Nerve injuries Flashcards

(43 cards)

1
Q

Define Bell’s palsy

A

Acute, unilateral, idiopathic facial nerve paralysis

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2
Q

What are the features of bell’s palsy?

A

Lower motor neurone facial nerve palsy - forehead affected
Post-auricular pain
Altered taste
Dry eyes

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3
Q

What is the difference between upper and lower motor neurone facial lesions?

A

Upper = forehead sparing

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4
Q

How is Bell’s palsy diagnosed?

A

Clinical diagnosis of exclusion

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5
Q

What are some RFs for Bell’s Palsy?

A

Intranasal flu vaccine

Pregnancy

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6
Q

What is the management for Bell’s palsy?

A

Corticosteroid
e.g. Prednisolone reduces time for full recovery
Usually within 3-4 months

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7
Q

What are the features of third nerve palsy?

A

Down and out eye

Ptosis

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8
Q

What is ptosis?

A

Drooping or downward displacement of the upper eyelid

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9
Q

What are some differentials for ptosis?

A

Thyroid eye disease
Stroke
Orbital tumours
Involutional changes as a result of squinting

Uncommonly - MS, Myasthenia gravis, giant cell arteritis, horner’s, third nerve palsy

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10
Q

What is multiple sclerosis?

A

Demyelinating CNS conditions

2 separate episodes of neuro dysfunction in different anatomy

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11
Q

Who is a typical MS pt?

A

White women
20-40 years
Temporary visual and sensory weakness

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12
Q

What are some presenting features of MS?

A
Visual disturbance in one eye
Peculiar sensory phenomena e.g. numbness, trigeminal neuralgia
Increased muscle tone
Increased reflexes 
Imbalance
Spastic weakness
Tremor
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13
Q

What are the investigations for MS?

A

MRI brain - periventricular plaques

Visual evoked potentials

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14
Q

What are the different forms of MS?

A

Relapsing-remitting
Secondary progressive disease
Primary progressive disease

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15
Q

What is the treatment for an acute MS relapse?

A

High dose steroids e.g. methylprednisolone

Hastens recovery

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16
Q

What are some disease modifying drugs used in MS?

A

Beta-interferon reduces relapse rate up-to 30%

Monoclonal ABs e.g. natalizumab

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17
Q

What can be used to treat spasticity?

A

Gabapentin
Diazepam
Physio

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18
Q

Define trigeminal neuralgia

A

Unilateral disorder characterised by brief electric shock-like pains, abrupt in onset and termination, limited to one or more divisions of the trigeminal nerve

19
Q

What evokes pain in trigeminal neuralgia?

A

Light touch e.g. washing, shaving, smoking, talking , brushing teeth

20
Q

What is first-line treatment for trigeminal neuralgia?

A

Carbamazepine

21
Q

What comprises the term paraesthesia?

A

Tingling
Prickling
Pins and needles
Burning

22
Q

What are some differentials for paraesthesia?

A
Carpal tunnel (3 digit weakness) 
Spinal cord compression
MS
DM
Peripheral vascular disease
23
Q

What are the main symptoms of peripheral neuropathy?

A
Pain
Tingling 
Loss of sensation
Loss of balance or weakness
Poor healing wounds/lcers
24
Q

What cases peripheral neuropathy?

A

Viral infection e.g. shingles
Alcohol excess
Medications
Diabetes

25
What is the initial management for neuropathic pain?
``` Amitriptyline Duloxetine Gabapentin Pregabalin One at a time ```
26
What conditions can case tremor?
``` Parkinsons Anxiety Essential tremor Thyrotoxicosis Hepatic encephalopathy CO2 retention Cerebellar disease ```
27
Define tremor
involuntary rhythmic oscillation of ≥1 body parts, mediated by alternating contractions of reciprocally acting muscles
28
Define essential tremor
progressive tremor of the upper extremities, present in posture and action, without other neurological signs or symptoms postural tremor: worse if arms outstretched improved by alcohol and rest most common cause of titubation (head tremor)
29
How do you diagnose essential tremor?
Clinically bilateral tremor with normal muscle tone and speed of movement; negative history and examination for Parkinson's disease, hyperthyroidism, medications, and alcohol use
30
When is medical treatment considered for essential tremor?
Dysfunction or embarrassment
31
What are the treatment options for essential tremor?
Propanolol
32
Define ALS
Amyotrophic lateral sclerosis Neurodegenerative disorder Progressive muscle weakness and disability Usually death from respiratory failure
33
What are some presenting feature of ALS?
``` Upper extremity weakness Stiffness Poor coordination and balance Painful muscle spasms Foot drop Muscle atrophy Hyper-reflexia Dyspnoea Slow speech ```
34
How is ALS diagnosed?
Clinically presence of upper and lower motor neuron signs, disease progression, and absence of any other explanation for the presentation
35
What is the first line treatment for ALS?
``` Riluzole - Prolongs survival Supportive care NIV Counselling regarding prognosis Advance directives ```
36
What are the types of motor neurone disease?
AML - 50% Primary lateral sclerosis - UMN signs only Progressive muscular atrophy - LMN signs only Progressive bulbar palsy
37
What are the features of progressive bulbar palsy?
palsy of the tongue, muscles of chewing/swallowing and facial muscles due to loss of function of brainstem motor nuclei carries worst prognosis
38
What can cause spinal cord compression?
``` Spine trauma Vertebral compression fracture Intervertebral disc herniation Primary or metastatic spinal tumour Infection ```
39
What can be presenting features of spinal cord compression?
``` Back pain Numbness Weakness or paralysis Bladder/bowel dysfunction Hyper-relflexia ```
40
What is the investigation for spinal cord decompression?
MRI Spine
41
What is the management for acute spinal cord injury?
Immobilisation e.g. cervical collar, backboard Decompressive/stabilisation surgery
42
What is the management for cauda equina syndrome?
Decompressive laminectomy
43
What is the management for malignant spinal cord compression?
Corticosteroids - oral dexamethasone Surgery - decompression laminectomy Radiation therapy