Nursing patients with chronic critical illness and their families: a qualitative study

被引:16
|
作者
Leung, Doris [1 ,2 ]
Blastorah, Margaret [1 ]
Nusdorfer, Linda [3 ]
Jeffs, Angie [3 ]
Jung, Judy [4 ]
Howell, Doris [5 ]
Fillion, Lise [6 ]
Rose, Louise [1 ,7 ,8 ,9 ,10 ]
机构
[1] Univ Toronto, Lawrence S Bloomberg Fac Nursing, 155 Coll St,Suite 130, Toronto, ON, Canada
[2] Polytech Univ, Sch Nursing, Hong Kong, Hong Kong, Peoples R China
[3] Sunnybrook Hlth Sci Ctr, Emergency & Crit Care Program, Toronto, ON, Canada
[4] Univ Hlth Network, Multiorgan Transplant Program, Toronto, ON, Canada
[5] Univ Hlth Network, Oncol Nursing Res & Educ, Toronto, ON, Canada
[6] Laval Univ, Quebec City, PQ, Canada
[7] Sunnybrook Hlth Sci Ctr, Crit Care Res, Toronto, ON, Canada
[8] Toronto East Gen Hosp, Prolonged Ventilat Weaning Ctr, Prov Ctr Weaning Excellence, Toronto, ON, Canada
[9] Mt Sinai Hosp, Toronto, ON, Canada
[10] St Michaels Hosp, Li Ka Shing Knowledge Inst, Toronto, ON, Canada
关键词
Communication; Family care in critical care; Hope; Intensive care nursing; Mechanical ventilation; ILL PATIENTS; CARE; LIFE; END; COMMUNICATION; EPIDEMIOLOGY; MANAGEMENT; DISEASE; NURSES; COSTS;
D O I
10.1111/nicc.12154
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
Background: chronic critical illness (CCI) is a complex syndrome with a high risk of dying in hospital. Intensive care unit nurses are well-positioned to lead conversations integrating palliative and end-of-life care, yet have reported limited involvement. Aim: To generate further understanding of nurses' experiences of patients with CCI and their families. Design and methods: This qualitative study followed Thorne's interpretive description methods. In 2012, 16 intensive care unit nurses from one academic hospital participated in interviews. Results: Our primary theme was that of internal tension generated through participants' knowledge of patients' anticipated and protracted dying, while wanting to shield families from suffering. This internal tension resulted from responsibilities to preserve hope for patients and families, while at the same time wanting to provide them prognostic information. Participants experienced challenges of: (i) preserving family trust, (ii) determining when and how to engage families in discussions and (iii) providing possibilities of a 'good' death. A secondary theme described constraints to acting on their insights because of interprofessional team dynamics or limited communication, within the team and with the family. Conclusion and relevance to clinical practice: Internal tension, as experienced by participants reflects the challenges of transition from acute to palliation and end-of-life care, made more complex in CCI, because of its poorly defined terminal stage. Nurses' ability to manage the complex process of supporting hope while gradually providing information to build family understanding of CCI highlights their central role in facilitating what and how prognostic information is given, while managing the emotional implications and family response. To better support nurses do this, we advocate for formal structures enabling nurses to participate in decision-making regarding timing of transitions using palliation and end-of-life care.
引用
收藏
页码:229 / 237
页数:9
相关论文
共 50 条
  • [31] Spiritual coping mechanisms in chronic illness: a qualitative study
    Narayanasamy, A
    [J]. JOURNAL OF CLINICAL NURSING, 2004, 13 (01) : 116 - 117
  • [32] Adolescent chronic illness: A qualitative study of psychosocial adjustment
    Olsson, CA
    Bond, L
    Johnson, MW
    Forer, DL
    Boyce, MF
    Sawyer, SM
    [J]. ANNALS ACADEMY OF MEDICINE SINGAPORE, 2003, 32 (01) : 43 - 50
  • [33] Integrated medicine in the management of chronic illness: a qualitative study
    Brien, Sarah B.
    Bishop, Felicity
    Riggs, Kirsty
    Stevenson, David
    Freire, Victoria
    Lewith, George
    [J]. BRITISH JOURNAL OF GENERAL PRACTICE, 2011, 61 (583): : e89 - e96
  • [34] IMPACT OF CHRONIC ILLNESS ON FAMILIES
    ATHREYA, BH
    MCCORMICK, MC
    [J]. RHEUMATIC DISEASE CLINICS OF NORTH AMERICA, 1987, 13 (01) : 123 - 131
  • [35] THE IMPACT OF CHRONIC ILLNESS ON FAMILIES
    RUSK, HA
    NOVEY, J
    [J]. MARRIAGE AND FAMILY LIVING, 1957, 19 (02): : 193 - 197
  • [36] Omani Families Caring for a Member with Mental Illness: A Descriptive Qualitative Study
    Aldiabat, Khaldoun
    Alsrayheen, Enam
    Alshammari, Muna A.
    Le Navenec, Carole -Lynne M.
    Griscti, Odette
    [J]. QUALITATIVE REPORT, 2023, 28 (07): : 1992 - 2010
  • [37] The psychology of chronic illness: The healing work of patients, therapists, and families
    Larsen, KE
    [J]. CONTEMPORARY PSYCHOLOGY, 1998, 43 (10): : 712 - 713
  • [38] Community families: A qualitative study of families who volunteer to support persons with severe mental illness
    Jensen, Lotte Groth
    Lou, Stina
    Aagaard, Jorgen
    Vaeggemose, Ulla
    [J]. INTERNATIONAL JOURNAL OF SOCIAL PSYCHIATRY, 2017, 63 (01) : 33 - 39
  • [39] Effect of Palliative Care-Led Meetings for Families of Patients With Chronic Critical Illness A Randomized Clinical Trial
    Carson, Shannon S.
    Cox, Christopher E.
    Wallenstein, Sylvan
    Hanson, Laura C.
    Danis, Marion
    Tulsky, James A.
    Chai, Emily
    Nelson, Judith E.
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2016, 316 (01): : 51 - 62
  • [40] Patients and families realising their future with chronic obstructive pulmonary disease-A qualitative study
    Bragadottir, Gudrun H.
    Halldorsdottir, Bryndis S.
    Ingadottir, Thorbjorg S.
    Jonsdottir, Helga
    [J]. JOURNAL OF CLINICAL NURSING, 2018, 27 (1-2) : 57 - 64