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Postictal psychosis - a complex challenge
Mariana Marinho1, João Marques2, Miguel Bragança1,3
1Clinic of Psychiatry and Mental Health of São João Hospital Centre, Portugal; 2Clinic of Psychiatry of Local Healthcare Unit of Matosinhos, Portugal
3Department of Clinical Neurosciences and Mental Health of Faculty of Medicine, University of Porto, Portugal
marianalemosmarinho@gmail.com
1.  INTRODUCTION AND OBJECTIVES
Patients with epilepsy have 6-12 times higher
risk of suffering from psychosis, with a
prevalence of about 7-8%, and the coexistence
of these two conditions is associated with
increased morbidity and mortality.
The psychosis of epilepsy is generally split into
two groups: interictal psychoses and postictal
psychosis (PIP). PIP has been estimated to
represent 25% of all types. However, many of
these episodes remain under-recognized and/
or are often misdiagnosed.
Objectives: To provide an overview of PIP.
2. METHODS
Literature review based on articles published
on PubMed/MEDLINE, between January 2006
and August 2016, using the keywords
“epilepsy” and “psychosis”.
3. RESULTS
• Only temporary measures - physical restriction or medical sedation - are needed to cope with risk behaviours aimed at
protecting the safety of patients and others
• Frequently responds very rapidly to low doses of antipsychotics and benzodiazepines (lorazepam, clobazam)
• To assess the need of continuous use of antipsychotics, seeking always the lowest dose for the shortest time
The pharmacological treatment of psychosis of epilepsy has particularities
• To avoid agents associated with a relatively greater risk of lowering the seizure threshold (clozapine, chlorpromazine)
• The potential seizure-threshold lowering properties of psychotropic drugs tend to be related to dose and escalation speed
•  Antipsychotics known or supposed to have low epileptogenic properties: olanzapine, risperidone, quetiapine, amisulpride
• To avoid sudden changes in the pharmacological treatment of epilepsy (reduction, increase or substitution of antiepileptics),
mainly in cases with history of psychoses
•  Side-effects, toxic effects and pharmacokinetic interactions of antiepileptics and antipsychotics may be additive
4. CONCLUSION
Given the negative impact of PIP in morbidity
and mortality among these patients, it is crucial
that neurologists and psychiatrists are able to
adequately recognize and treat this clinical
condition.
5. BIBLIOGRAPHY
Kanner AM and Rivas-Grajales AM, CNS Spectrums,
2016; Weisholtz DS et al, Journal of Neurological
Disorders & Stroke, 2014; Adachi N et al, Epilepsia,
2013; Guarnieria R et al, Rev Bras Psiquiatr, 2004.
•  Bilateral seizure foci in the limbic temporal regions
•  Processes associated with bilateral limbic lesions
•  Relative increase in seizure frequency preceding the
psychotic symptoms
•  Lower verbal IQ
•  Absence of febrile convulsions
•  Absence of temporal mesial sclerosis
Risk factors
Symptoms are variable
•  Auditory, visual or tactile hallucinations
•  Persecutory, religious or grandiose delusions
•  Sexual indiscretions
•  Irritability, agitation, aggressiveness
•  Affective symptoms
Clinical presentation
PIP is a psychiatric emergency
Management
PIP is defined by two features: chronologic relationship to seizures and nature of the mental state
PIP represents about 25% of epileptic psychosis
Episodes of psychosis that develop within 1 week after a seizure, or usually a cluster of seizures
EEG: Postictal slowing
There is often a short period of clear consciousness (12 to 72 hours) between
the end of the seizure and the onset of psychosis
PIP has been recognized since the 19th century, when Esquirol described postictal “fury”
PIP usually follows exacerbations, especially clusters, of complex partial seizures,
sometimes without, but more commonly with generalization
• Duration: generally short; days to 2 weeks; mean duration is nearly 70 hours
• PIP is essentially a benign, self-remitting condition
• In half of affected patients, PIP remains as a single episode
• In the other half, PIP episodes tend to repeat, which may occur even quasi regularly after
a cluster of complex focal seizures or secondary generalization in extreme cases
Course and Prognosis
PIP is heralded by severe
insomnia which, were it
recognised, would allow
preventive treatment of the
episode by prompt
administration of low doses of
benzodiazepines or
antipsychotics!	
