Development of the Serious Illness Care Program: a randomised controlled trial of a palliative care communication intervention

Rachelle Bernacki, Mathilde Hutchings, Judith Vick, Grant Smith, Joanna Paladino, Stuart Lipsitz, Atul A Gawande, Susan D Block, Rachelle Bernacki, Mathilde Hutchings, Judith Vick, Grant Smith, Joanna Paladino, Stuart Lipsitz, Atul A Gawande, Susan D Block

Abstract

Introduction: Ensuring that patients receive care that is consistent with their goals and values is a critical component of high-quality care. This article describes the protocol for a cluster randomised controlled trial of a multicomponent, structured communication intervention.

Methods and analysis: Patients with advanced, incurable cancer and life expectancy of <12 months will participate together with their surrogate. Clinicians are enrolled and randomised either to usual care or the intervention. The Serious Illness Care Program is a multicomponent, structured communication intervention designed to identify patients, train clinicians to use a structured guide for advanced care planning discussion with patients, 'trigger' clinicians to have conversations, prepare patients and families for the conversation, and document outcomes of the discussion in a structured format in the electronic medical record. Clinician satisfaction with the intervention, confidence and attitudes will be assessed before and after the intervention. Self-report data will be collected from patients and surrogates approximately every 2 months up to 2 years or until the patient's death; patient medical records will be examined at the close of the study. Analyses will examine the impact of the intervention on the patient receipt of goal-concordant care, and peacefulness at the end of life. Secondary outcomes include patient anxiety, depression, quality of life, therapeutic alliance, quality of communication, and quality of dying and death. Key process measures include frequency, timing and quality of documented conversations.

Ethics and dissemination: This study was approved by the Dana-Farber Cancer Institute Institutional Review Board. Results will be reported in peer-reviewed publications and conference presentations.

Trial registration number: Protocol identifier NCT01786811; Pre-results.

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Figures

Figure 1
Figure 1
Serious Illness Conversation Guide.
Figure 2
Figure 2
Research design.
Figure 3
Figure 3
Patient/family recruitment and assessment.
Figure 4
Figure 4
Family communication guide (front page only).
Figure 5
Figure 5
Pre-visit letter for patients.
Figure 6
Figure 6
Electronic module of the Serious Illness Conversation Guide. (c) 2015 Epic Systems Corporation. Used with permission.

