A Research Ethics Framework for the Clinical Translation of Healthcare Machine Learning

被引:64
作者
McCradden, Melissa D. [1 ,2 ,3 ]
Anderson, James A. [1 ,4 ]
Stephenson, Elizabeth A. [5 ,6 ]
Drysdale, Erik [2 ]
Erdman, Lauren [2 ,7 ,8 ]
Goldenberg, Anna [1 ,7 ,8 ,9 ]
Shaul, Randi Zlotnik [1 ,6 ,10 ]
机构
[1] Hosp Sick Children, Dept Bioeth, Toronto, ON, Canada
[2] Hosp Sick Children, Peter Gilgan Ctr Res & Learning, Genet & Genome Biol, Toronto, ON, Canada
[3] Dalla Lana Sch Publ Hlth, Div Clin & Publ Hlth, Toronto, ON, Canada
[4] Univ Toronto, Inst Hlth Management Policy & Evaluat, Toronto, ON, Canada
[5] Hosp Sick Children, Labatt Family Heart Ctr, Toronto, ON, Canada
[6] Hosp Sick Children, Dept Pediat, Toronto, ON, Canada
[7] Vector Inst, Toronto, ON, Canada
[8] Univ Toronto, Dept Comp Sci, Toronto, ON, Canada
[9] CIFAR, Toronto, ON, Canada
[10] Hosp Sick Children, Child Hlth Evaluat Sci, Toronto, ON, Canada
关键词
Ethics committees; health care delivery; human subjects research; informed consent; IRB (Institutional Review Board); research ethics; ARTIFICIAL-INTELLIGENCE; BIG DATA; STANDARDS; QUALITY; RISK; FOOD; BIAS;
D O I
10.1080/15265161.2021.2013977
中图分类号
B82 [伦理学(道德学)];
学科分类号
摘要
The application of artificial intelligence and machine learning (ML) technologies in healthcare have immense potential to improve the care of patients. While there are some emerging practices surrounding responsible ML as well as regulatory frameworks, the traditional role of research ethics oversight has been relatively unexplored regarding its relevance for clinical ML. In this paper, we provide a comprehensive research ethics framework that can apply to the systematic inquiry of ML research across its development cycle. The pathway consists of three stages: (1) exploratory, hypothesis-generating data access; (2) silent period evaluation; (3) prospective clinical evaluation. We connect each stage to its literature and ethical justification and suggest adaptations to traditional paradigms to suit ML while maintaining ethical rigor and the protection of individuals. This pathway can accommodate a multitude of research designs from observational to controlled trials, and the stages can apply individually to a variety of ML applications.
引用
收藏
页码:8 / 22
页数:15
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