27/3/22 Flashcards

1
Q

Epidural puncture site

Lumbar puncture site

A

Epidural - L3-4

Lumbar - L4-5

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2
Q

What bony feature do you feel for head engangment in childbirth

A

Ischial spine (4cm above bone = -4cm)

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3
Q

What muscles make up the levator ani?

label in diagram

A

Puborectalis
Pubococcygeus
Ileococcygeous

label in diagram

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4
Q

Name the bones of the hand

A

So long to pinky here comes the thumb

Scaphoid 
Lunate
Triquetrium 
Pisiform 
Hamate
Capitate
Trapezoid
Trapezium
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5
Q

Names the tarsal bones from cranial view

A

Call the cops nobody calls Colin cunt

Calcaneus
Talus
Cuboid
Navicular
3x cuneiform
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6
Q

Go look at xray of pelvis and complete it

A

DO IT

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7
Q

What is the word used to describe when someone’s affect is far more reactive than you think it should be

A

Labile

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8
Q

Multiple Sclerosis

Describe how a patient would present to clinic

What tests would you do to confirm

How would you explain the condition to them

What management and treatment would you give them

A

Multiple neurological deficits that are seperated by location and time frame
Classic triad =
- Nystagmus + optic neuritis + double vision
- Intention tremor + muscle spasms
- Dysarthria (difficulty talking)

MRI - check for white plaques
CSF (lumbar puncture at L4/5) - oligoclonal bands present

MS is an autoimmune condition (condition where body attacks itself). We have millions of nerves in our body that carry signals between each other. You can think of them like the cables for the telly - they have a thick layer around that protects them - this thick layer also means signals can run smoothly and quickly. In MS the immune system attacks that nice coating called myelin. This means signals are lost and can cause numerous symptoms like the ones you are experiencing. The most common type is relapsing-remitting - where you will have bad spells of symptoms and then will experience some recovery as the myelin repairs itself but it will never go back to normal. It’s important to stress that there is nothing you have done to cause this.

There is no cure.
In general use disease modifying therapy
Tecfedira and aubagio no1

With acute relapse

  • mild = symptomatic treatment
  • mod = oral steroids
  • severe = Iv steroids and admit
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9
Q

MND

Describe how a patient would present to clinic

What tests would you do to confirm

How would you explain the condition to them

What management and treatment would you give them

A

Mixed picture of UMN and LMN
With no sensory deficiet
In bulbar ALS can get early involvement of tongue and bulbar symptoms

MRI can be useful to rule out other causes

MND has many forms. It can cause lots of different motor symptoms and it is impossible to predict where these will occur and when. In a healthy individual signals get transmitted from the brain to the muscles down nerves called motor neurons. Unfortunately in MND these signals no longer trasmit properly and muscles affected can weaken and eventually stop working. Most cases are entirely random and it’s just an horrible hand that you have been dealt. Pause - ask questions.

There is no cure and there is only currently one drug that has been shown to improve survival by 3 months - riluzole. As this only adds time onto the end of life when symptoms are at their worst a lot of patients choose not to take it.
Other than that it is symptom control with botox and baclofen to reduce spasticity

Important for early discussion of advanced care planning.

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10
Q

Parkinson’s

Describe how a patient would present to clinic

What tests would you do to confirm

How would you explain the condition to them

What management and treatment would you give them.
What are the side effects of the medication

A

Pill-rolling tremor - improves on finger to nose test
Shuffling gait and stooped posture
Cog-wheel rigidity in upper and lower limbs
Bradykinesia
Blank expression

Usually a clinical diagnosis

Parkinson’s disease is the most common neurological disorder. It is caused by the breakdown of dopamine producing nerves (neurons) in the brain (substantia nigra in midbrain). Without enough dopamine our body struggles to control movement. This is a progressive disease so it will get worse as time goes on.

There is no cure. But drugs to help with symptoms.

