research statistics, methods and dilemmas in palliative
DESCRIPTION
Presentation given to KU Palliative Medicine Fellowship April 15th, 2010 Revised March 17, 2011TRANSCRIPT
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Research Methods and Dilemmasin Palliative Care
Christian Sinclair, MD, FAAHPMKansas City Hospice & Palliative Care
March 17, 2011
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D ISCL A IMER DI SCL A IMER
DI S D
This document:does not constitute professional medical advice does not constitute a doctor-patient relationship
Any medical decisions regarding your health should bediscussed with your health care providers.
Use common sense when researching health issues online.
The goal of sharing is to advance medical education.
References are included wherever possible.
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Please Click
lots of links includedin this slidedeck
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Objectives
1. Identify specific barriers to research in palliative care populations
2. Highlight strategies for increased availability for publication and research in academic and non-academic palliative care venues.
3. Discuss basic models of structuring research for symptom control
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Dogmatic Battle
“Don’t do research on the dying”
vs.
“All medicine needs to be evidence based”
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Current Approach to Research
• Experiential and anecdotal– ‘The serendipity model’
• Publish expert guidelines– Identifies knowledge gaps
• Few centers capable of consistent research
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Barriers to Palliative Care Research
• Funding• Infrastructure• Training/Mentor availability• Whole person approach• Rapidly changing patient population• Ethics• Research design
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Barrier: Lack of Funding
• <5 % of palliative investigators rec’d NIH grant• >50% from private sector philanthropy– Robert Woods Johnson Foundation– Open Society Institute– Fetzer Institute– Mayday Fund
• A significant minority with no funding at all• <1% of all NIH grants on palliative care issues
Gelfman LP, Morrison RS. Research funding for palliative medicine. J Palliat Med. 2008
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Solution: Lack of Funding
• Find money trees• Change development requests/distribution• Use private foundation to support
infrastructure over single studies• Write your congressional representatives• Find areas pharma would be interested in
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Barriers: Lack of Infrastructure
• Closely related to funding• Foundation dollars driven to clinical services• Community hospices– Provide bulk of palliative care– Yet little experience/culture of research
• Academic centers – Palliative care low priority compared to others
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Solution: Lack of Infrastructure
• Collaborate with related fields in an institution• Collaborate with research centers• NPCRC Grants for infrastructure/collaboration• Increase workforce to decrease clinical time• Co-opt QI/QA staff• Develop research networks– PoPCRN – Jean Kutner– PCRC – Amy Abernethy and Jean Kutner– KCPCRN? – KU, KCCC, KCHPC, TMC
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Barriers: Lack of Training/Mentors
• Palliative medicine fellowships– Most are 1-year, few do 2-year with research
• Just starting 2nd wave of key researchers– Morrison, Goldstein, Prigerson, Abernethy, Kutner
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Solution: Lack of Training/Mentors
• Research retreats– NPCRC – Annual research retreat– AAHPM –
Leadership Education and Academic Development project (LEAD)
– AAHPM – Mentors project• Find mentors in other fields within institution
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Barriers to Palliative Care Research
• Funding• Infrastructure• Training/Mentor availability• Whole person approach• Rapidly changing patient population• Ethics• Research design
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Barriers: Whole Person Approach
• Primacy of the individual as whole person– Ethical dilemma pitting four major bioethical
principles• Emphasis away from bio-medical model– Reinforced by an interdisciplinary approach
• Clinical duties of the day win over research
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Solutions: Whole Person Approach
• Research is more than a nice add-on• Ethical imperative to correctly treat the
individual• Reinforce good aspects of bio-medical model• Having research staff separate from clinical
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Barriers: Rapidly Changing Patients
• The prognostic dilemma – research attrition• Short temporal access to patients– US Hospice median LOS – Three weeks
• Altered mental status and informed consent• Patients don’t want to participate (?)• Heterogeneous patient population• Multi-system disease• Polypharmacy
NHPCO Facts & Figures Oct 2009.
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Solutions: Rapidly Changing Patients
• Research prognostication – objectively!• Automatic research enrollment at admission• Carefully screen for ability to consent• Develop consent procedures for proxies• Heterogeneous, polypharmacy can be helpful– It is who you are talking care of anyway– PPS studies are great examples
Harrold et al. Is PPS a useful predictor of mortality in a heterogeneous hospice population? J Palliat Med. 2005
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Do Patients Want to Participate?
• Positive themes emerge (60-90%)– Altruism– Benefit self– Maintaining hope
• Few negative themes (10-30%)
White C. 2009
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Do Patients Want to Participate?
