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Older persons' and health care professionals' design choices when co-designing a medication plan aiming to promote patient safety: Case study
Jönköping University, Hälsohögskolan, The Jönköping Academy for Improvement of Health and Welfare. Department of Public Health and Healthcare, Region Jönköping County, Jönköping, Sweden.ORCID-id: 0000-0003-3221-9800
Jönköping University, Hälsohögskolan, HHJ, Institutet för gerontologi. Jönköping University, Hälsohögskolan, HHJ. ARN-J (Aging Research Network - Jönköping).ORCID-id: 0000-0001-7101-3165
Jönköping University, Hälsohögskolan, HHJ, Avdelningen för kvalitetsförbättring och ledarskap. Jönköping University, Hälsohögskolan, The Jönköping Academy for Improvement of Health and Welfare.ORCID-id: 0000-0003-0123-6392
Jönköping University, Hälsohögskolan, The Jönköping Academy for Improvement of Health and Welfare. Jönköping University, Hälsohögskolan, HHJ, Avdelningen för kvalitetsförbättring och ledarskap.ORCID-id: 0000-0003-1814-4478
Vise andre og tillknytning
2023 (engelsk)Inngår i: JMIR Aging, E-ISSN 2561-7605, Vol. 6, artikkel-id e49154Artikkel i tidsskrift (Fagfellevurdert) Published
Hållbar utveckling
00. Hållbar utveckling, 3. God hälsa och välbefinnande
Abstract [en]

BACKGROUND: Harm from medications is a major patient safety challenge among older persons. Adverse drug events tend to arise when prescribing or evaluating medications; therefore, interventions targeting these may promote patient safety. Guidelines highlight the value of a joint plan for continued treatment. If such a plan includes medications, a medication plan promoting patient safety is advised. There is growing evidence for the benefits of including patients and health care professionals in initiatives for improving health care products and services through co-design.

OBJECTIVE: This study aimed to identify participants' needs and requirements for a medication plan and explore their reasoning for different design choices.

METHODS: Using a case study design, we collected and analyzed qualitative and quantitative data and compared them side by side. We explored the needs and requirements for a medication plan expressed by 14 participants (older persons, nurses, and physicians) during a co-design initiative in a regional health system in Sweden. We performed a directed content analysis of qualitative data gathered from co-design sessions and interviews. Descriptive statistics were used to analyze the quantitative data from survey answers.

RESULTS: A medication plan must provide an added everyday value related to safety, effort, and engagement. The physicians addressed challenges in setting aside time to apply a medication plan, whereas the older persons raised the potential for increased patient involvement. According to the participants, a medication plan needs to support communication, continuity, and interaction. The nurses specifically addressed the need for a plan that was easy to gain an overview of. Important function requirements included providing instant access, automation, and attention. Content requirements included providing detailed information about the medication treatment. Having the plan linked to the medication list and instantly obtainable information was also requested.

CONCLUSIONS: After discussing the needs and requirements for a medication plan, the participants agreed on an iteratively developed medication plan prototype linked to the medication list within the existing electronic health record. According to the participants, the medication plan prototype may promote patient safety and enable patient engagement, but concerns were raised about its use in daily clinical practice. The last step in the co-design framework is testing the intervention to explore how it works and connects with users. Therefore, testing the medication plan prototype in clinical practice would be a future step.

sted, utgiver, år, opplag, sider
JMIR Publications, 2023. Vol. 6, artikkel-id e49154
Emneord [en]
co-design, engagement, medication plan, medications, older adults, older people, participatory, patient experience, patient safety, remote
HSV kategori
Identifikatorer
URN: urn:nbn:se:hj:diva-62640DOI: 10.2196/49154ISI: 001085458100001PubMedID: 37796569Scopus ID: 2-s2.0-85176753115Lokal ID: GOA;;908748OAI: oai:DiVA.org:hj-62640DiVA, id: diva2:1803883
Tilgjengelig fra: 2023-10-10 Laget: 2023-10-10 Sist oppdatert: 2025-10-13bibliografisk kontrollert
Inngår i avhandling
1. Together towards safer medication treatment for older persons
Åpne denne publikasjonen i ny fane eller vindu >>Together towards safer medication treatment for older persons
2023 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

