Evidence map›Paper›PMID 40927648›Full record

ArticleFrontiers in human neuroscience2025

Slapping automatism in epileptic seizures: a case series.

Shenglin Hao, Ziyi Feng, Haifeng Zhao, Wei Liu, Shikun Zhan, Bomin Sun, Qiang Zhou, Chunyan Cao

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Article in Frontiers in human neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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8 authors.

Shenglin Hao *Department of Neurosurgery, Affiliated Ruijin Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Ziyi Feng *Department of Neurosurgery, Affiliated Ruijin Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Haifeng ZhaoDepartment of Neurosurgery, Affiliated Ruijin Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Wei LiuDepartment of Neurosurgery, Affiliated Ruijin Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Shikun ZhanDepartment of Neurosurgery, Affiliated Ruijin Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Bomin SunDepartment of Neurosurgery, Affiliated Ruijin Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Qiang ZhouDepartment of Laboratory Medicine, Gongli Hospital, Shanghai, China.
Chunyan CaoDepartment of Neurosurgery, Affiliated Ruijin Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Slapping automatism is a type of automatism observed during epileptic seizures, but its underlying electrophysiological mechanisms remain poorly understood. Stereo-electroencephalography (SEEG) provides a unique opportunity to investigate the associated cortical areas with epileptiform discharges during the slapping automatism. Case report: We report five cases of drug-resistant epilepsy in which SEEG recordings captured slapping automatism. In four patients, slapping movements coincided with ictal electrical evolution in the prefrontal lobe, specifically involving the orbitofrontal cortex (OFC), lateral prefrontal cortex (PFC), and anterior cingulate (ACC). Among them, two cases were temporal lobe epilepsy (TLE), while the other two were frontal lobe epilepsy (FLE). Additionally, we describe one patient with TLE and obsessive-compulsive disorder (OCD), whose SEEG recordings revealed frequent interictal epileptiform discharges in both the medial temporal and prefrontal regions. The seizures originated in the temporal lobe and rapidly evolved into generalized seizures. Although slapping automatism was not observed during seizures, the patient exhibited repetitive patting on the bed during the interictal period. Based on SEEG-defined epileptic networks, all patients underwent surgical interventions, including lesion resection and/or disconnection procedures. At follow-up, all three patients achieved Engel class I outcomes and two patients Engel class II. Conclusion: SEEG recordings in this study confirm a strong association between orbitofrontal lobe epileptic activity and slapping automatism. Notably, we report a case of TLE with comorbid OCD, characterized by frequent epileptiform discharges in the orbitofrontal lobe, providing direct electrophysiological evidence of prefrontal abnormalities in OCD. Together, these findings highlight a shared pathological network of orbitofrontal-striatal-pallidal-thalamic between frontal and temporal epilepsy with slapping automatism and OCD.

Indexed as

frontal lobe epilepsyobsessive-compulsive disorderslapping automatismstereo-electroencephalography (SEEG)temporal lobe epilepsy

Identifiers

PMID40927648
PMCPMC12415034

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