Neurology- core conditions Flashcards

1
Q

Parkinsons disease

A

Caused by the loss of dopaminergic neurones in the substantia nigra of the basal ganglia. The basal ganglia is essential for coordinating movement

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2
Q

Symptoms of parkinsons disease

A

• Bradykinesia- slow movement
• Tremor- rest, postural
• Rigiditity- cog wheeling, lead pipe
• Postural instability- late feature
• Early features- loss of sense of smell, REM sleep behaviour disorder, constipation, depression and anxiety
• Late complications- bladder and blood pressure problems, pyschosis and dementia

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3
Q

Differentials for Parkinsons disease

A

• Essential tremor
• Drug induced parkinsonism
• Dementia with Lewy bodies, multiple system atrophy, progressive supranuclear palsy, corticobasal degeneration
• Alzheimer’s and multiple cerebral infarctions

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4
Q

Clinical examination- Parkinsonian gait

A

• Stooped posture
• Forward flexion of the trunk and the knees
• Arms flexed at the elbows and wrists
• Known as shuffling gait due to small and fast steps
• Difficulty initiating turning around

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5
Q

Clinical examination- Parkinsonian tremor

A

• Resting tremor
• Pill rolling, looks like the patient is trying to roll a pill between their thumb and index finger
• 4-6Hz
• Asymmetrical, worse at rest
• Improves with movement
• No change with alcohol

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6
Q

Clinical diagnostic criteria
Step 1- diagnosis of Parkinsonian syndrome

A

• Bradykinesia
• At least one of muscle rigidity, resting tremor, postural instability

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7
Q

Clinical diagnostic criteria
Step 2- exclusion criteria for Parkinsons disease

A

• History of strokes/ head injury/ encephalitis
• Oculogyric crisis
• Neuroleptic treatment at onset of symptoms
• Sustained remission
• Cerebrallar signs
• Cerebral tumour

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8
Q

Clinical diagnostic criteria
Step 3- supportive positive criteria for Parkinsons disease

A

• Three or more are required alongside step one
• Unilateral onset
• Resting tremor present
• Disease is progressive
• Good response to levodopa

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9
Q

Parkinsons- investigations

A

DAT scan- less dye is taken up. Reduced uptake in the substantia nigra, particularly in the posterior part of the putamen. Motor symptoms begin in stage 4
MRI/CT- to rule out other things
Bedside- physical examination, anosmia testing
Bloods

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10
Q

Management plan- Parkinsons

A

First line treatment- levodopa. Addition of a dopamine agonist/ MAO-B inhibitor as an adjunct if motor symptoms are not controlled

Supportive therapies- include physiotherapy/ occupational therapy/ speech and language therapy/ diet advice

Can give deep brain stimulation

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11
Q

Levodopa

A

Usually combined with carbidopa to prolong action (peripheral inhibitor of dopamine metabolism). Side effects include dyskinesia when doses are high, impulsive behaviour, NV, loss of appetite, hypotension. Becomes less effective over time

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12
Q

Dyskinesia with levodopa (defenitions)

A

• Excessive motor activity when the dose is too high
• Dystonia - excessive muscle contraction leading to abnormal postures and movements
• Chorea - abnormal involuntary movements that are jerky and random
• Athetoid - involuntary twisting or writhing movements typically of the fingers / feet / hands

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13
Q

Dopamine agonists

A

• Stimulate dopamine receptors in the basal ganglia
• Side effects include pulmonary fibrosis / dizziness / drowsiness / tachycardia / dry mouth / NV / memory, concentration and confusion problems
• Usually used to delay the use of levodopa and then used in combination with levodopa to reduce the dose needed
• They increase impulsivity, shows as disinhibited behaviours i.e. gambling and hypersexuality
• E.g. pramipexole, ropinirole, bromocriptine

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14
Q

Monoamine oxidase B inhibitors

A

• These block the affects of monoamine oxidase B (an enzyme which breaks down dopamine)
• Used to delay the use of levodopa and used to reduce the required dose
• For example, Selegiline, Rasagiline

