期刊论文详细信息
BMC Medicine
Evaluating complex interventions in End of Life Care: the MORECare Statement on good practice generated by a synthesis of transparent expert consultations and systematic reviews
Chris Todd6  Morag Farquhar9  Marjolein Gysels4  Hamid Benalia8  Scott A Murray5  Matthew Hotopf1,11  Richard Harding8  Peter Fayers3  Penney Lewis1,10  Paul McCrone7  Myfanwy Morgan2  Nancy Preston1  Gunn Grande6  Catherine J Evans8  Irene J Higginson8 
[1]International Observatory on End of Life Care, Faculty of Health and Medicine, Lancaster University, Physics Avenue, Lancaster, LA1 4YT, UK
[2]Department of Primary Care and Public Health Sciences, King’s College London, Capital House, Weston Street, London, SE1 3QD, UK
[3]Department of Cancer Research and Molecular Medicine, Faculty of Medicine, NTNU, Prinsesse Kristinasgt. 1, NO-7006, Trondheim, Norway
[4]University of Amsterdam, Centre for Social Science and Global Health, Oudezijds Achterburgwal 185, Amsterdam, 1012 DK, The Netherlands
[5]Primary Palliative Care Research Group, Centre for Population Health Sciences, University of Edinburgh, Medical School, Teviot Place, Edinburgh, EH8 9AG, UK
[6]School of Nursing, Midwifery & Social Work, University of Manchester, Jean McFarlane Building, Oxford Road, Manchester, M13 9PL, UK
[7]Department of Health Services and Population Research, King’s College London, Institute of Psychiatry, 16 De Crespingy Park, London, SE5 8AF, UK
[8]King’s College London, Cicely Saunders Institute, Department of Palliative Care, Policy and Rehabilitation, Bessmer Road, Denmark Hill, London, SE5 9PJ, UK
[9]Primary Care Unit, Department of Public Health & Primary Care, University of Cambridge, Institute of Public Health, Forvie Site, Robinson Way, Cambridge, CB2 OSR, UK
[10]King’s College London, Centre of Medical Law and Ethics, Dickson Poon School of Law, Strand, London, WC2R 2LS, UK
[11]Department of Psychological Medicine, King’s College London, Institute of Psychiatry, Weston Education Centre, Cutcombe Rd, London, SE5 9RJ, UK
关键词: Consensus;    Review;    Evaluation studies;    Methods;    Research design;    Terminal care;    Palliative care;   
Others  :  857084
DOI  :  10.1186/1741-7015-11-111
 received in 2012-11-15, accepted in 2013-04-02,  发布年份 2013
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【 摘 要 】

Background

Despite being a core business of medicine, end of life care (EoLC) is neglected. It is hampered by research that is difficult to conduct with no common standards. We aimed to develop evidence-based guidance on the best methods for the design and conduct of research on EoLC to further knowledge in the field.

Methods

The Methods Of Researching End of life Care (MORECare) project built on the Medical Research Council guidance on the development and evaluation of complex circumstances. We conducted systematic literature reviews, transparent expert consultations (TEC) involving consensus methods of nominal group and online voting, and stakeholder workshops to identify challenges and best practice in EoLC research, including: participation recruitment, ethics, attrition, integration of mixed methods, complex outcomes and economic evaluation. We synthesised all findings to develop a guidance statement on the best methods to research EoLC.

Results

We integrated data from three systematic reviews and five TECs with 133 online responses. We recommend research designs extending beyond randomised trials and encompassing mixed methods. Patients and families value participation in research, and consumer or patient collaboration in developing studies can resolve some ethical concerns. It is ethically desirable to offer patients and families the opportunity to participate in research. Outcome measures should be short, responsive to change and ideally used for both clinical practice and research. Attrition should be anticipated in studies and may affirm inclusion of the relevant population, but careful reporting is necessitated using a new classification. Eventual implementation requires consideration at all stages of the project.

Conclusions

The MORECare statement provides 36 best practice solutions for research evaluating services and treatments in EoLC to improve study quality and set the standard for future research. The statement may be used alongside existing statements and provides a first step in setting common, much needed standards for evaluative research in EoLC. These are relevant to those undertaking research, trainee researchers, research funders, ethical committees and editors.

