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SEIZURE
DISORDERS
Linda H. Warren
EdD RN MSN CCRN
NUR 335
OBJECTIVES
Differentiate different types of seizures.
Demonstrate knowledge of diagnostic testing.
Demonstrate knowledge of assessment & management of seizures.
Discuss various pharmacological agents used in the treatment of
seizure disorders.
Demonstrate knowledge of patient & family teaching.
WHAT IS A SEIZURE?...
Abnormal electrical discharges
in the cerebral cortex.
Repetitive depolarization of
hyperactive, hypersensitive cells
at a rate of 300 – 1000 per sec.
Alteration in sensation, behavior,
movement, perception, or LOC.
• Seen at different levels r/t type of seizure.
EPILEPSY IS A
SPECTRUM OF
DISORDERS!!!
INTERNATIONAL CLASSIFICATION OF EPILEPTIC SEIZURES
Elementary (Simple) Partial:
• No impairment of consciousness.
• Motor or sensory
• Autonomic (repetitive)
• Psychic (déjà vu)
Complex Partial:
• Simple partial at onset
• Some impaired consciousness
PARTIAL: Activation of a restricted part of one hemisphere.
MOTOR:
• Myoclonic
• Clonic
• Tonic
• Tonic-Clonic
• Atonic
• Status Epilepticus
NONMOTOR:
• Absence Attacks
- Simple / typical
- Atypical
• Eyelid myoclonia
GENERALIZED: both hemispheres affected
INTERNATIONAL CLASSIFICATION OF EPILEPTIC SEIZURES
PHASES OF
SEIZURE ACTIVITY:
Prodromal:
 Changes in mood or behavior seen before a seizure.
Aural: signals the start of seizure activity.
 Lasts seconds to minutes
 Dreamlike, déjà vu, lightheaded, fear, smells (subjective)
Ictal: duration of seizure activity
 May be convulsive or non-convulsive
 Depends on seizure type & part of brain affected
Post-ictal: period after seizure, ”recovery stage”
 Can last minutes to hours
 Pt may not remember the seizure
 Pt may be confused, tired, weak, uncoordinated
PARTIAL SEIZURES:
Simple:
• Motor
• Sensory (visual, auditory, smell)
• Autonomic
- Hypotension / HTN
- Tachy/bradycardia
- Pallor, sweating
• Psychic
Complex:
• Automatisms:
- Lip smacking, pill rolling
PARTIAL SEIZURES:
GENERALIZED SEIZURES:
TONIC / CLONIC
TONIC PHASE: stiffening
• Rigid muscles
• Extremities extended
• Neck hyperextension
• Breathing ceases / Cyanosis
CLONIC PHASE: jerking
• Return of Breathing / Hyperventilation
• Muscles contract and relax
• Phase gradually subsides
“Grand Mal”
Loss of Consciousness
GENERALIZED SEIZURES:
ABSENCE SEIZURES
• “Petit Mal”
• Non-Convulsive
• Usually occurs in children:
- Blank Stare
- Impaired Consciousness (briefly)
- Cessation of movement (briefly)
STATUS EPILEPTICUS:
 Seizure activity lasts >30 mins.
 Sequential seizures without regaining
consciousness btwn seizures.
Frequent Causes / Precipitating Factors:
• Non-compliance taking anticonvulsants
• ETOH withdrawal (MI, stroke)
• Electrolyte imbalances
• Head trauma
• Brain tumor
• Azotemia (waste accumulation r.t renal failure)
MEDICAL EMERGENCY!!!
PHASE ONE:
• ↑ cerebral metabolism
• Hyperglycemia (release of glucose from brain)
• HTN (↑ cerebral blood flow)
• Hyperpyrexia / fever (r.t catecholamine release)
• Lactic acidosis (anaerobic metabolism)
• Cardiac dysrhythmias (↑ epi/NE)
• Autonomic dysfunction
PHASE TWO: 30-60 mins after phase one
• Decompensation r/t ↑ metabolic demands
• Metabolic / Respiratory acidosis
• Hypoglycemia (depleted energy stores)
• Electrolyte imbalances (sweating, dehydration)
• Pulmonary edema
• Aspiration (esp. if vomiting)
• Renal Failure (hyperkalemia, hyponatremia)
• Death!!
DOCUMENTATION
• Time seizure began & ended, duration of seizure
• Status before seizure
• Description of the seizure
• Type of motor movement
• Parts of the body involved, where did it start?
• LOC: Before, during & after seizure?
• Pupil Response: Deviation (deviates to side the focus initiated)
• Incontinence / Diaphoresis
• Complications during the seizure: injury, fractures, etc.
