Ch 88-Seizures Flashcards

1
Q

What percent of adults experience at least 1 seizure? what percent will be diagnosed with epilepsy?

A

seizure- 10%
epilepsy- 3%

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2
Q

Define Seizure

A

A seizure is a sudden change in behavior caused by electrical hypersynchronization of neuronal networks in the cerebral cortex. (UTD)

Seizures are excessive excitatory neuronal activity associated with hypersynchrony of neighboring cells, resulting in sensory, motor, autonomic, or cognitive function alterations (Rosens 10th edition)

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3
Q

Define convulsions

A

refers specifically to the motor manifestations of a seizure

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4
Q

Define ictal period and post ictal period

A

The ictal period is the time
during which a seizure or seizure-like
activity occurs.

A postictal period
is an interval of transient neurologic dysfunction (commonly AMS or weakness) immediately following a seizure, generally lasting < 1 hour.

Longer ictal activity is associated with more
prominent and prolonged postictal symptoms

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5
Q

How are seizures classified?

A
  1. Primary seizure- unprovoked vs Acute symptomatic seizure - provoked (secondary)
  2. Generalized vs focal vs unknown onset
  3. Convulsive vs non-convulsive
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6
Q

Define status epilepticus

A

> 5 min of continuous seizures
2 discrete seizures with incomplete recovery between seizures
convulsive vs non-convulsive (dx on eeg)

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7
Q

Define epilepsy

A

The International League Against Epilepsy defines epilepsy as a
(A) diagnosis of epilepsy syndrome (e.g., juvenile myoclonic epilepsy, Lennox-Gastault
syndrome, benign rolandic epilepsy, infantile spasms);
(B) two or more seizures occurring more than 24 hours apart without an identified trigger;
(C) one unprovoked seizure coupled with
a higher likelihood of recurrent seizures over the subsequent decade

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8
Q

Define Primary vs secondary seizures

A

Primary- unprovoked
Secondary- provoked (acute symptomatic seizure caused by underlying pathophysiologic process

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9
Q

Define generalized vs focal seizures

A

Generalized- abnormal neuronal activity in both hemispheres (LOC or aLOC)

Focal Seizures-occur in one hemisphere>patient maintains consciousness

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10
Q

How are generalized seizures categorized?

A

Motor
-tonic clonic
-myoclonic
-atonic
-tonic
-clonic
-myoclonic-tonic-clonic
-myoclonic-atonic
-epileptic spasms

Non-motor (absence)
-typical
-atypical
-myoclonic
-eyelid myoclonia

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11
Q

How are focal seizures classified

A

Aware vs impaired awareness

Motor onset:
-autospasms
-atonic
-clonic
-epileptic spasms
-hyperkinetic
-myoclonic
-tonic

non-motor onset
-autonomic
-behaviour arrest
-cognitive
-emotional
-sensory

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12
Q

Triggers of breakthrough seizures in epilepsy

A

sleep deprivation
emotional or physical stress
menses
illness
medication change or non compliance

**still considered unprovoked

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13
Q

Most common cause of SE and new epilepsy in the elderly?

A

cerebrovascular disease

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14
Q

Define NORSE

A

new onset refractory status epilepticus

Pts without a known diagnosis of epilepsy or clear triggers (absent toxic exposure, metabolic derangements, or structural brain injury) presenting with denovo refractory status epilepticus

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15
Q

Define FIRES

A

subcategory of NORSE to specify subset of patients with clear prodrome of febrile illness for 24hr up to 2 weeks prior to SE presentation

FIRES is common (but not exclusive to) pediatric population

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16
Q

List 10 causes of seizures and status epilepticus in adults (Rosens Box 88.1)

