Neurology Flashcards

1
Q

What is Hoover’s sign as it pertains to Somatisation disorder?

A

Hoover’s sign is the test used to help differentiate organic v non-organic / functional leg paresis
You place a hand under the affected leg while asking them to lift the unaffected leg against resistance - you will feel counter pressure in the ‘affected’ leg due to involuntary hip extension

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2
Q

When should phenytoin levels be checked?

A

Phenytoin levels do not need to be checked routinely but should be checked if suspect toxicity or if change of dose.
Need to check TROUGH levels so just before dose is due.

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3
Q

What is the classical presentation for normal pressure hydrocephalus?

A

Normal pressure hydrocephalus is an important differential to consider in patient’s presenting with confusion / memory loss as it is a REVERSIBLE cause of dementia.

It is caused by reduced resorption of CSF through the arachnoid villi.

Presents with WACKY, WET, WOBBLY
1. Cognitive disturbance / memory loss
2. Urinary incontinence
3. Wide, unstable gait (may present quite similar to parkinsons gait)

Management is ventricloperitoneal shunting

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4
Q

Which medications may cause peripheral neuropathy?

A

Nitrofurantoin
Metronidazole
Amiodarone
Isoniazid
Vincristine

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5
Q

In what ways does the classical presentation of migraines differ in children versus adults?

A

In children migraines are more likely to be *Bilateral *Last for shorter periods and have *Gastrointestinal disturbance / abdo pain associated

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6
Q

What DMARDs are available for those with MS?

A

Natalizumab - can reduce freq and severity of relapses by ~ 68%
Beta interferon (reduces relapses by ~ 30%)
The efficacy of cannabinoids is still debated

IF THE PATIENT HAS BEEN UNABLE TO WALK FOR 6 MONTHS THEN DMARDS ARE UNLIKELY TO BE EFFECTIVE

If there is disease progression despite treatment then normally that treatment should be stopped

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7
Q

Which patients with epilepsy would NOT be suitable to management under primary care and would require secondary care?

A

Any child / adolescent
Any adult with special needs
Any adult with ongoing seizures or with specific care needs e.g planning a pregnancy/

** Only adults with stable, well-controlled epilepsy should be managed in primary care **

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8
Q

What are the typical signs of lower and upper motor neurone lesions respectively?

A

UMN - hyperreflexia, spasticity, weakness, upgoing / extensor plantar response

LMN - reduced reflexes, flaccid paralysis, atrophy, fasciculations

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9
Q

What is the typical presentation of amyotrophic lateral sclerosis?

A

Mixed upper and lower motor neurone signs, involving initially one segment of the neuroaxis (i.e., cranial, cervical, thoracic, or lumbosacral), and then progressively spreading, typically to contiguous areas

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10
Q

What is the most common form of motor neurone disease?

A

Amyotrophic lateral sclerosis (ALS)

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11
Q

Which medication is shown to prolong survival in ALS and should be offered to all at diagnosis?

A

Riluzole

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12
Q

What is the first line drug for trigeminal neuralgia?

A

Carbamazapine

Carbamazepine is the only licensed anticonvulsant medication with proven efficacy to treat trigeminal neuralgia.
Initiate therapy at 100 mg up to twice daily, and titrate in steps of 100–200 mg every 2 weeks, until pain has been relieved.
In the majority of people a dosage of 200 mg three or four times a day is sufficient to prevent paroxysms of pain (maximum dosage 1600 mg daily).
Modified release preparations may be useful, particularly if the person experiences breakthrough pain at night. Once the pain is in remission, the dosage should be gradually reduced to the lowest possible maintenance level, or the drug can be discontinued until a further attack occurs

IF CARBAMAZEPINE DOES NOT WORK THEN REFER TO A SPECIALIST

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13
Q

According to NICE, within what window of time should people who sustain a head injury on anticoagulants (warfarin or NOAC) get a CT Head?

A

Within 8 hours

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14
Q

What is the typical presentation of diabetic amyotrophy?

A

PAINFUL mononeuropathy
Often affects the femoral nerve (normally unilateral) leading to wasting of the quadriceps, and LMN signs including loss of knee jerk as well as pain and numbness in the affected dermatome

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15
Q

What is the typical presentation of essential tremor?

A

Symmetrical, bilateral tremor - normally occurs during active movements and not present at present.

Worsened by caffeine, stress
Improved by alcohol, beta blockers and rest

May involve upper limbs, head and neck

Tx is with propranolol or primidone

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16
Q

What is the treatment window for suspected Bell’s Palsy?

A

If presents within 72 hours of symptom onset, start steroids:
- 60mg Pred for 5/7 then taper by 10mg per day (total course 10 days)
OR
50mg Pred for 10/7

Advise:
artificial tears / lubricants
taping eye closed with microporous tape during the night if can’t close eye
using sunglasses

REFER IF
- Nil improvement after 3 weeks
- Incomplete resolution by 3 months
- Atypical features
- New neurological symptoms develop

17
Q

Which patients with a head injury need to be referred to A&E for assessment?

A

Glasgow coma scale (GCS) less than 15
Any loss of consciousness
Any focal neurological deficit
Any signs of skull fracture
Persistent headaches
Vomiting episodes
Any seizures
History of previous neurosurgery
High-energy head injuries (fall of > 1m, or over 5 stairs or those attained during a significant RTA)
History of bleeding/clotting disorders
Current anticoagulation therapy
Current drug or alcohol intoxication
Safeguarding concerns
Ongoing clinical concerns