W16 61 neurological disease Flashcards

1
Q

What diseases classify as neurological diseases?

A

Epilepsy
Stroke
Multiple sclerosis (MS) and motor neurone disease (MND)
Headache, neuralgia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is a seizure?

A

A rapid and uncoordinated electrical firing in the brain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the types of seizures?

A

Provokes - cause for the seizure, eg high fevers, alcohol, drug withdrawal, low blood sugar
Unprovoked - spontaneous, or more than 7 days after an acute injury or insult such as stroke or brain haemorrhage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is epilepsy?

A

Disease of the brain defined by either:
- at least 2 unprovoked (or reflex) seizures occurring more than 24hrs apart
- 1 unprovoked (or reflex) seizure and a probability of further seizures similar to the general recurrence risk (at least 60%) after 2 unprovoked seizures occurring over the next 10 years

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the different types of epileptic seizure?

A

Focal, generalised, unknown onset

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is a focal onset seizure?

A

Seizures start in, and affect, one part of the brain
Can be aware or unaware, motor onset or non-motor onset (with or without physical movement)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is a generalised onset seizure?

A

Seizures start in, affect both sides of the brain at once and happen without warning.
Can be motor or non-motor.
Can be unknown onset in the brain or unclassified.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are some features of specific seizures?

A

Tonic seizure - short-lived (<1min), abrupt, generalised muscle stiffening with rapid recovery
Generalised tonic-clonic seizure - generalised stiffening and subsequent rhythmic jerking of the limbs, urinary incontinence, tongue biting
Absence seizure - more common in children, brief, sudden lapses of consciousness (look like daydreaming)
Atonic seizure - sudden onset of loss of muscle tone
Myoclonic seizure - brief, ‘shock-like’ involuntary single or multiple jerks

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What things are needed to diagnose epilepsy?

A

Blood glucose - first test
Blood test
CT head - to rule out intracranial pathologies eg brain haemorrhage or space occupying lesions like trauma
Electroencephalogram (EEG)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is the blood test done for epilepsy?

A

Sodium imbalance, uraemia, or other metabolic abnormalities
Evaluate for evidence of systemic or central nervous system (CNS)
Toxicology screen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What does an EEG show for epilepsy results?

A

Done last. Picks up uncoordinated signals in the brain.
Indicated after unprovoked seizure event
Can support diagnoses of generalised or focal onset epilepsy
Negative result does not mean pt does not have the disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What medical history in dental practice should you take for epilepsy?

A

Frequency of seizures and how they are controlled
Ask about triggers
Know the emergency drug box
Protect the airways
Take alcohol intake and drug intake
Alcohol increases risks of attack
Check post-seizure - check airway for tongue swelling, sublingual haematoma etc

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What should you do (less than 5 mins) for people having a tonic-clonic seizure?

A

Protect them from injury
Do not restrain them or put anything in their mouth
Monitor for 5 mins
If seizure stops, check their airway and place them in the recovery position
Observe them until they have recovered
Send them to A&E if this is their first seizure or there is breathing difficulty or altered consciousness level

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What should you do for people having a tonic-clonic seizure lasting more than 5min, or who have more than 3 seizures in 1 hour?

A

Buccal midazolam - first line
Rectal diazepam if this not available
Intravenous lorazepam if intravenous access is already established and resuscitation facilities are available - if your practice has the facilities or you are in a hospital setting
Call an ambulance for urgent hospital admission if seizures do not respond properly to treatment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What anti-epileptic drugs are there?

A

Valproic acid - gingival hyperplasia
Lamotrigine
Topiramate
Carbamazepine
Levetiracetam

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is stroke?

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What causes strokes?

A

85% - ischaemic (caused by thrombus)
15% - haemorrhagic (caused by blood vessel damage)
(Stroke increases the risk of more neurological events)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is a transient ischaemic attack (TIA)?

A

A transient (less than 24hrs) neurological dysfunction.
Caused by focal brain, spinal cord or retinal ischaemia, without evidence of acute infarction.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

How do you recognise a TIA?

A

Focal neurological deficit (resolves within 1hr but can persist for upto 24)
Unilateral weakness or sensory loss
Dysphasia - problems with speech
Ataxia, vertigo or loss of balance
Syncope
Sudden transient loss of vision in one eye, aplopia or homonymous hermianopia (loss of visual fields)
Cranial nerve defects

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

How do you recognise stroke?

A

Focal neurological deficit
Confusion
Headache - intracranial haemorrhage and subarachnoid haemorrhage. Usually sudden to set, gradual increase in intensity and failure to respond to pain relief.
Visual disturbances
Gaze paresis - often horizontal and unidirectional
Photophobia
Dizziness, vertigo or loss of balance
Nausea and/or vomitting - usually associated with intracranial pressure and haemorrhagic stroke
Specific cranial nerve deficits such as unilateral tongue weakness or Horner’s syndrome (miosis, ptosis, and facial anhidrosis)
Difficulty with fine motor coordination and gait
Neck or facial pain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

How do you manage stroke in dental practice?

