Suspected Seizure Flashcards

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1
Q

What is status epilepticus?

A

Single seizure >5 mins or 2 more seizures within a 5 min period without person returning to normal between them (no refractory period).

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2
Q

What is the management of status epilepticus?

A
  • ABC - airway adjunct, high flow O2, blood glucose
  • 1st line: if still seizing after 5 mins - benzodiazepines (diazepam/lorazepam)
  • Pre-hospital: can give diazepam rectally or buccal (oromucosal) midazolam (buccal midazolam is preferred) - rectal paraldehyde can be given but interacts with plastic so give it via glass syringe
  • In hospital: IV lorazepam (may be repeated once after 10-20 mins)
  • If still seizing (<10 mins) give 2nd line - phenytoin and phenobarbital infusion (paraldehyde PR 0.8ml/kg of the 50:50 mixture with oil, give while preparing or infusing phenytoin, use should not delay phenytoin)
  • Reconfirm it is a seizure and get senior help, seek anaesthetic/ICU advice
  • If no response within 45 mins of onset - induced coma via GA
  • Shouldn’t give >3 doses of benzos - respiratory depression
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3
Q

What are differentials for seizures?

A
  • Febrile seizure: triggered by high temperatures
  • Encephalopathy: fluctuation of altered consciousness
  • Encephalitis/meningitis
  • Brain tumour: focal neurology present
  • Epilepsy: need to have several seizures each on separate occasions
  • Metabolic disorder: the younger the unconscious child, the higher the possibility of a metabolic cause for being persistently unconscious/encephalopathic or intractable seizures - FH of infant deaths
  • Poisoning/intoxication
  • Post-ictal: if the child wakes up and returns to normal self (usually within an hour of seizure)
  • Sepsis/shock: illness prodrome
  • Trauma/head injury
  • HTN
  • Hydrocephalus
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4
Q

What questions do you want to ask about prior to the seizure?

A
  • Behavioural change
  • Health that day
  • Circumstances
  • Time of episode
  • Setting
  • Activity at onset
  • Warning: visual, hearing, fear, sweaty, lightheadedness
  • Objective warning
  • Triggers
  • Time of last meal
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5
Q

What questions do you want to ask about during episode?

A
  • Onset: sudden?
  • Unresponsive, awareness
  • Symmetrical
  • Facial movement, eye movements
  • Posturing, motor movements, clonic/myoclonic/spasm or tonic
  • Breathing changes
  • Incontinence
  • Autonomic
  • Visual disturbance
  • Duration of seizure
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6
Q

What questions do you want to ask about post episode?

A
  • Sleepy/disorientated
  • N+V
  • Amnesia for events
  • Strange behaviour
  • Weakness
  • Injuries: tongue
  • Time to recovery
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7
Q

What recent illness could correlate with a seizure?

A
  • Fever
  • Diarrhoea
  • Wheeze/chest symptoms
  • Weight loss
  • Recent headaches
  • Head injury/trauma
  • Visual disturbances
  • Vomiting or nausea/personality change
  • Poor co-ordination
  • New weakness
  • Taken drug/substance
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8
Q

What is a simple febrile seizure?

A
  • Short generalised seizure <5 mins - only 1 seizure
  • Not recurring within 24hrs
  • Occurring during a febrile episode and not acute disease on nervous system
  • In a child aged 6 months to 5yrs, with no hx of neurological deficits
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9
Q

What is a complex febrile seizure (CFS)?

A
  • Focal, generalised or prolonged seizure (>15 mins)
  • Recurring >1 within 24hrs
  • And/or associated with post-ictal neurological abnormalities - most commonly Todd’s palsy (usually localised to left/right side of body and usually subsides within 48hrs)
  • If CFS lasts >30 mins or there are shorter serial seizure, without consciousness regained in between seizures, the disorder is called ‘febrile status epilepticus’
  • Children have a slightly higher risk of developing epilepsy after complex febrile convulsions
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10
Q

What are indications for an urgent head CT or MRI?

A
  • Encephalopathic or coma
  • Suspected raised ICP
  • Progressive neurological deficit
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11
Q

What are indications for an elective head MRI?

A
  • In a child <2yrs at onset
  • Hard focal neurological signs
  • A focal epilepsy
  • Associated significant learning difficulties
  • Epilepsy resistant to full doses of 2 appropriate drugs
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12
Q

When would you do an EEG?

