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Metabolic Encephalopathy vs Seizures: Distinguishing between Triphasic Waves and Epileptiform Discharges

Cheng, Jocelyn Y
ORIGINAL:0012456
ISSN: n/a
CID: 2917022

Musicogenic Epilepsy and Treatment of Affective Disorders: Case Report and Review of Pathogenesis

Cheng, Jocelyn Y
Musicogenic epilepsy is a rare syndrome in which music triggers seizures. Affective network processing appears to play a key role in epileptogenesis. Many people with epilepsy suffer from comorbid affective disorders, the shared basis of which involves similar pathophysiologies, including deficiencies of serotonergic and noradrenergic function. Seizures and mood disorders may thus have reciprocal effects on one another, particularly in emotionally precipitated syndromes such as musicogenic epilepsy. I report a man with long-standing depression and anxiety who developed focal epilepsy that evolved into musicogenic seizures. His case suggests a pathophysiologic basis for this shared phenomenon.
PMID: 27984259
ISSN: 1543-3641
CID: 2411872

Latency to treatment of status epilepticus is associated with mortality and functional status

Cheng, Jocelyn Y
INTRODUCTION: Status epilepticus (SE) is a life-threatening neurologic emergency. Despite advances in management, in-hospital mortality remains unchanged. This is partly due to the pharmacoresistance which develops the longer that seizures persist. Therefore, rapid antiseizure medication (ASM) administration may represent a beneficial treatment option. The purpose of this study was to determine: 1) whether in-hospital mortality is reduced with shorter latencies to initial treatment of SE with an ASM (LTSE); and 2) the critical time frame during which LTSE is associated with reduced in-hospital mortality. MATERIALS AND METHODS: This was a retrospective, single-center study of adults diagnosed with SE between 1/1/2005 and 10/31/2012. Demographic characteristics included seizure history, etiology, semiology, and duration. Subjects were assigned to LTSE groups at the time frames of 5, 10, 30 and 60min. The primary outcome was in-hospital mortality, with poor functional status (mRS 3-6) as a secondary measure. Pearson's chi-square, Mann-Whitney-U, two-sample-t-tests, and binary logistic regression analysis were used as appropriate, with p<0.05. RESULTS: In unadjusted analysis, LTSE>30min demonstrated increased risk of mortality (OR 2.06, CI 1.01-4.17, p=0.046) and poor functional status (OR 2.48, CI 1.05-5.85, p=0.038) compared to LTSE
PMID: 27772779
ISSN: 1878-5883
CID: 2411572

Insomnia symptoms in South Florida military veterans with epilepsy

Lopez, M R; Cheng, J Y; Kanner, A M; Carvalho, D Z; Diamond, J A; Wallace, D M
BACKGROUND: Despite the high prevalence of insomnia in veterans with epilepsy, it remains understudied. Our aim was to identify the associations of insomnia with epilepsy, comorbidities, and treatment-related variables in South Florida veterans. METHODS: We performed a cross-sectional analysis of veterans attending an epilepsy clinic over 18 months. Participants completed standardized assessments of seizure and sleep. Insomnia was defined as 1) difficulty with sleep onset, maintenance, or premature awakenings with daytime consequences or 2) sedative-hypnotic use on most nights of the previous month. RESULTS: One hundred sixty-five veterans (87% male, age 56 +/- 15 years) were included: 66 reporting insomnia (40%). In logistic regression analysis, insomnia was significantly associated with post-traumatic seizure etiology, lamotrigine prescription, and mood and psychotic disorders. Female gender and levetiracetam treatment were associated with lower odds for insomnia. CONCLUSION: Insomnia was associated with post-traumatic epilepsy, mood/psychotic comorbidities, and antiepileptic regimen. Insomnia represents an under-recognized opportunity to improve comprehensive epilepsy care.
PMID: 23434722
ISSN: 1525-5069
CID: 2418822

Critical illness polyneuropathy/critical illness myopathy and acute motor-sensory axonal neuropathy. Response [Letter]

