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Prevalence of Clinical Electroencephalography Findings in Stroke Patients with Delirium

Overview
Publisher Elsevier
Specialties Neurology
Psychiatry
Date 2024 Mar 28
PMID 38548493
Authors
Affiliations
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Abstract

Objective: Delirium is an acute cognitive disorder associated with multiple electroencephalographic (EEG) abnormalities in non-neurological patients, though specific EEG characteristics in patients with stroke remain unclear. We aimed to compare the prevalence of EEG abnormalities in stroke patients during delirium episodes with periods that did not correspond to delirium.

Methods: We retrospectively analyzed clinical EEG reports for stroke patients who received daily delirium assessments as part of a prospective study. We compared the prevalence of EEG features corresponding to patient-days with vs. without delirium, including focal and generalized slowing, and focal and generalized epileptiform abnormalities (EAs).

Results: Among 58 patients who received EEGs, there were 192 days of both EEG and delirium monitoring (88% [n = 169] corresponding to delirium). Generalized slowing was significantly more prevalent on days with vs. without delirium (96% vs. 57%, p = 0.03), as were bilateral or generalized EAs (38% vs. 13%, p = 0.03). In contrast, focal slowing (53% vs. 74%, p = 0.11) and focal EAs were less prevalent on days with delirium (38% vs. 48%, p = 0.37), though these differences were not statistically significant.

Conclusions: We found a higher prevalence of generalized but not focal EEG abnormalities in stroke patients with delirium.

Significance: These findings may reinforce the diffuse nature of delirium-associated encephalopathy, even in patients with discrete structural lesions.

Citing Articles

Neuroimaging Markers of Brain Reserve and Associations with Delirium in Patients with Intracerebral Hemorrhage.

Rex N, Chuck C, Dandapani H, Zhou H, Yi T, Collins S Neurocrit Care. 2024; .

PMID: 39562387 DOI: 10.1007/s12028-024-02148-2.


Investigating delirium in stroke with an EEG lens: Focal lesions with global impact?.

Juarez Martinez E, Kimchi E Clin Neurophysiol. 2024; 162:219-221.

PMID: 38631924 PMC: 11682861. DOI: 10.1016/j.clinph.2024.03.028.

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