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Patient-Centered Communication During Oncology Follow-Up Visits for Breast Cancer Survivors: Content and Temporal Structure

Margaret F. Clayton

William N. Dudley

communication
ONF 2009, 36(2), E68-E79. DOI: 10.1188/09.ONF.E68-E79

Purpose/Objectives: To understand the content and temporal structure of survivor-provider communication during breast cancer survivor follow-up visits.

Design: Descriptive correlational.

Setting: Private outpatient oncology practice.

Sample: 55 breast cancer survivors; 6 oncology providers.

Methods: A secondary analysis of audio recordings of survivor follow-up visits.

Main Research Variables: Survivors: demographics, uncertainty, mood, length of survival, years receiving care from providers, survivor expectations. Providers: demographics, medical uncertainty, specialty (physician, nurse practitioner, or physician assistant). Outcomes: time spent in patient-centered communication, perception of patient-centeredness.

Findings: Most visit time (55%) was spent waiting. Of the remaining 45%, silence represented the most time spent with providers, followed by symptom conversations. More specific survivor discussion plans predicted more time spent discussing symptoms and in reassurance interactions. More specificity of visit purpose predicted survivor perceptions of less patient-centeredness; however, more time in contextual conversations predicted a greater perception of patient-centeredness. Provider factors were not associated with time spent in patient-centered communication or survivor perceptions of patient-centeredness. All dimensions of patient-centered communication occurred during each visit section (before, during, and after the physical examination).

Conclusions: Discussing symptoms and concerns with providers offers reassurance about cancer recurrence. When visit expectations are very high, achieving a survivor perception of patient-centered communication may be difficult. However, time spent understanding a survivor within the context of her life can enhance survivor perceptions of patient-centeredness.

Implications for Nursing: Providers must be sensitive to concerns that are presented throughout a visit. When visit time is short, a second appointment may be necessary to address survivor concerns.

