Psychiatric disorders in patients with psychogenic nonepileptic seizures and drug-resistant epilepsy: a study of an Argentine population.

Epidemiological data show that up to 20-30% of patients with psychogenic nonepileptic seizures (PNESs), resembling drug-resistant epilepsy (DRE), are referred to tertiary epilepsy centers. Furthermore, both disorders present high psychiatric comorbidity, and video-EEG is the gold standard to make differential diagnoses. In this study, we described and compared the clinical presentation and the frequency of psychiatric disorders codified in DSM IV in two groups of patients, one with PNESs and the other with DRE, admitted in a tertiary care epilepsy center of Buenos Aires, Argentina. We included 35 patients with PNESs and 49 with DRE; all were admitted in the video-EEG unit in order to confirm an epilepsy diagnosis and determine surgical treatment possibilities. All patients underwent a neurological and psychiatric assessment, according to standardized protocol (SCID I and II; DSM IV criteria). Student's t test was performed to compare continuous variables and Chi square test to compare qualitative variables. In this study, 33 (67%) patients with DRE and 35 (100%) patients with PNESs met criteria for at least one disorder codified in Axis I of DSM IV (p=0.003). Differences in the frequency of psychiatric disorder presentation were found between groups. Anxiety disorders (16.32% vs 40%; p=0.015), trauma history (24.5% vs 48.57%; p=0.02), posttraumatic stress disorder (4.08% vs 22.85%; p=0.009), and personality cluster B disorders (18.37% vs 42.86%; p=0.02) were more frequent in the group with PNESs. Psychotic disorders were more frequent in the group with DRE (20.4% vs 2.85%; p=0.019). Depression was equally prevalent in both groups. Standardized psychiatric assessment provides information that could be used by the mental health professional who receives the referral in order to improve quality of care and smooth transitions to proper PNES treatment, which should include a multidisciplinary approach including neurology and psychiatry.

Psychogenic nonepileptic seizures after head injury: a case report.

Psychogenic nonepileptic seizures (PNESs) are diagnosed when disruptive changes in behaviour, thinking, or emotion resemble epileptic seizures (ESs), but no paroxysmal discharges are seen on electroencephalogram (EEG) and do not originate from another medical illness. The gold standard for PNES diagnosis is video electroencephalogram (Video-EEG). PNESs are defined by modern psychiatry as conversion and dissociative disorders but these disorders may coexist with many others psychiatric disorders, including depression, posttraumatic stress disorder, and personality disorders. It is well known that epileptic seizures are a frequent and well-studied complication of traumatic head injury (THI). However, THI may also generate psychic symptoms including PNES. In this paper we describe a patient who developed PNES after THI in a bus accident and received a diagnosis of refractory epilepsy for 24 years until she underwent Video-EEG.

Epidemiological survey of epilepsy in the special school population in the city of Buenos Aires. A comparison with mainstream schools.

BACKGROUND: Previous studies in special schools have shown a high prevalence of epilepsy, which is strongly associated with cerebral palsy and severe mental retardation. The conditions regulating school placement have also been described in those studies. In the City of Buenos Aires, information is known only for mainstream schools. OBJECTIVE: To determine the prevalence and characteristics of epilepsy in special schools and to compare results with common primary education settings. DESIGN AND METHODS: A cross-sectional study was carried out in special schools in the City of Buenos Aires, by adopting the same definitions, diagnostic criteria and questionnaire as those used in a previous study in the common primary school population. Responses from 1,682 children, aged 6-16 years, residing in the City of Buenos Aires, with mental retardation, visual or hearing impairment, psychiatric disorders and motor disabilities were analyzed. RESULTS: A total of 121 children with epilepsy were detected. Lifetime prevalence was 71.9 per thousand and active prevalence was 64.8 per thousand (22-25 times greater than rates in mainstream schools). Prevalence was highest in girls and generalized seizures prevailed over other seizure types. Ninety-two percent of cases received antiepileptic drugs, 57.9% as a single drug treatment and 85.1% in adequate doses. Only 56% of the children with a diagnosis of epilepsy proved to be true-positive cases, and almost 40% received antiepileptic drugs for nonepileptic disorders. Malformations/degenerative disease were the most common etiology. CONCLUSIONS: Special schools contain clusters of children with epilepsy as a comorbid condition. False high frequency is due to misdiagnoses and unnecessary treatments. These schools are an important target for educational interventions.

