Socioeconomic and demographic patterning of family uptake of a paediatric electronic patient portal innovation.

PLOS digital health Pub Date : 2024-10-03 eCollection Date: 2024-10-01 DOI:10.1371/journal.pdig.0000496
Ameenat Lola Solebo, Lisanne Horvat-Gitsels, Christine Twomey, Siegfried Karl Wagner, Jugnoo S Rahi
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Abstract

Patient portals allowing access to electronic health care records and services can inform and empower but may widen existing sociodemographic inequities. We aimed to describe associations between activation of a paediatric patient portal and patient race/ethnicity, socioeconomic status and markers of previous engagement with health care. A retrospective single site cross-sectional study was undertaken to examine patient portal adoption amongst families of children receiving care for chronic or complex disorders within the United Kingdom. Descriptive and multivariable regression analysis was undertaken to describe associations between predictors (Race/Ethnicity, age, socio-economic deprivation status based on family residence, and previous non-attendance to outpatient consultations) and outcome. A sample of 3687 children, representative of the diverse 'real world' patient population, was identified. Of these 37% (1364) were from a White British background, 71% (2631) had English as the primary family spoken language (PSL), 14% (532) lived in areas of high deprivation, and 17% (643) had high (>33%) rates of non-attendance. The families of 73% (2682) had activated the portal. In adjusted analyses, English as a PSL (adjusted odds ratio [aOR] 1.58, 95% confidence interval 1.29-1.95) and multi-morbidity (aOR 1.26, 1.22-1.30) was positively associated with portal activation, whilst families from British Black African backgrounds (aOR 0.68, 0.50-0.93), and those with high rates of non-attendance (aOR 0.48, 0.40-0.58) were less likely to use the portal. Family race/ethnicity and previous low engagement with health care services are potentially key drivers of widening inequity in access to health care following the implementation of patient portals, a digital health innovation intended to inform and empower. Health care providers should be aware that innovative human-driven engagement approaches, targeted towards previously underserved communities, are needed to ensure equitable access to high quality patient-centred care.

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儿科电子患者门户网站创新的社会经济和人口结构模式。
患者门户网站允许访问电子医疗记录和服务,可以提供信息和增强能力,但也可能扩大现有的社会人口不平等。我们旨在描述儿科患者门户网站的激活与患者的种族/民族、社会经济地位和以往参与医疗保健的标志物之间的关联。我们开展了一项回顾性单点横断面研究,以考察英国接受慢性或复杂疾病治疗的儿童家庭采用患者门户网站的情况。研究人员通过描述性和多变量回归分析来描述预测因素(种族/民族、年龄、基于家庭居住地的社会经济贫困状况以及以前未参加门诊咨询的情况)与结果之间的关联。研究确定了 3687 名儿童样本,这些样本代表了 "现实世界 "中的不同患者群体。其中,37%(1364 名)的儿童来自英国白人背景,71%(2631 名)的儿童以英语为主要家庭口语(PSL),14%(532 名)的儿童居住在高度贫困地区,17%(643 名)的儿童未就诊率较高(>33%)。73%(2682 人)的家庭启动了门户网站。在调整后的分析中,英语作为PSL(调整后的几率比[aOR]1.58,95%置信区间1.29-1.95)和多病(aOR 1.26,1.22-1.30)与门户网站的激活呈正相关,而来自英国黑非洲背景的家庭(aOR 0.68,0.50-0.93)和未到会率高的家庭(aOR 0.48,0.40-0.58)使用门户网站的可能性较低。患者门户网站是一项旨在提供信息和增强能力的数字医疗创新,其实施后,家庭种族/民族和以前很少参与医疗服务可能是导致医疗服务不平等扩大的主要原因。医疗服务提供者应该意识到,需要针对以前服务不足的社区采取以人为本的创新参与方法,以确保公平地获得以患者为中心的高质量医疗服务。
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