A qualitative study of doctors' and nurses' barriers to communicating with seriously ill patients about their dependent children. Issue 12 (11th May 2017)

• Record Type: Journal Article
• Authors: Dencker, Annemarie; Rix, Bo Andreassen; Bøge, Per; Tjørnhøj‐Thomsen, Tine
• Is Part Of: Psycho-oncology. Volume 26:Issue 12(2017)
• Page Start: 2162
• Page End: 2167
• Publication Date: 2017-05-11
• Subjects: cancer -- family -- oncology -- psychosocial support -- training; Cancer -- Psychological aspects -- Periodicals; Cancer -- Social aspects -- Periodicals; Neoplasms -- psychology -- Periodicals; 616.9940019
• DOI: 10.1002/pon.4440
• Languages: English
• ISSNs: 1057-9249

Abstract

Abstract: Objective: Research indicates that health personnel caring for seriously ill patients with dependent children aged 0 to 18 years often avoid discussing with them the challenges of being a family with a parent in treatment. Children of seriously ill patients risk serious trauma and emotional difficulty later in life and depend on adult support to minimize these consequences. Patients suffer anxiety about supporting their children during their illness. Because of their potentially pivotal role in supporting patients in enabling parent‐child communication, we examined HP's structural and emotional barriers to communicating with patients about their children. Methods: The study was based on 49 semi‐structured, in‐depth interviews with doctors and nurses working with haematology, gynaecological cancer, and neurointensive care. Both interviews and analysis addressed emotional and structural barriers, drawing on the theoretical framework of Maturana's domains. Results: The study found structural barriers (eg, lack of space in the medical recording system, professional code, time pressure, and lack of training) and emotional barriers (eg, the painful nature of the situation and the perceived need of keeping professional distance). We found that emotional barriers tended to grow when structural barriers were not addressed. Conclusions: Our study indicates (1) the need to use templates and manual procedures to gather and process information about children in medical records; (2) the need for managerial backing for addressing children of seriously ill patients and time spent on it; and (3) the need for future HP training programmes to include how to implement procedures and how to address all barriers.