Early response or nonresponse at week 2 and week 3 predict ultimate response or nonresponse in adolescents with schizophrenia treated with olanzapine: results from a 6-week randomized, placebo-controlled trial

Verfasser / Beitragende:
[Marie Stentebjerg-Olesen, Stephen Ganocy, Robert Findling, Kiki Chang, Melissa DelBello, John Kane, Mauricio Tohen, Pia Jeppesen, Christoph Correll]
Ort, Verlag, Jahr:
2015
Enthalten in:
European Child & Adolescent Psychiatry, 24/12(2015-12-01), 1485-1496
Format:
Artikel (online)
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024 7 0 |a 10.1007/s00787-015-0725-1  |2 doi 
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245 0 0 |a Early response or nonresponse at week 2 and week 3 predict ultimate response or nonresponse in adolescents with schizophrenia treated with olanzapine: results from a 6-week randomized, placebo-controlled trial  |h [Elektronische Daten]  |c [Marie Stentebjerg-Olesen, Stephen Ganocy, Robert Findling, Kiki Chang, Melissa DelBello, John Kane, Mauricio Tohen, Pia Jeppesen, Christoph Correll] 
520 3 |a In adults with schizophrenia, early response/non-response (ER/ENR) to antipsychotics at 2weeks robustly predicts ultimate response/non-response (UR/UNR). However, less data about the predictive value of ER/ENR exist in adolescents with schizophrenia. Post hoc analysis of a 6-week trial in adolescents aged 13-17 with schizophrenia were randomized 2:1 to olanzapine or placebo. ER was defined as≥20% reduction in Brief Psychiatric Rating Scale-children (BPRS-C) total score at week 2 (ER2) or 3 (ER3); UR was defined with increasing stringency as total BPRS-C score reduction≥20,≥30,≥40 or≥50%; remission was defined cross-sectionally using Andreasen et al. (2005) criteria. By week 2 (n=69) and 3 (n=66), olanzapine-treated youth achieved 73.3 and 85.5% of their overall BPRS-C score reduction at 6weeks last observation carried forward. ER and ENR patients did not differ significantly regarding baseline demographic, illness and treatment variables. ER 2 (frequency=68.1%) and ER 3 (frequency=65.2%) significantly predicted UR and remission (p=0.0044-p<0.0001), with ER3 having more predictive power. A≥20% BPRS-C reduction threshold for ER had best predictive validity (area under the curve=0.88-0.92). At 6weeks, patients with ER had significantly greater improvements in BPRS-C, Clinical Global Impressions Improvement and Severity scores, greater cross-sectional remission and less all-cause discontinuation (p=0.047-p<0.0001). Adverse event profiles were similar in the ER and ENR groups. Adolescents with schizophrenia experienced the majority of symptomatic improvement early during olanzapine treatment. ER predicted UR and remission, with ER3 having best predictive power. A≥20% improvement threshold for defining ER was confirmed as a robust outcome indicator. 
540 |a Springer-Verlag Berlin Heidelberg, 2015 
690 7 |a Schizophrenia  |2 nationallicence 
690 7 |a Adolescents  |2 nationallicence 
690 7 |a Response  |2 nationallicence 
690 7 |a Remission  |2 nationallicence 
690 7 |a Prediction  |2 nationallicence 
700 1 |a Stentebjerg-Olesen  |D Marie  |u Mental Health Centre for Child and Adolescent Psychiatry, Copenhagen University Hospital, Glostrup, Denmark  |4 aut 
700 1 |a Ganocy  |D Stephen  |u Case Western Reserve University, University Hospitals Case Medical Center, Cleveland, OH, USA  |4 aut 
700 1 |a Findling  |D Robert  |u Johns Hopkins University and the Kennedy Krieger Institute, Baltimore, MD, USA  |4 aut 
700 1 |a Chang  |D Kiki  |u Stanford University School of Medicine, Stanford, CA, USA  |4 aut 
700 1 |a DelBello  |D Melissa  |u University of Cincinnati, Cincinnati, OH, USA  |4 aut 
700 1 |a Kane  |D John  |u Department of Psychiatry, The Zucker Hillside Hospital, Psychiatry Research, North Shore, Long Island Jewish Health System, 75-59 263rd Street, 11004, Glen Oaks, NY, USA  |4 aut 
700 1 |a Tohen  |D Mauricio  |u Department of Psychiatry, University of New Mexico Health Science Center, Albuquerque, NM, USA  |4 aut 
700 1 |a Jeppesen  |D Pia  |u Mental Health Centre for Child and Adolescent Psychiatry, Copenhagen University Hospital, Glostrup, Denmark  |4 aut 
700 1 |a Correll  |D Christoph  |u Department of Psychiatry, The Zucker Hillside Hospital, Psychiatry Research, North Shore, Long Island Jewish Health System, 75-59 263rd Street, 11004, Glen Oaks, NY, USA  |4 aut 
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950 |B NATIONALLICENCE  |P 700  |E 1-  |a Stentebjerg-Olesen  |D Marie  |u Mental Health Centre for Child and Adolescent Psychiatry, Copenhagen University Hospital, Glostrup, Denmark  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ganocy  |D Stephen  |u Case Western Reserve University, University Hospitals Case Medical Center, Cleveland, OH, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Findling  |D Robert  |u Johns Hopkins University and the Kennedy Krieger Institute, Baltimore, MD, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Chang  |D Kiki  |u Stanford University School of Medicine, Stanford, CA, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a DelBello  |D Melissa  |u University of Cincinnati, Cincinnati, OH, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kane  |D John  |u Department of Psychiatry, The Zucker Hillside Hospital, Psychiatry Research, North Shore, Long Island Jewish Health System, 75-59 263rd Street, 11004, Glen Oaks, NY, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Tohen  |D Mauricio  |u Department of Psychiatry, University of New Mexico Health Science Center, Albuquerque, NM, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Jeppesen  |D Pia  |u Mental Health Centre for Child and Adolescent Psychiatry, Copenhagen University Hospital, Glostrup, Denmark  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Correll  |D Christoph  |u Department of Psychiatry, The Zucker Hillside Hospital, Psychiatry Research, North Shore, Long Island Jewish Health System, 75-59 263rd Street, 11004, Glen Oaks, NY, USA  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t European Child & Adolescent Psychiatry  |d Springer Berlin Heidelberg  |g 24/12(2015-12-01), 1485-1496  |x 1018-8827  |q 24:12<1485  |1 2015  |2 24  |o 787