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31 Cards in this Set

  • Front
  • Back

Epilepsy

A group of disorders characterized by excessive excitation of neurons within the CNS


Usually a chronic condition

Seizure

A general term applied to all types of epileptic events

Convulsion

Abnormal motor phenomena (i.e. jerking movement)



Pathophysiology of Seizures

Seizures initiated by synchronous high frequency discharges from a group of hyper-excitable neurons (focus)

Partial (Focus) Seizures

Activity begins focally in Cerebral cortex areas


- Simple, Complex, Secondary Generalized

Simple Seizure

Discrete symptoms, depends on area of brain affected


S&S: twitching, numbness, hallucinations, salivation, incontinence, feelings of unreality


Lasts 20-60 seconds


No loss of consciousness

Complex Seizures

Impaired consciousness and lack of responsiveness


S&S: motionless, fixed gaze, repetitive purposeless movements


Lasts 45-90 seconds

Secondary Generalized

Begins as simple or complex and evolves to tonic-clonic (grand mal), lasts 1-2 minutes

Generalized Seizures

Focal seizure activity is conducted widely throughout both hemispheres


- Tonic-clonic, Absence (petit-mal), myoclonic, febrile

Tonic- Clonic (Grand Mal) Seizures

Neuronal discharge spreads throughout entire cerebral cortex


S&S: major convulsions, muscle rigidity, jerking, incontinence, loud cry, CNS depression (postictal state)

Absence (Petit Mal) Seizures

Brief loss of consciousness (10-30 seconds)


May or may not have motor activity

Myoclonic Seizures

Sudden muscle contractions


1 limb or whole body (1 sec)

Febrile Seziure

6mths- 5yo from increased fever


Does not increase risk of developing epilepsy later in life

Status Epilepticus (SE)

Seizures lasting 30 minutes or more; may be of various types; must go to ER; IV valium; O2 is limited to brain

Goal of Epilepsy Treatment

To reduce seizures to an extent that enables a person to live


Meds benefit 60-70% of pts with epilepsy


Evaluation of drug effect: seizures frequency chart

Drugs that potentiate GABA

- Barbiturates (Phenobarbital)


- Benzodiazepines (Lorazepam, Clonazepam)


- Misc. drugs (Gabapentin)

Drugs that suppress sodium influx

Decrease CNS activity by delaying the influx of sodium ions across neuronal membranes


- Hydontoins- Phenytoin (DIlantin)


- Hyentoin- like agents- Carbamozepine (Tegretol)

Drugs that suppress calcium influx

Delaying calcium influx into neuronal membranes


- Succinimides- Valproic Acid (Depakene)

Carbamazapine (Tegretol) treats...

Simple, complex partial seizures

Phenytoin (Dilantin) treats...

Secondary generalized seizures

Valproic Acid treats...

Tonic-clonic (grand mal) seizures


Absence seizures


Myoclonic seizures

Sodium Channel Physiology

Neuronal action potentials are moved along by Na moving into Na channels (gated pores in cell membrane)


For Na influx to occur, channel must be active


After Na entry, channel becomes inactivated, blocking further Na influx


Normally the channel recharges quickly to become active again

Phenytoin (Dilantin)/ Carbomazepine (Tegretol) MOA

Suppression of sodium influx


Reversibly bind to sodium channels while they are in the inactivated state


- Prolong Na channel inactivation


- Decrease ability of neurons to fire at high frequencies


- Decrease seizures that depend on high frequency neuronal discharge

Phenytoin (Dilantin)

Effective and safe dosage is difficult to establish- narrow therapeutic range


Absorption varies with formulation of drug (suspension, IV, tablets, capsules)


Overwhelms liver, ensure correct dosage


Contraindication: liver disease

Phenytoin (Dilantin) Adverse Effects

Sedation


Nystagmus


Diplopia


Skin rash


Ataxia


Gingival hyperplasia (gum tissue overgrowth)

Phenytoin (Dilantin) Drug Interactions

Warfarin, glucocorticoids, oral contraceptives (taking Dilantin may cause decrease effects)


Diazepam, alcohol, cimotidine (these increase Phenytoin plasma levels, toxicity)


Carbamozepine, Phenobarb (decrease Dilantin plasma levels to subtherapeutic levels)


Alcohol, CNS depressants, barbiturates (amplify the CNS depressant effects Phenytoin creates)

Phenytoin (DIlantin) Pharmacokinetics

Route: PO, IV


Initially doses even BID, maintained on OD doses


Very short half life, higher doses increase half-life (there is more drug present than the liver can process, can last up to 60 hrs as opposed to 8hr half life)


Serum levels: desired between 10-20 mcg

Carbamezepine (Tegretol) MOA

Delays recovery of Na channels from inactivated state

Carbamezepine (Tegretol) Pharmacokinetics

Half-life decreases as therapy progresses


(40-->15hrs)


Induces drug metabolizing enzymes- increase metabolism


Fewer side effects than Dilantin


Mood stabilizing effects- Bipolar disorder



Carbamezepine (Tegretol) Adverse Effects

Vertigo, nystagmus, blurred vision, diplopia, unsteadiness


Leukopenia, anemia, thrombocytopenia


Birth defects

Carbamezepine (Tegretol) Interactions

Oral contraceptives, Warfarin


Dilantin and Phenobarb


Grapefruit