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Erschienen in: Supportive Care in Cancer 12/2019

10.04.2019 | Original Article

Social disparities and symptom burden in populations with advanced cancer: specialist palliative care providers’ perspectives

verfasst von: Anna Santos Salas, Sharon M. Watanabe, Yoko Tarumi, Tracy Wildeman, Ana M. Hermosa García, Bisi Adewale, Wendy Duggleby

Erschienen in: Supportive Care in Cancer | Ausgabe 12/2019

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Abstract

Disparities in access to palliative care services for populations with social disparities have been reported in Western countries. Studies indicate that these populations tend to report higher symptom distress than other population groups. We need to further investigate how social disparities influence symptom burden to improve symptom relief in these populations.

Purpose

To examine the perspectives of specialist palliative care providers concerning the relationship between social disparities and symptom burden in populations with advanced cancer.

Methods

Two sequential qualitative studies that followed a combination of interpretive and critical methodologies. The interpretive approach was outlined by van Manen’s hermeneutic phenomenology while the critical component was informed by the works of Paulo Freire. Participants involved two specialist palliative care teams from a large acute care hospital and a large cancer center in Western Canada. Participants included 11 palliative care providers including registered nurses, nurse practitioners, physicians, and pharmacists.

Results

Participants perceived that social conditions that might aggravate symptom burden included low income, low education, lack of social support, language barriers, and rurality. The relationship between income and symptom burden reflected diverse views. Participants identified populations prone to complex symptom burden including homeless individuals, Indigenous people, people with a history of addictions, and people with mental health or psychosocial issues.

