Evidence map›Paper›PMID 42332278›Full record

ArticleJournal of neurology2026

Outcomes of intravenous thrombolysis in patients with acute ischemic stroke and direct oral anticoagulant use within 1 day before stroke onset.

Chia-Lin Liao, Hua Li, Hong-Jie Jhou, Jheng-Yan Wu, Meng-Chi Chiu, Tou-Yuan Tsai

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Article in Journal of neurology, 2026. 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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6 authors.

Chia-Lin LiaoDepartment of Neurosurgery, Dalin Tzuchi Hospital, The Buddist Tzuchi Medical Foundation, Chiayi, Taiwan.
Hua LiCenter for Health Data & Advanced Translational Analytics, Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Chiayi, Taiwan.
Hong-Jie JhouNeurological Institute, Changhua Christian Hospital, Changhua, Taiwan.
Jheng-Yan WuDepartment of Nutrition, Chi Mei Medical Center, Tainan, Taiwan.
Meng-Chi ChiuDepartment of Neurology, Dalin Tzuchi Hospital, The Buddist Tzuchi Medical Foundation, Chiayi, Taiwan.
Tou-Yuan TsaiSchool of Medicine, Tzu Chi University, Hualien, Taiwan. 96311123@gms.tcu.edu.tw.ORCID http://orcid.org/0000-0003-0071-9069

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6 · The paper itself

Abstract

backgroundEvidence regarding the outcomes of intravenous thrombolysis (IVT) in patients taking direct oral anticoagulants (DOACs) within 1 day before acute ischemic stroke remains limited. In this study, we aimed to evaluate the bleeding risk after IVT in patients with and without recent DOAC exposure.

methodsThis retrospective cohort study analyzed TriNetX global network data (January 2010-September 2024) in adults aged ≥ 20 years receiving IVT for acute ischemic stroke. Groups with DOAC and no anticoagulant (no-OAC) exposure within 1 day before stroke were compared. The primary outcome was intracranial hemorrhage (ICH) within 2 days after IVT. Secondary outcomes included major bleeding, blood transfusion within 2 days, and 30-day and 90-day mortality rates. Subgroup analyses examined individual DOACs (apixaban, rivaroxaban, edoxaban, and dabigatran). Propensity score matching controlled for confounders with risk differences (RDs) and odds ratios (ORs) to estimate outcome events.

resultsAmong 64,667 patients (mean age 65.1 ± 16.1 years; 50.1% women), 1183 (1.8%) received DOACs, and 63,462 (98.1%) received no anticoagulants. After propensity score matching, the DOAC cohort had lower risks of ICH (RD, - 2.88% [95% CI, - 4.28% to - 1.48%]; OR, 0.36 [95% CI, 0.21-0.60]) and major bleeding (RD, - 2.54% [95% CI, - 4.53% to - 0.55%]; OR, 0.66 [95% CI, 0.47-0.91]) than the no-OAC cohort. Mortality rates were similar at 30 (OR, 0.87 [95% CI, 0.69-1.08]) and 90 (OR, 1.04 [95% CI, 0.85-1.26]) days. In subgroup analyses, apixaban showed lower ICH and mortality risks than no-OAC.

conclusionDOAC exposure within 1 day before stroke does not result in higher bleeding or mortality risk in patients receiving IVT for acute ischemic stroke.

Indexed as

AnticoagulantsFibrinolytic AgentsIntracranial HemorrhagesIschemic StrokeThrombolytic TherapyAdministration, IntravenousAdministration, OralAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeAnticoagulantsFibrinolytic AgentsAcute ischemic strokeCohort studyDirect oral anticoagulantsIntravenous thrombolysis

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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.