AI Article Synopsis

  • Basilar artery occlusion leads to high mortality and disability rates in stroke patients, but treatments like intravenous thrombolysis can improve neurological outcomes if given within 4.5 hours.
  • Thrombectomy results are mixed for basilar artery occlusion, and recent trials show that specific patients with wake-up strokes can benefit from thrombolysis based on MRI criteria.
  • A case study highlights that treating a wake-up stroke with intravenous thrombolysis beyond the typical time frame can still be effective, supporting the use of MRI to guide treatment decisions even when standard criteria are not met.

Article Abstract

Stroke from basilar artery occlusion is associated with a poor natural history with high rates of death and disability. Intravenous thrombolysis administered within 4.5 hours of last known well time improves the odds of a good neurological outcome after ischemic stroke, including in patients with basilar artery occlusion. Thrombectomy for basilar artery occlusion has had mixed outcomes. The WAKE-UP randomized clinical trial demonstrated that administration of intravenous thrombolysis can benefit select patients with wake-up strokes whose brain MRI shows restricted diffusion but no accompanying T2 FLAIR change. We report a case of a wake-up acute ischemic stroke presenting with acute vertigo followed by progressive brainstem dysfunction from a basilar artery occlusion. The patient was successfully treated with intravenous thrombolysis beyond 4.5 hours of last known well and symptom discovery time according to an MRI tissue-based approach resulting in partial recanalization of her basilar artery and recovery to near normal. This case suggests that hyperacute MRI can serve as a tissue clock to select patients with wake-up stroke for acute reperfusion therapy even if they do not meet standard trial inclusion criteria, including patients with basilar artery occlusion.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9755624PMC
http://dx.doi.org/10.1177/19418744221119597DOI Listing

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