Evidence map›Paper›PMID 38563380›Full record

Trial reportJournal of the American Heart Association2024

Quantitative Benefit-Risk Evaluation of Rivaroxaban in Patients After Peripheral Arterial Revascularization: The VOYAGER PAD Trial.

Zhong Yuan, Bennett Levitan, Hsiaowei Deng, Michael Szarek, Rupert M Bauersachs, Scott D Berkowitz, Lloyd Haskell, Elliot S Barnathan, Marc P Bonaca

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Journal of the American Heart Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
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

9 authors at 4 institutions in 3 countries.

Zhong YuanJanssen Research & Development LLC Horsham PA.ORCID 0000-0002-5824-2040
Bennett LevitanJanssen Research & Development LLC Titusville NJ.ORCID 0000-0001-9069-8446
Hsiaowei DengJanssen Research & Development LLC Horsham PA.
Michael SzarekCPC Clinical Research, Department of Medicine University of Colorado Aurora CO.ORCID 0000-0002-0046-0264
Rupert M BauersachsCardioangiologisches Centrum Bethanien - CCB Gefäß-Centrum Frankfurt am Main Germany.ORCID 0000-0001-6192-1741
Scott D BerkowitzCPC Clinical Research, Department of Medicine University of Colorado Aurora CO.ORCID 0000-0002-9428-4408
Lloyd HaskellJanssen Research & Development LLC Horsham PA.ORCID 0000-0002-2468-2523
Elliot S BarnathanJanssen Research & Development LLC Horsham PA.ORCID 0000-0001-7744-1486
Marc P BonacaCPC Clinical Research, Department of Medicine University of Colorado Aurora CO.ORCID 0000-0002-9860-3584
Janssen (Belgium) · BEUniversity of Colorado Denver · USCardiovascular Center Bethanien · DEJanssen (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe VOYAGER PAD (Efficacy and Safety of Rivaroxaban in Reducing the Risk of Major Thrombotic Vascular Events in Subjects With Symptomatic Peripheral Artery Disease Undergoing Peripheral Revascularization Procedures of the Lower Extremities) trial compared rivaroxaban (2.5 mg twice a day) plus aspirin with aspirin alone in patients with symptomatic peripheral artery disease requiring endovascular or surgical limb revascularization, with 50% receiving clopidogrel background therapy. The New Drug Indication application includes benefit-risk assessments using clinical judgment to balance benefits against risks. During its review, the US Food and Drug Administration requested additional quantitative benefit-risk analyses with formal weighting approaches. METHODS AND

resultsBenefits and risks were assessed using rate differences between treatment groups (unweighted analysis). To account for clinical importance of the end points, a multi-criteria decision analysis was conducted using health state utility values as weights. Monte Carlo simulations incorporated statistical uncertainties of the event rates and utility weights. Intent-to-treat and on-treatment analyses were conducted. For unweighted intent-to-treat analyses, rivaroxaban plus aspirin would result in 120 (95% CI, -208 to -32) fewer events of the primary composite end point (per 10 000 patient-years) compared with aspirin alone. Rivaroxaban caused an excess of 40 (95% CI, 8-72) Thrombolysis in Myocardial Infarction major bleeding events, which was largely driven by nonfatal, nonintracranial hemorrhage Thrombolysis in Myocardial Infarction major bleeding events. For weighted analyses, rivaroxaban resulted in the utility equivalent of 13.7 (95% CI, -85.3 to 52.6) and 68.1 (95% CI, 7.9-135.7) fewer deaths per 10 000 patient-years (intent-to-treat and on-treatment, respectively), corresponding to probabilities of 64.4% and 98.7%, respectively, that benefits outweigh risks favoring rivaroxaban per Monte Carlo simulation.

conclusionsThese analyses show a favorable benefit-risk profile of rivaroxaban therapy in the VOYAGER PAD trial, with findings generally consistent between the unweighted and weighted approaches.

Indexed as

Myocardial InfarctionPeripheral Arterial DiseaseAspirinDrug Therapy, CombinationFactor Xa InhibitorsHemorrhageHumansPlatelet Aggregation InhibitorsRisk AssessmentRivaroxabanAspirinFactor Xa InhibitorsPlatelet Aggregation InhibitorsRivaroxabanhealth state utilitiesmodelingmulti‐criteria decision analysisperipheral artery diseaserivaroxaban

Identifiers

PMID38563380
PMCPMC11262494
OpenAlexW4393524423

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.