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Comparing the symptom experience of cancer patients and non-cancer patients

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Abstract

Purpose

Symptom burden is an established concept in oncology encompassing the presence and severity of symptoms experienced by cancer patients. Few studies have examined differences in symptom burden between cancer patients and non-cancer patients. This study seeks to examine the differences in symptom burden between cancer patients (CP) and non-cancer patients (NCP) in order to better understand symptom burden in both populations.

Methods

Two groups of patients completed the Memorial Symptom Assessment Scale: 301 patients from a general medical clinic and 558 cancer patients from a cancer tumor registry. Participants provided demographic information—age, race/ethnicity, and sex and completed the Memorial Symptom Assessment Scale. Medical comorbidity was also measured.

Results

Most symptoms were more common in CP, except for pain, which was more prevalent in the NCP (45% of CP vs. 54% of NCP, p < .05). There was no difference in prevalence for the following symptoms: dry mouth, mouth sores, feeling nervous, worry, cough, and dizziness. The CP had greater mean MSAS Total scores (0.53 vs. 0.43, p < .01), number of symptoms (9.11 vs. 6.13, p < .01), and psychological subscale scores (0.77 vs. 0.64, p < .05). There was no difference by group in the physical nor the GDI subscale scores.

Conclusion

The results of this study support the perception that cancer patients have greater symptom burden. There were some unexpected results, particularly in terms of pain, which was more common in NCP and other symptoms that were experienced equally in both patient populations.

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References

  1. American Cancer Society (2016) Cancer Facts & Figures 2016. American Cancer Society, Atlanta

    Google Scholar 

  2. Institute of Medicine and National Research Council (2006) From cancer patient to cancer survivor: lost in transition. National Academies Press, Washington, DC

    Google Scholar 

  3. Cleeland CS (2007) Symptom burden: multiple symptoms and their impact as patient-reported outcomes. J Natl Cancer Inst Monogr 37:16–21

    Article  Google Scholar 

  4. Wu H-S, Harden JK (2015) Symptom burden and quality of life in survivorship: a review of the literature. Cancer Nurs 38(1):E29–E54

    Article  Google Scholar 

  5. Deshields TL, Potter P, Olsen S, Liu J, Dye L (2011) Documenting the symptom experience of cancer patients. J Support Oncol 9(6):216–223

    Article  Google Scholar 

  6. Deshields T, Potter P, Olsen S, Liu J (2014) The persistence of symptom burden: symptom experience and quality of life of cancer patients across one year. Support Care Cancer 22(4):1089–1096

    Article  Google Scholar 

  7. Marvel MK, Epstein RM, Flowers K, Beckman HB (1999) Soliciting the patient’s agenda: have we improved? JAMA 281(3):283–287

    Article  CAS  Google Scholar 

  8. Tai-Seale M, McGuire T, Zhang W (2007) Time allocation in primary care visits. Health Serv Res 42(5):871–894

    Article  Google Scholar 

  9. Haas LJ, Glazer K, Houchins J, Terry S (2006) Improving the effectiveness of the medical visit: a brief visit-structuring workshop changes patients’ perceptions of primary care visits. Patient Educ Couns 62(3):374–378

    Article  Google Scholar 

  10. Kroenke K, Jackson JL, Chamberlin J (1997) Depressive and anxiety disorders in patients presenting with physical complaints: clinical predictors and outcome. Am J Med 103(5):339–347

    Article  CAS  Google Scholar 

  11. Bausewein C, Booth S, Gysels M et al (2010) Understanding breathlessness: cross-sectional comparison of symptom burden and palliative care needs in chronic obstructive pulmonary disease and cancer. J Palliat Med 13(9):1109–1118

    Article  Google Scholar 

  12. Goodridge D, Lawson J, Duggleby W et al (2008) Health care utilization of patients with chronic obstructive pulmonary disease and lung cancer in the last 12 months of life. Respir Med 102(6):885–891

    Article  Google Scholar 

  13. Bekelman DB, Rumsfeld JS, Havranek EP et al (2009) Symptom burden, depression, and spiritual well-being: a comparison of heart failure and advanced cancer patients. J Gen Intern Med 24(5):592–598

    Article  Google Scholar 

  14. Malik FA, Gysels M, Higginson IJ (2013) Living with breathlessness: a survey of caregivers of breathless patients with lung cancer or heart failure. Palliat Med 27(7):64–56

    Article  Google Scholar 

  15. Sherman DW, Ye XY, Beyer McSherry C et al (2007) Symptom assessment of patients with advanced cancer and AIDS and their family caregivers: the results of a quality-of-life pilot study. Am J Hosp Palliat Care 24(5):350–365

    Article  Google Scholar 

  16. Basch E, Reeve BB, Mitchell SA et al (2014) Development of the National Cancer Institute’s patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE). J Natl Cancer Inst 106(9):1–11

    Article  Google Scholar 

  17. Steindal SA, Bredal IS, Sorbye LW et al (2011) Pain control at the end of life: a comparative study of hospitalized cancer and noncancer patients. Scand J Caring Sci 25(4):771–779

    Article  Google Scholar 

  18. Charlson ME, Pompei P, Ales KL et al (1987) A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis 40(5):373–383

    Article  CAS  Google Scholar 

  19. Piccirillo JF, Creech CM, Zequeira R (1999) Anderson S, Johnston AS. Inclusion of comorbidity into oncology data registries. J Registry Manag 26(2):66–70

