# ESO annual stroke evidence update 2025

**Authors:** Diana Aguiar de Sousa, Aristeidis H Katsanos, Linxin Li, Nicolas Martinez-Majander, John McCabe, Lina Palaiodimou, Anna Ramos Pachon, Michele Romoli, Peter D Schellinger, Annaelle Zietz, Sven Poli, Melinda Roaldsen, Ashkan Shoamanesh, Marek Sýkora, Georgios Tsivgoulis

PMC · DOI: 10.1093/esj/aakag009 · European Stroke Journal · 2026-02-17

## TL;DR

The ESO 2025 Stroke Evidence Update summarizes recent clinical trials and findings to guide stroke treatment and management.

## Contribution

A curated synthesis of 2025 stroke research highlights new evidence and identifies priority research questions.

## Key findings

- Endovascular thrombectomy showed no benefit over medical therapy for MeVO strokes.
- Tenecteplase before thrombectomy improved outcomes in LVO stroke patients.
- Early intensive blood pressure lowering improved recovery in acute ICH.

## Abstract

Stroke medicine is evolving rapidly, with emerging evidence continuously informing clinical practice. The European Stroke Organisation (ESO) Annual Stroke Evidence Update is a new ESO Guideline Board initiative that bridges the interval between formal guideline revisions by providing a curated synthesis of recent advances that may inform stroke care.

This edition synthesises new evidence published or presented during 2025 across various key domains, including acute treatment, prevention, rehabilitation, imaging, systems of care and outcomes. We searched major stroke and internal medicine journals and reviewed abstract proceedings from the main international stroke conferences. Studies were shortlisted by domain leads and selected by consensus among ESO Guideline Board members based on methodological quality, clinical relevance and potential to impact stroke management.

Three randomised trials found no benefit for endovascular thrombectomy over best medical therapy in stroke due to MeVO. One trial showed that intravenous tenecteplase before thrombectomy was associated with improved functional independence at 90 days compared with thrombectomy alone in patients with stroke due to LVO. Individual patient data meta-analysis of 4 trials confirmed that intensive blood pressure lowering in the acute phase of ICH was safe and improved functional recovery, with greatest benefit when started within 3 h. A trial showed that triple-pill combination therapy achieved blood pressure control and reduced recurrent stroke after ICH. For ischaemic stroke associated with atrial fibrillation an individual participant data meta-analysis of 4 trials confirmed that early direct oral anticoagulant initiation within 4 days reduced recurrent ischaemic stroke without increasing symptomatic ICH. In non-cardioembolic stroke and high risk TIA, asundexian, a novel factor XIa inhibitor, reduced ischaemic stroke risk without increasing major bleeding in a large phase 3 trial. Mobile stroke units were shown to be cost-effective in high-volume systems. Promising therapeutic strategies for post-stroke cognitive impairment include brain stimulation, computerised cognitive training and cardiorespiratory training.

In 2025, trial evidence supported no routine role for EVT in MeVO, reinforced tenecteplase as bridging thrombolysis in eligible LVO patients undergoing EVT and strengthened the signal for early intensive blood pressure lowering in acute ICH. Priority research questions include identifying subgroups that may benefit from EVT in MeVO, defining the role of adjunct intra-arterial thrombolysis after successful EVT and clarifying which imaging-based selection pathways are most feasible and effective across different stroke systems.

Graphical Abstract

## Linked entities

- **Chemicals:** asundexian (PubChem CID 135206011)
- **Diseases:** stroke (MONDO:0005098), ischaemic stroke (MONDO:1060198), atrial fibrillation (MONDO:0004981), TIA (MONDO:0005264)

## Full-text entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, F10 (coagulation factor X) [NCBI Gene 2159] {aka FX, FXA}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** STROKE (MESH:D020521), intracranial atherosclerotic disease (MESH:D002537), CVT (MESH:D020767), obesity (MESH:D009765), bleeding (MESH:D006470), PSE (MESH:D004834), non (MESH:C580335), small-vessel disease (MESH:D059345), seizure (MESH:D012640), stenosis (MESH:D003251), cryptogenic stroke (MESH:D000083242), COI (MESH:D003103), Hypertensive Intracerebral Haemorrhage (MESH:D020299), coronary disease (MESH:D003327), inflammatory (MESH:D007249), Disease (MESH:D004194), Metabolic syndrome (MESH:D024821), Carotid tandem (MESH:D016893), flutter (MESH:D054141), ESUS (MESH:D000083262), hemianopia (MESH:D006423), artery dissection (MESH:D000094665), ICAC (MESH:D020765), PSD (MESH:C536311), cancer (MESH:D009369), diabetes (MESH:D003920), occlusive dissection (MESH:D000784), executive dysfunction (MESH:D006331), migraine with aura (MESH:D020325), amyloid (MESH:C000718787), dementia (MESH:D003704), TIA (MESH:D002546), type 2 diabetes (MESH:D003924), systemic embolism (MESH:D004617), infarction (MESH:D007238), heart failure (MESH:D006333), disability (MESH:D009069), CLOSURE (MESH:D015812), PSCI (MESH:D003072), CRAO (MESH:D015356), motor impairment (MESH:D000068079), LAAO (MESH:D059446), migraine (MESH:D008881), patent foramen ovale (MESH:D054092), venous thromboembolism (MESH:D054556), death (MESH:D003643), vascular dementia (MESH:D015140), basilar artery occlusion (MESH:D001157), hypertension (MESH:D006973), artery atherosclerosis (MESH:D050197), ICH (MESH:D002543), ischaemic (MESH:D018917), atrial cardiopathy (MESH:C536187), AF/flutter (MESH:D001282), cardioaortic thrombus (MESH:D013927), carotid atherosclerosis (MESH:D002340), cerebrovascular disease (MESH:D002561), cardiovascular (MESH:D002318), neurocognitive disorder (MESH:D019965), IRIS (MESH:C535535)
- **Chemicals:** aspirin (MESH:D001241), apixaban (MESH:C522181), edoxaban (MESH:C552171), cholesterol (MESH:D002784), colchicine (MESH:D003078), nerinetide (MESH:C542597), oxygen (MESH:D010100), milvexian (MESH:C000720754), telmisartan (MESH:D000077333), rivaroxaban (MESH:D000069552), glucose (MESH:D005947), levetiracetam (MESH:D000077287), Esmolol (MESH:C036604), indapamide (MESH:D007190), amlodipine (MESH:D017311), ANGEL (-), levodopa (MESH:D007980), levodopa/carbidopa (MESH:C009265)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

89 references — full list in the complete paper: https://tomesphere.com/paper/PMC12915583/full.md

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Source: https://tomesphere.com/paper/PMC12915583