遗传性出血性疾病社区国家研究蓝图基础:健康服务、多样性公平与包容及实施科学的研究优先级数据集
NHF社区咨询制定的遗传性出血性疾病研究优先级数据集,聚焦健康服务、公平包容及实施科学领域的研究倡议。

基本信息
资源简介
遗传性出血性疾病社区国家研究蓝图基础:健康服务、多样性公平与包容及实施科学的研究优先级数据集
【一句话概览】
本数据集是 figshare 公开的文本数据集,收录 4 个文件、合计 71.49 KB,主题涵盖 Community-based participatory research、diversity、equity、inclusion、Health equity,可用于医学自然语言处理(实体识别、信息抽取等),CC BY 4.0 许可开放获取。
【数据集背景】
本数据集源站标题为《Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities in health services; diversity, equity, and inclusion; and implementation science》。配套论文《Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities in health services; diversity, equity, and inclusion; and implementation science》发表于 Expert Review of Hematology(2023),DOI:10.1080/17474086.2023.2183836。项目资助方:The entire State of the Science Research Summit and this manuscript were funded by the National Hemophilia Foundation (NHF).。源站首次发布:2023-03-15。
【数据内容】
源站原始描述:The National Hemophilia Foundation (NHF) conducted extensive all-stakeholder inherited bleeding disorder (BD) community consultations to inform a blueprint for future research. Sustaining and expanding the specialized and comprehensive Hemophilia Treatment Center care model, to better serve all people with inherited BDs (PWIBD), and increasing equitable access to optimal health emerged as top priorities. NHF, with the American Thrombosis and Hemostasis Network (ATHN), convened multidisciplinary…
【数据结构与技术规格】
文件数 4 个,合计 71.49 KB。Suppl Table S2 WG5 SOSRS HSR DEI IS.xlsx:application/vnd.openxmlformats-officedocument.spreadsheetml.sheet,20.57 KB。Suppl Table S3 WG5 SOSRS HSR DEI IS.xlsx:application/vnd.openxmlformats-officedocument.spreadsheetml.sheet,14.62 KB。Suppl Table S4 WG5 SOSRS HSR DEI IS.xlsx:application/vnd.openxmlformats-officedocument.spreadsheetml.sheet,17.60 KB。数据集 DOI:10.6084/m9.figshare.22277845.v1。
【主题与分类】
源站学科分类:Medicine、Biotechnology、Science Policy。主题标签:Community-based participatory research、diversity、equity、inclusion、Health equity、Health services research、Implementation science、Inherited bleeding disorders、National Hemophilia Foundation、Public health。
【适用方向】
文本类数据可用于医学自然语言处理,如命名实体识别、信息抽取与文本分类。
【获取与许可】
源站页面:https://tandf.figshare.com/articles/dataset/Building_the_foundation_for_a_community-generated_national_research_blueprint_for_inherited_bleeding_disorders_research_priorities_in_health_services_diversity_equity_and_inclusion_and_implementation_science/22277845
使用许可:CC BY 4.0(https://creativecommons.org/licenses/by/4.0/)。
规范引用:Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities in health services; diversity, equity, and inclusion; and implementation science. Taylor & Francis. Byams, Vanessa R.; Baker, Judith R.; Bailey, Cindy; Connell, Nathan…
【使用注意】
· 源站最后修改于 2023-06-02,引用时请注意版本时效。
下载信息
注册下载
需要注册 Kaggle 账号并登录后下载,适合需要跟踪下载记录和使用 API 的用户。
暂未开放公开下载
无需注册即可直接获取公开样本或文档,适合快速预览和评估数据集质量。
免登录有偿下载
公开数据集受托下载与技术交付服务。
提供高速下载与技术交付服务(收技术服务费,非数据销售)
暂未开放当前数据集主要来源为 Kaggle 公开托管,完整影像包建议通过原始链接或 Kaggle API 获取。
使用方式
数据集获取(Figshare)
- 源站标题:Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities in health services; diversity, equity, and inclusion; and implementation science
- DOI:10.6084/m9.figshare.22277845.v1
- 发布日期:2023-03-15
- 文件数:4 个
- 文件总体积:71.49 KB
- 源站页面:https://tandf.figshare.com/articles/dataset/Building_the_foundation_for_a_community-generated_national_research_blueprint_for_inherited_bleeding_disorders_research_priorities_in_health_services_diversity_equity_and_inclusion_and_implementation_science/22277845
