Linking Activity Theory Within User-Centered Design: Novel Framework to Inform Design and Evaluation of Adverse Drug Reaction Reporting Systems in Pharmacy

被引:3
作者
Tagne, Joel Fossouo [1 ,2 ,3 ,8 ]
Yakob, Reginald Amin [4 ]
Mcdonald, Rachael [3 ,5 ,6 ]
Wickramasinghe, Nilmini [1 ,6 ,7 ]
机构
[1] Swinburne Univ Technol, Sch Hlth Sci & Biostat, Melbourne, Australia
[2] Murdoch Childrens Res Inst, Ctr Hlth Analyt, Melbourne, Australia
[3] Swinburne Univ Technol, MedTechVic, Melbourne, Australia
[4] Pharmaceut Soc Australia, Sydney, Australia
[5] Swinburne Univ Technol, Dept Nursing & Allied Hlth, Occupat Therapy, Melbourne, Australia
[6] Swinburne Univ Technol, Iverson Hlth Innovat Res Inst, Melbourne, Australia
[7] Epworth Healthcare, Melbourne, Australia
[8] Swinburne Univ Technol, Sch Hlth Sci & Biostat, John St, Melbourne 3122, Australia
关键词
pharmacovigilance; adverse drug reaction; pharmacist; user -centered design; activity theory; TASK-TECHNOLOGY FIT; CLUSTER-RANDOMIZED TRIAL; EVENTS; HEALTH;
D O I
10.2196/43529
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Adverse drug reactions (ADRs) may cause serious injuries including death. Timely reporting of ADRs may play a significant role in patient safety; however, underreporting exists. Enhancing the electronic communication of ADR information to regulators and between health care providers has the potential to reduce recurrent ADRs and improve patient safety. Objective: The main objectives were to explore the low rate of ADR reporting by community pharmacists (CPs) in Australia, evaluate the usability of an existing reporting system, and how this knowledge may influence the design of subsequent electronic ADR reporting systems. Methods: The study was carried out in 2 stages. Stage 1 involved qualitative semistructured interviews to identify CPs' perceived barriers and facilitators to ADR reporting. Data were analyzed by thematic analysis, and identified themes were subsequently aligned to the task-technology fit (TTF) framework. The second stage involved a usability evaluation of a commercial web-based ADR reporting system. A structured interview protocol that combined virtual observation, think-aloud moderating techniques, retrospective questioning of the overall user experience, and a System Usability Scale (SUS). The field notes from the interviews were subjected to thematic analysis. Results: In total, 12 CPs were interviewed in stage 1, and 7 CPs participated in stage 2. The interview findings show that CPs are willing to report ADRs but face barriers from environmental, organizational, and IT infrastructures. Increasing ADR awareness, improving workplace practices, and implementing user-focused electronic reporting systems were seen as facilitators of ADR reporting. User testing of an existing system resulted in above average usability (SUS 68.57); however, functional and user interpretation issues were identified. Design elements such as a drop-down menu, free-text entry, checkbox, and prefilled data fields were perceived to be extremely useful for navigating the system and facilitating ADR reporting. Conclusions: Existing reporting systems are not suited to report ADRs, or adapted to workflow, and are rarely used by CPs. Our study uncovered important contextual information for the design of future ADR reporting interventions. Based on our study, a multifaceted, theory-guided, user-centered, and best practice approach to design, implementation, and evaluation may be critical for the successful adoption of ADR reporting electronic interventions and patient safety. Future studies are needed to evaluate the effectiveness of theory-driven frameworks used in the design and implementation of ADR reporting systems.
引用
收藏
页数:12
相关论文
共 58 条
[1]  
Abbott AndrewDelano., 1988, SYSTEM PROFESSIONS, DOI 10.7208/chicago/9780226189666.001.0001
[2]   Focus Section Health IT Usability: Applying a Task-Technology Fit Model to Adapt an Electronic Patient Portal for Patient Work [J].
Ali, Sana B. ;
Romero, Juana ;
Morrison, Kevin ;
Hafeez, Baria ;
Ancker, Jessica S. .
APPLIED CLINICAL INFORMATICS, 2018, 9 (01) :174-184
[3]  
[Anonymous], 2019, Medicine Safety: take care
[4]  
[Anonymous], 2018, MED VACCINES POSTMAR
[5]  
Ayalew Mohammed Biset, 2019, Bull Emerg Trauma, V7, P339, DOI [10.29252/beat-070401, 10.29252/beat-070401]
[6]  
Baek E.-O., 2008, Handbook of research on educational communications and technology, V3rd, P660, DOI DOI 10.4324/9780203880869.CH49
[7]   Adverse drug event reporting systems: a systematic review [J].
Bailey, Chantelle ;
Peddie, David ;
Wickham, Maeve E. ;
Badke, Katherin ;
Small, Serena S. ;
Doyle-Waters, Mary M. ;
Balka, Ellen ;
Hohl, Corinne M. .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2016, 82 (01) :17-29
[8]   Epidemiology of Adverse Drug Reactions in Europe: A Review of Recent Observational Studies [J].
Bouvy, Jacoline C. ;
De Bruin, Marie L. ;
Koopmanschap, Marc A. .
DRUG SAFETY, 2015, 38 (05) :437-453
[9]   Lessons learnt from applying a human-centred design process to develop one of the largest mobile health communication programmes in the world [J].
Chamberlain, Sara ;
Dutt, Priyanka ;
Mitra, Radharani ;
Godfrey, Anna ;
LeFevre, Amnesty E. ;
Scott, Kerry ;
Katiyar, Soma ;
Mendiratta, Jai ;
Chaturvedi, Shefali .
BMJ INNOVATIONS, 2022, 8 (03) :240-246
[10]   Pilot-testing an adverse drug event reporting form prior to its implementation in an electronic health record [J].
Chruscicki, Adam ;
Badke, Katherin ;
Peddie, David ;
Small, Serena ;
Balka, Ellen ;
Hohl, Corinne M. .
SPRINGERPLUS, 2016, 5