Endovascular management of acute stroke
- PMID: 39341645
- DOI: 10.1016/S0140-6736(24)01410-7
Endovascular management of acute stroke
Abstract
Stroke related to large vessel occlusion is a leading cause of disability and death worldwide. Advances in endovascular therapy to reopen occluded arteries have been shown to reduce patient disability and mortality. Expanded indications to treat patients with large vessel occlusion in the late window (>6 h from symptom onset), with basilar artery occlusion, and with large ischaemic core at presentation have enabled treatment of more patients with simplified imaging methods. Ongoing knowledge gaps include an understanding of which patients with large ischaemic infarct are more likely to benefit from endovascular therapy, the role of endovascular therapy in patients who present with low National Institutes of Health Stroke Scale scores or medium or distal vessel occlusion, and optimal management of patients with underlying intracranial atherosclerotic disease. As reperfusion can now be facilitated by intravenous thrombolysis, mechanical thrombectomy, or both, the development of cytoprotective or adjunctive drugs to slow infarct growth, enhance reperfusion, or decrease haemorrhagic risk has gained renewed interest with the hope to improve patient outcomes.
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Conflict of interest statement
Declaration of interests TNN is a member of the advisory board for Aruna Bio and Brainomix; has received a research grant to institution from Medtronic; is the Associate Editor of Stroke; is a member of the data and safety monitoring committee of the SELECT2, TESLA, and ENDOLOW trials; is the President of Society of Vascular and Interventional Neurology; and is the co-principal investigator of the SUMMIT MAX and PICASSO trials. UF reports research support from the Swiss National Science Foundation and the Swiss Heart Foundation; reports research grants from Medtronic (for the BEYOND SWIFT and SWIFT DIRECT trials), Stryker, Rapid Medical, Penumbra, and Phenox (for the DISTAL trial); reports consultancies for Medtronic, Stryker, and CSL Behring; reports participation in an advisory board for Alexion/Portola, Boehringer Ingelheim, Biogen, and Acthera; is a member of a clinical event committee of the COATING study (Phenox) and a member of the data and safety monitoring committee of the TITAN, LATE_MT, and IN EXTREMIS trials; and reports presidency of the Swiss Neurological Society. All fees related to UF's declaration of interests are paid to institutions. UF is President-Elect of the European Stroke Organization. SN discloses stock options for Brainomix and was a speaker with Bayer, Boehringer Ingelheim, and Pfizer. ZM was principal investigator of the the ANGEL ASPECT trial and discloses that the trial was supported by grants from Covidien Healthcare International Trading (Shanghai), Johnson & Johnson MedTech, Genesis MedTech (Shanghai), and Shanghai HeartCare Medical Technology that were made to the institution. PK was the principal investigator of an unrestricted grant for the investigator-initiated clinical trial, ENDOLOW, supported by Cerenovus; was the National Leader of the PACIFIC-Stroke clinical trial supported by Bayer; consulted for Lumosa and Basking Biosciences (for scientific advisory board participation); and was a one-time consultant for Shionogi. All other authors declare no competing interests.
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