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Low fibrinogen after intravenous thrombolysis: a possible predictor of hemorrhagic intracranial complications?

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F27661989%3A_____%2F25%3A10003515" target="_blank" >RIV/27661989:_____/25:10003515 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://onlinelibrary.wiley.com/doi/full/10.1111/ene.70191" target="_blank" >https://onlinelibrary.wiley.com/doi/full/10.1111/ene.70191</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1111/ene.70191" target="_blank" >10.1111/ene.70191</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Low fibrinogen after intravenous thrombolysis: a possible predictor of hemorrhagic intracranial complications?

  • Popis výsledku v původním jazyce

    Background and aims: Current Czech guidelines for treatment with intravenous thrombolysis (IVT) include the examination of coagulation parameters, including fibrinogen levels, before IVT, 6 hours and 24 hours after IVT, but there is no official recommendation on when to substitute fibrinogen, and whether to do so at all. Substitution is available in hospitals (Hemocomplettan i.v.). Fibrinogen substitution may be a way to prevent the development of bleeding complications during IVT treatment. The aim of this study was to evaluate whether a decrease in fibrinogen levels below the reference range of 1.8 g/l is associated with a higher likelihood of intracranial hemorrhage in patients with ischemic stroke treated with IVT.Methods: This multicenter retrospective study was conducted in 7 Czech centers. The study population consists of 280 patients enrolled in the observational group (divided into subgroups according to the type of hemorrhagic complication after IVT) and the control group (without hemorrhagic complication) according to the model 1:1 principle (same NIHSS, age, sex).Results: In all treatment groups (all observational subgroups as well as the control group), a decrease in fibrinogen levels was noted after IVT administration, with varying degrees of signification. A statistically significant difference (p = 0.0394) was found at 6 h after IVT administration in patients with the most clinically serious form of bleeding (parenchymal hematoma type 2), fibrinogen value 1.84 g/l versus 2.53 g/l.

  • Název v anglickém jazyce

    Low fibrinogen after intravenous thrombolysis: a possible predictor of hemorrhagic intracranial complications?

  • Popis výsledku anglicky

    Background and aims: Current Czech guidelines for treatment with intravenous thrombolysis (IVT) include the examination of coagulation parameters, including fibrinogen levels, before IVT, 6 hours and 24 hours after IVT, but there is no official recommendation on when to substitute fibrinogen, and whether to do so at all. Substitution is available in hospitals (Hemocomplettan i.v.). Fibrinogen substitution may be a way to prevent the development of bleeding complications during IVT treatment. The aim of this study was to evaluate whether a decrease in fibrinogen levels below the reference range of 1.8 g/l is associated with a higher likelihood of intracranial hemorrhage in patients with ischemic stroke treated with IVT.Methods: This multicenter retrospective study was conducted in 7 Czech centers. The study population consists of 280 patients enrolled in the observational group (divided into subgroups according to the type of hemorrhagic complication after IVT) and the control group (without hemorrhagic complication) according to the model 1:1 principle (same NIHSS, age, sex).Results: In all treatment groups (all observational subgroups as well as the control group), a decrease in fibrinogen levels was noted after IVT administration, with varying degrees of signification. A statistically significant difference (p = 0.0394) was found at 6 h after IVT administration in patients with the most clinically serious form of bleeding (parenchymal hematoma type 2), fibrinogen value 1.84 g/l versus 2.53 g/l.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30210 - Clinical neurology

Návaznosti výsledku

  • Projekt

  • Návaznosti

    N - Vyzkumna aktivita podporovana z neverejnych zdroju

Ostatní

  • Rok uplatnění

    2025

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    European Journal of Neurology

  • ISSN

    1351-5101

  • e-ISSN

    1468-1331

  • Svazek periodika

    32

  • Číslo periodika v rámci svazku

    Supplement 1

  • Stát vydavatele periodika

    US - Spojené státy americké

  • Počet stran výsledku

    1

  • Strana od-do

    80

  • Kód UT WoS článku

    001628319700875

  • EID výsledku v databázi Scopus