Literature DB >> 21975207

Effect of public deliberation on attitudes toward surrogate consent for dementia research.

S Y H Kim1, H M Kim, D S Knopman, R De Vries, L Damschroder, P S Appelbaum.   

Abstract

OBJECTIVE: To assess the informed, deliberative views of the older general public toward a policy of allowing surrogate consent for Alzheimer disease (AD) research.
METHODS: A total of 503 persons aged 50+ recruited by random digit dialing were randomly assigned to 1 of 3 groups: deliberation, education, or control. The deliberation group attended an all-day education/peer deliberation session; the education group received written information only. Participants were surveyed at baseline, after deliberation session (or equivalent time), and 1 month after the session, regarding their attitudes toward a policy of allowing surrogate consent for research studies of varying risks and potential benefits (a lumbar puncture study, a drug randomized controlled trial, a vaccine randomized controlled trial, and an early phase gene transfer trial).
RESULTS: At baseline, a policy of surrogate consent for AD research was supported by 55%-91%, depending on the scenario. The education group had a transient increase in support for one research scenario after receiving the information materials. In the deliberation group, support for surrogate consent was higher after deliberation for all scenarios (67% to 97%), with much of the increase sustained 1 month after the deliberation session. No changes occurred in the control group. The study's limitations include self-selection of participants due to the demanding nature of attendance at the deliberation sessions.
CONCLUSIONS: This sample of the older general public generally supported a policy of surrogate consent for AD research at baseline. Their support increased with democratic deliberation involving informed, in-depth exploration of the relevant scientific and ethical issues.

Entities:  

Mesh:

Year:  2011        PMID: 21975207      PMCID: PMC3235352          DOI: 10.1212/WNL.0b013e31823648cb

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  14 in total

1.  Assessing the competence of persons with Alzheimer's disease in providing informed consent for participation in research.

Authors:  S Y Kim; E D Caine; G W Currier; A Leibovici; J M Ryan
Journal:  Am J Psychiatry       Date:  2001-05       Impact factor: 18.112

2.  Subacute meningoencephalitis in a subset of patients with AD after Abeta42 immunization.

Authors:  J-M Orgogozo; S Gilman; J-F Dartigues; B Laurent; M Puel; L C Kirby; P Jouanny; B Dubois; L Eisner; S Flitman; B F Michel; M Boada; A Frank; C Hock
Journal:  Neurology       Date:  2003-07-08       Impact factor: 9.910

3.  Proxy consent to participation of the decisionally impaired in medical resesarch--Maryland's policy initiative.

Authors:  D E Hoffman; J Schwartz
Journal:  J Health Care Law Policy       Date:  1998

4.  Proxy consent to research: the legal landscape.

Authors:  Elyn R Saks; Laura B Dunn; Jessica Wimer; Michael Gonzales; Scott Kim
Journal:  Yale J Health Policy Law Ethics       Date:  2008

5.  Deliberative assessment of surrogate consent in dementia research.

Authors:  Scott Y H Kim; Rebecca A Uhlmann; Paul S Appelbaum; David S Knopman; H Myra Kim; Laura Damschroder; Elizabeth Beattie; Laura Struble; Raymond De Vries
Journal:  Alzheimers Dement       Date:  2010-02-26       Impact factor: 21.566

6.  Deliberating about bioethics.

Authors:  A Gutmann; D Thompson
Journal:  Hastings Cent Rep       Date:  1997 May-Jun       Impact factor: 2.683

7.  A phase 1 clinical trial of nerve growth factor gene therapy for Alzheimer disease.

Authors:  Mark H Tuszynski; Leon Thal; Mary Pay; David P Salmon; Hoi Sang U; Roy Bakay; Piyush Patel; Armin Blesch; H Lee Vahlsing; Gilbert Ho; Gang Tong; Steven G Potkin; James Fallon; Lawrence Hansen; Elliott J Mufson; Jeffrey H Kordower; Christine Gall; James Conner
Journal:  Nat Med       Date:  2005-04-24       Impact factor: 53.440

8.  Medical decision-making capacity in patients with mild cognitive impairment.

Authors:  O Okonkwo; H R Griffith; K Belue; S Lanza; E Y Zamrini; L E Harrell; J C Brockington; D Clark; R Raman; D C Marson
Journal:  Neurology       Date:  2007-10-09       Impact factor: 9.910

9.  Surrogate consent for dementia research: a national survey of older Americans.

Authors:  S Y H Kim; H M Kim; K M Langa; J H T Karlawish; D S Knopman; P S Appelbaum
Journal:  Neurology       Date:  2009-01-13       Impact factor: 9.910

Review 10.  Proxy and surrogate consent in geriatric neuropsychiatric research: update and recommendations.

