英国活动过度型Ehlers-Danlos综合征和活动过度谱系障碍生活体验调查

基于英国全国横断面在线调查,收集2002名hEDS/HSD患者数据,揭示诊断延迟、护理获取、常见症状及社会影响。

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The lived experience of hypermobile Ehlers–Danlos syndrome and hypermobility spectrum disorders in the United Kingdom: findings from a national cross-sectional survey

基本信息

模态
表格
大小
0.000332732 GB
许可
CC BY 4.0
创建/更新时间
2026-10-09
版本
v1

资源简介

英国活动过度型Ehlers-Danlos综合征和活动过度谱系障碍生活体验调查

【一句话概览】

本数据集是 figshare 公开的结构化表格数据集,收录 5 个文件、合计 332.73 KB,主题涵盖 Hypermobility、health services、care pathways、disability、neurodivergence,可用于统计建模、特征工程与队列分析,CC BY 4.0 许可开放获取。

【数据集背景】

本数据集源站标题为《The lived experience of hypermobile Ehlers–Danlos syndrome and hypermobility spectrum disorders in the United Kingdom: findings from a national cross-sectional survey》。配套论文《The lived experience of hypermobile Ehlers–Danlos syndrome and hypermobility spectrum disorders in the United Kingdom: findings from a national cross-sectional survey》发表于 Disability and Rehabilitation(2026),DOI:10.1080/09638288.2026.2646723。项目资助方:The author(s) reported there is no funding associated with the work featured in this article.。源站首次发布:2026-04-03。

【数据内容】

源站原始描述:This study explored the lived experiences of individuals with hypermobile Ehlers-Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorder (HSD) in the United Kingdom, focusing on diagnosis, access to care, and impact on daily life. A cross-sectional, mixed-methods online survey was co-developed with patients and clinicians and disseminated via Ehlers-Danlos Support UK social media between September 2023 and January 2024. A total of 2002 valid responses were received. Respondents were predomina…

中文译文(机器翻译,仅供快速理解,请以原文为准):本研究探讨了英国高活动性埃勒斯-当洛斯综合征(hEDS)和高活动性谱系障碍(HSD)患者的亲身经历,重点关注诊断、获得医疗服务的机会以及对日常生活的影响。 一项横断面、混合方法在线调查由患者和临床医生共同开发,并于2023年9月至2024年1月期间通过Ehlers-Danlos Support UK的社交媒体传播。 共收到2002份有效回复。受访者以女性为主(90.9%)。平均诊断延迟为19.0–21.7年。研究注意到地区差异以及对私人医疗的高度依赖。常见症状包括慢性疼痛(83.9%)、关节半脱位(73.8%)和胃肠道表现(66.3%),并且我们观察到神经多样性比例较高。此外还报告了高失业率(45.6%)、教育中断(55.9%)和依赖福利(47.9%)。 我们的研究结果凸显了迫切需要与患者共同设计公平、多学科的照护路径,以减少诊断延迟、改善照护协调,并应对hEDS/HSD的广泛影响。 高活动性埃勒斯-当洛斯综合征(hEDS)和高活动性谱系障碍(HSD)患者常经历慢性疼痛、疲劳和多系统症状,这些问题会显著损害日常功能和生活质量。 获得协调的多学科管理(包括物理治疗、职业治疗和心理支持)的机会目前有限,且往往支离破碎。 支持性自我管理资源应具有神经多样性知情视角,并与患者共同设计,以可及的方式应对身体和社会心理两方面的挑战。 高活动性埃勒斯-当洛斯综合征(hEDS)和高活动性谱系障碍(HSD)患者常经历慢性疼痛、疲劳和多系统症状,这些问题会显著损害日常功能和生活质量。 获得协调的多学科管理(包括物理治疗、职业治疗和心理支持)的机会目前有限,且往往支离破碎。 支持性自我管理资源应具有神经多样性知情视角,并与患者共同设计,以可及的方式应对身体和社会心理两方面的挑战。

【数据结构与技术规格】

文件数 5 个,合计 332.73 KB。idre_a_2646723_sm4289.doc:application/msword,107.01 KB。idre_a_2646723_sm4288.docx:application/vnd.openxmlformats-officedocument.wordprocessingml.document,85.86 KB。idre_a_2646723_sm4287.pdf:application/pdf,97.39 KB。数据集 DOI:10.6084/m9.figshare.31932928.v1。

