IDEAS home Printed from https://ideas.repec.org/a/wly/jocnur/v26y2017i23-24p4877-4889.html
   My bibliography  Save this article

Patients' and their family members' experiences of participation in care following an acute exacerbation in chronic obstructive pulmonary disease: A phenomenological‐hermeneutic study

Author

Listed:
  • Ingrid Charlotte Andersen
  • Thora Grothe Thomsen
  • Poul Bruun
  • Uffe Bødtger
  • Lise Hounsgaard

Abstract

Aim and objectives To explore the experiences of patients with chronic obstructive pulmonary disease and their family members relating both to participation in care during hospitalisation for an acute exacerbation in chronic obstructive pulmonary disease, and to the subsequent day‐to‐day care at home. Background When recovering from an exacerbation, the challenges associated with an unpredictable health condition dominate everyday life for patients and can involve their family members. Proper patient and family participation in care during discharge and follow‐up can help patients to improve self‐management. However, knowledge of the significance of patient and family participation for recovery and subsequent everyday life is still limited. Design This study adopted a longitudinal design informed by ethnographic fieldwork principles. Methods Participant observations and interviews with 15 patients and 12 family members were conducted on a Danish hospital ward and twice at the participants' homes. A phenomenological‐hermeneutic approach inspired by Ricoeur's theory of interpretation guided the data analysis. Results Participation in care was perceived as valuable, but could be associated with tensions and increased uncertainty. While patients mostly demonstrated a reactive approach to care, family members strived to be more proactive. In hospital, preparing for discharge included an effort to find a balance between powerlessness and influence during interactions with healthcare professionals. At home, managing further recovery and self‐management were characterised by navigating between mutual pressure and consideration within the family. Conclusion Family members play an important role in ensuring that patients are seen, heard and understood, but want to be acknowledged more by healthcare professionals. Appropriate interactions with healthcare professionals are crucial in order to support discharge and daily self‐management. Relevance to clinical practice Knowledge of the challenges that patients with chronic obstructive pulmonary disease and their family members face in participating in care activities could inform future development of family‐centred care approaches tailored to individual needs.

Suggested Citation

  • Ingrid Charlotte Andersen & Thora Grothe Thomsen & Poul Bruun & Uffe Bødtger & Lise Hounsgaard, 2017. "Patients' and their family members' experiences of participation in care following an acute exacerbation in chronic obstructive pulmonary disease: A phenomenological‐hermeneutic study," Journal of Clinical Nursing, John Wiley & Sons, vol. 26(23-24), pages 4877-4889, December.
  • Handle: RePEc:wly:jocnur:v:26:y:2017:i:23-24:p:4877-4889
    DOI: 10.1111/jocn.13963
    as

    Download full text from publisher

    File URL: https://doi.org/10.1111/jocn.13963
    Download Restriction: no

    File URL: https://libkey.io/10.1111/jocn.13963?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Adeline Cooney & Lorraine Mee & Dympna Casey & Kathy Murphy & Collette Kirwan & Eimear Burke & Yvonne Conway & Denise Healy & Brona Mooney & Jill Murphy & The PRINCE Team, 2013. "Life with chronic obstructive pulmonary disease: striving for ‘controlled co‐existence’," Journal of Clinical Nursing, John Wiley & Sons, vol. 22(7-8), pages 986-995, April.
    2. Cara Bailey & Alistair Hewison & Eleni Karasouli & Sophie Staniszewska & Daniel Munday, 2016. "Hospital care following emergency admission: a critical incident case study of the experiences of patients with advanced lung cancer and Chronic Obstructive Pulmonary Disease," Journal of Clinical Nursing, John Wiley & Sons, vol. 25(15-16), pages 2168-2179, August.
    3. Helga Jonsdottir, 2013. "Self‐management programmes for people living with chronic obstructive pulmonary disease: a call for a reconceptualisation," Journal of Clinical Nursing, John Wiley & Sons, vol. 22(5-6), pages 621-637, March.
    4. Marit Kvangarsnes & Henny Torheim & Torstein Hole & Lennart S Öhlund, 2013. "Narratives of breathlessness in chronic obstructive pulmonary disease," Journal of Clinical Nursing, John Wiley & Sons, vol. 22(21-22), pages 3062-3070, November.
    5. Dorthe Gaby Bove & Ann‐Britt Zakrisson & Julie Midtgaard & Kirsten Lomborg & Dorthe Overgaard, 2016. "Undefined and unpredictable responsibility: a focus group study of the experiences of informal caregiver spouses of patients with severe COPD," Journal of Clinical Nursing, John Wiley & Sons, vol. 25(3-4), pages 483-493, February.
    6. Thorbjorg S Ingadottir & Helga Jonsdottir, 2010. "Partnership‐based nursing practice for people with chronic obstructive pulmonary disease and their families: influences on health‐related quality of life and hospital admissions," Journal of Clinical Nursing, John Wiley & Sons, vol. 19(19‐20), pages 2795-2805, October.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Marit Leine & Astrid Klopstad Wahl & Christine Råheim Borge & Magne Hustavenes & Hilde Bondevik, 2017. "Feeling safe and motivated to achieve better health: Experiences with a partnership‐based nursing practice programme for in‐home patients with chronic obstructive pulmonary disease," Journal of Clinical Nursing, John Wiley & Sons, vol. 26(17-18), pages 2755-2764, September.
    2. Karoline Stentoft Rybjerg Larsen & Annemette Krintel Petersen & Marianne Lisby & Marie Veje Knudsen, 2018. "Dyspnoea and self‐management strategies in patients admitted to the emergency department: A study of patients’ experiences," Journal of Clinical Nursing, John Wiley & Sons, vol. 27(21-22), pages 4112-4118, November.
    3. Jose Manuel Tinoco-Camarena & Montserrat Puig-Llobet & María Teresa Lluch-Canut & Juan Roldan-Merino & Mari Carmen Moreno-Arroyo & Antonio Moreno-Poyato & Judith Balaguer-Sancho & Zaida Agüera & Maria, 2022. "Effectiveness of the Online “Dialogue Circles” Nursing Intervention to Increase Positive Mental Health and Reduce the Burden of Caregivers of Patients with Complex Chronic Conditions. Randomized Clini," IJERPH, MDPI, vol. 20(1), pages 1-13, December.
    4. Flaminia Reale & Federica Segato & Daniela Tartaglini & Cristina Masella, 2020. "Action Research as a Method to Find Solutions for the Burden of Caregiving at Hospital Discharge," Systemic Practice and Action Research, Springer, vol. 33(2), pages 167-185, April.
    5. Wenjing Tu & Guihua Xu & Shizheng Du, 2015. "Structure and content components of self‐management interventions that improve health‐related quality of life in people with inflammatory bowel disease: a systematic review, meta‐analysis and meta‐reg," Journal of Clinical Nursing, John Wiley & Sons, vol. 24(19-20), pages 2695-2709, October.
    6. Lawless, Michael T. & Tieu, Matthew & Feo, Rebecca & Kitson, Alison L., 2021. "Theories of self-care and self-management of long-term conditions by community-dwelling older adults: A systematic review and meta-ethnography," Social Science & Medicine, Elsevier, vol. 287(C).

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:wly:jocnur:v:26:y:2017:i:23-24:p:4877-4889. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Wiley Content Delivery (email available below). General contact details of provider: https://doi.org/10.1111/(ISSN)1365-2702 .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.