Appropriate and inappropriate care in the last phase of life: an explorative study among patients and relatives

BMC Health Services Research - Tập 16 - Trang 1-11 - 2016
Eva Elizabeth Bolt1, H Roeline Willemijn Pasman1, Dick Willems2, Bregje Dorien Onwuteaka-Philipsen1
1Department of Public and Occupational Health, EMGO Institute for Health and Care Research, VUmc Expertise Center for Palliative Care, VU University Medical Center, Amsterdam, The Netherlands
2Department of General Practice, Section of Medical Ethics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands

Tóm tắt

Many people are in need of care in the last phase of life. However, the care they receive is not always appropriate. For instance, people can receive overly aggressive treatment or can have limited access to palliative care. The term appropriate care is often used by policy makers, while it is unclear what care recipients consider as appropriate care. This study aims to identify what care patients and relatives perceive as appropriate and as inappropriate in the last phase of life, for patients suffering from different conditions. We designed an online survey with open questions. Participants were recruited through organizations for patients, older people and medical professionals. Answers were analysed after data-driven coding. Forty-five patients and 547 relatives described the care they received and described why this care was appropriate or inappropriate. Participants described more cases of appropriate care than inappropriate care. The cases of appropriate care were diverse, but all involved care in (one or more of) five dimensions; supportive care, treatment decisions, location, the role of the patient’s wish and communication. Each of these dimensions was frequently described (39-62 %). When care was inappropriate, this mostly involved inappropriate treatment decisions (69 %; especially overtreatment was frequently mentioned), and poor communication (50 %). There was considerable consistency in what was seen as (in)appropriate care across different conditions. However, especially patients suffering from other physical diseases than cancer more often received inappropriate care. From the perspective of patients and relatives, appropriate care in the last phase of life is a broad concept. Caregivers should be aware of the diversity of care needs in the last phase of life. Especially treatment decisions and communication can be improved.

