51. Open trial of nefazodone for combat-related posttraumatic stress disorder.
- Author
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Hertzberg MA, Feldman ME, Beckham JC, Moore SD, and Davidson JR
- Subjects
- Adult, Ambulatory Care, Anger drug effects, Antidepressive Agents, Second-Generation administration & dosage, Antidepressive Agents, Second-Generation adverse effects, Combat Disorders diagnosis, Combat Disorders psychology, Depressive Disorder diagnosis, Depressive Disorder drug therapy, Depressive Disorder psychology, Drug Administration Schedule, Follow-Up Studies, Humans, Male, Middle Aged, Personality Inventory, Piperazines, Psychiatric Status Rating Scales, Sleep drug effects, Sleep Initiation and Maintenance Disorders drug therapy, Sleep Initiation and Maintenance Disorders psychology, Treatment Outcome, Triazoles administration & dosage, Triazoles adverse effects, Antidepressive Agents, Second-Generation therapeutic use, Combat Disorders drug therapy, Triazoles therapeutic use
- Abstract
Background: Because of its ability to block 5-HT2 receptors postsynaptically and inhibit 5-HT reuptake presynaptically and/or its enhancement of sleep quality, nefazodone may be useful for symptom management in posttraumatic stress disorder (PTSD) patients., Method: Ten patients with combat-related DSM-IV posttraumatic stress disorder (PTSD) entered an open-label 12-week trial of nefazodone with a 4-week follow-up, beginning with 100 mg/day and increasing as necessary to achieve a maximal response or until reaching a maximum dosage of 600 mg/day., Results: Nefazodone was well tolerated, and no significant changes in sexual function were reported. Based on Clinical Global Impressions-Improvement scores, all 10 patients were rated as much improved. All PTSD symptoms (except self-reported PTSD reexperiencing symptoms), sleep, and clinician-rated depression significantly improved at week 12. At follow-up, significant changes were maintained, and self-reported PTSD reexperiencing symptoms had also significantly improved. Effect sizes for all changed symptoms were moderate to large at week 12 and at follow-up. Self-reported and clinician-rated anger significantly improved. Self-reported depression failed to improve. Improvement in social and occupational functioning was minimal., Conclusion: These preliminary data suggest that nefazodone may be effective in reducing the 3 primary PTSD symptom clusters and may be particularly helpful in improving sleep and decreasing anger.
- Published
- 1998
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