A

Box 88.1

  1. Autoimmune
    -AI encephalitis
    -CREST, Goodpasture syndrome, SLE
    -MS
    -TTP
    -Acute disseminated encephalomyelitis (AEDM)
  2. Cerebrovascular disease
    -CVA
    -AVMs
    -CVST
    -ICH
    -SAH
    -PRES
    -RCVS
  3. Dementias
    - alzheimers
    -fronto-temporal dementia
    -vascular dementia
  4. Genetic syndromes & structural abnormalities
    - Focal cortical dysplasia
    -hydrocephalus
    -metabolic disease
    -mitochondrial disease
    -Porphyria
    -Tuberous scelrosis complex
    -wilsons disease
  5. Hypoxic ischemic brain injury
  6. Intracranial tumour
    -gangliogliomas
    -gliomas
    -lymphoma
    -meningioma
    -metastases
    -neuroectodermal tumor
  7. Metabolic
    - acidosis
    -elevated BUN
    -hypo/hyperglycemia
    -hyperammonia
    -hyper/hyponatremia
    -hypocalcemia
    -hypomagnesemia
    -wernicke encephalopathy
  8. Medications
    -EtOH and WD
    -alkylating agents
    -baclofen toxicity and WD
    -benzo WD
    -CAR-T
    -Carbapenums
    -cephalosporins (cefipime)
    -cylosporins
    -digoxin
    -fentanyl
    -heavy metals
    -lidocaine
    -metronidazole
    -tramadol
    -tacrolimus
    -subtherpeutic anti seizure meds
  9. Systemic disease
    -AoC renal failure
    -cirrhosis
  10. Trauma
    subdural/ epidural hematoma
    -SAH
    -DAI
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17
Q

Define ictal asystole

A

syndrome of focal epilepsies with left temporal onset, in females with PMHx of heart condition

ictal asystole lasting longer than 30 seconds is associated with
extra-temporal
seizure focus and secondary generalized tonic-clonic
seizures.

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18
Q

Most common cause for ED presentation of recurrent seizures

A

medication non compliance

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19
Q

List common causes of adult onset focal seizures in low and middle countries

A
  1. neurocysticerosis
  2. malaria
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20
Q

List 10 potential systemic complications related to seizures and status epilepticus

A
  1. Cardiac
    - arrhythmia’s
    - cardiac arrest
    - CM
    - HTN
    - thermodysregulation
  2. MSK
    -fracture/dislocation
  3. GI
    -hepatotoxicity and pancreatitis
    -ilieus and bowel ischemia
  4. Heme
    - rhabdo
    -leukocytosis/leukopenia
    -thrombocytopenia
  5. Pulmonary
    -AW obstruction
    -apnea/hypoventilation
    -aspiration
    -hypoxia
    -mucous plugging
    -pulmonary edema
  6. Renal/acid-base
    - ARF
    -Acidosis -lactic, respiratory
    -Hyperglycemia
    -hyperkalemia
    -myoglobinuria
  7. Prolonged ICU course complications
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21
Q

How to manage seizure caused by hyponatremia

A

Hypertonic saline (3%)
adult- 100 ml 3% NaCl / 10 min

children- 2-5ml/kg (up to 150 ml) over 20 min

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22
Q

How to manage seizures caused by hypocalcemia

A

calcium chloride or gluconate amps until seizure aborts

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23
Q

How to manage seizures caused by TCA OD

A

sodium bicarb
1 to 2 mEq/kg IV bolus; repeat as needed to maintain ECG QRS complex ≤ 100 msec

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24
Q

How t manage seizures caused by salicylate OD

A

Sodium bicarb or HD
Administer 1 to 2 mEq/kg IV bolus; repeat as needed to maintain a blood pH of 7.4 to 7.5

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25
Q

How to manage seizures caused by isoniazid toxicity

A

Pyridoxine 5 g IV (adult) or 70 mg/kg (pediatric)

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26
Q

How to manage seizures caused by lithium toxicity

A

HD

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27
Q

How to treat seizures caused by sympathomemetics/EtOH WD/ MDMA

A

Benzodiazepines

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28
Q

How to treat seizures caused by eclampsia

A

Magnesium sulfate IV loading dose of 4 to 6 g over 15 to 20 minutes, then 1 to 2 g/h infusion; monitor patients for
hyporeflexia; alternatively, lorazepam (Ativan) 4 mg IV over 2 to 5 minutes or diazepam (Valium) 5 to
10 mg IV slowly can be used to terminate the seizure, after which magnesium sulfate is administered

29
Q

Seizure + HTN+ bradycardia are suggestive of what intracranial pathology

A

herniation syndromes

30
Q

What are proposed seizure triggering thresholds for the following metabolic derangements: Glucose, sodium, calcium, magnesium, BUN, creatinine

A

Glc <2.0 or >25
Na <115
Ca <1.2
Mg <0.3
BUN >35.7
creatinine >884

31
Q

When do early post traumatic seizures typically occur? how many of those occur in the first 24h

A

Early post-traumatic
seizures occur
within the first week, with over 50% occurring within the first 24 hours

32
Q

Describe post traumatic seizure prophylaxis

A

Early post-traumatic
seizures occur
within the first week of initial brain insult, with over 50% occurring within the first 24 hours.

