Hostname: page-component-7479d7b7d-qlrfm Total loading time: 0 Render date: 2024-07-08T19:36:16.216Z Has data issue: false hasContentIssue false

Post-ictal psychosis: A case report

Published online by Cambridge University Press:  13 August 2021

M. Turki*
Affiliation:
Psychiatry “b” Department, Hedi Chaker University hospital, sfax, Tunisia
R. Ouali
Affiliation:
Psychiatry “b” Department, Hedi Chaker University hospital, sfax, Tunisia
S. Ellouze
Affiliation:
Psychiatry “b” Department, Hedi Chaker University hospital, sfax, Tunisia
R. Charfi
Affiliation:
Psychiatry “b” Department, Hedi Chaker University hospital, sfax, Tunisia
W. Abid
Affiliation:
Psychiatry “b” Department, Hedi Chaker University hospital, sfax, Tunisia
T. Babbah
Affiliation:
Psychiatry “b” Department, Hedi Chaker University hospital, sfax, Tunisia
N. Halouani
Affiliation:
Psychiatry “b” Department, Hedi Chaker University hospital, sfax, Tunisia
J. Alouou
Affiliation:
Psychiatry “b” Department, Hedi Chaker University hospital, sfax, Tunisia
*
*Corresponding author.

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Introduction

People suffering from chronic diseases, especially epilepsy, are more likely to suffer from neurobehavioral disorders, like psychotic states. Postictal psychosis (PIP) is one of these potentially serious complications, that classically follows exacerbations of seizures.

Objectives

The present paper aimed to study the clinical and therapeutic aspects of PIP.

Methods

We report a case of PIP, which involved a patient hospitalized in psychiatry department, and discuss it in light of the relevant literature.

Results

We report the case of a 27-year-old man, with medical history of generalized epilepsy which was well stabilized under treatment (carbamazepine 600 mg/day). The patient was hospitalized for dangerous behaviors after having experienced 2 episodes of seizure activity in context of poor therapeutic adherence. Psychiatric assessment revealed a psychomotor instability, a pressured speech and hallucinatory behavior. There were no delirium symptoms. Neurological examination showed no localization signs, and cerebral imaging was normal. The patient was treated with benzodiazepines (Diazepam), associated to antipsychotics (Haloperidol). His antiepileptic drug was quickly reintroduced. After 48 hours of treatment, psychiatric symptoms improved. The patient returned to its baseline condition after 7 days.

Conclusions

The short-term prognosis of PPI is often favorable, compared to other psychotic disorders. However, more severe psychiatric disorders can potentially develop in the long-term, raising diagnostic and therapeutic difficulties. Thus, a good collaboration between psychiatrists and neurologists is highly desirable in order to better adapt the treatment.

Disclosure

No significant relationships.

Type
Abstract
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© The Author(s), 2021. Published by Cambridge University Press on behalf of the European Psychiatric Association
Submit a response

Comments

No Comments have been published for this article.