Evidence map›Paper›PMID 36836514›Full record

ArticleJournal of personalized medicine2023

Peri-Interventional Triple Therapy with Dabigatran Modifies Vasomotion after Bare-Metal Stent Implantation in a Pig Coronary Artery Model.

Rayyan Hemetsberger, Serdar Farhan, Dominika Lukovic, Katrin Zlabinger, Judit Hajagos-Toth, Judit Bota, Hector M Garcia-Garcia, Cihan Ay, Eslam Samaha, Robert Gaspar and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2023. 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
1.0field-weighted citation impact, top 27% 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, 4 citations in OpenAlex.

  1. Article
  2. Review
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

14 authors at 6 institutions in 3 countries.

Rayyan HemetsbergerDepartment of Cardiology, 2nd Department of Internal Medicine, Medical University of Vienna, 1090 Vienna, Austria.
Serdar FarhanZena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Dominika LukovicDepartment of Cardiology, 2nd Department of Internal Medicine, Medical University of Vienna, 1090 Vienna, Austria.
Katrin ZlabingerDepartment of Cardiology, 2nd Department of Internal Medicine, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-3855-7643
Judit Hajagos-TothDepartment of Pharmacology and Pharmacotherapy, Albert Szent-Györgyi Medical School, University of Szeged, 6720 Szeged, Hungary.
Judit BotaDepartment of Pharmacology and Pharmacotherapy, Albert Szent-Györgyi Medical School, University of Szeged, 6720 Szeged, Hungary.
Hector M Garcia-GarciaMedstar Hospital Center, Department of Cardiology, Washington, DC 20010, USA.ORCID 0000-0001-5100-0471
Cihan AyClinical Division of Haematology and Haemostaseology, Department of Medicine I, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0003-2607-9717
Eslam SamahaDepartment of Cardiology, 2nd Department of Internal Medicine, Medical University of Vienna, 1090 Vienna, Austria.
Robert GasparDepartment of Pharmacology and Pharmacotherapy, Albert Szent-Györgyi Medical School, University of Szeged, 6720 Szeged, Hungary.
Rita GaramvölgyiInstitute of Diagnostics and Radiation Oncology, University of Kaposvar, 7400 Kaposvar, Hungary.
Kurt Huber3rd Medical Department with Cardiology, Wilhelminen Hospital, 1160 Vienna, Austria.
Andreas SpannbauerDepartment of Cardiology, 2nd Department of Internal Medicine, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-9819-0361
Mariann GyöngyösiDepartment of Cardiology, 2nd Department of Internal Medicine, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-7083-2107
Medical University of Vienna · ATUniversity of Szeged · HUIcahn School of Medicine at Mount Sinai · USMedStar Washington Hospital Center · USUniversity of Kaposvár · HUWilhelminen Hospital · AT

Funding

Boehringer Ingelheim Foundation
6 · The paper itself

Abstract

(1) Background: Coronary artery stenting leads to local inflammation, disturbs vasomotion, and slows endothelialization, increasing vascular thrombus risk. We used a pig stenting coronary artery model to assess how peri-interventional triple therapy with dabigatran ameliorates these effects. (2) Methods: In a total of 28 pigs bare-metal stents were implanted. Four days before the percutaneous coronary intervention (PCI), we started 16 of the animals on dabigatran, maintained through 4 days after the procedure. As controls, the remaining 12 pigs received no therapy. In both groups, dual antiplatelet therapy (DAPT) (clopidogrel, 75 mg plus aspirin, 100 mg) was administered until animals were euthanized. Just after the PCI and on day 3 after the procedure, we performed optical coherence tomography (OCT) in eight animals in the dabigatran group and four controls and euthanized them. We followed the eight remaining animals in each group with OCT and angiography for one month before euthanizing them and performed in vitro myometry and histology on harvested coronary arteries from all animals. (3) Results: The dabigatran group showed a significantly increased vasoconstriction at 3 days after PCI (10.97 ± 3.85 mN vs. 7.32 ± 5.41 mN,

Indexed as

bare metal stentdabigatranneointimal formationpreclinicalvasomotor function

Identifiers

PMID36836514
PMCPMC9962101
OpenAlexW4318778125

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.