Prazosin Dosing for PTSD-Associated Nightmares
Start prazosin at 1 mg at bedtime and titrate by 1-2 mg every few days until nightmares resolve, targeting 3-4 mg/day for civilians and 9.5-15.6 mg/day for military veterans, with monitoring for orthostatic hypotension after each dose increase. 1
Initial Dosing Strategy
- Begin with 1 mg at bedtime to minimize first-dose hypotension risk 2, 1
- Use lower starting doses in elderly patients or those on concurrent antihypertensive medications 1
- Monitor blood pressure after the initial dose and with each significant dose increase 1
Titration Protocol
- Increase by 1-2 mg every few days until clinical response is achieved 2, 1
- Assess nightmare frequency and intensity using standardized measures (such as CAPS Item No. 2 "recurrent distressing dreams") to guide titration 2
- Continue concurrent psychotherapy and psychotropic medications during prazosin treatment 2
Target Effective Doses
The effective dose varies substantially by population:
- Civilian trauma victims: Average effective dose is approximately 3-4 mg/day (mean 3.1 ± 1.3 mg) 2, 1
- Military veterans: Require significantly higher doses, with mean effective doses ranging from 9.5-15.6 mg/day 2, 1
- Active-duty military personnel: Dosing varies by gender, with men requiring mean effective dose of 15.6 ± 6.0 mg and women requiring 7.0 ± 3.5 mg 1
The guideline evidence shows treatment lengths of 3-9 weeks were effective, with doses ranging from 1 mg to over 10 mg across studies 2. While some case reports describe doses up to 45 mg 3, and one review suggests maximum dosing of 20 mg at bedtime 4, the American Academy of Sleep Medicine guideline data supports mean doses of 13.3 mg/day in military veterans 2.
Administration Schedule
- Give as a single bedtime dose initially for nightmare management 1
- For more severe cases, especially in military personnel, consider divided dosing 1
- One review suggests 20 mg at bedtime with 5 mg midmorning for maximum dosing, though this exceeds typical guideline recommendations 4
Monitoring and Side Effects
Common adverse effects to monitor:
- Dizziness and lightheadedness are common, especially after initial doses 1
- Orthostatic hypotension may occur but usually resolves during treatment 2, 1
- Monitor blood pressure systematically with each dose escalation 1
Critical Clinical Considerations
- SSRI interaction: If the patient is taking selective serotonin reuptake inhibitors, be aware that response to prazosin may be diminished 1, 5
- Discontinuation: Nightmares return to baseline intensity if prazosin is stopped, so this is not a curative treatment 1, 5
- Scope of use: Prazosin is specifically for PTSD-associated nightmares and trauma-related sleep disturbances, not as a general anxiolytic 5
- Therapeutic benefit timeline: Suppression of nightmare symptoms can occur within one week of prazosin initiation 6
Special Population Adjustments
For patients with comorbidities:
- Lower initial doses in elderly patients 1
- Exercise caution in patients on concurrent antihypertensive medications due to additive hypotensive effects 1
- Higher doses may be safe and tolerable in treatment-resistant cases, with case reports documenting doses up to 30-45 mg daily 3
Common Pitfalls to Avoid
- Underdosing military veterans: Don't stop at 3-4 mg in veterans—they typically require 9.5-15.6 mg/day for adequate response 2, 1
- Inadequate blood pressure monitoring: Always check orthostatic vital signs after initial dose and dose increases 2, 1
- Using as general anxiolytic: Prazosin only reduces anxiety symptoms if they stem from trauma-related nightmares causing sleep deprivation 5
- Premature discontinuation: Maintain treatment long-term as nightmares recur upon cessation 1, 5