Grosset K A, Bone I, Reid J L, Grosset D
Institute of Neurological Sciences, Department of Neurology, Southern General Hospital, Glasgow G51 4TF.
J Neurol Neurosurg Psychiatry. 2006 Feb;77(2):249-51. doi: 10.1136/jnnp.2005.064709.
The objective of this study was to assess different methods of measuring therapy adherence in Parkinson's disease (PD). In a single centre observational study, 112 patients with idiopathic PD were randomised to a crossover trial of active monitoring (n = 69, simple tablet count and electronic monitoring), or to no monitoring (n = 43, control group). All patients completed a self report and visual analogue scale (VAS) indicating therapy intake. In the active monitoring group, 56 (81% of cases) used > or = 80% of their medication, and 13 (19% of cases) used <80%, based on electronic monitoring. Median adherence for self report was 100% (interquartile range (IQR) 100 to 100) and for VAS was 100% (IQR 95 to 100), in both active and control groups. Patients taking > or = 80% of prescribed medication had a median total adherence of 98% (IQR 93 to 101) by electronic monitoring, which was similar to that from other
self report 100%, IQR 100 to 100; VAS 100%, IQR 95 to 100; simple tablet count 98%, IQR 89 to 100. Median total adherence in patients taking <80% of medication was significantly lower by electronic monitoring (69%, IQR 44 to 74) than by other methods: self report 100%, IQR 100 to 100; VAS 100%, IQR 95 to 100; and simple tablet count 90%, IQR 78 to 100 (all p<0.0001). Sensitivities of self report (10%), VAS (17%), and simple tablet count (50%) were all low for detecting suboptimal medicine intake. Self report, VAS, and simple tablet counts are insensitive as predictors of suboptimal medicine usage in PD. How patients take their medicines influences interpretation of the therapy response and consequent management decisions, with implications for clinical trial analysis and clinical practice.
本研究的目的是评估帕金森病(PD)中测量治疗依从性的不同方法。在一项单中心观察性研究中,112例特发性PD患者被随机分配到主动监测的交叉试验(n = 69,简单药片计数和电子监测)或无监测组(n = 43,对照组)。所有患者均完成了一份表明治疗药物摄入情况的自我报告和视觉模拟量表(VAS)。在主动监测组中,基于电子监测,56例(81%)患者服用了≥80%的药物,13例(19%)患者服用的药物<80%。主动监测组和对照组中,自我报告的中位依从性均为100%(四分位间距(IQR)100至100),VAS的中位依从性均为100%(IQR 95至100)。服用≥80%规定药物的患者通过电子监测的总中位依从性为98%(IQR 93至101),这与其他方法的结果相似:自我报告为100%,IQR 100至100;VAS为100%,IQR 95至100;简单药片计数为98%,IQR 89至100。服用<80%药物的患者通过电子监测的总中位依从性(69%,IQR 44至74)显著低于其他方法:自我报告为100%,IQR 100至100;VAS为100%,IQR 95至100;简单药片计数为90%,IQR 78至100(所有p<0.0001)。自我报告(10%)、VAS(17%)和简单药片计数(50%)检测次优药物摄入的敏感性均较低。自我报告、VAS和简单药片计数作为PD中次优药物使用的预测指标不敏感。患者服药方式会影响对治疗反应的解读以及后续的管理决策,这对临床试验分析和临床实践具有重要意义。