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15
Q

COMT inhibitors

A

• COMT metabolises levodopa, the inhibitors slow this down and extends the effect of levodopa
• For example, Tolcapone, entacapone

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16
Q

Multiple system atrophy

A

• Progressive degeneration of the neurones in multiple brain areas e.g. basal ganglia, cerebellum, autonomic and peripheral nervous system
• Basal ganglia degeneration leads to parkinsonian presentation but there are also other symptoms e.g. a lot of autonomic dysfunction causing hypotension/incontinence/impotence/sexual dysfunction etc
• Also profound cerebellar dysfunction
• Parkinsons with autonomic disturbance e.g. atomic bladder/postural hypotension points towards MSA

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17
Q

Progressive supranuclear palsy

A

• Rapidly progressive neurological disease characterised by accumulation of tau protein in basal ganglia, brainstem, prefrontal cortex, and cerebellum
• Symptoms include difficulty moving eyes, mood changes, dysphagia, backwards falls, slurred speech, memory loss, apraxia, resting tremor
• Involves psudeobulbar palsy (dysarthria and dysphagia)
• Bradykinesia, Backwards falls, Slow vertical saccades, Loss of a vertical gaze

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18
Q

Dementia with Lewy bodies

A

• Dementia associated with features of Parkinson’s disease - the parkinsonian features develop after the memory loss
• Other features = visual hallucinations / delusions / disorders of REM sleep / fluctuating consciousness

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19
Q

Neuroleptic malgnant syndrome

A

Life threatening muscle rigidity, fever and rhabdomyolysis in response to antipsychotics

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20
Q

Stroke

A

A clinical syndrome of presumed vascular origin characterised by rapidly developing signs of focal or global disturbance of cerebral functions which lasts longer than 24 hours or leads to death.

Types of stroke- Haemorrhagic (15%), Ischaemic (85%)

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21
Q

Types of stroke

A

Ischaemic- due to occlusion of arteries of cerebral circulation, normally due to an embolism as a result of atrial fibrillation

Haemorrhagic- a collection of blood from a blood vessel rupture.

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22
Q

Stroke risk factors (conditions)

A

• Ischaemic heart disease
• Peripheral arterial disease
• Carotid atherosclerosis -> carotid stenosis
• TIA
• Vascular heart disease and heart failure
• Clotting disorders
• Atrial fibrillation

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23
Q

Stroke symptoms

A

• Sudden onset
• F- face may have drooped to one side
• A- weakness or numbness in one arm
• S- speech may be slurred or cant speak
• T- call 999 immediately

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24
Q

Diagnosing a stroke

A

Diagnose with ROSIER score
Exclude hypoglycaemia in people with sudden onset neurological symptoms as the cause

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25
Q

Stroke- investigation findings

A

• CT head within an hour, possibly a CT angiogram
• Check blood pressure to look for hypertension
• ECG to look for atrial fibrillation (AF)
• Blood tests in order to check lipids, blood sugar, FBC and clotting
• Carotid duplex ultrasound to look for atherosclerotic plaque if its an anterior circulation stroke
• Echocardiogram to check for a clot in ventricles caused by AF

26
Q

Stroke- thrombolysis treatment

A

• Recombinant Tissue Plasminogen Activator- rTPA (alteplase)
• 0.9mg/kg (max 90mg)- 10% bolus and 90% infusion over 1 hour
• Medically: tPA (intravenous tissue plasminogen activator)
• NIHSS >4
• Administer within 4.5 hrs
• The earlier tPA is administered, the higher the likelihood of a positive neurologic outcome
• Activates blood clot removal system, restores blood supply, reducing the number of dead neurons
• Adverse outcome- intracerebral haemorrhage

27
Q

Absolute contraindications for tPA

A

• Major surgery in last 14 days
• GI or urinary tract bleeding in last 21 days
• Stroke < 3 months ago
• Platelets <100
• Symptoms suggestive of subarachnoid bleed (even if CT Head clear)
• BP greater than >185 systolic or >110 diastolic unresponsive to medical treatment
• INR >1.7 or NOAC (novel oral anticoagulant) within 24-48 hours