Fijación de prioridades en investigación en VIH/Sida. Uso de la matriz de estrategias combinadas, herramienta recomendada por el Foro Global de Investigación en Salud / Research priority setting in HIV/AIDS using the comined approach matrix, a tool recommended by TH Global Forum For Health Research

A partir de la aplicación de la matriz de estrategias cominadas, un equipo interdisciplinario de investigadores elaboró un diagnóstico sobre la epidemia de VIH/Sida en Argentina... En el taller se discutieron la situación epidemiológica argentina en VIH/SIDA, sus determinantes y las eventuales intervenciones útiles para mejorar o revertir dicha situación. Estas opiniones junto con las respuestas obetenidas de la encuesta y el material provisto por el equipo interdisciplinario, ayudaron a completar la matriz desde la cuál se elaboró un listado de prioridades en investigación en VIH/SIDA.

The combined approach matrix, tool recommended by the Global Forum for Health Research to set priorities for selection, organises information from different sources to establish the current situation on any sanitary problem form the point of view of the individual, the family, the community, the ministry of health, other institutions related or not to health and macroeconomic politics. By the application of the combined approach matrix, an interdisciplinary teams of researchers elaborated a diagnosis on HIV/aids epidemics in Argentina.

Periventricular nodular and subcortical neuronal heterotopia in adult epileptic patients.

Developmental malformations are brain abnormalities that occur during embryogenesis. Neuronal migration disorders, including heterotopic lesions, constitute one type of such abnormalities. The aim of the study was to compare the epileptic clinical patterns of patients with periventricular nodular heterotopia (PNH) (G1) with those affected by subcortical heterotopia (SCH) (G2) looking for differences between both groups which, eventually, might suggest the type of the underlying malformation. The variables studied in both groups were: type of the heterotopia depicted on MRI studies, sex, age, age at seizure onset, annual seizure frequency, localization of the ictal symptomatogenic zone, characteristics of the EEG, other associated anomalies on the magnetic resonance images (MRI) besides the heterotopia, and response to treatment. The only difference found between both groups was the type of heterotopia as shown by MRI studies. The other assessed variables did not significantly (p>0.05) differ between groups. No differences in the clinical features characterizing epilepsy could be found in patients with PNH or SCH, being the images the only tool able to differentiate them.

Periventricular nodular and subcortical neuronal heterotopia in adult epileptic patients

Developmental malformations are brain abnormalities that occur during embryogenesis. Neuronalmigration disorders, including heterotopic lesions, constitute one type of such abnormalities. Theaim of the study was to compare the epileptic clinical patterns of patients with periventricular nodular heterotopia(PNH) (G1) with those affected by subcortical heterotopia (SCH) (G2) looking for differences between bothgroups which, eventually, might suggest the type of the underlying malformation. The variables studied in bothgroups were: type of the heterotopia depicted on MRI studies, sex, age, age at seizure onset, annual seizure frequency,localization of the ictal symptomatogenic zone, characteristics of the EEG, other associated anomalies onthe magnetic resonance images (MRI) besides the heterotopia, and response to treatment. The only differencefound between both groups was the type of heterotopia as shown by MRI studies. The other assessed variablesdid not significantly (p>0.05) differ between groups. No differences in the clinical features characterizing epilepsycould be found in patients with PNH or SCH, being the images the only tool able to differentiate them.

