BHS occur most commonly within the first 18 months of age

Slides:



Advertisements
Similar presentations
Diagnostic Work-up. Electroencephalography (EEG) The only diagnostic test for absence seizures Ambulatory EEG monitoring over 24 hours may be useful to.
Advertisements

EEG findings in patients with Neurological Disorders Instructor: Dr. Gharibzadeh By: Fahime Sheikhzadeh.
Differential Diagnosis. Salient Features Often observed to be absent minded Brief episodes of blank staring and inattention Eye blinking Reflex scratching.
CARDIAC EFFECTS OF SEIZURES Meysam Golmohammadi. CARDIAC EFFECTS OF SEIZURES [Maromi Nei, 2009] Seizures frequently affect the heart rate and rhythm.
Date of download: 6/27/2016 Copyright © 2016 McGraw-Hill Education. All rights reserved. Panayiotopoulos Syndrome. A 5-year-old girl with nocturnal GTCS.
Automatisms with preserved responsiveness were observed exclusively during seizures arising from the right nondominant temporal lobe. They were not observed.
Benign infantile seizures are characterized by (1) familial or nonfamilial occurrence; (2) normal development prior to onset; (3) onset mostly during the.
Low Voltage EKG Activity Due to Scalp Edema; High Frequency Jet Respirator Artifact. An 18-day-old boy with diaphragmatic hernia, pulmonary hypoplasia,
The EEG features and their evolution change with age
In the scalp EEG, slow-wave activity was present in 62%
Transient Unilateral Attenuation of Background Activity During Sleep
A. “10-20” is a measurement system designed to reliably reproduce electrode positions on different patients, regardless of head size. Electrodes are placed.
The typical EEG of hydranencephaly shows a flat pattern but the EEG of severe hydrocephalus does not demonstrate a flat pattern. Visual evoked potential.
Additional electrodes can be used to supplement the standard System
A mild and inconsistent asymmetry of photic driving response is frequently seen in normal individuals. An asymmetry in photic driving response may result.
Generalized, frontally predominant, rhythmic fast activity is the most common ictal EEG accompaniment of generalized tonic seizures. Ictal EEG patterns.
Lateralized Background Suppression; Hemiplegic Migraine
Very Low-Voltage Background Activity; Hypoxic-Ischemic Encephalopathy (HIE). A 6-day-old infant who was born at term with Apgar scores of 0, 0, 0, 3, 4,
Outcomes after surgery, cortical resection, or hemispherectomy in infants with catastrophic focal epilepsy are very good. About 75–78% are seizure-free.
CBZ is the most common antiepileptic drug (AED) causing AED-induced seizure worsening. CBZ can both aggravate and induce new seizure types including absence,
In this patient, the ground electrode was placed on the forehead and the low-impedance active electrode occurred in the occipital region. Therefore, the.
Patients with IS caused by FCD frequently develop partial seizures that can precede, be simultaneous with, or follow the cluster of epileptic spasms. Spasms.
PFA may be a reflection of proximity of the epileptogenic zone to the recording electrodes. Seizures arising from the lateral frontal convexity began with.
The scalp EEG is frequently negative or maybe misleading; furthermore, spread of epileptic discharges from the parietal and occipital lobes to frontal.
The “H-response” is a prominent photic driving response at flash rates beyond 20 Hz. In a critical review of the literature, the reported sensitivity of.
Pyruvate dehydrogenase deficiency (PDH), a deficiency in the E1 (pyruvate dehydrogenase) component of the pyruvate dehydrogenase complex, is one of the.
The exact pathogenesis of atopic dermatitis remains a mystery
Abnormal EEGs were found in 43–75% of autistic children and 82% of their EEGs; 46% had clinical seizures. Nearly all children with seizures had epileptiform.
The causes of OS are symptomatic or organic; the causes of EME can be genetic, metabolic, or entirely unknown. OS causes tonic spasms and partial seizures.
Late posttraumatic epilepsy usually occurs within the first 2 years after the injury. Seizures are believed to originate from a cerebromeningeal scar.26.
Focal cortical dysplasia (FCD) is often associated with severe focal epilepsy. Intraoperative ECoG showed one of the following patterns: (1) repetitive.
MAS develop atonia immediately after a single or a series of 2–3 myoclonic seizures (MS). A sudden loss of tone causes either a drop attack or slight myatonia,
SEIZURE OF THE BRAIN.
A close relationship exists between heterotopic nodules and cortical regions in bilateral PNH, with an epileptogenic network including both structures.
The SSS phenomenon is defined as a pair of sequential ictal potentials separated by complete or almost complete cessation of seizure activity; the SSS.
Malignant rolandic-sylvian epilepsy (MRSE) differs from BECTS and LKS in its refractoriness to medication, clusters of seizures, change in semiology, and.
The incidence of epilepsy in children with hydrocephalus is approximately 30%. Myelomeningocele carries a low risk at approximately 7%, cerebral malformations.
Epilepsy is an important predictor of poor intellectual outcome in the children with hydrocephalus with shunts. Epilepsy was significantly affected by.
POLG1 mutations should be considered in teenagers and young adults reporting episodic visual symptoms with migraine-like headaches and sudden-onset intractable.
Eye Fluttering During Photic Stimulation
Seizures in Childhood A seizure: is a transient occurrence of signs and/or symptoms resulting from abnormal excessive or synchronous neuronal activity.
Six hundred and nine patients diagnosed clinically as brain dead were studied; 326 had final cardiac asystole while still being ventilated. The median.
Ohtahara syndrome is a very rare and devastating form of epileptic encephalopathy of very early infancy. Onset of seizures is mainly by 1 month of age.
After the seizure has been viewed using conventional frequencies and muscle activity has been removed, a search for baseline shifts should be performed.
Stroke or hemorrhage is the most common structural abnormality that causes focal clonic or tonic seizures. In addition, focal tonic or clonic seizures.
The extent of the PET hypometabolism may be substantially larger than the electrical focus.55 The relationship between the area of hypometabolism and the.
In this patient, the ground electrode was placed on the forehead and the low-impedance active electrode occurred in the occipital region. Therefore, the.
Patients presenting with clinical features compatible with MAE but with seizure semiology consistent with focal seizure or focal abnormality seen in the.
Photic driving responses in children <6 years are relatively small
BiPLEDs are PLEDs that are bilateral, generally asynchronous, and differ in amplitude, morphology, repetitive rate, and location. They are most commonly.
Only 23% of the survivors of RSE were normal at follow-up; 34% showed developmental deterioration and 36% developed new-onset epilepsy.230 Mortality is.
ECS is more common in females
Usually, scalp-recorded ictal DC shifts are not successfully recorded because movements during clinical seizures could cause artifacts. They are highly.
Secondarily generalized discharges are a common occurrence with frontal lobe epilepsy. The EEG findings that suggest secondary bilateral synchrony include.
POLG1 mutations should be considered in teenagers and young adults reporting episodic visual symptoms with migraine-like headaches and sudden-onset intractable.
“Zip-like electrical discharges (Zips)” is a common ictal EEG pattern in neonates, which consists of focal episodic rapid spikes of accelerating and decelerating.
The typical EEG in SWS is asymmetric, with local voltage depression and background slowing ipsilateral to the affected hemisphere. This asymmetry may be.
The presence of PDA and depression of beta and alpha activities is supportive of underlying structural abnormalities (both gray and white matter) in the.
ABSENCE SEIZURES.
The best predictor of surgical outcome is the presence of a focal epileptic generator that may or may not include the PNH. Invasive recording is required.
CEEG monitoring detected seizure activity in 19% of patients, and the seizures were almost always nonconvulsive. Coma, age 24 hours of monitoring to detect.
ESES may be the result of a secondary bilateral synchrony
AC is an EEG pattern in the alpha frequency range (8–13 Hz) that occurs with a generalized distribution in a comatose patient. It is monomorphic and does.
Combination of Continuous Polymorphic Delta Activity and FIRDA; Massive Brain Edema with Central Herniation Syndrome. EEG of a 28-month-old girl with a.
Take a detailed history of the description of the event, precipitants, duration, and postevent behavior. Does history suggest an epileptic seizure disorder?
In the study of 120 patients with defective alpha activity by mental arithmetic at Mayo Clinic, 32 patients had Bancaud phenomenon. Associated focal slowing.
An interictal EEG in BFNC was normal and discontinuous, and showed focal or multifocal sharp waves or “théta pointu alternant” pattern. The théta pointu.
Which of the following statements is false about the EEG shown:
An atypical case of Lennox-Gastaut syndrome not associated with mental retardation: A nosological issue  Hann-Yeh Shyu, Ji-Ho Lin, Chien Chen, Shang-Yeong.
PEDIATRIC EPILEPSY SYNDROMES
Presentation transcript:

