trigeminal neuralgia and facial pain Flashcards

1
Q

what is TN?

A

> A disorder of the trigeminal nerve that consists of episodes of unilateral, intense, stabbing, electric shock-like pain in the areas of the face where the branches of the nerve are distributed.

> Universally considered to be one of the most painful afflictions known: tic doloreux

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2
Q

what are the subtypes of TN?

A
  1. Idiopathic without other disease/cause
  2. Classical: signs of trigeminal nerve root comression
  3. Secondary TN may occur in presence of organic disease such as =
    > Tumours of trigeminal nerve (neuromas)
    > Lesions affecting the trigeminal nerve at the cerebellopontine angle
    > MS or demyelination
    > Cerebral neoplasms
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3
Q

what causes Primary/ idiopathic/ classical TN?

A

> No clinically obvious neurological cause

> May be due to pressure on the trigeminal nerve root in the posterior cranial fossa from an adjacent vessel pressing on nerve root causing demyelination/neuronal discharge)-classical

> No predisposing factors but emotional or physical stress can increase frequency and severity of attacks

> No neurological deficit in Primary TN but 2TN needs to be excluded eg is there any sign of demyelination, any tumours?

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4
Q

what is mandatory if you suspect TN?

A

> MRI scan

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5
Q

how many people in the population are affected by primary TN?

A

> 4/ 100000

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6
Q

what is the pain history of TN?

A

> Sudden, sharp, severe stabbing pain

> Lasts few seconds to <2mins

> Attacks may be more common in the morning

> Occurs spontaneously but can be triggered by touch/movement of face: shaving, cold air

> Affects normally one branch of trigeminal nerve V1, V2, V3 and unilateral: if different to this ? secondary cause

> Entirely asymptomatic between attacks (rarely patients report dull ache at other times): atypical variant (read articles by P. Eldridge)

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7
Q

is TN bilateral or unilateral?

A

> unilateral

> does not cross the midline

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8
Q

is TN more common in males or females?

A

> females

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9
Q

when is the onset of TN?

A

> onset usually 50-70 years old

> if younger think of MS

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10
Q

does TN effect sleep?

A

> no. doesn’t disturb

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11
Q

what do patients tend to do when experiencing TN?

A

> bring there hands up to their face

> Mask like expression

> quality of life severely affected?

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12
Q

how do you diagnose TN?

A

> Based on history

> Neurological assessment (negative)

> rule out dental cause

> May identify trigger areas on examination

> Otherwise NAD

> Special investigations

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13
Q

what special investigations do you carry out to diagnose TN?

A

> MRI brain

> MR angiography can identify neurovascular compression of trigeminal nerve

> Trial of Carbamazepine

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14
Q

what is the treatment for TN?

A

> Carbamazepine 100mg bd for 2 weeks

> If pain control not achieved, increase to 100mg tds

> Can continue further staged increases of Carbamazepine, or consider Phenytoin, Baclofen, Gabapentin, Pregabalin, Lamotrigine

> Medical management successful in >80% of cases, most respond to low dose

> FBC,U&E, LFT initially and monitored (quite easy to cause a drug induced hepatitis, and hyponeutrimia)

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15
Q

what type of drug is carbamazepine?

A

> Anticonvulsant, not an analgesic

> Most patients respond to 200-400mg tds daily

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16
Q

do patients suffer from adverse affects with carbamazepine and if so what are they ?

A

> yes, adverse effects occur in up to one third of patients

> Ataxia
Drowsiness
Visual disturbance
Headache
GI upset
Folate deficiency
Hypertension
Rashes
Pancytopenia or, rarely, leucopenia (typically within first 3 months of treatment)

> common that patients have problems at the start by symptoms will go away after they get used to the drug

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17
Q

what should patients on carbamazepine be monitored on ?

A

> Blood pressure

> U&E

> LFT

> FBC (bone marrow function)

> Folate

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18
Q

what is an alternative for carbamazepine?

A

> Oxcarbazepine may be better tolerated: doses slightly different-see BNF

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19
Q

what are the examples of surgery for TN management in patients?

A
  1. Peripheral surgery
    - Cryosurgery of affected branch of nerve
    - Radiofrequency thermocoagulation
  2. Intracranial surgery
    - Microvascular decompression (Gold Standard) - pad goes in between the artery and the nerve
  3. Percutaneous surgery
    - Radiofrequency lesioning (risk of anaesthesia dolorosa)
  4. Stereotactic gamma knife radiosurgery
    - 80% pain control, takes 6 weeks to work
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20
Q

what is giant cell arteritis?

A

> Immunological/vasculitic condition in which there is inflammation of medium sized arteries especially in the head and neck

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21
Q

what are the symptoms of giant cell arteritis?

A

> Severe burning pain in distribution of the affected vessel – temporal, tongue or masticatory muscle region

> Headache is intense, deep, aching, throbbing, persistent

> May be worse when lying flat in bed

> Affected artery may be enlarged and tender

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22
Q

who does Giant cell arteritis tend to affect?

A

> affects older patients (>50)

> F>M

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23
Q

what are the associated symtoms of giant cell arteritis?

A

> May experience jaw claudication (pain on chewing)

> Can cause pain and necrosis in tongue or lip

> If retinal artery affected, risk of blindness-DO NOT MISS THIS!

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24
Q

how do you diagnose Giant cell arteritis?

A

> Clinical history

> Raised ESR

> Arterial biopsy (numerous giant cells, deranged internal elastic lamina)

> ultrasound - characteristic halo sign over the temporal artery

25
Q

what is the management of Giant cell arteritis?