Heterotopía neuronal nodular y subcortical en pacientes adultos con epilepsia. Las malformacionesde la corteza cerebral son un grupo de entidades que se producen durante las etapasdel desarrollo embrionario y cuya manifestación clínica puede ser la epilepsia. Estas malformaciones puedenser diagnosticadas in vivo a través de las imágenes por resonancia magnética (IRM). Un subtipo particular deéstas lo constituyen los trastornos en la migración neuronal, dentro de los cuales se ubican las heterotopías(HT). El objetivo del estudio fue comparar enfermos portadores de HT periventriculares (G1) con aquellos portadoresde HT subcorticales (G2). Se analizaron las variables sexo, edad y edad de inicio de la epilepsia (EI) enaños, antecedentes familiares (AF) o prenatales (AP), frecuencia anual de crisis (FAC) y característicassemiológicas de las crisis, hallazgos en el EEG e IRM y respuesta al tratamiento farmacológico. G1 (n=13): 8mujeres (61.5%), edad promedio 32.9 ± 11.5 (rango 20-59), EI 13.7 ± 7.6 (rango 2-23), AF 1 caso (7.7%), AP en1 (7.7%), FAC 28.3 ± 31.4 (rango 0-120), crisis multifocales en 5 (38.5%), crisis temporales en 5 pacientes (38.5%),EEG epileptiforme (EEGE) en 7 casos (53.8%), anomalías asociadas en las IRM (AAIRM) en 8 sujetos (61.5%) y4 casos refractarios al tratamiento (30.7%). G2 (n=8): 6 mujeres (75%), edad promedio 30 ± 9.7 (rango 13-43), EI11.1 ± 6.3 (rango 1-19), AP 2 (25%), FAC 30 ± 39.5 (rango 0-120), crisis multifocales en 4 sujetos (50%), crisistemporales en 5 pacientes (62.5%), EEGE en 7 casos (87.5%), AAIRM en 3 casos (37.5%) y 1 caso refractario altratamiento (12.5%). El análisis de las diferentes variables clínicas analizadas no mostró diferencias significativasentre ambos grupos, siendo las imágenes el único elemento que permitió su diferenciación.

Periventricular nodular and subcortical neuronal heterotopia in adult epileptic patients

Developmental malformations are brain abnormalities that occur during embryogenesis. Neuronalmigration disorders, including heterotopic lesions, constitute one type of such abnormalities. Theaim of the study was to compare the epileptic clinical patterns of patients with periventricular nodular heterotopia(PNH) (G1) with those affected by subcortical heterotopia (SCH) (G2) looking for differences between bothgroups which, eventually, might suggest the type of the underlying malformation. The variables studied in bothgroups were: type of the heterotopia depicted on MRI studies, sex, age, age at seizure onset, annual seizure frequency,localization of the ictal symptomatogenic zone, characteristics of the EEG, other associated anomalies onthe magnetic resonance images (MRI) besides the heterotopia, and response to treatment. The only differencefound between both groups was the type of heterotopia as shown by MRI studies. The other assessed variablesdid not significantly (p>0.05) differ between groups. No differences in the clinical features characterizing epilepsycould be found in patients with PNH or SCH, being the images the only tool able to differentiate them. (AU)

Heterotopía neuronal nodular y subcortical en pacientes adultos con epilepsia. Las malformacionesde la corteza cerebral son un grupo de entidades que se producen durante las etapasdel desarrollo embrionario y cuya manifestación clínica puede ser la epilepsia. Estas malformaciones puedenser diagnosticadas in vivo a través de las imágenes por resonancia magnética (IRM). Un subtipo particular deéstas lo constituyen los trastornos en la migración neuronal, dentro de los cuales se ubican las heterotopías(HT). El objetivo del estudio fue comparar enfermos portadores de HT periventriculares (G1) con aquellos portadoresde HT subcorticales (G2). Se analizaron las variables sexo, edad y edad de inicio de la epilepsia (EI) enaños, antecedentes familiares (AF) o prenatales (AP), frecuencia anual de crisis (FAC) y característicassemiológicas de las crisis, hallazgos en el EEG e IRM y respuesta al tratamiento farmacológico. G1 (n=13): 8mujeres (61.5%), edad promedio 32.9 ± 11.5 (rango 20-59), EI 13.7 ± 7.6 (rango 2-23), AF 1 caso (7.7%), AP en1 (7.7%), FAC 28.3 ± 31.4 (rango 0-120), crisis multifocales en 5 (38.5%), crisis temporales en 5 pacientes (38.5%),EEG epileptiforme (EEGE) en 7 casos (53.8%), anomalías asociadas en las IRM (AAIRM) en 8 sujetos (61.5%) y4 casos refractarios al tratamiento (30.7%). G2 (n=8): 6 mujeres (75%), edad promedio 30 ± 9.7 (rango 13-43), EI11.1 ± 6.3 (rango 1-19), AP 2 (25%), FAC 30 ± 39.5 (rango 0-120), crisis multifocales en 4 sujetos (50%), crisistemporales en 5 pacientes (62.5%), EEGE en 7 casos (87.5%), AAIRM en 3 casos (37.5%) y 1 caso refractario altratamiento (12.5%). El análisis de las diferentes variables clínicas analizadas no mostró diferencias significativasentre ambos grupos, siendo las imágenes el único elemento que permitió su diferenciación. (AU)

