4.6 Review

Cerebral Autoregulation in Subarachnoid Hemorrhage

Journal

FRONTIERS IN NEUROLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fneur.2021.688362

Keywords

stroke; microvascular dysfunction; cerebral blood flow; cystic fibrosis transmembrane conductance regulator; delayed ischemia

Funding

  1. Ted Rogers Centre for Heart Research (University of Toronto)
  2. Heart and Stroke Foundation of Ontario Mid-Career Investigator award
  3. Brain Aneurysm Foundation

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Subarachnoid hemorrhage (SAH) is a devastating stroke subtype with a high mortality and morbidity rate. Current therapeutic interventions do not specifically target the microvascular dysfunction underlying the ischemic event, resulting in only modest improvement in clinical outcome.
Subarachnoid hemorrhage (SAH) is a devastating stroke subtype with a high rate of mortality and morbidity. The poor clinical outcome can be attributed to the biphasic course of the disease: even if the patient survives the initial bleeding emergency, delayed cerebral ischemia (DCI) frequently follows within 2 weeks time and levies additional serious brain injury. Current therapeutic interventions do not specifically target the microvascular dysfunction underlying the ischemic event and as a consequence, provide only modest improvement in clinical outcome. SAH perturbs an extensive number of microvascular processes, including the automated control of cerebral perfusion, termed cerebral autoregulation. Recent evidence suggests that disrupted cerebral autoregulation is an important aspect of SAH-induced brain injury. This review presents the key clinical aspects of cerebral autoregulation and its disruption in SAH: it provides a mechanistic overview of cerebral autoregulation, describes current clinical methods for measuring autoregulation in SAH patients and reviews current and emerging therapeutic options for SAH patients. Recent advancements should fuel optimism that microvascular dysfunction and cerebral autoregulation can be rectified in SAH patients.

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