Anxiety Disorder and OCD Clinical Pathway — Outpatient Behavioral Health and Primary Care
Anxiety Disorder and OCD Clinical Pathway — Outpatient Behavioral Health and Primary Care
Medication Management Recommendations
Consenting for Medication
Consent |
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Document |
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General Guidance for Medication Initiation
- SSRIs are the 1st line medications for treating moderate/severe anxiety disorders and OCD in children and adolescents
- FDA Approval/Evidence
- Use of SSRIs for anxiety treatment are based on ample evidence
- No SSRIs are FDA approved to treat core anxiety disorders in pediatric
- Sertraline and Fluoxetine are FDA approved to treat Pediatric OCD
- While SSRIs are not FDA approved for the core anxiety disorders, there is ample clinical evidence of safety and efficacy in using SSRIs for pediatric anxiety disorders
- Do not use with MAOIs (monoamine oxidase inhibitors)
- Recommend starting with lower doses in younger children
- If no clinical response to 1st line, PCP can consider consulting psychiatry
- Sertraline and Fluoxetine are available in liquid formulation
- Duloxetine is available in both capsule and sprinkle. Capsules may be added to liquids, and sprinkle may be added to food
- For additional information on medications, please refer to formulary
SSRI/SNRI Medication Dosing Recommendations and Adverse Effects
1st Line SSRI Selective Serotonin Reuptake Inhibitor | |||||
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Sertraline ZoloftTM |
FDA Approved Indication/Age | OCD, Age ≥ 6 years | |||
Typical Dosing Range |
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Typical Starting Dose | 12.5 mg - 25 mg daily | ||||
Typical Titration Increments | 12.5 – 25 mg for doses < 50 mg 25 mg for doses > 50 mg |
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Max Daily Dose | 200 mg | ||||
Common Adverse Effects | GI upset, headaches, insomnia | ||||
Fluoxetine ProzacTM |
FDA Approved Indication/Age | MDD, OCD, Age ≥ 8 years | |||
Typical Dosing Range |
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Typical Starting Dose | 5 - 10 mg daily | ||||
Typical Titration Increments | 5 mg for doses < 20 mg 10 mg for doses > 20 mg |
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Max Daily Dose | 60 mg | ||||
Common Adverse Effects | Nausea, headache, weight reduction, abdominal pain | ||||
2nd Line SNRI Serotonin-norepinephrine Reuptake Inhibitor | |||||
Duloxetine CymbaltaTM |
FDA Approved Indication/Age | GAD, Age ≥ 7 years | |||
Typical Dosing Range |
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Typical Starting Dose | 20 - 30 mg daily | ||||
Typical Titration Increments | 20 - 30 mg | ||||
Max Daily Dose | 120 mg | ||||
Common Adverse Effects | Nausea, headache, weight reduction, abdominal pain |
Titration Tips:
Initial increase: Can increase dose after 2 - 4 weeks after ensuring tolerability
Subsequent increases: Would wait 4 - 8 weeks between dose adjustments to allow medication to reach steady state before assessing for efficacy
Rare Potential Serious Side Effects
SSRI | Serotonin Syndrome, suicidal thoughts |
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SNRI | Serotonin Syndrome, suicidal thoughts, hepatic failure |
Please refer to CHOP formulary for detailed list of possible adverse effects.