Evidence map›Paper›PMID 32323190›Full record

Trial reportJournal of thrombosis and thrombolysis2020

Associations between model-predicted rivaroxaban exposure and patient characteristics and efficacy and safety outcomes in the prevention of venous thromboembolism.

Isabel Reinecke, Alexander Solms, Stefan Willmann, Theodore E Spiro, Gary Peters, Jeffrey I Weitz, Wolfgang Mueck, Dirk Garmann, Stephan Schmidt, Liping Zhang and 2 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of thrombosis and thrombolysis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 13% 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, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  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

12 authors at 6 institutions in 4 countries.

Isabel ReineckeBayer AB, Solna, Sweden.
Alexander SolmsClinical Pharmacometrics, Bayer AG, Berlin, Germany.
Stefan WillmannClinical Pharmacometrics, Bayer AG, Wuppertal, Germany.
Theodore E SpiroBayer U.S., LLC, Research & Development, Pharmaceuticals, 100 Bayer Boulevard, Whippany, NJ, 07981, USA.
Gary PetersJanssen Research & Development, LLC, Raritan, NJ, USA.
Jeffrey I WeitzMcMaster University, and the Thrombosis & Atherosclerosis Research Institute, Hamilton, ON, Canada.
Wolfgang MueckClinical Pharmacokinetics, Bayer AG, Wuppertal, Germany.
Dirk GarmannClinical Pharmacometrics, Bayer AG, Wuppertal, Germany.
Stephan SchmidtCenter for Pharmacometrics and Systems Pharmacology, Department of Pharmaceutics, College of Pharmacy, University of Florida, Orlando, FL, USA.
Liping ZhangJanssen Research & Development, LLC, Raritan, NJ, USA.
Keith A A FoxCentre for Cardiovascular Science, The University of Edinburgh, Edinburgh, UK.
Scott D BerkowitzBayer U.S., LLC, Research & Development, Pharmaceuticals, 100 Bayer Boulevard, Whippany, NJ, 07981, USA. scott.berkowitz@bayer.com.ORCID http://orcid.org/0000-0002-9428-4408
Bayer (Germany) · DEBayer (United States) · USJanssen (United States) · USThrombosis and Atherosclerosis Research Institute · CAUniversity of Edinburgh · GBUniversity of Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anticoagulant plasma concentrations and patient characteristics might affect the benefit-risk balance of therapy. The study objective was to assess the impact of model-predicted rivaroxaban exposure and patient characteristics on outcomes in patients receiving rivaroxaban for venous thromboembolism (VTE) prophylaxis (VTE-P) after hip/knee replacement surgery. Post hoc exposure-response analyses were conducted using data from the phase 3 RECORD1-4 studies, in which 12,729 patients were randomized to rivaroxaban 10 mg once daily or enoxaparin for ≤ 39 days. Multivariate regression approaches were used to correlate model-predicted individual rivaroxaban exposures and patient characteristics with outcomes. In the absence of measured rivaroxaban exposure, exposure estimates were predicted based on individual increases in prothrombin time (PT) and by making use of the known correlation between rivaroxaban plasma concentration and dynamics of PT. No significant associations between rivaroxaban exposure and total VTE or major bleeding were identified. A significant association between exposure and a composite of major or non-major clinically relevant (NMCR) bleeding from day 4 after surgery was observed. The relationship was shallow, with an approximate predicted absolute increase in a composite of major or NMCR bleeding from 1.08 [95% confidence interval (CI) 0.76-1.54] to 2.18% (95% CI 1.51-3.17) at the 5th and 95th percentiles of trough plasma concentration, respectively. In conclusion, based on the underlying data and analysis, no reliable target window for exposure with improved benefit-risk could be identified within the investigated exposure range. Hence, monitoring rivaroxaban levels is unlikely to be beneficial in VTE-P.

Indexed as

Drug MonitoringHemorrhagePostoperative ComplicationsRivaroxabanVenous ThromboembolismAnticoagulantsArthroplasty, Replacement, HipBiomarkers, PharmacologicalChemopreventionFemaleHumansMaleMiddle AgedModels, StatisticalPrognosisProthrombin TimeAnticoagulantsBiomarkers, PharmacologicalRivaroxabanDrug monitoringExposure–responseRivaroxabanVenous thromboembolism

Identifiers

PMID32323190
PMCPMC7293976
OpenAlexW3020565800

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.