Neuro Flashcards

1
Q

What is cerebral palsy?

A

disorder of movement and posture due to a non-progressive lesion of the motor pathways in the developing brain, due to CNS insult sustained before 2 years

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2
Q

What are some prenatal and postnatal causes of CP?

A

prenatal - APH, alcohol, rubella, HIV, placental abruption, cord prolapse, maternal shock
postnatal - birth trauma and hypoxia with cord around neck, HIE, severe neonatal jaundice

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3
Q

How does CP manifest?

A

weakness, paralysis, increased tone, coordination
premature handedness, delayed milestones
UMN signs
high steppage, waddling gait

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4
Q

What are some complications associated with CP?

A

learning disability, epilepsy, kyphoscoliosis, muscle contractures, hearing and visual impairments, GORD

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5
Q

How is CP managed?

A

MDT - physio for muscles, OT for ADL, SALT for swallow, ortho for contractures
paeds - optimise medications
social workers and charities

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6
Q

What are the medical managements for CP?

A

muscle relaxants - baclofen
anti-epileptics
glycopyrronium bromide - drooling

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7
Q

What is the pathophysiology of epilepsy?

A
  • seizures which are transient episodes of abnormal electrical activity in the brain
  • disrupted balance between excitatory glutamate and inhibitory GABA
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8
Q

How might a seizure present?

A
  • a general strange feelingthat’s hard to describe
  • a “rising” feeling inyourtummy–like the sensation in your stomach when on a fairground ride
  • a feeling that events have happened before (déjà vu)
  • unusual smells or tastes
  • tinglingin your arms and legs
  • an intense feeling of fear or joy
  • stiffness or twitching in part ofyour body, such as an arm or hand
  • witnessed general jerking of the whole body
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9
Q

What type of seizures are there?

A

tonic clonic - LOC
focal - focal signs
absence - stare blankly
atonic - muscle tones lapses briefly
myoclonic - brief contractions
infantile spasms

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10
Q

How would you manage status epilepticus?

A
  • Secure the airway
  • Give high-concentration oxygen
  • Assess cardiac and respiratory function
  • Check blood glucose levels
  • Gain intravenous access (insert a cannula)
  • IVlorazepam, repeated after 10 minutes if the seizure continues
  • then infusion of IV phenobarbital or phenytoin
  • ITU
  • community
    • Buccal midazolam
    • Rectal diazepam
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11
Q

How is epilepsy investigated?

A

EEG
MRI brain
ECG
electrolytes
glucose
blood cultures, urine cultures, LP

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12
Q

How do you manage seizure?

A

safety precautions for when seizures happen
medications
managing seizures
ketogenic diet, vagal nerve stimulation, epilepsy surgery

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13
Q

What is extradural haemorrhage?

A
  • tearing of middle meningeal artery as it passes through foramen spinosum of sphenoid
  • space between the dura and the overlying calvarium
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14
Q

How extradural haemorrhage present?

A
  • lucid interval until consciousness deteriorates
  • seizures secondary to increasing haematoma
  • initial presentation - anaemia and shock
  • dilation of ipsilateral pupil
  • paresis of contralateral limbs
  • false localising uL or bL 6th nerve paresis
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15
Q

how does a migraine present?

A

unilateral, throbbing, may take up to 48h to resolve and may present with visual aura, photophobia and phonophobia, N+V, abdominal pain

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16
Q

What is an aura in association to migraines?

A

aura - commonly visual disturbances like hemianopia, scotoma or fortification spectra (zig zag)

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17
Q

What are some red flags to be aware of in regards to migraines?

A
  • headache worse when lying down, coughing or straining, wakes child up from sleep (not in morning when waking up - migraines)
  • associated confusion, morning or persistent N+V
  • recent personality changes, behaviour or educational performance
18
Q

How are migraines managed?

A
  • acute - rest, fluids, low stimulus environment, paracetamol, ibuprofen, sumatriptan, antiemetics like domperidone
  • Prophylaxis - if impacting school and high frequency and severity, propranolol (not for asthma), pizotifen (drowsy), topiramate (teratogenic)
19
Q

What is Duchennes MD?

A
  • X linked recessive disorder of defective gene for dystrophin on X chromosome
    • dystrophin heps hold muscles together at cellular level
20
Q

How might MD present?

A
  • 3-5 year old with weakness in muscles around pelvis
  • progressive weakness
  • Frequent falls
  • Difficulty rising from a lying or sitting position
  • Trouble running and jumping
  • Gower’s signs
21
Q

What are the complications for MD?

A
  • breathing difficulties requiring CPAP etc
  • coughing difficulties due to weakness
  • swallowing difficulties and aspirations
  • heart disease - cardiomyopathy and CHF
  • scoliosis
  • osteoporosis
22
Q

How is MD managed?

