Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program...
-
Upload
gianna-standard -
Category
Documents
-
view
220 -
download
0
Transcript of Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program...
![Page 1: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/1.jpg)
Empowerment of Terminally Ill Research Subjects
Lauren Solberg, JD, MTSAssistant Professor,
Program in Bioethics, Law & Medical ProfessionalismDepartment of Community Health & Family Medicine;
Departments of Aging and Geriatric Research & Psychiatry
Uniformed Services University of the Health SciencesFebruary 10, 2014
![Page 2: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/2.jpg)
Goals of This Session
Discuss perceptions of terminally ill persons as vulnerable research subjects, present counterarguments
Identify ways terminally ill individuals are empowered under law to make clinical care decisions
Describe how informed consent process, other mechanisms can empower terminally ill individuals in research context, combat/counteract perceptions of vulnerability
![Page 3: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/3.jpg)
What is “Terminally Ill”?
Terminally ill person – one who is reasonably expected to die within a short period of time from a particular disease or condition
Ronald Bayer et al., The Care of the Terminally Ill: Mortality and Economics, 309 NEJM 1490 (1983).
“Short period” not necessarily set period
Sometimes individual lives beyond anticipated timeframe
![Page 4: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/4.jpg)
Perceptions of Terminally Ill as Vulnerable Research Population
Google “terminally ill research population” (without quotes)
What results do you see?
![Page 5: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/5.jpg)
![Page 6: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/6.jpg)
![Page 7: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/7.jpg)
Vulnerability Perceived Regardless of Research Type?
Yes
Concerns about potential vulnerability in biomedical research (i.e. clinical trials)
Also concerns about potential vulnerability in social/behavioral research
![Page 8: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/8.jpg)
Perception of Vulnerability of Terminally Ill Based On…
Interpretation of federal regulations, other documents
Possibility of therapeutic misconception
Hope for survival
Potential diminished capacity for consent– Either at the time of enrollment or at some point
during the study
Pressure from physicians (esp. those who may also be researchers)
No right to unapproved drugs
![Page 9: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/9.jpg)
How persuasive are each of these?
Some more so than others…
Let’s discuss!
![Page 10: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/10.jpg)
Vulnerability Under the Regulations
IRBs that regularly review research involving vulnerable populations (such as children, pregnant women, prisoners, or handicapped or mentally disabled persons) should include one or more people with knowledge/experience about working with those populations
45 C.F.R. §46.111(a)(3); 21 C.F.R. §56.107(a); 32 C.F.R. §219.107(a)
![Page 11: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/11.jpg)
Vulnerability Under the Regulations (cont’d)
IRBs must ensure subject selection is equitable – should be cognizant of involvement of vulnerable populations (such as children, prisoners, pregnant women, handicapped, or mentally disabled persons, or economically or educationally disadvantaged persons)
45 C.F.R. §46.107(a)(3); 21 C.F.R. §56.111(a)(3); 32 C.F.R. §219.111(a)(3)
![Page 12: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/12.jpg)
Vulnerability Under the Regulations (cont’d)
When some/all subjects likely to be vulnerable to coercion or undue influence (such as children, prisoners, pregnant women, handicapped, or mentally disabled persons, or economically or educationally disadvantaged persons), IRBs must ensure additional safeguards have been included in the study to protect rights and welfare of these subjects
45 C.F.R. § 46.111(b); 21 C.F.R. §56.111(b); 32 C.F.R. §219.111(b)
![Page 13: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/13.jpg)
The Belmont Report
Published 1979
Terminally ill listed among populations that may be “incompetent”
Concern that comprehension may be limited
http://www.hhs.gov/ohrp/humansubjects/guidance/belmont.html
![Page 14: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/14.jpg)
OHRP’s IRB Guidebook
Last updated in 1993
Chapter 6 – Special Classes of Subjects
Terminally ill considered vulnerable population of research subjects
But should not be excluded from research participation just because of their status
http://www.hhs.gov/ohrp/archive/irb/irb_chapter6ii.htm#g8
![Page 15: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/15.jpg)
Vulnerable Under the Regs?
