SOAP Note: 30-Year-Old Male with Anxiety on Lexapro (Escitalopram) - 2 Week Follow-Up
SUBJECTIVE
- Chief Complaint: Follow-up for anxiety management on escitalopram (Lexapro) started 2 weeks ago
- History of Present Illness: Patient reports mild improvement in anxiety symptoms since starting escitalopram. Continues to experience persistent worries and difficulty sleeping, though notes some reduction in overall symptom severity
- Current Medications: Escitalopram (dose to be confirmed - typically 10mg daily for initial treatment)
- Medication Adherence: Patient reports taking medication as prescribed
- Side Effects: None reported at this visit
OBJECTIVE
- Vital Signs: (to be documented)
- Mental Status Examination:
- Appearance: (to be documented)
- Mood/Affect: Anxious but showing mild improvement
- Thought Process: Organized, reports persistent worries
- Sleep: Impaired, difficulty initiating/maintaining sleep
ASSESSMENT
Primary Diagnosis: Generalized Anxiety Disorder (GAD), partial response to initial SSRI therapy
Clinical Reasoning:
- Two weeks is insufficient time to assess full therapeutic response - escitalopram typically requires 4-8 weeks for full anxiolytic effect, though some improvement may be seen within 1-2 weeks 1, 2
- Patient demonstrates early positive response (mild improvement), which is encouraging and suggests medication is appropriate
- Persistent sleep disturbance and worries are expected at this early treatment stage
- No adverse effects reported, indicating good tolerability 3
PLAN
1. Continue Current Escitalopram Dose and Monitor Response
The most appropriate next step is to continue the current escitalopram regimen for at least 4-8 weeks before making any medication adjustments, as full therapeutic response requires this duration 4, 1, 2. The American Academy of Child and Adolescent Psychiatry recommends evaluating response after 8-12 weeks of treatment 4.
2. Add Cognitive Behavioral Therapy (CBT)
- Combination of escitalopram with CBT has demonstrated superior efficacy compared to medication monotherapy 4
- Refer patient to therapist specializing in anxiety disorders for evidence-based CBT
- CBT can specifically target worry patterns and sleep hygiene while medication takes full effect
3. Sleep Management Strategies
- Provide sleep hygiene education (consistent sleep schedule, avoid caffeine after 2pm, limit screen time before bed, relaxation techniques)
- Consider short-term use of low-dose trazodone 25-50mg at bedtime if insomnia persists and significantly impairs function (off-label use, generally well-tolerated) 5
- Avoid benzodiazepines for routine sleep management due to dependence risk and potential to worsen anxiety long-term 5
4. Monitoring Plan
- Schedule follow-up in 2-4 weeks to reassess anxiety symptoms using standardized scales (HAM-A or GAD-7) 4, 6
- Monitor for:
5. Dose Optimization Strategy (If Needed at 4-8 Weeks)
If inadequate response after 4-8 weeks at current dose:
- Increase escitalopram to 20mg daily (maximum FDA-approved dose for anxiety) 4, 1, 2
- Studies demonstrate dose-dependent efficacy, with 20mg showing statistically significant superiority over placebo in anxiety reduction 4, 6, 7
- Allow additional 4 weeks at increased dose before considering alternative strategies 4
6. Alternative Strategies (If 20mg Escitalopram Fails After 8 Weeks)
If patient shows insufficient response to escitalopram 20mg after adequate trial:
- Switch to SNRI (venlafaxine) - demonstrated greater efficacy in treatment-resistant cases 4
- Consider augmentation with bupropion if sexual side effects emerge or if additional activating properties needed 8
- Alternative SSRI (sertraline, paroxetine) may be considered 4
7. Patient Education
- Explain that full therapeutic effect requires 4-8 weeks, and current mild improvement is encouraging 1, 2, 6
- Advise patient to continue medication even as symptoms improve 3
- Warn about discontinuation syndrome if medication stopped abruptly 3
- Instruct to report immediately: worsening anxiety, new depression, suicidal thoughts, unusual behavioral changes 3
- Discuss that insomnia often improves as anxiety symptoms resolve with continued treatment 6
8. Safety Monitoring
- Screen for suicidal ideation at each visit (critical in first months of SSRI treatment) 3
- Assess for activation/agitation, particularly in younger patients 4
- Monitor for serotonin syndrome if adding any serotonergic agents 3
- Avoid NSAIDs/aspirin/anticoagulants when possible due to increased bleeding risk with SSRIs 3
9. Long-Term Considerations
- Once remission achieved (HAM-A ≤10), continue escitalopram for minimum 6-12 months to prevent relapse 7
- Studies show escitalopram reduces relapse risk by 4-fold compared to placebo in GAD (19% vs 56% relapse rate) 7
- Maintain combined medication and CBT approach for optimal outcomes 4
Follow-up: 2-4 weeks for symptom reassessment and medication tolerance evaluation 4, 6
Prescriptions:
- Continue escitalopram (current dose) - 30-day supply
- (Consider trazodone 25-50mg qhs PRN for sleep if insomnia severe and impairing function)