Paediatric Neurology 2 - Chronic Flashcards

1
Q

Define status epilepticus:

A

This is the term used when someone has been seizing for over 30 minutes without recovery.

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2
Q

What are the 3 phases of generalised childhood epilepsy?

A

Tonic phase
Clonic Phase
Postictal phase

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3
Q

What type of epilepsy is benign with centro-temporal spikes and accounts for 15% of all childhood epilepsy?

A

Rolandic Epilepsy

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4
Q

What type of seizure is seen in Rolandic Epilepsy?

A

Infrequent, partial fits with unilateral facial or oropharyngeal sensory motor symptoms, speech arrest and hypersalivation

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5
Q

What are some of the common generalised epilepsy coditions?

A

Tonic-Clonic (grand mal)
Absences
Infantile spasms (west’s syndrome)

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6
Q

What is the peak age for West’s syndrome?

A

5 months

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7
Q

What are some of the characteristic features of infantile spasms / West’s syndrome?

A

sudden clusters of head nodding (tonic flexor spasm of head)
Salaam attack
Arm jerking
Relaxation after 3-30 seconds, spasms may occur up to 20 times a day

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8
Q

How is West’s syndrome managed?

A

ACTH or prednisolone first line

Vigabatrin second line

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9
Q

What is commonly seen on an EEG in a child with West’s syndrome?

A

Chaotic Hypsarrhythmia

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10
Q

A child presents with altered/ impaired consciousness, lip smacking, hallucinations and chewing motions. When they come round they show signs of postictal amnesia? What is the most likely diagnosis?

A

Temporal Lobe partial seizures

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11
Q

WHat will occur in the tonic phase of a generalise seizure?

A

Sudden loss of consciousness with limbs extended, back arched and breathing stops.

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12
Q

What will occur in the clonic phase of a generalised seizure?

A

Intermittent jerking and irregular breathing

Involuntary urination and salivation

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13
Q

What is the management for an epileptic convulsion?

A
Buccal midazolam / rectal diazepam if fitting more than ten minutes
IV lorazepam (up to 2 doses)
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14
Q

What is the prevalence or cerebral palsy?

A

1/400 children

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15
Q

What are some additional problems often associated with cerebral palsy?

A
Epilepsy
Learning difficulties
Visual impairment
Squint
Hearing loss
Speech disorders
Behavioural disorders
Undernutrition and poor growth
GORD and swallowing problems
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16
Q

Define cerebral palsy:

A

This is a disorder of movement caused by permanent, non progressive brain damage acquired in early brain development, before 2 y/o, often due to hypoxia of the brain.

17
Q

What are the features of hemiplegia cerebral palsy?

A

One side is affected
arm usually more involved than leg
Delayed walking
Tiptoe gait when running

18
Q

What are some clinical features of diplegia cerebral pasly?

A

Both legs are involved with arms more or less unaffected
Scissoring of legs and excessive hip adduction
Equinovarus of feet
Tiptoe walking

19
Q

What causes ataxic cerebral palsy and what are the features?

A

Cerebellar damage

Poor coordination and ataxic gait

20
Q

What are some neonatal signs of cerebral palsy?

A
Difficulty sucking
Irritable
Convulsions
Abnormal neurological exam
Head lag
Persistent moro reflex
21
Q

What members of the MDT are essential in the management of cerebral palsy?

A

Physiotherapy
Occupational therapy
Dietician
Speech therapist

22
Q

What are some common orthopaedic complications which can occur in cerebral palsy?

A

Hip dislocation due to spasticity
Equinus deformity of the ankle
Scoliosis

23
Q

What is given to treat spasticity in cerebral palsy?

A

Baclofen first line

Botulinum injections second line

24
Q

What is given to treat dystonia in cerebral palsy?

A

Trihexyphenidyl first line

Deep brain stimulation is a more invasive option for later