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Abstract Details

Hemodynamic Patterns Associated with Arterial Baroreflex Dysfunction in Stimulation-induced Seizures
Epilepsy/Clinical Neurophysiology (EEG)
P4 - Poster Session 4 (8:00 AM-9:00 AM)
11-001

We aimed to investigate associations between pre-to-post-ictal BRS changes with hemodynamic patterns during stimulation-induced seizures (SIS).

Ictal cardiovascular autonomic dysfunction (CAD) is widely recognized, but may present with a variety of hemodynamic types. Disruption of central autonomic control, specifically arterial baroreflex sensitivity (BRS) dysfunction, may be more profound during a distinct combinations of heart rate (HR) and blood pressure (BP) changes.

We analyzed HR and beat-to-beat BP data from 35 patients (median age with interquartile range 30 years [25-39 years], 22 women) with drug resistant focal epilepsy undergoing stereo-EEG (SEEG) monitoring with electrical stimulation. Ictal CAD was defined as newly appeared hypertension (systolic or diastolic BP ≥140/90 mmHg), hypotension (systolic or diastolic BP <90/60 mmHg), tachycardia (HR >100 bpm), and bradycardia (HR <60 bpm) during the first minute of seizures if changes of HR/BP exceeded 3 standard deviation thresholds from prestimulation baseline mean values. Hemodynamic patterns were categorized based on constellations of HR and BP changes. BRS was assessed during 1-minute preictal and ictal periods. Wilcoxon signed-rank test was used to compare pre-to-post-ictal changes of BRS (p < 0.05).

We registered 54 SIS, 20 of them revealed three hemodynamic patterns. Pattern 1 (n=5): ictal hypotension – bradycardia; Pattern 2 (n=5) ictal hypotension – tachycardia; Pattern 3 (n=10) hypertension – tachycardia. We did not reveal significant pre-to-post-ictal changes of BRS for Pattern 1 (p=0,3) and Pattern 2 (p=0,06). Significant decrease of BRS values was found in SIS manifesting with Pattern 3 (p=0,002).

Our findings demonstrate diverse ictal hemodynamic patterns during SIS. Significant blunting of BRS was associated with the ictal hypertension-tachycardia pattern and reflected transient impairment of central autonomic regulation during stimulation-induced seizures.

Authors/Disclosures
Anna Marchenko, MD
PRESENTER
Dr. Marchenko has nothing to disclose.
Dmitry Zhuravlev, MD, PhD Dr. Zhuravlev has nothing to disclose.
Marina Lebedeva, PhD Mrs. Lebedeva has nothing to disclose.
Igor Trifonov, PhD Dr. Trifonov has nothing to disclose.
Anastasia Skalnaya, MD (Research Center of Neurology) Dr. Skalnaya has nothing to disclose.
Mikhail Sinkin, MD, PhD Prof. Sinkin has nothing to disclose.
Flora Rider, PhD Mrs. Rider has nothing to disclose.
Alla Borisovna Guekht, PhD (Centre of Psychoneurology Named By Solovyeva) The institution of Prof. Guekht has received research support from Russian Science Foundation .
Vladimir Krylov, MD, PhD Prof. Krylov has nothing to disclose.