Ethical Challenges of Risk, Informed Consent, and Posttrial Responsibilities in Human Research With Neural Devices: A Review.


Journal

JAMA neurology
ISSN: 2168-6157
Titre abrégé: JAMA Neurol
Pays: United States
ID NLM: 101589536

Informations de publication

Date de publication:
01 Dec 2019
Historique:
medline: 18 10 2019
pubmed: 18 10 2019
entrez: 18 10 2019
Statut: ppublish

Résumé

Developing more and better diagnostic and therapeutic tools for central nervous system disorders is an ethical imperative. Human research with neural devices is important to this effort and a critical focus of the National Institutes of Health Brain Research Through Advancing Innovative Neurotechnologies (BRAIN) Initiative. Despite regulations and standard practices for conducting ethical research, researchers and others seek more guidance on how to ethically conduct neural device studies. This article draws on, reviews, specifies, and interprets existing ethical frameworks, literature, and subject matter expertise to address 3 specific ethical challenges in neural devices research: analysis of risk, informed consent, and posttrial responsibilities to research participants. Research with humans proceeds after careful assessment of the risks and benefits. In assessing whether risks are justified by potential benefits in both invasive and noninvasive neural device research, the following categories of potential risks should be considered: those related to surgery, hardware, stimulation, research itself, privacy and security, and financial burdens. All 3 of the standard pillars of informed consent-disclosure, capacity, and voluntariness-raise challenges in neural device research. Among these challenges are the need to plan for appropriate disclosure of information about atypical and emerging risks of neural devices, a structured evaluation of capacity when that is in doubt, and preventing patients from feeling unduly pressured to participate. Researchers and funders should anticipate participants' posttrial needs linked to study participation and take reasonable steps to facilitate continued access to neural devices that benefit participants. Possible mechanisms for doing so are explored here. Depending on the study, researchers and funders may have further posttrial responsibilities. This ethical analysis and points to consider may assist researchers, institutional review boards, funders, and others engaged in human neural device research.

Identifiants

pubmed: 31621797
pii: 2752422
doi: 10.1001/jamaneurol.2019.3523
pmc: PMC9395156
mid: NIHMS1811494
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1506-1514

Subventions

Organisme : Intramural NIH HHS
ID : Z99 CL999999
Pays : United States

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Auteurs

Saskia Hendriks (S)

Clinical Center, Department of Bioethics, National Institutes of Health, Bethesda, Maryland.
National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland.

Christine Grady (C)

Clinical Center, Department of Bioethics, National Institutes of Health, Bethesda, Maryland.

Khara M Ramos (KM)

National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland.

Winston Chiong (W)

Department of Neurology, University of California, San Francisco.

Joseph J Fins (JJ)

Division of Medical Ethics, Weill Cornell Medical College, New York, New York.
Consortium for the Advanced Study of Brain Injury, Weill Cornell Medical College, New York, New York.

Paul Ford (P)

Center for Bioethics, Cleveland Clinic, Cleveland, Ohio.

Sara Goering (S)

Department of Philosophy, University of Washington, Seattle.
Center for Neurotechnology, University of Washington, Seattle.

Henry T Greely (HT)

Stanford Law School, Stanford University, Stanford, California.

Katrina Hutchison (K)

Department of Philosophy, Macquarie University, Sydney, New South Wales, Australia.
Australian Research Council, Centre of Excellence for Electromaterials Science, Wollongong, Australia.

Michael L Kelly (ML)

MetroHeath Medical Center, School of Medicine, Department of Neurosurgery, Case Western Reserve University, Cleveland, Ohio.

Scott Y H Kim (SYH)

Clinical Center, Department of Bioethics, National Institutes of Health, Bethesda, Maryland.

Eran Klein (E)

Department of Philosophy, University of Washington, Seattle.
Center for Neurotechnology, University of Washington, Seattle.
Department of Neurology, Oregon Health and Sciences, University of Portland, Portland, Oregon.

Sarah H Lisanby (SH)

Division of Translational Research, National Institute of Mental Health, Bethesda, Maryland.

Helen Mayberg (H)

Center of Advanced Circuit Therapeutics, Icahn School of Medicine at Mount Sinai, New York, New York.

Hannah Maslen (H)

The Oxford Uehiro Centre for Practical Ethics, University of Oxford, Oxford, United Kingdom.

Franklin G Miller (FG)

Division of Medical Ethics, Weill Cornell Medical College, New York, New York.

Karen Rommelfanger (K)

Department of Neurology, Emory University, Atlanta, Georgia.

Sameer A Sheth (SA)

Cognitive Science and Neuromodulation Program, Department of Neurological Surgery, Columbia University College of Physicians and Surgeons, New York, New York.

Anna Wexler (A)

Department of Medical Ethics and Health Policy, University of Pennsylvania, Philadelphia.

Classifications MeSH