An open-label randomised comparison of aripiprazole, olanzapine and risperidone for the acute treatment of first-episode schizophrenia: Eight-week outcomes. (October 2019)
- Record Type:
- Journal Article
- Title:
- An open-label randomised comparison of aripiprazole, olanzapine and risperidone for the acute treatment of first-episode schizophrenia: Eight-week outcomes. (October 2019)
- Main Title:
- An open-label randomised comparison of aripiprazole, olanzapine and risperidone for the acute treatment of first-episode schizophrenia: Eight-week outcomes
- Authors:
- Cheng, Zhang
Yuan, Yanbo
Han, Xue
Yang, Lei
Cai, Shangli
Yang, Fude
Lu, Zheng
Wang, Chuanyue
Deng, Hong
Zhao, Jingping
Xiang, Yutao
Correll, Christoph U
Yu, Xin - Abstract:
- Purpose: This study aimed to investigate the efficacy and tolerability of aripiprazole, olanzapine and risperidone in first-episode schizophrenia (FES). Methods: The eight-week, open, randomised study was conducted in six Chinese medical centres. Altogether, 498 FES subjects were randomised to aripiprazole ( n = 165), olanzapine ( n = 168) or risperidone ( n = 165). Efficacy was measured with the Positive and Negative Syndrome Scale (PANSS), tolerability with the Udvalg for Kliniske Undersogelser Side Effect Rating Scale (UKU) and functioning with the Personal and Social Performance Scale (PSP). Results: All three antipsychotics significantly improved the baseline to end-point PANSS total and each of the sub-scale scores ( p < 0.001). Risperidone was superior to olanzapine and aripiprazole regarding PANSS total end-point scores ( p < 0.05). Cumulative response (PANSS total score reduction ⩾30%) was similar between risperidone, olanzapine and aripiprazole (74.8%, 73.5% and 70.1%; p = 0.707), but risperidone was superior to aripiprazole regarding PANSS total score reduction ⩾50% (37.8% vs. 26.6%; p < 0.05). Olanzapine was associated with the largest weight gain at week 4 and 8 ( p < 0.01), weight gain ⩾7% (olanzapine = 49.0% vs. risperidone = 32.5% vs. aripiprazole = 17.0%; p < 0.01), more psychic side effects at week 8 ( p < 0.01 each) and more 'other' side effects at week 4 ( p < 0.001) and week 8 ( p < 0.05) but fewer neurological side effects at week 4 ( p < 0.05) and weekPurpose: This study aimed to investigate the efficacy and tolerability of aripiprazole, olanzapine and risperidone in first-episode schizophrenia (FES). Methods: The eight-week, open, randomised study was conducted in six Chinese medical centres. Altogether, 498 FES subjects were randomised to aripiprazole ( n = 165), olanzapine ( n = 168) or risperidone ( n = 165). Efficacy was measured with the Positive and Negative Syndrome Scale (PANSS), tolerability with the Udvalg for Kliniske Undersogelser Side Effect Rating Scale (UKU) and functioning with the Personal and Social Performance Scale (PSP). Results: All three antipsychotics significantly improved the baseline to end-point PANSS total and each of the sub-scale scores ( p < 0.001). Risperidone was superior to olanzapine and aripiprazole regarding PANSS total end-point scores ( p < 0.05). Cumulative response (PANSS total score reduction ⩾30%) was similar between risperidone, olanzapine and aripiprazole (74.8%, 73.5% and 70.1%; p = 0.707), but risperidone was superior to aripiprazole regarding PANSS total score reduction ⩾50% (37.8% vs. 26.6%; p < 0.05). Olanzapine was associated with the largest weight gain at week 4 and 8 ( p < 0.01), weight gain ⩾7% (olanzapine = 49.0% vs. risperidone = 32.5% vs. aripiprazole = 17.0%; p < 0.01), more psychic side effects at week 8 ( p < 0.01 each) and more 'other' side effects at week 4 ( p < 0.001) and week 8 ( p < 0.05) but fewer neurological side effects at week 4 ( p < 0.05) and week 8 ( p < 0.01). PSP improved more with risperidone than with aripiprazole at week 4 and 8 ( p < 0.05). Conclusions: For FES, risperidone might be a better choice than aripiprazole due to improved efficacy and functional improvement, without inferior tolerability. Aripiprazole is a better choice to avoid relevant short-term weight gain. Olanzapine could be chosen to avoid neurological adverse effects. … (more)
- Is Part Of:
- Journal of psychopharmacology. Volume 33:Number 10(2019)
- Journal:
- Journal of psychopharmacology
- Issue:
- Volume 33:Number 10(2019)
- Issue Display:
- Volume 33, Issue 10 (2019)
- Year:
- 2019
- Volume:
- 33
- Issue:
- 10
- Issue Sort Value:
- 2019-0033-0010-0000
- Page Start:
- 1227
- Page End:
- 1236
- Publication Date:
- 2019-10
- Subjects:
- First-episode -- schizophrenia -- antipsychotic -- efficacy -- safety
Psychopharmacology -- Periodicals
615.78 - Journal URLs:
- http://jop.sagepub.com/ ↗
http://www.uk.sagepub.com/home.nav ↗ - DOI:
- 10.1177/0269881119872193 ↗
- Languages:
- English
- ISSNs:
- 0269-8811
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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