Restarting Escitalopram After Discontinuation
For a patient who has been off escitalopram 20mg since April (approximately 6-8 months), it is recommended to restart at 10mg for one week before increasing to the previous 20mg dose to minimize potential side effects. 1
Rationale for Gradual Reintroduction
The FDA drug label for escitalopram provides guidance on dosing that supports a gradual approach:
- The recommended starting dose of escitalopram for adults is 10mg once daily 1
- If increasing to 20mg, this should occur after a minimum of one week 1
- This gradual titration helps minimize potential side effects during reintroduction
Recommended Restart Protocol
- Week 1: Start with 10mg once daily (morning or evening, with or without food)
- Week 2 and beyond: If tolerated and clinically indicated, increase to 20mg once daily
Pharmacokinetic Considerations
Escitalopram has specific pharmacokinetic properties that support this approach:
- Reaches steady-state concentrations within 7-10 days of administration 2
- Has an elimination half-life of approximately 27-33 hours 2
- After several months off medication, the patient should be considered treatment-naïve from a pharmacokinetic perspective
Safety Considerations
Starting at a lower dose helps minimize potential adverse effects:
- Reduces risk of initial side effects such as nausea, insomnia, or increased anxiety
- Lowers potential for dose-related treatment-emergent adverse events
- Case reports suggest dose-related risk of treatment-emergent mania/hypomania with escitalopram, supporting a gradual titration approach 3
Special Considerations
- Monitoring: Assess for return of therapeutic effect and any adverse reactions during the first 1-2 weeks
- Timing: Administer once daily, either morning or evening, with or without food 1
- Prior to restarting: Screen for any changes in health status, particularly development of bipolar disorder, as recommended in the FDA label 1
Common Pitfalls to Avoid
- Restarting at full dose: Beginning immediately at 20mg may increase risk of side effects and reduce tolerability
- Inadequate monitoring: Failing to assess response during the titration period
- Prolonged low-dose treatment: Unnecessarily remaining at 10mg if 20mg was previously effective and well-tolerated
This approach balances the need for therapeutic efficacy with minimizing potential adverse effects during medication reintroduction.