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C Jalin

Publications and source records attributed to C Jalin.

At least 19 recordsLinked to original sources
PubMed2004

Behavioural epileptic seizures: a clinical and intracranial EEG study in 8 children with frontal lobe epilepsy.

We report on eight children who underwent prolonged invasive video-EEG recording (IC-EEG) for intractable frontal lobe epilepsy and whose seizures consisted of behaviour changes. Seizures were recorded on a BMSI computer with 128 channels connected to the Gotman software of a stellate system; their identification was made both clinically and by automatic detection of paroxysmal electrical events. Behavioural epileptic seizures (BES) consisted of various clinical signs comprising mood change, sudden agitation, unexpected quietness, and subtle change of awareness or awakening. In 2 patients, seizures consisted in repetitive movements that we referred to as epileptic stereotypes. BES came from the prefrontal areas of the brain. Most of them were overlooked or misdiagnosed as behavioural manifestations, especially in children with mental deficiency and autistic features. Given the improvement of behaviour and mental functions following surgery, we assume that BES may contribute to generate mental and behavioural dysfunction.

Autistic Disorder↗
PubMed2004

[Surgery for intractable focal epilepsy in children].

Surgery of drug resistant epilepsy in children is a functional surgery which aims at the suppression of the epileptogenic focus. The surgical decision is adopted or rejected as a result of the clinical examination and complementary investigations following a multidisciplinary discussion in which the benefit-risk ratio is being carefully weighed. The objective of the presurgical investigations, dominated by scalp-recorded video-electroencephalography and magnetic resonance imaging, is the localization of the epileptogenic focus. The invasive surgical investigations with intracranial electrode placement are indicated when the limits of a planned resection have to be defined precisely or when the focus is located nearby a functionally eloquent region (sensori-motor and language region). Their identification is possible by means of electrical stimulation. Two methods of exploration are available: The combination of subdural and intracerebral electrode placement through craniotomy and the stereotactic placement of intracerebral depth electrodes (Stereo-EEG). The choice of either of these two methods depends on the child's age and on the topography of the epileptogenic focus. Surgery can be either palliative, with the purpose of reducing the intensity and/or the frequency of a certain seizure type (callosotomy, multiple subpial transsections) or curative, aiming at a suppression of the epileptogenic focus through a resective or a disconnective surgical procedure. We have operated on a population of 148 children and infants between 3 months and 10 years of age during the years 1993 to 2001: In the infant group, dysplastic lesions represented the predominant etiology. In the age group of 3 to 10 years, the underlying pathology was more distributed (dysplastic lesions, epileptogenic tumors, Rasmussen's encephalitis, hypothalamic hamartomas). Extratemporal focal resections required, in the majority of cases, an invasive preoperative exploration and hemispherotomy was frequent in this group (44 p. 100). Sixty-seven percent of the children were seizure-free, with an acceptable morbidity rate, primarily due to shunt placement following hemispherotomy in children with dysplastic lesions. Our preliminary results concerning quality of life and socialization are encouraging and favor surgical treatment at an early stage.

Anticonvulsants↗
PubMed2003

Ictal SPECT in children with epilepsy: comparison with intracranial EEG and relation to postsurgical outcome.

In order to validate the ability of ictal single photon emission computed tomography (SPECT) to localize the epileptogenic zone (EZ) in children, we compared in 20 patients aged from 10 months to 17 years (mean 6.5 years) the topography of the area of increased ictal perfusion (IPA), determined on the basis of ictal minus interictal scan values, with that of the EZ determined by intracranial EEG recordings and assessed its relationship with the postsurgical outcome. Eighteen patients had symptomatic epilepsy and 10 had extratemporal epilepsy. All patients except one had an ictal injection (mean time lag from clinical seizure onset was 18 s). Ictal and interictal SPECT images were successively co-registered, normalized, subtracted, smoothed and superimposed on MRI. All patients with ictal injection exhibited one or several IPAs. The topography of the 'highest' IPA, i.e. the maximal cerebral blood flow (CBF) change between ictal and interictal SPECT, significantly colocalized with the site of onset of the discharge, and that of the lower IPAs with that of the area of propagation (P < 0.0001). At a threshold of 30% of the maximal CBF change, the IPAs detected the onset of the discharge with a sensitivity of 0.80 and a specificity of 0.70. The highest IPA localized the EZ in 12 out of 15 patients. In the three others it missed the EZ and showed the area of propagation because of rapid seizure propagation or of infraclinical seizure onset. Among the patients with favourable surgery outcome, the highest IPA colocalized with the resected area in 70% of cases. Ictal SPECT could therefore plays an important role as a non-invasive presurgical method of investigation by optimizing the placement of intracranial electrodes, thus improving the postsurgery outcome of paediatric partial epilepsy.

