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Design and Quality Considerations for Developing Mobile Apps for Medication Management最新文献

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Acceptability and Adoption of mHealth Interventions for Medication Adherence 移动医疗干预药物依从性的可接受性和采用
Pub Date : 1900-01-01 DOI: 10.4018/978-1-7998-3832-6.ch005
The success of medication adherence apps depends on user acceptance and usage of the apps in their daily lives. It is essential for app developers to gain an in-depth understanding of the factors that can influence the acceptance of mHealth apps for adherence. It has been suggested that end users' acceptance of a technology-based health intervention can be studied through evaluation of their behavioral intention to use the intervention. Hence, it is important to continuously engage the target audience (e.g. clinicians, patients, caregivers) for their perceptions, experiences and feedback about the technological intervention, in this case, medication adherence apps. Factors such as socio-demographics and prior use of mobile technologies can influence user acceptance and adoption of mHealth apps. This chapter introduces the evolution of the Technology Acceptance Model (TAM) and the Unified Theory of Acceptance and Use of Technology (UTAUT). In addition, the application of the UTAUT2 model is described through a case study in Singapore that determined the factors which influenced the acceptability of mHealth-based adherence interventions among healthcare institutions in Singapore.
药物依从应用程序的成功取决于用户在日常生活中对应用程序的接受和使用。对于应用程序开发人员来说,深入了解可能影响人们接受移动健康应用程序的因素是至关重要的。有人建议,可以通过评估最终用户使用干预措施的行为意愿来研究他们对基于技术的健康干预措施的接受程度。因此,不断吸引目标受众(如临床医生、患者、护理人员)对技术干预的看法、经验和反馈是很重要的,在这种情况下,是药物依从性应用程序。社会人口统计和先前使用移动技术等因素会影响用户对移动健康应用程序的接受和采用。本章介绍了技术接受模型(TAM)和技术接受与使用统一理论(UTAUT)的演变。此外,通过新加坡的一个案例研究描述了UTAUT2模型的应用,该案例研究确定了影响新加坡医疗机构中基于移动健康的依从性干预措施可接受性的因素。
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引用次数: 0
The Need for Quality Assessment of mHealth Interventions 移动医疗干预措施质量评估的必要性
Pub Date : 1900-01-01 DOI: 10.4018/978-1-7998-3832-6.ch004
With growing numbers of mHealth interventions, there is a need to evaluate the quality of existing apps based on quality assessment criteria that are grounded in published literature and health behavior research. These criteria can help identify the quality of mHealth apps from the perspectives of reliability, feature usefulness and feature convenience. This chapter will discuss the various quality criteria that are relevant for mHealth apps that target drug-related problems, as well as for medication management, through the development of two quality assessment tools. In addition to reliability, usability and privacy criteria, other feature criteria related to tele-monitoring, interaction checkers, dose calculators, medication information provision, medication records, as well as tele-support, tele-collaboration and personalization/contextualization, will be discussed. This chapter aims to provide guidance to mobile app developers, clinicians and patients on the types of quality parameters to consider in apps that are designed for pharmaceutical care and medication management.
随着移动医疗干预的数量不断增加,有必要根据基于已发表文献和健康行为研究的质量评估标准来评估现有应用程序的质量。这些标准可以从可靠性、功能有用性和功能便利性的角度来帮助识别移动健康应用程序的质量。本章将通过开发两种质量评估工具,讨论与针对药物相关问题的移动健康应用程序以及药物管理相关的各种质量标准。除了可靠性、可用性和隐私标准外,还将讨论与远程监测、交互检查器、剂量计算器、药物信息提供、药物记录以及远程支持、远程协作和个性化/情境化相关的其他特征标准。本章旨在为移动应用程序开发人员、临床医生和患者提供指导,指导他们在为药物护理和药物管理设计的应用程序中考虑的质量参数类型。
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引用次数: 1
A Pharmaco-cybernetics Approach to Designing an Oncology Drug Interaction Database for Clinical Practice 用药物控制论方法设计临床肿瘤药物相互作用数据库
Pub Date : 1900-01-01 DOI: 10.4018/978-1-7998-3832-6.ch007
This chapter describes how OncoRx-MI, a pharmaco-informatics platform for detecting chemotherapy interactions, was designed through a pharmaco-cybernetics approach targeting the 5 activities of the digital health innovation process. This is the first database of its kind that is able to provide interaction information for anticancer drugs and chemotherapy regimen cocktails. In order to identify the gap and determine the usefulness of this database in clinical oncology practice, the quality of online anticancer drug interactions was assessed, and the perceptions of oncology practitioners were sought. The results showed that the accuracy of drug interaction content and the clinical usefulness of the database was highly regarded by these practitioners. In addition, evidence of its relevance and credibility was demonstrated through user feedback on the database.