  

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Postictal psychosis - a complex challenge

  • 1. Postictal psychosis - a complex challenge Mariana Marinho1, João Marques2, Miguel Bragança1,3 1Clinic of Psychiatry and Mental Health of São João Hospital Centre, Portugal; 2Clinic of Psychiatry of Local Healthcare Unit of Matosinhos, Portugal 3Department of Clinical Neurosciences and Mental Health of Faculty of Medicine, University of Porto, Portugal marianalemosmarinho@gmail.com 1.  INTRODUCTION AND OBJECTIVES Patients with epilepsy have 6-12 times higher risk of suffering from psychosis, with a prevalence of about 7-8%, and the coexistence of these two conditions is associated with increased morbidity and mortality. The psychosis of epilepsy is generally split into two groups: interictal psychoses and postictal psychosis (PIP). PIP has been estimated to represent 25% of all types. However, many of these episodes remain under-recognized and/ or are often misdiagnosed. Objectives: To provide an overview of PIP. 2. METHODS Literature review based on articles published on PubMed/MEDLINE, between January 2006 and August 2016, using the keywords “epilepsy” and “psychosis”. 3. RESULTS • Only temporary measures - physical restriction or medical sedation - are needed to cope with risk behaviours aimed at protecting the safety of patients and others • Frequently responds very rapidly to low doses of antipsychotics and benzodiazepines (lorazepam, clobazam) • To assess the need of continuous use of antipsychotics, seeking always the lowest dose for the shortest time The pharmacological treatment of psychosis of epilepsy has particularities • To avoid agents associated with a relatively greater risk of lowering the seizure threshold (clozapine, chlorpromazine) • The potential seizure-threshold lowering properties of psychotropic drugs tend to be related to dose and escalation speed •  Antipsychotics known or supposed to have low epileptogenic properties: olanzapine, risperidone, quetiapine, amisulpride • To avoid sudden changes in the pharmacological treatment of epilepsy (reduction, increase or substitution of antiepileptics), mainly in cases with history of psychoses •  Side-effects, toxic effects and pharmacokinetic interactions of antiepileptics and antipsychotics may be additive 4. CONCLUSION Given the negative impact of PIP in morbidity and mortality among these patients, it is crucial that neurologists and psychiatrists are able to adequately recognize and treat this clinical condition. 5. BIBLIOGRAPHY Kanner AM and Rivas-Grajales AM, CNS Spectrums, 2016; Weisholtz DS et al, Journal of Neurological Disorders & Stroke, 2014; Adachi N et al, Epilepsia, 2013; Guarnieria R et al, Rev Bras Psiquiatr, 2004. •  Bilateral seizure foci in the limbic temporal regions •  Processes associated with bilateral limbic lesions •  Relative increase in seizure frequency preceding the psychotic symptoms •  Lower verbal IQ •  Absence of febrile convulsions •  Absence of temporal mesial sclerosis Risk factors Symptoms are variable •  Auditory, visual or tactile hallucinations •  Persecutory, religious or grandiose delusions •  Sexual indiscretions •  Irritability, agitation, aggressiveness •  Affective symptoms Clinical presentation PIP is a psychiatric emergency Management PIP is defined by two features: chronologic relationship to seizures and nature of the mental state PIP represents about 25% of epileptic psychosis Episodes of psychosis that develop within 1 week after a seizure, or usually a cluster of seizures EEG: Postictal slowing There is often a short period of clear consciousness (12 to 72 hours) between the end of the seizure and the onset of psychosis PIP has been recognized since the 19th century, when Esquirol described postictal “fury” PIP usually follows exacerbations, especially clusters, of complex partial seizures, sometimes without, but more commonly with generalization • Duration: generally short; days to 2 weeks; mean duration is nearly 70 hours • PIP is essentially a benign, self-remitting condition • In half of affected patients, PIP remains as a single episode • In the other half, PIP episodes tend to repeat, which may occur even quasi regularly after a cluster of complex focal seizures or secondary generalization in extreme cases Course and Prognosis PIP is heralded by severe insomnia which, were it recognised, would allow preventive treatment of the episode by prompt administration of low doses of benzodiazepines or antipsychotics!