Efficacy of sertraline in preventing relapse of posttraumatic stress disorder: Results of a 28-week double-blind, placebo-controlled study

被引:129
作者
Davidson, J
Pearlstein, T
Londborg, P
Brady, KT
Rothbaum, B
Bell, J
Maddock, R
Hegel, MT
Farfel, G
机构
[1] Duke Univ, Med Ctr, Dept Psychiat & Behav Sci, Anxiety & Traumat Stress Program, Durham, NC 27710 USA
[2] Butler Hosp, Providence, RI 02906 USA
[3] Brown Univ, Providence, RI 02912 USA
[4] Seattle Clin Res Ctr, Seattle, WA USA
[5] Med Univ S Carolina, Charleston, SC 29425 USA
[6] Emory Univ, Atlanta, GA 30322 USA
[7] Dartmouth Coll, Hanover, NH USA
[8] Univ Calif Davis, Davis, CA 95616 USA
[9] Pfizer Inc, New York, NY USA
关键词
D O I
10.1176/appi.ajp.158.12.1974
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
objective: The study examined the efficacy of sertraline, compared with placebo, in sustaining improvement and preventing relapse over 28 weeks in patients with posttraumatic stress disorder (PTSD) who had completed a 12-week double-blind, placebo-controlled acute treatment study and a subsequent 24-week open-label study of continuation treatment with sertraline. Method: Ninety-six patients were randomly assigned, in a double-blind design, to 28 weeks of maintenance treatment with sertraline (50-200 mg, N=46; 78% were women) or placebo (N=50; 62% were women). Measures used in biweekly assessments included the Clinician-Administered PTSD Scale, the Impact of Event Scale, and the Clinical Global Impression severity and improvement ratings. Kaplan-Meier analyses were used to estimate time to discontinuation from the study due to relapse, relapse or study discontinuation due to clinical deterioration, and acute exacerbation. Results: Continued treatment with sertraline yielded lower PTSD relapse rates than placebo (5% versus 26%). Patients who received placebo were 6.4 times as likely to experience relapse as were patients who received sertraline. Kaplan-Meier analyses confirmed the protective effect of sertraline in significantly extending time in remission. The ability of sertraline to sustain improvement was comparable across the three core PTSD symptom clusters (reexperiencing/intrusion, avoidance/numbing, and hyperarousal). A regression analysis found early response during acute treatment to be associated with a more than 16-fold reduced risk of relapse after placebo substitution. Sertraline, at a mean endpoint dose of 137 mg, was well tolerated, with no sertraline-related adverse events observed at a rate of 10% or higher. Conclusions: The results provide evidence for the ability of sertraline both to sustain improvement in PTSD symptoms and to provide prophylactic protection against relapse.
引用
收藏
页码:1974 / 1981
页数:8
相关论文
共 44 条
  • [1] *AG HLTH CAR POL R, 1993, TREATM MAJ DEPR CLIN, V5
  • [2] Functional impairment and utilization of services associated with posttraumatic stress in the community
    Amaya-Jackson, L
    Davidson, JR
    Hughes, DC
    Swartz, M
    Reynolds, V
    George, LK
    Blazer, DG
    [J]. JOURNAL OF TRAUMATIC STRESS, 1999, 12 (04) : 709 - 724
  • [3] Blake D.D., 1990, The Behavior Therapist, V18, P187, DOI [10.1002/jts.2490080106, DOI 10.1007/BF02105408]
  • [4] PHYSIOLOGICAL-RESPONSE TO COMBAT MEMORIES AND PRELIMINARY TREATMENT OUTCOME IN VIETNAM VETERAN PTSD PATIENTS TREATED WITH DIRECT THERAPEUTIC EXPOSURE
    BOUDEWYNS, PA
    HYER, L
    [J]. BEHAVIOR THERAPY, 1990, 21 (01) : 63 - 87
  • [5] Efficacy and safety of sertraline treatment of posttraumatic stress disorder - A randomized controlled trial
    Brady, K
    Pearlstein, T
    Asnis, GM
    Baker, D
    Rothbaum, B
    Sikes, CR
    Farfel, GM
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (14): : 1837 - 1844
  • [6] BRADY KT, 1995, J CLIN PSYCHIAT, V56, P502
  • [7] BRESLAU N, 1992, AM J PSYCHIAT, V149, P671
  • [8] BRIEF PSYCHOTHERAPY FOR POSTTRAUMATIC STRESS DISORDERS
    BROM, D
    KLEBER, RJ
    DEFARES, PB
    [J]. JOURNAL OF CONSULTING AND CLINICAL PSYCHOLOGY, 1989, 57 (05) : 607 - 612
  • [9] Does EMDR work? And if so, why?: A critical review of controlled outcome and dismantling research
    Cahill, SP
    Carrigan, MH
    Frueh, BC
    [J]. JOURNAL OF ANXIETY DISORDERS, 1999, 13 (1-2) : 5 - 33
  • [10] Fluoxetine in post-traumatic stress disorder - Randomised, double-blind study
    Connor, KM
    Sutherland, SM
    Tupler, LA
    Malik, ML
    Davidson, JRT
    [J]. BRITISH JOURNAL OF PSYCHIATRY, 1999, 175 : 17 - 22