Evidence map›Paper›PMID 35888060›Full record

ArticleLife (Basel, Switzerland)2022

Dabigatran in Cerebral Sinus Vein Thrombosis and Thrombophilia.

Lukas Kellermair, Matthias W G Zeller, Caterina Kulyk, Josef Tomasits, Tim J von Oertzen, Milan R Vosko

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 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
0.4field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
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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

6 authors at 1 institution in 1 country.

Lukas KellermairDepartment of Neurology 2, Kepler University Hospital, Med Campus III, 4020 Linz, Austria.ORCID 0000-0003-4986-5657
Matthias W G ZellerDepartment of Neurology 2, Kepler University Hospital, Med Campus III, 4020 Linz, Austria.
Caterina KulykDepartment of Neurology 2, Kepler University Hospital, Med Campus III, 4020 Linz, Austria.
Josef TomasitsMedical Faculty, Johannes Kepler University, 4040 Linz, Austria.
Tim J von OertzenDepartment of Neurology 2, Kepler University Hospital, Med Campus III, 4020 Linz, Austria.
Milan R VoskoDepartment of Neurology 2, Kepler University Hospital, Med Campus III, 4020 Linz, Austria.
Johannes Kepler University of Linz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeThrombophilic gene alterations are a major risk factor for cerebral sinus vein thrombosis (CSVT). Up to 30% of all patients with cerebral sinus vein thrombosis (CSVT) are found to have thrombophilic defects such as prothrombin mutation (PTM) or factor V Leiden (FVL). Their repercussions on the plasma levels of dabigatran etexilate are unclear. In this prospective case-control study, we aimed to investigate whether thrombophilia in CSVT has an influence on dabigatran peak-plasma levels.

methodsWe monitored 10 patients over 12 months with acute CSVT, genetic thrombophilia with off-label use of dabigatran etexilate 150 mg twice a day and measured dabigatran peak-plasma levels and radiological outcome. We also monitored patients without genetic thrombophilia with dabigatran etexilate 150 mg twice a day and compared the efficiency and dabigatran peak-plasma levels.

resultsPatients with homozygote PTM had significantly lower dabigatran peak concentration compared to patients with FVL or the control group (23 ± 4.2 vs. 152.3 ± 27.5 and 159.6 ± 63.08;

conclusionsDabigatran peak concentration was stable in patients with heterozygote FVL and heterozygote PTM, but not in homozygote PTM, compared to controls. Genetic screening for thrombophilia in patients after CSVT may be useful to make patient tailored therapeutic decisions regarding oral anticoagulation and may decrease thrombotic events.

Indexed as

cerebral sinus vein thrombosisdabigatran peak concentrationfactor II mutationfactor V Leidenthrombus dissolution

Identifiers

PMID35888060
PMCPMC9316430
OpenAlexW4283701402

What OpenQuestion holds

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LicenceCC BY
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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.