• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
HIV patients' willingness to share personal health information electronically.艾滋病毒感染者对电子方式分享个人健康信息的意愿。
Patient Educ Couns. 2011 Aug;84(2):e9-12. doi: 10.1016/j.pec.2010.07.013. Epub 2010 Aug 17.
2
Processes and outcomes of developing a continuity of care document for use as a personal health record by people living with HIV/AIDS in New York City.制定一份连续性护理文件的过程和结果,供在纽约市生活的艾滋病毒/艾滋病患者用作个人健康记录。
Int J Med Inform. 2012 Oct;81(10):e63-73. doi: 10.1016/j.ijmedinf.2012.06.004. Epub 2012 Jul 26.
3
Sociotechnical Analysis of Health Information Exchange Consent Processes in an HIV Clinic.艾滋病诊所健康信息交换同意流程的社会技术分析
J Assoc Nurses AIDS Care. 2016 Nov-Dec;27(6):792-803. doi: 10.1016/j.jana.2016.08.001. Epub 2016 Aug 16.
4
Trust, confidentiality, and the acceptability of sharing HIV-related patient data: lessons learned from a mixed methods study about Health Information Exchanges.信任、保密性和共享 HIV 相关患者数据的可接受性:来自健康信息交换混合方法研究的经验教训。
Implement Sci. 2012 Apr 19;7:34. doi: 10.1186/1748-5908-7-34.
5
Willingness to Exchange Health Information via Mobile Devices: Findings From a Population-Based Survey.通过移动设备交换健康信息的意愿:基于人群调查的结果。
Ann Fam Med. 2016 Jan-Feb;14(1):34-40. doi: 10.1370/afm.1888.
6
Sharing medical data for health research: the early personal health record experience.用于健康研究的医学数据共享:早期个人健康记录经验。
J Med Internet Res. 2010 May 25;12(2):e14. doi: 10.2196/jmir.1356.
7
Putting the Focus Back on the Patient: How Privacy Concerns Affect Personal Health Information Sharing Intentions.将焦点重新放回患者身上:隐私担忧如何影响个人健康信息共享意愿。
J Med Internet Res. 2017 Sep 13;19(9):e169. doi: 10.2196/jmir.6877.
8
The Impact of Trust and the Role of the Opt-Out Mechanism in Willingness to Share Health Data via Electronic Health Records in Germany: Telephone Survey Study.信任的影响以及退出机制在德国通过电子健康记录共享健康数据意愿中的作用:电话调查研究
JMIR Hum Factors. 2025 Apr 15;12:e65718. doi: 10.2196/65718.
9
Trust and Health Information Exchanges: Qualitative Analysis of the Intent to Share Personal Health Information.信任与健康信息交流:个人健康信息共享意向的定性分析。
J Med Internet Res. 2023 Aug 30;25:e41635. doi: 10.2196/41635.
10
Consent and widespread access to personal health information for the delivery of care: a large scale telephone survey of consumers' attitudes using vignettes in New Zealand.为提供医疗服务而获取个人健康信息的同意与广泛获取:一项在新西兰使用 vignettes 对消费者态度进行的大规模电话调查。
BMJ Open. 2016 Aug 23;6(8):e011640. doi: 10.1136/bmjopen-2016-011640.

