Oxford Outcomes Ltd, Oxford, UK.
Mult Scler. 2011 Dec;17(12):1504-13. doi: 10.1177/1352458511414039. Epub 2011 Jul 14.
The Functional Assessment of Multiple Sclerosis (FAMS) is widely used in clinical trial programmes; however, it was developed before the rise in trials targeted at early stage multiple sclerosis (MS) and clinically isolated syndrome (CIS).
The aim of this study was to assess the psychometric properties of the FAMS within two clinically distinct populations, CIS and early relapsing-remitting MS (RRMS), and discern the appropriateness of the FAMS within these populations.
Secondary analysis was conducted on FAMS data from two clinical trials assessing interferon beta-1b in early RRMS and CIS. The statistical analysis assessed the scale acceptability, reliability, validity and responsiveness of the FAMS. Item response theory (IRT) was also conducted on the early RRMS sample in order to assess how well the FAMS discriminated amongst individuals with less severe MS.
Results from both trials demonstrated an improvement in the FAMS psychometric properties with increased baseline disease severity. However, high ceiling effects were evident amongst less severe patients, and there was an overall lack of responsiveness to improvement and poor construct validity. IRT also demonstrated its lack of discrimination/sensitivity in early RRMS.
In trials involving patients with early stage RRMS and CIS, modifications to the FAMS based on a qualitative assessment of its content validity in these populations would be required in order to potentially improve the FAMS psychometric properties and sensitivity.
多发性硬化症功能评估量表(FAMS)广泛应用于临床试验方案中;然而,它是在针对早期多发性硬化症(MS)和临床孤立综合征(CIS)的试验兴起之前开发的。
本研究旨在评估 FAMS 在两个具有临床差异的人群(CIS 和早期复发缓解型 MS(RRMS))中的心理测量特性,并确定 FAMS 在这些人群中的适用性。
对两项评估干扰素β-1b 在早期 RRMS 和 CIS 中的临床试验的 FAMS 数据进行二次分析。统计分析评估了 FAMS 的量表可接受性、可靠性、有效性和反应性。还对早期 RRMS 样本进行了项目反应理论(IRT)分析,以评估 FAMS 在区分轻度 MS 个体方面的效果。
两项试验的结果表明,随着基线疾病严重程度的增加,FAMS 的心理测量特性得到了改善。然而,轻度患者中存在较高的天花板效应,且总体上缺乏对改善的反应性和较差的结构有效性。IRT 还表明其在早期 RRMS 中缺乏区分力/敏感性。
在涉及早期 RRMS 和 CIS 患者的试验中,需要对 FAMS 进行修改,方法是基于对这些人群中其内容有效性的定性评估,以潜在改善 FAMS 的心理测量特性和敏感性。