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Palliative care outcomes in surgical oncology patients with advanced malignancies: a mixed methods approach

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Abstract

Purpose

To prospectively compare outcomes and processes of hospital-based early palliative care with standard care in surgical oncology patients (N = 152).

Methods

A randomized, mixed methods, longitudinal study evaluated the effectiveness of a hospital-based Pain and Palliative Care Service (PPCS). Interviews were conducted presurgically and at follow-up visits up to 1 year. Primary outcome measures included the Gracely Pain Intensity and Unpleasantness Scales and the Symptom Distress Scale. Qualitative interviews assessed social support, satisfaction with care, and communication with providers. Survival analysis methods explored factors related to treatment crossover and study discontinuation. Models for repeated measures within subjects over time explored treatment and covariate effects on patient-reported pain and symptom distress.

Results

None of the estimated differences achieved statistical significance; however, for those who remained on study for 12 months, the PPCS group performed better than their standard of care counterparts. Patients identified consistent communication, emotional support, and pain and symptom management as positive contributions delivered by the PPCS.

Conclusions

It is unclear whether lower pain perceptions despite greater symptom distress were clinically meaningful; however, when coupled with the patients’ perceptions of their increased resources and alternatives for pain control, one begins to see the value of an integrated PPCS.

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Abbreviations

PPCS:

Pain and Palliative Care Service

NIH:

Institutes of Health

CC:

Clinical Center

NCI:

National Cancer Institute

IRB:

Institutional Review Board

ICU:

Intensive Care Unit

APACHE II:

The Acute Physiology and Chronic Health Evaluation

GPS:

Gracely Pain Scales

SDS:

Symptom Distress Scale

CES-D:

Center for Epidemiologic Studies Depression Scale

References

  1. Arnold, B. L. (2011). Mapping hospice patients” perception and verbal communication of end-of-life needs: An exploratory mixed methods inquiry. BMC Palliative Care, 10(1), 1–10.

    Article  PubMed  Google Scholar 

  2. Bakitas, M., Lyons, K. D., Hegel, M. T., Balan, S., Brokaw, F. C., Seville, J., et al. (2009). Effects of a palliative care intervention on clinical outcomes in patients with advanced cancer: The project ENABLE II randomized controlled trial. Journal of the American Medical Association, 302(7), 741–749.

    Article  PubMed  CAS  Google Scholar 

  3. Barrera, M. (1986). Distinctions between social support concepts, measures, and models. American Journal of Community Psychology, 14(4), 413–445.

    Article  Google Scholar 

  4. Carr, A. J., & Higginson, I. J. (2001). Measuring quality of life: Are quality of life measures patient centered? British Medical Journal, 322, 1357–1360.

    Article  PubMed  CAS  Google Scholar 

  5. Cleeland, C. S. (2001). Cross-cutting research issues: A research agenda for reducing distress of patients with cancer. In K. M. Foley & H. Gellband (Eds.), Improving palliative care for cancer (pp. 233–276). Washington, DC: National Academy Press.

  6. Creswell, J. W. (2009). Research design: Qualitative, quantitative, and mixed methods (3rd ed). Thousand Oaks, CA: Sage.

  7. Creswell, J. W., & Plano Clark, V. L. (2007). Designing and conducting mixed methods research. Thousand Oaks, CA: Sage.

  8. Creswell, J. W., & Zhang, W. (2009). The application of mixed methods designs to trauma research. Journal of Traumatic Stress, 22(6), 612–621.

    Google Scholar 

  9. Del Bufalo, C., Morelli, A., Bassein, L., Fasano, L., Quarta, C. C., Pacilli, A. M., et al. (1995). Severity scores in respiratory intensive care: Apache ii predicted mortality better than saps ii. Respiratory Care, 40(10), 1042–1047.

    PubMed  Google Scholar 

  10. Devery, K., Lennie, I., & Cooney, N. (1999). Health outcomes for people who use palliative care services. Journal of Palliative Care, 15(2), 5–12.

    PubMed  CAS  Google Scholar 

  11. Gracely, R. H., Dubner, R., & McGrath, P. A. (1982). Fentanyl reduces the intensity of painful tooth pulp sensations: Controlling for detection of active drugs. Anesthesia and Analgesia, 61(9), 751–755.

