For seizure

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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
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Doc for ABSENCE (Petit mal) SEIZURES
Imipramine
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● (bilateral massive epileptic myoclonus)
● present as involuntary jerking of the facial, limb, or trunk
muscles, possibly in rhythmic manner.
MYOCLONIC SEIZURES
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consist 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
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● 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
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● 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)
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● 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
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● have no identifiable cause.
PRIMARY (idiopathic) SEIZURES
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● occur secondary to an identifiable cause
SECONDARY SEIZURES (symptomatic or acquired seizures)
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one drug is used for the maintenance of certain conditions
Monotherapy
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● valproic acid, carbamazepine, phenytoin
GTC and PARTIAL SEIZURES
16
GTC and PARTIAL SEIZURES
DOC: Valproic Acid
Alternative: Carbamazepine, Phenytoin
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ethosuximide, valproic acid
ABSENCE
18
ABSENCE
○ DOC: Ethosuximide
○ Alternative: Valproic acid
19
clonazepam, valproic acid
MYOCLONIC
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MYOCLONIC
○ DOC: Clonazepam
○ Alternative: Valproic acid
21
diazepam, lorazepam, phenytoin
STATUS EPILEPTICUS
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STATUS EPILEPTICUS
○ DOC: Diazepam / Lorazepam
○ Alternative: Phenytoin
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FEBRILE SEIZURES
DOC: Phenobarbital
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Lamotrigene, VPA, Topiramide
TONIC CLONIC
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TONIC CLONIC
Alternative: Valproic acid, Topirmaide
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○ 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
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blocks 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
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● 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)
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– loss of muscle control
Ataxia
30
– vision condition that causes repetitive
uncontrolled movement
Nystagmus
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– double vision (Banlag)
Diplopia
32
– hypertrichosis – unwanted hair growth
Hirsutism
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(20-40%) – overgrowth gums
Gingival hyperplasia
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– cleft palate, congenital heart disease, microcephaly, growth and
mental retardation
“Fetal hydantoin syndrome
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Phenytoin is an
ENZYME INDUCER
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