Evidence map›Paper›PMID 27769294›Full record

Trial reportEuropean journal of medical research2016

Incidence of left atrial abnormalities under treatment with dabigatran, rivaroxaban, and vitamin K antagonists.

Stefan Reers, Tolga Agdirlioglu, Michael Kellner, Matthias Borowski, Holger Thiele, Johannes Waltenberger, Michael Reppel

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in European journal of medical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 21% 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, 2 syntheses or guidelines pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
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

7 authors at 3 institutions in 1 country.

Stefan ReersDepartment of Cardiovascular Medicine, University Hospital Muenster, 48149, Muenster, Germany. stefan.reers@ukmuenster.de.
Tolga AgdirliogluDepartment of Cardiology/Angiology/Intensive Care Medicine, University Heart Center Luebeck, Luebeck, Germany.
Michael KellnerDepartment of Cardiology/Angiology/Intensive Care Medicine, University Heart Center Luebeck, Luebeck, Germany.
Matthias BorowskiInstitute of Biostatistics and Clinical Research, University of Muenster, Muenster, Germany.
Holger ThieleDepartment of Cardiology/Angiology/Intensive Care Medicine, University Heart Center Luebeck, Luebeck, Germany.
Johannes WaltenbergerDepartment of Cardiovascular Medicine, University Hospital Muenster, 48149, Muenster, Germany.
Michael ReppelDepartment of Cardiology/Angiology/Intensive Care Medicine, University Heart Center Luebeck, Luebeck, Germany.
University Hospital Münster · DEUniversity Hospital Schleswig-Holstein · DEUniversity of Lübeck · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-vitamin K antagonist oral anticoagulants (NOACs) such as dabigatran or rivaroxaban are alternatives to vitamin K antagonists (VKAs) for prevention of stroke and systemic embolism in patients with atrial fibrillation (AF) and atrial flutter (AFL). Incidences of risk factors for left atrium (LA) and left atrial appendage (LAA) thrombus formation, such as dense spontaneous echo contrast (SEC), low LAA velocity (LAAV) <20 cm/s under treatment with dabigatran and rivaroxaban in comparison with VKAs are unknown.

methodsWe studied 306 patients with AF (94 %) and AFL (6 %) undergoing transesophageal echocardiography. Patients received VKAs (n = 138), dabigatran (n = 68), or rivaroxaban (n = 100) for at least 3 weeks prior to investigation. Time in therapeutic range was 67 % for VKA. Mean CHADS

resultsAny LA abnormality occurred in 9, 3, and 5 % of patients receiving VKA, dabigatran, and rivaroxaban, respectively. The most frequent abnormality was LAA thrombus (VKA: 4 %, dabigatran: 0 %, rivaroxaban: 2 %) and low LAAV of less than 20 cm/s (VKA: 4 %, dabigatran: 1 %, rivaroxaban: 1 %), followed by dense SEC (VKA: 2 %, dabigatran: 1 %, rivaroxaban: 2 %). Results of uni- and multivariate analyses revealed a numerically lower but not significantly different frequency of any LA abnormality under dabigatran (OR 0.4, 95 % Cl 0.08 - 1.88, p = 0.25) and rivaroxaban (OR 0.65, 95 % Cl 0.22 - 1.98, p = 0.45) compared to VKA.

conclusionWith respect to the incidence of LA abnormalities, dabigatran and rivaroxaban are not inferior to VKA.

Indexed as

AgedAtrial FibrillationAtrial FlutterAtrial Function, LeftDabigatranElectrocardiographyFemaleHeart AtriaHumansMaleMiddle AgedRivaroxabanThrombosisVitamin KDabigatranRivaroxabanVitamin KAtrial fibrillationDabigatranLeft atrial appendageRivaroxabanThrombusVitamin K antagonist

Identifiers

PMID27769294
PMCPMC5073429
OpenAlexW2534592337

What OpenQuestion holds

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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 OpenQuestion graph.