Adolescent↗
PubMed2000

Hot water epilepsy: a benign and unrecognized form.

Hot water epilepsy is a reflex epilepsy. Seizures are provoked by hot water, and result from the association of both cutaneous and heat stimuli. Described mainly in India and Japan, the condition seems to be rare in Europe, where it occurs in young children. We report five infants aged from 6 months to 2 years. They had brief seizures during bathing with activity arrest, hypotonia, and vasoactive modification; clonic movements were observed. A simple treatment-decreasing the bath temperature-can be sufficient. Sometimes an antiepileptic drug is required. Seizure course and psychomotor development are favorable. Hot water epilepsy is a benign form of epilepsy. Its incidence could be underestimated because of confusion with febrile convulsions, vagal fits, or aquagenic urticaria.

Electroencephalography↗
PubMed1999

[Hot water epilepsy: a benign and underestimated form].

BACKGROUND: Hot water epilepsy belongs to the group of reflex epilepsies. Seizures are provoked by hot water, due to the association of both cutaneous and heat stimuli. Described mainly in India and Japan, it seems to be rare in Europe where it occurs in young children. CASE REPORTS: Five infants aged between 6 months to 2 years had seizures during bathing with activity arrest, hypotonia and vasoactive modification. Sometimes clonic movements could be observed. The diagnosis was confirmed by EEG recorded during bath in the fives cases, with video for two of them. The course of the seizures and of the psychomotor development were favorable. CONCLUSION: Hot water epilepsy is a benign epilepsy. Its incidence could be underestimated because seizures can be confused with febrile convulsions or vagal fits.

Baths↗
PubMed1998

[Surgery and epilepsy].

Corpus callosotmy was introduced in 1940 as a palliative treatment for generalized epilepsies. The improvement of the surgical technique, and the simplification of the initial "total commissurotomy" made that procedure proposed in order to decrease the frequency and the severity of the seizures occurring in the secondary geralzed epilepsies. However the indication criteria remain unclear, due to the difficulty for analysing the results and the feterogenity of the series. A careful selection requiring a comprehensive epilepsy team remains mandatory despite the relative simplicity of the procedure.

Brain Diseases↗
PubMed1996

[Problems related to neurosurgical treatment of epilepsy in children].

Neurosurgery of epilepsy in children has undergone rapid development during the past decade. This was justified by the high incidence of intractable epilepsy and its consequences on cognitive development. Any decision in the area of surgery must take in account specific etiology and the rapid maturation of the infant's brain. As in adulthood, both the epileptogenic and the functional zones must be identified, but this is a challenge when the brain is not mature and the functions not yet developed. In addition, the ability to recover must be determined. At the present time no precise methodology can be advised for presurgical work-up and surgical indications.

Age Factors↗
PubMed1987

[Ambulatory 24-hour EEG recording in epileptic infantile spasms].

Twenty-four h cassette recording (MEDILOG 9000) where obtained in 22 untreated infants (23 records) with a West syndrome (idiopathic: n = 12, symptomatic: n = 10). All these infants had had a 3 h polygraphic recording. Tracings were visually analyzed for sleep stages. Electro-clinical seizures and infraclinical discharges were listed according to their type and the stage of vigilance. Two hundred twenty-eight critical events were recorded in 22 cassette recordings: isolated spasms, clusters of spasms, partial or generalized discharges followed or not by clusters of spasms. Sixty per cent of these fits occurred during wakefulness, 27% during non REM sleep, 13% during awakening and none during REM sleep. Partial discharges, followed or not by clusters of spasms, were only present in cases with unfavourable outcome. In benign spasms the hypsarrhythmic pattern was present between spasms in each cluster, but not in cases with unfavourable outcome. Compared with 3 h polygraphic recordings, 24 h cassette recordings gave supplementary data on the presence, type and timing of seizures in 16 of out 22 cases.

Ambulatory Care↗
PubMed1986

[Seizures recorded upon awakening in the child: diagnostic difficulties].

We describe the EEG patterns and the clinical modifications of spontaneous awakening in 34 infants and children. An "awakening seizure" could be confirmed in 27 children, including 18 with various epilepsies and 9 infants with West syndrome. In other 7 children, the analysis of the tracing could not conclude whether or not the pathological awakening patterns were critical. The frequency of seizures occurring with awakening in various epileptic syndromes might be underestimated: it rated 18% in our series of 150 children with a recorded seizure in a two years period. Since the EEG patterns occurring with awakening have been poorly studied in epileptic children, it may be difficult to distinguish a pathological arousal from an "awakening seizure".

