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Patient-centred care: making cancer treatment centres accountable

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Abstract

Patient-centred care is argued to be an essential component in the delivery of quality health and cancer care. This manuscript discusses the need to generate credible data which indicates the quality of patient-centred care provided by cancer treatment centres. Patient-centred care covers six domains including physical comfort; emotional support; respect for patients’ preferences and values; integration and coordination; involvement of family and friends; and the provision of information, communication and education to enable patients to understand and make informed decisions about their care. First, we identify priority areas within each domain. Next, we propose three questions that should be asked of every patient across the six domains of patient-centred care. The first question explores whether patients were specifically asked by a healthcare provider at the cancer treatment centre about their concerns, values and preferences. Research indicates that it cannot be assumed that clinicians are aware of patient’s needs or preferences in these six areas. Second, if the answer from the patient suggests that they would like assistance, then it would be expected that this would be offered. Thirdly, if the patient indicates that they would like such assistance and it is provided, then it might be expected that the patient would report that the provided assistance did relieve their suffering, or the assistance provided was consistent with their preferences, needs and values. Regular measurement and reporting of these aspects of patient-centred cancer care has the potential to identify deficits and inequities in care delivery, allow for comparisons across treatment centres and stimulate an improvement in the patient-centred care provided to cancer patients.

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References

  1. IOM (2001) Crossing the quality chasm: a new health system for the 21st century. National Academies Press, Washington

    Google Scholar 

  2. Mead N, Bower P (2000) Patient-centredness: a conceptual framework and review of the empirical literature. Soc Sci Med 51(7):1087–1110

    Article  CAS  PubMed  Google Scholar 

  3. Gerteis M, Edgman-Levitan S, Daley J (1993) Through the patient’s eyes. Understanding and promoting patient-centered care. Jossey-Bass, San Francisco

    Google Scholar 

  4. Wild C, Patera N (2013) Measuring quality in cancer care: overview of initiatives in selected countries. Eur J Cancer Care 22(6):773–781

    Article  CAS  Google Scholar 

  5. Robert G (2013) Rethinking policy approaches to measuring and improving patient experience. J Health Serv Res Pol 18(2):67–69

    Article  Google Scholar 

  6. Hudon C, Fortin M, Haggerty JL, Lambert M, Poitras ME (2011) Measuring patients’ perceptions of patient-centered care: a systematic review of tools for family medicine. Ann Fam Med 9(2):155–164

    Article  PubMed Central  PubMed  Google Scholar 

  7. Lipscomb J, Gotay CC, Snyder CF (2007) Patient-reported Outcomes in cancer: a review of recent research and policy initiatives. CA Cancer J Clin 57(5):278–300

    Article  PubMed  Google Scholar 

  8. Harrison J, Young J, Price M, Butow P, Solomon M (2009) What are the unmet supportive care needs of people with cancer? A systematic review. Support Care Cancer 17:1117–1128

    Article  PubMed  Google Scholar 

  9. Coulter A (2006) Can patients assess the quality of health care?: Patients’ surveys should ask about real experiences of medical care. BMJ: Br M J 333(7557):1

    Article  Google Scholar 

  10. Uphoff EPMM, Wennekes L, Punt CJA, Grol RPTM, Wollersheim HCH, Hermens RPMG, Ottevanger PB (2012) Development of generic quality indicators for patient-centered cancer care by using a RAND modified Delphi method. Cancer Nurs 35(1):29

    Article  PubMed  Google Scholar 

  11. Ouwens M, Hermens R, Hulscher M, Vonk-Okhuijsen S, Tjan-Heijnen V, Termeer R, Marres H, Wollersheim H, Grol R (2010) Development of indicators for patient-centred cancer care. Support Care Cancer 18(1):121–130

    Article  PubMed Central  PubMed  Google Scholar 

  12. Kaplan W, Wirtz V, Mantel-Teeuwisse A, Stolk P, Duthey B, Laing R (2013) 2013 Report priority medicines for Europe and the World. World Health Organization, Geneva

