Evidence map›Paper›PMID 16679474›Full record

ArticlePostgraduate medical journal2006

A single centre cohort experience with a new once daily antiretroviral drug.

J Stebbing, M Bower, P Holmes, B Gazzard, M Nelson

Open access · bronzeAbstract read
In one paragraph

Article in Postgraduate medical journal, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. 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

5 authors at 1 institution in 1 country.

J StebbingDepartment of HIV Medicine, Chelsea and Westminster Hospital, London, UK.
M Bower
P Holmes
B Gazzard
M Nelson
Chelsea and Westminster Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAtazanavir, an azadipeptide protease inhibitor (PI) with once daily dosing, a lack of insulin resistance, lipid increase, and gastrointestinal toxicities, is approved in combination with other antiretrovirals for the treatment of patients infected with HIV. Unboosted atazanavir is also used in highly active antiretroviral therapy (HAART) naive patients.

methodsThe study prospectively followed up an established cohort of patients who received atazanavir, and for whom one year of follow up data were available.

resultsIt was found that use of atazanavir in intent to treat and on treatment analyses, maintained and led to virological suppression and increases in CD4 count in both PI naive and experienced patients. Virological failure occurred in 7% of patients and the main toxicity was hyperbilirubinaemia, which led to treatment withdrawal in 2%. Its efficacy and safety profile was similar to that seen in previous randomised studies investigating its use.

conclusionsThese data should provide reassurance for clinicians wishing to introduce a new antiretroviral into an established cohort.

Indexed as

Anti-HIV AgentsAntiretroviral Therapy, Highly ActiveAtazanavir SulfateCohort StudiesDrug Administration ScheduleHIV InfectionsHIV Protease InhibitorsHumansOligopeptidesProspective StudiesPyridinesTreatment OutcomeAnti-HIV AgentsAtazanavir SulfateHIV Protease InhibitorsOligopeptidesPyridines

Identifiers

PMID16679474
PMCPMC2563794
OpenAlexW2062382961

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.