Terminally ill populations not specifically mentioned in federal human subjects research regulations as vulnerable populations– In either Common Rule or FDA regulations
So decision that terminally ill people are vulnerable subjects is based on local IRB/researcher interpretation (perhaps in conjunction with analysis of other sources)– Other sources only advisory
![Page 16: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/16.jpg)
Therapeutic Misconception
“Research subjects will assume (especially, but not exclusively, in therapeutic research) that decisions about their care are being made solely with their benefit in mind.”
Appelbaum, P. S.; Roth, L. H.; Lidz, C. (1982). "The therapeutic misconception: Informed consent in psychiatric research". International Journal of Law and Psychiatry 5 (3–4): 319–329.
Subject’s false belief that study will provide him/her with therapeutic benefit
Shira Bender et al. (2007). Access for the Terminally Ill to Experimental Medical Innovations: A Three-Pronged Threat. AM J BIOETHICS, 7(10): 3-6.
![Page 17: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/17.jpg)
Misunderstanding of Research = Vulnerability
But this can be said for anyone!
Not just limited to terminally ill individuals
Not even limited to people with “serious” diseases or terminal diseases– Appelbaum study shows therapeutic
misconception in participants in studies about plantar warts, Sjogren’s syndrome
Paul S. Appelbaum, Charles W. Lidz, and Thomas Grisso, “Therapeutic Misconception in Clinical Research: Frequency and Risk Factors,” IRB: Ethics & Human Research 26 No. 2 (2004): 1-8.
![Page 18: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/18.jpg)
Hope for SurvivalTerminally ill cancer patients tend to overestimate survival time
Possible denial of poor prognosis, unrealistic hope of survival
Unrealistic expectations about clinical trials, potential benefits (different from therapeutic misconception)
Manish Agrawal & Mario Danis, End-of-life Care for Terminally Ill Participants in Clinical Research, 5 J. Palliative Med. 729, 732-33 (2002).
BUT…studies report Phase I oncology study participants hope their condition will improve, yet still understand the study
Emily Abdoler et al., The Ethics of Phase 0 Oncology Trials, 14 CLIN. CANCER RES. 3692, 3694 (2008)
![Page 19: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/19.jpg)
“Therapeutic Doublethink”
Doublethink – from Orwell’s 1984 - having 2 contradictory beliefs, accepting both of them
Unrealistic optimism on part of patient doesn’t mean he/she hasn’t accepted terminal diagnosis
Beneficial for patients with cancer– Psychological benefits
Therapeutic Doublethink: A Novel Concept to Ethically Justify Unrealistic Optimism in Patients with Advanced Cancer; Irene Ying, University of Toronto, as presented at ASBH meeting, Oct. 2013
![Page 20: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/20.jpg)
Judging Enrollment Decisions
In general, subjects who understand – and demonstrate understanding of – the study’s purpose(s), risks and benefits, etc. are permitted to consent– More about consent later!
Must subject’s decision to enroll be based on the researcher’s stated purpose of the study? – Can a subject enroll in a study for another reason?– Should subjects enroll in a study only if they enroll
for the “right reasons” (i.e., study’s true purpose)?– Is hope for survival a “wrong reason”?
![Page 21: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/21.jpg)
Subject Compensation – A “Right Reason”?
Ex: community-engaged research/CBPR– Studies show motivation for enrolling is often the
compensation that is offered
Ex: FDA-regulated research– FDA guidance says subject payment incentivizes
research participation, is not a benefit http://www.fda.gov/regulatoryinformation/guidances/ucm126429.htm
So why question other reasons for enrolling in research?
![Page 22: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/22.jpg)
Capacity Concerns
10-40% of terminally ill patients experience cognitive impairment in last months of life
Up to 85% of terminally ill patients experience cognitive impairment in last days of life
Clinical depression could affect capacity – and 5-25% of terminally ill patients suffer from depression
David Casarett, Ethical Considerations in End-of-Life Care and Research, 8 J. Palliative Med. S-148,S-156 (2005).
![Page 23: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/23.jpg)
Cognitive Impairment = Vulnerability
But this can be said for anyone!