Conclusion

Participants perceived that social disparities may increase symptom complexity in populations with advanced cancer. Participants did not identify ethnicity and gender as influencing symptom burden. Further research is needed to examine the interactions of social disparities, patient individuality, and symptom burden.
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Literatur
4.
Zurück zum Zitat Canada. Parliament. House of Commons. Parliamentary Committee on Palliative and Compassionate Care (2011) Not to be forgotten care of vulnerable Canadians. In: Editor (ed)^(eds) Book Not to be forgotten care of vulnerable Canadians. Parliamentary Committee on Palliative and Compassionate Care, City Canada. Parliament. House of Commons. Parliamentary Committee on Palliative and Compassionate Care (2011) Not to be forgotten care of vulnerable Canadians. In: Editor (ed)^(eds) Book Not to be forgotten care of vulnerable Canadians. Parliamentary Committee on Palliative and Compassionate Care, City
5.
Zurück zum Zitat Canadian Partnership Against Cancer (2017) Cancer system performance: 2017 report. The Canadian Partnership Against Cancer, Toronto Canadian Partnership Against Cancer (2017) Cancer system performance: 2017 report. The Canadian Partnership Against Cancer, Toronto
6.
Zurück zum Zitat World Health Organization (2007) Cancer control: knowledge into action: WHO guide for effective programmes. Palliative Care. World Health Organization, Geneva World Health Organization (2007) Cancer control: knowledge into action: WHO guide for effective programmes. Palliative Care. World Health Organization, Geneva
7.
Zurück zum Zitat Ferrell BR, Temel JS, Temin S, Alesi ER, Balboni TA, Basch EM, Firn JI, Paice JA, Peppercorn JM, Phillips T, Stovall EL, Zimmermann C, Smith TJ (2016) Integration of palliative care into standard oncology care: American Society of Clinical Oncology Clinical Practice Guideline Update. J Clin Oncol 35:96–112CrossRef Ferrell BR, Temel JS, Temin S, Alesi ER, Balboni TA, Basch EM, Firn JI, Paice JA, Peppercorn JM, Phillips T, Stovall EL, Zimmermann C, Smith TJ (2016) Integration of palliative care into standard oncology care: American Society of Clinical Oncology Clinical Practice Guideline Update. J Clin Oncol 35:96–112CrossRef
8.
Zurück zum Zitat Leeman J, Sandelowski M (2012) Practice-based evidence and qualitative inquiry. J Nurs Scholarsh 44:171–179CrossRef Leeman J, Sandelowski M (2012) Practice-based evidence and qualitative inquiry. J Nurs Scholarsh 44:171–179CrossRef
9.
Zurück zum Zitat Whitehead M, Dahlgren G (2006) Levelling up (part 1): a discussion paper on concepts and principles for tackling social inequities in health. World Health Organization Regional Office for Europe, Copenhagen Whitehead M, Dahlgren G (2006) Levelling up (part 1): a discussion paper on concepts and principles for tackling social inequities in health. World Health Organization Regional Office for Europe, Copenhagen
10.
Zurück zum Zitat Morrison S, Augustin R, Souvanna P, Meier D (2011) America’s care of serious illness: a state-by-state report card on access to palliative care in our nation’s hospitals. J Palliat Med 14:1094–1096CrossRef Morrison S, Augustin R, Souvanna P, Meier D (2011) America’s care of serious illness: a state-by-state report card on access to palliative care in our nation’s hospitals. J Palliat Med 14:1094–1096CrossRef
11.
Zurück zum Zitat Evans N, Meñaca A, Andrew EV, Koffman J, Harding R, Higginson IJ, Pool R, Gysels M, Prisma (2012) Systematic review of the primary research on minority ethnic groups and end-of-life care from the United Kingdom. J Pain Symptom Manag 43:261–286CrossRef Evans N, Meñaca A, Andrew EV, Koffman J, Harding R, Higginson IJ, Pool R, Gysels M, Prisma (2012) Systematic review of the primary research on minority ethnic groups and end-of-life care from the United Kingdom. J Pain Symptom Manag 43:261–286CrossRef
12.
Zurück zum Zitat Bossuyt N, Van den Block L, Cohen J, Meeussen K, Bilsen J, Echteld M, Deliens L, Van Casteren V (2011) Is individual educational level related to end-of-life care use? Results from a nationwide retrospective cohort study in Belgium. J Palliat Med 14:1135–1141CrossRef Bossuyt N, Van den Block L, Cohen J, Meeussen K, Bilsen J, Echteld M, Deliens L, Van Casteren V (2011) Is individual educational level related to end-of-life care use? Results from a nationwide retrospective cohort study in Belgium. J Palliat Med 14:1135–1141CrossRef
