Opler Mark G A, Claxton Amy, McGrory James, Gasper Sabina, Wang Meihua, Yagoda Sergey
Dr. Opler is with WCG, Inc. in New York, New York.
Drs. Claxton, McGrory, Wang, and Yagoda and Ms. Gasper are with Alkermes, Inc. in Waltham, Massachusetts.
Innov Clin Neurosci. 2024 Mar 1;21(1-3):43-51. eCollection 2024 Jan-Mar.
Clinical practice guidelines support efforts to improve functioning in patients with schizophrenia. Discrepancies in the perception of cognitive status between clinicians, patients with schizophrenia, and their caregivers have been associated with impaired functional abilities in patients; medication side effects might worsen both cognition and daily functioning. We assessed daily/social functioning and cognition in stable patients with schizophrenia who switched to the long-acting injectable (LAI) antipsychotic aripiprazole lauroxil (AL).
Clinically stable adults with residual symptoms of schizophrenia or intolerance following three or more doses of paliperidone palmitate or risperidone LAI were switched to flexibly dosed open-label AL treatment (441mg, 662mg, or 882mg every 4 weeks or 882mg every 6 weeks) for six months (ClinicalTrials.gov identifier: NCT02634320). Daily/social functioning was assessed using the Personal and Social Performance Scale (PSP); total and subscale scores were summarized using descriptive statistics. The cognitive status of patients was assessed using the New York Assessment of Adverse Cognitive Effects of Neuropsychiatric Treatment (NY-AACENT) at baseline and Month 6 or early termination, providing patient, caregiver, and clinician perspectives. A analysis assessed level of agreement in ratings of cognitive status among respondents, evaluated at baseline and last assessment, using weighted kappa coefficients (0.01-0.20, slight agreement; 0.21-0.40, fair agreement; 0.41-0.60, moderate agreement; 0.61-0.80, substantial agreement.).
All 51 enrolled patients received one or more AL doses; 35 completed the study, and 45 contributed data at last assessment. Mean age was 40.6 years; 72.5 percent of patients were male. Based on PSP total score, functioning was maintained from baseline (mean [standard deviation (SD)]: 55.1 [10.5]) through six months of AL treatment (mean [SD]: 57.7 [13.2]). Proportions of patients rating personal and social functioning issues as "not present" or "mild" remained stable between baseline and Month 6 for each PSP subscale. At baseline (n=50), cognitive difficulties were most commonly rated "not present" or "mild" in all NY-AACENT domains by patients (58-86% across domains), clinicians (62-94%), and caregivers (50-92%), and these rates were maintained or increased at last assessment for all reporters. Weighted kappa coefficients indicated fair-to-substantial agreement between patients and clinicians across domains at last assessment (0.32-0.64; baseline: 0.14-0.55); patient-caregiver agreement ranged from 0.07 to 0.50 at last assessment (baseline: 0.25-0.60).
In clinically stable patients with schizophrenia who initiated AL, self-reported functioning was maintained over six months of treatment. Clinician-, caregiver-, and patient-reported cognitive function was stable at baseline and maintained in all NY-AACENT domains; patient-clinician agreement on level of cognitive impairment increased over six months of treatment with AL.
临床实践指南支持改善精神分裂症患者功能的努力。临床医生、精神分裂症患者及其照料者对认知状态的认知差异与患者功能能力受损有关;药物副作用可能会使认知和日常功能恶化。我们评估了换用长效注射用(LAI)抗精神病药物阿立哌唑月桂酸盐(AL)的病情稳定的精神分裂症患者的日常/社交功能和认知情况。
临床上病情稳定、有残留症状或在接受三剂或更多剂棕榈酸帕利哌酮或利培酮长效注射剂后不耐受的成年人,换用灵活给药的开放标签AL治疗(每4周441mg、662mg或882mg,或每6周882mg),为期6个月(ClinicalTrials.gov标识符:NCT02634320)。使用个人和社会表现量表(PSP)评估日常/社交功能;使用描述性统计总结总分和子量表分数。在基线以及第6个月或提前终止时,使用纽约神经精神治疗不良认知效应评估量表(NY - AACENT)评估患者的认知状态,提供患者、照料者和临床医生的观点。一项分析使用加权kappa系数(0.01 - 0.20,轻度一致;0.21 - 0.40,一般一致;0.41 - 0.60,中度一致;0.61 - 0.80,高度一致)评估了在基线和最后评估时受访者之间认知状态评分的一致程度。
所有51名入组患者均接受了一剂或多剂AL;35名患者完成了研究,45名患者在最后评估时提供了数据。平均年龄为40.6岁;72.5%的患者为男性。根据PSP总分,从基线(均值[标准差(SD)]:55.1[10.5])到接受AL治疗6个月(均值[SD]:57.7[13.2]),功能得以维持。在基线和第6个月之间,每个PSP子量表中,将个人和社交功能问题评为“不存在”或“轻度”的患者比例保持稳定。在基线时(n = 50),患者(各领域58 - 86%)、临床医生(62 - 94%)和照料者(50 - 92%)在所有NY - AACENT领域中最常将认知困难评为“不存在”或“轻度”,并且在最后评估时,所有报告者的这些比例保持或有所增加。加权kappa系数表明,在最后评估时,患者和临床医生在各领域之间的一致性为一般到高度一致(0.32 - 0.64;基线:0.14 - 0.55);在最后评估时,患者与照料者的一致性范围为0.07至0.50(基线:0.25 - 0.60)。
在开始使用AL的病情稳定的精神分裂症患者中,自我报告的功能在6个月的治疗期间得以维持。临床医生、照料者和患者报告的认知功能在基线时稳定,并且在所有NY - AACENT领域中保持稳定;在接受AL治疗的6个月期间,患者与临床医生在认知损害程度上的一致性有所增加。