< half of terminally ill patients experience cognitive impairment in last months of life
So why consider the population as a whole to be vulnerable?– Instead: terminally ill people who are
cognitively impaired are vulnerable because of limited ability to make decisions
– Not vulnerable because of terminally ill status
![Page 24: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/24.jpg)
Inability to Make Voluntary Decisions
Not because of course of disease, but…
In clinical trials, unreasonable to expect people to accept 50/50 chance of receiving placebo when doing nothing = certain death
“True volunteer” would have reasonable alternative to possibly receiving placebo in clinical trial– Not offering experimental drugs outside of clinical
trial coerces people into studies that aren’t necessarily in their best interests
Can autonomous choice be made if subject has no idea if intervention will work?
![Page 25: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/25.jpg)
Counter-ArgumentSubject doesn’t need to know if intervention will work
Subject just needs to understand limited knowledge about intervention, resulting risk that would be undertaken by enrolling– Especially if study not designed to directly
benefit participant (i.e. Phase I study)
“Decision about what risks a competent person takes in the face of death is fundamentally a personal choice”
Udo Schüklenk & Christopher Lowry. (2009). Terminal Illness and Access to Phase 1 Experimental Agents, Surgeries and Devices: Reviewing the Ethical Arguments. BRIT MED BULLETIN; 89: 7-22.
![Page 26: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/26.jpg)
Physician Pressure to Participate
7% of Phase I oncology study subjects feel moderate or significant pressure to participate
9% think patients in general (not just Phase I-eligible subjects) are subject to physician pressures to participate
Emily Abdoler et al., The Ethics of Phase 0 Oncology Trials, 14 CLIN. CANCER RES. 3692, 3694 (2008).
BUT…these are small numbers
And COI regulations, IRB scrutiny of recruitment procedures helps control this
![Page 27: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/27.jpg)
Limited Access to Unapproved Drugs
Clinical trials likely only way someone with terminal illness will access investigational drug– But not everyone is eligible
Access through expanded access (aka “compassionate use”) possible– But requirements are stringent for receiving
drug this way
![Page 28: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/28.jpg)
U.S. v. Rutherford (1979)
Terminally ill cancer patients sued because U.S. government prohibited sale of unapproved drug (laetrile)
Court of Appeals, 10th circuit held terminally ill patients exempt from FDA restrictions
SCOTUS reversed – FDCA does not provide for exceptions to allow terminally ill to have access to unapproved drugs
![Page 29: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/29.jpg)
SCOTUS’ Reasoning
Pre-FDCA (1938) – Congress concerned about people with fatal illnesses being “shielded from fraudulent cures”
Irreversible consequences if conventional therapy rejected in favor of unproven therapy
Clinical testing ok under FDCA, unfettered access is not
U.S. v. Rutherford, 442 U.S. 544 (1979)
![Page 30: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/30.jpg)
Abigail Alliance v. von Eschenbach
Abigail Burroughs’ dad sued FDA for access to investigational drug being studied in colon cancer patients– She had head/neck cancer
Argued FDA should allow terminally ill to access drugs after completing Phase I investigation, before FDA approval– Compassionate use – after Phase II (or later)
studies complete
![Page 31: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/31.jpg)
Outcome of Abigail Alliance Case
2007 – U.S. Court of Appeals, D.C. held there is no constitutional right to access to drugs not yet approved by FDA– 495 F.3d 695 (D.C. Cir. 2007)
SCOTUS refused to hear appeal
Did the court get it right?
![Page 32: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/32.jpg)
Empowerment Under the Law
Statutes and Regulations
Court opinions
![Page 33: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/33.jpg)
Right to Withhold/Withdraw Treatment
“It cannot be disputed that the Due Process Clause protects an interest in life as well as an interest in refusing life-sustaining medical treatment.”
Cruzan v. MO Dep’t of Health, 497 U.S. 261 (1990)
*Competent people have Due Process right to refuse life-sustaining treatment
![Page 34: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/34.jpg)
Minors Rights Under the Law26 states plus DC allow minors 12+ to consent to contraceptive services
All states plus DC allow all minors to receive STI treatment without parental consent
32 states plus DC allow minors to consent to all prenatal treatment
Abortion – varies (some parental consent, some parental notification, 2 states allow all minors to consent)
http://www.guttmacher.org/statecenter/spibs/spib_OMCL.pdf
![Page 35: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/35.jpg)
Oregon, Washington
OR Death with Dignity Act (1997)
WA Death with Dignity Act (2009)
Patients 18+, residents of OR/WA, can make own health care decisions, diagnosed with terminal illness (< 6 months to live), voluntarily stated wish to die
May voluntarily self-administer medication to end their lives with drugs prescribed by physician for this purpose
Accompanying regulations provide reporting requirements, etc.
