Bell's palsy Flashcards
Bells palsy: RFs, features, management, f/u and prognosis
Facial nerve paralysis - motor
RFs: 20-40y, pregnancy
Possible cause: HSV
Features:; unilateral (if bilateral needs urgent ENT referral)
- lower motor neuron facial nerve palsy - affectrs forehead (UMN spares upper face)
- post-auricular pain
- altered taste anterior 2/3 tongue
- dry eyes
**- hyperacusis ** - palsy of stapedius muscle, can’t dampen sound
Management:
1) Prednisolone within 72h of onset - 25mg BD for 10 days or 60mg OD for 5 days followed by daily reduction of 10mg (total - 10 days treatment)
2) Antivirals alone not recommended, may consider with specialist advice if severe
3) Eye care to prevent exposure keratopathy - artificial tears and lubricants and tape eye closed at night
4) **If recurrent - urgent ENT referral **
Follow-up:
- if no improvement in 3 weeks - urgent ENT referral
- if long standing weakness for several months - plastic surgery referral
Prognosis:
- most recover fullly within 3-4 months
- if untreataed 15% will have permanent moderate-severe weakness
Referral:
1) Urgent ENT if bilateral or recurrent or paralysis not improving at 3 weeks
2) Opthalmology if cornea remains exposed after attempting to close eyelid
If sensory and motor loss = facial nerve compression eg. parotid tumour or acoustic neuroma
Stongest risk factor for Bell’s Palsy
3x more likely in pregnancy
Guillain-Barre Syndrome
Immune mediated demyelination of peripheral nervous system triggered by infection (campylobacter jejuni)
Antu-GMI abs in 25%
Rapidly progresive symmetrical weakness of limbs - ascending
Reduced power, normal/mild sensory loss, reduced/absent reflexes
Additional symptoms: respiraotry muscle weakness, diplopia, BL facial nerve palsy, oropharyngeal weakness, urinary retention, diarrrhoea
Investigations:
1) Lumbar puncture - raised protein, normal WCC
2) Nerve conduction studies - redcued motor conduction
Miller-Fisher syndrome
Variant of GBS
Ophthalmoplegia, areflexia, ataxia
Eyes affected first
Descending paralysis (rather than ascending in other GBS)
Anti-GQ1b abs in 90%
Charcot-Marie Tooth
Most common hereditary peripheral neuropathy
Features:
1) History of frequently sprained ankles
2) Foot drop
3) High-arched feet - pes cavus
4) Hammer toes
5) Distal muscle weakness
6) Distal muscle atrophy
7) Hyporeflexia
8) Stork leg deformity
No cure - focus on physio and OT
Drugs that can cause peripheral neuropathy
1) Amiodarone
2) Isoniazid
3) Vincristine
4) Nitrofurantoin
5) Metronidazole
Neuropathic pain
DM neuropathy, post-herpetic neuralgia, trigeminak neuralgia, prolapsed disc
1st line: amitriptyline, duloxetine, gabapentin, pregabalin - all as monotherapy
Rescue therapy: tramadol
Localised neuropathic pain eg. post-hereptic neuralgia - topical capsaicin