2018
Intravenous Thrombolysis in Patients with Acute Ischemic Stroke after a Reversal of Dabigatran Anticoagulation with Idarucizumab: A Real-World Clinical Experience
ŠAŇÁK, Daniel, Stanislava JAKUBÍČEK, David ČERNÍK, Roman HERZIG, Zdeněk KUNÁŠ et. al.Základní údaje
Originální název
Intravenous Thrombolysis in Patients with Acute Ischemic Stroke after a Reversal of Dabigatran Anticoagulation with Idarucizumab: A Real-World Clinical Experience
Autoři
ŠAŇÁK, Daniel (203 Česká republika, garant), Stanislava JAKUBÍČEK (703 Slovensko, domácí), David ČERNÍK (203 Česká republika), Roman HERZIG (203 Česká republika), Zdeněk KUNÁŠ (203 Česká republika), Robert MIKULÍK (203 Česká republika), Svatopluk OSTRÝ (203 Česká republika), Michal REIF (203 Česká republika), Vladimír ROHAN (203 Česká republika), Aleš TOMEK (203 Česká republika) a Tomáš VEVERKA (203 Česká republika)
Vydání
JOURNAL OF STROKE & CEREBROVASCULAR DISEASES, AMSTERDAM, ELSEVIER SCIENCE BV, 2018, 1052-3057
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30103 Neurosciences
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 1.646
Kód RIV
RIV/00216224:14110/18:00104196
Organizační jednotka
Lékařská fakulta
UT WoS
000441086000034
Klíčová slova anglicky
Acute ischemic stroke; intravenous thrombolysis; anticoagulation; dabigatran; antidote; reversal
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 10. 2. 2019 15:01, Soňa Böhmová
Anotace
V originále
Background: Intravenous thrombolysis (IVT) is contraindicated in patients with acute ischemic stroke (AIS) using oral anticoagulants. A specific human monoclonal antibody was introduced to reverse immediately the anticoagulation effect of the direct inhibitor of thrombin, dabigatran. Until now, mostly individual cases presenting with successful IVT after a reversal of dabigatran anticoagulation in patients with AIS were published. Thus, we aimed to report real-world data from clinical practice. Methods: Patients with AIS on dabigatran treated with IVT after antidote reversal were enrolled in the retrospective nationwide study. Neurological deficit was scored using the National Institutes of Health Stroke Scale (NIHSS) and 90-day clinical outcome using modified Rankin scale (mRS) with a score 0-2 for a good outcome. Intracerebral hemorrhage (ICH) was defined as a presence of any sign of bleeding on control imaging after IVT, and symptomatic intracerebral hemorrhage (SICH) was assessed according to the Safe Implementation of Thrombolysis in Stroke-Monitoring Study (SITS-MOST) criteria. Results: In total, 13 patients (7 men, mean age 70.0 +/- 9.1 years) with a median NIHSS admission score of 7 points were analyzed. Of these patients, 61.5% used 2 x 150 mg of dabigatran daily. Antidote was administrated 427 +/- 235 minutes after the last intake of dabigatran, with a mean activated prothrombin time of 38.1 +/- 27.8 seconds and a mean thrombin time of 72.2 +/- 56.1 seconds. Of the 13 patients, 2 had ICH and 1 had SICH, and no other bleeding complications were observed after IVT. Of the total number of patients, 76.9% had a good 3-month clinical outcome and 3 patients (23.1%) died. Recurrent ischemic stroke occurred in 2 patients (15.4%). Conclusion: The data presented in the study support the safety and efficacy of IVT after the reversal of the anticoagulation effect of dabigatran with antidote in a real-world clinical practice.