![Page 36: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/36.jpg)
Vermont
Patient Choice and Control at End of Life Act, passed in 2013
Modeled after OR statute
First statute legalizing physician-assisted suicide to be passed by legislature
OR initiative approved by 51.3% of voters, WA initiative approved by 57.72% of voters
ASBH presentation, Legal update 2013: top 10 Legal Developments in Bioethics
![Page 37: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/37.jpg)
Montana
Baxter v. MT, 224 P.3d 1211 (2009)– No right to die under MT state constitution– But assisted suicide not against MT public
policy– Consent exception under MT law could apply
to physicians assisting in suicide (no homicide prosecution)
![Page 38: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/38.jpg)
New Mexico
Morris v. Brandenberg (2014)– State of New Mexico, Bernalillo County,
Second Judicial District
“This court cannot envision a right more fundamental, more private or more integral to the liberty, safety and happiness of a New Mexican than the right of a competent, terminally ill patient to choose aid in dying.”
https://newmexico.tylerhost.net/ServeDocument.ashx?SID=0730da82-c2ce-4331-9d34-98fe74190124&RID=001664dd-e045-4d6c-b5ce-1294189b0a7a
![Page 39: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/39.jpg)
Some Statistics
OR – 2013 – 122 prescriptions written under Act– Written by 62 different drs
63 deaths were from prescriptions written in 2013– 71 people died, 8 from 2011, 2012 prescriptions
28 people died from other causes
Remaining 31, ingestion status currently unknown– 7 died but cause unknown, status of remaining
24 unknown
***Most frequently stated end-of-life concern – loss of autonomy
![Page 40: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/40.jpg)
MI, 1997Dignified Death Act (amendments since ‘97)
Patients diagnosed with “reduced life expectancy” or their decision-makers, where appropriate must be informed about:– Recommended medical treatment and alternatives,
and advantages/disadvantages, risks of each– Right to appoint someone to make health care
decisions for them in event of incapacity– Right to make decision about receiving, continuing,
refusing, discontinuing treatment– Right to palliative care– Right to pain and symptom management
![Page 41: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/41.jpg)
CA, 2009
Right to Know End of Life Options Act
When diagnosis of terminal illness made, upon patient’s request, health care provider must provide patient w/ comprehensive information and counseling on end of life care options
Statute details information that must be included – such as right to refuse/withdraw treatment, right to pain management, etc.
![Page 42: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/42.jpg)
NY, 2010
Palliative Care Information Act
Terminally ill patients (with illness/condition reasonably expected to cause death within 6 months) MUST be offered information by health care provider about palliative care, end of life options
![Page 43: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/43.jpg)
Empowerment to Tweet!