13.
Zurück zum Zitat Lewis JM, Digiacomo M, Currow DC, Davidson PM (2011) Dying in the margins: understanding palliative care and socioeconomic deprivation in the developed world. J Pain Symptom Manag 42:105–118CrossRef Lewis JM, Digiacomo M, Currow DC, Davidson PM (2011) Dying in the margins: understanding palliative care and socioeconomic deprivation in the developed world. J Pain Symptom Manag 42:105–118CrossRef
14.
Zurück zum Zitat Green CR, Montague L, Hart-Johnson TA (2009) Consistent and breakthrough pain in diverse advanced cancer patients: a longitudinal examination. J Pain Symptom Manag 37:831–847CrossRef Green CR, Montague L, Hart-Johnson TA (2009) Consistent and breakthrough pain in diverse advanced cancer patients: a longitudinal examination. J Pain Symptom Manag 37:831–847CrossRef
15.
Zurück zum Zitat Reyes-Gibby CC, Shete S, Anderson KO, Bruera E, Yennurajalingam S (2012) Early referral to supportive care specialists for symptom burden in lung cancer patients: a comparison of non-Hispanic whites, Hispanics, and non-Hispanic blacks. Cancer 118:856–863CrossRef Reyes-Gibby CC, Shete S, Anderson KO, Bruera E, Yennurajalingam S (2012) Early referral to supportive care specialists for symptom burden in lung cancer patients: a comparison of non-Hispanic whites, Hispanics, and non-Hispanic blacks. Cancer 118:856–863CrossRef
16.
Zurück zum Zitat Bell C, Kuriya M, Fischberg D (2011) Pain outcomes of inpatient pain and palliative care consultations: differences by race and diagnosis. J Palliat Med 14:1142–1148CrossRef Bell C, Kuriya M, Fischberg D (2011) Pain outcomes of inpatient pain and palliative care consultations: differences by race and diagnosis. J Palliat Med 14:1142–1148CrossRef
17.
Zurück zum Zitat Goodridge D, Buckley A, Marko J, Whitehead S (2011) Home care clients in the last year of life: is material deprivation associated with service characteristics? J Aging Health 23:954–973CrossRef Goodridge D, Buckley A, Marko J, Whitehead S (2011) Home care clients in the last year of life: is material deprivation associated with service characteristics? J Aging Health 23:954–973CrossRef
18.
Zurück zum Zitat Neergaard M, Olesen F, Sondergaard J, Vedsted P, Jensen A (2015) Are cancer patients’ socioeconomic and cultural factors associated with contact to general practitioners in the last phase of life? Int J Family Med 2015:1–8CrossRef Neergaard M, Olesen F, Sondergaard J, Vedsted P, Jensen A (2015) Are cancer patients’ socioeconomic and cultural factors associated with contact to general practitioners in the last phase of life? Int J Family Med 2015:1–8CrossRef
19.
Zurück zum Zitat Van Manen M (1997) Researching lived experience: human science for an action sensitive pedagogy. Althouse Press, London Van Manen M (1997) Researching lived experience: human science for an action sensitive pedagogy. Althouse Press, London
20.
Zurück zum Zitat Freire P (2007) Pedagogía de la tolerancia. Fondo de Cultura Economica de Argentina, Buenos Aires Freire P (2007) Pedagogía de la tolerancia. Fondo de Cultura Economica de Argentina, Buenos Aires
21.
Zurück zum Zitat Rozendo CA, Santos Salas A, Cameron B (2017) Problematizing in nursing education: Freire’s contribution to transformative practice. Nurse Educ Today 51:120–123CrossRef Rozendo CA, Santos Salas A, Cameron B (2017) Problematizing in nursing education: Freire’s contribution to transformative practice. Nurse Educ Today 51:120–123CrossRef
22.
Zurück zum Zitat Creswell JW, Poth CN (2017) Qualitative inquiry and research design: choosing among five approaches. SAGE Publications, Thousand Oaks Creswell JW, Poth CN (2017) Qualitative inquiry and research design: choosing among five approaches. SAGE Publications, Thousand Oaks
23.
Zurück zum Zitat Martinez KA, Snyder CF, Malin JL, Dy SM (2014) Is race/ethnicity related to the presence or severity of pain in colorectal and lung cancer? J Pain Symptom Manag 48:1050–1059CrossRef Martinez KA, Snyder CF, Malin JL, Dy SM (2014) Is race/ethnicity related to the presence or severity of pain in colorectal and lung cancer? J Pain Symptom Manag 48:1050–1059CrossRef
24.
Zurück zum Zitat Rannestad T, Skjeldestad F (2012) Socioeconomic conditions and number of pain sites in women. BMC Womens Health 12:1–7CrossRef Rannestad T, Skjeldestad F (2012) Socioeconomic conditions and number of pain sites in women. BMC Womens Health 12:1–7CrossRef
25.
