Evidence map›Paper›PMID 30383768›Full record

ArticlePloS one2018

Real-world comparison of bleeding risks among non-valvular atrial fibrillation patients prescribed apixaban, dabigatran, or rivaroxaban.

Ping G Tepper, Jack Mardekian, Cristina Masseria, Hemant Phatak, Shital Kamble, Younos Abdulsattar, William Petkun, Gregory Y H Lip

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
–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

29 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
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  16. P- and E- selectin in venous thrombosis and non-venous pathologies.Journal of thrombosis and haemostasis : JTH · 2022
    Review
  17. Article
  18. Acute haemorrhage rate in 28,000 Out-of-Hours CT heads.The British journal of radiology · 2022
    Article
  19. Article
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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.

Ping G TepperDepartment of Epidemiology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.ORCID 0000-0001-7402-1662
Jack MardekianDepartment of Outcomes & Evidence, Pfizer, Inc; New York, New York, United States of America.
Cristina MasseriaDepartment of Outcomes & Evidence, Pfizer, Inc; New York, New York, United States of America.
Hemant PhatakDepartment of Global Health Economics and Outcomes Research, Bristol-Myers Squibb; Princeton, New Jersey, United States of America.
Shital KambleDepartment of Global Health Economics and Outcomes Research, Bristol-Myers Squibb; Princeton, New Jersey, United States of America.
Younos AbdulsattarDepartment of Outcomes & Evidence, Pfizer, Inc; New York, New York, United States of America.
William PetkunDepartment of Global Medical Affairs, Bristol-Myers Squibb; Princeton, New Jersey, United States of America.
Gregory Y H LipInstitute of Cardiovascular Sciences, University of Birmingham, City Hospital, Birmingham, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Limited real-world data are available regarding the comparative safety of non-vitamin K antagonist oral anticoagulants (NOACs). The objective of this retrospective claims observational cohort study was to compare the risk of bleeding among non-valvular atrial fibrillation (NVAF) patients prescribed apixaban, dabigatran, or rivaroxaban. NVAF patients aged ≥18 years with a 1-year baseline period were included if they were new initiators of NOACs or switched from warfarin to a NOAC. Cox proportional hazards modelling was used to estimate the adjusted hazard ratios of any bleeding, clinically relevant non-major (CRNM) bleeding, and major inpatient bleeding within 6 months of treatment initiation for rivaroxaban and dabigatran compared to apixaban. Among 60,227 eligible patients, 8,785 were prescribed apixaban, 20,963 dabigatran, and 30,529 rivaroxaban. Compared to dabigatran or rivaroxaban patients, apixaban patients were more likely to have greater proportions of baseline comorbidities and higher CHA2DS2-VASc and HAS-BLED scores. After adjusting for baseline clinical and demographic characteristics, patients prescribed rivaroxaban were more likely to experience any bleeding (HR: 1.35, 95% confidence interval [CI]: 1.26-1.45), CRNM bleeding (HR: 1.38, 95% CI: 1.27-1.49), and major inpatient bleeding (HR: 1.43, 95% CI: 1.17-1.74), compared to patients prescribed apixaban. Dabigatran patients had similar bleeding risks as apixaban patients. In conclusion, NVAF patients treated with rivaroxaban appeared to have an increased risk of any bleeding, CRNM bleeding, and major inpatient bleeding, compared to apixaban patients. There was no significant difference in any bleeding, CRNM bleeding, or inpatient major bleeding risks between patients treated with dabigatran and apixaban.

Indexed as

Administration, OralAdolescentAdultAgedAged, 80 and overAnticoagulantsAnti-Inflammatory Agents, Non-SteroidalAtrial FibrillationCohort StudiesDabigatranFemaleHemorrhageHumansInpatientsMaleMiddle AgedAnticoagulantsAnti-Inflammatory Agents, Non-SteroidalapixabanDabigatranPyrazolesPyridonesRivaroxabanVitamin KWarfarin

Identifiers

PMID30383768
PMCPMC6211674

What OpenQuestion holds

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Registered trials

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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.