From the Division of Intramural Research, National Institute on Minority Health and Health Disparities, National Institutes of Health, Bethesda, MD (SET); Division of Intramural Research, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD (SET, AM); School of Medicine, Indiana University, Indianapolis (AM); School of Medicine, Emory University, Atlanta, GA (SC); Division of Intramural Research, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD (EJPS); Office of the Director, National Institute on Minority Health and Health Disparities, Bethesda, MD (EJPS).
J Am Board Fam Med. 2020 Nov-Dec;33(6):953-968. doi: 10.3122/jabfm.2020.06.190402.
Patient access to their medical records through patient portals (PPs) facilitates information exchange and provision of quality health care. Understanding factors that characterize patients with limited access to and use of PPs is needed.
Data were from the 2017-2018 Health Information National Trends Survey 5, Cycles 1 and 2, a nationally representative survey of US adults ≥ 18 years old (n = 6789). Weighted multivariate logistic regressions modeled the associations between patient characteristics and access to, facilitators of use, and use of PPs and their functions.
Individuals without (vs with) a regular doctor (adjusted odds ratio [aOR], 0.4; CI, 0.3-0.5) or health insurance (aOR, 0.4; CI, 0.2-0.7), those with high school (aOR 0.4; CI, 0.3-0.5) or with vocational/some college (aOR, 0.5; CI, 04.-0.7) education (vs college/postgraduate), or those with limited English proficiency (vs those who speak English very well) (aOR, 0.7; CI, 0.5-0.9) were less likely to report accessing their personal medical records. Women (vs men) were more likely to report accessing their medical records (aOR, 1.5; CI, 1.2-1.8). Similar patterns were found for PPs access and facilitators of use. Less consistent associations emerged between patient characteristics and use of PP functionalities.
PP access and use are low. Having a primary care clinician, patient's educational attainment, and being a woman were factors associated with PP access and use, but not race/ethnicity. Once access was achieved, use of PP functionalities was generally uniform across demographic segments. Facilitating PP access and use among all patient populations is warranted.
患者通过患者门户(PP)访问其病历,有助于信息交流和提供高质量的医疗保健。需要了解限制患者访问和使用 PP 的因素。
数据来自 2017-2018 年健康信息国家趋势调查 5 号,循环 1 和 2,这是一项针对美国≥18 岁成年人的全国代表性调查(n=6789)。加权多变量逻辑回归模型分析了患者特征与访问、使用促进因素以及使用 PP 及其功能之间的关联。
与有固定医生(调整后的优势比 [aOR],0.4;95%置信区间 [CI],0.3-0.5)或医疗保险(aOR,0.4;CI,0.2-0.7)的个体相比,没有固定医生或医疗保险的个体(aOR,0.4;CI,0.3-0.5),高中(aOR,0.4;CI,0.3-0.5)或职业/大专(aOR,0.5;CI,0.4-0.7)教育程度(与大学/研究生相比),或英语水平有限(与英语非常好的人相比)(aOR,0.7;CI,0.5-0.9)的个体不太可能报告访问个人医疗记录。女性(与男性相比)更有可能报告访问其医疗记录(aOR,1.5;CI,1.2-1.8)。PP 访问和使用促进因素也存在类似的模式。患者特征与 PP 功能的使用之间存在不太一致的关联。
PP 的访问和使用率较低。拥有初级保健临床医生、患者的教育程度和女性是与 PP 访问和使用相关的因素,但与种族/族裔无关。一旦获得访问权限,PP 功能的使用在各个人口统计群体中通常是一致的。有必要促进所有患者群体对 PP 的访问和使用。