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通过使用雾化器时间记录器提高临床试验中吸入器的依从性。

Improving inhaler adherence in a clinical trial through the use of the nebulizer chronolog.

作者信息

Nides M A, Tashkin D P, Simmons M S, Wise R A, Li V C, Rand C S

机构信息

Division of Pulmonary Medicine, University of California, Los Angeles School of Medicine.

出版信息

Chest. 1993 Aug;104(2):501-7. doi: 10.1378/chest.104.2.501.

Abstract

This study examined whether utilizing an electronic medication monitor (Nebulizer Chronolog) to provide participants with detailed feedback on their metered-dose inhaler (ipratropium bromide or placebo) usage patterns would result in closer adherence to the prescribed regimen of two inhalations three times daily compared to a control group not receiving feedback. Adherence was also measured by canister weighing and self-report. Two-hundred fifty-one consecutive special intervention participants from the University of California, Los Angeles, and Johns Hopkins University centers of a National Heart, Lung, and Blood Institute-sponsored clinical trial were enrolled in this ancillary study. Compared to controls, feedback participants at the 4-month follow-up adhered more closely to the prescribed three sets per day (mean 1.95 vs 1.65) and used the prescribed two actuations in a greater percentage of sets (80 percent vs 60.3 percent). These results indicate that electronic monitoring of metered-dose inhaler use with a Nebulizer Chronolog in a clinical trial not only provides a more accurate assessment of adherence to prescribed inhaler use, but also enhances adherence when participants are given feedback of the monitoring results.

摘要

本研究探讨了使用电子药物监测器(雾化器时间记录器)向参与者提供其定量吸入器(异丙托溴铵或安慰剂)使用模式的详细反馈,与未接受反馈的对照组相比,是否会使参与者更严格地遵守每日三次、每次两喷的规定治疗方案。还通过药罐称重和自我报告来衡量依从性。来自加利福尼亚大学洛杉矶分校和约翰·霍普金斯大学中心的251名连续参与一项由美国国立心肺血液研究所赞助的临床试验的特殊干预参与者被纳入了这项辅助研究。与对照组相比,在4个月的随访中,接受反馈的参与者更严格地遵守了每天规定的三组用药(平均1.95组对1.65组),并且在更大比例的用药组中使用了规定的两喷(80%对60.3%)。这些结果表明,在临床试验中使用雾化器时间记录器对定量吸入器的使用进行电子监测,不仅能更准确地评估对规定吸入器使用的依从性,而且当向参与者提供监测结果反馈时,还能提高依从性。

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