Patient perspectives on breast cancer treatment plan and summary documents in community oncology care
dc.contributor.author | Blinder, Victoria S. | en_US |
dc.contributor.author | Norris, Virginia W. | en_US |
dc.contributor.author | Peacock, Nancy W. | en_US |
dc.contributor.author | Griggs, Jennifer J. | en_US |
dc.contributor.author | Harrington, David P. | en_US |
dc.contributor.author | Moore, Anne | en_US |
dc.contributor.author | Theriault, Richard L. | en_US |
dc.contributor.author | Partridge, Ann H. | en_US |
dc.date.accessioned | 2013-01-03T19:45:05Z | |
dc.date.available | 2014-03-03T15:09:23Z | en_US |
dc.date.issued | 2013-01-01 | en_US |
dc.identifier.citation | Blinder, Victoria S.; Norris, Virginia W.; Peacock, Nancy W.; Griggs, Jennifer J.; Harrington, David P.; Moore, Anne; Theriault, Richard L.; Partridge, Ann H. (2013). "Patient perspectives on breast cancer treatment plan and summary documents in community oncology care ." Cancer 119(1): 164-172. <http://hdl.handle.net/2027.42/95515> | en_US |
dc.identifier.issn | 0008-543X | en_US |
dc.identifier.issn | 1097-0142 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/95515 | |
dc.description.abstract | BACKGROUND: Although the routine use of treatment plans and summaries (TPSs) has been recommended to improve the quality of cancer care, limited data exist about their impact on quality, including patient satisfaction and coordination of care. METHODS: Patients received TPSs as part of the American Society of Clinical Oncology Breast Cancer Registry (BCR) pilot program of 20 community oncology practices. Participants were surveyed 2 to 4 weeks after receiving a TPS to evaluate their perceptions of the document. Patients who were receiving chemotherapy received the TPS as separate plan and summary documents (at the start and the end of treatment) and could complete 2 surveys. Others received a single integrated TPS. Eligible survey participants had stage 0 through III breast cancer and were enrolled in the BCR. RESULTS: Of 292 consented patients, 174 (60%) completed at least 1 survey. Of 157 patients who recalled receiving a TPS, 148 (94%) believed that the documents improved patient‐physician communication, and 128 (82%) believed that they improved communication between physicians; 113 (72%) said the documents increased their peace of mind, whereas 2 (1%) had less peace of mind. Of 152 patients (97%) who still had their documents, 147 (97%) said they were useful, and 94 (62%) had given or planned to give the documents to another physician. All 63 patients who were surveyed after receiving a summary recommended that practices continue to provide TPSs to patients. CONCLUSIONS: Participants in this study expressed high satisfaction with TPSs. Additional research is needed to study the broad‐scale implementation of the BCR and to evaluate the impact of routine use of TPSs on the quality of care delivered. Cancer 2013. © 2012 American Cancer Society. Breast cancer survivors express high levels of satisfaction with the integration of treatment plan and summary documents into their clinical care. Participants recommended that practices continue to provide these documents to their patients. | en_US |
dc.publisher | Wiley Subscription Services, Inc., A Wiley Company | en_US |
dc.subject.other | Breast Cancer | en_US |
dc.subject.other | Survivorship | en_US |
dc.subject.other | Survivorship Care Plan | en_US |
dc.subject.other | Treatment Summary | en_US |
dc.subject.other | Treatment Plan | en_US |
dc.title | Patient perspectives on breast cancer treatment plan and summary documents in community oncology care | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Public Health | en_US |
dc.subject.hlbsecondlevel | Oncology and Hematology | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Internal Medicine, Division of Hematology/Oncology, University of Michigan Medical School, Ann Arbor, Michigan | en_US |
dc.contributor.affiliationother | Department of Epidemiology and Biostatistics, Center for Health Policy and Outcomes, Memorial Sloan‐Kettering Cancer Center, 300 East 66th Street, 14th Floor, New York, NY, 10065 | en_US |
dc.contributor.affiliationother | Department of Epidemiology and Biostatistics, Memorial Sloan‐Kettering Cancer Center, New York, New York | en_US |
dc.contributor.affiliationother | American Society of Clinical Oncology, Alexandria, Virginia | en_US |
dc.contributor.affiliationother | Tennessee Oncology, PLLC, Nashville, Tennessee | en_US |
dc.contributor.affiliationother | Department of Biostatistics, Dana‐Farber Cancer Institute, Boston, Massachusetts | en_US |
dc.contributor.affiliationother | Department of Medicine, Weill Cornell Medical College, New York, New York | en_US |
dc.contributor.affiliationother | Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas | en_US |
dc.contributor.affiliationother | Department of Medical Oncology, Dana‐Farber Cancer Institute and Brigham and Women's Hospital, Boston, Massachusetts | en_US |
dc.identifier.pmid | 23197335 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/95515/1/27856_ftp.pdf | |
dc.identifier.doi | 10.1002/cncr.27856 | en_US |
dc.identifier.source | Cancer | en_US |
