United BioSource Corporation, Bethesda, MD 20814, USA.
Schizophr Res. 2010 May;118(1-3):271-8. doi: 10.1016/j.schres.2010.01.021. Epub 2010 Feb 20.
The Medication Satisfaction Questionnaire (MSQ) is a single-item questionnaire which evaluates satisfaction with antipsychotic medication in schizophrenia patients. This study evaluated the reliability and validity for its use in research and clinical settings. Data pooled across treatment groups (control vs. Paliperidone ER) from a randomized 6-week study were used to conduct four psychometric assessments of the MSQ: (1) test-retest reliability, (2) convergent validity, (3) known-groups validity, and (4) minimally important difference (MID). This analysis included 191 randomized subjects. Test-retest reliability was evaluated for patients with no change in satisfaction from weeks 2 to 4 and weeks 4 to 6 (ICC=0.80; 0.83, respectively). Convergent validity was demonstrated through large correlations with Treatment Satisfaction Questionnaire for Medication (TSQM) global score (r=0.72-0.77), and through small correlations with variables measuring clinical symptoms and functioning (e.g., Positive and Negative Syndrome Scale (PANSS) total score [r=-0.30 to -0.17], CGI-S [r=-0.35 to -0.27], SF-36 Physical Functioning Score [r=0.18] and side effects and extrapiramidal measures (including UKU, ESRS-A, SAS). Mean MSQ scores were significantly different between those who completed and discontinued the study, and between different satisfaction groups based on TSQM, demonstrating good known-groups validity. MID estimates for the MSQ ranged from 0.47 (standard error of measurement) to 0.58 (anchor-based method). Results suggest that the MSQ has acceptable reliability and validity, making this single-item questionnaire appropriate and easy to use in clinical research and potentially in clinical practice. A 1-point change on the MSQ may be considered clinically meaningful.
《药物满意度问卷》(MSQ)是一个单项问卷,用于评估精神分裂症患者对抗精神病药物的满意度。本研究评估了其在研究和临床环境中的可靠性和有效性。这项来自一项随机 6 周研究的跨治疗组(对照组与帕利哌酮长效)数据用于对 MSQ 进行四项心理测量学评估:(1)重测信度,(2)聚合效度,(3)已知组有效性,和(4)最小有意义差异(MID)。该分析包括 191 名随机受试者。对于第 2 周到第 4 周和第 4 周到第 6 周满意度无变化的患者,评估重测信度(ICC=0.80;0.83)。通过与治疗满意度问卷药物评分(TSQM)总分(r=0.72-0.77)的大相关性以及与测量临床症状和功能的变量(例如阳性和阴性症状量表(PANSS)总分 [r=-0.30 至-0.17]、CGI-S [r=-0.35 至-0.27]、SF-36 身体功能评分 [r=0.18])和副作用及锥体外系测量值(包括 UKU、ESRS-A、SAS)的小相关性,证明了聚合效度。完成和退出研究的患者之间,以及基于 TSQM 的不同满意度组之间的 MSQ 平均评分差异显著,表明具有良好的已知组有效性。MSQ 的 MID 估计值范围为 0.47(测量误差)至 0.58(基于锚的方法)。结果表明,MSQ 具有可接受的可靠性和有效性,使这个单项问卷适合并易于在临床研究中使用,并且可能在临床实践中使用。MSQ 上的 1 点变化可能被认为具有临床意义。