Neurology Flashcards

1
Q

Risk factors for developing cerebral palsy (CP)

A
  • Breech
  • Maternal infection during pregnancy e.g. toxoplasmosis
  • Meningitis
  • Encephalitis
  • Severe untreated jaundice
  • Signs of resp/cardio distress during labour
  • Low birth weight
  • Premature
  • Multiple babies
  • Rh incompatibility
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2
Q

List and describe types of CP

A

Spastic - damage to upper motor neuron, incr tone + brisk relfexes. Tone is velocity dependant -> faster you move the muscle the more its tone. This leads to hallmark dynamic catch where the mm contracts intensly. Divided into limb involvement: hemiplegia (1 side affected), quadriplegia (all limbs affected), diplegia (all limbs legs>arms)

Dyskinetic - involuntary movements, divided into: chorea (irregular, sudden, brief non-repetitive), athetosis (slow, writhing in distal joints e.g. fanning of fingers), dystonia (simultaneous contraction of agonist and antagonst mm proximally usually twisting of trunk)

Ataxic (hypotonic) - usually genetic, early trunk and limb hypotonia, poor balance and delayed motor development. Incoordinate movements, intention tremor and ataxic gate later on.

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3
Q

Treatments of CP and when to use them

A

Therapy - All sorts available depends on problems examples: physio, speech and language, occupational, recreational.

Antispadmodic drugs - Whihc one depends on type of and extent of spasticity. Examples include botox injections (isolated spasticity), for more general diazepam, baclofen may be used in pump

Orthopaedic surgery - May be required to put bones in correct position to improve mobility. In severe cases nerves may be cut to prevent them stimulating affected mms.

Baclofen pumps - Antispadmodic drug given for generalised via pump in skin of abdo

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4
Q

Common types of childhood epilepsies/convulsions/fits and how they differ

A

Febrile convulsions

  • 6 months to 6 years
  • Preceeding infection/fever
  • Voilent shaking of all 4 limbs
  • Self resolving
  • Complete recovery

Focal tonic-clonic with secondary generalisation

  • 2-12 years peak 8-9 yrs
  • Preceeded by stress inducing event e.g. emotional/illness/lack of sleep
  • Starts in one area then spreads everywhere, eyes deviate to right and lip smacking
  • EEG shows abnormal features in one area

Absence

  • 4-8 years peaking 6-7 yrs
  • No trigger
  • Unresponsive, stares into distance, last a few seconds, worse when tired, immediate recovery
  • EEG shows 3 sec spike/wave pattern

Infantile spasms/West syndrome - choas eeg?

  • Presents 4months age
  • No trigger
  • Sudden cry, stiffening of upper body, flexion of head and neck, arms thrown out, occur in clusters, lasts 1-2 seconds
  • Losing skills
  • Unsettled for few minutes after otherwise fine
  • EEG shows hypsarrhythmia (choas eeg)

Relfex anoxic seizure/reflex asystolic syncope

  • Brief stoppage of the heart through excessive activity of the vagus nerve
  • Preceeded by bump on head
  • 0-6 years but can occur at any age
  • Loss of consciossness pale and stiff
  • Full recovery

Syncope/faint

  • Hx that may suggest stress getting blood to brain, e.g. exercise, heat, long period of standing
  • Usually teenager
  • No convulsions, may tremor
  • Other sx feeling hot nauseous, light headidness
  • Short lived and fully recovers

Expiratory apnoea syncope/blue breath holding

  • Usually cry and fail to breath in and go blue and faint
  • Will then start breathing again
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5
Q

Describe what an EEG shows

A

Electroencephalogram

  • Sensors attached to head that detect electrical activity
  • Mainly used to investigate epilepsy
  • Can help identify seizure type, triggering factors and best treatment
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6
Q

Describe what an MRI shows

A

Magnetic resonance imaging

  • Uses magnetic resonance to generate detailed images
  • Claustrophobic warning
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7
Q

Initial investigations into seizures and treatment options

A

Initial investigations

  • EEG
  • MRI
  • Bloods: U+E, glucose, calcium
  • ECG
  • Urine dip
  • LP
  • Temp

Treatment

  • Pharmalogical - AED e.g. sodium valproate (contraindicated in women of child bearing age)
  • CBT and psychological therapy
  • Ketogenic diet
    *
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8
Q

Common AEDs and their side effects

A

Carbamazepine - Blurry vision, dizziness, rashes, unsteadiness, birth defects, induces metabolism therefore interacts w/ lots of drugs

