Evidence map›Paper›PMID 39574230›Full record

ArticleClinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis

Total Thrombus-Formation System in Patients with Peripheral Artery Disease.

Christian Pfrepper, Careen Franke, Michael Metze, Maria Weise, Annelie Siegemund, Roland Siegemund, Martin Federbusch, Reinhard Henschler, Sirak Petros, Manuela Konert

Abstract read
In one paragraph

Article in Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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.

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

10 authors.

Christian PfrepperDivision of Hemostaseology, University of Leipzig Medical Center, Leipzig, Germany.ORCID 0000-0002-0485-7402
Careen FrankeDivision of Hemostaseology, University of Leipzig Medical Center, Leipzig, Germany.
Michael MetzeDepartment of Cardiology, University of Leipzig Medical Center, Leipzig, Germany.
Maria WeiseDivision of Hemostaseology, University of Leipzig Medical Center, Leipzig, Germany.
Annelie SiegemundDivision of Hemostaseology, University of Leipzig Medical Center, Leipzig, Germany.
Roland SiegemundMedical ICU, University of Leipzig Medical Center, Leipzig, Germany.
Martin FederbuschInstitute for Laboratory Medicine, University of Leipzig Medical Center, Leipzig, Germany.ORCID 0000-0002-1126-5763
Reinhard HenschlerInstitute for Transfusion Medicine, University of Leipzig Medical Center, Leipzig, Germany.
Sirak PetrosDivision of Hemostaseology, University of Leipzig Medical Center, Leipzig, Germany.ORCID 0000-0002-2345-756X
Manuela KonertDepartment of Angiology, University of Leipzig Medical Center, Leipzig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Total Thrombus-formation Analysis System (T-TAS) is an automated device using coated microchips to assess thrombus formation under flow conditions. Its value to monitor coagulation function in patients under antiplatelet therapy awaits further clarification. This study evaluated T-TAS to detect response to dual antiplatelet therapy (DAPT) in patients with peripheral artery disease (PAD).T-TAS using the platelet-chip (PL-chip) and atheroma-chip (AR-chip) was performed in 60 patients with PAD on the day after lower extremity revascularization. Results were compared with light transmission aggregometry (LTA) and multiple electrode aggregometry (MEA, ADP- and ASPI-test). To determine T-TAS reference ranges, 30 healthy blood donors were enrolled.The area under the curve of the PL-chip (AUC-PL) was outside the reference range in 91.2% and AUC-AR in 21.1% of the PAD patients. Low responders in MEA ASPI, MEA ADP or both tests and low responders in LTA induced by ADP had a significantly higher AUC-PL compared to responders (204 vs 70, p = .016 and 140 vs 32, p < .001), respectively. Median AUC-PL in low responders in LTA and MEA, LTA or MEA and in responders in LTA and MEA was 301, 104 and 32 (p = .001), respectively. Our results suggest that the PL-chip can continuously assess the level of response to DAPT and might be helpful to monitor PAD patients.

Indexed as

Peripheral Arterial DiseaseThrombosisAgedAged, 80 and overFemaleHumansMaleMiddle AgedPlatelet Aggregation InhibitorsPlatelet Aggregation Inhibitorsantiplatelet monitoringclopidogreldual antiplatelet therapyperipheral artery diseaseT-TAS

Identifiers

PMID39574230
PMCPMC11585050

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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.