ReviewJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism2026
Haemorrhage, hypercoagulability and ischaemia: Evolution of brain injury after aneurysmal subarachnoid haemorrhage.
Review in Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 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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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
4 authors.
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Abstract
Aneurysmal subarachnoid haemorrhage (aSAH) is a catastrophic cerebrovascular event associated with high early mortality and substantial long-term disability. Delayed cerebral ischaemia (DCI) is among its most severe complications and a principal driver of secondary neurological injury. Despite decades of research describing diverse pathophysiological mechanisms, a unifying framework for DCI pathogenesis is still lacking, and its clinical prediction remains challenging. We therefore conducted a narrative review to synthesise current understanding of the spatiotemporal evolution of brain injury following aSAH, with emphasis on integrating mechanisms across overlapping clinical phases. Acute phase events from physical effects of bleeding, including intracranial pressure elevation, hyperacute vasospasm and microvascular thrombosis, sets off the evolution of downstream brain injuries. During the early phase, converging mechanisms such as neuroinflammation, oxidative stress, spreading depolarisation and blood-brain barrier disruption coalesce into pan-vascular dysfunction and systemic hypercoagulability. Rather than representing a singular vasospastic complication, these processes collectively evolve into pathobiological states characterised by large-artery vasospasm, microvascular constriction, diffuse capillary occlusion and supply-demand mismatch, ultimately precipitating DCI and cortical infarction. This review examines the key mechanisms underlying these aforementioned processes and aims to establish mechanistic continuity across the evolving phases of injury following aSAH.
Indexed as
Identifiers
42499004What Socratic holds
Registered trials
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 Socratic graph.