    Article  PubMed  CAS  Google Scholar 

  12. Gracely, R. H., & Kwilosz, D. M. (1988). The descriptor differential scale: Applying psychophysical principles to clinical pain assessment. Pain, 35(3), 279–288.

    Article  PubMed  CAS  Google Scholar 

  13. Gracely, R. H., McGrath, P., & Dubner, R. (1978). Ratio scales of sensory and affective verbal pain descriptors. Pain, 5(1), 5–18.

    Article  PubMed  CAS  Google Scholar 

  14. Grande, G., & Todd, C. J. (2000). Why are trials in palliative care so difficult? Palliative Medicine, 14(1), 69–74.

    Article  PubMed  CAS  Google Scholar 

  15. Helgeson, V. S., & Cohen, S. (1996). Social support and adjustment to cancer: Reconciling descriptive, correlational, and intervention research. Health Psychology, 15(2), 135–148.

    Article  PubMed  CAS  Google Scholar 

  16. Higginson, I. J. (1999). Evidence based palliative care. There is some evidence-and there needs to be more. BMJ, 319(7208), 462–463.

    Article  PubMed  CAS  Google Scholar 

  17. Higginson, I. J., & Carr, A. J. (2001). Measuring quality of life: Using quality of life measures in the clinical setting. BMJ, 322(7297), 1297–1300.

    Article  PubMed  CAS  Google Scholar 

  18. Higginson, I. J., Finlay, I., Goodwin, D. M., Cook, A. M., Hood, K., Edwards, A. G., et al. (2002). Do hospital-based palliative teams improve care for patients or families at the end of life? Journal of Pain and Symptom Management, 23(2), 96–106.

    Google Scholar 

  19. Hutchison, C. (1999). Social support: Factors to consider when designing studies that measure social support. Journal of Advanced Nursing, 29(6), 1520–1526.

    Article  PubMed  CAS  Google Scholar 

  20. Israel, B. A., & Schurman, S. J. (1990). Social support, control and the stress process. In K. Glanz, B. K. Rimer, & F. M. Lewis (Eds.), Health behavior and health education: Theory, research, and practice. San Francisco: Jossey-Bass.

    Google Scholar 

  21. Jackson, B. S., Strauman, J., Frederickson, K., & Strauman, T. J. (1991). Long-term biopsychosocial effects of interleukin-2 therapy. Oncology Nursing Forum, 18, 683–690.

    PubMed  CAS  Google Scholar 

  22. Karim, K. (2000). Conducting research involving palliative patients. Nursing Standard, 15(2), 34–36.

    Google Scholar 

  23. Knaus, W. A., Draper, E. A., Wagner, D. P., & Zimmerman, J. E. (1985). APACHE II: A severity of disease classification system. Critical Care Medicine, 13(10), 818–829.

    Article  PubMed  CAS  Google Scholar 

  24. Krueger, R. A. (1998). Analyzing & reporting focus groups. Thousand Oaks, CA: Sage Publications, Inc.

    Google Scholar 

  25. Lesage, P., & Portenoy, R. K. (2001). Ethical challenges in the care of patients with serious illness. Pain Medicine, 2(2), 121–130.

    Article  PubMed  CAS  Google Scholar 

  26. Max, M. B., Lynch, S. A., Muir, J., Shoaf, S. E., Smoller, B., & Dubner, R. (1992). Effects of desipramine, amitriptyline, and fluoxetine on pain in diabetic neuropathy. New England Journal of Medicine, 326(19), 1250–1256.

    Article  PubMed  CAS  Google Scholar 

  27. Mazzocato, C., Sweeney, C., & Bruera, E. (2001). Clinical research in palliative care: Patient populations, symptoms, interventions and endpoints. Palliative Medicine, 15(2), 163–168.

    Article  PubMed  CAS  Google Scholar 

  28. McArthur, J. C., Yiannoutsos, C., Simpson, D. M., Adornato, B. T., Singer, E. J., Hollander, H., et al. (2000). A phase II trial of nerve growth factor for sensory neuropathy associated with hiv infection. Neurology, 54(5), 1080–1088.