    Google Scholar 

  13. Chassin MR, Loeb JM, Schmaltz SP, Wachter RM (2010) Accountability measures—using measurement to promote quality improvement. N Engl J Med 363(7):683–688

    Article  CAS  PubMed  Google Scholar 

  14. Sofaer S, Firminger K (2005) Patient perceptions of the quality of health services. Annu Rev Public Health 26:513–559

    Article  PubMed  Google Scholar 

  15. Van den Beuken-van EM, De Rijke J, Kessels A, Schouten H, Van Kleef M, Patijn J (2007) Prevalence of pain in patients with cancer: a systematic review of the past 40 years. Ann Oncol 18(9):1437–1449

    Article  Google Scholar 

  16. Tavoli A, Montazeri A, Roshan R, Tavoli Z, Melyani M (2008) Depression and quality of life in cancer patients with and without pain: the role of pain beliefs. BMC Cancer 8(1):177

    Article  PubMed Central  PubMed  Google Scholar 

  17. Buckwalter AE, Karnell LH, Smith RB, Christensen AJ, Funk GF (2007) Patient-reported factors associated with discontinuing employment following head and neck cancer treatment. Arch Otolaryngol Head Neck Surg 133(5):464

    Article  PubMed  Google Scholar 

  18. Tanaka K, Akechi T, Okuyama T, Nishiwaki Y, Uchitomi Y (2002) Impact of dyspnea, pain, and fatigue on daily life activities in ambulatory patients with advanced lung cancer. J Pain Symptom Manag 23(5):417–423

    Article  Google Scholar 

  19. Lipscomb J, Gillespie T, Ward K, Goodman M Early termination of adjuvant therapy for breast and colorectal cancers. In: J Clin Oncol (Meeting Abstracts), 2007. p 6610

  20. Green E, Zwaal C, Beals C, Fitzgerald B, Harle I, Jones J, Tsui J, Volpe J, Yoshimoto D, Wiernikowski J (2010) Cancer-related pain management: a report of evidence-based recommendations to guide practice. Clin J Pain 26(6):449

    Article  PubMed  Google Scholar 

  21. Lawrence DP, Kupelnick B, Miller K, Devine D, Lau J (2004) Evidence report on the occurrence, assessment, and treatment of fatigue in cancer patients. JNCI Monogr 2004(32):40–50

    Article  Google Scholar 

  22. Curt GA, Breitbart W, Cella D, Groopman JE, Horning SJ, Itri LM, Johnson DH, Miaskowski C, Scherr SL, Portenoy RK, Vogelzang N (2000) Impact of cancer-related fatigue on the lives of patients: new findings from the Fatigue Coalition. Oncologist 5:353–340

    Article  CAS  PubMed  Google Scholar 

  23. Stone P, Richardson A, Ream E, Smith A, Kerr D, Kearney N (2000) Cancer-related fatigue: inevitable, unimportant and untreatable? Results of a multi-centre patient survey. Ann Oncol 11(8):971–975

    Article  CAS  PubMed  Google Scholar 

  24. Campos M, Hassan B, Riechelmann R, Del Giglio A (2011) Cancer-related fatigue: a practical review. Ann Oncol 22(6):1273–1279

    Article  CAS  PubMed  Google Scholar 

  25. Zabora J, Brintzenhofeszoc K, Curbow B, Hooker C, Piantadosi S (2001) The prevalence of psychological distress by cancer site. Psycho-Oncology 10(1):19–28

    Article  CAS  PubMed  Google Scholar 

  26. Boyes AW, Girgis A, D’Este CA, Zucca AC, Lecathelinais C, Carey ML (2013) Prevalence and predictors of the short-term trajectory of anxiety and depression in the first year after a cancer diagnosis: a population-based longitudinal study. J Clin Oncol 31(21):2724–2729