dc.identifier.citedreference | Malin JL, Schneider EC, Epstein AM, Adams J, Emanuel EJ, Kahn KL. Results of the National Initiative for Cancer Care Quality: how can we improve the quality of cancer care in the United States? J Clin Oncol. 2006; 24: 626 ‐ 634. | en_US |
dc.identifier.citedreference | Partridge A, Norris V, Blinder V, et al. Implementing a breast cancer registry and treatment plan/summary program in clinical practice: a pilot program. Cancer. 2012; 000: 000 ‐ 000. | en_US |
dc.identifier.citedreference | American Society for Clinical Oncology (ASCO). ASCO Breast Cancer Treatment Plan and Summary Resources. Available at: http://www.asco.org/ASCOv2/Practice+%26+Guidelines/Quality+ Care/Quality+Measurement+%26+Improvement/Chemotherapy+ Treatment+Plan+and+Summary/Breast+Cancer+Treatment+Plan+ and+Summary+Resources?cpsextcurrchannel=1. Accessed March 26, 2012. | en_US |
dc.identifier.citedreference | Grunfeld E, Julian JA, Pond GR, et al. Evaluating survivorship care plans: results of a randomized, clinical trial of patients with breast cancer. J Clin Oncol. 2011; 29: 4755 ‐ 4762. | en_US |
dc.identifier.citedreference | Hewitt ME, Bamundo A, Day R, Harvey C. Perspectives on post‐treatment cancer care: qualitative research with survivors, nurses, and physicians. J Clin Oncol. 2007; 25: 2270 ‐ 2273. | en_US |
dc.identifier.citedreference | Kantsiper M, McDonald EL, Geller G, Shockney L, Snyder C, Wolff AC. Transitioning to breast cancer survivorship: perspectives of patients, cancer specialists, and primary care providers. J Gen Intern Med. 2009; 24 ( suppl 2 ): S459 ‐ S466. | en_US |
dc.identifier.citedreference | Nissen MJ, Beran MS, Lee MW, Mehta SR, Pine DA, Swenson KK. Views of primary care providers on follow‐up care of cancer patients. Fam Med. 2007; 39: 477 ‐ 482. | en_US |
dc.identifier.citedreference | Erikson C, Salsberg E, Forte G, Bruinooge S, Goldstein M. Future supply and demand for oncologists: challenges to assuring access to oncology services. J Oncol Pract. 2007; 3: 79 ‐ 86. | en_US |
dc.identifier.citedreference | Ganz PA. Quality of care and cancer survivorship: the challenge of implementing the Institute of Medicine recommendations. J Oncol Pract. 2009; 5: 101 ‐ 105. | en_US |
dc.identifier.citedreference | National Cancer Institute; Surveillance, Epidemiology, and End Results (SEER) Program. Fast Stats: An interactive tool for access to SEER cancer statistics. Bethesda, MD: Surveillance Research Program, National Cancer Institute; 2012. | en_US |
dc.identifier.citedreference | Bober SL, Recklitis CJ, Campbell EG, et al. Caring for cancer survivors: a survey of primary care physicians. Cancer. 2009; 115 ( 18 suppl ): 4409 ‐ 4418. | en_US |
dc.identifier.citedreference | Hoffman B, Stovall E. Survivorship perspectives and advocacy. J Clin Oncol. 2006; 24: 5154 ‐ 5159. | en_US |
dc.identifier.citedreference | Feuerstein M. The cancer survivorship care plan: health care in the context of cancer. J Oncol Pract. 2009; 5: 113 ‐ 115. | en_US |
dc.identifier.citedreference | Earle CC. Failing to plan is planning to fail: improving the quality of care with survivorship care plans. J Clin Oncol. 2006; 24: 5112 ‐ 5116. | en_US |
dc.identifier.citedreference | Hewitt M, Greenfield S, Stovall E. From Cancer Patient to Cancer Survivor: Lost in Transition. Washington, DC: The National Academies Press; 2006. | en_US |
dc.identifier.citedreference | Ganz PA, Hahn EE. Implementing a survivorship care plan for patients with breast cancer. J Clin Oncol. 2008; 26: 759 ‐ 767. | en_US |
dc.identifier.citedreference | Marbach TJ, Griffie J. Patient preferences concerning treatment plans, survivorship care plans, education, and support services. Oncol Nurs Forum. 2011; 38: 335 ‐ 342. | en_US |
dc.identifier.citedreference | Mao JJ, Bowman MA, Stricker CT, et al. Delivery of survivorship care by primary care physicians: the perspective of breast cancer patients. J Clin Oncol. 2009; 27: 933 ‐ 938. | en_US |
dc.identifier.citedreference | Smith SL, Singh‐Carlson S, Downie L, Payeur N, Wai ES. Survivors of breast cancer: patient perspectives on survivorship care planning. J Cancer Surviv. 2011; 5: 337 ‐ 344. | en_US |
dc.identifier.citedreference | Burg MA, Lopez ED, Dailey A, Keller ME, Prendergast B. The potential of survivorship care plans in primary care follow‐up of minority breast cancer patients. J Gen Intern Med. 2009; 24 ( suppl 2 ): S467 ‐ S471. | en_US |
dc.identifier.citedreference | Miller R. Implementing a survivorship care plan for patients with breast cancer. Clin J Oncol Nurs. 2008; 12: 479 ‐ 487. | en_US |
dc.identifier.citedreference | Royak‐Schaler R, Passmore SR, Gadalla S, et al. Exploring patient‐physician communication in breast cancer care for African American women following primary treatment. Oncol Nurs Forum. 2008; 35: 836 ‐ 843. | en_US |
dc.identifier.citedreference | Smith TJ, Snyder C. Is it time for (survivorship care) plan B? J Clin Oncol. 2011; 29: 4740 ‐ 4742. | en_US |
dc.identifier.citedreference | Ware JE Jr, Snyder MK, Wright WR, Davies AR. Defining and measuring patient satisfaction with medical care. Eval Program Plann. 1983; 6: 247 ‐ 263. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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