Evidence map›Paper›PMID 29992490›Full record

Trial reportDrugs in R&D2018

Evaluation of Cardiovascular Disease Risk in HIV-1-Infected Patients Treated with Darunavir.

Magda Opsomer, Dessislava Dimitrova, Johan Verspeelt, Amy Purrington, Abdul Mehbob, Scott Chavers, Helen Pai, Simon Vanveggel, Donghan Luo, Kimberley Brown and 3 more

Erratum issuedOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in Drugs in R&D, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Stroke in HIV.The Canadian journal of cardiology · 2019
    Review
  6. Observational
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 4 countries.

Magda OpsomerJanssen Research and Development, Beerse, Belgium. mopsomer@its.jnj.com.
Dessislava DimitrovaJanssen Research and Development, LLC, Titusville, NJ, USA.
Johan VerspeeltJanssen Research and Development, Beerse, Belgium.
Amy PurringtonJanssen Research and Development, LLC, Horsham, PA, USA.
Abdul MehbobJanssen-Cilag Ltd, High Wycombe, UK.
Scott ChaversJanssen Research and Development, LLC, Titusville, NJ, USA.
Helen PaiJanssen Research and Development, LLC, Raritan, NJ, USA.
Simon VanveggelJanssen Research and Development, Beerse, Belgium.
Donghan LuoJanssen Research and Development, LLC, Titusville, NJ, USA.
Kimberley BrownJanssen Scientific Affairs, LLC, Titusville, NJ, USA.
Christiane MoecklinghoffJanssen EMEA, Neuss, Germany.
Richard E NettlesJanssen Scientific Affairs, LLC, Titusville, NJ, USA.
Katia BovenJanssen Research and Development, LLC, Titusville, NJ, USA.
Janssen (United States) · USJanssen (Belgium) · BEJanssen Scientific Affairs (United States)Janssen (Germany) · DEJanssen (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWe evaluated cardiovascular disease (CVD) risk associated with darunavir treatment and examined the demographic/clinical characteristics of darunavir users based on data from Janssen-sponsored clinical trials, post-marketing pharmacovigilance databases, and administrative claims databases.

methodsFirst, selected CVD events [myocardial infarction, stroke, sudden death, invasive cardiovascular procedures (coronary artery angioplasty or bypass, or carotid endarterectomy)] were analyzed in 19 Janssen-sponsored phase 2-4 studies (incidence rates estimated from pooled data; 95% confidence intervals derived from Poisson distribution). Second, analyses were conducted to identify spontaneously reported CVD events in post-marketing pharmacovigilance databases and evaluate disproportional reporting of CVD events for darunavir (using Empirical Bayesian Geometric Mean scores). Third, baseline demographic/clinical characteristics of human immunodeficiency virus-1 (HIV-1)-infected patients in general and new users of darunavir and atazanavir were explored using three US administrative claims databases.

resultsAmong 19 Janssen-sponsored clinical trials (treatment durations ≤ 6 years), the CVD event rate (95% CI) per 1000 person-years (pooled population; n = 5713) was 6.15 (2.91-11.89), and was lower for patients who used once-daily darunavir/ritonavir 800/100 mg [0.71 (0.16-3.05); n = 1326] versus twice-daily darunavir/ritonavir 600/100 mg [9.21 (4.94-16.04); n = 3058]. Trend analysis of post-marketing pharmacovigilance data showed that cumulative CVD event reporting rates for darunavir users (any dose) generally declined over time. Spontaneously reported CVD events were not disproportionately reported with darunavir versus other protease inhibitors. Compared with the general HIV-1-infected population and atazanavir users, higher proportions of darunavir users were male, older, and had comorbidities associated with CVD risk based on results from US administrative claims databases.

conclusionsThis comprehensive review of Janssen-sponsored clinical trial, post-marketing, and epidemiological data does not suggest that CVD should be considered an important risk for users of darunavir.

Indexed as

AdolescentAdultAgedAged, 80 and overCardiovascular DiseasesDarunavirFemaleHIV InfectionsHIV Protease InhibitorsHumansMaleMiddle AgedRisk FactorsYoung AdultDarunavirHIV Protease Inhibitors

Identifiers

PMID29992490
PMCPMC6131121
OpenAlexW2815215413

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.