• Vital Signs including Pulse-Ox: may be apneic for a period of time
• Post-ictal status
• Motor / Sensory / neuro status (GCS, can they follow commands or talk)
• Behavior: Confusion , Headache, Drowsiness
EPILEPSY
• Seizure Disorder
• A condition of recurring seizures
• Occur over days, weeks or years
• Primary: Idiopathic
• Secondary: Symptom of an underlying condition
(tumor, facial injury, previous brain injury)
HISTORY & PHYSICAL
• Birth and developmental history (forceps? Difficult labor?)
• Illnesses or injuries
• Family history
• Febrile seizures as children
• Neurological Assessment: GCS (best eye opening, verbal, mvmt)
• Seizure History
• Precipitating Factors (a certain smell/taste/sensory experience?)
• Antecedent Event (what happened before seizure began?)
• Seizure Description
DIAGNOSTIC TESTS
• Labs
- BMP, electrolytes, BUN/creatinine r/t azotemia, glucose, LFT
- Monitor for therapeutic serum levels of anticonvulsant
• Lumbar Puncture (meningitis?)
• CT Scan (tumors, lesions)
• MRI / MRA
• PET Scan (tumors)
• EEG
ASSESSMENT
• Neurological
• Respiratory
• Precipitating Factors
• Cardiac Monitoring
MANAGEMENT
Airway: ensure adequate oxygenation
• Be prepared to intubate
• Meds to TX can also cause respiratory depression
Vascular Access
Seizure precautions: pad side rails, low bed, lower to floor
MEDICAL MANAGEMENT
 Lorazepam (Ativan): drug of choice (1-2mg, consecutive doses)
• Benzodiazepines (Lorazepam, midazolam, diazepam)
• Dilantin (phenytoin): anticonvulsant
- ONLY given with NS.
- <50mg/min bc it can cause cardiac arrest (apply cardiac monitor).
- Requires a filter added to IV tubing if given as a gtt.
- NEVER mixed w dextrose (precipitates & clogs up tubing).
• Phenobarbital: anticonvulsant
• takes a while to reach therapeutic levels, given as maintenance dose.
• Propofol: mg/kg when used for seizure activities (not mcg/kg)
- Assess for hypotension & respiratory depression.
COLLABORATIVE MANAGEMENT
Drug Therapy
Surgery
Vagal Nerve Stimulation
GOALS OF DRUG THERAPY
Reduce number of seizures.
Return to normal ADLs with minimal restrictions.
• Significant lifestyle changes
• May not be able to drive
• May not be able to participate in contact sports
ANTI-SEIZURE MEDICATIONS
• Carbamazepine (Tegretol)
• Divalproex (Depakote)  also an antipsychotic
• Gabapentin (Neurontin)  also used for neuropathy
• Phenytoin (Dilantin) not used as much bc side effects
• Causes dental decay…ensure pt has frequent dental visits.
• Valproic Acid (Depakane)
• Lorazapam (Ativan)
• Diprivan (Propofol)
ANTI-SEIZURE MEDS:
ABSENCE & MYOCLONIC SEIZURES
• Clonazepam (Klonapin)
• Divalproex (Depakote)
• Ethosuzimide (Zarontin)
• Phenobarbitol
• Valproic Acid (Depakene)
EEG helps to determine if pt is seizing when it can’t be
visually observed (when pt is on anticonvulsants)
NURSING DIAGNOSIS
• Risk for Injury
• Risk for Ineffective Breathing Pattern
• Risk for Ineffective Airway Clearance
• Risk for Altered Tissue Perfusion
• Risk for Volume Excess
• Altered Thought Process
• Impaired Verbal Communication
• Risk for Ineffective Family Coping
• Knowledge Deficit
• Self-Esteem Disturbance / Anxiety
PRIORITIES:
• Maintain Patent Airway
• Provide Adequate Oxygenation
• Maintain / Obtain Vascular Access
• Maintain Seizure Precautions
• Preparation / Administration of Appropriate Medications
• Assess for therapeutic drug levels
PATIENT & FAMILY
EDUCATION
• Medications need to be taken as
prescribed to maintain therapeutic
levels & prevent complications.
• Use of non-drug techniques
• Medic alert bracelet
• Community resources
AVOID:
• Alcohol
• Elicit drug use
• Fatigue
• Sleep deprivation

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Seizure disorders

  • 2. OBJECTIVES Differentiate different types of seizures. Demonstrate knowledge of diagnostic testing. Demonstrate knowledge of assessment & management of seizures. Discuss various pharmacological agents used in the treatment of seizure disorders. Demonstrate knowledge of patient & family teaching.
  • 3. WHAT IS A SEIZURE?... Abnormal electrical discharges in the cerebral cortex. Repetitive depolarization of hyperactive, hypersensitive cells at a rate of 300 – 1000 per sec. Alteration in sensation, behavior, movement, perception, or LOC. • Seen at different levels r/t type of seizure.
