FP 4: Trigeminal Neuralgia Flashcards

1
Q

What is Neuralgia?

A
  • intense stabbing pain
  • pain is brief but may be severe
  • pain extends along course of affected nerve
  • usually caused by irritation/ damage to nerve
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2
Q

What nerves are involved?

A
  • trigeminal
  • glossopharyngeal and vagus
  • nervus intermedius
  • occipital
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3
Q

Epidemiology of TN

A
  • 4.3: 100000 population in usa
  • more F > M
  • usually elderly patients
  • 60 yrs and above
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4
Q

Causes of Trigeminal neuralgia

A
  • idiopathic
  • classical: vascular compression of trigeminal nerve
  • secondary: multiple sclerosis, space-occupying lesions, skull base bone deformity, CT disease, arteriovenous malformation
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5
Q

Presentation of TN

A
  • unilateral maxillary/ mandibular division pain > ophthalmic division
  • stabbing pain
  • 5-10s duration
  • Triggers: cutaneous, wind, cold, touch, chewing
  • purely paroxymal/ with concomitant continuous pain
  • remissions and relapse
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6
Q

TN on continuum with other cranial nerve pain disorders

A
  • acute spasms of sharp shooting pain
  • may be more than on division
  • bilateral
  • burning component
  • vasomotor component
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7
Q

How does a typical pt with TN present

A
  • older pt, >60
  • mask like face
  • having excruciating pain
  • no obvious precipitating pathology
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8
Q

TN Red Flags

A
  • younger patient >40
  • sensory deficit in facial region
  • hearing loss acoustic neuroma
  • other cranial nerve lesions
  • always test for cranial nerves to identify sensory deficit
  • all patients now get MRI
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9
Q

Medications for TN

A

First line
- Carbamazepine: modified release
- Oxcarbamazepine
- Lamotrigine (Slow onset)

Second line
- Gabapentin
- Pregabalin
- Phenytoin
- Baclofen

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10
Q

Management of TN

A
  • should be responsive to Carbamazepine if tolerated
  • maximise efficacy and minimise side effects
  • often difficult to control pain first thing in the morning
  • pain diary to identify modifications neccessary to therapy
  • responsive to LA
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11
Q

Side Effects of Carbamazepine

A

Blood dyscrasias
- Thrombocytopenia
- Neutropenia
- Pancytopenia

Electrolyte imbalance
- Hyponatraemia (a lower than normal level of sodium in the bloodstream)

Neurological deficits
- Paraesthesia
- vestibular problems

Liver toxicity
Skin reactions

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12
Q

Should you prescribe Carbamazepine in GDP?

A
  • BNF dental preparations
  • SDCEP guidelines
  • Expertise
  • have facilities to monitor toxicity
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13
Q

Surgery indications for TN

A
  • usually not recommended if patient managing on medical therapy with moderate drug dose and no significant side effects
  • only consider when approaching maximum tolerable medical management
  • consider when young patients with significant drug use
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14
Q

Surgical options for TN

A
  1. Microvascular decompression (MVD)
    - preferred surgical treatment
    - requires a vessel impinging on TN root
    - 12 months; 1% mortality, 10% morbidity
  2. Destructive Central procedures
    - radiofrequency thermocoagulation
    - retrogasserian glycerol injection
    - balloon compression
    - 9 months; 2% mortality
  3. Sterotactic radiosurgery
    - gamma knife
    - targeted radiation at trigeminal ganglion to kill trigeminal nerve cells
  4. Destructive Peripheral Neurectomies
    - only performed as a last resort after trial local anesthesia
    - 6 months pain free without medication
    - can result in allodynia as well as TN
  5. Glycerol injection
  6. Balloon compression
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15
Q

Complications after surgery

A
  • local effects: peripheral treatments (cryotherapy)
  • sensory loss: corneal reflex, general sensation, hearing loss
  • motor deficit
  • may be reversible/ irreversible
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16
Q

Causes of Painful Trigeminal Neuropathy

A

Causes
- Herpes Zoster Virus (active VZV infection, post herpetic neuralgia)
- Trauma (develops < 6 months after traumatic event)
- idiopathic

17
Q

Characteristics of painful trigeminal neuropathy

A
  • pain is localised to distribution of TN
  • burning/ squeezing/ pins and needles
  • primary pain is usually continuous/ near- continuous
  • superimposed brief pain paroxysms may occur
  • commonly accompanied by clinically evident cutaneous allodynia and/ or sensory deficits
18
Q

Trigeminal Autonomic cephalalgias

A
19
Q

Cluster headache vs Paroxysmal vs SUNCT

A
20
Q

Cluster headache

A
  • mainly orbital and temporal
  • attacks are unilateral
  • rapid onset
  • duration: 15 mins to 3 hours; majority 45-90 mins
  • rapid cessation of pain
  • excruciating severe headache
  • prominent ipsilateral autonomic symptoms

Migraine symptoms often present
- tiredness and yawning
- nausea, vomitting, photophobia, phonophobia
- aura in 14%

21
Q

Extra about cluster headaches (the bout)

A

-

22
Q

Paroxysmal Hemicrania

A

Pain: mainly orbital and temporal

  • attacks are unilateral
  • rapid onset
  • duration: 2-30 mins
  • rapid cessation of pain
  • frequency: 2-40 attacks per day (no circadian rhythm)
  • excruciating severe
  • 50% are restless and agitated during attack
  • prominent ipsilateral autonomic symptoms
  • 10% attacks may be precipitated by bending or rotating head
  • 80& have chronic PH, 20% episodic
  • absolute response to indometacin
23
Q

Drug therapy for Cluster headache (Abortive- attack)

A
  • subcutaneous sumatriptan 6mg or nasal zolmatriptan 5mg
  • 100% oxygen 7-12l/min via a non- rebreathing mask (effective and safe)
24
Q

Drug therapy for cluster headaches (Abortive- bout)

A
  • occipital depomedrone/ lidocaine injection
  • tapering course of oral prednisolone
25
Q

Preventative therapy for CH

A
  • Verapamil (high doses)
  • Lithium
  • Methysergide (retroperitoneal fibrosis)
  • Topiramate
26
Q

Drug management for Paroxysmal Hemicrania

A
  • no abortive tx
  • prophylaxis with indomethacin
  • Alternatives: COX-II inhibitors, Topiramate