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The MOBID-2 pain scale: Reliability and responsiveness to pain in patients with dementia

机译:MOBID-2疼痛量表:痴呆患者对疼痛的可靠性和反应性

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Background Mobilization-Observation-Behavior-Intensity-Dementia-2 (MOBID-2) pain scale is a staff-administered pain tool for patients with dementia. This study explores MOBID-2's test-retest reliability, measurement error and responsiveness to change.Methods Analyses are based upon data from a cluster randomized trial including 352 patients with advanced dementia from 18 Norwegian nursing homes. Test-retest reliability between baseline and week 2 (n = 163), and weeks 2 and 4 (n = 159) was examined in patients not expected to change (controls), using intraclass correlation coefficient (ICC2.1), standard error of measurement (SEM) and smallest detectable change (SDC). Responsiveness was examined by testing six priori-formulated hypotheses about the association between change scores on MOBID-2 and other outcome measures.Results ICCs of the total MOBID-2 scores were 0.81 (0-2 weeks) and 0.85 (2-4 weeks). SEM and SDC were 1.9 and 3.1 (0-2 weeks) and 1.4 and 2.3 (2-4 weeks), respectively. Five out of six hypotheses were confirmed: MOBID-2 discriminated (p < 0.001) between change in patients with and without a stepwise protocol for treatment of pain (SPTP). Moderate association (r = 0.35) was demonstrated with Cohen-Mansfield Agitation Inventory, and no association with Mini-Mental State Examination, Functional Assessment Staging and Activity of Daily Living. Expected associations between change scores of MOBID-2 and Neuropsychiatric Inventory - Nursing Home version were not confirmed.Conclusion The SEM and SDC in connection with the MOBID-2 pain scale indicate that the instrument is responsive to a decrease in pain after a SPTP. Satisfactory test-retest reliability across test periods was demonstrated. Change scores ≥ 3 on total and subscales are clinically relevant and are beyond measurement error.
机译:背景动员-观察-行为强度-痴呆2(MOBID-2)疼痛量表是痴呆症患者的人工管理疼痛工具。这项研究探讨了MOBID-2的重测信度,测量误差和对变化的响应能力。方法分析是基于一项随机试验的数据,该试验包括来自18个挪威养老院的352例晚期痴呆患者。使用组内相关系数(ICC2.1),标准误为±1,对基线和第2周(n = 163),第2周和第4周(n = 159)之间的预期重测可靠性进行了检查测量(SEM)和最小可检测变化(SDC)。通过测试关于MOBID-2上的变化评分与其他结局指标之间的关联的六个先天假设假设来检验反应性。结果,MOBID-2总评分的ICC为0.81(0-2周)和0.85(2-4周) 。 SEM和SDC分别为1.9和3.1(0-2周)和1.4和2.3(2-4周)。六种假设中的五种得到了证实:MOBID-2在有和没有逐步治疗疼痛(SPTP)的患者中区分出变化(p <0.001)。 Cohen-Mansfield焦虑量表显示中等程度的关联(r = 0.35),而与迷你精神状态检查,功能评估分期和日常生活活动没有关联。未确认MOBID-2的变化评分与神经精神病学目录-疗养院版本之间的预期关联。结论SEM和SDC与MOBID-2疼痛量表相关,表明该仪器对SPTP术后疼痛减轻有反应。整个测试期间的重测信度都令人满意。总分和分量表的变化得分≥3与临床相关,并且超出测量误差。

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