Evidence map›Paper›PMID 36562754›Full record

ArticleBlood advances2023

Comparison of the effectiveness and safety of direct oral anticoagulants: a nationwide propensity score-weighted study.

Arnar B Ingason, Johann P Hreinsson, Arnar S Agustsson, Sigrun H Lund, Edward Rumba, Daniel A Palsson, Indridi E Reynisson, Brynja R Gudmundsdottir, Pall T Onundarson, Einar S Bjornsson

Open access · goldAbstract readComparative Study
In one paragraph

Article in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
2.1field-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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
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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

10 authors at 5 institutions in 2 countries.

Arnar B IngasonFaculty of Medicine, University of Iceland, Reykjavik, Iceland.
Johann P HreinssonDepartment of Internal Medicine & Clinical Nutrition, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Sweden.
Arnar S AgustssonFaculty of Medicine, University of Iceland, Reykjavik, Iceland.
Sigrun H LundDeCODE Genetics, Reykjavik, Iceland.
Edward RumbaFaculty of Medicine, University of Iceland, Reykjavik, Iceland.
Daniel A PalssonFaculty of Medicine, University of Iceland, Reykjavik, Iceland.
Indridi E ReynissonPrimary Health Care of the Capital Area, Reykjavik, Iceland.
Brynja R GudmundsdottirHematology Laboratory and Thrombosis and Hemostasis Center, Landspitali University Hospital, Reykjavik, Iceland.
Pall T OnundarsonFaculty of Medicine, University of Iceland, Reykjavik, Iceland.
Einar S BjornssonFaculty of Medicine, University of Iceland, Reykjavik, Iceland.
National University Hospital of Iceland · ISAdministration of Occupational Safety and Health · ISdeCODE Genetics (Iceland) · ISUniversity of Gothenburg · SEUniversity of Iceland · IS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the pivotal randomized controlled trials (RCTs) for patients with atrial fibrillation, direct oral anticoagulants (DOACs) had similar or even superior efficacy and safety compared with warfarin. However, RCTs comparing different DOACs are nonexistent and previous observational studies have yielded conflicting results. In this nationwide cohort study, rates of any stroke or systemic embolism (stroke/SE) and major bleeding were compared among new users of apixaban, dabigatran, and rivaroxaban with atrial fibrillation from 2014 to 2019. Inverse probability weighting was used to yield balanced study groups, and outcomes were compared using Cox regression. Stroke/SE rates were similar in patients receiving apixaban, dabigatran, and rivaroxaban. Dabigatran was associated with twofold higher rates of myocardial infarction (MI) than rivaroxaban (1.4 events/100 person-years (py) vs 0.7 events/100-py, hazard ratio [HR] 2.21, 95% confidence interval [CI], 1.00-4.90) and apixaban (1.4 events/100-py vs 0.7 events/100-py, HR 2.26, 95% CI, 0.90-5.67), although the second comparison included the possibility of a null effect. Rivaroxaban was associated with higher major bleeding rates compared with apixaban (2.9 events/100-py vs 1.8 events/100-py, HR 1.64, 95% CI, 1.13-2.37) and dabigatran (2.9 events/100-py vs 1.4 events/100-py, HR 2.18, 95% CI, 1.21-3.93). Specifically, rivaroxaban had higher rates of major gastrointestinal bleeding and other major bleeding than apixaban. In conclusion, although stroke/SE rates were similar for DOACs, rivaroxaban was associated with higher rates of major bleeding than other DOACs and lower rates of MI than dabigatran. These results may help guide oral anticoagulant selection, especially in patients at high risk of bleeding or MI.

Indexed as

Atrial FibrillationMyocardial InfarctionStrokeAnticoagulantsDabigatranHemorrhageHumansPropensity ScoreRivaroxabanAnticoagulantsDabigatranRivaroxaban

Identifiers

PMID36562754
PMCPMC10242633
OpenAlexW4312114542

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.