Skip to main content
Erschienen in: Supportive Care in Cancer 8/2018

03.03.2018 | Original Article

Exploring symptom meaning: perspectives of palliative care physicians

verfasst von: Celina F. Estacio, Phyllis N. Butow, Melanie R. Lovell, Skye T. Dong, Josephine M. Clayton

Erschienen in: Supportive Care in Cancer | Ausgabe 8/2018

Einloggen, um Zugang zu erhalten

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.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat Hanson LC, Eckert JK, Dobbs D, Williams CS, Caprio AJ, Sloane PD, Zimmerman S (2008) Symptom experience of dying long-term care residents. J Am Geriatr Soc 56:91–98CrossRefPubMed Hanson LC, Eckert JK, Dobbs D, Williams CS, Caprio AJ, Sloane PD, Zimmerman S (2008) Symptom experience of dying long-term care residents. J Am Geriatr Soc 56:91–98CrossRefPubMed
2.
Zurück zum Zitat Peters L, Sellick K (2006) Quality of life of cancer patients receiving inpatient and home-based palliative care. J Adv Nurs 53:524–533CrossRefPubMed Peters L, Sellick K (2006) Quality of life of cancer patients receiving inpatient and home-based palliative care. J Adv Nurs 53:524–533CrossRefPubMed
3.
4.
Zurück zum Zitat Jones RA, Wiese HJ, Moore RW, Haley JV (1981) On the perceived meaning of symptoms. Med Care 19:710–717CrossRefPubMed Jones RA, Wiese HJ, Moore RW, Haley JV (1981) On the perceived meaning of symptoms. Med Care 19:710–717CrossRefPubMed
5.
Zurück zum Zitat Richer MC, Ezer H (2000) Understanding beliefs and meanings in the experience of cancer: a concept analysis. J Adv Nurs 32:1108–1115CrossRefPubMed Richer MC, Ezer H (2000) Understanding beliefs and meanings in the experience of cancer: a concept analysis. J Adv Nurs 32:1108–1115CrossRefPubMed
6.
Zurück zum Zitat Lindqvist O, Widmark A, Rasmussen BH (2006) Reclaiming wellness—living with bodily problems, as narrated by men with advanced prostate cancer. Cancer Nurs 29:327–337CrossRefPubMed Lindqvist O, Widmark A, Rasmussen BH (2006) Reclaiming wellness—living with bodily problems, as narrated by men with advanced prostate cancer. Cancer Nurs 29:327–337CrossRefPubMed
8.
Zurück zum Zitat Lovely MP, Stewart-Amidei C, Page M, Mogensen K, Arzbaecher J, Lupica K, Maher ME (2013) A new reality: long-term survivorship with a malignant brain tumor. Oncol Nurs Forum 40:267–274CrossRefPubMed Lovely MP, Stewart-Amidei C, Page M, Mogensen K, Arzbaecher J, Lupica K, Maher ME (2013) A new reality: long-term survivorship with a malignant brain tumor. Oncol Nurs Forum 40:267–274CrossRefPubMed
9.
Zurück zum Zitat Lindqvist O, Widmark A, Rasmussen BH (2004) Meanings of the phenomenon of fatigue as narrated by 4 patients with cancer in palliative care. Cancer Nurs 27:237–243CrossRefPubMed Lindqvist O, Widmark A, Rasmussen BH (2004) Meanings of the phenomenon of fatigue as narrated by 4 patients with cancer in palliative care. Cancer Nurs 27:237–243CrossRefPubMed
10.
Zurück zum Zitat Doumit MAA, Abu-Saad Huijer H, Kelley JH (2007) The lived experience of Lebanese oncology patients receiving palliative care. Eur J Oncol Nurs 11:309–319CrossRefPubMed Doumit MAA, Abu-Saad Huijer H, Kelley JH (2007) The lived experience of Lebanese oncology patients receiving palliative care. Eur J Oncol Nurs 11:309–319CrossRefPubMed
11.
Zurück zum Zitat Carter H, MacLeod R, Brander P, McPherson K (2004) Living with a terminal illness: patients’ priorities. J Adv Nurs 45:611–620CrossRefPubMed Carter H, MacLeod R, Brander P, McPherson K (2004) Living with a terminal illness: patients’ priorities. J Adv Nurs 45:611–620CrossRefPubMed
12.
Zurück zum Zitat Potter J (2004) Fatigue experience in advanced cancer: a phenomenological approach. Int J Palliat Nurs 10:15–23CrossRefPubMed Potter J (2004) Fatigue experience in advanced cancer: a phenomenological approach. Int J Palliat Nurs 10:15–23CrossRefPubMed
13.