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    References

    Agency for Healthcare Research and Quality. (2005). 2005 CAHPS Health Plan Survey Chartbook: What consumers say about the quality of their health plans and medical care. Washington, DC: U. S. Department of Health and Human Services.
    American Cancer Society. (2005). Breast cancer facts and figures 2005-2006. Atlanta, GA: Author.
    American Cancer Society. (2007a). Breast cancer facts and figures 2007-2008. Atlanta GA: Author.
    American Cancer Society. (2007b). Cancer facts and figures, 2007. Atlanta, GA: Author.
    Beach, M. C., & Roter, D. L. (2000). Interpersonal expectations in the patient-physician relationship. Journal of General Internal Medicine, 15(11), 825-827.
    Beach, M. C., Roter, D. L., Wang, N. Y., Duggan, P. S., & Cooper, L. A. (2006). Are physicians' attitudes of respect accurately perceived by patients and associated with more positive communication behaviors? Patient Education and Counseling, 62(3), 347-354.
    Brown, J., Stewart, M., & Ryan, B. (2001). Assessing communication between patients and physicians: The measure of patient-centered communication (MPCC). London, Canada: Thames Valley Family Practice Research Unit and Centre for Studies in Family Medicine.
    Cameron, S., & Horsburgh, M. E. (1998). Comparing issues faced by younger and older women with breast cancer. Canadian Oncology Nursing Journal, 8(1), 40-44.
    Carver, C. S., Smith, R. G., Petronis, V. M., & Antoni, M. H. (2006). Quality of life among long-term survivors of breast cancer: Different types of antecedents predict different classes of outcomes. Psycho-Oncology, 15(9), 749-758.
    Cassileth, B. R., Zupkis, R. V., Sutton-Smith, K., & March, V. (1980). Information and participation preferences among cancer patients. Annals of Internal Medicine, 92(6), 832-836.
    Clayton, M. F., Dudley, W. N., & Musters, A. (2008). Communication with breast cancer survivors. Health Communication, 23(3), 207-221.
    Clayton, M. F., Mishel, M. H., & Belyea, M. (2006). Testing a model of symptoms, communication, uncertainty, and well-being, in older breast cancer survivors. Research in Nursing and Health, 29(1), 18-39.
    Cooper-Patrick, L., Gallo, J. J., Gonzales, J. J., Vu, H. T., Powe, N. R., Nelson, C., et al. (1999). Race, gender, and partnership in the patient-physician relationship. JAMA, 282(6), 583-589.
    Curran, L. S., Andrykowski, M. A., & Studts, J. L. (1995). Short form of the Profile of Mood States (POMS-SF): Psychometric information. Psychological Assessment, 7(1), 80-83.
    Curtis, R., Ron, E., Hankey, B., & Hoover, R. (2006). New malignancies following breast cancer (NIH Publication No. 05-5302). Bethesda, MD: National Cancer Institute.
    Druss, B. G., Marcus, S. C., Olfson, M., Tanielian, T., & Pincus, H. A. (2003). Trends in care by nonphysician clinicians in the United States. New England Journal of Medicine, 348(2), 130-137.
    Epstein, R. M., Franks, P., Fiscella, K., Shields, C. G., Meldrum, S. C., Kravitz, R. L., et al. (2005). Measuring patient-centered communication in patient-physician consultations: Theoretical and practical issues. Social Science and Medicine, 61(7), 1516-1528.
    Epstein, R. M., & Street, R. L. (2007). Patient-centered communication in cancer care: Promoting healing and reducing suffering (NIH Publication No. 07-6225). Bethesda, MD: National Cancer Institute.
    Feldman-Stewart, D., Brundage, M. D., & Tishelman, C. (2005). A conceptual framework for patient-professional communication: An application to the cancer context. Psycho-Oncology, 14(10), 801-809.
    Foley, K. L., Farmer, D. F., Petronis, V. M., Smith, R. G., McGraw, S., Smith, K., et al. (2006). A qualitative exploration of the cancer experience among long-term survivors: comparisons by cancer type, ethnicity, gender, and age. Psycho-Oncology, 15(3), 248-258.
    Ganz, P. A., Coscarelli, A., Fred, C., Kahn, B., Polinsky, M. L., & Petersen, L. (1996). Breast cancer survivors: Psychosocial concerns and quality of life. Breast Cancer Research and Treatment, 38(2), 183-199.
    Ganz, P. A., Desmond, K. A., Leedham, B., Rowland, J. H., Meyerowitz, B. E., & Belin, T. R. (2002). Quality of life in long-term, disease-free survivors of breast cancer: A follow-up study. Journal of the National Cancer Institute, 94(1), 39-49.
    Gaudine, A., Sturge-Jacobs, M., & Kennedy, M. (2003). The experience of waiting and life during breast cancer follow-up. Research and Theory for Nursing Practice, 17(2), 153-168.
    Gerrity, M. S., White, K. P., DeVellis, R. F., & Dittus, R. S. (1995). Physicians' reactions to uncertainty: Refining the constructs and scales. Motivation and Emotion, 19(3), 175-191.
    Gil, K. M., Mishel, M., Belyea, M., Germino, B., Germino, L. S., Porter, L., et al. (2004). Triggers of uncertainty about recurrence and long-term treatment side effects in older African American and Caucasian breast cancer survivors. Oncology Nursing Forum, 31(3), 633-639.
    Gil, K. M., Mishel, M. H., Belyea, M., Germino, B., Porter, L., & Clayton, M. F. (2006). Benefits from an uncertainty management intervention for older long-term breast cancer: 20 month outcomes. International Journal of Behavioral Medicine, 13(4), 286-294.