【 授权许可】

   
2013 Higginson et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]End-of-life care: the neglected core business of medicine Lancet 2012, 379:1171.
  • [2]Department of Health: End of Life Care Strategy - Promoting High Quality Care for Adults at the End of Life. London: Department of Health; 2008.
  • [3]Higginson IJ: It would be NICE to have more evidence? Palliat Med 2004, 18:85-86.
  • [4]Kendall M, Harris F, Boyd K, Sheikh A, Murray SA, Brown D, Mallinson I, Kearney N, Worth A: Key challenges and ways forward in researching the “good death”: qualitative in-depth interview and focus group study. BMJ 2007, 334:521.
  • [5]Sleeman KE, Gomes B, Higginson IJ: Research into end-of-life cancer care–investment is needed. Lancet 2012, 379:519.
  • [6]Shipman C, Gysels M, White P, Worth A, Murray SA, Barclay S, Forrest S, Shepherd J, Dale J, Dewar S, Peters M, White S, Richardson A, Lorenz K, Koffman J, Higginson IJ: Improving generalist end of life care: national consultation with practitioners, commissioners, academics, and service user groups. BMJ 2008, 337:a1720.
  • [7]Lorenz KA, Lynn J, Dy SM, Shugarman LR, Wilkinson A, Mularski RA, Morton SC, Hughes RG, Hilton LK, Maglione M, Rhodes SL, Rolon C, Sun VC, Shekelle PG: Evidence for improving palliative care at the end of life: a systematic review. Ann Intern Med 2008, 148:147-159.
  • [8]Chochinov HM, Kristjanson LJ, Breitbart W, McClement S, Hack TF, Hassard T, Harlos M: Effect of dignity therapy on distress and end-of-life experience in terminally ill patients: a randomised controlled trial. Lancet Oncol 2011, 12:753-762.
  • [9]Gysels M, Higginson IJ: Improving Supportive and Palliative Care for Adults with Cancer: Research Evidence. London: NICE; 2004.
  • [10]Higginson IJ, Finlay IG, Goodwin DM, Hood K, Edwards AG, Cook A, Douglas HR, Normand CE: Is there evidence that palliative care teams alter end-of-life experiences of patients and their caregivers? J Pain Symptom Manage 2003, 25:150-168.
  • [11]Craig P, Dieppe P, Macintyre S, Michie S, Nazareth I, Petticrew M: Developing and evaluating complex interventions: the new Medical Research Council guidance. BMJ 2008, 337:a1655.
  • [12]Zwarenstein M, Treweek S, Gagnier JJ, Altman DG, Tunis S, Haynes B, Oxman AD, Moher D, group C, Pragmatic Trials in Healthcare group: Improving the reporting of pragmatic trials: an extension of the CONSORT statement. BMJ 2008, 337:a2390.
  • [13]von Elm E, Altman DG, Egger M, Pocock SJ, Gotzsche PC, Vandenbroucke JP, STROBE Initiative: The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. Lancet 2007, 370:1453-1457.
  • [14]National Institutes of Health: National Institutes of Health State-of-the-Science Conference Statement on Improving End-of-Life Care. USA: NIH Concensus Development Program; 2004.
  • [15]Walshe C, Caress A, Chew-Graham C, Todd C: Implementation and impact of the Gold Standards Framework in community palliative care: a qualitative study of three primary care trusts. Palliat Med 2008, 22:736-743.
  • [16]Higginson IJ, Evans CJ: What is the evidence that palliative care teams improve outcomes for cancer patients and their families? Cancer J 2010, 16:423-435.
  • [17]Gysels MH, Evans C, Higginson IJ: Patient, caregiver, health professional and researcher views and experiences of participating in research at the end of life: a critical interpretive synthesis of the literature. BMC Med Res Methodol 2012, 12:123. BioMed Central Full Text
  • [18]Evans CJ, Harding R, Higginson IJ, on behalf of MORECare: ‘Best practice’ in developing and evaluating palliative and end-of-life care services: a meta-synthesis of research methods for the MORECare project. Palliat Med 2013.
  • [19]Yardley L, Beyer N, Hauer K, McKee K, Ballinger C, Todd C: Recommendations for promoting the engagement of older people in activities to prevent falls. Qual Saf Health Care 2007, 16:230-234.
  • [20]Gysels M, Evans CJ, Lewis P, Speck P, Benalia A, Preston NJ, Grande G, Short V, Owen-Jones E, Todd C, Higginson IJ, on behalf of MORECare: MORECare research methods guidance development: Recommendations for ethical issues in palliative and end-of-life care research. Palliat MedIn press