Zurück zum Zitat Estacio CF, Butow PN, Lovell MR, Dong ST, Clayton JM (2017) What is symptom meaning? A framework analysis of communication in palliative care consultations. Patient Educ Couns 100:2088–2094CrossRefPubMed Estacio CF, Butow PN, Lovell MR, Dong ST, Clayton JM (2017) What is symptom meaning? A framework analysis of communication in palliative care consultations. Patient Educ Couns 100:2088–2094CrossRefPubMed
14.
Zurück zum Zitat Gibbins J, Bhatia R, Forbes K, Reid CM (2004) What do patients with advanced incurable cancer want from the management of their pain? A qualitative study. Palliat Medicine 28:71–78CrossRef Gibbins J, Bhatia R, Forbes K, Reid CM (2004) What do patients with advanced incurable cancer want from the management of their pain? A qualitative study. Palliat Medicine 28:71–78CrossRef
15.
Zurück zum Zitat Jakobsson S, Ekman T, Ahlberg K (2008) Components that influence assessment and management of cancer-related symptoms: an interdisciplinary perspective. Oncol Nurs Forum 35:691–698CrossRefPubMed Jakobsson S, Ekman T, Ahlberg K (2008) Components that influence assessment and management of cancer-related symptoms: an interdisciplinary perspective. Oncol Nurs Forum 35:691–698CrossRefPubMed
16.
Zurück zum Zitat Detmar SB, Muller MJ, Wever LDV, Schornagel JH, Aaronson NK (2001) Patient-physician communication during outpatient palliative treatment visits. JAMA 285:1351–1357CrossRefPubMed Detmar SB, Muller MJ, Wever LDV, Schornagel JH, Aaronson NK (2001) Patient-physician communication during outpatient palliative treatment visits. JAMA 285:1351–1357CrossRefPubMed
17.
Zurück zum Zitat Liamputtong P (2013) Qualitative research methods, 4th edn. Oxford University Press, Melbourne Liamputtong P (2013) Qualitative research methods, 4th edn. Oxford University Press, Melbourne
18.
Zurück zum Zitat Shuy RW (2003) In-person versus telephone interviewing. In: Holstein JA, Gubrium JF (eds) Inside interviewing: new lenses, new concerns. Sage Publications Inc, Thousand Oaks, pp 174–193 Shuy RW (2003) In-person versus telephone interviewing. In: Holstein JA, Gubrium JF (eds) Inside interviewing: new lenses, new concerns. Sage Publications Inc, Thousand Oaks, pp 174–193
19.
Zurück zum Zitat Gale NK, Heath G, Cameron E, Rashid S, Redwood S (2013) Using the framework method for the analysis of qualitative data in multi-disciplinary health research. BMC Med Res Methodol 13:117CrossRefPubMedPubMedCentral Gale NK, Heath G, Cameron E, Rashid S, Redwood S (2013) Using the framework method for the analysis of qualitative data in multi-disciplinary health research. BMC Med Res Methodol 13:117CrossRefPubMedPubMedCentral
20.
21.
Zurück zum Zitat Kitto SC, Chesters J, Grbich C (2008) Quality in qualitative research. Med J Aust 188:243–246PubMed Kitto SC, Chesters J, Grbich C (2008) Quality in qualitative research. Med J Aust 188:243–246PubMed
22.
Zurück zum Zitat Larsson A, Wijk H (2007) Patient experiences of pain and pain management at the end of life: a pilot study. Pain Manag Nurs 8:12–16CrossRefPubMed Larsson A, Wijk H (2007) Patient experiences of pain and pain management at the end of life: a pilot study. Pain Manag Nurs 8:12–16CrossRefPubMed
23.
Zurück zum Zitat Koffman J, Morgan M, Higginson IJ (2008) Cultural meanings of pain: a qualitative study of Black Caribbean and White British patients with advanced cancer. Palliat Medicine 22:350–359CrossRef Koffman J, Morgan M, Higginson IJ (2008) Cultural meanings of pain: a qualitative study of Black Caribbean and White British patients with advanced cancer. Palliat Medicine 22:350–359CrossRef
24.
Zurück zum Zitat Blomberg K, Sahlberg-Blom E (2007) Closeness and distance: a way of handling difficult situations in daily care. J Clin Nurs 16:244–254CrossRefPubMed Blomberg K, Sahlberg-Blom E (2007) Closeness and distance: a way of handling difficult situations in daily care. J Clin Nurs 16:244–254CrossRefPubMed