![Page 44: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/44.jpg)
![Page 45: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/45.jpg)
Empowerment to Make Clinical Decisions…
Should = empowerment to make decisions about research participation– Concerns about vulnerability of terminally ill not necessarily
strong arguments in favor of vulnerability– Terminally ill can make decisions about
withdrawal/termination of medical care, PAS– Should therefore be presumption that they are not vulnerable– Could be rebuttable presumption based on particular
study, study population
And…We have a mandatory informed consent process under federal regulations to combat vulnerability concerns
![Page 46: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/46.jpg)
Informed Consent Empowers Research Subjects
Because…
By regulation, informed consent process is detailed– 8 required elements of consent– 6 additional elements that shall be provided to
subjects where appropriate
Unless waiver granted by IRB, subjects must explicitly consent to all aspects of non-exempt research
![Page 47: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/47.jpg)
8 Required Elements of Consent
Purpose of the research, description of procedures involved, duration of participation (1)
Risks, benefits of participation (2,3)
Alternatives to participation, if any (4)
How confidentiality of data will be protected (5)
Compensation/treatment in event of injury information (for > minimal risk studies) (6)
Statement that participation is voluntary, withdrawal ok at any time (7)
Contact information for PI, IRB, other key study team members (8)
![Page 48: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/48.jpg)
6 Additional ElementsStatement that treatment/procedure may involve currently unforeseeable risks
Circumstances under which PI may terminate subject's participation without subject's consent
Additional costs to subject for participation
Consequences of decision to withdraw, procedures for terminating participation
Statement that significant new findings which may relate to subject's willingness to continue participation will be provided to the subject
Approx. # of subjects participating in study
![Page 49: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/49.jpg)
Criticisms of Informed Consent
Many criticisms detailed in July 2011 ANPRM
Consent forms too long, too detailed
Really protecting institutions, not participants
Easy to miss important info in consent forms
IRBs too rigid about requiring written consent form where it may not be necessary
ANPRM includes number of possible ways to overcome these issues– http://www.gpo.gov/fdsys/pkg/FR-2011-07-26/pdf/2011-18792.pdf
![Page 50: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/50.jpg)
Good Verbal Discussion Can Help Compensate
Thorough discussion with potential participants (not just vulnerable ones) can help compensate for many of these issues
Especially important with potentially vulnerable population to include this component of consent process
![Page 51: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/51.jpg)
Additional Consent Suggestions
Consider who best person from research team is to consent participant
Discuss potential benefit(s) and potential lack of benefit(s) to allow for voluntary decision-making– Be sure that it is clear what subjects are giving up
in order to participate
Periodic reminders (at designated intervals) of alternatives to participation– Consent is ongoing process– Even if no indication that subject may change
his/her mind
![Page 52: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/52.jpg)
In Event of Incapacity…
Subjects may differ re: desire to participate
May wish to discontinue/not participate – Reaching stage of incapacity = total loss of hope
May wish to participate/continue participation – Hope of regaining capacity– Belief that their families, research teams would
want them to continue– Desire to contribute to research to benefit future
populations
Manish Agrawal & Mario Danis, End-of-life Care for Terminally Ill Participants in Clinical Research, 5 J. Palliative Med. 729, 732 (2002).
![Page 53: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/53.jpg)
Relying on LARs
In event of incapacity, subject’s LAR would make decision about research participation
Predictions by surrogate decision-makers re: end of life care decisions made with 68% accuracy – (U.S. Dep’t of Health & Human Services, Advance Directives and Advance Care Planning: Report
to Congress, Aug. 2008, http://aspe.hhs.gov/daltcp/reports/2008/ADCongRpt.pdf)
– Surrogate may guess incorrectly about desire of individual to participate or not
Advance directive will help ensure participant’s wishes will be carried out
![Page 54: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/54.jpg)
Advance Directives
“Advance Directive” is umbrella
Several types of advance directives that can be executed– Living will– Health Care Surrogate/Proxy, Durable Power of
Attorney
Executing advance directives that specifically address research participation (esp. with re: to specific study/studies), who LAR is, can help ensure wishes re: research participation are honored
![Page 55: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/55.jpg)
![Page 56: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/56.jpg)
A Few Words of Caution
Some criticize ADs, saying they aren’t followed, aren’t produced in time
Some surrogates/proxies may disagree with participant’s stated wishes– Ugly situation!!!
If not study-specific, an AD pertaining to research could be harder to follow
![Page 57: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/57.jpg)
Ethics of Research Still Important!
This is not an argument for allowing any research to go forward as long as subjects consent
Autonomy is not letting subjects make whatever decision they want about whatever may be offered
IRB review and judgment, ethical research is still important!
![Page 58: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/58.jpg)
ConclusionsTerminally ill persons perceived as vulnerable research subjects for variety of reasons
Some of these reasons more persuasive than others
But law empowers terminally ill to make lots of decisions autonomously outside of research context
That empowerment should translate to research setting because of required informed consent process, possibility of executing advance directive addressing research participation
![Page 59: Empowerment of Terminally Ill Research Subjects Lauren Solberg, JD, MTS Assistant Professor, Program in Bioethics, Law & Medical Professionalism Department.](https://reader036.fdocuments.in/reader036/viewer/2022062423/56649c9c5503460f9495b568/html5/thumbnails/59.jpg)
Thank You!
Lauren Solberg, JD, MTS
UF College of Medicine
352-273-5142