    Gosselin-Acomb, T. K., Schneider, S. M., Clough, R. W., & Veenstra, B. A. (2007). Nursing advocacy in North Carolina. Oncology Nursing Forum, 34(5), 1070-1074.
    Hesse, B. (2003). The Health Information National Trends Survey (HINTS): Main study instrument. Bethesda, MD: National Cancer Institute.
    Krippendorff, K. (1980). Content analysis: An introduction to its methodology. Beverly Hills, CA: Sage.
    Lechner, S. C., Carver, C. S., Antoni, M. H., Weaver, K. E., & Phillips, K. M. (2006). Curvilinear associations between benefit finding and psychosocial adjustment to breast cancer. Journal of Consulting and Clinical Psychology, 74(5), 828-840.
    Mast, M. E. (1998). Survivors of breast cancer: Illness uncertainty, positive reappraisal, and emotional distress. Oncology Nursing Forum, 25(3), 555-562.
    Mead, N., & Bower, P. (2000). Patient-centredness: A conceptual framework and review of the empirical literature. Social Science and Medicine, 51(7), 1087-1110.
    Mishel, M. H. (1988). Uncertainty in illness. Image: The Journal of Nursing Scholarship, 20(4), 225-232.
    Mishel, M. H. (1997). Uncertainty in illness scales manual. Available upon request from M. H. Mishel, University of North Carolina, Chapel Hill.
    Mishel, M. H., & Clayton, M. F. (2003). Uncertainty in illness theories. In M. J. Smith &, P. Liehr (Eds.), Middle range theory in advanced practice nursing (pp. 25-48). New York: Springer.
    Nissen, M. J., Swenson, K. K., & Kind, E. A. (2002). Quality of life after postmastectomy breast reconstruction. Oncology Nursing Forum, 29(3), 547-553.
    Ogden, J., Ambrose, L., Khadra, A., Manthri, S., Symons, L., Vass, A., et al. (2002). A questionnaire study of GPs' and patients' beliefs about the different components of patient centredness. Patient Education and Counseling, 47(3), 223-227.
    Reschovsky, J. D., Hadley, J., & Landon, B. E. (2006). Effects of compensation methods and physician group structure on physicians' perceived incentives to alter services to patients. Health Services Research, 41(4, Pt. 1), 1200-1220.
    Roter, D. L., & Hall, J. A. (2004). Physician gender and patient-centered communication: A critical review of empirical research. Annual Review of Public Health, 25, 497-519.
    Rutgers, E. J. (2004). Follow-up care in breast cancer. Expert Review of Anticancer Therapy, 4(2), 212-218.
    Sapir, R., Catane, R., Kaufman, B., Isacson, R., Segal, A., Wein, S., et al. (2000). Cancer patient expectations of and communication with oncologists and oncology nurses: The experience of an integrated oncology and palliative care service. Supportive Care in Cancer, 8(6), 458-463.
    Schmid Mast, M., Hall, J. A., & Roter, D. L. (2007). Disentangling physician sex and physician communication style: Their effects on patient satisfaction in a virtual medical visit. Patient Education and Counseling, 68(1), 16-22.
    Snyder, L., & Neubauer, R. L. (2007). Pay-for-performance principles that promote patient-centered care: An ethics manifesto. Annals of Internal Medicine, 147(11), 792-794.
    Stewart, M., Brown, J. B., Donner, A., McWhinney, I. R., Oates, J., Weston, W. W., et al. (2000). The impact of patient-centered care on outcomes. Journal of Family Practice, 49(9), 796-804.
    Tabachnick, B. G., & Fidell, L. S. (2001). Using multivariate statistics. Needham Heights, MA: Allyn and Bacon.
    Thomas, S., Glynne-Jones, R., & Chait, I. (1997). Is it worth the wait? A survey of patients' satisfaction with an oncology outpatient clinic. European Journal of Cancer Care, 6(1), 50-58.
    Thorne, S. E. (1999). Communication in cancer care: What science can and cannot teach us. Cancer Nursing, 22(5), 370-378.
    Thorne, S. E., Bultz, B. D., & Baile, W. F. (2005). Is there a cost to poor communication in cancer care? A critical review of the literature. Psycho-Oncology, 14(10), 875-884.
    Thorne, S. E., Kuo, M., Armstrong, E. A., McPherson, G., Harris, S. R., & Hislop, T. G. (2005). Being known: Patients' perspectives of the dynamics of human connection in cancer care. Psycho-Oncology, 14(10), 887-898.
    Tomich, P. L., & Helgeson, V. S. (2002). Five years later: A cross-sectional comparison of breast cancer survivors with healthy women. Psycho-Oncology, 11(2), 154-169.
    Tomich, P. L., & Helgeson, V. S. (2004). Is finding something good in the bad always good? Benefit finding among women with breast cancer. Health Psychology, 23(1), 16-23.
    Turk-Charles, S., Meyerowitz, B. E., & Gatz, M. (1997). Age differences in information-seeking among cancer patients. International Journal of Aging and Human Development, 45(2), 85-98.
    Walker, D. L. (2000). Physician compensation: Rewarding productivity. Journal of Ambulatory Care Management, 23(4), 48-59.
    Waltz, C. F., Strickland, O. L., & Lenz, E. R. (2005). Measurement in nursing and health research (3rd ed.). New York: Springer.
    White, J., Levinson, W., & Roter, D. (1994). "Oh, by the way…": The closing moments of the medical visit. Journal of General Internal Medicine, 9(1), 24-28.
    Wilensky, G. R. (2004). Framing the public policy questions: Financial incentives for efficiency and effectiveness. Medical Care Research and Review, 61(3, Suppl.), 31S-36S.
    Wonghongkul, T., Dechaprom, N., Phumivichuvate, L., & Losawatkul, S. (2006). Uncertainty appraisal coping and quality of life in breast cancer survivors. Cancer Nursing, 29(3), 250-257.