Valproate - sedation, weight gain, tremor, CONTRAINDICATED IN PREGNANCY

Lamotrigine - bone marrow toxicity, stop if flu or rash ensues

Levetiracetam - GI sx

Ethosuximde - GI sx

Phenytoin - increased gum growth, nystagmus, birth defects

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9
Q

What is SUDEP and what safety information should you give

A

SUDEP - Sudden unexpected death in epilepsy

Safety advice

  • Minimise the number of seizures you experience
  • There are safety devices you can get
  • There’s a good website on SUDEP contains lots of good information
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10
Q

Explain febrile convultions to parents, their prevalence and how to offer basic first aid

A

Explanation

  • We all have a threshold of brain activity when we get above it we have a seizure
  • A quick change in body temperature can put us above this threshold
  • Childrens’ threshold is lower than adults because their brains aren’t fully developed
  • Children are very good at rapidly increasing their body temperature

Prevalence

  • 1 in 30 children will have a febrile convulsion
  • If they have 1 they are 3x more likely to have another
  • If one of their sibilings has had one they have a 30% chance of having 1

Basic safety info

  • If convulsion lasts more than 5 mins call 999
  • Stay calm put them in a soft place, don’t put anything in their mouth or restrain them
  • When your child gets a fever give them paracetamol asap and regularly
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11
Q

Common causes of ataxia and their investigations

A

Ataxia - loss of control of bodily movement

Causes

  • Infection
  • Toxin
  • Tumour
  • Hydrocephalus
  • CP
  • Trauma
  • Hereditary

Investigations

  • Infection screen - bloods and LP
  • Toxin screen
  • MRI head
  • Hereditary/genetic screen
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12
Q

Presenting features of brain tumour

A
  • Raised ICP
    • Headache
    • Nausea vomiting
    • Inc BP
    • Confusion
    • Double vision
  • Focal neuro signs
  • Weight loss
  • Night sweats
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13
Q

What are the common causes of development regression

A

Battens Disease

Retts syndrome

Leukodystrophies

Wilson’s

SSPE (Subacute sclerosing panencephalitis)

Infantile spasm (west syndrome)

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14
Q

What’s the difference between obstructive, communicating and external hydrocephalus

A

Obstructive - obstruction stops CSF flowing through ventricles

Communicating - impairment of CSF reabsorption w/out obstruction

External - Widening subarachnoid space w/out ventricular enlargement

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15
Q

Common causes of macrocephaly

A
  • Hydrocephalus
  • Tall stature
  • Familial macrocephaly
  • Tumour
  • Intracranial bleeding
  • Hurlers syndrome
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16
Q

Common causes of microcephaly

A
  • Familial (presenting from birth)
  • Autosomal recessive condition when associated w/ developmental delay
  • Congenital infection
  • Brain injury e.g. perinatal hypoxia
17
Q

Pathophysiology and presenting features of craniosynostosis

A

Craniosynostosis - sutures of skull start to fuse during infancy and finish in late childhood

Can be causes by some syndromes

  • Apert syndrome
  • Pfeiffer syndrome
  • Crouzon syndrome

Presenting features

  • Distorted head shape
  • Raised ICP
  • Syndrome features
18
Q

How do you differentiate tension type and secondary headaches?

A
  1. Systemic S&S: fever, wght loss, this could point to meningitis, cancer
  2. Abnormal neurologic point to secondary cause rather than simple tension type headaches
  3. Onset: sudden = possible secondary (aneurysm, meningitis) >6months = reassuring of benign headache
  4. Age of onset if <5 yrs or >50 yrs w/ new onset headache, shoul be investigated.
  5. Insidious? if headache is getting progressively worse, check for secondary causes
19
Q

Management of a seizure > 15 mins

A
  • Buccal midazolam (benzo)
  • O2
  • IV paracetamol
  • Bloods: culture, U+E, FBC, glucose

10 more minutes fitting

  • 2nd buccal midazolam
  • IV lorazepam (benzo)

10 more minutes fitting

  • IV phenytoin

10 more minutes

  • Induce medical coma
  • Ventilate + intubate
20
Q

What is Todd’s paresis and what is the prognosis

A

Definition: Focal weakness after seizure

Usually resolves in 48 hrs

21
Q

How can an absence seizure be induced

A

Hypoventilation

22
Q

1st line in focal seizures

A

Carbamazepine

23
Q

1st line in absence seizures

A

Ethosuximide

24
Q

1st line in absence with generalised tonic clonic seizures

A

Valproate if teenage girl lamotrogine

25
Q

Features of Duschennes Muscular Dystrophy

A
  • Gait instability
  • Growers manouver
  • Single palmar crease
  • Calf pseudohypertrophy
  • Inc creatinine kinase