  • 4.
  • 5.
  • 6.
  • 7. EPILEPSY IS A SPECTRUM OF DISORDERS!!!
  • 8. INTERNATIONAL CLASSIFICATION OF EPILEPTIC SEIZURES Elementary (Simple) Partial: • No impairment of consciousness. • Motor or sensory • Autonomic (repetitive) • Psychic (déjà vu) Complex Partial: • Simple partial at onset • Some impaired consciousness PARTIAL: Activation of a restricted part of one hemisphere.
  • 9. MOTOR: • Myoclonic • Clonic • Tonic • Tonic-Clonic • Atonic • Status Epilepticus NONMOTOR: • Absence Attacks - Simple / typical - Atypical • Eyelid myoclonia GENERALIZED: both hemispheres affected INTERNATIONAL CLASSIFICATION OF EPILEPTIC SEIZURES
  • 10.
  • 11. PHASES OF SEIZURE ACTIVITY: Prodromal:  Changes in mood or behavior seen before a seizure. Aural: signals the start of seizure activity.  Lasts seconds to minutes  Dreamlike, déjà vu, lightheaded, fear, smells (subjective) Ictal: duration of seizure activity  May be convulsive or non-convulsive  Depends on seizure type & part of brain affected Post-ictal: period after seizure, ”recovery stage”  Can last minutes to hours  Pt may not remember the seizure  Pt may be confused, tired, weak, uncoordinated
  • 12.
  • 13.
  • 14.
  • 15. PARTIAL SEIZURES: Simple: • Motor • Sensory (visual, auditory, smell) • Autonomic - Hypotension / HTN - Tachy/bradycardia - Pallor, sweating • Psychic Complex: • Automatisms: - Lip smacking, pill rolling
  • 17. GENERALIZED SEIZURES: TONIC / CLONIC TONIC PHASE: stiffening • Rigid muscles • Extremities extended • Neck hyperextension • Breathing ceases / Cyanosis CLONIC PHASE: jerking • Return of Breathing / Hyperventilation • Muscles contract and relax • Phase gradually subsides “Grand Mal” Loss of Consciousness
  • 18.
  • 19. GENERALIZED SEIZURES: ABSENCE SEIZURES • “Petit Mal” • Non-Convulsive • Usually occurs in children: - Blank Stare - Impaired Consciousness (briefly) - Cessation of movement (briefly)
  • 20. STATUS EPILEPTICUS:  Seizure activity lasts >30 mins.  Sequential seizures without regaining consciousness btwn seizures. Frequent Causes / Precipitating Factors: • Non-compliance taking anticonvulsants • ETOH withdrawal (MI, stroke) • Electrolyte imbalances • Head trauma • Brain tumor • Azotemia (waste accumulation r.t renal failure) MEDICAL EMERGENCY!!!
  • 21. PHASE ONE: • ↑ cerebral metabolism • Hyperglycemia (release of glucose from brain) • HTN (↑ cerebral blood flow) • Hyperpyrexia / fever (r.t catecholamine release) • Lactic acidosis (anaerobic metabolism) • Cardiac dysrhythmias (↑ epi/NE) • Autonomic dysfunction PHASE TWO: 30-60 mins after phase one • Decompensation r/t ↑ metabolic demands • Metabolic / Respiratory acidosis • Hypoglycemia (depleted energy stores) • Electrolyte imbalances (sweating, dehydration) • Pulmonary edema • Aspiration (esp. if vomiting) • Renal Failure (hyperkalemia, hyponatremia) • Death!!
  • 22.
  • 23. DOCUMENTATION • Time seizure began & ended, duration of seizure • Status before seizure • Description of the seizure • Type of motor movement • Parts of the body involved, where did it start? • LOC: Before, during & after seizure? • Pupil Response: Deviation (deviates to side the focus initiated) • Incontinence / Diaphoresis • Complications during the seizure: injury, fractures, etc. • Vital Signs including Pulse-Ox: may be apneic for a period of time • Post-ictal status • Motor / Sensory / neuro status (GCS, can they follow commands or talk) • Behavior: Confusion , Headache, Drowsiness
  • 24. EPILEPSY • Seizure Disorder • A condition of recurring seizures • Occur over days, weeks or years • Primary: Idiopathic • Secondary: Symptom of an underlying condition (tumor, facial injury, previous brain injury)
  • 25. HISTORY & PHYSICAL • Birth and developmental history (forceps? Difficult labor?) • Illnesses or injuries • Family history • Febrile seizures as children • Neurological Assessment: GCS (best eye opening, verbal, mvmt) • Seizure History • Precipitating Factors (a certain smell/taste/sensory experience?) • Antecedent Event (what happened before seizure began?) • Seizure Description
  • 26. DIAGNOSTIC TESTS • Labs - BMP, electrolytes, BUN/creatinine r/t azotemia, glucose, LFT - Monitor for therapeutic serum levels of anticonvulsant • Lumbar Puncture (meningitis?) • CT Scan (tumors, lesions) • MRI / MRA • PET Scan (tumors) • EEG
  • 27. ASSESSMENT • Neurological • Respiratory • Precipitating Factors • Cardiac Monitoring
  • 28. MANAGEMENT Airway: ensure adequate oxygenation • Be prepared to intubate • Meds to TX can also cause respiratory depression Vascular Access Seizure precautions: pad side rails, low bed, lower to floor
  • 29.