A
  • no curative
  • aim for highest quality of life for longest time possible
  • occupational therapy, physio, medical appliances like wheelchairs and braces
  • complication management for spinal scoliosis and heart failure
  • DMD - oral steroids may slow progression of weakness by 2 years, creatine supplementation slight improvement for strength, genetic trials ongoing
23
Q

What could cause a raised ICP?

A
  • traumatic brain injury
  • hydrocephalus, brain tumors
  • intracranial infections
  • hepatic encephalopathy
  • impaired central nervous system venous outflow
24
Q

How might you identify a paeds raised ICP?

A
  • extremely irritable
  • increased sleepiness
  • high pitched cry
  • vomiting
  • headache
  • loss of consciousness
25
What examination findings would you look for in raised ICP?
- drowsy - seizures - papilloedema - pupil changes - ipsilateral dilation - abnormal posturing - decorticate or decerebrate - cushings triad - bradycardia, raised BP, irregular breathing
26
What initial investigations might you do in suspected raised ICP?
- Cardiovascular monitoring - Pulse oximetry - Laboratory investigations (to include U&Es, FBC, blood and urine cultures) - CT scan urgently once vital signs stabilised - Contra-indication to LP
27
What is the management of raised ICP?
- A-E and maintaining cerebral perfusion pressure vital - manage in ICU with intubation and ventilation - help venous drainage by keeping head in midline elevated at 30 degrees - reduce metabolic demand - normothermia (36-37c), oxygenation, muscle relax, prevent seizures and hypoglycaemia - optimise CPP - normal pCO2, high - normal BP - hypertonic saline or mannitol - fluid restriction and diuresis, avoid hypovolaemia - emergent neurosurgical transfer if intervention possible - steroids maybe useful - dexamethasone - no LP
28
What is spinal muscle atrophy?
autosomal recessive condition causing progressive loss of motor neurones, leading to progressive muscular weakness affects lower motor neurones in spinal cord
29
What are the symptoms of spinal atrophy?
- floppy or weak arms and legs - movement problems – such as difficulty sitting up, crawling or walking - twitching or shaking muscles - tremors - bone and joint problems – such as an unusually curved spine - scoliosis - swallowing problems - breathing difficulties
30
What examination findings would you look for in spinal atrophy?
- fasciculations - reduced muscle bulk - reduced tone - reduced power - reduced or absent reflexes
31
How might you manage spinal atrophy?
- no cure - MDT - physiotherapy - maximise strength, retain resp function - splints, braces, wheelchair - resp - non-invasive ventilation to prevent hypo and failure - type 1 - tracheostomy, mechanical ventilation - PEG feeding as weak swallow
32
What are ways of spinal cord injury?
*where neck bent or squeezed - during delivery - falls - RTA - driving accidents - sporting injuries - trampoline incidents - gunshot or stab - infecction forming an abscess on spinal cord - injury blocking circulation to spinal cord
33
How might spinal cord injury present?
spinal shock complete - no movement or feeling incomplete - some muscle weakness loss of voluntary movement breathing problems, bladder and bowel and autonomic regulation issues
34
What are some investigations carried out in spinal cord injury?
- blood tests - infection - XR - visualise injury - CT - MRI - Somatosensory evoked potential (SSEP)
35
What is the immediate management of spinal cord injuries?
- Close watch in the intensive care unit - Medicines such as corticosteroids to help decrease the swelling in the spinal cord - mechanical ventilator or respirator - catheter to drain urine into a bag - NGT to give nutrition - Surgery to check the cord, treat broken backbones, release pressure from the injured area, or to manage other injuries - longterm rehab and follow up as required with MDT care
36
What could cause subarachnoid haemorrhage in children?
aneurysm or arteriovenous malformation, trauma, non accidental injury, infections causing vessel weakening, coagulation disorders
37
How is an SAH managed?
stabilise pt diagnostic imaging treat underlying cause medical - control HTN, prevent vasospasm, manage seizures, pain management neuro monitor rehab long term follow up
38
what could cause tension headache in children?
stress and anxiety muscle strain eye strain dehydration and poor nutrition underlying condition poor sleep
39
What is a febrile seizure?
seizure accompanied by a fever in the absence of intracranial infection occuring in children 6m-6y
40
How would you manage a febrile seizure?
- reassurance and information for parents - antipyretics but not shown to prevent seizures - first aid management of seizures - rescue therapy if history of prolonged seizures - buccal midozolam - oral prophylactic antiepileptics not used as not shown to reduce recurrence rate and have relative high risk side effects *call ambulance if longer than 5 min