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Patient perspectives on digital patient reported outcomes in routine care of inflammatory bowel disease

BACKGROUND: Digital patient reported outcomes are used increasingly in daily care and treatment of inflammatory bowel disease. Their purpose includes increased focus on patient wellbeing, reduction in avoidable follow-up consultations and increased patient self-management. However, implementation is...

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Autores principales: Nielsen, Amalie Søgaard, Appel, Charlotte W., Larsen, Birgit Furstrand, Kayser, Lars, Hanna, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448812/
https://www.ncbi.nlm.nih.gov/pubmed/34533682
http://dx.doi.org/10.1186/s41687-021-00366-2
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author Nielsen, Amalie Søgaard
Appel, Charlotte W.
Larsen, Birgit Furstrand
Kayser, Lars
Hanna, Lisa
author_facet Nielsen, Amalie Søgaard
Appel, Charlotte W.
Larsen, Birgit Furstrand
Kayser, Lars
Hanna, Lisa
author_sort Nielsen, Amalie Søgaard
collection PubMed
description BACKGROUND: Digital patient reported outcomes are used increasingly in daily care and treatment of inflammatory bowel disease. Their purpose includes increased focus on patient wellbeing, reduction in avoidable follow-up consultations and increased patient self-management. However, implementation issues occur and studies indicate patients may have concerns, particularly regarding having fewer face-to-face consultations. This study aims to explore patients’ perspectives of use and non-use of digital patient reported outcomes and to understand the mechanisms underpinning patient reluctance to engage with this health technology. RESULTS: Sixteen patients with inflammatory bowel disease at a regional hospital in Denmark were interviewed about their experiences of, and perspectives on, digital patient reported outcomes. A certain level of eHealth literacy was found to be a fundamental condition for use, while other factors were barriers or facilitators for use of digital PROs. Patients’ main concerns were about potential consequences for their care and relationship with the clinic. Most patients in stable remission were satisfied with the hospital being a “life-line” if their symptoms worsened, and perceived digital patient reported outcomes to be an efficient tool to establish that “life-line”. Patients with severe symptoms and a high degree of emotional distress related to their disease valued the potential for digital patient reported outcomes to increase their clinicians’ focus on mental health and extra-intestinal symptoms. CONCLUSION: This study found that if patients had sufficient digital literacy, they perceived digital patient reported outcomes to be a useful replacement for face-to-face consultations. However, they were concerned about digital patient reported outcomes’ effect on the patient–clinician relationship and its ability to detect worsening of symptoms. These concerns may be mitigated by good patient–clinician relationships, and the option for patients to maintain direct telephone contact with their gastroenterology specialist. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41687-021-00366-2.
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spelling pubmed-84488122021-10-01 Patient perspectives on digital patient reported outcomes in routine care of inflammatory bowel disease Nielsen, Amalie Søgaard Appel, Charlotte W. Larsen, Birgit Furstrand Kayser, Lars Hanna, Lisa J Patient Rep Outcomes Research BACKGROUND: Digital patient reported outcomes are used increasingly in daily care and treatment of inflammatory bowel disease. Their purpose includes increased focus on patient wellbeing, reduction in avoidable follow-up consultations and increased patient self-management. However, implementation issues occur and studies indicate patients may have concerns, particularly regarding having fewer face-to-face consultations. This study aims to explore patients’ perspectives of use and non-use of digital patient reported outcomes and to understand the mechanisms underpinning patient reluctance to engage with this health technology. RESULTS: Sixteen patients with inflammatory bowel disease at a regional hospital in Denmark were interviewed about their experiences of, and perspectives on, digital patient reported outcomes. A certain level of eHealth literacy was found to be a fundamental condition for use, while other factors were barriers or facilitators for use of digital PROs. Patients’ main concerns were about potential consequences for their care and relationship with the clinic. Most patients in stable remission were satisfied with the hospital being a “life-line” if their symptoms worsened, and perceived digital patient reported outcomes to be an efficient tool to establish that “life-line”. Patients with severe symptoms and a high degree of emotional distress related to their disease valued the potential for digital patient reported outcomes to increase their clinicians’ focus on mental health and extra-intestinal symptoms. CONCLUSION: This study found that if patients had sufficient digital literacy, they perceived digital patient reported outcomes to be a useful replacement for face-to-face consultations. However, they were concerned about digital patient reported outcomes’ effect on the patient–clinician relationship and its ability to detect worsening of symptoms. These concerns may be mitigated by good patient–clinician relationships, and the option for patients to maintain direct telephone contact with their gastroenterology specialist. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41687-021-00366-2. Springer International Publishing 2021-09-17 /pmc/articles/PMC8448812/ /pubmed/34533682 http://dx.doi.org/10.1186/s41687-021-00366-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Nielsen, Amalie Søgaard
Appel, Charlotte W.
Larsen, Birgit Furstrand
Kayser, Lars
Hanna, Lisa
Patient perspectives on digital patient reported outcomes in routine care of inflammatory bowel disease
title Patient perspectives on digital patient reported outcomes in routine care of inflammatory bowel disease
title_full Patient perspectives on digital patient reported outcomes in routine care of inflammatory bowel disease
title_fullStr Patient perspectives on digital patient reported outcomes in routine care of inflammatory bowel disease
title_full_unstemmed Patient perspectives on digital patient reported outcomes in routine care of inflammatory bowel disease
title_short Patient perspectives on digital patient reported outcomes in routine care of inflammatory bowel disease
title_sort patient perspectives on digital patient reported outcomes in routine care of inflammatory bowel disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448812/
https://www.ncbi.nlm.nih.gov/pubmed/34533682
http://dx.doi.org/10.1186/s41687-021-00366-2
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