Cheng, Jocelyn; Kahn, D Ethan; Wang, Michael Y
PMID: 23667929
ISSN: 1547-5646
CID: 2411892

Nocturnal frontal lobe epilepsy presenting as excessive daytime sleepiness

Cheng, Jocelyn Y; Wallace, Douglas M; Lopez, Maria R; Carrazana, Enrique J
Excessive daytime sleepiness (EDS) is common in the general population. Etiologies include insufficient sleep and primary sleep disorders. Due to its high prevalence, physicians often overlook EDS as a significant problem. However, EDS may also be the presenting symptom of seizures, in particular Nocturnal Frontal Lobe Epilepsy (NFLE). Due to the clinical similarity between the nocturnal behaviors of NFLE and parasomnias, and poor patient-related history, NFLE remains a challenging diagnosis. We report the case of a patient with NFLE who presented with a primary complaint of EDS, and discuss the differential diagnosis and evaluation of patients with EDS associated with nocturnal behaviors. In the context of a patient presenting with EDS and stereotyped nocturnal events, clinical suspicion should be high for NFLE.
PMCID:3894023
PMID: 24479058
ISSN: 2249-4863
CID: 2411882

Occipital seizures manifesting as visual loss with post-ictal Anton's syndrome [Case Report]

Cheng, Jocelyn; Posas, Jose; Selas, George; Lowe, Merredith; Carrazana, Enrique
PMID: 22154042
ISSN: 1872-6968
CID: 2190162

Electroencephalographic Correlation in Postanoxic Mycolonus: A Case Series [Meeting Abstract]

Cheng, Jocelyn
ISI:000303204801101
ISSN: 0028-3878
CID: 2411942

The acute motor-sensory axonal neuropathy variant of Guillain-Barre syndrome after thoracic spine surgery [Case Report]

Cheng, Jocelyn; Kahn, D Ethan; Wang, Michael Y
Guillain-Barre syndrome (GBS) is the eponym used to describe acute inflammatory polyradiculoneuropathies, which manifest with weakness and diminished reflexes. Although the classic form of GBS is considered to be an ascending demyelinating polyneuropathy, several variants have been described in the literature, including the Miller-Fisher syndrome, acute panautonomic neuropathy, acute motor axonal neuropathy, and acute motor-sensory axonal neuropathy (AMSAN). Few cases of postoperative GBS have been documented, particularly for the AMSAN variant. The authors describe the case of a patient who developed AMSAN after thoracic spine surgery and highlight the importance of investigating new-onset weakness in the postoperative period.
PMID: 21923235
ISSN: 1547-5646
CID: 2411912

St Theresa's dart and a case of religious ecstatic epilepsy [Historical Article]

Carrazana, Enrique; Cheng, Jocelyn
OBJECTIVE: : We report a case of ecstatic seizures with religious overtones in a patient whose semiology resembles that of Saint Theresa of Avila (1515 to 1582), and review the anatomical basis of this phenomenon. BACKGROUND: : Seizures with an emotional component are typically associated with negative sensations. Ecstatic seizures, particularly those with a religious character, are rarely reported, although they hold an important place in history, as a number of religious figures have been posited to be epileptic. Here, we present a patient with ecstatic seizures whose semiology and religious overtones resemble those of Saint Theresa of Avila (1515 to 1582), and discuss the anatomical basis of this phenomenon. METHOD: : Case report. RESULTS: : Evaluation of the patient demonstrated right temporal encephalomalacia on magnetic resonance imaging of the brain. Electroencephalogram showed focal slowing and poorly defined sharp waves in the right frontotemporal region. This area of pathology concurs with prior studies that localize ecstatic seizures to the anterior insula or temporal lobes. CONCLUSIONS: : Ecstatic seizures may involve the right temporal region. Although interpretation of ecstatic seizures is subject to individual variation, a similar localization and our patient's religious background may explain the resemblance between the semiology of his seizures, and that of Saint Theresa's visions as described almost 5 centuries ago.
PMID: 21945987
ISSN: 1543-3641
CID: 2411902