1● Entire brain is involved
● motor manifestations are bilateral.
● diffuse, affecting both cerebral hemispheres.
● clinical and EEG changes indicate initial involvement of both
hemispheres.
GENERALIZED SEIZURES
2● Common in children
○ They experience brief loss of consciousness to the point that
they are staring blankly as well
● present as alterations of consciousness (absences) lasting
10-30 seconds.
ABSENCE (Petit mal) SEIZURES
3● It can happen for more than 100 times per day
● Staring (with occasional eye blinking) and loss or reduction in
postural tone is typical.
ABSENCE (Petit mal) SEIZURES
4Doc for ABSENCE (Petit mal) SEIZURES
Imipramine
5● (bilateral massive epileptic myoclonus)
● present as involuntary jerking of the facial, limb, or trunk
muscles, possibly in rhythmic manner.
MYOCLONIC SEIZURES
6consist of sporadic jerks, usually on both sides of the body.
Patients sometimes describe the jerks as brief electrical shocks.
When violent, these seizures may result in dropping or
involuntarily throwing objects.
MYOCLONIC SEIZURES
7● characterized by sustained muscle contractions alternating
with relaxation
● are repetitive, rhythmic jerks that involve both sides of the
body at the same time.
○ Continuous jerking movement throughout the seizure
process
CLONIC SEIZURES
8● involve sustained tonic muscle extension (muscle stiffening).
○ Muscle stiffness particularly in arms / legs (usually their arms
and legs are extended)
TONIC SEIZURES
9● cause sudden loss of consciousness.
● Combination of Tonic and Clonic seizure
○ Muscle stiffness (Tonic) + Jerking movements (Clonic)
GENERALIZED TONIC-CLONIC SEIZURES (Grand mal)
10● characterized by a sudden loss of postural tone so that the
individual falls to the ground. They occur primarily in children.
○ It’s like having Spastic Paralysis because there in no muscle
tone at all
ATONIC SEIZURES (Drop Attacks)
11● Some epileptics have serial grand mal seizures, regaining
consciousness briefly between attacks. In some cases, grand
mal seizures occur repeatedly with no recovery of
consciousness between attacks (status epilepticus)
STATUS EPILEPTICUS
12● have no identifiable cause.
PRIMARY (idiopathic) SEIZURES
13● occur secondary to an identifiable cause
SECONDARY SEIZURES (symptomatic or acquired seizures)
14one drug is used for the maintenance of certain conditions
Monotherapy
15● valproic acid, carbamazepine, phenytoin
GTC and PARTIAL SEIZURES
16GTC and PARTIAL SEIZURES
DOC: Valproic Acid
Alternative: Carbamazepine, Phenytoin
17ethosuximide, valproic acid
ABSENCE
18ABSENCE
○ DOC: Ethosuximide
○ Alternative: Valproic acid
19clonazepam, valproic acid
MYOCLONIC
20MYOCLONIC
○ DOC: Clonazepam
○ Alternative: Valproic acid
21diazepam, lorazepam, phenytoin
STATUS EPILEPTICUS
22STATUS EPILEPTICUS
○ DOC: Diazepam / Lorazepam
○ Alternative: Phenytoin
23FEBRILE SEIZURES
DOC: Phenobarbital
24Lamotrigene, VPA, Topiramide
TONIC CLONIC
25TONIC CLONIC
Alternative: Valproic acid, Topirmaide
26○ Inhibition of voltage-gated Na+ channels to slow neuron firing.
○ Enhancement of the inhibitory effects of the neurotransmitter GABA.
○ Inhibition of calcium channels
MOA of Epileptic Drugs
27blocks voltage-gated sodium channels by selectively binding
to the channel in the inactive state and slowing its rate of
recovery (Sodium channel blockers)
NA+ CHANNEL INHIBITORS
28● MOA: closes Na channels
● Oldest non-sedative antiepileptic drug
● Elimination rate constant: From First Order it becomes Zero
Order at higher therapeutic level
PHENYTOIN (Dilantin, Epilantin)
29 – loss of muscle control
Ataxia
30 – vision condition that causes repetitive
uncontrolled movement
Nystagmus
31 – double vision (Banlag)
Diplopia
32 – hypertrichosis – unwanted hair growth
Hirsutism
33 (20-40%) – overgrowth gums
Gingival hyperplasia
34– cleft palate, congenital heart disease, microcephaly, growth and
mental retardation
“Fetal hydantoin syndrome
35Phenytoin is an
ENZYME INDUCER