    Article  PubMed  Google Scholar 

  27. Delgado-Sanz MC, García-Mendizábal MJ, Pollán M, Forjaz MJ, López-Abente G, Aragonés N, Pérez-Gómez B (2011) Heath-related quality of life in Spanish breast cancer patients: a systematic review. Health Qual Life Outcome 9(3)

  28. Turner J, Zapart S, Pedersen K, Rankin N, Luxford K, Fletcher J (2005) Clinical practice guidelines for the psychosocial care of adults with cancer. Psycho-Oncology 14(3):159–173

    Article  PubMed  Google Scholar 

  29. Okamoto I, Wright D, Foster C (2012) Impact of cancer on everyday life: a systematic appraisal of the research evidence. Health Expect 15(1):97–111

    Article  PubMed  Google Scholar 

  30. Walker J, Hansen CH, Martin P, Sawhney A, Thekkumpurath P, Beale C, Symeonides S, Wall L, Murray G, Sharpe M (2013) Prevalence of depression in adults with cancer: a systematic review. Ann Oncol 24(4):895–900

    Article  CAS  PubMed  Google Scholar 

  31. DiMatteo MR, Lepper HS, Croghan TW (2000) Depression is a risk factor for noncompliance with medical treatment: meta-analysis of the effects of anxiety and depression on patient adherence. Arch Intern Med 160(14):2101–2107

    Article  CAS  PubMed  Google Scholar 

  32. Zaza C, Baine N (2002) Cancer pain and psychosocial factors: a critical review of the literature. J Pain Symptom Manag 24(5):526–542

    Article  Google Scholar 

  33. Keating NL, Weeks JC, Borbas C, Guadagnoli E (2003) Treatment of early stage breast cancer: do surgeons and patients agree regarding whether treatment alternatives were discussed? Breast Cancer Res Treat 79(2):225–231

    Article  PubMed  Google Scholar 

  34. Fraenkel L (2007) What are the essential elements to enable patient participation in medical decision making? J Gen Intern Med 22(5):614–619

    Article  PubMed Central  PubMed  Google Scholar 

  35. Hack TF, Degner LF, Parker PA (2005) The communication goals and needs of cancer patients: a review. Psycho-Oncology 14(10):831–845

    Article  PubMed  Google Scholar 

  36. Shields CG, Coker CJ, Poulsen SS, Doyle JM, Fiscella K, Epstein RM, Griggs JJ (2009) Patient-centered communication and prognosis discussions with cancer patients. Patient Educ Couns 77(3):437–442

    Article  PubMed Central  PubMed  Google Scholar 

  37. Diefenbach M, Turner G, Carpenter KM, Sheldon LK, Mustian KM, Gerend MA, Rini C, von Wagner C, Gritz ER, McQueen A (2009) Cancer and patient–physician communication. J Health Commun 14(S1):57–65

    Article  PubMed Central  PubMed  Google Scholar 

  38. Mazor KM, Gaglio B, Nekhlyudov L, Alexander GL, Stark A, Hornbrook MC, Walsh K, Boggs J, Lemay CA, Firneno C (2013) Assessing patient-centered communication in cancer care: stakeholder perspectives. J Oncol Pract 9(5):e186–e193

    Article  PubMed  Google Scholar 

  39. Moumjid N, Charles C, Morelle M, Gafni A, Brémond A, Farsi F, Whelan T, Carrère M-O (2009) The statutory duty of physicians to inform patients versus unmet patients’ information needs: the case of breast cancer in France. Health Policy 91(2):162–173. doi:10.1016/j.healthpol.2008.11.010

    Article  PubMed  Google Scholar 

  40. Rutten LJF, Arora NK, Bakos AD, Aziz N, Rowland J (2005) Information needs and sources of information among cancer patients: a systematic review of research (1980–2003). Patient Educ Couns 57(3):250–261

    Article  PubMed  Google Scholar 

  41. Mallinger JB, Griggs JJ, Shields CG (2005) Patient-centered care and breast cancer survivors’ satisfaction with information. Patient Educ Couns 57(3):342