【主题与分类】

源站学科分类:Medicine、Cell Biology、Biotechnology、Ecology、Biological Sciences not elsewhere classified、Science Policy。主题标签:Hypermobility、health services、care pathways、disability、neurodivergence、mental health、socioeconomic impact。

【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://tandf.figshare.com/articles/dataset/The_lived_experience_of_hypermobile_Ehlers_Danlos_syndrome_and_hypermobility_spectrum_disorders_in_the_United_Kingdom_findings_from_a_national_cross-sectional_survey/31932928

使用许可:CC BY 4.0(https://creativecommons.org/licenses/by/4.0/)。

规范引用:The lived experience of hypermobile Ehlers–Danlos syndrome and hypermobility spectrum disorders in the United Kingdom: findings from a national cross-sectional survey. Taylor & Francis. Berg, Kathryn M.; Dockrell, Dervil M

【使用注意】

· 源站最后修改于 2026-09-26,引用时请注意版本时效。

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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。

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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)

命令行下载

curl -L -o "idre_a_2646723_sm4289.doc" "https://ndownloader.figshare.com/files/63427228"
curl -L -o "idre_a_2646723_sm4288.docx" "https://ndownloader.figshare.com/files/63427231"
curl -L -o "idre_a_2646723_sm4287.pdf" "https://ndownloader.figshare.com/files/63427234"
curl -L -o "idre_a_2646723_sm4286.docx" "https://ndownloader.figshare.com/files/63427237"
curl -L -o "idre_a_2646723_sm4285.docx" "https://ndownloader.figshare.com/files/63427240"

文件清单

  • idre_a_2646723_sm4289.doc(107.01 KB)
  • idre_a_2646723_sm4288.docx(85.86 KB)
  • idre_a_2646723_sm4287.pdf(97.39 KB)
  • idre_a_2646723_sm4286.docx(19.67 KB)
  • idre_a_2646723_sm4285.docx(22.81 KB)

文件总体积 332.73 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

This study explored the lived experiences of individuals with hypermobile Ehlers-Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorder (HSD) in the United Kingdom, focusing on diagnosis, access to care, and impact on daily life.
A cross-sectional, mixed-methods online survey was co-developed with patients and clinicians and disseminated via Ehlers-Danlos Support UK social media between September 2023 and January 2024.
A total of 2002 valid responses were received. Respondents were predominantly female (90.9%). The mean diagnostic delay was 19.0–21.7 years. Regional differences and heavy reliance on private healthcare were noted. Common symptoms included chronic pain (83.9%), joint subluxations (73.8%), and gastrointestinal manifestations (66.3%), and we observed high rates of neurodivergence. High rates of unemployment (45.6%), disrupted education (55.9%), and benefit dependence (47.9%) were also reported.
Our findings highlight the urgent need for equitable, multidisciplinary care pathways co-designed with patients to reduce diagnostic delay, improve care coordination, and address the wide-ranging impacts of hEDS/HSD.

Individuals with hypermobile Ehlers-Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorders (HSD) commonly experience chronic pain, fatigue, and multisystem symptoms that significantly impair daily functioning and quality of life.
Access to coordinated, multidisciplinary management (including physiotherapy, occupational therapy, and psychological support) is currently limited and often fragmented.
Supported self-management resources should be neurodivergence-informed and co-designed with patients to address both physical and psychosocial challenges in an accessible manner.

Individuals with hypermobile Ehlers-Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorders (HSD) commonly experience chronic pain, fatigue, and multisystem symptoms that significantly impair daily functioning and quality of life.
Access to coordinated, multidisciplinary management (including physiotherapy, occupational therapy, and psychological support) is currently limited and often fragmented.
Supported self-management resources should be neurodivergenc

许可

CC BY 4.0

引用

学术使用请引用 DOI 10.6084/m9.figshare.31932928.v1(source: https://tandf.figshare.com/articles/dataset/The_lived_experience_of_hypermobile_Ehlers_Danlos_syndrome_and_hypermobility_spectrum_disorders_in_the_United_Kingdom_findings_from_a_national_cross-sectional_survey/31932928)。

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