Neuro 2 Flashcards
Concerns after first seizure (4)
- It is a brain tumor
- He stopped breathing and we want oxygen at home
- We do not want to start drugs–
a. Asking why you will find they read the package insert
b. Drug is not FDA approved for children
c. The Internet - Things to remember about seizures and parental concerns
a. All children look terrible during the seizure but they are breathing
b. Seizures are common 1 in 200
c. Children with seizures are normal children
d. They need to sleep in their own beds, go to school, take out the garbage and do most sports except
i. Sky diving
ii. Archery
iii. Hunting
iv. Scuba diving
Generalized Absence, Typical (5)
- 3-8 year old, common at 6-7
- May present with convulsion
- Usually several months of staring and unresponsive spells
- 3 hz spike wave
- Strong genetic disposition
Generalized Absence, Typical Treatment (3)
- Ethosuximide (Zarontin) is excellent
- Valproate
- Lamotrigine (Lamictal) → Steven Johnsons Syndrome
* Always worry* start slow and watch for skin rashes
Generalized Tonic-Clonic Seizure: Benign Rolandic Epilepsy (8)
- School aged child 5-10
- Boys >girls
- Usually nocturnal, strong genetic disposition
- High voltage centrotemporal spike
- Brief seizure after falling asleep with face and shoulder twitching occasionally with preserved awareness
- Can have migraines and learning disability
- Seizures are sporadic and remit in puberty
- Most AED work but you can wait to see if a second seizure reoccurs
Juvenile Myoclonic Epilepsy (9)
- Adolescent (12-18) with seizure on wakening
- Reports early am arm and body jerks which resolve by breakfast
- Tend to recur
- Lifelong disease
- Normal Intelligence
- Will not usually remit without anticonvulsants
a. Valproate (Depekene)
b. Levetiracetam (Keppra)
c. Zonisamide (Zonagran) - Does not go away, adolescent, first thing in the morning when they have seizure, sleep deprivation
- Keppra is a nice safe drug, push levels high* drug of choice for generalized epilepsy
- Need to monitor blood levels before you renew prescription
a. Every 3 months for the first few then every 6 months
Treatment Considerations (5)
- Potential risks of additional seizures
- Likelihood of seizure recurrence
- Likelihood of multiple recurrences
- Risk factors for recurrence
- Efficacy of treatment for prevention of recurrences
a. Which drug
b. Adverse effects
Focal Epilepsy Anticonvulsants (3)
- Oxcarbazepine (trileptal) 20 mg/kg/day bid
- Carbamazepine (tegretol, carbatrol) is acceptable alternative
- Levetiracetam 20 mg/kg/kay bid
Generalized Epilepsy Anticonvulsants (2)
- Valproate 20mg/kg/day bid – increase side effects and monitor liver function
- Lamotrigine (Lamictal) 1mg/kg/day
Systemic Side Effect of Antiepileptic drugs (4)
- Rash, hirsutism, and weight gain.
- Severe reactions such as hepatic toxicity, bone marrow toxicity, and Stevens–Johnson syndrome
- Side effects of AED include effects on behavior and higher cortical function, which are often dose related
- Under-recognized
Differential Diagnosis for Epilepsy (14)
- Night terrors
- Apnea
- Breath holding spells
- Syncope
- Vertigo
- Migraine confusional state
- Nightmares
- Hyperventilation
- Daydreaming attentional disorder
- Hyperplexia (exaggerated startle
- Paroxysmal behavior outburst*** weird things
- Psychogenic seizure
- GER
- Arrhythmia (long QT)
*ALL PATIENTS W SEIZURES DESERVE AN ECG
Paroxysmal Non-Epileptic Disorders (8)
- Diverse Group
- Breath holding spells
* Pallid
* Cyanotic Breath holding spells - Sandifer syndrome
- Tics
- Spasmus Nutans
a. Differential = optic glioma
b. Nystagmus and head tilt
c. Head tilt = always differential for head tumor - Benign Neonatal myoclonus = when they are going to sleep or sucking body will jump
- Shudder Attacks – paroxysmal event
- Paroxysmal dystonic dyskinesia
Tics (5)
- Common 5-24% with stereotypic repetitive movements or vocalization
- Increase with anxiety, frustration
- Diminishes with sleep
- Most common tick = eye blinker, or lip smacking
- A lot of times the kids are under stress
Spasmus Nutans (6)
- Age 4-12 months
- Benign, self-limited
- Clinical triad
a. Head tilt
b. Head nodding
c. Nystagmus-asymmetric - Differential Optic glioma
- Anterior visual pathway disease
- Referred to ophthalmology or neurology = need to get MRI
Benign Neonatal Myoclonus (4 with 4 clinical features)
- Infants
- Benign, self limiting
- Clinical Features
a. Paroxysmal myoclonic jerks
b. May cluster
c. Primarily of upper body
d. Occurs during sleep - Normal infant development
Landau Reflex (2)
- Infant will lift head and extend the neck and trunk
2. Present by 6 months
Parachute Reflex (2)
- Present by 6-8 months
2. Look for symmetric response
Propping Reflex (2)
- Anterior propping when sitting up
2. Lateral propping to maintain balance
Headache (5)
- Common pediatric disorder which has become more common in adolescents
- Overall, prevalence is between 37-51% in 7 year olds with an increase to as high as 82% in 15 year olds
- Males have slightly higher prevalence pre-puberty
- Reeldx case 434
a. Post-inflammatory hyperpigmentation
b. Sandpaper acne; papules of acne - Not drinking water in schools