Ismail Zahinoor, Peters-Strickland Timothy, Miguelez Maia, Baker Ross A, Hertel Peter, Eramo Anna, Jin Na, Perry Pamela, Sanchez Raymond, McQuade Robert D, Kane John M
From the Departments of *Psychiatry and †Neurology, Hotchkiss Brain Institute, University of Calgary, Calgary, Canada; ‡Otsuka Pharmaceutical Development & Commercialization, Inc, Princeton, NJ; §Otsuka Canada Pharmaceutical, Inc, Quebec, Canada; ∥H. Lundbeck A/S, Copenhagen-Valby, Denmark; ¶Lundbeck LLC, Deerfield, IL; #Otsuka Pharmaceutical Development & Commercialization, Inc, Rockville, MD; **The Zucker Hillside Hospital, Glen Oaks and ††Hofstra Northwell School of Medicine, Hempstead, NY.
J Clin Psychopharmacol. 2017 Jun;37(3):347-350. doi: 10.1097/JCP.0000000000000710.
Long-acting injectable antipsychotics are treatment options for acute and long-term treatment of patients with schizophrenia. In a previously published 12-week randomized, double-blind, placebo-controlled clinical trial of patients with schizophrenia experiencing an acute psychotic episode, aripiprazole once-monthly 400 mg (AOM 400) produced significantly greater improvement than placebo on the primary endpoint, Positive and Negative Syndrome Scale (PANSS) total score at week 10.
To examine the efficacy of AOM 400 across a broader representation of schizophrenia symptoms, including agitation, a post hoc analysis of this trial was carried out to assess the change in PANSS Marder factor domains (positive symptoms, negative symptoms, disorganized thought, uncontrolled hostility/excitement, and anxiety/depression) and the PANSS excited component (equivalent to Marder factor domain uncontrolled hostility/excitement plus the tension item) by comparing differences in change from baseline between AOM 400 and placebo using a mixed model for repeated measures.
The differences between treatment and placebo for all factors were statistically significant, with improvements seen as early as week 1 or 2, and maintained through week 12. Thus, AOM 400, supplemented with oral aripiprazole in the first 2 weeks, showed significantly greater efficacy versus placebo in acutely ill patients with schizophrenia in all 5 Marder illness domains, as well as in agitation as conceptualized by the PANSS excited component score.
These findings indicate that AOM 400 is efficacious across the spectrum of schizophrenia symptoms in acutely ill patients, with implications for both short-term and, by extension, long-term patient outcomes.
长效注射用抗精神病药物是治疗精神分裂症患者急性发作和长期治疗的选择。在之前发表的一项针对经历急性精神病发作的精神分裂症患者的为期12周的随机、双盲、安慰剂对照临床试验中,每月一次400mg阿立哌唑(AOM 400)在主要终点指标(第10周时的阳性和阴性症状量表(PANSS)总分)上比安慰剂产生了显著更大的改善。
为了在更广泛的精神分裂症症状表现中检验AOM 400的疗效,包括激越症状,对该试验进行了一项事后分析,以评估PANSS马德因子域(阳性症状、阴性症状、思维紊乱、失控的敌意/兴奋和焦虑/抑郁)的变化,以及通过使用重复测量的混合模型比较AOM 400和安慰剂组从基线开始的变化差异,来评估PANSS激越成分(相当于马德因子域失控的敌意/兴奋加上紧张项目)。
所有因子的治疗组与安慰剂组之间的差异具有统计学意义,早在第1周或第2周就出现改善,并持续到第12周。因此,在前2周补充口服阿立哌唑的AOM 400,在所有5个马德疾病域中,以及在由PANSS激越成分评分所概念化的激越方面,对急性精神分裂症患者显示出比安慰剂显著更大的疗效。
这些发现表明,AOM 400对急性病精神分裂症患者的一系列症状有效,对短期以及由此延伸的长期患者预后均有影响。