遗传性出血性疾病患者护理不平等性的医疗服务提供者视角数据集
一项关于医疗服务提供者对遗传性出血性疾病患者获取护理不平等性看法的调查数据集。

基本信息
资源简介
遗传性出血性疾病患者护理不平等性的医疗服务提供者视角数据集
【数据集背景】
本数据集源站标题为《Healthcare provider perspectives on inequities in access to care for patients with inherited bleeding disorders》。配套论文《Healthcare provider perspectives on inequities in access to care for patients with inherited bleeding disorders》发表于 PLOS ONE(2020),DOI:10.1371/journal.pone.0229099。源站首次发布:2020-02-20。
【数据内容】
源站原始描述:Introduction The ways in which social determinants of health affect patients with inherited bleeding disorders remains unclear. The objective of this study was to understand healthcare provider perspectives regarding access to care and diagnostic delay amongst this patient population. Methods A healthcare provider survey comprising 24 questions was developed, tested, and subsequently disseminated online with recruitment to all members of The Association of Hemophilia Clinic Directors of Canada (…
【数据结构与技术规格】
文件数 2 个,合计 50.59 KB。pone.0229099.s001.docx:application/vnd.openxmlformats-officedocument.wordprocessingml.document,22.98 KB。pone.0229099.s002.xlsx:application/vnd.openxmlformats-officedocument.spreadsheetml.sheet,27.61 KB。数据集 DOI:10.1371/journal.pone.0229099。
【主题与分类】
源站学科分类:Biotechnology、Ecology、Cancer、Mental Health、Infectious Diseases。主题标签:healthcare provider survey、access、HCP、Hemophilia Clinic Directors、Hemophilia Care、healthcare provider perspectives、member。
【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://plos.figshare.com/articles/dataset/Healthcare_provider_perspectives_on_inequities_in_access_to_care_for_patients_with_inherited_bleeding_disorders/11878827
使用许可:CC BY 4.0(https://creativecommons.org/licenses/by/4.0/)。
规范引用:Arya, Sumedha; Wilton, Pamela; Page, David; Boma-Fischer, Laurence; Floros, Georgina; Dainty, Katie N.; et al. (2020). Healthcare provider perspectives on inequities in access to care for patients with inherited bleeding disorders. PLOS ONE. Dataset
【使用注意】
· 源站最后修改于 2023-06-01,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:Healthcare provider perspectives on inequities in access to care for patients with inherited bleeding disorders
- DOI:10.1371/journal.pone.0229099
- 发布日期:2020-02-20
- 文件数:2 个
- 文件总体积:50.59 KB
- 源站页面:https://plos.figshare.com/articles/dataset/Healthcare_provider_perspectives_on_inequities_in_access_to_care_for_patients_with_inherited_bleeding_disorders/11878827
命令行下载
curl -L -o "pone.0229099.s001.docx" "https://ndownloader.figshare.com/files/21780162"
curl -L -o "pone.0229099.s002.xlsx" "https://ndownloader.figshare.com/files/21780165"
文件清单
pone.0229099.s001.docx(22.98 KB)pone.0229099.s002.xlsx(27.61 KB)
文件总体积 50.59 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
Introduction
The ways in which social determinants of health affect patients with inherited bleeding disorders remains unclear. The objective of this study was to understand healthcare provider perspectives regarding access to care and diagnostic delay amongst this patient population.
Methods
A healthcare provider survey comprising 24 questions was developed, tested, and subsequently disseminated online with recruitment to all members of The Association of Hemophilia Clinic Directors of Canada (N = 73), members of the Canadian Association of Nurses in Hemophilia Care (N = 40) and members of the Canadian Physiotherapists in Hemophilia Care (N = 44).
Results
There were 70 respondents in total, for a total response rate of 45%. HCPs felt that there were diagnostic delays for patients with mild symptomatology (71%, N = 50), women presenting with abnormal uterine bleeding as their only or primary symptom (59%, N = 41), and patients living in rural Canada (50%, N = 35). Fewer respondents felt that factors such as socioeconomic status (46%, N = 32) or race (21%, N = 15) influenced access to care, particularly as compared to the influence of rural location (77%, N = 54).
Discussion
We found that healthcare providers identified patients with mild symptomatology, isolated abnormal uterine bleeding, and residence in rural locations as populations at risk for inequitable access to care. These factors warrant further study, and will be investigated further by our group using our nation-wide patient survey and ongoing in-depth qualitative patient interviews.
许可
CC BY 4.0
引用
学术使用请引用 DOI 10.1371/journal.pone.0229099(source: https://plos.figshare.com/articles/dataset/Healthcare_provider_perspectives_on_inequities_in_access_to_care_for_patients_with_inherited_bleeding_disorders/11878827)。
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。
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