Evidence map›Paper›PMID 28772696›Full record

ArticleMaterials (Basel, Switzerland)2017

Effect of Immobilized Antithrombin III on the Thromboresistance of Polycarbonate Urethane.

Karin Lukas, Karin Stadtherr, Andre Gessner, Daniel Wehner, Thomas Schmid, Hans Peter Wendel, Christof Schmid, Karla Lehle

Open access · goldAbstract read
In one paragraph

Article in Materials (Basel, Switzerland), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 4 institutions in 1 country.

Karin LukasIMHR, Institute for Medical Microbiology and Hygiene, University of Regensburg, Franz-Josef-Strauss-Allee 11, 93042 Regensburg, Germany. Karin.Lukas@UKR.de.
Karin StadtherrIMHR, Institute for Medical Microbiology and Hygiene, University of Regensburg, Franz-Josef-Strauss-Allee 11, 93042 Regensburg, Germany. Karin.Stadtherr@gmail.com.
Andre GessnerIMHR, Institute for Medical Microbiology and Hygiene, University of Regensburg, Franz-Josef-Strauss-Allee 11, 93042 Regensburg, Germany. Andre.Gessner@UKR.de.
Daniel WehnerDualis Medtech GmbH, Am Technologiepark 8+10, 82229 Seefeld, Germany. Daniel.Wehner@dualis-medtech.de.
Thomas SchmidDualis Medtech GmbH, Am Technologiepark 8+10, 82229 Seefeld, Germany. Thomas.Schmid@hotmail.de.
Hans Peter WendelDepartment of Thoracic, Cardiac, and Vascular Surgery, University Hospital Tübingen, Hoppe-Seyler-Str. 3, 72076 Tübingen, Germany. Hans-Peter.Wendel@med.uni-tuebingen.de.
Christof SchmidDepartment of Cardiothoracic Surgery, University Medical Center Regensburg, Josef-Strauss-Allee 11, 93042 Regensburg, Germany. Christof.Schmid@UKR.de.
Karla LehleDepartment of Cardiothoracic Surgery, University Medical Center Regensburg, Josef-Strauss-Allee 11, 93042 Regensburg, Germany. Karla.Lehle@UKR.de.
University Hospital Regensburg · DEUniversity of Regensburg · DEInstitute of Medical Microbiology and Hygiene · DEUniversity Children's Hospital Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The surface of foils and vascular grafts made from a thermoplastic polycarbonate urethanes (PCU) (Chronoflex AR) were chemically modified using gas plasma treatment, binding of hydrogels-(1) polyethylene glycol bisdiamine and carboxymethyl dextran (PEG-DEX) and (2) polyethyleneimine (PEI)-and immobilization of human antithrombin III (AT). Their biological impact was tested in vitro under static and dynamic conditions. Static test methods showed a significantly reduced adhesion of endothelial cells, platelets, and bacteria, compared to untreated PCU. Modified PCU grafts were circulated in a Chandler-Loop model for 90 min at 37 °C with human blood. Before and after circulation, parameters of the hemostatic system (coagulation, platelets, complement, and leukocyte activation) were analyzed. PEI-AT significantly inhibited the activation of both coagulation and platelets and prevented the activation of leukocytes and complement. In conclusion, both modifications significantly reduce coagulation activation, but only PEI-AT creates anti-bacterial and anti-thrombogenic functionality.

Indexed as

anti-bacterialantithrombin IIIhemocomaptibilitypolycarbonate urethanethromboresistance

Identifiers

PMID28772696
PMCPMC5506919
OpenAlexW2599504714

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.