This thesis focuses on promoting patient safety in older persons using medications. Given that medications can unintentionally harm patients, the World Health Organisation emphasises “Medication without harm” as a global patient safety challenge. Older persons are more likely to experience harm, and harm tends to occur when prescribing or monitoring medications. Co-production of healthcare with patients may reduce the risk of adverse events and can serve as a resource to promote safety in healthcare. Accordingly, this thesis aims to increase knowledge of how older persons and healthcare professionals can co-produce a solution for improved medication evaluation and thereby promote patient safety.

Co-design is an approach that emphasises patient involvement in improvements of healthcare services. Therefore, the thesis was guided by the four phases of the Double Diamond framework for co-design. In the Discover phase experiences of medication evaluations were collected. Older persons were interviewed and data were analysed using qualitative inductive content analysis (Paper I). Critical Incident Technique was used to collect and analyse data from interviews with healthcare professionals in primary care (Paper II). In the Define and Develop phases, a case study design was used to explore older persons’, nurses’ and physicians’ design choices for a medication and their experiences of a remote co-design approach. Collected data were analysed using descriptive statistics along with directed content analysis (Paper III) and thematic analysis (Paper IV). In the Deliver phase, the feasibility of applying a medication plan in primary care, as well as the study methods used were examined. Data were analysed using descriptive statistics and inductive content analysis (Paper V).

The findings showed that older persons reported having a responsibility to engage in their medication evaluations, even if some felt unable to do so or considered themselves unconcerned. Continuity of care and participation facilitate evaluations, but a comprehensive medication evaluation was lacking (Paper I). Healthcare professionals experienced that medication evaluations for older persons were influenced by working conditions and working in partnership. Actions taken to manage medication evaluations were carried out through working with a plan and collaborative problem-solving (Paper II). A medication plan, linked to the medication list, had to provide an added everyday value related to safety, effort and engagement, and support communication, continuity and interaction. Important functional requirements were to provide instant access, automation and attention, and content requirements were detailed information about the medication treatment (Paper III). Remote co-design can complement or substitute for face-to-face co-design sessions. The approach allowed an accessible environment, and sharing everyday life experiences created learning and awareness of possible risks and strategies that could promote patient safety (Paper IV). The feasibility of applying a medication plan, assessed as usability, varied and the participants’ experiences of usability concerned a de-prioritised medication plan, functionalities, individualisation and resources. The participants’ perceptions of patient safety addressed awareness and information, challenges beyond the medication plan and patient involvement (Paper V).

Healthcare services could promote patient safety by involving older persons in medication evaluations and in co-designing patient safety solutions. However, implementing a medication plan in clinical practice is complex and requires continuous co-produced improvements at different levels within the healthcare system.

sted, utgiver, år, opplag, sider
Jönköping: Jönköping University, School of Health and Welfare, 2023. s. 99
Serie
Dissertation Series. School of Health and Welfare, ISSN 1654-3602 ; 132
Emneord
case study, co-design, co-production, feasibility study, medications, nurses, older persons, patient safety, physicians, primary care, qualitative research methods
HSV kategori
Identifikatorer
urn:nbn:se:hj:diva-62892 (URN)978-91-88669-39-1 (ISBN)978-91-88669-40-7 (ISBN)
Disputas
2023-12-08, Originalet, Qulturum, Länssjukhuset Ryhov, Jönköping, 13:00 (svensk)
Opponent
Veileder
Tilgjengelig fra: 2023-11-17 Laget: 2023-11-17 Sist oppdatert: 2025-10-13bibliografisk kontrollert

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