Seizure Disorders Disease

DESCRIPTION
A sudden alteration of behavior, characterized by a sensory perception or motor activity without or with change in awareness or consciousness, due to aberrant cortical electrical activity
  • Classification of seizures
    • I. Partial seizures (seizures begin locally) - (A) without impairment of consciousness, (B) with complex symptoms (with impairment of consciousness)
    • II. Generalized seizures (bilaterally symmetrical and without local onset)
    • III. Unclassified epileptic seizures
  • System(s) affected: Nervous
  • Genetics: Three times the prevalence of seizures in close relatives of seizure patients
  • Incidence/Prevalence in USA:
    • 1.5 million for epilepsy
    • Annual incidence is 1.2/1000 for all types of seizures and 0.54/1000 for recurrent seizures
    • The age-adjusted prevalence is 0.625% or 6.25/1000; isolated seizures may occur in 10% of the general population
    • 10–20% of all patients have intractable epilepsy
  • Predominant age: All ages
  • Predominant sex: Male = Female
SIGNS AND SYMPTOMS
  • General
    • Fever – indicative of infectious etiology
    • Focal neurologic finding – may indicate tumor or localized injury to the brain
    • Papilledema – suggestive of increased intracranial pressure
    • Hemorrhagic eye grounds – suggests underlying hypertension
    • Meningismus – may be present with meningitis
    • Headache – sometimes associated with infectious or hemorrhagic causes of seizures
  • Generalized seizures
    • Absence – loss of consciousness or posture
    • Myoclonic – repetitive muscle contractions
    • Tonic-clonic – sustained contraction followed by rhythmic contractions of all four extremities
  • Partial seizures
    • Simple – Focal seizures without alteration of awareness/consciousness
    • Complex – Focal seizures with alteration of awareness/consciousness
  • Febrile seizures (see separate chapter on febrile seizures)
    • Occurs between three months and five years of age
    • Fever without evidence of any other defined cause for seizures
    • If febrile seizures occur in the first year, the recurrence rate is 51%
    • If febrile seizures occur in the 2nd year, the recurrence rate is 25%
    • 88% of all recurrences of febrile seizures occur in the first 2 years
    • The earlier the age of onset, the more likely repetitive febrile seizures will occur
    • Recurrent febrile seizures probably do not increase the risk of epilepsy
  • Status epilepticus (see separate chapter)
    • Repetitive generalized seizures without return to consciousness between seizures
    • Considered a neurological emergency
CAUSES
  • Brain tumor
  • Cerebral hypoxia (breath holding, carbon monoxide poisoning, anesthesia)
  • Cerebrovascular accident (infarct or hemorrhage)
  • Convulsive or toxic agents (lead, alcohol, picrotoxin, strychnine)
  • Eclampsia
  • Exogenous factors (sound, light, cutaneous stimulation)
  • Fever (see chapter on febrile seizures)
  • Head injury
  • Heat stroke
  • Infection
  • Metabolic disturbances
  • Withdrawal from, or hereditary intolerance of, alcohol
RISK FACTORS
  • Susceptibility to seizures determined by a complex interplay between genetic factors and acquired brain disorders
  • Children delivered breech have a prevalence rate of 3.8% compared with 2.2% in children delivered vertex
LABORATORY
  • Serum tests – glucose, sodium, potassium, calcium, phosphorus, magnesium, BUN, ammonia
  • Anticonvulsant levels – inadequate level of anticonvulsant medication is the most common cause of recurrent seizures in children, and many adults
  • Drug and toxic screens – include alcohol
  • Complete blood count – helpful in evaluating infection

Drugs that may alter lab results:

  • Anticonvulsant therapy may dramatically affect the EEG results
  • Levels of anticonvulsants may be altered by a variety of common medications such as erythromycin, sulfonamides, warfarin, and cimetidine, as well as alcohol

Disorders that may alter lab results: Pregnancy decreases serum concentration. Frequent monitoring and dosage adjustments are necessary.

PATHOLOGICAL FINDINGS

None

SPECIAL TESTS
  • Electroencephalogram (EEG) – A negative EEG does not rule out a seizure disorder. Sensitivity, specificity, and predictive value of the test depend on the underlying cause and anatomic location of the seizure focus.
  • 24-hour ambulatory EEG – allows for continuous monitoring of cortical activity during regular activities
  • Video-monitoring – useful in conjunction with simultaneous EEG monitoring in separating true events from pseudoseizures
IMAGING
  • MRI of brain – superior in evaluation of the temporal lobes
  • CT scan of brain – indicated routinely in work-up of tonic-clonic seizures
DIAGNOSTIC PROCEDURES
None
APPROPRIATE HEALTH CARE

Outpatient therapy except for status epilepticus

GENERAL MEASURES

Protect the patient's airway

SURGICAL MEASURES

N/A

ACTIVITY

As tolerated

DIET

Regular

PATIENT EDUCATION
  • Stress the importance of compliance with anticonvulsant therapy
  • Printed patient information available from: Epilepsy Foundation of America, 4351 Garden City Drive, Landover, MD 20785-2267, (800) EFA-1000
PREVENTION/AVOIDANCE

Maintain adequate epileptic drug therapy. Patient education on compliance.

POSSIBLE COMPLICATIONS

Drug toxicity

EXPECTED COURSE AND PROGNOSIS
  • Depends on the pathophysiology of seizure within a particular patient
  • Seizure activity may become quiescent. If a patient has been seizure-free for two years, withdrawal of therapy may be considered. Relapse rate after three years of being off medications is 33%.
ASSOCIATED CONDITIONS
  • Infections
  • Tumors
  • Drug abuse
  • Metabolic disorders
AGE-RELATED FACTORS

Pediatric: Breastfeeding is not contraindicated in mothers receiving epileptic medication, although drug concentration in the infant may require monitoring if problems such as sedation occur
Geriatric: N/A
Others: N/A

PREGNANCY

Serum levels of anticonvulsants may decline, frequent monitoring recommended. There is a two-fold increased risk of congenital malformation in mothers taking anticonvulsant medication

OTHER NOTES

Jacksonian epilepsy - characterized by unilateral clonic movements that start in one group of muscles and spread systematically to adjacent groups, reflecting the march of epileptic activity through the motor cortex. Usual course - chronic; recurrent; intermittent.

ABBREVIATIONS

N/A

Clinical Investigations

ROLE OF HOMOEOPATHY

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