    Article  PubMed  Google Scholar 

  42. Brown R, Butow P, Wilson-Genderson M, Bernhard J, Ribi K, Juraskova I (2012) Meeting the decision-making preferences of patients with breast cancer in oncology consultations: impact on decision-related outcomes. J Clin Oncol 30(8):857–862

    Article  PubMed  Google Scholar 

  43. Gattellari M, Butow PN, Tattersall MH (2001) Sharing decisions in cancer care. Soc Sci Med 52(12):1865–1878

    Article  CAS  PubMed  Google Scholar 

  44. Keating NL, Guadagnoli E, Landrum MB, Borbas C, Weeks JC (2002) Treatment decision making in early-stage breast cancer: should surgeons match patients’ desired level of involvement? J Clin Oncol 20(6):1473–1479

    Article  PubMed  Google Scholar 

  45. Street RL, Elwyn G, Epstein RM (2012) Patient preferences and healthcare outcomes: an ecological perspective. Expert Rev Pharmacoeconomics Outcomes Res 12(2):167–180

    Article  Google Scholar 

  46. Stacey D, Bennett CL, Barry MJ, Col NF, Eden KB, Holmes-Rovner M, Llewellyn-Thomas H, Lyddiatt A, Légaré F, Thomson R (2011) Decision aids for people facing health treatment or screening decisions. Cochrane Database Syst Rev 10(10)

  47. Mack JW, Weeks JC, Wright AA, Block SD, Prigerson HG (2010) End-of-life discussions, goal attainment, and distress at the end of life: predictors and outcomes of receipt of care consistent with preferences. J Clin Oncol 28(7):1203–1208

    Article  PubMed Central  PubMed  Google Scholar 

  48. Shin DW, Park JH, Shim EJ, Park JH, Choi JY, Kim SG, Park EC (2011) The development of a comprehensive needs assessment tool for cancer caregivers in patient–caregiver dyads. Psycho-Oncology 20(12):1342–1352

    Article  PubMed  Google Scholar 

  49. Hodgkinson K, Butow P, Hunt G, Pendlebury S, Hobbs K, Lo S, Wain G (2007) The development and evaluation of a measure to assess cancer survivors’ unmet supportive care needs: the CaSUN (Cancer Survivors’ Unmet Needs measure). Psycho-Oncology 16(9):796–804

    Article  CAS  PubMed  Google Scholar 

  50. Adams E, Boulton M, Watson E (2009) The information needs of partners and family members of cancer patients: a systematic literature review. Patient Educ Couns 77(2):179–186

    Article  PubMed  Google Scholar 

  51. Hardin SR, Bernhardt-Tindal K, Hart A, Stepp A, Henson A (2011) Critical-care visitation: the patients’ perspective. Dimens Crit Care Nurs 30(1):53

    Article  PubMed  Google Scholar 

  52. Given BA, Given CW, Sherwood PR (2012) Family and caregiver needs over the course of the cancer trajectory. J Support Oncol 10(2):57–64

    Article  PubMed  Google Scholar 

  53. Harding R, Higginson IJ (2003) What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness. Palliat Med 17(1):63–74

    Article  CAS  PubMed  Google Scholar 

  54. Wolff JL, Roter DL (2011) Family presence in routine medical visits: a meta-analytical review. Soc Sci Med 72(6):823–831. doi:10.1016/j.socscimed.2011.01.015

    Article  PubMed Central  PubMed  Google Scholar 

  55. Fradgley L, Bryant J, Paul C, Sanson-Fisher R (2013) Making it real: operationalising medical oncology outpatients’ preferences for health service change in Hunter New England clinics. 11th Behavioural Research in Cancer Control (BRCC) Conference, Adelaide

