Abstract | BACKGROUND: METHOD: Four consecutively identified combat veterans with chronic DSM-IV PTSD and severe intractable combat trauma nightmares participated in an 8-week open trial of escalating-dose prazosin. Nightmare severity response was rated using the nightmare item of the Clinician Administered PTSD Scale and the Clinical Global Impressions-Change scale. RESULTS: The 2 patients who achieved a daily prazosin dose of at least 5 mg were markedly improved, with complete elimination of trauma nightmares and resumption of normal dreaming. The 2 subjects limited to 2 mg of prazosin to avoid excessive blood pressure reduction were moderately improved with at least 50% reduction in nightmare severity. CONCLUSION: These clinical observations, together with neurobiological evidence for alpha1-adrenergic regulation of CNS neurobiological systems relevant to PTSD, provide rationale for placebo-controlled trials of prazosin for PTSD combat trauma nightmares.
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Authors | M A Raskind, D J Dobie, E D Kanter, E C Petrie, C E Thompson, E R Peskind |
Journal | The Journal of clinical psychiatry
(J Clin Psychiatry)
Vol. 61
Issue 2
Pg. 129-33
(Feb 2000)
ISSN: 0160-6689 [Print] United States |
PMID | 10732660
(Publication Type: Case Reports, Clinical Trial, Journal Article, Research Support, U.S. Gov't, Non-P.H.S.)
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Chemical References |
- Adrenergic alpha-Antagonists
- Prazosin
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Topics |
- Adrenergic alpha-Antagonists
(therapeutic use)
- Aged
- Ambulatory Care
- Chronic Disease
- Combat Disorders
(drug therapy, epidemiology, psychology)
- Comorbidity
- Dreams
(drug effects)
- Drug Administration Schedule
- Humans
- Male
- Middle Aged
- Prazosin
(therapeutic use)
- Prostatic Hyperplasia
(drug therapy, epidemiology)
- Psychiatric Status Rating Scales
- Severity of Illness Index
- Treatment Outcome
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