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本文引用的文献

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Effects of an online personal health record on medication accuracy and safety: a cluster-randomized trial.在线个人健康记录对药物准确性和安全性的影响:一项集群随机试验。
J Am Med Inform Assoc. 2012 Sep-Oct;19(5):728-34. doi: 10.1136/amiajnl-2011-000723. Epub 2012 May 3.
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Access to the medical record for patients and involved providers: transparency through electronic tools.患者及相关医疗服务提供者获取病历:通过电子工具实现透明度。
Ann Intern Med. 2011 Dec 20;155(12):853-4. doi: 10.7326/0003-4819-155-12-201112200-00010.
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Inviting patients to read their doctors' notes: patients and doctors look ahead: patient and physician surveys.邀请患者阅读医生的记录:患者和医生展望未来:患者和医生调查。
Ann Intern Med. 2011 Dec 20;155(12):811-9. doi: 10.7326/0003-4819-155-12-201112200-00003.
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Patient interest in sharing personal health record information: a web-based survey.患者对分享个人健康记录信息的兴趣:一项基于网络的调查。
Ann Intern Med. 2011 Dec 20;155(12):805-10. doi: 10.7326/0003-4819-155-12-201112200-00002.
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Randomized controlled trial of health maintenance reminders provided directly to patients through an electronic PHR.通过电子个人健康档案直接向患者提供健康维护提醒的随机对照试验。
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Personal health records: a scoping review.个人健康记录:范围综述。
J Am Med Inform Assoc. 2011 Jul-Aug;18(4):515-22. doi: 10.1136/amiajnl-2011-000105.
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A method and knowledge base for automated inference of patient problems from structured data in an electronic medical record.一种从电子病历的结构化数据中自动推断患者问题的方法和知识库。
J Am Med Inform Assoc. 2011 Nov-Dec;18(6):859-67. doi: 10.1136/amiajnl-2011-000121. Epub 2011 May 25.
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The digital divide in adoption and use of a personal health record.个人健康记录采用与使用方面的数字鸿沟。
Arch Intern Med. 2011 Mar 28;171(6):568-74. doi: 10.1001/archinternmed.2011.34.
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The "meaningful use" regulation for electronic health records.电子健康记录的“有意义使用”规定。
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Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.研究电子数据采集(REDCap)——一种用于提供转化研究信息学支持的元数据驱动方法和工作流程。
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提高患者参与度:患者对在线查看问题列表的反应。

Increasing patient engagement: patients' responses to viewing problem lists online.

作者信息

Wright A, Feblowitz J, Maloney F L, Henkin S, Ramelson H, Feltman J, Bates D W

机构信息

Division of General Internal Medicine, Brigham & Women's Hospital , Boston, MA ; Partners HealthCare , Boston, MA ; Harvard Medical School , Boston, MA.

Partners HealthCare , Boston, MA.

出版信息

Appl Clin Inform. 2014 Nov 26;5(4):930-42. doi: 10.4338/ACI-2014-07-RA-0057. eCollection 2014.

DOI:10.4338/ACI-2014-07-RA-0057
PMID:25589908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4287672/
Abstract

OBJECTIVE

To characterize the opinions, emotions, and actions taken by patients who viewed their electronic problem list via an online personal health record (PHR).

MATERIALS AND METHODS

An online survey of patients who viewed their problem lists, as maintained by their healthcare provider, in a web-based PHR linked to an electronic health record for the first time.

RESULTS

A total 3,649 patients completed the survey, yielding a response rate of 42.1%. Patient attitudes towards the problem list function were positive overall, with 90.4% rating it at least somewhat useful and 86.7% reporting they would probably or definitely use it again. Nearly half (45.6%) of patients identified at least one major or minor problem missing from their list. After viewing the list, 56.1% of patients reported taking at least one action in response, with 32.4% of patients reporting that they researched a condition on the Internet, 18.3% reported that they contacted their healthcare provider and 16.7% reported changing or planning to change a health behavior (patients could report multiple actions). 64.7% of patients reported feeling at least somewhat happy while viewing their problem list, though others reported feeling sad (30.4%), worried (35.7%) or scared (23.8%) (patients could report multiple emotions). A smaller number of patients reported feeling angry (16.6%) or ashamed (14.3%). Patients who experienced an emotional response were more likely to take action.

CONCLUSION

Overall, patients found the ability to view their problem lists very useful and took action in response to the information. However, some had negative emotions. More research is needed into optimal strategies for supporting patients receiving this information.

摘要

目的

描述通过在线个人健康记录(PHR)查看其电子问题列表的患者的意见、情绪和采取的行动。

材料与方法

对首次在与电子健康记录相关联的基于网络的PHR中查看其医疗服务提供者所维护的问题列表的患者进行在线调查。

结果

共有3649名患者完成了调查,回复率为42.1%。患者对问题列表功能的总体态度是积极的,90.4%的患者认为它至少有些用处,86.7%的患者表示他们可能或肯定会再次使用它。近一半(45.6%)的患者发现其列表中至少遗漏了一个主要或次要问题。查看列表后,56.1%的患者报告至少采取了一项应对行动,32.4%的患者报告他们在互联网上研究了某种病症,18.3%的患者报告他们联系了医疗服务提供者,16.7%的患者报告改变或计划改变健康行为(患者可报告多项行动)。64.7%的患者报告在查看问题列表时至少感到有些高兴,不过也有其他患者报告感到悲伤(30.4%)、担忧(35.7%)或害怕(23.8%)(患者可报告多种情绪)。较少患者报告感到愤怒(16.6%)或羞愧(14.3%)。经历过情绪反应的患者更有可能采取行动。

结论

总体而言,患者发现查看问题列表的功能非常有用,并根据信息采取了行动。然而,一些患者有负面情绪。需要对支持患者接收此信息的最佳策略进行更多研究。