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来源类型 | Issue Brief |
规范类型 | 简报 |
Child health, big data & ethics | |
Quianta Moore; Tara Blagg | |
发表日期 | 2017-05-23 |
出版年 | 2017 |
语种 | 英语 |
概述 | The Advancing Care for Exceptional Kids Act proposes a national database that would serve as a centralized source of information ... |
摘要 | By Quianta Moore, Tara Blagg and Hannah Todd The Advancing Care for Exceptional Kids Act proposes a national database that would serve as a centralized source of information on children with medically complex conditions. The aim is to improve treatment and care coordination. The authors of this brief argue, however, that the database could put children and their families at risk of discrimination by making their health information public, and therefore accessible to employers and health insurers. |
主题 | Domestic Health Policy |
URL | https://www.bakerinstitute.org/research/ethical-considerations-national-database-children-medical-complexity/ |
来源智库 | James A. Baker III Institute for Public Policy (United States) |
资源类型 | 智库出版物 |
条目标识符 | http://119.78.100.153/handle/2XGU8XDN/80019 |
推荐引用方式 GB/T 7714 | Quianta Moore,Tara Blagg . Child health, big data & ethics. 2017. |
条目包含的文件 | ||||||
文件名称/大小 | 资源类型 | 版本类型 | 开放类型 | 使用许可 | ||
BI-Brief-052317-CHB_(201KB) | 智库出版物 | 限制开放 | CC BY-NC-SA | 浏览 |
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