- Background: The use of patient-reported outcome measures (PROM) and caregiver-reported outcome measures can raise the patient centeredness of treatment and improve the quality of palliative care. Nevertheless, the everyday implementation of self-report in patients and caregivers is complex, and should be adapted for use in specific settings. We aimed to implement a set of outcome measures that included patient and caregiver self- and proxy-reported outcome measures in specialised outpatient palliative care (SOPC). In this study, we explore how the Integrated Palliative Outcome Scale (IPOS), IPOS Views on Care (IPOS VoC) and the Short-form Zarit Caregiver Burden Interview (ZBI-7) can be feasibly, acceptably and appropriately implemented in the daily care routines of SOPC.
Methods: Five SOPC teams were trained, and used the outcome measures in daily practice. Team members were mainly nurses and physicians. To investigate their feedback, we used a multi-method qualitative design consisting of focus groups with SOPC-team members (n = 14), field notes of meetings and conversations with the SOPC teams. In an iterative process, we analysed the findings using qualitative content analysis and refined use of the outcome measures.
Results: We found that integrating patient and caregiver outcome measures into daily care routines in SOPC is feasible. To improve feasibility, acceptability and appropriateness, the resulting burden on patients and relatives should be kept to a minimum, the usefulness of the measures must be understood, they should be used considerately, and administration must be manageable. We removed ZBI-7 from the set of measures as a result of feedback on its content and wording.
Conclusions: SOPC-team members have reservations about the implementation of PROM in SOPC, but with appropriate adjustments, its application in daily care is feasible, accepted and perceived as appropriate. Previous to use, SOPC-team members should be trained in how to apply the measures, in the design of manageable processes that include integration into electronic documentation systems, and in ongoing evaluation and support. They should also be taught how useful the measures can be.
MetadatenAuthor: | Hannah SeippORCiDGND, Jörg HaasenritterORCiDGND, Michaela HachGND, Dorothée Becker, Dania SchützeORCiDGND, Jennifer EnglerORCiDGND, Cornelia PloegerGND, Stefan Bösner, Katrin KussORCiDGND |
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URN: | urn:nbn:de:hebis:30:3-837922 |
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DOI: | https://doi.org/10.1186/s12904-022-00944-1 |
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ISSN: | 1472-684X |
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Parent Title (English): | BMC palliative care |
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Publisher: | BioMed Central |
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Place of publication: | London |
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Document Type: | Article |
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Language: | English |
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Date of Publication (online): | 2022/05/02 |
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Date of first Publication: | 2022/05/02 |
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Publishing Institution: | Universitätsbibliothek Johann Christian Senckenberg |
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Release Date: | 2024/04/23 |
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Tag: | Home Care Services [MeSH]; Needs Assessment [MeSH]; Palliative Care [MeSH]; Patient Outcome Assessment [MeSH]; Patient Reported Outcome Measures [MeSH]; Qualitative Research [MeSH]; Quality of Health Care [MeSH]; Routinely Collected Health Data [MeSH] |
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Volume: | 21 |
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Issue: | art. 60 |
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Article Number: | 60 |
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Page Number: | 12 |
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First Page: | 1 |
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Last Page: | 12 |
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Note: | Open Access funding enabled and organized by Projekt DEAL. The trial was funded by the Innovation fund (‘Innovationsfonds’) of the Federal Joint Committee of Germany (grant number: 01VSF16006). The funders had no impact on data collection, analysis, interpretation of data and writing this article. |
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Note: | The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
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HeBIS-PPN: | 519153391 |
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Institutes: | Medizin |
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Dewey Decimal Classification: | 6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit |
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Sammlungen: | Universitätspublikationen |
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Licence (German): | Creative Commons - CC BY - Namensnennung 4.0 International |
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