Evidence map›Paper›PMID 35785369›Full record

ArticleJournal of arrhythmia2022

Impact of different dose reduction criteria for anti-Xa direct oral anticoagulants on bleeding complications: A single center observational study.

Hidehira Fukaya, Jun Oikawa, Hironori Nakamura, Tazuru Igarashi, Tamami Fujiishi, Naruya Ishizue, Tomoharu Yoshizawa, Akira Satoh, Jun Kishihara, Shinichi Niwano and 1 more

Abstract read
In one paragraph

Article in Journal of arrhythmia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Hidehira FukayaDepartment of Cardiovascular Medicine Kitasato University School of Medicine Sagamihara Japan.ORCID https://orcid.org/0000-0002-7588-554X
Jun OikawaDepartment of Cardiovascular Medicine Kitasato University School of Medicine Sagamihara Japan.ORCID https://orcid.org/0000-0003-2223-9541
Hironori NakamuraDepartment of Cardiovascular Medicine Kitasato University School of Medicine Sagamihara Japan.ORCID https://orcid.org/0000-0003-4463-6185
Tazuru IgarashiDepartment of Cardiovascular Medicine Kitasato University School of Medicine Sagamihara Japan.ORCID https://orcid.org/0000-0003-0890-2757
Tamami FujiishiDepartment of Cardiovascular Medicine Kitasato University School of Medicine Sagamihara Japan.ORCID https://orcid.org/0000-0002-8494-9621
Naruya IshizueDepartment of Cardiovascular Medicine Kitasato University School of Medicine Sagamihara Japan.ORCID https://orcid.org/0000-0002-2448-616X
Tomoharu YoshizawaDepartment of Cardiovascular Medicine Kitasato University School of Medicine Sagamihara Japan.
Akira SatohDepartment of Cardiovascular Medicine Kitasato University School of Medicine Sagamihara Japan.
Jun KishiharaDepartment of Cardiovascular Medicine Kitasato University School of Medicine Sagamihara Japan.ORCID https://orcid.org/0000-0002-5920-4417
Shinichi NiwanoDepartment of Cardiovascular Medicine Kitasato University School of Medicine Sagamihara Japan.ORCID https://orcid.org/0000-0002-0702-0800
Junya AkoDepartment of Cardiovascular Medicine Kitasato University School of Medicine Sagamihara Japan.ORCID https://orcid.org/0000-0001-6645-6404

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Each direct oral anticoagulant (DOAC) has different dose reduction criteria. Here, we evaluated the differences in the doses of three anti-Xa DOACs and clinical events based on the dose reduction criteria in patients with atrial fibrillation (AF). Methods: Consecutive AF patients prescribed with anti-Xa DOACs [rivaroxaban (Riva), apixaban (Apix), and edoxaban (Edox)] between April 2011 and May 2016 were retrospectively evaluated. The incidences of thromboembolic and bleeding events were evaluated by the end of December 2020, focusing on the dose proportion. Results: A total of 786 patients (72 ± 10 years old, 66.9% male) were enrolled in this study [Riva ( Conclusions: The patients with a standard dose of Apix had a higher incidence of minor bleeding events than the other dosages. A reduced dose of apixaban was not prone to being chosen because of the dose reduction criteria, which may have been associated with a higher minor bleeding rate in patients with Apix.

Indexed as

anti‐Xa direct oral anticoagulantsatrial fibrillationbleeding complicationsdose reduction criteria

Identifiers

PMID35785369
PMCPMC9237315

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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.