Pharmacopsychiatry 2017; 50(01): 26-31
DOI: 10.1055/s-0042-107794
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Doxazosin, an α-1-adrenergic-receptor Antagonist, for Nightmares in Patients with Posttraumatic Stress Disorder and/or Borderline Personality Disorder: a Chart Review

Stefan Roepke
1   Department of Psychiatry, Campus Benjamin Franklin, Charité – Universitätsmedizin Berlin, Berlin, Germany
,
Heidi Danker-Hopfe
2   Competence Center for Sleep Medicine, Campus Benjamin Franklin, Charité – Universitätsmedizin Berlin, Berlin, Germany
,
Dimitris Repantis
1   Department of Psychiatry, Campus Benjamin Franklin, Charité – Universitätsmedizin Berlin, Berlin, Germany
,
Behnoush Behnia
1   Department of Psychiatry, Campus Benjamin Franklin, Charité – Universitätsmedizin Berlin, Berlin, Germany
,
Florian Bernard
1   Department of Psychiatry, Campus Benjamin Franklin, Charité – Universitätsmedizin Berlin, Berlin, Germany
,
Marie-Luise Hansen
2   Competence Center for Sleep Medicine, Campus Benjamin Franklin, Charité – Universitätsmedizin Berlin, Berlin, Germany
,
Christian Otte
1   Department of Psychiatry, Campus Benjamin Franklin, Charité – Universitätsmedizin Berlin, Berlin, Germany
› Author Affiliations
Further Information

Publication History

received 17 August 2015
revised 25 March 2016

accepted 25 April 2016

Publication Date:
08 June 2016 (online)

Abstract

Objective: Centrally active α-1-adrenergic-receptor antagonists such as prazosin are effective in the treatment of nightmares in patients with posttraumatic stress disorder (PTSD). A pharmacological alternative is doxazosin, which has a longer half-life and fewer side effects. However, doxazosin is currently being used without solid empirical evidence. Furthermore, no study so far has assessed the effects of α-1-antagonists on nightmares in patients with borderline personality disorder (BPD). We retrospectively assessed the effectiveness of doxazosin on nightmares in PTSD and BPD.

Method: A retrospective chart review of patients treated with doxazosin for trauma-associated nightmares in our clinic was performed. As in previous prazosin studies, the B2 score of the Clinician-Administered PTSD Scale (CAPS) was used as the primary outcome measure. Furthermore, the Pittsburgh Sleep Quality Index-Addendum for PTSD (PSQI-A) and sleep logs were analyzed.

Results: We identified 51 patients with PTSD and/or BPD (mean age 35.7 years, 92.3% women) who received doxazosin for nightmares. Of these, 46 patients continued doxazosin over a 4-week period and 31 patients over a 12-week period. Within the 12-week period, doxazosin treatment significantly reduced nightmares regardless of PTSD/BPD. 25 percent of patients treated for 12 weeks had full remission of nightmares. PSQI-A scores indicated that additional trauma-associated sleep symptoms improved over 12 weeks. Furthermore, recuperation of sleep improved with doxazosin within the first 4 weeks of treatment.

Conclusion: Doxazosin might improve trauma associated nightmares and more general sleep parameters in patients with PTSD and BPD. Randomized controlled trials are warranted.

 
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