    Google Scholar 

  56. Bradley CJ, Bednarek HL (2002) Employment patterns of long-term cancer survivors. Psycho-Oncology 11(3):188–198

    Article  PubMed  Google Scholar 

  57. Main DS, Nowels CT, Cavender TA, Etschmaier M, Steiner JF (2005) A qualitative study of work and work return in cancer survivors. Psycho-Oncology 14(11):992–1004

    Article  PubMed  Google Scholar 

  58. Carroll JK, Humiston SG, Meldrum SC, Salamone CM, Jean-Pierre P, Epstein RM, Fiscella K (2010) Patients’ experiences with navigation for cancer care. Patient Educ Couns 80(2):241–247

    Article  PubMed Central  PubMed  Google Scholar 

  59. Bennion A, Molassiotis A (2013) Qualitative research into the symptom experiences of adult cancer patients after treatments: a systematic review and meta-synthesis. Support Care Cancer 21(1):9–25

    Article  CAS  PubMed  Google Scholar 

  60. Sandoval GA, Brown AD, Sullivan T, Green E (2006) Factors that influence cancer patients’ overall perceptions of the quality of care. Int J Qual Health Care 18(4):266–274

    Article  PubMed  Google Scholar 

  61. Hewitt ME, Greenfield S, Stovall E (2006) From cancer patient to cancer survivor: lost in transition. National Academies, Washington

    Google Scholar 

  62. Salz T, Oeffinger KC, McCabe MS, Layne TM, Bach PB (2012) Survivorship care plans in research and practice. CA Cancer J Clin 62(2):101–117

    Article  Google Scholar 

  63. Snyder CF, Earle CC, Herbert RJ, Neville BA, Blackford AL, Frick KD (2008) Preventive care for colorectal cancer survivors: a 5-year longitudinal study. J Clin Oncol 26(7):1073–1079

    Article  PubMed  Google Scholar 

  64. Baravelli C, Krishnasamy M, Pezaro C, Schofield P, Lotfi-Jam K, Rogers M, Milne D, Aranda S, King D, Shaw B (2009) The views of bowel cancer survivors and health care professionals regarding survivorship care plans and post treatment follow up. J Cancer Survivorship 3(2):99–108

    Article  Google Scholar 

  65. Smith S, Nicol K, Devereux J, Cornbleet M (1999) Encounters with doctors: quantity and quality. Palliat Med 13(3):217–223

    Article  CAS  PubMed  Google Scholar 

  66. Haggerty JL, Reid RJ, Freeman GK, Starfield BH, Adair CE, McKendry R (2003) Continuity of care: a multidisciplinary review. BMJ 327(7425):1219–1221

    Article  PubMed Central  PubMed  Google Scholar 

  67. Cook RI, Render M, Woods DD (2000) Gaps in the continuity of care and progress on patient safety. BMJ 320(7237):791–794

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  68. Sharma G, Freeman J, Zhang D, Goodwin JS (2009) Continuity of care and ICU utilization during end of life. Arch Intern Med 169(1):81

    Article  PubMed Central  PubMed  Google Scholar 

  69. Pandhi N, Saultz JW (2006) Patients’ perceptions of interpersonal continuity of care. J Am Board Fami Med 19(4):390–397

    Article  Google Scholar 

  70. Aubin M, Giguère A, Verreault R, Fitch MI, Kazanjian A (2012) Interventions to improve continuity of care in the follow-up of patients with cancer. Cochrane Libr 7, CD007672

    Google Scholar 

  71. McGlynn EA, Asch SM, Adams J, Keesey J, Hicks J, DeCristofaro A, Kerr EA (2003) The quality of health care delivered to adults in the United States. N Engl J Med 348(26):2635–2645

    Article  PubMed  Google Scholar 

  72. Jenkinson C, Coulter A, Bruster S (2002) The Picker Patient Experience Questionnaire: development and validation using data from in-patient surveys in five countries. Int J Qual Health Care 14(5):353–358

    Article  PubMed  Google Scholar 

  73. Pargeon KL, Hailey BJ (1999) Barriers to effective cancer pain management: a review of the literature. J Pain Symptom Manag 18(5):358–368

