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患者对预包装多药电子配药装置的看法:门诊环境中的定性评估

Patient views on an electronic dispensing device for prepackaged polypharmacy: a qualitative assessment in an ambulatory setting.

作者信息

Allemann Samuel S, Hersberger Kurt E, Arnet Isabelle

机构信息

Pharmaceutical Care Research Group, Department of Pharmaceutical Sciences, University of Basel, Basel, Switzerland.

出版信息

Integr Pharm Res Pract. 2015 Nov 6;4:167-174. doi: 10.2147/IPRP.S90923. eCollection 2015.

Abstract

OBJECTIVE

To collect opinions on medication management aids (MMAs) in general and on an electronic MMA (e-MMA) dispensing prepackaged polypharmacy in sealed pouches.

STUDY SETTING

The setting involved community-dwelling older adults in Basel, Switzerland, in 2013.

STUDY DESIGN

The study involved 1) a 14-day trial with the e-MMA and 2) a focus group to identify general attributes of MMAs, their applicability to the e-MMA, and possible target groups for the e-MMA.

DATA COLLECTION METHODS

Six participants using long-term polypharmacy and willing to try new technologies completed the 14-day trial and participated in the focus group. Inductive content analysis was performed to extract data.

PRINCIPAL FINDINGS

Participants rated ten of 17 general attributes as clearly applicable to the e-MMA and five as unsuitable. Attributes pertained to three interrelating themes: product design, patient support, and living conditions. Envisaged target groups were patients with time-sensitive medication regimens, patients with dementia, the visually impaired, and several patients living together to prevent accidental intake of the wrong medication.

CONCLUSION

The evaluated e-MMA for prepackaged polypharmacy met the majority of the requirements set for an MMA. Patients' living conditions, such as mobility, remain the key determinants for acceptance of an e-MMA.

摘要

目的

收集关于药物管理辅助工具(MMAs)的总体意见,以及关于一种电子药物管理辅助工具(e-MMA)的意见,该工具用于预包装多药复方的密封药袋配药。

研究背景

该研究于2013年在瑞士巴塞尔针对社区居住的老年人展开。

研究设计

该研究包括1)一项为期14天的e-MMA试验,以及2)一个焦点小组,以确定MMAs的一般属性、其对e-MMA的适用性以及e-MMA的可能目标群体。

数据收集方法

六名长期使用多药复方且愿意尝试新技术的参与者完成了为期14天的试验并参与了焦点小组。采用归纳性内容分析法提取数据。

主要发现

参与者认为17项一般属性中的10项明显适用于e-MMA,5项不适用。这些属性涉及三个相互关联的主题:产品设计、患者支持和生活条件。设想的目标群体包括用药方案有时间要求的患者、痴呆患者、视力受损者以及一些共同居住以防误服药物的患者。

结论

评估的预包装多药复方e-MMA符合为MMAs设定的大多数要求。患者的生活条件,如行动能力,仍然是接受e-MMA的关键决定因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ee5/5741022/6a8806234129/iprp-4-167Fig1.jpg

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