Insights from parents of a child with leukaemia and healthcare professionals about sharing illness and treatment information: A qualitative research study

被引:12
|
作者
Gibson, Faith [1 ,2 ]
Kumpunen, Stephanie [3 ]
Bryan, Gemma [4 ]
Forbat, Liz [5 ,6 ]
机构
[1] Great Ormond St Hosp Children NHS Fdn Trust, Ctr Outcomes & Experience Res Childrens Hlth Illn, Great Ormond St, London WC1N 3JH, England
[2] Univ Surrey, Sch Hlth Sci, Guildford, Surrey, England
[3] Nuffield Trust, London, England
[4] UCL Great Ormond St Inst Child Hlth, Louis Dundas Ctr Childrens Palliat Care, London, England
[5] Calvary Hlth Care Bruce, Canberra, ACT, Australia
[6] Australian Catholic Univ, Canberra, ACT, Australia
关键词
Cancer; Children and parents; Communication patterns; Communication intervention; DAY ONE TALK; PEDIATRIC ONCOLOGY; DECISION-MAKING; UNCERTAINTY MANAGEMENT; NURSING-RESEARCH; GROUNDED THEORY; YOUNG-PEOPLE; CANCER CARE; COMMUNICATION; LIFE;
D O I
10.1016/j.ijnurstu.2018.04.008
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
Background: Many parents report a strong desire to take on information-giving roles, and believe they are best positioned to discuss their child's illness with their child. Healthcare professionals have a supporting role to reduce the burden on parents who feel responsible for conveying information to their child and other family members. Objective: To examine parents' and healthcare professionals' perceptions of roles in receiving and communicating information when a child is diagnosed with and treated for acute lymphoblastic leukaemia. Design, setting and participants: We used the principles of a grounded theory approach. This was a single site study, recruiting from a principal children's cancer treatment centre in the United Kingdom. The sample included parents of children receiving and completed treatment for acute lymphoblastic leukaemia (n = 28), and healthcare professionals (n = 34). Methods: Methods included individual interviews, face-to-face and telephone, focus groups, and an online forum. Findings: Communication 'touch points' are many over the course of a child's cancer journey. We describe often 'mismatched' communication encounters where those seeking information and those providing information have different goals. Healthcare professionals in the encounter have expertise at the outset while parents have less expertise, but this expertise grows over time and this can increase the perceptions of this 'mismatch' and create different challenges. Conclusions: Considered in the context of middle range transition theory, we might suggest that parental foreground (seeking information directly) and background (passive actors) roles are the result of differing levels of uncertainty, and depend on the situation and preferences and child and family needs that may present differently over time in different contexts. Our work contributes to the emerging consensus that communication is more than a core set of skills that healthcare professionals just need to learn: clear specifications of mutual roles, responsibilities and a shared understanding of goals is also essential.
引用
收藏
页码:91 / 102
页数:12
相关论文
共 5 条
  • [1] Anticipating the future of the child and family in pediatric palliative care: a qualitative study into the perspectives of parents and healthcare professionals
    Verberne, Lisa M.
    Fahner, Jurrianne C.
    Sondaal, Stephanie F. V.
    Schouten-van Meeteren, Antoinette Y. N.
    de Kruiff, Chris C.
    van Delden, Johannes J. M.
    Kars, Marijke C.
    EUROPEAN JOURNAL OF PEDIATRICS, 2021, 180 (03) : 949 - 957
  • [2] Anticipating the future of the child and family in pediatric palliative care: a qualitative study into the perspectives of parents and healthcare professionals
    Lisa M. Verberne
    Jurrianne C. Fahner
    Stephanie F. V. Sondaal
    Antoinette Y. N. Schouten–van Meeteren
    Chris C. de Kruiff
    Johannes J. M. van Delden
    Marijke C. Kars
    European Journal of Pediatrics, 2021, 180 : 949 - 957
  • [3] Views and experiences of young people, their parents/carers and healthcare professionals of the advance care planning process: A summary of the findings from a qualitative study
    Hughes, Ben
    O'Brien, Mary
    Flynn, Anita
    Knighting, Katherine
    PALLIATIVE MEDICINE, 2022, 36 (05) : 841 - 854
  • [4] Healthcare professionals' adoption and use of a clinical information system (CIS) in primary care: Insights from the Da Vinci study
    Vedel, Isabelle
    Lapointe, Liette
    Lussier, Marie-Therese
    Richard, Claude
    Goudreau, Johanne
    Lalonde, Lyne
    Turcotte, Alain
    INTERNATIONAL JOURNAL OF MEDICAL INFORMATICS, 2012, 81 (02) : 73 - 87
  • [5] The experiences of professionals with using information from patient-reported outcome measures to improve the quality of healthcare: a systematic review of qualitative research
    Boyce, Maria B.
    Browne, John P.
    Greenhalgh, Joanne
    BMJ QUALITY & SAFETY, 2014, 23 (06) : 508 - 518