    Article  CAS  Google Scholar 

  74. Donabedian A (2005) Evaluating the quality of medical care. Milbank Q 83(4):691–729

    Article  PubMed Central  PubMed  Google Scholar 

  75. Velikova G, Wright P, Smith AB, Stark D, Perren T, Brown J, Selby P (2001) Self-reported quality of life of individual cancer patients: concordance of results with disease course and medical records. J Clin Oncol 19(7):2064–2073

    CAS  PubMed  Google Scholar 

  76. Newell S, Sanson-Fisher RW, Girgis A, Bonaventura A (1998) How well do Medical oncologists’ perceptions reflect their patients’ reported physical and psychosocial problems? Cancer 83(8):1640–1651

    Article  CAS  PubMed  Google Scholar 

  77. Rhondali W, Hui D, Kim SH, Kilgore K, Kang JH, Nguyen L, Bruera E (2012) Association between patient-reported symptoms and nurses’ clinical impressions in cancer patients admitted to an acute palliative care unit. J Palliat Med 15(3):301–307

    PubMed Central  PubMed  Google Scholar 

  78. Keller M, Sommerfeldt S, Fischer C, Knight L, Riesbeck M, Löwe B, Herfarth C, Lehnert T (2004) Recognition of distress and psychiatric morbidity in cancer patients: a multi-method approach. Ann Oncol 15(8):1243–1249

    Article  CAS  PubMed  Google Scholar 

  79. Fallowfield L, Ratcliffe D, Jenkins V, Saul J (2001) Psychiatric morbidity and its recognition by doctors in patients with cancer. Br J Cancer 84(8):1011–1015

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  80. Söllner W, DeVries A, Steixner E, Lukas P, Sprinzl G, Rumpold G, Maislinger S (2001) How successful are oncologists in identifying patient distress, perceived social support, and need for psychosocial counselling? Br J Cancer 84(2):179

    Article  PubMed Central  PubMed  Google Scholar 

  81. Bruera E, Sweeney C, Calder K, Palmer L, Benisch-Tolley S (2001) Patient preferences versus physician perceptions of treatment decisions in cancer care. J Clin Oncol 19(11):2883–2885

    CAS  PubMed  Google Scholar 

  82. Rothenbacher D, Lutz M, Porzsolt F (1997) Treatment decisions in palliative cancer care: patients’ preferences for involvement and doctors’ knowledge about it. Eur J Cancer 33(8):1184–1189

    Article  CAS  PubMed  Google Scholar 

  83. Wessels H, de Graeff A, Wynia K, de Heus M, Kruitwagen CL, Teunissen SC, Voest EE (2010) Are health care professionals able to judge cancer patients’ health care preferences correctly? A cross-sectional study. BMC Health Serv Res 10(1):198

    Article  PubMed Central  PubMed  Google Scholar 

  84. Schubart JR, Toran L, Whitehead M, Levi BH, Green MJ (2013) Informed decision making in advance care planning: concordance of patient self-reported diagnosis with physician diagnosis. Support Care Cancer 21(2):637–641

    Article  PubMed  Google Scholar 

  85. Quirt C, Mackillop W, Ginsburg A, Sheldon L, Brundage M, Dixon P, Ginsburg L (1997) Do doctors know when their patients don’t?: a survey of doctor–patient communication in lung cancer. Lung Cancer 18(1):1–20

    Article  CAS  PubMed  Google Scholar 

  86. Arora NK, Reeve BB, Hays RD, Clauser SB, Oakley-Girvan I (2011) Assessment of quality of cancer-related follow-up care from the cancer survivor’s perspective. J Clin Oncol 29(10):1280–1289

    Article  PubMed Central  PubMed  Google Scholar 

  87. Street J, Richard L, Gordon HS, Ward MM, Krupat E, Kravitz RL (2005) Patient participation in medical consultations: why some patients are more involved than others. Med Care 43(10):960–969

