Betahistine for Menière's Disease
Direct Recommendation
Start betahistine 48 mg daily (24 mg twice daily or single modified-release tablet) for maintenance therapy in patients with definite or probable Menière's disease, continuing for at least 3 months with reassessment at 6-9 months, though be aware that the highest quality evidence (BEMED trial) shows no significant benefit over placebo. 1
Critical Evidence Caveat
The American Academy of Otolaryngology-Head and Neck Surgery explicitly states they cannot make a definitive recommendation for betahistine due to conflicting evidence. 1, 2 The most recent high-quality BEMED trial found no significant difference between betahistine and placebo in reducing vertigo attacks over 9 months. 1, 2 Despite this, betahistine remains widely used and may be offered as maintenance therapy with appropriate patient counseling about uncertain efficacy. 3, 1
Diagnostic Confirmation Required
Before prescribing betahistine, confirm the patient meets criteria for definite Menière's disease: 2 or more episodes of vertigo lasting 20 minutes to 12 hours PLUS fluctuating or nonfluctuating sensorineural hearing loss, tinnitus, or pressure in the affected ear. 3 For probable Menière's disease, vertigo episodes may last up to 24 hours. 3
Ensure true rotational vertigo (spinning sensation) rather than vague dizziness or lightheadedness, as betahistine is indicated specifically for vestibular disorders. 1
Absolute Contraindications
Never prescribe betahistine in patients with pheochromocytoma. 3, 1, 2
Relative Contraindications and Cautions
Use betahistine cautiously in patients with: 3, 1, 2
- Active asthma
- Active peptic ulcer disease
- History of peptic ulcer disease
Dosing Protocol
Initial dose: 48 mg daily, administered as either 24 mg twice daily or a single 48 mg modified-release tablet. 1
Duration: Minimum 3 months to properly evaluate therapeutic efficacy. 1
Reassessment timeline: Evaluate response at 6-9 months. 1 If no improvement occurs by 6-9 months, discontinue betahistine as continued therapy is unlikely to provide benefit. 1
Higher doses: 144 mg/day shows no advantage over the standard 48 mg/day dose. 1
Expected Outcomes and Monitoring
Document changes in: 3
- Vertigo frequency and severity
- Tinnitus
- Hearing loss
- Aural fullness
- Quality of life measures
Consider obtaining follow-up audiograms to monitor hearing function. 3
Italian consensus experts (87% agreement) consider betahistine useful for reducing dizziness and vertigo during the intercritical phase of disease, but less effective during acute attacks. 4
Common Side Effects
- Headache
- Balance disorder
- Nausea
- Upper gastrointestinal symptoms
- Nasopharyngitis
- Feeling hot
- Eye irritation
- Palpitations
Alternative and Adjunctive Treatments
For acute vertigo attacks: Offer a limited course of vestibular suppressants (medications with direct antiemetic effects like prochlorperazine are preferred over betahistine for acute episodes). 3, 1
Combination therapy: Intratympanic steroids combined with oral betahistine may improve vertigo control (73% improvement versus 44% without betahistine). 5, 1
Alternative maintenance therapy: Diuretics may be offered as an alternative or in addition to betahistine. 3
For refractory disease: Intratympanic gentamicin provides 70-87% complete vertigo control, though with 12.5-15.4% risk of hearing loss. 5, 1 Titration therapy with gentamicin achieves 81.7% vertigo control. 5
Vestibular rehabilitation: Consider for patients who have failed less definitive therapy and have nonusable hearing. 3
Important Clinical Pitfalls
Do not use betahistine for benign paroxysmal positional vertigo (BPPV) - this is a different condition requiring different treatment. 3
Screen for vestibular migraine: This commonly mimics Menière's disease. 5 Vestibular migraine patients may describe "hearing loss" as difficulty processing sound rather than hearing it, often have bilateral auditory complaints, and experience visual auras, motion intolerance, and light sensitivity. 5 Vertigo duration in vestibular migraine may be shorter (<15 minutes) or longer (>24 hours) than typical Menière's attacks. 5
Patient preference is critical given the uncertain evidence for benefit. 3, 2 Discuss the conflicting evidence openly with patients before initiating therapy.