Evidence map›Paper›PMID 30599063›Full record

Trial reportHeart and vessels2019

Comparison of anti-inflammatory effects of rivaroxaban vs. dabigatran in patients with non-valvular atrial fibrillation (RIVAL-AF study): multicenter randomized study.

Shinnosuke Kikuchi, Kengo Tsukahara, Kentaro Sakamaki, Yukiko Morita, Takeshi Takamura, Kazuki Fukui, Tsutomu Endo, Makoto Shimizu, Reimin Sawada, Teruyasu Sugano and 10 more

Abstract readComparative StudyMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Heart and vessels, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Observational
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. 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

20 authors at 12 institutions in 1 country.

Shinnosuke KikuchiDivision of Cardiology, Yokohama City University Medical Center, 4-57 Urafune-cho, Minami-ku, Yokohama, 232-0024, Japan.
Kengo TsukaharaDivision of Cardiology, Yokohama City University Medical Center, 4-57 Urafune-cho, Minami-ku, Yokohama, 232-0024, Japan. k-tsuka@urahp.yokohama-cu.ac.jp.ORCID http://orcid.org/0000-0002-9115-2880
Kentaro SakamakiDepartment of Biostatistics, Yokohama City University Hospital, Yokohama, Japan.
Yukiko MoritaDivision of Cardiology, National Hospital Organization Sagamihara National Hospital, Sagamihara, Japan.
Takeshi TakamuraDivision of Cardiology, Nagatsuda Kousei General Hospital, Yokohama, Japan.
Kazuki FukuiDivision of Cardiology, Kanagawa Cardiovascular and Respiratory Center, Yokohama, Japan.
Tsutomu EndoDivision of Cardiology, Saiseikai Yokohama City Southern Hospital, Yokohama, Japan.
Makoto ShimizuDivision of Cardiology, International Goodwill Hospital, Yokohama, Japan.
Reimin SawadaDivision of Cardiology, Hadano Red Cross Hospital, Hadano, Japan.
Teruyasu SuganoDivision of Cardiology, Yokohama City University Hospital, Yokohama, Japan.
Hideo HimenoDivision of Cardiology, Fujisawa City Hospital, Fujisawa, Japan.
Syunichi KobayashiDivision of Cardiology, Yokohama Hodogaya Central Hospital, Yokohama, Japan.
Kentaro ArakawaDivision of Cardiology, Fujisawa Shounandai Hospital, Fujisawa, Japan.
Yasuyuki MochidaDivision of Cardiology, Omori Red Cross Hospital, Tokyo, Japan.
Takashi TsunematsuDivision of Cardiology, Ashigarakami Hospital, Ashigara, Japan.
Tomohiko ShigemasaDivision of Cardiology, International University of Health and Welfare Atami Hospital, Atami, Japan.
Jun OkudaDivision of Cardiology, Yokosuka City Hospital, Yokosuka, Japan.
Toshiyuki IshikawaDivision of Cardiology, Yokohama City University Hospital, Yokohama, Japan.
Kazuo KimuraDivision of Cardiology, Yokohama City University Medical Center, 4-57 Urafune-cho, Minami-ku, Yokohama, 232-0024, Japan.
Kouichi TamuraDepartment of Medical Science and Cardiorenal Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Yokohama City University Hospital · JPYokohama City University Medical Center · JPFujisawa City Hospital · JPHiratsuka City Hospital · JPInternational Goodwill Hospital · JPInternational University Of Health And Welfare Atami Hospital · JPJapanese Red Cross Hadano Hospital · JPKanagawa Cardiovascular and Respiratory Center · JPNational Sagamihara Hospital · JPSaiseikai Yokohama Eastern Hospital · JPSocial Insurance Yokohama Central Hospital · JPYokohama City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some experimental studies have shown that direct oral anticoagulants (DOACs) have anti-inflammatory effects. However, the interval changes in inflammatory markers in patients with non-valvular atrial fibrillation (AF) who receive DOACs remain unknown. Between July 2013 and April 2014, a total of 187 AF patients randomly assigned to receive rivaroxaban (n = 91) or dabigatran (n = 96) were assessed for eligibility. The levels of the following inflammatory markers were serially evaluated: high-sensitivity C-reactive protein, pentraxin-3, interleukin (IL)-1β, IL-6, IL-18, tumor necrosis factor-α, monocyte chemotactic protein-1, growth and differentiation factor-15, and soluble thrombomodulin (sTM). The aim in this study was to evaluate the anti-inflammatory effects of rivaroxaban and dabigatran in patients with AF, in addition to the impact of markers on bleeding events. Finally, 117 patients (rivaroxaban: n = 55, dabigatran: n = 62) were included in the analysis at 12 months. Although the interval changes in sTM levels tended to be greater in the dabigatran group [0.3 (0-0.7) vs. 0.5 (0-1.0) FU/ml, p = 0.061], there were no significant differences in the interval changes in any inflammatory marker between 2 groups. There were no significant differences in bleeding events between 2 groups. The interval changes in sTM levels were significantly greater in patients with bleeding compared with those without [0.8 (0.5-1.3) vs. 0.4 (- 0.1-0.8) FU/ml, p = 0.017]. There were no significant differences in the interval changes in any inflammatory marker between rivaroxaban and dabigatran treatments in patients with AF. The increased levels of sTM after DOACs treatment might be related to bleeding events.

Indexed as

AgedAnticoagulantsAtrial FibrillationDabigatranFemaleHemorrhageHumansJapanMaleMiddle AgedMultivariate AnalysisProspective StudiesRegression AnalysisRivaroxabanSeverity of Illness IndexStrokeAnticoagulantsDabigatranRivaroxabanAtrial fibrillationBleedingDirect oral anticoagulationInflammationThrombomodulin

Identifiers

PMID30599063
OpenAlexW2908052388

What OpenQuestion holds

Textmetadata
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.