References

    1. Institute of Medicine. Dying in America: improving quality and honoring individual preferences near end of life. Washington, DC, 2014.
    1. Wright AA, Mack JW, Kritek PA et al. . Influence of patients’ preferences and treatment site on cancer patients’ end-of-life care. Cancer 2010;116:4656–63. 10.1002/cncr.25217
    1. Detering KM, Hancock AD, Reade MC et al. . The impact of advance care planning on end of life care in elderly patients: randomised controlled trial. BMJ 2010;340:c1345 10.1136/bmj.c1345
    1. Temel JS, Greer JA, Muzikansky A et al. . Early palliative care for patients with metastatic non-small-cell lung cancer. N Engl J Med 2010;363:733–42. 10.1056/NEJMoa1000678
    1. Mack JW, Cronin A, Taback N et al. . End-of-life care discussions among patients with advanced cancer: a cohort study. Ann Intern Med 2012;156:204–10. 10.7326/0003-4819-156-3-201202070-00008
    1. Curtis JR, Patrick DL, Caldwell ES et al. . Why don't patients and physicians talk about end-of-life care? Barriers to communication for patients with acquired immunodeficiency syndrome and their primary care clinicians. Arch Intern Med 2000;160:1690–6. 10.1001/archinte.160.11.1690
    1. Anderson WG, Chase R, Pantilat SZ et al. . Code status discussions between attending hospitalist physicians and medical patients at hospital admission. J Gen Intern Med 2011;26:359–66. 10.1007/s11606-010-1568-6
    1. Hagerty RG, Butow PN, Ellis PA et al. . Cancer patient preferences for communication of prognosis in the metastatic setting. J Clin Oncol 2004;22:1721–30. 10.1200/JCO.2004.04.095
    1. Smith AK, McCarthy EP, Paulk E et al. . Racial and ethnic differences in advance care planning among patients with cancer: impact of terminal illness acknowledgment, religiousness, and treatment preferences. J Clin Oncol 2008;26:4131–7. 10.1200/JCO.2007.14.8452
    1. Buss MK, Lessen DS, Sullivan AM et al. . Hematology/oncology fellows’ training in palliative care: results of a national survey. Cancer 2011;117:4304–11. 10.1002/cncr.25952
    1. Block SD. Medical education in end-of-life care: the status of reform. J Palliat Med 2002;5:243–8. 10.1089/109662102753641214
    1. Fallowfield L, Jenkins V, Farewell V et al. . Efficacy of a Cancer Research UK communication skills training model for oncologists: a randomised controlled trial. Lancet 2002;359:650–6. 10.1016/S0140-6736(02)07810-8
    1. Back AL, Arnold RM, Baile WF et al. . Faculty development to change the paradigm of communication skills teaching in oncology. J Clin Oncol 2009;27:1137–41. 10.1200/JCO.2008.20.2408
    1. Sullivan AM, Lakoma MD, Billings JA et al. . Teaching and learning end-of-life care: evaluation of a faculty development program in palliative care. Acad Med 2005;80:657–68. 10.1097/00001888-200507000-00008
    1. Sullivan AM, Lakoma MD, Billings JA et al. . Creating enduring change: demonstrating the long-term impact of a faculty development program in palliative care. J Gen Intern Med 2006;21:907–14. 10.1111/j.1525-1497.2006.00486.x
    1. Rao JK, Anderson LA, Inui TS et al. . Communication interventions make a difference in conversations between physicians and patients: a systematic review of the evidence. Med Care 2007;45:340–9. 10.1097/01.mlr.0000254516.04961.d5
    1. Fellowes D, Wilkinson S, Moore P. Communication skills training for health care professionals working with cancer patients, their families and/or carers. Cochrane Database Syst Rev 2004;(2):CD003751 10.1002/14651858.CD003751.pub2
    1. Jacobsen J, Jackson V, Dahlin C et al. . Components of early outpatient palliative care consultation in patients with metastatic nonsmall cell lung cancer. J Palliat Med 2011;14:459–64. 10.1089/jpm.2010.0382
    1. Lupu D. Estimate of current hospice and palliative medicine physician workforce shortage. J Pain Symptom Manage 2010;40:899–911. 10.1016/j.jpainsymman.2010.07.004
    1. Block SD, Billings JA. A need for scalable outpatient palliative care interventions. Lancet 2014;383:1699–700. 10.1016/S0140-6736(13)62676-8
    1. Bernacki RE, Block SD, American College of Physicians High Value Care Task Force. Communication about serious illness care goals: a review and synthesis of best practices. JAMA Intern Med 2014;174:1994–2003. 10.1001/jamainternmed.2014.5271
    1. Billings JA, Bernacki R. Strategic targeting of advance care planning interventions: the Goldilocks phenomenon. JAMA Intern Med 2014;174:620–4. 10.1001/jamainternmed.2013.14384
    1. Brach C, Fraser I, Paez K. Crossing the language chasm. Health Aff (Millwood) 2005;24:424–34. 10.1377/hlthaff.24.2.424
    1. Thornton JD, Pham K, Engelberg RA et al. . Families with limited English proficiency receive less information and support in interpreted intensive care unit family conferences. Crit Care Med 2009;37:89–95. 10.1097/CCM.0b013e3181926430
    1. Moss AH, Ganjoo J, Sharma S et al. . Utility of the “surprise” question to identify dialysis patients with high mortality. Clin J Am Soc Nephrol 2008;3:1379–84. 10.2215/CJN.00940208