BHS occur most commonly within the first 18 months of age BHS occur most commonly within the first 18 months of age. Virtually all breath-holders cease experiencing episodes by 7–8 years of age. 70 EEGs in 129 children with breath-holding spells were almost always normal.71 Cardiac arrest was observed following ocular compression. With an arrest lasting 3–6 sec, there were no clinical or electrical abnormalities. However, with a longer cardiac arrest (7–13 sec) bisynchronous slow waves appeared. This was usually accompanied by clouding or loss of consciousness. When the arrest lasted more than 14 sec, one or two generalized clonic jerks appeared without affecting the EEG. This could be followed by a generalized tonic contraction resembling decerebrate rigidity and accompanied by complete flattening of the EEG. Thus, during a syncopal event the EEG initially shows mild generalized slowing. This is followed by high-voltage frontal delta activity. If the cerebral hypoperfusion persists, the EEG flattens. With recovery, the EEG normalizes in a reverse sequence.71–73 Occasionally, patients may experience protracted seizures or status epilepticus following BHS.74,75 Typically, interictal EEG findings in these patients are normal or rarely vertex spikes. They were termed episodes anoxic-epileptic seizures. Administration of an AED frequently ablates the lengthy seizures, although BHS may continue to occur.76 Patients with cyanotic BHS may follow this EEG evolution without significant bradycardia or asystole. Prolonged QT syndrome is a rare, but potentially malignant, cause of anoxic seizure. It is recommended that an EKG to screen for prolonged QT syndrome be performed in all cases.77 Source: Generalized Epilepsy, Atlas of Pediatric EEG Citation: Laoprasert P. Atlas of Pediatric EEG; 2011 Available at: http://neurology.mhmedical.com/DownloadImage.aspx?image=/data/books/1042/lao001_fig_08-50.gif&sec=59079911&BookID=1042&ChapterSecID=59078730&imagename= Accessed: October 07, 2017 Copyright © 2017 McGraw-Hill Education. All rights reserved