Personal and Social Functioning and Health-Related Quality of Life in Patients with Schizophrenia Treated with the Long-Acting Injectable Antipsychotic Risperidone ISM

被引:6
|
作者
Litman, Robert [1 ,2 ]
Naber, Dieter [3 ]
Anta, Lourdes [4 ]
Martinez, Javier [4 ,9 ]
Filts, Yuriy [5 ]
Correll, Christoph U. [6 ,7 ,8 ]
机构
[1] CBH Hlth LLC, Gaithersburg, MD USA
[2] Georgetown Univ Med Sch, Dept Psychiat, Washington, DC USA
[3] Hamburg Eppendorf Univ, Dept Psychiat & Psychotherapy, Hamburg, Germany
[4] Labs Farmaceut ROVI SA, Med Dept, Madrid, SA, Spain
[5] Lviv Reg Clin Psychiat Hosp, Communal Noncommercial Enterprise Lviv Reg Council, Lvov, Ukraine
[6] Zucker Hillside Hosp, Dept Psychiat Res, Glen Oaks, NY USA
[7] Donald & Barbara Zucker Sch Med Hofstra Northwell, Dept Psychiat & Mol Med, Hempstead, NY USA
[8] Charite, Dept Child & Adolescent Psychiat, Berlin, Germany
[9] Labs Farmaceut ROVI SA, Calle Alfonso Gomez 45A, Madrid 28037, Spain
关键词
risperidone; long -acting injectable; antipsychotics; schizophrenia; social functioning; quality of life; PERFORMANCE SCALE PSP; PALIPERIDONE PALMITATE; MAINTENANCE TREATMENT; OPEN-LABEL; MEDICATIONS; EFFICACY; PLACEBO; SAFETY; TOLERABILITY; METAANALYSIS;
D O I
10.2147/NDT.S392351
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To analyze the effect of Risperidone ISM on social functioning and health-related quality of life (HR-QoL) in both shortand long-term treatment of patients with schizophrenia. Patients and Methods: This analysis was based on data from both phases of the PRISMA-3 study, including 433 relapsed patients from the double-blind (DB) phase of the PRISMA-3 trial who were treated for 12-weeks with once-monthly (every 28 days) intramuscular Risperidone ISM 75 mg or 100 mg (n = 288), or placebo (n = 145), as well as 174 patients transitioning from the DB to an open-label 52-week extension (OLE) phase, plus 41 de novo patients treated on a stable maintenance dose of oral risperidone. The clinician-administered Personal and Social Performance (PSP) scale and the patient-reported 20-item Subjective Wellbeing under Neuroleptics scale (SWN-20) were used to measure social functioning and HR-QoL outcomes, respectively. Results: Risperidone ISM significantly improved PSP total score from baseline to endpoint (Day 85) versus placebo in the DB phase with mean change total score (95% CI) of 10.7 (9; 12) compared to 4.8 (3; 7) for placebo (p < 0.0001). The statistically significant improvement was present from the first measurement time point (Day 29). SWN-20-measured HR-QoL increased on average in patients treated with Risperidone ISM in the DB phase. A significant improvement was also observed for PSP and SWN-20 scores from the OLE baseline to week 52 for patients transitioning from the DB phase. Stable de novo patients maintained similar PSP and SWN-20 scores during the whole OLE phase. Conclusion: Risperidone ISM provided a rapid and sustained improvement in personal and social functioning, and HR-QOL without need of oral risperidone supplementation or loading doses. These findings, along with a fast onset of efficacy, could contribute to reinforcing the therapeutic alliance and possibly an earlier discharge. Moreover, patient functioning continued improving or was maintained with long-term treatment.
引用
收藏
页码:219 / 232
页数:14
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