What antiemetics are used in Multiple System Atrophy (MSA)?

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Last updated: October 22, 2025View editorial policy

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Antiemetics in Multiple System Atrophy (MSA)

For patients with Multiple System Atrophy experiencing nausea and vomiting, 5-HT3 receptor antagonists (such as ondansetron 8 mg once or twice daily) should be used as first-line antiemetic therapy, with metoclopramide as a second-line option at 5-20 mg doses, while carefully monitoring for extrapyramidal side effects.

First-Line Antiemetic Options

  • 5-HT3 Receptor Antagonists: These are preferred first-line agents due to their efficacy and lower risk of extrapyramidal side effects 1

    • Ondansetron: 8 mg oral/IV once or twice daily 2
    • Granisetron: 1-2 mg oral daily or 1 mg oral twice daily 1
    • Palonosetron: Single dose on day 1 only (longer-acting) 1
  • Corticosteroids: Can be used in combination with 5-HT3 antagonists for enhanced effect 1

    • Dexamethasone: 4-12 mg oral/IV daily 1

Second-Line Antiemetic Options

  • Dopamine Receptor Antagonists: Use with caution due to risk of worsening parkinsonian symptoms in MSA 1

    • Metoclopramide: 5-20 mg oral/IV every 4-6 hours 3
    • Monitor closely for extrapyramidal symptoms and dystonic reactions 1
    • Consider diphenhydramine for prevention/treatment of dystonic reactions 1
  • Antihistamines: Useful for managing both nausea and anxiety symptoms 1

    • H1 blockers: Diphenhydramine 25-50 mg every 4-6 hours 1
    • H2 blockers: Can be added to regimens for gastrointestinal symptoms 1

Breakthrough Nausea and Vomiting

  • For breakthrough symptoms, add one agent from a different drug class 1:
    • Olanzapine: 5-10 mg daily (category 1 recommendation) 1
    • Lorazepam: 0.5-2 mg oral/sublingual/IV every 6 hours 1
    • Haloperidol: 0.5-2 mg oral/IV every 4-6 hours (use with caution in MSA) 1
    • Scopolamine: 1.5 mg transdermal patch every 72 hours 1

Special Considerations in MSA

  • Avoid medications that may worsen orthostatic hypotension, which is common in MSA 4
  • Position patients upright during and after meals to reduce risk of aspiration, as dysphagia is common in MSA 5
  • Monitor for dysphagia which can worsen as MSA progresses and increase aspiration risk 5
  • Consider alternative administration routes (IV, transdermal, sublingual) if oral intake is compromised 1

Monitoring and Follow-up

  • Assess QT interval when using ondansetron, particularly in patients with cardiac risk factors 2
  • Monitor for extrapyramidal symptoms when using dopamine antagonists, which may be difficult to distinguish from underlying MSA symptoms 1
  • Evaluate for drug interactions with other medications commonly used in MSA 6

Treatment Algorithm

  1. Start with ondansetron 8 mg once or twice daily 2
  2. If inadequate response, add dexamethasone 4-8 mg daily 1
  3. For persistent symptoms, add lorazepam 0.5-1 mg every 6 hours 1
  4. Consider metoclopramide only if symptoms persist despite above measures, starting at lowest effective dose (5 mg) 3
  5. For refractory cases, consider olanzapine 5 mg daily 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Ondansetron Dosing Guidelines for Antiemetic Therapy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Metoclopramide Dosage and Administration for Hiccups

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Multiple system atrophy: current and future approaches to management.

Therapeutic advances in neurological disorders, 2010

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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