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Patients’ accounts of living with and managing inflammatory bowel disease in rural Southern New Zealand: a qualitative study
OBJECTIVE: To explore how adults living with inflammatory bowel disease (IBD) in rural New Zealand manage their condition and engage with healthcare providers. DESIGN: Qualitative exploratory design with semi-structured interviews analysed thematically. SETTING AND PARTICIPANTS: Interviews were cond...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662529/ https://www.ncbi.nlm.nih.gov/pubmed/33184085 http://dx.doi.org/10.1136/bmjopen-2020-041789 |
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author | Richard, Lauralie Noller, Geoff Derrett, Sarah Sullivan, Trudy Doolan-Noble, Fiona McCombie, Andrew Schultz, Michael Ho, Christine Stokes, Tim |
author_facet | Richard, Lauralie Noller, Geoff Derrett, Sarah Sullivan, Trudy Doolan-Noble, Fiona McCombie, Andrew Schultz, Michael Ho, Christine Stokes, Tim |
author_sort | Richard, Lauralie |
collection | PubMed |
description | OBJECTIVE: To explore how adults living with inflammatory bowel disease (IBD) in rural New Zealand manage their condition and engage with healthcare providers. DESIGN: Qualitative exploratory design with semi-structured interviews analysed thematically. SETTING AND PARTICIPANTS: Interviews were conducted with 18 people living with IBD in the Otago region of the South Island. RESULTS: Five important constructs were identified: (1) journey to confirming and accepting diagnosis; (2) importance of the relationship with the healthcare team; (3) support from others; (4) learning how to manage IBD and (5) care at a distance—experiences of rurality. Pathways to confirming diagnosis involved two contrasting journeys: a long and slow process where diagnosis remained unclear for a prolonged period, and a more acute process where diagnosis typically came as a shock. Central to the acceptance process was acknowledging the chronicity of the condition, which involved feelings of grief but also the fear of judgement and stigma. Building a strong relationship with the specialist was central to medical management, particularly in the initial stage following diagnosis. Support from others was critical, enabling participants to progress through acceptance of the disease and developing confidence in its everyday management. Participants shared different strategies on how to manage IBD, describing a ‘trial and error’ process of ‘finding what is right’ at different stages of the condition. Managing IBD rurally involved challenges of access to specialist care, with perceptions of delayed referrals and concerns about disparities in specialist access compared with urban counterparts. Rural living also had financial implications—cost of time and cost of mobilising resources for long travels to the urban centre for treatments. CONCLUSIONS: Findings from this study provide a rich understanding of the complex health journeys of people living with IBD and the challenges of managing the condition rurally. |
format | Online Article Text |
id | pubmed-7662529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-76625292020-11-20 Patients’ accounts of living with and managing inflammatory bowel disease in rural Southern New Zealand: a qualitative study Richard, Lauralie Noller, Geoff Derrett, Sarah Sullivan, Trudy Doolan-Noble, Fiona McCombie, Andrew Schultz, Michael Ho, Christine Stokes, Tim BMJ Open Gastroenterology and Hepatology OBJECTIVE: To explore how adults living with inflammatory bowel disease (IBD) in rural New Zealand manage their condition and engage with healthcare providers. DESIGN: Qualitative exploratory design with semi-structured interviews analysed thematically. SETTING AND PARTICIPANTS: Interviews were conducted with 18 people living with IBD in the Otago region of the South Island. RESULTS: Five important constructs were identified: (1) journey to confirming and accepting diagnosis; (2) importance of the relationship with the healthcare team; (3) support from others; (4) learning how to manage IBD and (5) care at a distance—experiences of rurality. Pathways to confirming diagnosis involved two contrasting journeys: a long and slow process where diagnosis remained unclear for a prolonged period, and a more acute process where diagnosis typically came as a shock. Central to the acceptance process was acknowledging the chronicity of the condition, which involved feelings of grief but also the fear of judgement and stigma. Building a strong relationship with the specialist was central to medical management, particularly in the initial stage following diagnosis. Support from others was critical, enabling participants to progress through acceptance of the disease and developing confidence in its everyday management. Participants shared different strategies on how to manage IBD, describing a ‘trial and error’ process of ‘finding what is right’ at different stages of the condition. Managing IBD rurally involved challenges of access to specialist care, with perceptions of delayed referrals and concerns about disparities in specialist access compared with urban counterparts. Rural living also had financial implications—cost of time and cost of mobilising resources for long travels to the urban centre for treatments. CONCLUSIONS: Findings from this study provide a rich understanding of the complex health journeys of people living with IBD and the challenges of managing the condition rurally. BMJ Publishing Group 2020-11-12 /pmc/articles/PMC7662529/ /pubmed/33184085 http://dx.doi.org/10.1136/bmjopen-2020-041789 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Gastroenterology and Hepatology Richard, Lauralie Noller, Geoff Derrett, Sarah Sullivan, Trudy Doolan-Noble, Fiona McCombie, Andrew Schultz, Michael Ho, Christine Stokes, Tim Patients’ accounts of living with and managing inflammatory bowel disease in rural Southern New Zealand: a qualitative study |
title | Patients’ accounts of living with and managing inflammatory bowel disease in rural Southern New Zealand: a qualitative study |
title_full | Patients’ accounts of living with and managing inflammatory bowel disease in rural Southern New Zealand: a qualitative study |
title_fullStr | Patients’ accounts of living with and managing inflammatory bowel disease in rural Southern New Zealand: a qualitative study |
title_full_unstemmed | Patients’ accounts of living with and managing inflammatory bowel disease in rural Southern New Zealand: a qualitative study |
title_short | Patients’ accounts of living with and managing inflammatory bowel disease in rural Southern New Zealand: a qualitative study |
title_sort | patients’ accounts of living with and managing inflammatory bowel disease in rural southern new zealand: a qualitative study |
topic | Gastroenterology and Hepatology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662529/ https://www.ncbi.nlm.nih.gov/pubmed/33184085 http://dx.doi.org/10.1136/bmjopen-2020-041789 |
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