引用本文的文献

1
Measuring the willingness to share personal health information: a systematic review.测量个人健康信息共享意愿:系统评价。
Front Public Health. 2023 Jul 20;11:1213615. doi: 10.3389/fpubh.2023.1213615. eCollection 2023.
2
Understanding the attitudes and experiences of people living with potentially stigmatised long-term health conditions with respect to collecting and sharing health and lifestyle data.了解患有可能遭受污名化的长期健康状况的人群在收集和共享健康及生活方式数据方面的态度和经历。
Digit Health. 2022 Apr 18;8:20552076221089798. doi: 10.1177/20552076221089798. eCollection 2022 Jan-Dec.
3
Behavioral Health Professionals' Perceptions on Patient-Controlled Granular Information Sharing (Part 2): Focus Group Study.行为健康专业人员对患者控制的细粒度信息共享的看法(第2部分):焦点小组研究。
JMIR Ment Health. 2022 Apr 20;9(4):e18792. doi: 10.2196/18792.
4
Considerations for an integrated population health databank in Africa: lessons from global best practices.非洲综合人口健康数据库的考量:全球最佳实践的经验教训
Wellcome Open Res. 2021 Aug 23;6:214. doi: 10.12688/wellcomeopenres.17000.1. eCollection 2021.
5
Factors Associated With Willingness to Share Health Information: Rapid Review.与健康信息分享意愿相关的因素:快速综述
JMIR Hum Factors. 2022 Feb 9;9(1):e20702. doi: 10.2196/20702.
6
Understanding the Barriers and Facilitators to Sharing Patient-Generated Health Data Using Digital Technology for People Living With Long-Term Health Conditions: A Narrative Review.理解使用数字技术为长期健康状况患者共享患者生成的健康数据的障碍和促进因素:叙事评论。
Front Public Health. 2021 Nov 23;9:641424. doi: 10.3389/fpubh.2021.641424. eCollection 2021.
7
The public's comfort with sharing health data with third-party commercial companies.公众对于与第三方商业公司共享健康数据的接受程度。
Humanit Soc Sci Commun. 2020;7(1). doi: 10.1057/s41599-020-00641-5. Epub 2020 Nov 11.
8
Longitudinal analysis of social and behavioral determinants of health in the EHR: exploring the impact of patient trajectories and documentation practices.电子健康记录中健康的社会和行为决定因素的纵向分析:探索患者轨迹和记录实践的影响。
AMIA Annu Symp Proc. 2020 Mar 4;2019:399-407. eCollection 2019.
9
Mental health professional perspectives on health data sharing: Mixed methods study.心理健康专业人士对健康数据共享的看法:混合方法研究。
Health Informatics J. 2020 Sep;26(3):2067-2082. doi: 10.1177/1460458219893848. Epub 2020 Jan 11.
10
Mental health professionals' perceptions on patients control of data sharing.心理健康专业人员对患者数据共享控制权的看法。
Health Informatics J. 2020 Sep;26(3):2011-2029. doi: 10.1177/1460458219893845. Epub 2020 Jan 8.

本文引用的文献

1
Development of an electronic medical record-based clinical decision support tool to improve HIV symptom management.开发一种基于电子病历的临床决策支持工具,以改善艾滋病毒症状管理。
AIDS Patient Care STDS. 2009 Jul;23(7):521-9. doi: 10.1089/apc.2008.0209.
2
Electronic health records in ambulatory care--a national survey of physicians.门诊医疗中的电子健康记录——一项针对医生的全国性调查。
N Engl J Med. 2008 Jul 3;359(1):50-60. doi: 10.1056/NEJMsa0802005. Epub 2008 Jun 18.
3
Development and psychometric assessment of a multidimensional measure of internalized HIV stigma in a sample of HIV-positive adults.对一组HIV阳性成年人样本中内化HIV耻辱感的多维测量方法的开发与心理测量评估。
AIDS Behav. 2008 Sep;12(5):748-58. doi: 10.1007/s10461-008-9375-3. Epub 2008 Apr 4.
4
Health information exchange and patient safety.健康信息交换与患者安全。
J Biomed Inform. 2007 Dec;40(6 Suppl):S40-5. doi: 10.1016/j.jbi.2007.08.011. Epub 2007 Sep 7.
5
Predictors of antiretroviral treatment failure in an urban HIV clinic.城市艾滋病诊所中抗逆转录病毒治疗失败的预测因素
J Acquir Immune Defic Syndr. 2007 Jan 1;44(1):30-7. doi: 10.1097/01.qai.0000248351.10383.b7.
6
Systematic review: impact of health information technology on quality, efficiency, and costs of medical care.系统评价:健康信息技术对医疗质量、效率和成本的影响
Ann Intern Med. 2006 May 16;144(10):742-52. doi: 10.7326/0003-4819-144-10-200605160-00125. Epub 2006 Apr 11.
7
Variations in self-rated health among patients with HIV infection.感染艾滋病毒患者自我评估健康状况的差异。
Qual Life Res. 2006 Apr;15(3):503-14. doi: 10.1007/s11136-005-1946-4.
8
The clinical document architecture and the continuity of care record: a critical analysis.临床文档架构与连续护理记录:批判性分析
J Am Med Inform Assoc. 2006 May-Jun;13(3):245-52. doi: 10.1197/jamia.M1963. Epub 2006 Feb 24.
9
Patients' attitudes towards sharing their health information.患者对分享其健康信息的态度。
Int J Med Inform. 2006 Jul;75(7):530-41. doi: 10.1016/j.ijmedinf.2005.08.009. Epub 2005 Sep 28.
10
Can electronic medical record systems transform health care? Potential health benefits, savings, and costs.电子病历系统能否改变医疗保健?潜在的健康益处、节省的费用和成本。
Health Aff (Millwood). 2005 Sep-Oct;24(5):1103-17. doi: 10.1377/hlthaff.24.5.1103.

