Magnitude of placebo response and drug-placebo differences across psychiatric disorders

被引:88
作者
Khan, A
Kolt, RL
Rapaport, MH
Krishnan, KRR
Brodhead, AE
Brown, WA
机构
[1] NW Clin Res Ctr, Bellevue, WA USA
[2] Duke Univ, Med Ctr, Dept Psychiat & Behav Sci, Durham, NC USA
[3] Eastern Washington Univ, Dept Psychol, Cheney, WA 99004 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA USA
[5] Cedars Sinai Med Ctr, Dept Psychiat, Los Angeles, CA 90048 USA
[6] Brown Univ, Sch Med, Dept Psychiat, Providence, RI 02912 USA
[7] Tufts Univ, Sch Med, Boston, MA 02111 USA
关键词
D O I
10.1017/S0033291704003873
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background. Placebo response, drug response, and drug-placebo differences appear to vary among psychiatric conditions. Method. We evaluated the Food and Drug Administration (FDA) Summary Basis of Approval (SBA) reports to compare the magnitude of placebo response, magnitude of psychotopic drug response, and drug-placebo differences among various diagnostic groups such as depression, anxiety, and psychotic disorders. Results. Six diagnostic groups (psychosis, obsessive-compulsive disorder (OCD), generalized anxiety disorder (GAD), depression, post-traumatic stress disorder, panic) varied in response to both placebo and active drug treatments. Response to placebo was high among patients participating in GAD, depression, and panic disorder clinical trials. Conversely, patients participating in psychotic disorder and OCD trials experienced low response to placebo. Conclusion. Our findings indicate that the magnitude of placebo response and drug response were heterogeneous and were statistically significantly different among various psychiatric disorders. Although a noticeable degree of heterogeneity was detected in the drug-placebo ratio among various disorders, the differences did not reach statistical significance. This finding suggests that placebo use should be continued for newer agents being tested for all of the psychiatric disorders. These findings may help in the development of psychopharmacology trial designs and in the deliberations of ethics committees.
引用
收藏
页码:743 / 749
页数:7
相关论文
共 14 条
[1]   THE POWERFUL PLACEBO [J].
BEECHER, HK .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1955, 159 (17) :1602-1606
[2]  
Frank J.D., 1991, Persuasion Healing: A Comparative Study of Psychotherapy, V3rd, DOI 10.56021/9780801840678
[3]   Treatment of bulimia nervosa with topiramate in a randomized, double-blind, placebo-controlled trial, Part 2: Improvement in psychiatric measures [J].
Hedges, DW ;
Reimherr, FW ;
Hoopes, SP ;
Rosenthal, NR ;
Kamin, M ;
Karim, R ;
Capece, JA .
JOURNAL OF CLINICAL PSYCHIATRY, 2003, 64 (12) :1449-1454
[4]   A double-blind, placebo-controlled study of the efficacy and safety of controlled-release fluvoxamine in patients with obsessive-compulsive disorder [J].
Hollander, E ;
Koran, LM ;
Goodman, WK ;
Greist, JH ;
Ninan, PT ;
Yang, HC ;
Li, D ;
Barbato, LM .
JOURNAL OF CLINICAL PSYCHIATRY, 2003, 64 (06) :640-647
[5]   Are placebo controls necessary to test new antidepressants and anxiolytics? [J].
Khan, A ;
Khan, S ;
Brown, WA .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2002, 5 (03) :193-197
[6]  
Khan A, 2001, INT J NEUROPSYCHOPH, V4, P113, DOI 10.1017/S1461145701002322
[7]  
Lanctôt KL, 2003, CAN MED ASSOC J, V169, P557
[8]   Evaluating treatments for the mood disorders: time for the evidence to get real [J].
Parker, G .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY, 2004, 38 (06) :408-414
[9]   SSRI treatment of borderline personality disorder: A randomized, placebo-controlled clinical trial for female patients with borderline personality disorder [J].
Rinne, T ;
van den Brink, W ;
Wouters, L ;
van Dyck, R .
AMERICAN JOURNAL OF PSYCHIATRY, 2002, 159 (12) :2048-2054
[10]  
Srisurapanont Manit, 1999, Journal of the Medical Association of Thailand, V82, P341