Guidelines recommend 7 days in traumatic brain injury and short-term
therapy in subarachnoid hemorrhage.

33
Q

How are seizures in pregnancy classified

A
  1. Diagnosed epilepsy + pregnant
  2. new onset seizure in pregnant pts
  3. seizure 2/2 to eclampsia
34
Q

Define recruitment as it relates to seizure development and progression

A

Defined as the activation of neurons by increased electrical activity of adjacent
neurons.

Neuronl impulses that track into deep circuits of the subcortex (ie RAS) or cross the midline cause alterations in LOC.

The process of recruitment explains seizure auras (i.e., alterations in sensation, autonomic deregulations, aphasia, deja vu, lip smacking,
repeated swallowing, picking at clothing secondary to abnormal neuronal activity) and how focal seizures can secondarily become generalized

35
Q

List 4 clinical findings that differentiate seizures from syncope

A

Features of Seizure:
1. Post ictal state
2. Longer duration of motor manifestations
3. loss of bladder/bowel control
4. tongue biting or laceration

Features of syncope
1. rapid recovery/ spontaneous return of conciousness
2. less likely to have motor involvement, if present lasts seconds
3. no loss of bladder/bowel function
4. No tongue biting

36
Q

List 5 features that differentiate neurogenic and psychogenic seizures

A

Features of PNES
- often longer in duration compared to neurogenic
-recollection of events during psychogenic seizure
- forward thrusting pelvic movements
-head turning from side to side during event
-gaze deviation away from examiner during event
-avoid noxious stimuli during event
-typical metabolic acidosis not present after event

37
Q

List 5 diagnosis that can mimic seizures

A

Cardiac
1. Vasodepressive (vagal) syncope
2. Orthostatic syncope
3. Cardiogenic syncope

Neurologic
1. Stroke, transient ischemic attack
2. Atypical migraine
3. Movement disorders
4. Mass lesions

Toxicologic
1. Intoxication, inebriation
2. Oversedation, over-analgesia

  1. Extrapyramidal symptoms
    Metabolic
  2. Hypo-, hyperglycemia
  3. Thyrotoxicosis
  4. Delirium tremens

Infectious
1. CNS infections
2. Tetanus

Psychiatric
1. Pseudoseizure
2. Panic attacks
3. Cataplexy

38
Q

List 10 causes of status epilepticus in adults (crack cast)

A

Metabolic Disturbances
1. Hepatic encephalopathy
2. Hypocalcemia
3. Hypoglycemia or hyperglycemia
4. Hyponatremia
5. Uremia

Infectious Processes
1. Central nervous system abscess
2. Encephalitis
3. Meningitis

Withdrawal Syndromes
1. Alcohol
2. Antiepileptic drugs
3. Baclofen
4. Barbiturates
5. Benzodiazepines

Central Nervous System Lesions
1. Acute hydrocephalus
2. Anoxic or hypoxic insult
3. Arteriovenous malformations
4. Brain metastases
5. Cerebrovascular accident
6. Eclampsia
7. Head trauma: acute and remote
8. Intracerebral hemorrhage
9. Neoplasm
10. PRES

Intoxication
1. Bupropion
2. Camphor
3. Clozapine
4. Cyclosporine
5. Flumazenil
6. Fluoroquinolones
7. Imipenem
8. Isoniazid
9. Lead
10. Lidocaine
11. Lithium
12. MDMA
13. Metronidazole
14. Synthetic cannabinoids
15. Theophylline
16. Tricyclic antidepressants

39
Q

Outline the management of SE in the pre hospital setting

A

Assess ABCs
Attach monitors -Pulse oximetry
ECG
BG- treat if low
Place pt in position of safety (left lateral decubitus)
Give one of the following medications:
- Midazolam 10 mg IV/IM/IN - FIRST LINE IF NO IV
- Lorazepam 2 mg up to max of 10 mg IV - FIRST LINE IF IV
- Diazepam 5 mg up to max of 20 mg PR - do not use re: poor absorption

40
Q

Outline the management of SE in the ED

A
  1. Ongoing seizure activity:
    -Midazolam 10 mg IV/IM/IN - FIRST LINE IF NO IV
    - Lorazepam 2 mg up to max of 10 mg IV - FIRST LINE IF IV