A
Urgent indications:
- Suspected non-convulsive status
- Non-traumatic encephalopathy
- Coma of unknown cause
Elective standard EEG:
- Strong suspicion of epilepsy (to support classification)
- Developmental or language regression
- NOT generally after a first afebrile seizure or febrile seizures.
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13
Q

What is an epileptic seizure?

A

An epileptic seizure is a transient occurrence of signs +/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain.

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14
Q

What is epilepsy?

A

A disorder of the brain characterised by an enduring predisposition to generate epileptic seizures and by the neurobiologic, cognitive, psychological and social consequences of this condition. The definition of epilepsy requires the occurrence of at least one epileptic seizure.

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15
Q

How is epilepsy defined?

A

A disease of the brain defined by ant of the following conditions:

  1. At least 2 unprovoked seizures occurring >24hrs apart
  2. One unprovoked seizure and a probability of further seizures similar to the general recurrence risk (at least 60%) after 2 unprovoked seizures, occurring over the next 10yrs
  3. Diagnosis of an epilepsy syndrome
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16
Q

What do you counsel parents about on seizures?

A
  • Counselling on recurrence risk of fever related seizures and risk of epilepsy
  • Parents need first aid training and what not to do in a convulsive seizure i.e. not putting something into the child’s mouth or do chest compressions
  • May be considered for training to administer rescue medication, buccal midazolam e.g. at 5 mins
  • Need to be aware of when to call ambulance e.g. after 5 mins of a convulsive seizure or if rescue medication was ineffective after 5 mins
  • Follow up arrangements, by either consultant or epilepsy specialist
17
Q

What causes a higher risk of hemiplegia?

A

Children who show an early hand preference before 12 months have a higher risk of hemiplegia of the non-dominant side.

18
Q

What are causes of delayed walking?

A
  • Central causes: delayed maturation (constitutional); global developmental causes (e.g. genetic/chromosomal disorder with often hypotonia or dysmorphism); all causes of hemiplegia often with hypertonia including cerebral palsy
  • Peripheral: spina bifida
  • Muscular and neuromuscular diseases: Duchenne muscular dystrophy
  • Environmental: bottom shufflers, institutionalised (chronically ill, prematurity, gross psycho-social deprivation)
  • Orthopaedic: developmental dysplasia of hip
  • Metabolic/hormonal: hypothyroidism, rickets, mucopolysaccharidosis
19
Q

What is cerebral palsy?

A
  • This is a group of lifelong conditions that affect movement and co-ordination, caused by a problem with the brain that occurs before, during or soon after birth
  • Disorder of movement and posture due to a non-progressive lesion of motor pathways in developing brain - usually with neuroimaging changes
20
Q

What are the causes of cerebral palsy?

A
  • Antenatal (80%) - e.g. cerebral malformation and congenital infection (rubella, toxoplasmosis, CMV)
  • Intrapartum (10%) - birth asphyxia/trauma (can be preventable)
  • Postnatal (10%) - intraventricular haemorrhage, meningitis, head trauma
21
Q

What are the features of cerebral palsy?

A
  • Abnormal tone seen in early years
  • Delayed motor milestones
  • Abnormal gait
  • Feeding difficulty (can have dysphagia due to dysfunctional swallowing muscles)
  • Majority are spastic (70%) - hemiplegia (unilateral arm and leg involved), diplegia (symmetrical paralysis e.g. both arms), quadriplegia (all 4 limbs)
  • Other forms are ataxic (balance, coordination, depth perception) and dyskinetic (muscle movement control)
22
Q

What are the non-motor features of cerebral palsy?

A
  • Learning difficulties (60%)
  • Epilepsy (30%)
  • Squint (30%)
  • Hearing impairment (20%)
23
Q

What is the management for cerebral palsy?

A
  • MDT approach
  • Treatments for spasticity include oral diazepam, oral and intrathecal baclofen, botulinum toxin type A, orthopaedic surgery and selective dorsal rhizotomy (cuts nerve rootlets in spinal cord that sends abnormal signals to muscles)
  • Anticonvulsants, analgesia as required
24
Q

What are the types of cerebral palsy?

A
  • Spastic: most common, UMN findings
  • Ataxic
  • Dyskinetic (or choreo-athetoid)
  • Many have mixed clinical presentation
25
Q

What are the causes of cerebral palsy?

A
  • Obstetric interventions have little impact on incidence
  • A small number have autosomal recessive inheritance
  • Peri-ventricular cysts are generally due to hypoxic/ischaemic insult and take 7-10 days to develop. Their presence can be important in determining when insult occurred, if present on day 1 then probably not caused by birth