    Google Scholar 

  20. Portenoy RK, Thaler HT, Kornblith AB et al (1994) The memorial symptom assessment scale: an instrument for the evaluation of symptom prevalence, characteristics and distress. Eur J Cancer 30A(9):1326–1236

    Article  CAS  Google Scholar 

  21. Tranmer JE, Heyland D, Dudgeon D et al (2003) Measuring the symptom experience of seriously ill cancer and non-cancer hospitalized patients near the end of life with the memorial symptom assessment scale. J Pain Symptom Manag 25(5):420–429

    Article  Google Scholar 

  22. Esther Kim JE, Dodd MJ, Aouizerat BE et al (2009) Review of the prevalence and impact of multiple symptoms in oncology patients. J Pain Symptom Manag 37(4):715–736

    Article  Google Scholar 

  23. Chang VT, Hwang SS, Feuerman M et al (2000) Symptom and quality of life survey of medical oncology patients at a veteran’s affairs medical center: a role for symptom assessment. Cancer 88(5):1175–1183

    Article  CAS  Google Scholar 

  24. Van den Beuken-van Everdingen MHJ, De Rijke JM, Kessels AG et al (2007) Prevalence of pain in patients with cancer: a systematic review of the past 40 years. Ann Oncol 18(9):1437–1449

    Article  CAS  Google Scholar 

  25. Kroenke K. A (2014) Practical and evidence-based approach to common symptoms. Ann Intern Med 161:579–586

    Article  Google Scholar 

  26. Schumacher S, Rief W, Brähler E et al (2014) Disagreement in doctor’s and patient’s rating about medically unexplained symptoms and health care use. Int J Behav Med 20(1):30–37

    Article  Google Scholar 

  27. Fries JF, Koop CE, Beadle CE et al (1993) Reducing health care costs by reducing the need and demand for medical services. N Engl J Med 329:321–325

    Article  CAS  Google Scholar 

  28. Jensen SB, Pedersen AM, Vissink A et al (2010) A systematic review of salivary gland hypofunction and xerostomia induced by cancer therapies: prevalence, severity and impact on quality of life. Support Care Cancer 18(8):1039–1060

    Article  CAS  Google Scholar 

  29. Chambers MS, Garden AS, Kies MS, Martin JW (2004) Radiation-induced xerostomia in patients with head and neck cancer: pathogenesis, impact on quality of life, and management. Head & Neck 26(9):796–807

    Article  Google Scholar 

  30. Barkokebas A1, Silva IH, de Andrade SC et al (2014) Impact of oral mucositis on oral-health-related quality of life of patients diagnosed with cancer. J Oral Pathol Med 44(9):746–751

    Article  Google Scholar 

  31. Smith RG, Burtner AP (1994) Oral side-effects of the most frequently prescribed drugs. Spec Care Dentist 14(3):96–102

    Article  CAS  Google Scholar 

  32. Reyes-Gibby C, Anderson K, Morrow P et al (2012) Depressive symptoms and health-related quality of life in breast cancer survivors. J Women's Health 21(3):311–318

    Article  Google Scholar 

  33. Graça Pereira M1, Figueiredo AP, Fincham FD (2012) Anxiety, depression, traumatic stress and quality of life in colorectal cancer after different treatments: a study with Portuguese patients and their partners. Eur J Oncol Nurs 16(3):227–232

    Article  Google Scholar 

  34. Collins C (2009) Integrating behavioral and mental health services into the primary care setting. N C Med J 70:248–252

    PubMed  Google Scholar 

  35. Perkins A (1994) Saving money by reducing stress. Harvard Bus Rev 72:12

    Google Scholar 

  36. Cummings N, VandenBos G (1981) The twenty years Kaiser-Permanente experience with psychotherapy and medical utilization: implications for national health policy and national health insurance. Health Policy Q 1(2):159–175

    CAS  PubMed  Google Scholar 

  37. Integrating Primary Care and Behavioral Health Services: A Compass and a Horizon (2015) Bureau of Primary Health Care: Mountain view Consulting Group, Inc. http://www.apa.org/rural/strosahl.pdf. Accessed April 10 2015

  38. American College of Surgeons Commission on Cancer. Cancer Program Standards 2012 Version 1.2.1:ensuringpatient-centeredcare. https://www.facs.org/quality-programs/cancer/coc/standards. Accessed August 26 2015

  39. Nesic VS, Petrovic AM, Sipetic SB et al (2012) Comparison of the adult comorbidity evaluation 27 and the Charlson comorbidity indices in patients with laryngeal squamous cell carcinoma. J Laryngol Otol 126:516–524

    Article  CAS  Google Scholar 

  40. Kallogjeri D, Gaynor SM, Piccirillo ML et al (2014) Comparison of comorbidity collection methods. J Am Coll Surg 219(2):245–255

    Article  Google Scholar 

Download references

Acknowledgments

The authors wish to thank Cara Jacobsen and Nebu Kolenchery for their contributions to this project and Dr. Raymond Tait for his editorial assistance with the manuscript. There was no support from any organization for the submitted work; no financial relationships with any organizations that might have an interest in the submitted work in the previous 3 years; and no other relationships or activities that could appear to have influenced the submitted work.

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Correspondence to Teresa L. Deshields.

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Deshields, T.L., Penalba, V., Liu, J. et al. Comparing the symptom experience of cancer patients and non-cancer patients. Support Care Cancer 25, 1103–1109 (2017). https://doi.org/10.1007/s00520-016-3498-2

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  • DOI: https://doi.org/10.1007/s00520-016-3498-2

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