本章描述了OncoRx-MI(一个用于检测化疗相互作用的药物信息学平台)是如何通过药物控制论方法设计的,该方法针对数字健康创新过程的5项活动。这是同类数据库中第一个能够提供抗癌药物和化疗方案鸡尾酒相互作用信息的数据库。为了确定差距并确定该数据库在临床肿瘤学实践中的有用性,评估了在线抗癌药物相互作用的质量,并寻求肿瘤学从业者的看法。结果表明,药物相互作用内容的准确性和数据库的临床实用性得到了从业人员的高度评价。此外,用户对数据库的反馈证明了数据库的相关性和可信性。
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引用次数: 0
Introduction to Pharmaceutical Care and Medication Adherence 药学护理和药物依从性导论
Pub Date : 1900-01-01 DOI: 10.4018/978-1-7998-3832-6.ch001
Pharmaceutical care is a concept that involves identifying, solving and preventing drug-related problems, such as drug interactions, with regards to a patient's drug therapy. Cancer patients are at high risk of drug interactions due to the complex pharmacological profiles and narrow therapeutic indices of anticancer drugs. Furthermore, these patients tend to consume complementary and alternative medicines, thus predisposing them to a risk of herb-drug interactions. This can impact their adherence to anticancer therapies. Various factors are involved in medication non-adherence, such as the cost of medications and patients' beliefs about the value of their treatments. There is a need to understand the impact of non-adherence and optimize intervention strategies from a macro-, meso-, and micro-level. Chapter 1 introduces the concept of pharmaceutical care and the impact of oncology drug interactions and medication non-adherence in patients with cancer. The chapter will also provide an insight to the factors influencing medication adherence and the intervention strategies that have targeted non-adherence.
药学保健是一个概念,涉及识别、解决和预防与药物有关的问题,如药物相互作用,涉及到患者的药物治疗。由于抗癌药物的药理特征复杂,治疗指标狭窄,癌症患者存在药物相互作用的高风险。此外,这些患者倾向于服用补充和替代药物,从而使他们容易受到草药相互作用的风险。这可能会影响他们对抗癌治疗的坚持。药物不依从性涉及各种因素,例如药物的成本和患者对其治疗价值的信念。有必要从宏观、中观和微观层面了解不依从的影响并优化干预策略。第1章介绍了药学服务的概念以及肿瘤药物相互作用和药物依从性对癌症患者的影响。本章还将提供对影响药物依从性的因素和针对不依从性的干预策略的见解。
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引用次数: 0
Application of Health Behavior Frameworks in the Design of an Oral Anticancer Medication Adherence App 健康行为框架在口服抗癌药物依从性应用程序设计中的应用
Pub Date : 1900-01-01 DOI: 10.4018/978-1-7998-3832-6.ch006
L. Dayer
This chapter describes the application of the Intervention Mapping (IM) framework through a case study of the development of an in-house medication adherence mHealth app for oral anticancer medications (called MedFC). Using the behavioral intervention frameworks described previously, this chapter discusses how patients' medication adherence needs, mobile app usage, perceptions and experiences with the prototype helped inform the development of MedFC. Through iterative evaluations, this chapter will illustrate how a mHealth intervention can be developed in a holistic manner, involving its target audience in the design process.
