Evidence map›Paper›PMID 28879581›Full record

ArticleJournal of thrombosis and thrombolysis2017

Activation of blood coagulation and thrombin generation in acute ischemic stroke treated with rtPA.

Sarah Goldman, Shannon M Prior, Jan P Bembenek, Maciej Niewada, Elżbieta Broniatowska, Anna Członkowska, Saulius Butenas, Anetta Undas

Open access · hybridAbstract read
In one paragraph

Article in Journal of thrombosis and thrombolysis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

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  4. 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

8 authors at 5 institutions in 2 countries.

Sarah GoldmanKrakow Center for Medical Research and Technology, John Paul II Hospital, Krakow, Poland.
Shannon M PriorDepartment of Biochemistry, University of Vermont, Colchester, VT, USA.
Jan P Bembenek2nd Department of Neurology, Institute of Psychiatry and Neurology, Warsaw, Poland.
Maciej Niewada2nd Department of Neurology, Institute of Psychiatry and Neurology, Warsaw, Poland.
Elżbieta BroniatowskaDepartment of Bioinformatics and Telemedicine, Jagiellonian University Medical College, Krakow, Poland.
Anna Członkowska2nd Department of Neurology, Institute of Psychiatry and Neurology, Warsaw, Poland.
Saulius ButenasDepartment of Biochemistry, University of Vermont, Colchester, VT, USA.
Anetta UndasKrakow Center for Medical Research and Technology, John Paul II Hospital, Krakow, Poland. mmundas@cyf-kr.edu.pl.
Institute of Psychiatry and Neurology · PLUniversity of Vermont · USInstitute of Cardiology · PLJagiellonian University · PLJohn Paul II Hospital · PL

Funding

Analysis and Characterization of Trauma-Induced CoagulopathyUM1HL120877 · NHLBI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI MORRISSEY, JAMES H., WISNIEWSKI, STEPHEN R · 2013 to 2019
$26.6M
National Institutes of Health UM1 HL120877NHLBI NIH HHS UM1 HL120877
6 · The paper itself

Abstract

The impact of thrombolysis with recombinant tissue plasminogen activator (rtPA) on blood coagulation in acute ischemic stroke (AIS) patients is not completely understood. We studied the effect of thrombolysis on the thrombin generation (TG) profile as well as coagulant activity of activated factors IX (FIXa), XI (FXIa) and tissue factor (TF) in AIS patients. In a case-control study, TG parameters as well as FIXa, FXIa and TF levels were assessed in 95 AIS patients, including individuals receiving rtPA treatment within 4.5 h since AIS onset (n = 71, 74.7%) and those ineligible for thrombolysis (n = 24, 25.3%). Blood samples were collected at baseline and after 24 h since admission. The two groups were similar with regard to demographics and clinical factors. In thrombolysed patients, all TG parameters measured after 24 h were markedly decreased, with strongest impact on lag time (LT), when compared with the baseline values (81.3% longer LT, p < 0.0001), as well as when compared to the non-thrombolysed group (86% longer LT, p = 0.002). In non-thrombolysed AIS patients the TG remained unaltered. Logistic regression adjusted for potential confounders showed that high baseline ETP value (the top quartile) was solely predicted by the presence of circulating FIXa, whereas after 24 h FXIa predicted high ETP in the subgroup of thrombolysed and in all AIS patients. Thrombolysis in AIS patients markedly attenuates the TG. Elevated FXIa contributes to thrombin formation capacity after 24 h, highlighting a role of this factor in the regulation of blood coagulation in AIS.

Indexed as

Blood CoagulationThrombolytic TherapyAgedAged, 80 and overBrain IschemiaCase-Control StudiesFactor IXaFactor XIaFemaleHumansMaleStrokeThrombinThromboplastinTissue Plasminogen ActivatorFactor IXaFactor XIaThrombinThromboplastinTissue Plasminogen ActivatorCoagulation factorStrokeThrombin generationThrombolysis

Identifiers

PMID28879581
PMCPMC5617868
OpenAlexW2752648761

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.