    Google Scholar 

  29. McCorkle, R., Cooley, M. E., & Shea, J. A. (1998). A user’s manual for the symptom distress scale. Philadelphia: University of Pennsylvania.

    Google Scholar 

  30. Moreno, R., Apolone, G., & Reis Miranda, D. (1998). Evaluation of the uniformity of fit of general outcome prediction models. Intensive Care Medicine, 24(1), 40–47. doi:10.1007/s001340050513.

    Article  PubMed  CAS  Google Scholar 

  31. Morgan, D. L. (1998). Computerized analysis. In R. A. Krueger (Ed.), Analyzing & reporting focus groups. Thousand Oaks, CA: Sage Publications, Inc.

    Google Scholar 

  32. O’Mara, A. M., Germain, D., Ferrell, B., & Bornemann, T. (2009). Challenges to and lessons learned from conducting palliative care research. Journal of Pain and Symptom Management, 37(3), 387–394.

    Article  PubMed  Google Scholar 

  33. Portenoy, R. K., Thaler, H. T., Kornblith, A. B., McCarthy L. J., Friedlander-Klar, H., Kiyasu, E., et al. (1994). The memorial symptom assessment scale: An instrument for the evaluation of symptom prevalence, characteristics and distress. European Journal of Cancer Part A: General Topics, 30(9), 1326–1336.

    Google Scholar 

  34. Radloff, L. S. (1977). The CES-D scale: A self-report depression scale for research in the general population. Applied Psychological Measurement, 1(3), 385–401.

    Article  Google Scholar 

  35. Sarna, L. (1998). Effectiveness of structured nursing assessment of symptom distress in advanced lung cancer. Oncology Nursing Forum, 25, 1041–1048.

    PubMed  CAS  Google Scholar 

  36. Sarna, L., Lindsey, A. M., Dean, H., Brecht, M. L., & McCorkle, R. (1993). Nutritional intake, weight change, symptom distress, and functional status over time in adults with lung cancer. Oncology Nursing Forum, 20, 481–489.

    PubMed  CAS  Google Scholar 

  37. Shaver, P. R., & Brennan, K. A. (1991). Measures of depression and loneliness. In J. P. Robinson, P. R. Shaver, & L. S. Wrightsman (Eds.), Measures of personality and social psychological attitudes. San Diego: Academic Press Inc.

    Google Scholar 

  38. Standing Medical Advisory Committee, & Committee, Standing Nursing and Midwifery Advisory. (1992). The principles and provision of palliative care. London.

  39. Taylor, E. J. (1993). Factors associated with meaning in life among people with recurrent cancer. Onclology Nursing Forum, 20, 1399–1407.

    CAS  Google Scholar 

  40. Ternel, J. S., Greer, J. A., Musilkansky, M. A., Gallagher, E. R., Admane, S., Jackson, V. A., et al. (2010). Early palliative care for patients with metastatic non-small-cell lung cancer. The New England Journal of Medicine, 363, 733–742.

    Article  Google Scholar 

  41. Wallen, G. R., & Berger, A. (2004). Mixed methods: In search of truth in palliative care medicine. Journal of Palliative Medicine, 7(3), 403–404.

    Article  PubMed  Google Scholar 

  42. Wallen, G. R., Ulrich, C., & Grady, C. (2005). Learning about a “Good Death”: Ethical considerations in palliative care nursing research. DNA Reporter, 30(2), 8–9.

    Google Scholar 

  43. Wills, T. A., & Shinar, O. (2000). Measuring perceived and received social support. In S. Cohen, L. G. Underwood, & B. H. Gottlieb (Eds.), Social support measurement and intervention: A guide for health and social scientists (pp. 86–135). New York: Oxford University Press.

    Google Scholar 

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Correspondence to Gwenyth R. Wallen.

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Wallen, G.R., Baker, K., Stolar, M. et al. Palliative care outcomes in surgical oncology patients with advanced malignancies: a mixed methods approach. Qual Life Res 21, 405–415 (2012). https://doi.org/10.1007/s11136-011-0065-7

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