    Article  PubMed  Google Scholar 

  88. Epstein R, Street R (2007) Patient-centered communication in cancer care: promoting healing and reducing suffering. National Cancer Institute, NIH Publication No 07-6225, Bethesda

    Google Scholar 

  89. DeWalt DA, Berkman ND, Sheridan S, Lohr KN, Pignone MP (2004) Literacy and health outcomes. J Gen Intern Med 19(12):1228–1239

    Article  PubMed Central  PubMed  Google Scholar 

  90. Ryan H, Schofield P, Cockburn J, Butow P, Tattersall M, Turner J, Girgis A, Bandaranayake D, Bowman D (2005) How to recognize and manage psychological distress in cancer patients. Eur J Cancer Care 14(1):7–15

    Article  CAS  Google Scholar 

  91. Gunnarsdottir S, Serlin RC, Ward S (2005) Patient-related barriers to pain management: the Icelandic Barriers Questionnaire II. J Pain Symptom Manag 29(3):273–285

    Article  Google Scholar 

  92. Clayton JM, Natalia C, Butow PN, Simpson JM, O’Brien AM, Devine R, Tattersall MH (2012) Physician endorsement alone may not enhance question-asking by advanced cancer patients during consultations about palliative care. Support Care Cancer 20(7):1457–1464

    Article  PubMed  Google Scholar 

  93. Grad FP (2002) The preamble of the constitution of the World Health Organization. Bull World Health Organ 80(12):981–981

    PubMed Central  PubMed  Google Scholar 

  94. Street RL Jr, Makoul G, Arora NK, Epstein RM (2009) How does communication heal? Pathways linking clinician–patient communication to health outcomes. Patient Educ Couns 74(3):295–301

    Article  PubMed  Google Scholar 

  95. Ha JF, Longnecker N (2010) Doctor-patient communication: a review. Ochsner J 10(1):38–43

    PubMed Central  PubMed  Google Scholar 

  96. Coyne JC, Lepore SJ, Palmer SC (2006) Efficacy of psychosocial interventions in cancer care: evidence is weaker than it first looks. Ann Behav Med 32(2):104–110

    Article  PubMed  Google Scholar 

  97. Tzelepis F, Rose SK, Sanson-Fisher R, Clinton-McHarg T, Carey ML, Paul CL (2014) Are we missing the Institute of Medicine’s mark? A systematic review of patient-reported outcome measures assessing quality of patient-centred cancer care. BMC Cancer 14:41

    Article  PubMed Central  PubMed  Google Scholar 

  98. Rozenblum R, Lisby M, Hockey PM, Levtzion-Korach O, Salzberg CA, Efrati N, Lipsitz S, Bates DW (2013) The patient satisfaction chasm: the gap between hospital management and frontline clinicians. BMJ Qual Saf 22(3):242–250

    Article  PubMed  Google Scholar 

  99. Scobie S, Thomson R, McNeil JJ, Phillips PA (2006) Measurement of the safety and quality of health care. Med J Aust 184(10):S51

    PubMed  Google Scholar 

  100. Clarke AL, Shearer W, McMillan AJ, Ireland PD (2010) Investigating apparent variation in quality of care: the critical role of clinician engagement. Med J Aust 193(8):S111

    PubMed  Google Scholar 

  101. Australian Commission on Safety and Quality in Health Care (2011) Patient-centred care: improving quality and safety through partnerships with patient and consumers. ACSQHC, Sydney

    Google Scholar 

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Acknowledgments

This manuscript was also supported by a Strategic Research Partnership Grant from Cancer Council NSW to the Newcastle Cancer Control Collaborative.

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Correspondence to Alison Zucca.

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Zucca, A., Sanson-Fisher, R., Waller, A. et al. Patient-centred care: making cancer treatment centres accountable. Support Care Cancer 22, 1989–1997 (2014). https://doi.org/10.1007/s00520-014-2221-4

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