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Personal health records in a public hospital: experience at the HIV/AIDS clinic at San Francisco General Hospital.公立医院的个人健康记录:旧金山总医院艾滋病诊所的经验。
J Am Med Inform Assoc. 2010 Mar-Apr;17(2):224-8. doi: 10.1136/jamia.2009.000315.
2
Embracing a health services research perspective on personal health records: lessons learned from the VA My HealtheVet system.从 VA 我的健康档案系统中汲取个人健康记录的卫生服务研究视角的经验教训。
J Gen Intern Med. 2010 Jan;25 Suppl 1(Suppl 1):62-7. doi: 10.1007/s11606-009-1114-6.
3
Disparities in use of a personal health record in a managed care organization.在管理式医疗组织中,个人健康记录的使用存在差异。
J Am Med Inform Assoc. 2009 Sep-Oct;16(5):683-9. doi: 10.1197/jamia.M3169. Epub 2009 Jun 30.
4
Determinants of personal health record use: a large population study at Cleveland Clinic.个人健康记录使用的决定因素:克利夫兰诊所的一项大型人群研究。
J Healthc Inf Manag. 2007 Summer;21(3):44-8.
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A research agenda for personal health records (PHRs).个人健康记录(PHR)的研究议程。
J Am Med Inform Assoc. 2008 Nov-Dec;15(6):729-36. doi: 10.1197/jamia.M2547. Epub 2008 Aug 28.
6
Screening for chronic conditions using a patient internet portal: recruitment for an internet-based primary care intervention.使用患者互联网门户筛查慢性病:基于互联网的初级保健干预措施的招募
J Gen Intern Med. 2008 Apr;23(4):472-5. doi: 10.1007/s11606-007-0443-6.
7
Interest in the use of computerized patient portals: role of the provider-patient relationship.对使用计算机化患者门户网站的兴趣:医患关系的作用。
J Gen Intern Med. 2008 Jan;23 Suppl 1(Suppl 1):20-6. doi: 10.1007/s11606-007-0273-6.
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Early experiences with personal health records.个人健康记录的早期经历。
J Am Med Inform Assoc. 2008 Jan-Feb;15(1):1-7. doi: 10.1197/jamia.M2562. Epub 2007 Oct 18.
9
Rethinking health numeracy: a multidisciplinary literature review.重新思考健康数字素养:一项多学科文献综述。
J Am Med Inform Assoc. 2007 Nov-Dec;14(6):713-21. doi: 10.1197/jamia.M2464. Epub 2007 Aug 21.
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Understanding African Americans' views of the trustworthiness of physicians.了解非裔美国人对医生可信度的看法。
J Gen Intern Med. 2006 Jun;21(6):642-7. doi: 10.1111/j.1525-1497.2006.00485.x.

利用电子病人门户服务于弱势群体。

Use of an electronic patient portal among disadvantaged populations.

机构信息

Department of Pediatrics and of Public Health, Weill Cornell Medical College, New York, NY 10065, USA.

出版信息

J Gen Intern Med. 2011 Oct;26(10):1117-23. doi: 10.1007/s11606-011-1749-y. Epub 2011 Jun 7.

DOI:10.1007/s11606-011-1749-y
PMID:21647748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3181304/
Abstract

BACKGROUND

Electronic patient portals give patients access to information from their electronic health record and the ability to message their providers. These tools are becoming more widely used and are expected to promote patient engagement with health care.

OBJECTIVE

To quantify portal usage and explore potential differences in adoption and use according to patients' socioeconomic and clinical characteristics in a network of federally qualified health centers serving New York City and neighboring counties.

DESIGN

Retrospective analysis of data from portal and electronic health records.

PARTICIPANTS

74,368 adult patients seen between April 2008 and April 2010.

MAIN MEASURES

Odds of receiving an access code to the portal, activating the account, and using the portal more than once

KEY RESULTS

Over the 2 years of the study, 16% of patients (n = 11,903) received an access code. Of these, 60% (n = 7138) activated the account, and 49% (n = 5791) used the account two or more times. Patients with chronic conditions were more likely to receive an access code and to become repeat users. In addition, the odds of receiving an access code were significantly higher for whites, women, younger patients, English speakers, and the insured. The odds of repeat portal use, among those with activated accounts, increased with white race, English language, and private insurance or Medicaid compared to no insurance. Racial disparities were small but persisted in models that controlled for language, insurance, and health status.

CONCLUSIONS

We found good early rates of adoption and use of an electronic patient portal during the first 2 years of its deployment among a predominantly low-income population, especially among patients with chronic diseases. Disparities in access to and usage of the portal were evident but were smaller than those reported recently in other populations. Continued efforts will be needed to ensure that portals are usable for and used by disadvantaged groups so that all patients benefit equally from these technologies.

摘要

背景

电子患者门户使患者能够访问其电子健康记录中的信息,并与医疗服务提供者进行信息交流。这些工具的使用越来越广泛,预计将促进患者参与医疗保健。

目的

在为纽约市及其周边县提供服务的一个联邦合格医疗中心网络中,量化患者使用门户的情况,并根据患者的社会经济和临床特征,探索采用和使用电子患者门户的潜在差异。

设计

对来自门户和电子健康记录的数据进行回顾性分析。

参与者

2008 年 4 月至 2010 年 4 月间就诊的 74368 名成年患者。

主要测量指标

获得门户访问码、激活账户和多次使用门户的几率。

主要结果

在研究的 2 年期间,有 16%的患者(n=11903)收到了访问码。在这些患者中,有 60%(n=7138)激活了账户,有 49%(n=5791)两次或以上使用了账户。患有慢性病的患者更有可能收到访问码并成为重复使用者。此外,白人、女性、年轻患者、英语使用者和有保险的患者获得访问码的几率明显更高。在已激活账户的患者中,与没有保险的患者相比,使用门户的几率随着白种人、英语和私人保险或医疗补助的增加而增加。在控制语言、保险和健康状况后,种族差异仍然存在,但有所缩小。

结论

我们发现,在电子患者门户部署的头 2 年中,在一个以低收入人群为主的人群中,该门户的采用和使用情况良好,尤其是在患有慢性病的患者中。虽然在获得和使用门户方面存在差异,但与最近在其他人群中报告的差异相比,这些差异较小。需要继续努力,确保门户可供弱势群体使用并被其使用,以便所有患者都能平等受益于这些技术。