Authors:  Scott Y H Kim; Paul S Appelbaum; Dilip V Jeste; Jason T Olin
Journal:  Am J Psychiatry       Date:  2004-05       Impact factor: 18.112

View more
  15 in total

1.  A framework for assessing the quality of democratic deliberation: enhancing deliberation as a tool for bioethics.

Authors:  Raymond De Vries; Aimee E Stanczyk; Kerry A Ryan; Scott Y H Kim
Journal:  J Empir Res Hum Res Ethics       Date:  2011-09       Impact factor: 1.742

2.  Acceptable Approaches to Enrolling Adults Who Cannot Consent in More Than Minimal Risk Research.

Authors:  Marion Danis; David Wendler; Scott Kim
Journal:  Am J Bioeth       Date:  2015       Impact factor: 11.229

3.  Informed consent, participation in research, and the Alzheimer's patient.

Authors:  Edmund Howe
Journal:  Innov Clin Neurosci       Date:  2012-05

Review 4.  The ethics of informed consent in Alzheimer disease research.

Authors:  Scott Y H Kim
Journal:  Nat Rev Neurol       Date:  2011-05-24       Impact factor: 42.937

5.  Impact of non-welfare interests on willingness to donate to biobanks: an experimental survey.

Authors:  Michele C Gornick; Kerry A Ryan; Scott Y H Kim
Journal:  J Empir Res Hum Res Ethics       Date:  2014-08-11       Impact factor: 1.742

6.  Effect of deliberation on the public's attitudes toward consent policies for biobank research.

Authors:  Tom Tomlinson; Raymond G De Vries; H Myra Kim; Linda Gordon; Kerry A Ryan; Chris D Krenz; Scott Jewell; Scott Y H Kim
Journal:  Eur J Hum Genet       Date:  2018-01-18       Impact factor: 4.246

7.  Effect of Public Deliberation on Patient Attitudes Regarding Consent and Data Use in a Learning Health Care System for Oncology.

Authors:  Reshma Jagsi; Kent A Griffith; Rochelle D Jones; Chris Krenz; Michele Gornick; Rebecca Spence; Raymond De Vries; Sarah T Hawley; Robin Zon; Sage Bolte; Navid Sadeghi; Richard L Schilsky; Angela R Bradbury
Journal:  J Clin Oncol       Date:  2019-10-02       Impact factor: 44.544

8.  Effect of Public Deliberation on Attitudes toward Return of Secondary Results in Genomic Sequencing.

Authors:  Michele C Gornick; Aaron M Scherer; Erica J Sutton; Kerry A Ryan; Nicole L Exe; Ming Li; Wendy R Uhlmann; Scott Y H Kim; J Scott Roberts; Raymond G De Vries
Journal:  J Genet Couns       Date:  2016-06-16       Impact factor: 2.537

9.  Public's approach to surrogate consent for dementia research: cautious pragmatism.

Authors:  Raymond De Vries; Kerry A Ryan; Aimee Stanczyk; Paul S Appelbaum; Laura Damschroder; David S Knopman; Scott Y H Kim
Journal:  Am J Geriatr Psychiatry       Date:  2013-01-12       Impact factor: 4.105

10.  Processes of consent in research for adults with impaired mental capacity nearing the end of life: systematic review and transparent expert consultation (MORECare_Capacity statement).

Authors:  C J Evans; E Yorganci; P Lewis; J Koffman; K Stone; I Tunnard; B Wee; W Bernal; M Hotopf; I J Higginson
Journal:  BMC Med       Date:  2020-07-22       Impact factor: 8.775

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.