Abstract
Introduction
Patients with advanced cancer often experience symptoms including pain, nausea, anorexia, fatigue, and depression. High symptom burden can be alleviated by multidisciplinary palliative care (PC) teams practicing symptom-directed management. Patients who are unable to access such services may be at higher risk of increased symptoms and poor outcomes.
Methods
A sequential exploratory mixed methods study was performed to explore the burden of symptoms experienced by Northern Alberta patients with advanced cancer. The symptom burden among patients from rural and remote communities was characterized in a retrospective review capturing basic demographic and clinicopathologic information, in addition to patient-reported outcomes. Symptom prevalence was evaluated against the nature and range of supportive care services available. Service accessibility was assessed at community level by surveying health care providers (HCPs) and performing thematic analysis on their responses.
Results
From January 1 to December 31, 2017, 607 outpatients were seen in consultation in an integrated palliative radiotherapy clinic in Edmonton, Alberta. A total of 166 (27.3%) patients resided in Alberta communities designated as rural or remote. Patient-reported symptom prevalence and intensity of scores did not differ significantly between rural/remote and urban populations. Unmet practical needs were flagged significantly more often by patients from rural communities (p = 0.05). HCPs from rural community health centers in Northern Alberta were knowledgeable regarding PC services availability and referral processes within their communities.
Conclusion
Although the symptom burden experienced by patients living with advanced cancer in rural and remote areas of Northern Alberta does not differ significantly from their urban counterparts, and community HCPs are knowledgeable regarding PC services, unmet needs within these communities remain. Continuing support for PC services in rural communities, as well as establishing care pathways for patients from rural populations traveling to urban centers to receive treatment, will help to minimize the unmet needs these patients experience.
Similar content being viewed by others
References
Senate of Canada (1995) Of life and death: a report of the Special Committee on Euthanasia and Assisted Suicide. Issues Law Med 11(2):209–213
Stukenborg GJ, Blackhall LJ, Harrison JH, Dillon PM, Read PW (2016) Longitudinal patterns of cancer patient reported outcomes in end of life care predict survival. Support Care Cancer 24(5):2217–2224
Rauenzahn SL, Schmidt S, Aduba IO, Jones JT, Ali N, Tenner LL (2017) Integrating palliative care services in ambulatory oncology: an application of the Edmonton Symptom Assessment System. J Oncol Pract 13(4):e401–e407
Strasser F, Sweeney C, Willey J, Benisch-Tolley S, Palmer JL, Bruera E (2004) Impact of a half-day multidisciplinary symptom control and palliative care outpatient clinic in a comprehensive cancer center on recommendations, symptom intensity, and patient satisfaction: a retrospective descriptive study. J Pain Symptom Manag 27(6):481–491
Smith TJ, Temin S, Alesi ER, Abernethy AP, Balboni TA, Basch EM, Ferrell BR, Loscalzo M, Meier DE, Paice JA, Peppercorn JM, Somerfield M, Stovall E, von Roenn JH (2012) American Society of Clinical Oncology provisional clinical opinion: the integration of palliative care into standard oncology care. J Clin Oncol 30(8):880–887
Tedder T, Elliott L, Lewis K (2017) Analysis of common barriers to rural patients utilizing hospice and palliative care services: an integrated literature review. J Am Assoc Nurse Pract 29(6):356–362
Pesut B, Robinson CA, Bottorff JL, Fyles G, Broughton S (2010) On the road again: patient perspectives on commuting for palliative care. Palliat Support Care 8(2):187–195
Dumont S, Jacobs P, Turcotte V, Turcotte S, Johnston G (2015) Palliative care costs in Canada: a descriptive comparison of studies of urban and rural patients near end of life. Palliat Med 29(10):908–917