本章通过一个内部服药依从性移动健康应用程序(称为MedFC)的案例研究,描述了干预映射(IM)框架的应用。使用前面描述的行为干预框架,本章讨论了患者的药物依从性需求、移动应用程序的使用、对原型的感知和体验如何帮助告知MedFC的发展。通过迭代评估,本章将说明如何以整体方式开发移动医疗干预,使其目标受众参与设计过程。
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引用次数: 0
The Role of mHealth in Improving Health and Medication Management 移动医疗在改善健康和药物管理中的作用
Pub Date : 1900-01-01 DOI: 10.4018/978-1-7998-3832-6.ch002
Mobile health (mHealth) involves the application of mobile devices and their related technologies in the provision of healthcare. In recent years, mHealth has become one of the most promising fields in improving healthcare quality and outcomes. There were over 325,000 mHealth apps in 2017, and this number is expected to grow tremendously due to continued investments in health apps. With advancements in mobile technologies and connectivity, mobile app developers now have the flexibility to develop and implement various mHealth-based interventions for medication management. Through improved functionalities and integration with electronic medical records, mHealth can potentially enable the provision of macro-, meso-, micro- and patient-level interventions in a more efficient manner. Chapter 2 provides an overview of the various mHealth interventions that have targeted medication management and medication non-adherence throughout the years, such as short-messaging services (SMSes) and smartphone apps. The functionalities that are useful in mHealth apps will also be discussed.
移动医疗(mHealth)涉及在提供医疗保健方面应用移动设备及其相关技术。近年来,移动医疗已成为提高医疗质量和结果最有前途的领域之一。2017年有超过32.5万个移动健康应用程序,由于对健康应用程序的持续投资,这一数字预计将大幅增长。随着移动技术和连通性的进步,移动应用程序开发人员现在可以灵活地开发和实施各种基于移动健康的药物管理干预措施。通过改进功能和与电子医疗记录的集成,移动医疗有可能以更有效的方式提供宏观、中观、微观和患者层面的干预措施。第2章概述了多年来针对药物管理和药物依从性的各种移动健康干预措施,如短信服务(sms)和智能手机应用程序。在移动健康应用程序中有用的功能也将被讨论。
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引用次数: 0
Design Principles in the Development of Digital Health Applications 数字健康应用开发中的设计原则
Pub Date : 1900-01-01 DOI: 10.4018/978-1-7998-3832-6.ch003
The roles of patients and healthcare professionals have evolved with the digital age. The convergence of digital technologies with health and healthcare services has led to the birth of disciplines such as digital health and pharmaco-cybernetics. Development of digital health innovations and mHealth applications need to be useful and user-friendly. For example, ease-of-use associated with mobile app interfaces can be more important to patients than the number and type of functionalities. Therefore, the application of health behavior theories and patient-centered approaches is needed to develop clinically relevant digital health systems and mHealth apps. This chapter introduces the pharmaco-cybernetic frameworks that are relevant for designing digital health innovations and an Intervention Mapping (IM) framework that can help inform behavioral change techniques. Concepts such as the Pharmaco-cybernetic Maxims, user-centered (UCD), experience-centered (ECD) and activity-centered designs (ACD), and the Ecological Systems Theory applied to technological and mHealth systems will be described. In addition, the consideration factors for technological product design based on UCD, ECD and ACD, as well as for iOS and Android platforms will be discussed.
随着数字时代的到来,患者和医疗保健专业人员的角色也在不断演变。数字技术与健康和保健服务的融合导致了数字健康和药物控制论等学科的诞生。数字医疗创新和移动医疗应用的开发必须是有用的和用户友好的。例如,对患者来说,与移动应用界面相关的易用性可能比功能的数量和类型更重要。因此,需要应用健康行为理论和以患者为中心的方法来开发临床相关的数字卫生系统和移动健康应用程序。本章介绍了与设计数字健康创新相关的药物控制论框架和可以帮助告知行为改变技术的干预映射(IM)框架。将描述诸如药物控制论格言、以用户为中心(UCD)、以体验为中心(ECD)和以活动为中心的设计(ACD)以及应用于技术和移动医疗系统的生态系统理论等概念。此外,还将讨论基于UCD、ECD和ACD以及iOS和Android平台的技术产品设计的考虑因素。
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引用次数: 0
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Design and Quality Considerations for Developing Mobile Apps for Medication Management
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