28
Q

tPa relative exclusion criteria

A

• Minor stroke symptoms or rapidly resolving symptoms
• Major surgery or trauma in the last 14 days
• GI or GU bleeding in last 14 days
• MI in last 3 months
• Seizure at onset of stroke symptoms
• Pregnancy

29
Q

Endovascular treatment for stroke

A

The clot is caught in a stent and removed, used for moderate to severe stroke when there is large vessel occlusion. Must be administered within 6 hours, can follow tPa or be done when its contraindicated.

30
Q

Relative exclusion criteria for EVT

A

• Minor stroke symptoms or rapidly resolving symptoms
• Major surgery or trauma in the last 14 days
• GI or GU bleeding in the last 21 days
• MI in last 3 months
• Seizure at onset of stroke symptoms
• Pregnancy

31
Q

Stroke medication

A

• Aspirin (300mg daily) for two weeks, offer a PPI as well if they have dyspepsia
• Clopidogrel (75mg)

DVLA states no driving for a month after a stroke
Stop anticoagulation treatment in people with haemorrhagic stroke. Reverse the effects of warfarin through prothrombin complex concentrate and intravenous vitamin K.

32
Q

TIA

A

Transient (less than 24 hours) neurological dysfunction caused by focal brain ischaemia without evidence of acute infarction. Tends to last less than an hour.
Give aspirin (300mg daily)
MRI can show extent of ischaemia

33
Q

Meningitis

A

Inflammation of the meninges

Causes- most commonly Neisseria meningitidis or streptococcus pneumonia. In children/neonates its normally group B strep/ E.coli. Can also be viral/fungal. Neisseria meningitidis is a gram negative diplococci.

34
Q

Symptoms of meningitis

A

• Neck stiffness
• Photophobia
• Non-blanching rash
• Severe headache
• Fever
• Neurological deficits e.g. seizures / difficulty concentrating
Vomiting

35
Q

Meningitis- Kernigs test

A

• Patient is supine
• Their leg is passively flexed 90 degrees with the hip and knee flexed
• The knee is then extended
• This will stretch the meninges and lead to pain = positive test

36
Q

Meningitis- Brudzinskis test

A

• Patient is supine
• Head of the patient is passively flexed
• This stretches the meninges and spinal cord
• If positive this causes the patient to flex their hip and knees due to the neck stiffness

37
Q

Meningitis diagnosis

A

Bedside- Kernigs and Brudzinski. Lumbar puncture (definitive diagnosis)
Bloods- Blood cultures, FBC, UE, clotting, glucose, ABG
Imaging- CT for unclear diagnosis

38
Q

Meningitis diagnosis

A

Bedside- Kernigs and Brudzinski. Lumbar puncture (definitive diagnosis)
Bloods- Blood cultures, FBC, UE, clotting, glucose, ABG
Imaging- CT for unclear diagnosis

39
Q

Lumbar puncture results

A

• Cloudy/ pink/ yellow- bleeding
• Green- bilirubin
• Elevated protein- inflammatory condition/infection
• Elevated white blood cells- infection
• Low glucose- infection with bacteria

40
Q

Treatment for bacterial meningitis

A

• Urgent IV antibiotics e.g. ceftriaxone for 7 days
• Monitor and correct any hypoglycaemia / acidosis / anaemia / electrolyte disturbances
• Dexamethasone for 4 days to help reduce the inflammatory response and prevent long lasting neurological damage
Give IM benzylpenicillin prior to urgent hospital transfer

41
Q

Treatment for viral meningitis

A

• Usually self-limiting so requires just supportive treatment
• Can use acyclovir

42
Q

Meningitis prophylaxis

A

Ciprofloxacine single dos, given as soon as possible after exposure. Risk of devloping meningitis after exposure is 7 days