Adolescent↗
PubMed1985

[Ambulatory EEG monitoring (Medilog 9000). Initial results in a pediatric population].

The authors report their experience of ambulatory EEG monitoring (Medilog 9000, Oxford Instruments) in a paediatric population. They describe the method of recording, the system of lecture and the paper reproduction possibilities. Thirty-four 24 h cassettes have been recorded and analysed in 30 children aged from 1 month to 17 years. Six infants (under 1 year) had convulsions or spasms; 20 children were epileptic and 5 children were recorded for different reasons. Sleep was obtained in all cases. Seizures were recorded in 5 of 6 infants under 1 year of age, and in 11 of 20 epileptic children. The advantages and applications of this method are discussed.

Adolescent↗
PubMed1983

[Prognostic value of EEG in pneumococcal meningitis in children].

We studied the prognostic value of initial EEG in 36 children with a pneumococcal meningitis. The children were divided into 2 groups: infants under 1 year old, and children over 1 year old. The evolution was favourable in 5 cases out of 6 with normal or subnormal initial EEG. The evolution was unfavourable every time we recorded a status epilepticus. When the initial EEG is 'altered' or 'very altered' the prognosis is more difficult to determine but we did not find any sequelae after transitory localised abnormalities with a clinical neurological deficit. The EEG seems to be important for the surveillance and the prognosis of pneumococcal meningitis.

Brain↗
PubMed1983

[Electroencephalographic aspects of classic agyria-pachygyria].

Four infants had agyria confirmed by CT scan. All were mentally retarded, microcephalic, 3 of them having characteristic facial dysmorphy and 2 infantile spasms. EEG was characterized by very high amplitude rhythms in the alpha range, associated with delta waves and with infrequent spikes. The tracing was poorly modified by sleep. Drugs reduced its amplitude and rapid rhythms appeared with benzodiazepines. The authors point to the usefulness of the EEG in suggesting diagnosis before the CT scan, as was the case in 2 patients. They point to the urgent need of studying infantile epilepsies according to etiology, and not only to seizure types.

Cerebral Cortex↗
PubMed1983

[Unilateral status epilepticus during the neonatal period].

Twenty-one newborns displaying a strictly unilateral status epilepticus were studied. Three groups have been isolated according to the aetiology: neonatal anoxia (n = 5), postcardiac surgery (n = 8), cerebral hemispheric lesions confirmed by CT scan (n = 7). The authors relate in detail the clinical features and the EEG abnormalities, ictal and interictal in each group, and comment on their results. They show the importance of EEG in establishing or detecting a unilateral status epilepticus and in helping the aetiologic diagnosis.

Brain Diseases↗
PubMedDate not supplied

Progabide for previously untreated absence epilepsy.

Ten patients suffering from absence epilepsy and showing generalized spike-wave paroxysms in the EEG were treated by progabide monotherapy. Findings concerning clinical data and serial 24 h long-term EEG recordings were compared for the pre-treatment and treatment period. The average total spike-wave duration in 24 h decreased slightly from 810 sec to 699 sec; at follow-up, in 4 cases this trend was found to have reversed. Concerning seizure frequency, a marked anticonvulsant effect could not be confirmed; an initial slight anti-absence activity in some cases seemed to be subjected to the development of tolerance. Side effects were rarely observed and if so were not severe.

Adolescent↗
PubMedDate not supplied

Twenty-four-hour ambulatory EEG monitoring in infantile spasms.

Twenty-four-hour ambulatory EEG (AEEG) recordings were performed in 74 infants with West Syndrome (WS) who had not received corticosteroids before the recording. EEG analysis was performed visually for interictal background activity as well as for ictal events: spasms (isolated or in clusters) and other seizures either generalized or partial. Six hundred fifty-four seizures were recorded in 67 patients. Partial seizures (PS) were noted in 31 infants (51% of symptomatic WS cases, 33% of cryptogenic WS cases). In 14 patients, PS were immediately followed by a cluster of spasms consisting of a single ictal event. Patients with PS had an asymmetrical interictal background activity in 85% of cases, with no return to hypsarrhythmia between spasms in a given cluster. AEEG is a reliable method to detect and analyze ictal events in infants with WS. In this population, patients with unfavorable outcome of both epilepsy and psychomotor development have PS. Therefore, the existence of PS may contribute to etiologic diagnosis and prognostic evaluation.

Child, Preschool↗