What is the recommended tapering schedule for Namenda (memantine) after catatonia has resolved?

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Tapering Namenda (Memantine) After Catatonia Resolution

Taper memantine over 2-4 weeks with gradual dose reductions of approximately 10% of the original dose per week, monitoring closely for catatonia recurrence at each step.

Recommended Tapering Protocol

The most appropriate approach is to reduce memantine by 10% of the original dose weekly over 2-4 weeks, extrapolating from general deprescribing principles for CNS-active medications in older adults 1. This gradual approach minimizes the risk of symptom recurrence while allowing safe discontinuation.

Specific Tapering Schedule

  • Reduce the dose by approximately 2.5-5 mg per week depending on the starting dose 1
  • Total taper duration should be 2-4 weeks minimum 1
  • Monitor for catatonia recurrence after each dose reduction before proceeding to the next step 2, 3
  • If catatonia symptoms re-emerge, return to the previous well-tolerated dose and slow the taper further 2, 3

Critical Monitoring Considerations

Watch specifically for early signs of catatonia recurrence, including:

  • Mutism or decreased verbal output 4
  • Waxy flexibility or posturing 4
  • Immobility or psychomotor retardation 4
  • Staring or decreased responsiveness 4
  • Rigidity or grimacing 4

Resurgence of catatonia can occur rapidly—within one week of medication changes—so close monitoring during and immediately after tapering is essential 5.

Special Circumstances Requiring Slower Tapers

Consider extending the taper to 4-6 weeks or longer if:

  • The patient required higher doses of memantine (>10 mg/day) 4
  • Catatonia was severe or prolonged before treatment 6
  • The patient has been on memantine for an extended period (>3 months) 1
  • There is a history of catatonia recurrence with previous medication changes 5

Managing Catatonia Recurrence During Taper

If catatonia symptoms return during tapering:

  • Immediately return to the last effective dose 5, 6
  • Consider maintaining that dose for several more weeks before attempting a slower taper 5
  • Some patients may require indefinite maintenance treatment if multiple taper attempts fail 6
  • Ensure benzodiazepines (particularly lorazepam) remain available as first-line rescue therapy if needed 5, 6

Common Pitfalls to Avoid

  • Never abruptly discontinue memantine, as this increases risk of symptom recurrence 5, 6
  • Do not use a fixed schedule for all patients—be prepared to slow the taper based on individual response 3, 7
  • Avoid tapering during periods of psychosocial stress or other medication changes that could confound assessment 6
  • Do not assume successful acute treatment means the patient can be rapidly tapered—some cases require prolonged or indefinite maintenance 6

Documentation and Follow-Up

  • Schedule follow-up within 1 week of each dose reduction to assess for early recurrence 7, 5
  • Continue monitoring for at least 2-4 weeks after complete discontinuation, as late recurrences can occur 5
  • Document the patient's response to guide future treatment decisions if catatonia recurs 7

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Citalopram Tapering Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Tapering Aripiprazole

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Catatonic schizophrenia and the use of memantine.

The Annals of pharmacotherapy, 2006

Research

Maintenance treatment of catatonia with benzodiazepines: A case series and literature review.

Neuropsychopharmacologia Hungarica : a Magyar Pszichofarmakologiai Egyesulet lapja = official journal of the Hungarian Association of Psychopharmacology, 2024

Guideline

Buspirone Tapering Protocol

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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