艾滋病毒感染者对电子方式分享个人健康信息的意愿。

HIV patients' willingness to share personal health information electronically.

机构信息

Department of Biomedical Informatics, Columbia University, New York, NY 10032, USA.

出版信息

Patient Educ Couns. 2011 Aug;84(2):e9-12. doi: 10.1016/j.pec.2010.07.013. Epub 2010 Aug 17.

DOI:10.1016/j.pec.2010.07.013
PMID:20724095
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3010305/
Abstract

OBJECTIVE

To assess the attitudes of persons living with HIV/AIDS (PLWH) towards having their personal health information (PHI) stored and shared electronically.

METHODS

PLWH (n = 93) in New York City completed surveys using audio computer-assisted self-interview (ACASI) that assessed willingness to share their PHI with various people and entities via a secure electronic network. The survey also included questions on satisfaction with and trust of health care providers, current health, HIV-associated stigma, and frequency of internet access. Data were analyzed with descriptive and multivariate statistical methods.

RESULTS

The majority (84%) of individuals were willing to share their PHI with clinicians involved in their care. Fewer individuals (39%) were as willing to share with non-clinical staff. Willingness to share PHI was positively associated with trust and respect of clinicians.

CONCLUSION

PLWH accepted clinicians' need for access to accurate information. Patients' trust in their primary care providers highlights the importance of the clinician-patient relationship which can be used to engage patients support for health information exchange initiatives.

PRACTICE IMPLICATIONS

As electronic storage and sharing of PHI is increasing, clinicians and PLWH should discuss patients' attitudes towards sharing PHI electronically.

摘要

目的

评估艾滋病毒/艾滋病感染者(PLWH)对其个人健康信息(PHI)进行电子存储和共享的态度。

方法

纽约市的 PLWH(n=93)通过音频计算机辅助自我访谈(ACASI)完成了调查,该调查评估了他们通过安全的电子网络与各种人员和实体共享其 PHI 的意愿。该调查还包括对医疗服务提供者的满意度和信任度、当前健康状况、与 HIV 相关的耻辱感以及互联网访问频率的问题。使用描述性和多变量统计方法对数据进行分析。

结果

大多数(84%)个体愿意与参与其护理的临床医生共享其 PHI。较少的个体(39%)愿意与非临床人员共享。愿意共享 PHI 与对临床医生的信任和尊重呈正相关。

结论

PLWH 接受临床医生对获取准确信息的需求。患者对初级保健提供者的信任突显了医患关系的重要性,这可以用于促使患者支持健康信息交换计划。

实践意义

随着 PHI 的电子存储和共享不断增加,临床医生和 PLWH 应讨论患者对电子共享 PHI 的态度。