命令行下载
curl -L -o "Suppl Table S2 WG5 SOSRS HSR DEI IS.xlsx" "https://ndownloader.figshare.com/files/39620242"
curl -L -o "Suppl Table S3 WG5 SOSRS HSR DEI IS.xlsx" "https://ndownloader.figshare.com/files/39620245"
curl -L -o "Suppl Table S4 WG5 SOSRS HSR DEI IS.xlsx" "https://ndownloader.figshare.com/files/39620248"
curl -L -o "Supplementary Table S1 WG5 SOSRS HSR DEI IS.docx" "https://ndownloader.figshare.com/files/39620251"
文件清单
Suppl Table S2 WG5 SOSRS HSR DEI IS.xlsx(20.57 KB)Suppl Table S3 WG5 SOSRS HSR DEI IS.xlsx(14.62 KB)Suppl Table S4 WG5 SOSRS HSR DEI IS.xlsx(17.60 KB)Supplementary Table S1 WG5 SOSRS HSR DEI IS.docx(18.70 KB)
文件总体积 71.49 KB(源站 API 实测)。
数据说明
The National Hemophilia Foundation (NHF) conducted extensive all-stakeholder inherited bleeding disorder (BD) community consultations to inform a blueprint for future research. Sustaining and expanding the specialized and comprehensive Hemophilia Treatment Center care model, to better serve all people with inherited BDs (PWIBD), and increasing equitable access to optimal health emerged as top priorities.
NHF, with the American Thrombosis and Hemostasis Network (ATHN), convened multidisciplinary expert working groups (WG) to distill priority research initiatives from consultation findings. WG5 was charged with prioritizing health services research (HSR); diversity, equity, and inclusion (DEI); and implementation science (IS) research initiatives to advance community-identified priorities.
WG5 identified multiple priority research themes and initiatives essential to capitalizing on this potential. Formative studies using qualitative and mixed methods approaches should be conducted to characterize issues and meaningfully investigate interventions. Investment in HSR, DEI and IS education, training, and workforce development are vital.
An enormous amount of work is required in the areas of HSR, DEI, and IS, which have received inadequate attention in inherited BDs. This research has great potential to evolve the experiences of PWIBD, deliver transformational community-based care, and advance health equity.
Research into how people get their health care, called health services research, is important to understand if care is being delivered equitably and efficiently. This research figures out how to provide the best care at the lowest cost and finds out if everyone gets equally good care. Diversity and inclusion research focuses on whether all marginalized and minoritized populations (such as a given social standing, race, ethnicity, sex, gender identity, sexuality, age, income, disability status, language, culture, faith, geographic location, or country of birth) receive equitable care. This includes checking whether different populations are all getting the care they need and looking for ways to improve the care. Implementation science studies how to make a poten
许可
CC BY 4.0
引用
学术使用请引用 DOI 10.6084/m9.figshare.22277845.v1(source: https://tandf.figshare.com/articles/dataset/Building_the_foundation_for_a_community-generated_national_research_blueprint_for_inherited_bleeding_disorders_research_priorities_in_health_services_diversity_equity_and_inclusion_and_implementation_science/22277845)。
数据缺失?
依托陕西、四川两大基地,我们与超过十家三甲医院建立直接合作关系,覆盖合规授权、采集治理、专业标注、数据交付的全流程,为AI医疗团队提供即拿即用的高质量临床数据。
⚡️ 需要数据支持或标注服务?立即联系我们获取专业方案。




