Literature DB >> 29502155

Exploring symptom meaning: perspectives of palliative care physicians.

Celina F Estacio1, Phyllis N Butow2, Melanie R Lovell1,3, Skye T Dong1, Josephine M Clayton1,3.   

Abstract

CONTEXT: Understanding patients' symptom experiences is essential to providing effective clinical care. The discussion between patients and physicians of symptom meaning and its significance, however, is ill understood.
OBJECTIVES: To investigate palliative care physicians' understanding of symptom meaning, and their experiences of and attitudes towards the discussion of symptom meaning with patients.
METHODS: Semi-structured interviews were conducted (N = 17) across Sydney, Australia. Transcripts were analysed using framework analysis.
RESULTS: Six key themes were identified: (1) definitions of symptom meaning (causal meanings, functional impact, existential impact, and cascade of meanings); (2) meanings are personal (demographic, culture, spiritual, and family differences); (3) eliciting meanings requires subtlety and trust (following the patient's cues); discussing meaning can be (4) hard (for the patient and health professional); (5) therapeutic (assuaging fears, feeling listened to and valued, increased sense of control, and reduced symptom distress); and (6) enhances clinicians' practice and work satisfaction (provision of more tailored care, reassurance through the provision of information, and strengthening of doctor-patient relationship).
CONCLUSIONS: Exploring symptom meaning can serve to provide information, alleviate anxiety, and facilitate individualised care, but only when patients present cues or are open to discuss symptom-related concerns. However, various barriers hinder such dialogue in consultations. Greater awareness of symptom meaning and its influence may facilitate physicians exploring symptom meaning more with patients in the future.

Entities:  

Keywords:  Advanced cancer; Health professionals; Palliative care; Qualitative research; Symptom experience; Symptom meaning

Mesh:

Year:  2018        PMID: 29502155     DOI: 10.1007/s00520-018-4126-0

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  39 in total

1.  Hospital based palliative care teams improve the symptoms of cancer patients.

Authors:  Barbara Jack; Valerie Hillier; Anne Williams; Jackie Oldham
Journal:  Palliat Med       Date:  2003-09       Impact factor: 4.762

2.  Meanings of the phenomenon of fatigue as narrated by 4 patients with cancer in palliative care.

Authors:  Olav Lindqvist; Anders Widmark; Birgit H Rasmussen
Journal:  Cancer Nurs       Date:  2004 May-Jun       Impact factor: 2.592

Review 3.  Continuing or forgoing treatment at the end of life? Preferences of the general public and people with an advance directive.

Authors:  Matthijs P S van Wijmen; H Roeline W Pasman; Guy A M Widdershoven; Bregje D Onwuteaka-Philipsen
Journal:  J Med Ethics       Date:  2014-09-02       Impact factor: 2.903

4.  The patient-physician relationship. Patient-physician communication during outpatient palliative treatment visits: an observational study.

Authors:  S B Detmar; M J Muller; L D Wever; J H Schornagel; N K Aaronson
Journal:  JAMA       Date:  2001-03-14       Impact factor: 56.272

5.  Patient experiences of pain and pain management at the end of life: a pilot study.

Authors:  Annika Larsson; Helle Wijk
Journal:  Pain Manag Nurs       Date:  2007-03       Impact factor: 1.929

6.  Quality of life of cancer patients receiving inpatient and home-based palliative care.

Authors:  Louise Peters; Ken Sellick
Journal:  J Adv Nurs       Date:  2006-03       Impact factor: 3.187

7.  Components that influence assessment and management of cancer-related symptoms: an interdisciplinary perspective.

Authors:  Sofie Jakobsson; Tor Ekman; Karin Ahlberg
Journal:  Oncol Nurs Forum       Date:  2008-07       Impact factor: 2.172

8.  Living with a terminal illness: patients' priorities.

Authors:  Helen Carter; Rod MacLeod; Penny Brander; Kath McPherson
Journal:  J Adv Nurs       Date:  2004-03       Impact factor: 3.187

9.  Ethical issues in palliative care. Views of patients, families, and nonphysician staff.

Authors:  Anna Towers; Neil MacDonald; Ellen Wallace
Journal:  Can Fam Physician       Date:  2003-12       Impact factor: 3.275

10.  Using the framework method for the analysis of qualitative data in multi-disciplinary health research.

Authors:  Nicola K Gale; Gemma Heath; Elaine Cameron; Sabina Rashid; Sabi Redwood
Journal:  BMC Med Res Methodol       Date:  2013-09-18       Impact factor: 4.615

View more
  1 in total

1.  Importance of and Satisfaction with Domains of Health-Related Quality of Life in Cancer Rehabilitation.

Authors:  Andreas Hinz; Thomas Schulte; Jochen Ernst; Anja Mehnert-Theuerkauf
Journal:  Cancers (Basel)       Date:  2022-04-14       Impact factor: 6.575

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.