Tài liệu tham khảo

Hales S, Zimmermann C, Rodin G. The quality of dying and death. Arch Intern Med. 2008;168:912–8. Steinhauser KE, Clipp EC, McNeilly M, Christakis NA, McIntyre LM, Tulsky JA. In search of a good death: observations of patients, families, and providers. Ann Intern Med. 2000;132:825–32. Ferrell BR. Overview of the domains of variables relevant to end-of-life care. J Palliat Med. 2005;8 Suppl 1:S22–9. Buiting HM, Rurup ML, Wijsbek H, van Zuylen L, den Hartogh G. Understanding provision of chemotherapy to patients with end stage cancer: qualitative interview study. BMJ. 2011;342:d1933. Earle CC, Landrum MB, Souza JM, Neville BA, Weeks JC, Ayanian JZ. Aggressiveness of cancer care near the end of life: is it a quality-of-care issue? J Clin Oncol. 2008;26:3860–6. Ho TH, Barbera L, Saskin R, Lu H, Neville BA, Earle CC. Trends in the aggressiveness of end-of-life cancer care in the universal health care system of Ontario, Canada. J Clin Oncol. 2011;29:1587–91. Foley KM, Gelband H. Improving Palliative Care for Cancer. Washington D.C.: National Cancer Policy Board; 2001. Zwart-Olde I, Jacobs J, Broese van Groenou M. [Care networks of frail elderly-Research report for caregivers, researchers and policymakers in elderly care], in Dutch, Nationaal Programma Ouderenzorg, 2013. Quaglia A, Lillini R, Mamo C, Ivaldi E, Vercelli M. Socio-economic inequalities: a review of methodological issues and the relationships with cancer survival. Crit Rev Oncol Hematol. 2013;85:266–77. Marik P. The cost of inappropriate care at the end of life: implications for an aging population. Am J Hosp Palliat Care. 2014. Berman N. End-of-life matters in chronic renal failure. Curr Opin Support Palliat Care. 2014;8:371–7. Butola S. Inappropriate referrals at the end of life--the existing Indian scenario. Support Care Cancer. 2014;22:2219–22. de Neeling J. Appropriate medical care. On choosing and guidelines. Final report KNMG-project appropriate care. Utrecht: Dutch, Royal Dutch Medical Organization (KNMG); 2000. World Health Organization. Appropriateness in health care services. Copenhagen: Report on a WHO Workshop; 2000. The ABIM Foundation. Choosing wisely. An initiative of the ABIM Foundation, 2015. Online Source. www.choosingwisely.org. Accessed 2 Mar 2015. Nelson ML, Schrader SL, Eidsness LM. "South Dakota's Dying to Know": personal experiences with end-of-life care. J Palliat Med. 2009;12:905–13. Moens K, Higginson IJ, Harding R. Are there differences in the prevalence of palliative care-related problems in people living with advanced cancer and eight non-cancer conditions? A systematic review. J Pain Symptom Manage. 2014;48:660–77. Lynn J, Adamson DM. Living Well at the End of Life, White paper. Santa Monica: RAND Health; 2003. National Institutes of Health. National institutes of health state-of-the-science conference statement of improving end-of-life care, 2004. online source. http://consensus.nih.gov/2004/2004EndOfLifeCareSOS024html.htm. Accessed 7 Apr 2015. Steinhauser KE, Christakis NA, Clipp EC, McNeilly M, McIntyre L, Tulsky JA. Factors considered important at the end of life by patients, family, physicians, and other care providers. JAMA. 2000;284:2476–82. Singer PA, Martin DK, Kelner M. Quality end-of-life care: patients' perspectives. JAMA. 1999;281:163–8. Habraken JM, Willems DL, de Kort SJ, Bindels PJE. Health care needs in end-stage COPD: a structured literature review. Patient Educ Couns. 2007;68:121–30. Hanson LC, Danis M, Garrett J. What is wrong with end-of-life care? Opinions of bereaved family members. J Am Geriatr Soc. 1997;45:1339–44. Emanuel LL, von Gunten CF, Ferris FD. Gaps in end-of-life care. Arch Fam Med. 2000;9:1176–80. Detering KM, Hancock AD, Reade MC, Silvester W. The impact of advance care planning on end of life care in elderly patients: randomised controlled trial. BMJ. 2010;340:c1345. Audrey S, Abel J, Blazeby JM, Falk S, Campbell R. What oncologists tell patients about survival benefits of palliative chemotherapy and implications for informed consent: qualitative study. BMJ. 2008;337:a752. Hoff L, Hermeren G. Information from physicians and retention of information by patients - obstacles to the awareness of patients of progressing disease when life is near the end. BMC Palliat Care. 2008;7:2. Solano JP, Gomes B, Higginson IJ. A comparison of symptom prevalence in far advanced cancer, AIDS, heart disease, chronic obstructive pulmonary disease and renal disease. J Pain Symptom Manage. 2006;31:58–69. Murray SA, Sheikh A. Palliative Care Beyond Cancer: Care for all at the end of life. BMJ. 2008;336:958–9. Remillard ML, Mazor KM, Cutrona SL, Gurwitz JH, Tjia J. Systematic review of the use of online questionnaires of older adults. J Am Geriatr Soc. 2014;62:696–705. Statistics Netherlands (CBS), [ICT use of people], in Dutch, online source. http://statline.cbs.nl/Statweb/publication/?DM=SLNL&PA=71098ned&D1=33-133&D2=0-2&D3=a&VW=T. Accessed 7 Apr 2015. Statistics Netherlands (CBS), [Population: Generation, age, gender and place of origin, January 1], in Dutch, online source. http://statline.cbs.nl/statweb/publication/?vw=t&dm=slnl&pa=37325&d1=a&d2=0&d3=0&d4=0&d5=0-4,137,152,220,237&d6=0,4,9,14,18-19&hd=151214-1201&hdr=g2,g1,g3,t&stb=g4,g5. Accessed 29 Oct 2016. Central Committee on Research Involving Human Subjects. Online source. www.ccmo.nl/en. Accessed 24 Apr 2015.