AND (Keppra first line)
- Phenytoin 20 mg/kg IV at max rate 50 mg/min
- Fosphenytoin 20 PE/kg IM or IV at max rate of 150 mg/min
- Valproic Acid 20-40 mg/kg at 3-6 mg/kg/min
- Keppra 1000-3000 mg over 15 minutes

If seizure still not aborted
- Intubation and EEG recommended
- Treat with one of the following third-line medications:
- Phenobarbitol 20 mg/kg IV at 50-75 mg/min
- Midazolam 0.2mg/kg IV, then 0.1-0.4 mg/kg/hr
- Propofol 2 mg/kg IV at 2-5 mg/kg/hr, then 5-10 mg/kg/hr as
needed

41
Q

Diazepam dosing for seizure in adult and peds

A

Adult 5 mg IV, up to max 20 mg or 10-20 mg PRN

Peds 0.2-0.5 mg/kg IV/ET
or 0.5-1.0 mg/kg PR
(max 20 mg)

May repeat in 10
minutes; monitor
respiratory status

42
Q

Lorazepam dosing for seizure in adult and peds

A

Adult- 2 mg IV at 2 mg/min,
up to max 10 mg IV

Peds- 0.05-0.1 mg/kg IV
(max 2 mg)

Preferred IV benzo;
may repeat in 10
minutes; monitor
respiratory status

43
Q

Midazolam dosing for seizure in adult and peds

A

Adult- 5 mg, up to a max of
10 mg IV/IM/IN

Peds-0.2 mg/kg IV/IM/IN
(max 5 mg)

Preferred IM
benzodiazepine; may
repeat in 10 minutes;
monitor respiratory
status

44
Q

List 10 indications for CT head for first seizure

A
  • New focal deficit
  • Persistent altered mental status
  • Fever
  • Recent trauma
  • Persistent headache
  • History of cancer
  • Anticoagulant use
  • Suspicion or known history of AIDS
  • Age > 40 years
  • Presence of partial complex seizure
45
Q

List 5 characteristics of ictal events

A
  1. Abrupt onset:
    -History should focus on any evidence of an aura.
  2. Brief duration.
    -Seizures rarely last longer than 90 to 120 seconds, Status epilepticus is the important exception.
  3. Alteration of consciousness.
    -Generalized seizures are manifest by loss of
    consciousness; focal seizures are often accompanied by an alteration in consciousness.
  4. Purposeless activity. -Automatisms and undirected tonic-clonic movements are common
    in ictal events. Tonic-clonic movements are rhythmic and generally do not involve head shaking.
  5. Postictal state.
    -can last from minutes to hours, depending on
    which specific region of the brain triggered the seizure, seizure duration, age, and use of an antiepileptic drug (AED).
46
Q

Name 3 metabolic causes of seizures

A

The top 6 metabolic abnormalities causing seizures are:

  1. Hyponatremia
  2. Hypocalcemia
  3. Hypoglycemia
  4. Hyperglycemia
  5. Uremia
  6. Hyperammonemia
47
Q

What percentage of patients with convulsive status epilepticus will
develop non-convulsive status epilepticus?

A

up to 15% of patients who are successfully treated for convulsive status
epilepticus remain in non-convulsive status afterwards.

48
Q

List 5 causes of persistent AMS in a patient who has seized

A

Metabolic- hypoglycaemic; encephalopathy

CNS- ICH, migraine, Transient global amnesia

Infectious

Drug intoxication or WD

Psychogenic

49
Q

What is Todds Paralysis?

A
  • Transient post-ictal paralysis
  • Common (13%) following focal motor seizure affecting one side of the body
  • Can also affect speech, gaze or vision
  • Usually subsides within 24hrs

**high likelihood of underlying structural cause of seizure

50
Q

List 4 features that increase the likelihood the event was a seizure

A

> 45 yo

Abrupt onset and brief duration

Confirmed unresponsiveness

Postictal confusion

Rhythmic limb shaking or dystonic posturing

Tongue biting

Head or eye turning to one side

Cyanosis

Preceding déjà vu or aura

NOTE
Incontinence and trauma were not discriminative findings between seizure, syncope, and nonepileptic attack disorder..