A

> Systemic corticosteroids – Prednisolone 60mg daily (1mg/kg)

> quick treatment = stop the patient going blind

> Ref Rheumatology

26
Q

what is glossopharyngeal neuralgia?

A

> Similar condition to TN but rarer

> Severe paroxysmal pain in post tongue/tonsillar region

27
Q

where may the pain radiate to in glossopharyngeal neuralgia?

A

> the ear

28
Q

what triggers pain in glossopharyngeal neuralgia?

A

> swallowing

> coughing

29
Q

what has a similar presentation to glossopharyngeal neuralgia?

A

> similar presentation to nasopharyngeal malignancy

30
Q

how do you manage glossopharyngeal neuralgia?

A

> carbamazepine

31
Q

what is periodic migrainous neuralgia?

A

> “cluster headaches”

> Unilateral, excruciating pain in the maxilla or behind the eye, notably in the very early morning hours, occurring repeatedly over several days

> attacks often last 30-60mins, awaken from sleep and end suddenly

32
Q

what are examples of trigeminal autonomic cephalgias (TACS) ?

A

> Cluster headache, hemicrania, SUNCT, SUNA

> important to rule these out if thinking TN

> found in V1 area, forehead

> ask in pain history

33
Q

what are symptoms related to the autonomic nervous system?

A
  • redness in face, redness in eye, blurring of the eye, running of the nose
34
Q

who does periodic migrainous neuralgia affect?

A

> males > females

> middle age

35
Q

what is periodic migrainous neuralgia often accompanied with?

A

> Often accompanied by
- ipsilateral lacrimation
- conjunctival redness
- photophobia
- nasal stuffiness/rhinorrhoea

36
Q

what is the pathology behind cluster head aches?

A

> Vasodilation in extra cranial carotid arteries and increased hypothalmic activity

37
Q

what may attacks in cluster headaches be precipitated by?

A

> alcohol

> high altitudes

> hypoxia in REM sleep

38
Q

what is the management for cluster headaches when attack is coming on?

A

> neurolgy input needed

> Oxygen therapy (100% oxygen at 10-15 litres/min for 10-20mins)

> Sumatriptan (subcut or nasal spray)

39
Q

what is the prophylactic management of cluster headaches?

A

> Verapamil

> Nifedipine

> Ergotamine

> Lithium

40
Q

what is paroxysmal hemicranias?

A

> Frequent, short-lasting (few minutes) attacks of unilateral pain

41
Q

what is the difference between a paroxysmal hemicranias and a hemicrania?

A

> hemicrania is constant pains

42
Q

where does paroxysmal hemicranias usually affect?

A

Usually orbital, supraorbital or temporal region

43
Q

how many attacks a day are common for paroxysmal hemicranias?

A

> 5-40 attacks per day

44
Q

what are the associated symptoms of paroxysmal hemicranias?

A

> Conjunctival redness

> Rhinorrhoea

> Nasal congestion

> Lacrimation

> Ptosis

> Eyelid oedema

45
Q

what is the treatment for paroxysmal hemicranias?

A

> indometacin (NSAID)

> (if happy with diagnosis you carry out a trial with this)

46
Q

what is persistent idiopathic facial pain (PIFP)?

A

> A constant chronic orofacial discomfort or pain, for which no organic cause can be found

47
Q

who does PIFP commonly affect?

A

> Affects 1-2% of population

> Older females (70%)

48
Q

what are the symptoms of PIFP?

A

> Pain poorly localised

> Objective signs absent

> Often multiple oral and/or other psychogenic related symptoms

> Deep, dull, boring pain

> Persists for most or all of day

> Doesn’t disturb sleep

49
Q

does PIFP respond to treatment well?

A

> no, poor response

> Psychogenic origin – many patients have history of depression

50
Q

what is PIFP also referred to as?

A

> atypical facial pain

51
Q

where is the pain usually found in PIFP

A

> Usually upper jaw pain, unrelated to distribution of trigeminal nerve (may cross midline)

52
Q

how do you diagnose PIFP?

A

> clinical history

> Diagnosis made by exclusion of organic disease

> patients often have not tried simple analgesics to control pain

53
Q

what is the management of PIFP?

A

> Amitriptyline/Nortriptyline, Duloxetine, Pregabalin, Gabapentin

> Cognitive behavioural therapy (if they show a low mood)

54
Q

what is a migraine?

A

> Recurrent, incapacitating, unilateral headaches

> Usually supraorbital

> Last hours/days

> Spontaneous remission not uncommon

55
Q

who is affected by migraines?

A

> Common problem

> F>M

> middle age

56
Q

what are some associations of migraines?

A

> Nausea/vomiting/photophobia

57
Q

what causes migraines?

A

> Serotonin release – cerebral artery dilatation – increased midbrain grey matter metabolic activity

> Attacks may be precipitated by stress, alcohol, ripe bananas, chocolate, OCP

> May have preceding warning symptoms (aura) – lights, smells, etc.

58
Q

how do you diagnose migraines?

A

> clinically

59
Q

what is the treatment for migraines?

A
  1. Aspirin/Paracetamol/NSAID
  2. Lysine acetylsalicylate with metoclopramide in acute attacks (MigraMax)
  3. Sumatriptan
  4. Prophylaxis: usually NSAID but can use =
    - Pizotifen
    - Propranolol
    - Tricyclics
    - Sodium valproate
    - Gabapentin
  5. Botulinum toxin (BOTOX) (NICE guidelines)