Elective inpatient video-EEG monitoring during the COVID-19 pandemic.

To evaluate the safety and feasibility of admission for elective video-EEG monitoring during the SARS-CoV-2 pandemic. We performed a retrospective review of elective inpatient epilepsy monitoring unit admissions at our institution from May 3rd, 2020 to August 12th, 2020. All patients were screened by telephone for symptoms concerning infection or recent diagnosis of SARS-CoV-2 or excess medical risk prior to admission. Patients deemed eligible for admission underwent testing via a nasopharyngeal swab for SARS-CoV-2 within three days of admission, and were directed to self-quarantine between testing and admission. The community seven-day case rate for SARS-CoV-2 (new cases per 100,000 population) ranged from 2.8 to 28.9 during the study period in our region. A total of 95 patients (63 adults and 32 children) were admitted. One adult patient developed mild SARS-CoV-2 infection and one adult patient tested positive for asymptomatic SARS-CoV-2 infection. These findings illustrate that inpatient epilepsy monitoring can be safely performed in carefully selected patients when appropriate processes are in place, even in the setting of the SARS-CoV-2 pandemic. There is a risk of nosocomial spread, and the potential benefits of admission should be balanced against the risks of infection.

Intraoperative seizures during craniotomy under general anesthesia.

PURPOSE: An acute symptomatic seizure is a clinical seizure occurring at the time of or in close temporal association with a brain insult. We report an acute symptomatic seizure occurring during a surgical procedure in a patient who did not have a prior history of epilepsy and who did not have a lesion associated with an increased risk of epilepsy. To characterize the incidence and clinical features of intraoperative seizures during craniotomy under general anesthesia, we reviewed cases where continuous EEG was acquired during craniotomy. METHOD: Records of 400 consecutive cases with propofol as general anesthesia during craniotomy were reviewed. Demographic data, indication for surgery, clinical history, history of prior seizures, duration of surgery and duration of burst suppression were recorded. Cases where seizures were observed were analyzed in detail. RESULTS: Two out of 400 patients experienced intraoperative seizures, including one patient who appeared to have an acute symptomatic seizure related to the surgical procedure itself and a second patient who experienced two seizures likely related to an underlying diagnosis of epilepsy. CONCLUSIONS: This is the first report of an acute symptomatic seizure secondary to a neurosurgical procedure. Overall, 0.5% of patients monitored experienced seizures, indicating that intraoperative seizures are rare, and EEG monitoring during craniotomies is of low yield in detecting seizures.

A rapid course through the five electrographic stages of status epilepticus.

A 54-year-old woman was transferred to a university hospital for severe sepsis and multiorgan failure. A complex partial seizure was noted and she was placed on continuous electroencephalography (EEG). During EEG monitoring she developed generalized convulsive status epilepticus. After consultation with family it was decided not to escalate treatment due to her overall medical condition. She proceeded sequentially through the five stages of status epilepticus, described by Treiman et al. (1990) over 22 h and 30 min and then developed electrocerebral silence. This case is significant in that it is the first report of a single individual experiencing all five stages of status epilepticus displayed on a continuous EEG. The case further demonstrates the rapid progression of status epilepticus and exemplifies the need for prompt treatment.

Stimulus-induced diffuse voltage attenuation (SIDVA): a previously undescribed EEG pattern in a critically ill child.

We report the case of a 15-month-old critically ill child with stimulus-induced diffuse voltage attenuation, a previously unreported electroencephalogram pattern. No clinical evidence of seizure activity was associated with these EEG changes. The patient went on to have a full recovery. This case suggests that critically ill children have distinct stimulus induced electrographic patterns from those seen in adults. Additional research is needed to define the significance of these patterns.

Time to first interictal epileptiform discharge in extended recording EEGs.

The presence of interictal epileptiform discharges (IEDs) in the outpatient interictal EEG can provide evidence for a diagnosis of epilepsy and support for a specific epilepsy syndrome. However, there is variation in the duration of outpatient EEGs, and prolonged EEGs may have a higher yield for IEDs. The authors retrospectively reviewed 172 routine, extended, outpatient EEGs of at least 60 minutes duration in adults to determine the time to the first IED. The mean duration was 187 minutes. Twenty-six percent captured IEDs. The initial IED occurred in the first 20 minutes in 53% and after 20 minutes in 47%. The mean time to the first IED was 32.8 minutes with a range of 1 to 216 minutes and a standard deviation of 48.2 minutes. Results were skewed to the right (skew 2.22) with a median time to the first IED of 10 minutes. There was a longer time to the first IED in temporal epileptiform discharges compared with generalized discharges.

The Hitchhiker's guide to the child neurologist's genetic evaluation of epilepsy.

Over the past several decades, familial aggregation studies as well as twin studies have supported a genetic component to seizures. The recent advent of the genome project has served as a catalyst in the search for elucidating the hereditary influences of various epilepsies. Overlapping seizure features may lead to ambiguity when attempting to isolate a single phenotype. Conversely, the phenomenon of genetic heterogeneity implies that multiple genetic mutations may give rise to a similar phenotype. Despite valiant attempts at strictly defining epilepsy phenotype and mode of penetrance, one must also consider the role of environment in gene expression. Genetics (testing) in epilepsy is no longer limited to the idiopathic epilepsies but may have an equally significant role in the symptomatic epilepsies. This article guides the reader through the genetics of epilepsy via discussion of the phenotypic description of known genetic childhood epilepsy syndromes, illustration of the associated gene mutations identified thus far, and the implications of genetic testing in clinical practice.