A

A-E approach - oxygen, check glucose, reassurance, CPR if needed
Call an ambulance - tell them time of onset: FAST:
Facial weakness - can person smile, has their mouth or eye dropped
Arm weakness - can the person raise both arms
Speech problems - can the person speak clearly and understand what you say?
Time to call 999 - stroke is a medical emergency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

How do you manage stroke/TIA (specialists)?

A

Stroke team review immediately upon arrival
Offer aspirin (300mg daily), unless contraindicated, to people who have had a suspected TIA, to be started immediately
Perform brain imaging immediately with a non-enhanced CT
Thrombolysis with alter place for people with acute ischaemic stroke - within 4.5hrs of onset of stroke symptoms
Thrombectomy - aspirin and anticoagulant treatment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

What do patients who have had a stroke take in the long term?

A

Long-term anticoagulant and anti-platelets
(Increases risks of bleeding)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

When should you call an ambulance if you suspect a stroke?

A

Immediately

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

What are the issues for dentists with post-stroke patients?

A

Communication
Manual dexterity and mobility - oral hygiene and access of dental care

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

What is multiple sclerosis (MS)?

A

An acquired immune-mediated inflammatory condition of the central nervous system. Causes demyelination, gliosis and secondary neural damage throughout the CNS.
Can affect nearly any part of the CNS.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

What are the 3 main patterns of MS?

A

Relapsing-remitting MS (RRMS) - most common
Secondary progressive MS (SPMS)
Primary progressive MS (PPMS)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

What is relapsing remitting MS?

A

Episodes of exacerbations of symptoms (relapses) are followed by recovery (remissions) and periods of stability

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

What is secondary progressive MS?

A

A gradual accumulation of disability unrelated to relapses, which become less frequent or stop completely.

30
Q

What is primary progressive MS?

A

In PPMS there is a steady progression and worsening of the disease from the onset, without remissions

31
Q

What is the presentation of MS?

A

Depends on which nerve is affected first
Optic neuritis = inflammation of optic nerve
Loss or reduction of vision in one eye with painful eye movements
Problems telling colour
Diplopia
Ascending sensory disturbance and/or weakness
Problems with speech
Transverse meilitis = focal inflammation within the spinal cord
Balance or gait problems, unsteadiness, or clumsiness
Altered sensation radiating down the back and sometimes into the limbs on neck flexion (Lhermitte’s syndrome)
Diagnosis of MS is made by a consultant neurologist
Finger nose test might be negative

32
Q

How do you treat MS?

A

No cure and unpredictable, lack of evidence of long-term benefit of treatments

33
Q

What is the general management for MS?

A

Lifestyle: exercise, don’t smoke, ensure conditions like depression, anxiety and vascular risk factors are well controlled
Pregnancy advise: relapse might reduce during pregnancy and increase 3-6months post-partum before returning to pre-pregnancy rates.

34
Q

How do you manage a relapse of MS?

A

Short courses of high-dose corticosteroids - oral methylprednisolone
Social need and hospital admission
Significant recovery can be expected within 2-3months, improvement can continue for upto 12months

35
Q

What is motor neurone disease (MND)?

A

A rare condition that progressively damages motor neurones of the nervous system

36
Q

What is ALS?

A

Amyotrophic lateral sclerosis (ALS) is the most common form of motor neurone disease (MND).
Progressive muscle weakness that can start in limb, axial, bulbar or respiratory muscles and then generalised relentlessly, causing progressive disability and ultra intent death, usually from respiratory failure.

37
Q

How does MND present - early?

A

Limb-onset - weakened grip, can’t lift arms/shoulders
Bulbar-onset
Respiratory onset

38
Q

How does MND present - advance symptoms?

A

Speech and swallow difficulties, muscle weakness, reduced saliva, excessive yawning, emotional changes, difficulties with concentration/planning/communication
Sometimes misdiagnosed as stroke or obstruction in throat

39
Q

How does MND present - end-stage?

A

Paralysis
Respiratory failure

40
Q

How do you treat MND?

A

No cure but can delay progression and manage symptoms

41
Q

How do you manage MND?

A

Medication: riluzole
Multidisciplinary approach - neurologist and specialist nurse, speech and language therapist, dietician, respiratory physician, mental health

42
Q

How do you manage MS and MND in dental practice?

A

Difficult management
Modified oral hygiene regime due to reduced manual dexterity
All biological disease modifying therapies have an increased risk of common and serious infections, including bacterial, fungal and viral infections.
Refer to special care service is unable to treat in a dental practice

43
Q

What is trigeminal neuralgia?