Periventricular nodular and subcortical neuronal heterotopia in adult epileptic patients

Developmental malformations are brain abnormalities that occur during embryogenesis. Neuronalmigration disorders, including heterotopic lesions, constitute one type of such abnormalities. Theaim of the study was to compare the epileptic clinical patterns of patients with periventricular nodular heterotopia(PNH) (G1) with those affected by subcortical heterotopia (SCH) (G2) looking for differences between bothgroups which, eventually, might suggest the type of the underlying malformation. The variables studied in bothgroups were: type of the heterotopia depicted on MRI studies, sex, age, age at seizure onset, annual seizure frequency,localization of the ictal symptomatogenic zone, characteristics of the EEG, other associated anomalies onthe magnetic resonance images (MRI) besides the heterotopia, and response to treatment. The only differencefound between both groups was the type of heterotopia as shown by MRI studies. The other assessed variablesdid not significantly (p>0.05) differ between groups. No differences in the clinical features characterizing epilepsycould be found in patients with PNH or SCH, being the images the only tool able to differentiate them. (AU)

Heterotopía neuronal nodular y subcortical en pacientes adultos con epilepsia. Las malformacionesde la corteza cerebral son un grupo de entidades que se producen durante las etapasdel desarrollo embrionario y cuya manifestación clínica puede ser la epilepsia. Estas malformaciones puedenser diagnosticadas in vivo a través de las imágenes por resonancia magnética (IRM). Un subtipo particular deéstas lo constituyen los trastornos en la migración neuronal, dentro de los cuales se ubican las heterotopías(HT). El objetivo del estudio fue comparar enfermos portadores de HT periventriculares (G1) con aquellos portadoresde HT subcorticales (G2). Se analizaron las variables sexo, edad y edad de inicio de la epilepsia (EI) enaños, antecedentes familiares (AF) o prenatales (AP), frecuencia anual de crisis (FAC) y característicassemiológicas de las crisis, hallazgos en el EEG e IRM y respuesta al tratamiento farmacológico. G1 (n=13): 8mujeres (61.5%), edad promedio 32.9 ± 11.5 (rango 20-59), EI 13.7 ± 7.6 (rango 2-23), AF 1 caso (7.7%), AP en1 (7.7%), FAC 28.3 ± 31.4 (rango 0-120), crisis multifocales en 5 (38.5%), crisis temporales en 5 pacientes (38.5%),EEG epileptiforme (EEGE) en 7 casos (53.8%), anomalías asociadas en las IRM (AAIRM) en 8 sujetos (61.5%) y4 casos refractarios al tratamiento (30.7%). G2 (n=8): 6 mujeres (75%), edad promedio 30 ± 9.7 (rango 13-43), EI11.1 ± 6.3 (rango 1-19), AP 2 (25%), FAC 30 ± 39.5 (rango 0-120), crisis multifocales en 4 sujetos (50%), crisistemporales en 5 pacientes (62.5%), EEGE en 7 casos (87.5%), AAIRM en 3 casos (37.5%) y 1 caso refractario altratamiento (12.5%). El análisis de las diferentes variables clínicas analizadas no mostró diferencias significativasentre ambos grupos, siendo las imágenes el único elemento que permitió su diferenciación. (AU)

Mesial temporal lobe epilepsy and hippocampal sclerosis: cognitive function assessment in Hispanic patients.

PURPOSE: The goal of this study was to assess the cognitive function status in patients with mesial temporal lobe epilepsy and hippocampal sclerosis (TLE+HS) to determine their cognitive function profile and to correlate material-specific memory deficits with HS laterality diagnosed by MRI. METHODS: Seventy-one patients were assessed with a neuropsychological protocol that includes IQ, attention, handedness, verbal memory, visual memory, language, and the executive function. chi(2) and correlation tests were used. RESULTS: Memory impairment was found in 46 patients (66%): patients without any memory deficit (n=25), patients with verbal memory deficit (n=21), patients with visual memory deficit (n=17), patients with deficit for both types of memory (n=8). Correlation between MRI lesion and memory was 66%. Language was impaired in 33 patients (46%). Eighteen patients (25%) had a deficit of the executive function. CONCLUSIONS: Patients with TLE+HS presented with a deficit in material-specific episodic memory correlating in large proportion with HS lateralization. We also found language and executive function impairments.