使用个性化风险筛查时间表优化糖尿病视网膜病变筛查项目的工作量和停留时间:一项回顾性队列研究
包含苏格兰糖尿病视网膜病变筛查数据,用于分析个性化风险筛查时间表对工作量、停留时间和疾病风险差异的影响。

基本信息
资源简介
使用个性化风险筛查时间表优化糖尿病视网膜病变筛查项目的工作量和停留时间:一项回顾性队列研究
【数据集背景】
本数据集源站标题为《Use of personalised risk-based screening schedules to optimise workload and sojourn time in screening programmes for diabetic retinopathy: A retrospective cohort study》。配套论文《Use of personalised risk-based screening schedules to optimise workload and sojourn time in screening programmes for diabetic retinopathy: A retrospective cohort study》发表于 PLOS Medicine(2019),DOI:10.1371/journal.pmed.1002945。源站首次发布:2019-10-17。
【数据内容】
源站原始描述:Background National guidelines in most countries set screening intervals for diabetic retinopathy (DR) that are insufficiently informed by contemporary incidence rates. This has unspecified implications for interval disease risks (IDs) of referable DR, disparities in ID between groups or individuals, time spent in referable state before screening (sojourn time), and workload. We explored the effect of various screening schedules on these outcomes and developed an open-access interactive policy t…
【数据结构与技术规格】
文件数 5 个,合计 630.80 KB。pmed.1002945.s001.pdf:application/pdf,569.04 KB。pmed.1002945.s002.docx:application/vnd.openxmlformats-officedocument.wordprocessingml.document,15.02 KB。pmed.1002945.s003.docx:application/vnd.openxmlformats-officedocument.wordprocessingml.document,16.78 KB。数据集 DOI:10.1371/journal.pmed.1002945。
【主题与分类】
源站学科分类:Medicine、Biotechnology、Chemical Sciences not elsewhere classified、Infectious Diseases、Virology。主题标签:grade strata、diabetes registry data、policy、personalised risk-based screening schedules、findings Scottish Diabetic Retinopathy Screening Programme data、workload、1 January 2007、31 December 2016、type 2 diabetes、risk factor data。
【适用方向】
结构化表格数据可直接用于统计建模、特征工程与队列分析。
【获取与许可】
源站页面:https://plos.figshare.com/articles/dataset/Use_of_personalised_risk-based_screening_schedules_to_optimise_workload_and_sojourn_time_in_screening_programmes_for_diabetic_retinopathy_A_retrospective_cohort_study/9996314
使用许可:CC BY 4.0(https://creativecommons.org/licenses/by/4.0/)。
规范引用:Ochs, Andreas; McGurnaghan, Stuart; Black, Mike W.; Leese, Graham P.; Philip, Sam; Sattar, Naveed; et al. (2019). Use of personalised risk-based screening schedules to optimise workload and sojourn time in screening programmes for diabetic retinopathy: A retrospective cohort study. PLOS Medicine. Da…
【使用注意】
· 源站最后修改于 2023-06-04,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:Use of personalised risk-based screening schedules to optimise workload and sojourn time in screening programmes for diabetic retinopathy: A retrospective cohort study
- DOI:10.1371/journal.pmed.1002945
- 发布日期:2019-10-17
- 文件数:5 个
- 文件总体积:630.80 KB
- 源站页面:https://plos.figshare.com/articles/dataset/Use_of_personalised_risk-based_screening_schedules_to_optimise_workload_and_sojourn_time_in_screening_programmes_for_diabetic_retinopathy_A_retrospective_cohort_study/9996314
命令行下载
curl -L -o "pmed.1002945.s001.pdf" "https://ndownloader.figshare.com/files/18029393"
curl -L -o "pmed.1002945.s002.docx" "https://ndownloader.figshare.com/files/18029396"
curl -L -o "pmed.1002945.s003.docx" "https://ndownloader.figshare.com/files/18029399"
curl -L -o "pmed.1002945.s004.docx" "https://ndownloader.figshare.com/files/18029402"
curl -L -o "pmed.1002945.s005.docx" "https://ndownloader.figshare.com/files/18029405"
文件清单
pmed.1002945.s001.pdf(569.04 KB)pmed.1002945.s002.docx(15.02 KB)pmed.1002945.s003.docx(16.78 KB)pmed.1002945.s004.docx(15.27 KB)pmed.1002945.s005.docx(14.68 KB)
文件总体积 630.80 KB(源站 API 实测)。
数据加载示例(图像类)
from PIL import Image
import glob, os
files = (glob.glob(os.path.join(path, "**", "*.png"), recursive=True)
+ glob.glob(os.path.join(path, "**", "*.jpg"), recursive=True)
+ glob.glob(os.path.join(path, "**", "*.tif"), recursive=True))
print("图像文件数:", len(files))
img = Image.open(files[0]); print("尺寸/模式:", img.size, img.mode)
# torchvision Dataset 方式:
# from torchvision import datasets
# ds = datasets.ImageFolder(path) # 要求 子目录=类别
目录组织与标注格式以源站说明和下载后实际文件为准。
数据说明
Background
National guidelines in most countries set screening intervals for diabetic retinopathy (DR) that are insufficiently informed by contemporary incidence rates. This has unspecified implications for interval disease risks (IDs) of referable DR, disparities in ID between groups or individuals, time spent in referable state before screening (sojourn time), and workload. We explored the effect of various screening schedules on these outcomes and developed an open-access interactive policy tool informed by contemporary DR incidence rates.
Methods and findings
Scottish Diabetic Retinopathy Screening Programme data from 1 January 2007 to 31 December 2016 were linked to diabetes registry data. This yielded 128,606 screening examinations in people with type 1 diabetes (T1D) and 1,384,360 examinations in people with type 2 diabetes (T2D). Among those with T1D, 47% of those without and 44% of those with referable DR were female, mean diabetes duration was 21 and 23 years, respectively, and mean age was 26 and 24 years, respectively. Among those with T2D, 44% of those without and 42% of those with referable DR were female, mean diabetes duration was 9 and 14 years, respectively, and mean age was 58 and 52 years, respectively. Individual probability of developing referable DR was estimated using a generalised linear model and was used to calculate the intervals needed to achieve various IDs across prior grade strata, or at the individual level, and the resultant workload and sojourn time. The current policy in Scotland—screening people with no or mild disease annually and moderate disease every 6 months—yielded large differences in ID by prior grade (13.2%, 3.6%, and 0.6% annually for moderate, mild, and no prior DR strata, respectively, in T1D) and diabetes type (2.4% in T1D and 0.6% in T2D overall). Maintaining these overall risks but equalising risk across prior grade strata would require extremely short intervals in those with moderate DR (1–2 months) and very long intervals in those with no prior DR (35–47 months), with little change in workload or average sojourn time. Changing to intervals of 12, 9, and 3 months in T1D and to 24, 9, and 3 months in T2D for no
许可
CC BY 4.0
引用
学术使用请引用 DOI 10.1371/journal.pmed.1002945(source: https://plos.figshare.com/articles/dataset/Use_of_personalised_risk-based_screening_schedules_to_optimise_workload_and_sojourn_time_in_screening_programmes_for_diabetic_retinopathy_A_retrospective_cohort_study/9996314)。
数据缺失?
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