A

A facial pain syndrome in the distribution of more than or equal to 1 division of the trigeminal nerve. Thought to be caused by vascular compression of the trigeminal nerve,

44
Q

How do you diagnose trigeminal neuralgia?

A

History: paroxysms of sharp, stabbing, intense pain lasting upto 2 minutes.
Can be associated with cold air, shaving

45
Q

How do you exclude other causes of pain than trigeminal neuralgia?

A

Dental x-rays
TMJ examination
Ear, nose, throat infection
Assess for sensation and motor changes +/- MRI, malignancy?

46
Q

What is the first line and second line pain relief for trigeminal neuralgia?

A

Carbamazepine - anticonvulsant that can achieve pain control, but can lose efficacy after a while. First line.
Second line - gabapentin or pregabalin

47
Q

What other procedures can be done to aid the pain from trigeminal neuralgia?

A

Percutaneous procedures - targeting Gasserian ganglion to cause delivery damage to nerve and stop signal passing through.
Surgical therapy (no guarantee will work). Eg micro vascular decompression, cryotherapy.

48
Q

How do you manage severe TN in hospital?

A

Long acting local anaesthetics such as bupivicaine

49
Q

Once you have excluded dental causes of facial pain like TMD, dental infection and pulpitis, who do you refer to?

A

OMFS, TN specialist service, neurology team

50
Q

What are some common headaches? IMG PG566!

A

Tension headaches
Migraine
Cluster headaches

51
Q

What are some rare but important causes of headache?

A

Raised intracranial pressure
Temporal arteritis

52
Q

What are some features of a tension headache?

A

Dull, non-pulsatile, bilateral, constricting pain (not severe
Pericranial tenderness
Stress and mental tension
Can be either episodic or chronic

53
Q

What is treatment for a tension headache?

A

Simple analgesic, eg paracetamol
Non-pharmacological: relaxation, CBT, physiotherapy.

54
Q

What is a migraine?

A

A chronic, episodic, neurological disorder
Strong genetic component
Diagnosis is clinical

55
Q

Symptoms of a migraine

A

Intermittent headache
Associated symptoms, such as visual disturbance, nausea, vomiting, and sensitivity to light or noise (photophobia and phonophobia)

56
Q

What is treatment for a migraine?

A

Avoid triggers
NSAIDs used early
Paracetamol
Triptan for severe cases
Ergotamine

57
Q

What are cluster headaches?

A

The most common trigeminal autonomic cephalgia. Attacks of severe unilateral pain localised to the orbital, peri-orbital and/or temporal areas that last from 15-180mins.
Restless or agitated during attacks.

58
Q

What are risk factors for cluster headaches?

A

Male
Family history
Head injury
Cigarette smoking

59
Q

What is the treatment for acute cluster headaches?

A

Subcutaneous sumatriptan (without cardiovascular disease)
High flow oxygen
Non-invasive vagus nerve stimulation
Verapamil is considered first-line preventative therapy

60
Q

Summary of the different types of headaches

A

TABLE PG 567 READ!

61
Q

What are some red flag neurological conditions?

A

Raised intracranial pressure
Giant cell arteritis (GCA) - temporal arteritis

62
Q

What can raised ICP cause?

A

Subarachnoid haemorrhage
Subdural haematoma
Idiopathic intracranial hypertension (IIH)
Meningitis
Haemorrhagic stroke

63
Q

What is subarachnoid haemorrhage (SAH)?

A

A sudden, severe headache that peaks within 1-5mins and lasts more than an hour
Vomiting, photophobia
Non-focal neurological signs

64
Q

When does subdural haematoma usually happen?

A

In patients with a history of alcohol abuse, anticoagulants, frequent falls, seizure disorder

65
Q

What are the common symptoms of meningitis?

A

(commonly in HIV or immunocompromised)
Classic triad of fever, headache, stiff neck
Other symptoms include nausea, seizures focal deficits, rash etc
When patients become septic they also present with hypotension and altered mental status

66
Q

Some symptoms of haemorrhagic stroke?

A

Neurological deficit, nausea, vomiting, vertigo, altered mental status

67
Q

What is giant cell arteritis (GCA) or temporal arteritis?

A

A common form of vasculitis in people agesd 50 or older. Commonly affects extracranial branches of the carotid artery.
Can cause irreversible blindness

68
Q

What can GCA present with on examination”

A

Jaw claudication, diplopia, and an abnormal temporal artery on examination

69
Q

What should you do immediately if you suspect GCA?

A

Prednisolone should be started immediately if suspected GCA
Immediate referal to a specialist (eg rheumatology, ophthalmology, neurology)

70
Q

What is the diagnosis for GCA?

A

Blood test - CRP, ESR
Vascular ultrasonography
Temporal artery biopsy
High-resolution MRI of cranial arteries

71
Q

What will a specialist consider for patients with GCA who relapse?

A

Tocilizumab or methotrexate in combination with a glucocorticoid taper in patients with GCA who relapse