Levodopa (dopamine agonist that carries BBB) and carbidopa (dopa decarboxylase i. - which breaks down levodopa before it reaches BBB)
Can cause N+V and hallucinations and make you v tried throughout the day
Given initally along with domperidone (anti-emetic)

These drugs also have the ‘on-off phenomenon’ -> work better at certain times of day randomly

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11
Q

What condition is this sign associated with:

Forward flexion of the neck sends an electric shock down back and radiates to limbs

A

Multiple sclerosis

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12
Q

What can help you differentiate from drug induced Parkinsonism and Parkinson’s Disease?

What drugs can cause drug induced?

A

Drug - symmetrical
PD - asymmetrical

Metoclopramide
Typical anti-psychotics

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13
Q

What neuro condition is assoc. with pesticide use?

A

Parkinson’s disease

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14
Q

What can be used to reduce spasicity in patients?

A

Botox

Baclofen

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15
Q

What are the signs and symptoms of UMN vs LMN defect

A

UMN

  • hyperreflexia
  • increased tone
  • spastic gait
  • exaggerated jaw-jerk
  • extensor plantar response

LMN

  • muscle wasting
  • weakness
  • fasciculations
  • absent or reduced deep tendon reflexes

UMN = tight and tense

LMN = slow and wasting and fitting

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16
Q

What is the most common cause of encephalitis?

A

HSV

17
Q

What signs and symptoms are characterisitc of Lewy Body dementia

A
  • visual hallucinations
  • fluctuating cognition = “good days and bad days”
  • loss of concentration and attention
  • parkinsonism
  • early phase: loss of exectutive function (ability to carry out tasks) but recognition and recall preserved
18
Q

Name some classical features of fronto-temporal dementia

A

Personality change

  • lack of attention to personal hygiene
  • hoarding/criminal behaviour
  • ignoring social etiquette
  • new eating habits
  • repetitive behaviours

In early stages tend to perform well on cognition

19
Q

What type of headache presents more commonly in men than women?

Describe it’s presentation and how you would manage the condition and acute attacks

A

Cluster headache

Periorbital pain 
Eye symptoms e.g. lacrimation, ptosis
Acute onset
Very painful
Occur 1-2 day for 4-12wk period and then nothing followed by another 'cluster'
Last 15mins-3hrs
  1. Avoid triggers
  2. Prophylaxis - verapamil
    Acute attack
    = 100% O2
    = subcutaneous/nasal triptan
20
Q

How is trigeminal neuralgia managed?

A
  1. Carbamazepine (anti-convulsant)

~microvascular decompression

21
Q

Describe the differences in presentation between a migraine and tension headache

How do you manage both

A

Migraine

  • unilateral
  • sometimes with visual symptoms
  • pulsitile
  • photophobia and can’t hear loud noises
  • lasts 4-72hrs

Keep a migraine diary to find triggers and then avoid
Reduce caffiene intake, drink H20 and sleep well
Prophylaxis - propranolol/toprimate

Acute = sumatriptan and pain relief and anti-emetic

Tension headache

  • bilateral
  • non-pulsitile
  • around head like a headband

Minimise stressers
Pain relief

22
Q

What aspects of a headache make you think raised ICP?

A

Worse in morning, coughing, when bent over and lying down

Improve after standing up and vomiting

~disturb sleep

New onset focal neuro deficet/personality change

Reduced level of conciousness

23
Q

What red flag symptoms do you need to ask about for headache

A
  • new onset focal neuro defiect/personality change/cognitive dysfunction -> raised ICP, enecphelitis, meningitis
  • neck stiffness and altered mental state - bacterial/fungal/viral meningitis
  • temporal region of headache with jaw claudication (pain and discomfort on chewing) - temporal arteritis in GCA
  • weight loss - malignancy
  • rash - meningococcal sepsis
  • loss/reduced level of conciousness - raised ICP
  • recent head trauma - subdural
  • headache with severe eye pain, reduced vision and N+V - acute closed angle glucoma
  • limb and facial weakness
  • aura?
  • balance
  • new seizures - malignancy
24
Q

If someone presents with migraine with aura when do you tell them to take their acute medicine - at beginning of headache or beginning of aura.

Also what is the drug again?

A

Sumatriptan - beginning of headache

25
Q

When does meningitis become a notifiable disease?

How is it managed?

A

Upon clinical suspicion

With IM benzyl penicillin