Watanabe SM, Fairchild A, Pituskin E, Borgersen P, Hanson J, Fassbender K (2013) Improving access to specialist multidisciplinary palliative care consultation for rural cancer patients by videoconferencing: report of a pilot project. Support Care Cancer 21(4):1201–1207
Olson RA et al (2014) Prospective evaluation of unmet needs of rural and aboriginal cancer survivors in Northern British Columbia. Curr Oncol 21(2):e179
Fairchild A, Pituskin E, Rose B, Ghosh S, Dutka J, Driga A, Tachynski P, Borschneck J, Gagnon L, Macdonnell S, Middleton J, Thavone K, Carstairs S, Brent D, Severin D (2009) The rapid access palliative radiotherapy program: blueprint for initiation of a one-stop multidisciplinary bone metastases clinic. Support Care Cancer 17(2):163–170
Danielson B, Fairchild A (2012) Beyond palliative radiotherapy: a pilot multidisciplinary brain metastases clinic. Support Care Cancer 20(4):773–781
Wu JSY et al (2010) Patterns of practice in palliative radiotherapy for painful bone metastases: impact of a regional rapid access clinic on access to care. Int J Radiat Oncol Biol Phys 78(2):533–538
Bruera E et al. (1991) The Edmonton Symptom Assessment System (ESAS): a simple method for the assessment of palliative care patients. J Palliat Care
Feldstain A et al (2014) Screening for distress in patients with cancer: methodologic considerations. Curr Oncol 21(2):e330
Watson L, Groff S, Tamagawa R, Looyis J, Farkas S, Schaitel B, DeIure A, Faris P, Bultz BD (2016) Evaluating the impact of provincial implementation of screening for distress on quality of life, symptom reports, and psychosocial well-being in patients with cancer. J Natl Compr Cancer Netw 14(2):164–172
Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG (2009) Research electronic data capture (REDCap)—a metadata-driven methodology and workflow process for providing translational research informatics support. J Biomed Inform 42(2):377–381
“Census metropolitan influenced zone” Statistics Canada (2015) http://www12.statcan.gc.ca/census-recensement/2011/ref/dict/geo010-eng.cfm. Accessed June 2018
Tamagawa R, Groff S, Anderson J, Champ S, Deiure A, Looyis J, Faris P, Watson L (2016) Effects of a provincial-wide implementation of screening for distress on healthcare professionals' confidence and understanding of person-centered care in oncology. J Natl Compr Cancer Netw 14(10):1259–1266
“My Health Alberta” Government of Alberta (2018) https://myhealth.alberta.ca/journey/healthier-together/Pages/default.aspx. Accessed June 2018
Brazil K et al. (2013) "Comparing the experiences of rural and urban family caregivers of the terminally ill." Rural Remote Health 13.1
Robinson CA et al (2009) Rural palliative care: a comprehensive review. J Palliat Med 12(3):253–258
Evans R, Stone D, Elwyn G (2003) Organizing palliative care for rural populations: a systematic review of the evidence. Fam Pract 20(3):304–310
Gillan C et al (2012) Barriers to accessing radiation therapy in Canada: a systematic review. Radiat Oncol 7(1):167
Beck SL, Towsley GL, Caserta MS, Lindau K, Dudley WN (2009) Symptom experiences and quality of life of rural and urban older adult cancer survivors. Cancer Nurs 32(5):359–369
DiSipio T et al (2010) Does quality of life among breast cancer survivors one year after diagnosis differ depending on urban and non-urban residence? A comparative study. Health Qual Life Outcomes 8(1):3
Fitch MI et al (2005) Travelling for radiation cancer treatment: patient satisfaction. Can Oncol Nurs J 15(2):107–112
Qato DM et al (2014) ‘Pharmacy deserts’ are prevalent in Chicago’s predominantly minority communities, raising medication access concerns. Health Aff 33(11):1958–1965
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest. The authors are in full control of the primary data and will provide if requested.
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Appendix
Appendix
Rights and permissions
About this article
Cite this article
Spence, W., Ghosh, S., Palen, M. et al. Symptom burden among Northern Alberta radiotherapy patients with advanced cancer: mapping needs and gaps. Support Care Cancer 28, 4963–4969 (2020). https://doi.org/10.1007/s00520-020-05330-2
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00520-020-05330-2