25.
Zurück zum Zitat Towers A, MacDonald N, Wallace E (2003) Ethical issues in palliative care: views of patients, families, and nonphysician staff. Can Fam Physician 49:1626–1631PubMedPubMedCentral Towers A, MacDonald N, Wallace E (2003) Ethical issues in palliative care: views of patients, families, and nonphysician staff. Can Fam Physician 49:1626–1631PubMedPubMedCentral
26.
Zurück zum Zitat Deschepper R, Bernheim JL, Vander Stichele R et al (2008) Truth-telling at the end of life: a pilot study on the perspective of patients and professional caregivers. Patient Educ Couns 71:52–56CrossRefPubMed Deschepper R, Bernheim JL, Vander Stichele R et al (2008) Truth-telling at the end of life: a pilot study on the perspective of patients and professional caregivers. Patient Educ Couns 71:52–56CrossRefPubMed
27.
Zurück zum Zitat Willard C, Luker K (2006) Challenges to end of life care in the acute hospital setting. Palliat Med 20:611–615CrossRefPubMed Willard C, Luker K (2006) Challenges to end of life care in the acute hospital setting. Palliat Med 20:611–615CrossRefPubMed
28.
Zurück zum Zitat Butow P, Cockburn J, Girgis A, Bowman D, Schofield P, D'Este C, Stojanovski E, Tattersall MHN, the CUES Team (2008) Increasing oncologists’ skills in eliciting and responding to emotional cues: evaluation of a communication skills training program. Psychooncology 17:209–218CrossRefPubMed Butow P, Cockburn J, Girgis A, Bowman D, Schofield P, D'Este C, Stojanovski E, Tattersall MHN, the CUES Team (2008) Increasing oncologists’ skills in eliciting and responding to emotional cues: evaluation of a communication skills training program. Psychooncology 17:209–218CrossRefPubMed
29.
Zurück zum Zitat Miccinesi G, Bianchi E, Brunelli C, Borreani C (2012) End-of-life preferences in advanced cancer patients willing to discuss issues surrounding their terminal condition. Eur J Cancer Care 21:623–633CrossRef Miccinesi G, Bianchi E, Brunelli C, Borreani C (2012) End-of-life preferences in advanced cancer patients willing to discuss issues surrounding their terminal condition. Eur J Cancer Care 21:623–633CrossRef
30.
Zurück zum Zitat Marcusen C (2010) Information and communication needs of individuals living with advanced cancer. Semin Oncol Nurs 26:151–156CrossRefPubMed Marcusen C (2010) Information and communication needs of individuals living with advanced cancer. Semin Oncol Nurs 26:151–156CrossRefPubMed
31.
Zurück zum Zitat Gourdji I, McVey L, Purden M (2009) A quality end of life from a palliative care patient’s perspective. J Palliat Care 25:40–50PubMed Gourdji I, McVey L, Purden M (2009) A quality end of life from a palliative care patient’s perspective. J Palliat Care 25:40–50PubMed
32.
Zurück zum Zitat Jack B, Hillier V, Williams A, Oldham J (2003) Hospital based palliative care teams improve the symptoms of cancer patients. Palliat Med 17:498–502CrossRefPubMed Jack B, Hillier V, Williams A, Oldham J (2003) Hospital based palliative care teams improve the symptoms of cancer patients. Palliat Med 17:498–502CrossRefPubMed
33.
Zurück zum Zitat Jack B, Hillier V, Williams A, Oldham J (2004) Hospital based palliative care teams improve the insight of cancer patients into their disease. Palliat Med 18:46–52CrossRefPubMed Jack B, Hillier V, Williams A, Oldham J (2004) Hospital based palliative care teams improve the insight of cancer patients into their disease. Palliat Med 18:46–52CrossRefPubMed
34.
Zurück zum Zitat Walczak A, Butow PN, Davidson PM, Bellemore FA, Tattersall MHN, Clayton JM, Young J, Mazer B, Ladwig S, Epstein RM (2013) Patient perspectives regarding communication about prognosis and end-of-life issues: how can it be optimised? Patient Educ Couns 90:307–314CrossRefPubMed Walczak A, Butow PN, Davidson PM, Bellemore FA, Tattersall MHN, Clayton JM, Young J, Mazer B, Ladwig S, Epstein RM (2013) Patient perspectives regarding communication about prognosis and end-of-life issues: how can it be optimised? Patient Educ Couns 90:307–314CrossRefPubMed
