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Effectiveness of a new tool for self‐evaluation of adherence to antimuscarinic drug treatment in older patients of both sexes with urge incontinence

机译:一种新工具的依从性依赖于抗尿失禁患者抗血清药物治疗的新工具的有效性

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Aim The present study was a comparison of the validity of the Medication Adherence Self‐Report Inventory (MASRI) questionnaire with other methods of assessing adherence to antimuscarinic drugs treatment in older patients with urge incontinence. Methods The experiment involved 733 men and women aged 65 years who had noted no less than one urge incontinence episode per day. At the beginning of the experiment, and after 4, 8 and 12 weeks, their adherence to treatment was monitored using the MASRI. Results The construct validity of the tool was confirmed by data on the correlation of the percentage of non‐adherent patients according to the MASRI and the percentage of patients having a belief barrier on the Brief Medication Questionnaire screen ( r = 0.89, P ≤ 0.01; r = 0.91, P ≤ 0.01; and r = 0.91, P ≤ 0.05 at the 4th, 8th and 12th week of the follow up). The hypothesis of competitive validity was supported by comparing the percentage of non‐adherent patients according to the MASRI and the number of missed doses on the Brief Medication Questionnaire screen ( r = 0.94, P ≤ 0.01; r = 0.85, P ≤ 0.05; and r = 0.7, P ≤ 0.05), and according to a visual count of pills. The area under the curve at the 4th, 8 th , and 12th week was 0.95 ± 0.04, 0.92 ± 0.03 and 0.94 ± 0.04, respectively. Conclusion The MASRI questionnaire has high validity, and is effective for evaluating adherence to treatment among older patients with urge incontinence taking antimuscarinic drugs. Using the MASRI would imply lower costs and greater availability of diagnostics, and it is the tool of choice in clinical practice. Geriatr Gerontol Int 2018; 18: 115–122 .
机译:目的本研究表比较了药物依据自我报告库存(Masri)问卷的有效性与其他方法评估依然尿失禁患者患者依赖于抗血清胰岛素药物治疗的方法。方法实验涉及733名男子和女性效果; 65岁,人们每天注意到不少于一个冲击尿失禁。在实验开始,在4,8和12周后,使用Masri监测它们对治疗的粘附。结果通过根据MASRI的非粘附患者百分比的相关性证实了该工具的构建有效性,并且在短暂的药物调查问卷筛网上具有信仰屏障的患者的百分比(R = 0.89,P≤0.01; r = 0.91,p≤0.01;和后续第4周,第4周和第12周的r = 0.91,p≤0.05)。通过比较Masri的非粘附剂患者的百分比和短暂的药物调查问卷筛网(r = 0.94,p≤0.01; r = 0.85,p≤0.05;和r = 0.7,p≤0.05),并根据药丸的视觉计数。 4,第8周和第12周的曲线下的区域分别为0.95±0.04,0.92±0.03和0.94±0.04。结论马斯里问卷有效,有效评估老年患者尿尿尿动蛋白药物尿毒蛋白药物的患者治疗的依从性。使用Masri将意味着降低成本和更高的诊断可用性,并且是临床实践中的选择工具。 GeriaTr Gerontol int 2018; 18:115-122。

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