    1. Moss AH, Lunney JR, Culp S et al. . Prognostic significance of the “surprise” question in cancer patients. J Palliat Med 2010;13:837–40. 10.1089/jpm.2010.0018
    1. Curtis JR, Patrick DL, Engelberg RA et al. . A measure of the quality of dying and death. Initial validation using after-death interviews with family members. J Pain Symptom Manage 2002;24:17–31. 10.1016/S0885-3924(02)00419-0
    1. Engelberg RA, Patrick DL, Curtis JR. Correspondence between patients’ preferences and surrogates’ understandings for dying and death. J Pain Symptom Manage 2005;30:498–509. 10.1016/j.jpainsymman.2005.06.006
    1. Patrick DL, Curtis JR, Engelberg RA et al. . Measuring and improving the quality of dying and death. Ann Intern Med 2003;139(5 Pt 2):410–15. 10.7326/0003-4819-139-5_Part_2-200309021-00006
    1. Kristjanson LJ. Validity and reliability testing of the FAMCARE Scale: measuring family satisfaction with advanced cancer care. Soc Sci Med 1993;36:693–701. 10.1016/0277-9536(93)90066-D
    1. Steinhauser KE, Christakis NA, Clipp EC et al. . Factors considered important at the end of life by patients, family, physicians, and other care providers. JAMA 2000;284:2476–82. 10.1001/jama.284.19.2476
    1. Steinhauser KE, Clipp EC, McNeilly M et al. . In search of a good death: observations of patients, families, and providers. Ann Intern Med 2000;132:825–32.
    1. Quill T, Norton S, Shah M et al. . What is most important for you to achieve? An analysis of patient responses when receiving palliative care consultation. J Palliat Med 2006;9:382–8. 10.1089/jpm.2006.9.382
    1. Barnato AE, Llewellyn-Thomas HA, Peters EM et al. . Communication and decision making in cancer care: setting research priorities for decision support/patients’ decision aids. Med Decis Making 2007;27:626–34. 10.1177/0272989X07306788
    1. Clayton J, Butow P, Tattersall M et al. . Asking questions can help: development and preliminary evaluation of a question prompt list for palliative care patients. Br J Cancer 2003;89:2069–77. 10.1038/sj.bjc.6601380
    1. Mack JW, Weeks JC, Wright AA et al. . 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 2010;28:1203–8. 10.1200/JCO.2009.25.4672
    1. [No authors listed]. A controlled trial to improve care for seriously ill hospitalized patients. The study to understand prognoses and preferences for outcomes and risks of treatments (SUPPORT). The SUPPORT Principal Investigators. JAMA 1995;274:1591–8. 10.1001/jama.1995.03530200027032
    1. Mack JW, Nilsson M, Balboni T et al. . Peace, Equanimity, and Acceptance in the Cancer Experience (PEACE): validation of a scale to assess acceptance and struggle with terminal illness. Cancer 2008;112:2509–17. 10.1002/cncr.23476
    1. Cameron IM, Crawford JR, Lawton K et al. . Psychometric comparison of PHQ-9 and HADS for measuring depression severity in primary care. Br J Gen Pract 2008;58:32–6. 10.3399/bjgp08X263794
    1. Spitzer RL, Kroenke K, Williams JB et al. . A brief measure for assessing generalized anxiety disorder: the GAD-7. Arch Intern Med 2006;166:1092–7. 10.1001/archinte.166.10.1092
    1. Martin A, Rief W, Klaiberg A et al. . Validity of the Brief Patient Health Questionnaire Mood Scale (PHQ-9) in the general population. Gen Hosp Psychiatry 2006;28:71–7. 10.1016/j.genhosppsych.2005.07.003
    1. Mack JW, Block SD, Nilsson M et al. . Measuring therapeutic alliance between oncologists and patients with advanced cancer: the Human Connection Scale. Cancer 2009;115:3302–11. 10.1002/cncr.24360
    1. Wenrich MD, Curtis JR, Shannon SE et al. . Communicating with dying patients within the spectrum of medical care from terminal diagnosis to death. Arch Intern Med 2001;161:868–74. 10.1001/archinte.161.6.868
    1. Engelberg R, Downey L, Curtis JR. Psychometric characteristics of a quality of communication questionnaire assessing communication about end-of-life care. J Palliat Med 2006;9:1086–98. 10.1089/jpm.2006.9.1086
    1. Ware J Jr., Kosinski M, Keller SD. A 12-Item Short-Form Health Survey: construction of scales and preliminary tests of reliability and validity. Med Care 1996;34:220–33. 10.1097/00005650-199603000-00003
    1. Pargament K, Feuille M, Burdzy D. The brief RCOPE: current psychometric status of a short measure of religious coping. Religions 2011;2:51–76. 10.3390/rel2010051
    1. Natarajan S, Lipsitz SR, Fitzmaurice GM et al. . An extension of the Wilcoxon Rank-Sum test for complex sample survey data. J R Stat Soc Ser C Appl Stat 2012;61:653–64. 10.1111/j.1467-9876.2011.01028.x
    1. Donner A, Klar N. Pitfalls of and controversies in cluster randomization trials. Am J Public Health 2004;94:416–22. 10.2105/AJPH.94.3.416
    1. Haybittle JL. Repeated assessment of results in clinical trials of cancer treatment. Br J Radiol 1971;44:793–7. 10.1259/0007-1285-44-526-793
    1. O'Brien PC, Fleming TR. A multiple testing procedure for clinical trials. Biometrics 1979;35:549–56. 10.2307/2530245
    1. Robins JM, Hernan MA, Brumback B. Marginal structural models and causal inference in epidemiology. Epidemiology 2000;11:550–60. 10.1097/00001648-200009000-00011

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