4.4 Article

Early symptom response to antipsychotic medication as a marker of subsequent symptom change: An eighteen-month follow-up study of recent episode schizophrenia

Journal

SCHIZOPHRENIA RESEARCH
Volume 141, Issue 2-3, Pages 168-172

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.schres.2012.08.030

Keywords

Treatment response; PANSS; Schizophrenia; Recent-episode; Early-response; Delayed-response; Clinical trial

Categories

Funding

  1. Eli Lilly
  2. F. Hoffmann-LaRoche

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Background: Differences between early- and delayed-responders to antipsychotic medication as a marker of subsequent symptom change to 18 months are unknown. Aims: To examine the association between initial non-, early- and delayed-response and subsequent symptom change up to 18 months in the antipsychotic treatment of the symptoms of recent-episode schizophrenia. Method: Participants were from a double-blind randomized clinical trial of recent episode schizophrenia (n=263). Based on attainment of a 20% PANSS total change in the initial four weeks, the following groups were created and compared: non- (i.e., no-response): early- (i.e. within 2 weeks) and delayed- (i.e. 3-4 weeks) responders. Mixed modeling was used to predict PANSS percent change with group, time and the time-group interaction. Results: Analysis of the PANSS total percent change showed significant (p<.01) group, time, and time-group interaction effects. Compared to non-responders, early-responders maintained significantly greater total response from week 5 to 44, and delayed-responders from week 5 to 20. After this time, non-responders and the other groups did not significantly differ on change. Generally, differences between the delayed- and early-responders were not statistically significance. Results were similar on the PANSS positive, negative and general psychopathology symptom subscales. Conclusions: Early-response is marked by up to 39 weeks of longer subsequent symptom response than non-response, and infrequently differs to delayed-response. This has implications for consideration of switching and clinical trial design. (C) 2012 Elsevier B.V. All rights reserved.

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