Pearls & Oy-sters: Severe Case of Ictal Asystole in Temporal Lobe Epilepsy.

Neurology

From the Warren Alpert Medical School at Brown University (A.C.F., S.D., N.A.); and Department of Neurology (S.D., N.A.), Rhode Island Hospital, Providence.

Published: August 2023


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Ictal asystole is a rare condition associated primarily with temporal lobe epilepsy that can cause syncope, falls, and head trauma. It is also associated with increased rates of sudden unexplained death in epilepsy. We present a case of a 33-year-old woman with a history of childhood epilepsy who presented with 3 years of recurrent syncope. Video-EEG revealed temporal lobe seizures with ictal asystole. EKG showed stepwise progression of bradycardia, asystole, and tachycardia. MRI showed focal cortical thickening at the right insular cortex with blurring of the gray-white matter interface, consistent with insular focal cortical dysplasia. The patient was transitioned from lacosamide to clobazam because of concern for PR interval prolongation and was referred to cardiology for pacemaker placement. Ictal asystole should be considered as a rare but serious cause of unexplained recurrent syncope, particularly in patients with a history of seizures. Management includes antiepileptic drug regimen optimization, consideration of epilepsy surgery, and referral for cardiac pacing when asystole lasts longer than 6 seconds.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501100PMC
http://dx.doi.org/10.1212/WNL.0000000000207396DOI Listing

Publication Analysis

Top Keywords

ictal asystole
16
temporal lobe
12
lobe epilepsy
8
recurrent syncope
8
focal cortical
8
asystole
6
epilepsy
5
pearls oy-sters
4
oy-sters severe
4
severe case
4

Similar Publications

We report the first known case of a 9-year-old male with early-onset epilepsy, syncope, and ictal asystole-requiring pacemaker implantation at the age of seven-associated with a pathogenic variant in FGF12.

View Article and Find Full Text PDF

Objective: Prognostication in patients with disorders of consciousness (DOCs) remains challenging because of heterogeneous etiologies, pathophysiologies and, consequently, highly variable electroencephalograms (EEGs). Here, we use EEG patterns that are well-characterizable to create a latent map that positions novel EEGs along a continuum. We asses this map as a generalizable tool to extract prognostically valuable information from long-term EEG, by predicting outcome post-cardiac arrest as a first use case.

View Article and Find Full Text PDF

Background: Long QT Syndrome Type-2 (LQT2) is due to loss-of-function KCNH2 variants. KCNH2 encodes K11.1 that forms a delayed-rectifier potassium channel in the brain and heart.

View Article and Find Full Text PDF