The Psychopharmacology Algorithm Project at the Harvard South Shore Program: An Update on Posttraumatic Stress Disorder

被引:54
作者
Bajor, Laura A. [2 ,3 ]
Ticlea, Ana Nectara [2 ,3 ]
Osser, David N. [1 ]
机构
[1] VA Boston Healthcare Syst, Brockton Div, Brockton, MA 02301 USA
[2] Harvard Univ, Sch Med, Brockton, MA 02401 USA
[3] Harvard S Shore Psychiat Residency Training Progr, Brockton, MA USA
关键词
algorithms; posttraumatic stress disorder; psychopharmacology; stress disorders; PLACEBO-CONTROLLED-TRIAL; VENLAFAXINE EXTENDED-RELEASE; OPEN-LABEL TRIAL; RANDOMIZED CONTROLLED-TRIAL; DOUBLE-BLIND; COMBAT VETERANS; QUETIAPINE TREATMENT; SLEEP DISTURBANCES; ADJUNCTIVE THERAPY; MAJOR DEPRESSION;
D O I
10.3109/10673229.2011.614483
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: This project aimed to provide an organized, sequential, and evidence-supported approach to the pharmacotherapy of posttraumatic stress disorder (PTSD), following the format of previous efforts of the Psychopharmacology Algorithm Project at the Harvard South Shore Program. Method: A comprehensive literature review was conducted to determine the best pharmacological choices for PTSD patients and to update the last published version (1999) of the algorithm. We focused on optimal pharmacological interventions to address the prominent symptoms of PTSD, with additional attention to the impact that common comorbidities have on treatment choices. Results: We found that SSRIs and SNRIs are not as effective as previously thought, and that awareness of their long-term side effects has increased. New evidence suggests that addressing fragmented sleep and nightmares can improve symptoms (in addition to insomnia) that are frequently seen with PTSD (e. g., hyperarousal, reexperiencing). Prazosin and trazodone are emphasized at this initial step; if significant PTSD symptoms remain, an antidepressant may be tried. For PTSD-related psychosis, an antipsychotic may be added. In resistant cases, two or three antidepressants may be used in sequence. Following that, or with partial improvement and residual symptomatology, augmentation may be tried; the best options are antipsychotics, clonidine, topiramate, and lamotrigine. Conclusion: This heuristic may be helpful in producing faster symptom resolution, fewer side effects, and increased compliance. (HARV REV PSYCHIATRY 2011; 19: 240-258.)
引用
收藏
页码:240 / 258
页数:19
相关论文
共 146 条
  • [1] Quetiapine as an adjunctive treatment for post-traumatic stress disorder: an 8-week open-label study
    Ahearn, EP
    Mussey, M
    Johnson, C
    Krohn, A
    Krahn, D
    [J]. INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 2006, 21 (01) : 29 - 33
  • [2] [Anonymous], TREATM POSTTR STRESS
  • [3] [Anonymous], J CLIN PSYCHIAT S16
  • [4] [Anonymous], 2005, POSTTRAUMATIC STRESS
  • [5] [Anonymous], 2004, AM J PSYCHIAT
  • [6] [Anonymous], 2006, CAN J PSYCHIAT
  • [7] [Anonymous], 2000, DIAGN STAT MAN MENT, DOI DOI 10.1176/APPI.BOOKS.9780890425787
  • [8] The Psychopharmacology Algorithm Project at the Harvard South Shore Program: An Update on Bipolar Depression
    Ansari, Arash
    Osser, David N.
    [J]. HARVARD REVIEW OF PSYCHIATRY, 2010, 18 (01) : 36 - 55
  • [9] Effects of mirtazapine in patients with post-traumatic stress disorder in Korea: a pilot study
    Bahk, WM
    Pae, CU
    Tsoh, J
    Chae, JH
    Jun, TY
    Chul-Lee
    Kim, KS
    [J]. HUMAN PSYCHOPHARMACOLOGY-CLINICAL AND EXPERIMENTAL, 2002, 17 (07) : 341 - 344
  • [10] Post-traumatic stress disorder: emerging concepts of pharmacotherapy
    Baker, Dewleen G.
    Nievergelt, Caroline M.
    Risbrough, Victoria B.
    [J]. EXPERT OPINION ON EMERGING DRUGS, 2009, 14 (02) : 251 - 272