35.
Zurück zum Zitat Kvåle K (2007) Do cancer patients always want to talk about difficult emotions? A qualitative study of cancer inpatients communication needs. Eur J Oncol Nurs 11:320–327CrossRefPubMed Kvåle K (2007) Do cancer patients always want to talk about difficult emotions? A qualitative study of cancer inpatients communication needs. Eur J Oncol Nurs 11:320–327CrossRefPubMed
36.
Zurück zum Zitat Enguidanos S, Housen P, Penido M, Mejia B, Miller JA (2014) Family members’ perceptions of inpatient palliative care consult services: a qualitative study. Palliat Med 28:42–48CrossRefPubMed Enguidanos S, Housen P, Penido M, Mejia B, Miller JA (2014) Family members’ perceptions of inpatient palliative care consult services: a qualitative study. Palliat Med 28:42–48CrossRefPubMed
37.
Zurück zum Zitat Hürny C (2002) Do patients with advanced cancer get appropriate information. Support Care Cancer 10:383–384CrossRefPubMed Hürny C (2002) Do patients with advanced cancer get appropriate information. Support Care Cancer 10:383–384CrossRefPubMed
38.
Zurück zum Zitat Reid J, McKenna HP, Fitzsimons D, McCance TV (2010) An exploration of the experience of cancer cachexia: what patients and their families want from healthcare professionals. Eur J Cancer Care 19:682–689CrossRef Reid J, McKenna HP, Fitzsimons D, McCance TV (2010) An exploration of the experience of cancer cachexia: what patients and their families want from healthcare professionals. Eur J Cancer Care 19:682–689CrossRef
39.
Zurück zum Zitat Armes PJ, Addington-Hall JM (2003) Perspectives on symptom control in patients receiving community palliative care. Palliat Med 17:608–615CrossRefPubMed Armes PJ, Addington-Hall JM (2003) Perspectives on symptom control in patients receiving community palliative care. Palliat Med 17:608–615CrossRefPubMed
40.
Zurück zum Zitat van Wijmen MPS, Pasman HRW, Widdershoven GAM, Onwuteaka-Philipsen BD (2015) Continuing or forgoing treatment at the end of life? Preferences of the general public and people with an advance directive. J Med Ethics 41:599–606CrossRefPubMed van Wijmen MPS, Pasman HRW, Widdershoven GAM, Onwuteaka-Philipsen BD (2015) Continuing or forgoing treatment at the end of life? Preferences of the general public and people with an advance directive. J Med Ethics 41:599–606CrossRefPubMed
41.
Zurück zum Zitat Graham J, Ramirez AJ, Cull A, Finlay I, Hoy A, Richards MA (1996) Job stress and satisfaction among palliative physicians. Palliat Med 10:185–194CrossRefPubMed Graham J, Ramirez AJ, Cull A, Finlay I, Hoy A, Richards MA (1996) Job stress and satisfaction among palliative physicians. Palliat Med 10:185–194CrossRefPubMed
42.
Zurück zum Zitat Jackson VA, Mack J, Matsuyama R, Lakoma MD, Sullivan AM, Arnold RM, Weeks JC, Block SD (2008) A qualitative study of oncologists’ approaches to end-of-life care. J Palliat Med 11:893–906CrossRefPubMedPubMedCentral Jackson VA, Mack J, Matsuyama R, Lakoma MD, Sullivan AM, Arnold RM, Weeks JC, Block SD (2008) A qualitative study of oncologists’ approaches to end-of-life care. J Palliat Med 11:893–906CrossRefPubMedPubMedCentral
Metadaten
Titel
Exploring symptom meaning: perspectives of palliative care physicians
verfasst von
Celina F. Estacio
Phyllis N. Butow
Melanie R. Lovell
Skye T. Dong
Josephine M. Clayton
Publikationsdatum
03.03.2018
Verlag
Springer Berlin Heidelberg
Erschienen in
Supportive Care in Cancer / Ausgabe 8/2018
Print ISSN: 0941-4355
Elektronische ISSN: 1433-7339
DOI
https://doi.org/10.1007/s00520-018-4126-0

Weitere Artikel der Ausgabe 8/2018

Supportive Care in Cancer 8/2018 Zur Ausgabe

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.