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本文引用的文献

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Association of Race and Ethnicity and Medicare Program Type With Ambulatory Care Access and Quality Measures.种族和民族以及医疗保险计划类型与门诊护理可及性和质量指标的关联。
JAMA. 2021 Aug 17;326(7):628-636. doi: 10.1001/jama.2021.10413.
2
Race and the Patient-Physician Relationship in 2021.2021年的种族与医患关系
JAMA. 2021 Aug 17;326(7):595-596. doi: 10.1001/jama.2021.12454.
3
Patient characteristics associated with the successful transition to virtual care: Lessons learned from the first million patients.与成功过渡到虚拟护理相关的患者特征:从第一百万患者中吸取的经验教训。
J Telemed Telecare. 2023 Sep;29(8):621-631. doi: 10.1177/1357633X211015547. Epub 2021 Jun 13.
4
Quantifying Patient Portal Use: Systematic Review of Utilization Metrics.量化患者门户使用情况:利用指标的系统评价。
J Med Internet Res. 2021 Feb 25;23(2):e23493. doi: 10.2196/23493.
5
Reducing Administrative Waste in the US Health Care System.减少美国医疗保健系统中的行政浪费。
JAMA. 2021 Feb 2;325(5):427-428. doi: 10.1001/jama.2020.24767.
6
Virtual Care, Telemedicine Visits, and Real Connection in the Era of COVID-19: Unforeseen Opportunity in the Face of Adversity.COVID-19 时代的虚拟护理、远程医疗就诊与真实连接:逆境中的意外机遇
JAMA. 2021 Feb 2;325(5):437-438. doi: 10.1001/jama.2020.27304.
7
National Health Care Spending In 2019: Steady Growth For The Fourth Consecutive Year.2019 年国家医疗保健支出:连续第四年稳步增长。
Health Aff (Millwood). 2021 Jan;40(1):14-24. doi: 10.1377/hlthaff.2020.02022. Epub 2020 Dec 16.
8
COVID-19 and Health Equity-A New Kind of "Herd Immunity".新冠疫情与健康公平——一种新型的“群体免疫”
JAMA. 2020 Jun 23;323(24):2478-2480. doi: 10.1001/jama.2020.8051.
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Disparities in Secure Messaging Uptake Between Patients and Physicians: Longitudinal Analysis of Two National Cross-Sectional Surveys.患者与医生之间安全消息传递使用情况的差异:两项全国性横断面调查的纵向分析
J Med Internet Res. 2020 May 1;22(5):e12611. doi: 10.2196/12611.
10
Failing Another National Stress Test on Health Disparities.在健康差距问题上再次未能通过全国压力测试。
JAMA. 2020 May 19;323(19):1905-1906. doi: 10.1001/jama.2020.6547.

美国老年人的护理协调体验:来自健康与退休研究的证据。

Experiences of care coordination among older adults in the United States: Evidence from the Health and Retirement Study.

机构信息

Center for Social Epidemiology and Population Health, Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, MI, USA.

Center for Social Epidemiology and Population Health, Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, MI, USA; Research Center for Group Dynamics, Institute for Social Research, University of Michigan, Ann Arbor, MI, USA.

出版信息

Patient Educ Couns. 2022 Jul;105(7):2429-2435. doi: 10.1016/j.pec.2022.03.015. Epub 2022 Mar 17.

DOI:10.1016/j.pec.2022.03.015
PMID:35331572
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9203919/
Abstract

INTRODUCTION

The goal of this study was to examine variation in patient experiences and perceptions of care coordination across sociodemographic and health factors.

METHODS

Data come from the 2016 Health and Retirement Study (N = 1, 216). Three domains of coordination were assessed: 1) Perceptions (e.g., patient impressions of provider-provider communication), 2) Tangible supports (e.g., meeting with a care coordinator, being accompanied to appointments), and 3) Technical supports (e.g., use of a "patient portal"). Logistic regression was used to quantify the frequency of each domain and examine variation by racial minority status, socioeconomic status, and health status.

RESULTS

Approximately 42% of older adults perceived poor care coordination, including 14.8% who reported receiving seemingly conflicting advice from different providers. Only one-third had ever met with a formal care coordinator, and 40% were occasionally accompanied to appointments. Although racial minorities were less likely to have access to technical supports, they were more likely to use them. Better perceived coordination was associated with higher care satisfaction (Odds Ratio: 1.43, 95% CI: 1.27-1.61).

CONCLUSIONS

Important gaps in care coordination remain for older adults.

PRACTICE IMPLICATIONS

Providers should consider assessing patient perceptions of care coordination to address these gaps in an equitable manner.

摘要

简介

本研究旨在考察社会人口学和健康因素对患者对医疗协调体验和感知的差异。

方法

数据来自 2016 年健康与退休研究(N=1216)。评估了三个协调领域:1)感知(例如,患者对医生间沟通的印象);2)有形支持(例如,与协调员会面、陪同就诊);3)技术支持(例如,使用“患者门户”)。使用逻辑回归来量化每个领域的频率,并根据种族少数群体状况、社会经济地位和健康状况来检查差异。

结果

约 42%的老年人认为医疗协调不佳,包括 14.8%的人报告说从不同的提供者那里得到了似乎相互矛盾的建议。只有三分之一的人曾见过正式的协调员,40%的人偶尔会陪同就诊。尽管少数族裔获得技术支持的机会较少,但他们更有可能使用这些支持。更好的协调感知与更高的护理满意度相关(优势比:1.43,95%置信区间:1.27-1.61)。

结论

老年人的医疗协调仍存在重要差距。

实践意义

提供者应考虑评估患者对医疗协调的感知,以公平的方式解决这些差距。