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
—