Zurück zum Zitat Canadian Partnership Against Cancer (2014) Examining disparities in cancer control: a system performance special focus report. The Canadian Partnership Against Cancer, Toronto Canadian Partnership Against Cancer (2014) Examining disparities in cancer control: a system performance special focus report. The Canadian Partnership Against Cancer, Toronto
26.
Zurück zum Zitat Klop HT, de Veer AJE, van Dongen SI, Francke AL, Rietjens JAC, Onwuteaka-Philipsen BD (2018) Palliative care for homeless people: a systematic review of the concerns, care needs and preferences, and the barriers and facilitators for providing palliative care. BMC Palliat Care 17:67CrossRef Klop HT, de Veer AJE, van Dongen SI, Francke AL, Rietjens JAC, Onwuteaka-Philipsen BD (2018) Palliative care for homeless people: a systematic review of the concerns, care needs and preferences, and the barriers and facilitators for providing palliative care. BMC Palliat Care 17:67CrossRef
27.
Zurück zum Zitat Gourlay DL, Heit HA, Almahrezi A (2005) Universal precautions in pain medicine: a rational approach to the treatment of chronic pain. Pain Med 6:107–112CrossRef Gourlay DL, Heit HA, Almahrezi A (2005) Universal precautions in pain medicine: a rational approach to the treatment of chronic pain. Pain Med 6:107–112CrossRef
28.
Zurück zum Zitat Fisch M, Mendoza T, Cleeland C, Lee J, Manola J, Weiss M, Wagner L, Chang V, Cella D, Minasian L, McCaskill-Stevens W (2012) Prospective, observational study of pain and analgesic prescribing in medical oncology outpatients with breast, colorectal, lung, or prostate cancer. J Clin Oncol 30:1980–1988CrossRef Fisch M, Mendoza T, Cleeland C, Lee J, Manola J, Weiss M, Wagner L, Chang V, Cella D, Minasian L, McCaskill-Stevens W (2012) Prospective, observational study of pain and analgesic prescribing in medical oncology outpatients with breast, colorectal, lung, or prostate cancer. J Clin Oncol 30:1980–1988CrossRef
29.
Zurück zum Zitat Kwok W, Bhuvanakrishna T (2014) The relationship between ethnicity and the pain experience of cancer patients: a systematic review. Indian J Palliat Care 20:194–200CrossRef Kwok W, Bhuvanakrishna T (2014) The relationship between ethnicity and the pain experience of cancer patients: a systematic review. Indian J Palliat Care 20:194–200CrossRef
30.
Zurück zum Zitat Bell CL, Kuriya M, Fischberg D (2011) Hospice referrals and code status: outcomes of inpatient palliative care consultations among Asian Americans and Pacific Islanders with cancer. J Pain Symptom Manag 42:557–564CrossRef Bell CL, Kuriya M, Fischberg D (2011) Hospice referrals and code status: outcomes of inpatient palliative care consultations among Asian Americans and Pacific Islanders with cancer. J Pain Symptom Manag 42:557–564CrossRef
31.
Zurück zum Zitat Chuang E, Hope AA, Allyn K, Szalkiewicz E, Gary B, Gong MN (2017) Gaps in provision of primary and specialty palliative care in the acute care setting by race and ethnicity. J Pain Symptom Manag 54:645–653CrossRef Chuang E, Hope AA, Allyn K, Szalkiewicz E, Gary B, Gong MN (2017) Gaps in provision of primary and specialty palliative care in the acute care setting by race and ethnicity. J Pain Symptom Manag 54:645–653CrossRef
32.
Zurück zum Zitat Withrow DR, Nishri ED, Marrett LD, Pole JD, Tjepkema M (2017) Cancer survival disparities between First Nations and non-Aboriginal adults in Canada: follow-up of the 1991 census mortality cohort. Cancer Epidemiol Biomark Prev 26:145–151CrossRef Withrow DR, Nishri ED, Marrett LD, Pole JD, Tjepkema M (2017) Cancer survival disparities between First Nations and non-Aboriginal adults in Canada: follow-up of the 1991 census mortality cohort. Cancer Epidemiol Biomark Prev 26:145–151CrossRef
34.
Zurück zum Zitat Sumalinog R, Hwang SW, Harrington K, Dosani N (2017) Advance care planning, palliative care, and end-of-life care interventions for homeless people: a systematic review. Palliat Med 31:109–119CrossRef Sumalinog R, Hwang SW, Harrington K, Dosani N (2017) Advance care planning, palliative care, and end-of-life care interventions for homeless people: a systematic review. Palliat Med 31:109–119CrossRef
35.
Zurück zum Zitat Surbone A, Halpern MT (2016) Unequal cancer survivorship care: addressing cultural and sociodemographic disparities in the clinic. Support Care Cancer 24:4831–4833CrossRef Surbone A, Halpern MT (2016) Unequal cancer survivorship care: addressing cultural and sociodemographic disparities in the clinic. Support Care Cancer 24:4831–4833CrossRef
36.