  • [21]Preston NJ, Fayers P, Walters SJ, Pilling M, Grande G, Short V, Owen-Jones E, Evans CJ, Benalia A, Higginson IJ, Todd C, on behalf of MORECare: Recommendations for managing missing data, attrition and response shift in palliative and end of life care research: Part of the MORECare research methods guidance on statistical issues. Palliat MedIn press
  • [22]Evans CJ, Benalia A, Preston NJ, Grande G, Gysels M, Short V, Daveson BA, Bausewein C, Todd C, Higginson IJ, on behalf of MORECare: The selection and use of outcome measures in palliative and end-of- life care research: the MORECare international consensus workshop. J Pain Symptom ManageIn press
  • [23]Farquhar M, Preston NJ, Short V, Evans CJ, Walshe C, Grande G, Benalia H, Anscombe E, Higginson IJ, Todd C: MORECare research methods guidance development: Recommendations for using mixed methods to develop and evaluate complex interventions in palliative and end of life care [abstract]. Palliat Med 2012, 26:419.
  • [24]Preston NJ, Short V, Hollingworth W, McCrone P, Grande G, Evans CJ, Anscombe E, Benalia A, Higginson IJ, Todd C: MORECare research methods guidance development: Recommendations for health economic evaluation in palliative and end of life care research [abstract]. Palliat Med 2012, 26:541.
  • [25]Perera R, Heneghan C, Yudkin P: Graphical method for depicting randomised trials of complex interventions. BMJ 2007, 334:127-129.
  • [26]Koffman J, Morgan M, Edmonds P, Speck P, Higginson IJ: Vulnerability in palliative care research: findings from a qualitative study of black Caribbean and white British patients with advanced cancer. J Med Ethics 2009, 35:440-444.
  • [27]Dumville JC, Torgerson DJ, Hewitt CE: Reporting attrition in randomised controlled trials. BMJ 2006, 332:969-971.
  • [28]Hewitt CE, Kumaravel B, Dumville JC, Torgerson DJ, Trial attrition study group: Assessing the impact of attrition in randomized controlled trials. J Clin Epidemiol 2010, 63:1264-1270.
  • [29]Bausewein C, Simon ST, Benalia H, Downing J, Mwangi-Powell FN, Daveson BA, Harding R, Higginson IJ: Implementing patient reported outcome measures (PROMs) in palliative care–users’ cry for help. Health Qual Life Outcomes 2011, 9:27. BioMed Central Full Text
  • [30]Tang ST, McCorkle R: Appropriate time frames for data collection in quality of life research among cancer patients at the end of life. Qual Life Res 2002, 11:145-155.
  • [31]Mokkink LB, Terwee CB, Patrick DL, Alonso J, Stratford PW, Knol DL, Bouter LM, de Vet HC: The COSMIN study reached international consensus on taxonomy, terminology, and definitions of measurement properties for health-related patient-reported outcomes. J Clin Epidemiol 2010, 63:737-745.
  • [32]Harding R, Simon ST, Benalia H, Downing J, Daveson BA, Higginson IJ, Bausewein C: The PRISMA Symposium 1: outcome tool use. Disharmony in European outcomes research for palliative and advanced disease care: too many tools in practice. J Pain Symptom Manage 2011, 42:493-500.
  • [33]Simon ST, Higginson IJ, Harding R, Daveson BA, Gysels M, Deliens L, Echteld MA, Radbruch L, Toscani F, Krzyzanowski DM, Costantini M, Downing J, Ferreira PL, Benalia A, Bausewein C, PRISMA: Enhancing patient-reported outcome measurement in research and practice of palliative and end-of-life care. Support Care Cancer 2012, 20:1573-1578.
  • [34]Harvey S, Rowan K, Harrison D, Black N: Using clinical databases to evaluate healthcare interventions. Int J Technol Assess Health Care 2010, 26:86-94.
  • [35]Morrison SR, Penrod J, Cassel B, Caust-Ellenbogen M, Litke A, Spragens L, Meier DE, Palliative Care Leadership Centers’ Outcomes Group: Cost savings associated with US hospital palliative care consultation programs. Arch Int Med 2008, 168:1783-1790.
  • [36]Costantini M, Ottonelli S, Canavacci L, Pellegrini F, Beccaro M: The effectiveness of the Liverpool care pathway in improving end of life care for dying cancer patients in hospital. BMC Health Serv Res 2011, 11:13. BioMed Central Full Text
  • [37]Higginson IJ, Costantini M, Silber E, Burman R, Edmonds P: Evaluation of a new model of short-term palliative care for people severely affected with multiple sclerosis: a randomised fast-track trial to test timing of referral and how long the effect is maintained. Postgrad Med J 2011, 87:769-775.
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