Pautex S et al. Is Research Really Problematic in Palliative Care? A Pilot Study. JPSM 2005
Anorexia Delirium
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Barriers: Research Ethics
• IRB approval• Harm of asking dying people about dying (?)• Informed consent• Appropriate methodology• Obligation to do research to please staff• Pediatric populations
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Solutions: Research Ethics
• Work closely with IRB, explain study well• Patients interested in research• Careful informed consent• Understand research methodology• Separate research and clinical staff
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Research Methods
• Data types:– Qualitative– Quantitative
• Study designs:– Observational v. Interventional– Size of study– Singe vs. multi-center design– Quality initiative– Domain of study
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Qualitative Research Methods
• Theories:– Ethnographic– Grounded theory
• Data:– Interviews– Observation
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Research Methods
• Observational– Case study/series– Severity– Prevalence– Descriptive– Narrative– Retrospective– Case-control v cohort
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Wikipedia
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Research Methods
• Interventional– Tool validation– Randomized– Blinded– Quasi-experimental
Research Methods Knowledge Base
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Areas of Study
Grant et al. Current Status of Pall. Care—Clinical Implementation, Education, & Research. 2009
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National Palliative Care Research Center
• Established 2005• Headed by Sean Morrison, MD– Current AAHPM president
• Based out of Mt. Sinai SOM• Funded by
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Dartmouth Atlas
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Future
• American Cancer Society– $1.5M towards palliative care research– 136 applicants with majority in the funding range– Only 7 applicants were given grants• Lack of funds
• Palliative Care Research Collaborative– $7.5M from NINR– Headed by Kutner and Abernethy
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Summary
• Many barriers exist to good palliative care research
• With applied effort they may be overcome• Patients are not afraid of research – Don’t be afraid to ask
• Funding and mentorship opportunities exist
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References Bruera E. Ethical issues in palliative care research. J Palliat Care. 1994 Autumn;10(3):7-9. PubMed PMID: 7531237
. Gelfman LP, Morrison RS. Research funding for palliative medicine. J Palliat Med. 2008 Jan-Feb;11(1):36-43.
Review. PubMed PMID: 18370891. Grant M, Elk R, Ferrell B, Morrison RS, von Gunten CF. Current status of palliative care--clinical implementation,
education, and research. CA Cancer J Clin. 2009 Sep-Oct;59(5):327-35. PubMed PMID: 19729681. Jocham HR, Dassen T, Widdershoven G, Halfens R. Quality of life in palliative care cancer patients: a literature
review. J Clin Nurs. 2006 Sep;15(9):1188-95. Review. PubMed PMID: 16911060. Kaasa S, Caraceni A. Palliative cancer care research. Palliat Med. 2010 Apr;24(3):259-60. PubMed PMID:
20371636. Kaasa S, Radbruch L. Palliative care research--priorities and the way forward. Eur J Cancer. 2008 May;44(8):1175-
9. Epub 2008 Apr 18. PubMed PMID: 18374560.
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ReferencesKaasa S, Hjermstad MJ, Loge JH. Methodological and structural challenges in palliative care research: how
have we fared in the last decades? Palliat Med. 2006 Dec;20(8):727-34. Review. PubMed PMID: 17148527.
Kaasa S, De Conno F. Palliative care research. Eur J Cancer. 2001 Oct;37 Suppl 8:S153-9. Review. PubMed
PMID: 11602381. Kramer BJ, Christ GH, Bern-Klug M, Francoeur RB. A national agenda for social work research in palliative
and end-of-life care. J Palliat Med. 2005 Apr;8(2):418-31. Review. PubMed PMID: 15890053. Rinck GC, van den Bos GA, Kleijnen J, de Haes HJ, Schadé E, Veenhof CH. Methodologic issues in
effectiveness research on palliative cancer care: a systematic review. J Clin Oncol. 1997 Apr;15(4):1697-707. Review. PubMed PMID: 9193371.
Saunders C. Hospice Care. Am J Medicine. 1978. 65, 76-8. PMID: 81612
White C, Hardy J. What do palliative care patients and their relatives think about research in palliative care?-a systematic review. Support Care Cancer. 2009 Aug 25. [Epub ahead of print] PubMed PMID: 19705165.
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ReferencesTodd AMH et al. A Systematic Review Examining the Literature on Attitudes of Patients with Advanced
Cancer Toward Research. JPSM 2009 37(6), p. 1078-1085, DOI: 10.1016/j.jpainsymman.2008.07.009
Pautex S et al. Is Research Really Problematic in Palliative Care? A Pilot Study. JPSM 2005 Vol. 30, Issue 2, Pages 109-111, DOI: 10.1016/j.jpainsymman.2005.05.010
Lipman AG, Jackson KC, Tyler LS. Evidence Based Symptom Control in Palliative Care, 2000informa Healthcare.
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Christian Sinclair, MD, FAAHPM
• Email– [email protected]
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Let’s get connected!Skype: ctsinclair
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