple therapyVictrelis

Identifiers

PMID24052911
PMCPMC3764547

What OpenQuestion holds

Textmetadata
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.