Evidence map›Paper›PMID 37261475›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2023

Comparison of edoxaban and enoxaparin in a rat model of AlCl

M Hachenberger, M Yeniguen, L Suenner, D Hinchliffe, C Mueller, A Wietelmann, T Gerriets, M Tschernatsch, M Juenemann, S T Gerner and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

13 authors at 4 institutions in 1 country.

M Hachenberger *Department of Neurology, Justus-Liebig University Giessen, Klinikstraße 33, 35385, Giessen, Germany.
M Yeniguen *Department of Neurology, Justus-Liebig University Giessen, Klinikstraße 33, 35385, Giessen, Germany.
L SuennerDepartment of Neurology, Justus-Liebig University Giessen, Klinikstraße 33, 35385, Giessen, Germany.
D HinchliffeDepartment of Neurology, Justus-Liebig University Giessen, Klinikstraße 33, 35385, Giessen, Germany.
C MuellerDepartment of Radiology, Kerckhoff-Klinik Bad Nauheim, 61231, Bad Nauheim, Germany.
A WietelmannScientific Service Group Magnetic Resonance Imaging, Max Planck Institute for Heart and Lung Research, 61231, Bad Nauheim, Germany.
T GerrietsDepartment of Neurology, Justus-Liebig University Giessen, Klinikstraße 33, 35385, Giessen, Germany.
M TschernatschDepartment of Neurology, Justus-Liebig University Giessen, Klinikstraße 33, 35385, Giessen, Germany.
M JuenemannDepartment of Neurology, Justus-Liebig University Giessen, Klinikstraße 33, 35385, Giessen, Germany.
S T GernerDepartment of Neurology, Justus-Liebig University Giessen, Klinikstraße 33, 35385, Giessen, Germany.
T R DoeppnerDepartment of Neurology, Justus-Liebig University Giessen, Klinikstraße 33, 35385, Giessen, Germany.
H B HuttnerDepartment of Neurology, Justus-Liebig University Giessen, Klinikstraße 33, 35385, Giessen, Germany.
T BraunDepartment of Neurology, Justus-Liebig University Giessen, Klinikstraße 33, 35385, Giessen, Germany. tobias.braun@neuro.med.uni-giessen.de.
Brain (Germany) · DEUniversity of Giessen · DEKerckhoff Klinik · DEMax Planck Institute for Heart and Lung Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebral sinus venous thrombosis (CSVT) is an uncommon disease that is usually treated with anticoagulation (heparin, low-molecular heparin, or vitamin K-antagonists). We compared treatment with edoxaban, an oral factor Xa-antagonist, that has not been approved in patients with CSVT, with enoxaparin, a well-established therapy, in a rat model of CSVT. Fifty male Wistar rats were randomized into 5 groups (10 animals each) and subjected to aluminum chloride (AlCl3)-induced thrombosis of the superior sagittal sinus (SSS) or sham procedure. Animals with thrombosis of the SSS were treated with edoxaban, enoxaparin, or placebo. Diagnostic workup included neurological examination, MRI imaging, MR-flow measurements of the SSS, and immunohistochemical staining. Neurological examination revealed no differences between treatment groups. Seven days after initial thrombosis, flow in the SSS was lower in the active treatment group as compared to sham-operated animals (p < 0.05). Flow in the SSS in the active treatment groups (edoxaban 1 h prior to thrombosis: 0.16 cm/s ± 0.06 cm/s; edoxaban 6 h after thrombosis: 0.13 cm/s ± 0.05 cm/s; enoxaparin: 0.13 cm/s ± 0.04 cm/s; placebo: 0.07 cm/s ± 0.02 cm/s) was higher as compared to placebo (p < 0.05), but there were no differences between the active treatment groups (p > 0.05). Immunohistochemical staining showed no differences in the actively treated animals. Edoxaban proved to be similar to enoxaparin in a model of experimental AlCl

Indexed as

EnoxaparinThrombosisAnimalsFactor Xa InhibitorsHeparinHumansMalePyridinesRatsRats, WistarSuperior Sagittal SinusThiazolesedoxabanEnoxaparinFactor Xa InhibitorsHeparinPyridinesThiazolesCerebral venous thrombosisEdoxabanRatSinus thrombosisStroke

Identifiers

PMID37261475
PMCPMC10643418
OpenAlexW4378952017

What OpenQuestion holds

Textmetadata
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.