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Safety and efficacy of idarucizumab-assisted thrombolysis in dabigatran-related acute ischemic stroke: a systematic review and single-arm meta-analysis

Journal
Frontiers in neurology (Q2)
Published
20 August 2026
Study design
Systematic review / meta-analysis of RCTs
Evidence level
Level 1, High (CEBM 1a)
Authors
Xiaoyuan Guo, Hang Xiong, Wenping Li, Qian Liu, Wei Li, Lingbo Kong, et al.
PMID
42694037
DOI
10.3389/fneur.2026.1884021

Why clinicians should know about it

  • Picked for Pharmacology (medical) (top studies of the week, 6 September 2026): Idarucizumab reversal safety meta-analysis

Abstract

BACKGROUND: Intravenous thrombolysis (IVT) in patients with acute ischemic stroke (AIS) related to dabigatran use requires prior anticoagulation reversal. This study aimed to evaluate the safety and efficacy of IVT following idarucizumab-mediated reversal through a systematic single-arm meta-analysis. METHODS: We systematically searched multiple databases. Single-arm studies (≥5 patients) on idarucizumab-facilitated IVT for dabigatran-related AIS were included. Outcome data from DOAC patients without reversal in the Meinel 2023 cohort (n = 580) served as a descriptive external reference. Pooled proportions for safety (symptomatic intracranial hemorrhage, sICH) and efficacy (90-day good functional outcome, mRS 0-2) were calculated using a random-effects GLMM. RESULTS: Eleven single-arm studies (226 patients) were included. The pooled sICH rate was 5.4% (95% CI 2.6-10.6%; τ 2 = 0.362, Q p = 0.12). The pooled 90-day good functional outcome rate was 66.6% (95% CI 54.2-77.1%; τ 2 = 0.116). In the external reference cohort, the sICH rate was 3.1% and the good outcome rate was 42.4%. Due to baseline imbalances and lack of confounder adjustment, descriptive comparisons were hypothesis-generating only. The certainty of evidence was rated very low (GRADE). CONCLUSION: Current evidence is insufficient to guide routine clinical practice. However, these findings provide useful effect-size estimates (sICH ~5%, good outcome ~67%) for designing future randomised controlled trials. Multicenter prospective registries or pragmatic RCTs are warranted.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.