Zurück zum Zitat Hudson BF, Candy B, Shulman C, Flemming K (2016) Challenges to access and provision of palliative care for people who are homeless: a systematic review of qualitative research. BMC Palliat Care 15:96CrossRef Hudson BF, Candy B, Shulman C, Flemming K (2016) Challenges to access and provision of palliative care for people who are homeless: a systematic review of qualitative research. BMC Palliat Care 15:96CrossRef
37.
Zurück zum Zitat Canadian Partnership Against Cancer (2017) Palliative and end-of-life care: a cancer system performance report. Canadian Partnership Against Cancer, Toronto, ON Canadian Partnership Against Cancer (2017) Palliative and end-of-life care: a cancer system performance report. Canadian Partnership Against Cancer, Toronto, ON
38.
Zurück zum Zitat McGrath P, Holewa H (2012) Reconceptualising relocation for specialist treatment: insights from New Zealand. Support Care Cancer 20:499–505CrossRef McGrath P, Holewa H (2012) Reconceptualising relocation for specialist treatment: insights from New Zealand. Support Care Cancer 20:499–505CrossRef
39.
Zurück zum Zitat Im E-O, Chee W, Guevara E, Liu Y, Lim H-J, Tsai H-M, Clark M, Bender M, Suk kim K, Hee Kim Y, Shin H (2007) Gender and ethnic differences in cancer pain experience: a multiethnic survey in the United States. Nurs Res 56:296–306CrossRef Im E-O, Chee W, Guevara E, Liu Y, Lim H-J, Tsai H-M, Clark M, Bender M, Suk kim K, Hee Kim Y, Shin H (2007) Gender and ethnic differences in cancer pain experience: a multiethnic survey in the United States. Nurs Res 56:296–306CrossRef
40.
Zurück zum Zitat Montague L, Green CR (2009) Cancer and breakthrough pain's impact on a diverse population. Pain Med 10:549–561CrossRef Montague L, Green CR (2009) Cancer and breakthrough pain's impact on a diverse population. Pain Med 10:549–561CrossRef
41.
Zurück zum Zitat Maddison AR, Asada Y, Burge F, Johnston GW, Urquhart R (2012) Inequalities in end-of-life care for colorectal cancer patients in Nova Scotia, Canada. J Palliat Care 28:90–96CrossRef Maddison AR, Asada Y, Burge F, Johnston GW, Urquhart R (2012) Inequalities in end-of-life care for colorectal cancer patients in Nova Scotia, Canada. J Palliat Care 28:90–96CrossRef
42.
Zurück zum Zitat Barbera L, Seow H, Sutradhar R, Chu A (2015) Quality of end-of-life cancer care in Canada: a retrospective four-province study using administrative health care data. Curr Oncol 22:341–355CrossRef Barbera L, Seow H, Sutradhar R, Chu A (2015) Quality of end-of-life cancer care in Canada: a retrospective four-province study using administrative health care data. Curr Oncol 22:341–355CrossRef
43.
Zurück zum Zitat Bubis LD, Davis L, Mahar A, Barbera L, Li Q, Moody L, Karanicolas P, Sutradhar R, Coburn NG (2018) Symptom burden in the first year after cancer diagnosis: an analysis of patient-reported outcomes. J Clin Oncol 36:1103–1121CrossRef Bubis LD, Davis L, Mahar A, Barbera L, Li Q, Moody L, Karanicolas P, Sutradhar R, Coburn NG (2018) Symptom burden in the first year after cancer diagnosis: an analysis of patient-reported outcomes. J Clin Oncol 36:1103–1121CrossRef
44.
Zurück zum Zitat Butler H, O’Brien AJ (2018) Access to specialist palliative care services by people with severe and persistent mental illness: a retrospective cohort study. Int J Ment Health Nurs 27:737–746CrossRef Butler H, O’Brien AJ (2018) Access to specialist palliative care services by people with severe and persistent mental illness: a retrospective cohort study. Int J Ment Health Nurs 27:737–746CrossRef
45.
Zurück zum Zitat McNamara B, Same A, Rosenwax L, Kelly B (2018) Palliative care for people with schizophrenia: a qualitative study of an under-serviced group in need. BMC Palliat Care 17:1–11CrossRef McNamara B, Same A, Rosenwax L, Kelly B (2018) Palliative care for people with schizophrenia: a qualitative study of an under-serviced group in need. BMC Palliat Care 17:1–11CrossRef
Metadaten
Titel
Social disparities and symptom burden in populations with advanced cancer: specialist palliative care providers’ perspectives
verfasst von
Anna Santos Salas
Sharon M. Watanabe
Yoko Tarumi
Tracy Wildeman
Ana M. Hermosa García
Bisi Adewale
Wendy Duggleby
Publikationsdatum
10.04.2019
Verlag
Springer Berlin Heidelberg
Erschienen in
Supportive Care in Cancer / Ausgabe 12/2019
Print ISSN: 0941-4355
Elektronische ISSN: 1433-7339
DOI
https://doi.org/10.1007/s00520-019-04726-z

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