Publication

Microvascular cerebral blood flow response to intrathecal nicardipine is associated with delayed cerebral ischemia

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Last modified
  • 06/17/2025
Type of Material
Authors
    Eashani Sathialingam, Emory UniversityKyle R Cowdrick, Emory UniversityAmanda Y Liew, Emory UniversityZhou Fang, Emory UniversitySeung Lee, Emory UniversityCourtney E McCracken, Kaiser Permanente Georgia, AtlantaFeras Akbik, Emory UniversityOwen Samuels, Emory UniversityPrem Kandiah, Emory UniversityOfer Sadan, Emory UniversityErin Buckley, Emory University
Language
  • English
Date
  • 2023-03-17
Publisher
  • FRONTIERS MEDIA SA
Publication Version
Copyright Statement
  • © 2023 Sathialingam, Cowdrick, Liew, Fang, Lee, McCracken, Akbik, Samuels, Kandiah, Sadan and Buckley.
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Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 14
Start Page
  • 1052232
End Page
  • 1052232
Grant/Funding Information
  • This study was supported in part by the National Center for Advancing Translational Sciences of the National Institutes of Health under Award Numbers UL1TR002378 and R01NS130036-01 (OS), and 1F31HL154703-01A1 (ES).
Supplemental Material (URL)
Abstract
  • One of the common complications of non-traumatic subarachnoid hemorrhage (SAH) is delayed cerebral ischemia (DCI). Intrathecal (IT) administration of nicardipine, a calcium channel blocker (CCB), upon detection of large-artery cerebral vasospasm holds promise as a treatment that reduces the incidence of DCI. In this observational study, we prospectively employed a non-invasive optical modality called diffuse correlation spectroscopy (DCS) to quantify the acute microvascular cerebral blood flow (CBF) response to IT nicardipine (up to 90 min) in 20 patients with medium-high grade non-traumatic SAH. On average, CBF increased significantly with time post-administration. However, the CBF response was heterogeneous across subjects. A latent class mixture model was able to classify 19 out of 20 patients into two distinct classes of CBF response: patients in Class 1 (n = 6) showed no significant change in CBF, while patients in Class 2 (n = 13) showed a pronounced increase in CBF in response to nicardipine. The incidence of DCI was 5 out of 6 in Class 1 and 1 out of 13 in Class 2 (p < 0.001). These results suggest that the acute (<90 min) DCS-measured CBF response to IT nicardipine is associated with intermediate-term (up to 3 weeks) development of DCI.
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Research Categories
  • Engineering, Biomedical

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