51
Q

List 8 causes of toxin-induced seizure

A
  1. organophosphate
  2. TCA
  3. Salicylate
  4. sympathomemetic
  5. Camphor
  6. Methylxanthine
  7. Benzo WD
  8. EtOH WD
  9. lithium
  10. lidocaine
52
Q

Name 5 infectious causes of provoked seizures

A

Bacterial meningitis (s. pneumonia most common in adults, GBS in <2mo

Viral encephalitis (HSV, EBV, enterovirus, west nile)

Abscess (gram + strep and staph most common)

syphillis

cysticercosis

Malaria

53
Q

List 5 causes of seizure with immediate reversible treatment

A

Hyponatremia
Hypoglycemia
Hypocalcemia
TCA
ASA
Isoniazide
cocaine
etoh
lithium
MDMA
eclampsia

54
Q

List 3 causes of seizure in HIV patients

A
  1. Toxoplasmosis
    Clinical: Fever; HA; AMS; seizures; weeks
    Imaging: ring enhancing
    Dx: PCR for Toxo
  2. Cryptococcous
    Clinical:Fever; HA; AMS; seizures
    Imaging: ring enhancing
    Dx: india ink
  3. CNS lymphoma
    Clinical: fever; wt loss; sweats; months
    Imaging: ring enhancing
    Dx: PCR for EBV
  4. PML
    Clinical: FND; ataxia; VF loss; months
    Imaging: demyelinatoin
    Dx: PCT for JC
  5. HIV encephalopathy
    Clinical: depression, movement, memory
    Imaging: T2 signals
    Dx: PCR for HIV
  6. CMV
    Clinical: FND; confusion
    Imaging: micronodules
    Dx: PCR for CMV
  7. Abscess
    Clinical: Fever; FND; bacteremia
    Imaging: ring enhancing
    Dx: culture
  8. TB
    Clinical: FND; TB SxS
    Imaging: Ring enhancing
    Dx: Culture
55
Q

Phenytoin dosing

A

Phenytoin 20 mg/kg IV at max rate 50 mg/min

56
Q

Fosphenytoin dosing

A

Fosphenytoin 20 PE/kg IM or IV at max rate of 150 mg/min

57
Q

Valproic Acid dosing

A

Valproic Acid 20-40 mg/kg at 3-6 mg/kg/min

58
Q

Keppra dosing

A

Keppra 1000-3000 mg over 15 minutes

59
Q

phenobarbitol dosing

A

Phenobarbitol 20 mg/kg IV at 50-75 mg/min

60
Q

Midazolam infusion dosing for third line therapay

A

Midazolam 0.2mg/kg IV, then 0.1-0.4 mg/kg/hr

61
Q

Propofol infusion dose 93rd line)

A

Propofol 2 mg/kg IV at 2-5 mg/kg/hr, then 5-10 mg/kg/hr as
needed

62
Q

Carbamezipine loading dose and route of administration of AEDs when resuming in the ED

A

8mg/kg po suspension x1

63
Q

Keppra loading dose and route of administration of AEDs when resuming in the ED

A

1500 mg po load or rapid IV up to 60 mg/kg

64
Q

phenytoin loading dose and route of administration of AEDs when resuming in the ED

A

20 mg/kg divided into max doses of 400 mg q 2 h po.

or

18 mg/kg IV at <50 mg/min

65
Q

VPA loading dose and route of administration of AEDs when resuming in the ED

A

up to 30 mg/kg IV to max rate of 10 mg/kg/min

66
Q

What anticonvulsants can paradoxically cause seizures in supratherapeutic levels?

A

Phenytoin
Carbamazepine
Valproic Acid
Lamotrigine

Therefore… if known to take Rx, give HALF loading dose (in case they are seizing because of supratherapeutic levels)

67
Q

What options do you have for anti-epileptics if you can’t get IV access?

A

Midazolam IM, IN, Buccal
Lorazepam SL (can also give IM)
Diazepam PR

68
Q

When would you consider starting a patient with first time seizure on an antiepileptic?What DC instructions will you provide

A

Decision to start on anticonvulsant based on:
Risk of seizure recurrence – more common in partial seizures, status, hx, intracranial sx/trauma, presence of Todd’s paralysis
Presence of any underlying predisposing disease – particularly HIV
Have to consider risk of anticonvulsant tx – side effects and drug interactions

In most cases, no need to tx after 1st unprovoked seizure
Refer to neuro – let them decide

PATIENT EDUCATION MOST IMPORTANT!
d/c instructions: avoid swimming w/o lifeguard, don’t work w/ hazardous tools/equipment/ladders, report to driving agencies as required, document instructions precisely