  • 30. MEDICAL MANAGEMENT  Lorazepam (Ativan): drug of choice (1-2mg, consecutive doses) • Benzodiazepines (Lorazepam, midazolam, diazepam) • Dilantin (phenytoin): anticonvulsant - ONLY given with NS. - <50mg/min bc it can cause cardiac arrest (apply cardiac monitor). - Requires a filter added to IV tubing if given as a gtt. - NEVER mixed w dextrose (precipitates & clogs up tubing). • Phenobarbital: anticonvulsant • takes a while to reach therapeutic levels, given as maintenance dose. • Propofol: mg/kg when used for seizure activities (not mcg/kg) - Assess for hypotension & respiratory depression.
  • 32. GOALS OF DRUG THERAPY Reduce number of seizures. Return to normal ADLs with minimal restrictions. • Significant lifestyle changes • May not be able to drive • May not be able to participate in contact sports
  • 33. ANTI-SEIZURE MEDICATIONS • Carbamazepine (Tegretol) • Divalproex (Depakote)  also an antipsychotic • Gabapentin (Neurontin)  also used for neuropathy • Phenytoin (Dilantin) not used as much bc side effects • Causes dental decay…ensure pt has frequent dental visits. • Valproic Acid (Depakane) • Lorazapam (Ativan) • Diprivan (Propofol)
  • 34. ANTI-SEIZURE MEDS: ABSENCE & MYOCLONIC SEIZURES • Clonazepam (Klonapin) • Divalproex (Depakote) • Ethosuzimide (Zarontin) • Phenobarbitol • Valproic Acid (Depakene) EEG helps to determine if pt is seizing when it can’t be visually observed (when pt is on anticonvulsants)
  • 35. NURSING DIAGNOSIS • Risk for Injury • Risk for Ineffective Breathing Pattern • Risk for Ineffective Airway Clearance • Risk for Altered Tissue Perfusion • Risk for Volume Excess • Altered Thought Process • Impaired Verbal Communication • Risk for Ineffective Family Coping • Knowledge Deficit • Self-Esteem Disturbance / Anxiety
  • 36. PRIORITIES: • Maintain Patent Airway • Provide Adequate Oxygenation • Maintain / Obtain Vascular Access • Maintain Seizure Precautions • Preparation / Administration of Appropriate Medications • Assess for therapeutic drug levels
  • 37. PATIENT & FAMILY EDUCATION • Medications need to be taken as prescribed to maintain therapeutic levels & prevent complications. • Use of non-drug techniques • Medic alert bracelet • Community resources AVOID: • Alcohol • Elicit drug use • Fatigue • Sleep deprivation

Editor's Notes

  1. GOAL: STOP SEIZURES (brain cells are dying)
  2. Focus in cerebrum that is activated through a brain injury, congenital causes, etc.
  3. Myoclonic: Brief jerking motions of one or more muscle groups Clonic: repetitive jerking Tonic: stiffening phase Tonic-clonic: stiffening followed by jerking Atonic: drop attack, abrupt cessation of muscle tone Absence: common in children, stare of into space for a few secs Atypical: staring spell with myoclonic jerking & automatisms (lip smacking, pill rolling—unconscious repetitive motions)
  4. Jacksonian: starts with one muscle group & moves to other areas. (ex: starts in hand and moves up arm)
  5. Stop what they are doing for a few seconds & then return to activity shortly after
  6. Therapeutic levels of anticonvulsant falls r/t noncompliance
  7. No bite blocks  inc. risk of aspiration if teeth break As pt comes out of seizure  recovery position to prevent aspiration
  8. No bite blocks  inc. risk of aspiration if teeth break As pt comes out of seizure  recovery position to prevent aspiration
  9. Seizure free for 6 months before they are able to drive again.
  10. Know that these drugs have multiple uses (not just for seizures)
  11. EEG helps to determine if pt is seizing when it cant be visually observed (when pt is on anticonvulsants)
  12. INVOLVE FAMILY & encourage familial support