43
Q

Lumbar puncture contraindications

A

• Local skin infection
• Raised ICP - can cause brain herniation
• Suspicion of a mass
• Acute spinal trauma
• Anticoagulants
• Always do a CT head before lumbar puncture

44
Q

Fungal meningitis

A

Cryptococcus neoformans - typically found in immunosuppressed patients e.g. HIV / AIDS
CSF: clear/cloudy, elevated opening pressure, WBC elevated, low glucose and elevated protein

45
Q

Migraine symptoms

A

• Severe throbbing headache
• Usualy unilateral
• Sensitivity to light
• Nausea and vomiting
• Aura

Lasts from 4 hours to 3 days

46
Q

Phases of a migraine

A

• Prodrome- symptoms before the migraine i.e. stiff neck/ irritability/ tiredness/ food cravings
• Aura- Perceptual disturbances. 90% are visual i.e. fortification spectra/ scotoma. Lasts up to an hour. Can also be sensory i.e. paraesthesia
• Headache
• Postdrome

47
Q

Migraine diagnosis

A

At least 5 attacks lasting 4-72 hours with
• Nausea/vomiting
• Photo/phonophobia

And 2 of
• Unilateral headache
• Pulsating character
• Worsening by daily activities

48
Q

Acute management of migraine

A

• Analgesia e.g. paracetamol, NSAIDs and aspirin
• Antiemetics
• Triptans e.g. sumatriptan - take when the headache starts not during aura

49
Q

Migraines- prophylactic management

A

• Propranolol - CI asthma
• Topiramate i.e. anti-epileptic drug
• Antidepressants e.g. amitriptyline

50
Q

Tension headache

A

• Headaches caused by muscle contractions in the head and neck - associated with stress
• Mild/moderate pain
• Feels like a tight band around the head
• Tend to last 30 mins to 7 days

51
Q

Cluster headache

A

• Severe pain
• Unilateral pain around the eye / behind the eye
• Associated with ipsilateral autonomic symptoms e.g. rhinorrhoea / ptosis / eye watering
• ‘Suicide headache’
• Rapid onset
• Common in males and smokers
• Tends to last 15 mins to 3 hours

52
Q

Thunderclap headache

A

• Indicative of a subarachnoid haemorrhage
• Reaches peak intensity within 3 seconds
• Get nausea and vomiting, alongside meningitis like symptoms

53
Q

Giant cell arteritis

A

• Vasculitis of the extra cranial branches of the carotid artery, normally the temporal artery
• Symptoms- headache, scalp tenderness, jaw claudication, amorosis fugax and potential blindness, polymyalgia rheumatica i.e. shoulder/pelvic girdle pain
• Investigate with ESR, FBC, LFT
• Definitive investigation- temporal artery biopsy of 3-5cm
• Treat with high dose steroids i.e. 60mg OD prednisolone

54
Q

Headache red flags

A

• New severe/unexpected headache
• Progressive headache
• Associated features e.g. fever / seizure / neck stiffness / papilloedema / neurological deficits
• Contacts with similar symptoms
• Head trauma within the past 3 months
• Co-morbidity
• Pregnancy

55
Q

What blood tests correlates with seizure

A

Lactate
also dysregulated in sepsis

56
Q

Symptoms of space occupying lesion

A
  • Present on waking
  • Worse I’m bending and straining
57
Q

Meningitits- arterial blood gas reading

A

Shows metabolic acidosis

58
Q

Features of upper motor neurone lesions

A

Extensor plantar responses, increased muscle tone, spasticity

59
Q

Neurological symptoms- random

A

Echopraxia- the patient is imitating or copying what another person is doing

Inattention- a feature of non-dominant hemisphere lesions and patients will be noted to ignore their affected side

Perseveration- the patient keeps doing the same thing over and over again

Dyspraxia- inability to carry out a learned pattern of movement i.e. dressing

60
Q

Visual field defects

A

Optic nerve- Monocular vision loss

Optic chiasm- Bitemporal hemianopia. Most likely due to pituitary adenoma

Optic tract- homonymous hemianopia

Optic radiation- quandrantopia