Solebo Ameenat Lola, Horvat-Gitsels Lisanne, Twomey Christine, Wagner Siegfried Karl, Rahi Jugnoo S
Population, Policy and Practice Research and Teaching Department, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
PLOS Digit Health. 2024 Oct 3;3(10):e0000496. doi: 10.1371/journal.pdig.0000496. eCollection 2024 Oct.
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.
允许访问电子医疗记录和服务的患者门户可以提供信息并赋予患者权力,但可能会扩大现有的社会人口不平等现象。我们旨在描述儿科患者门户的激活与患者种族/民族、社会经济地位以及先前参与医疗保健的标志之间的关联。我们进行了一项回顾性单中心横断面研究,以调查在英国接受慢性或复杂疾病治疗的儿童家庭中患者门户的采用情况。我们进行了描述性和多变量回归分析,以描述预测因素(种族/民族、年龄、基于家庭住址的社会经济剥夺状况以及先前未参加门诊咨询)与结果之间的关联。我们确定了一个由3687名儿童组成的样本,该样本代表了多样化的“现实世界”患者群体。其中,37%(1364名)来自英国白人背景,71%(2631名)以英语作为主要家庭语言(PSL),14%(532名)生活在高度贫困地区,17%(643名)的未就诊率较高(>33%)。73%(2682名)的家庭激活了该门户。在调整分析中,以英语作为PSL(调整后的优势比[aOR]为1.58,95%置信区间为1.29 - 1.95)和多种疾病(aOR为1.26,1.22 - 1.30)与门户激活呈正相关,而来自英国黑人非洲背景的家庭(aOR为0.68,0.50 - 0.93)以及未就诊率较高的家庭(aOR为0.48,0.40 - 0.58)使用该门户的可能性较小。家庭种族/民族以及先前对医疗保健服务的低参与度可能是实施患者门户(一项旨在提供信息并赋予患者权力的数字健康创新)后医疗保健获取不平等加剧的潜在关键驱动因素。医疗保健提供者应意识到,需要针对先前服务不足的社区采用创新的人为驱动的参与方法,以确保公平获得高质量的以患者为中心的护理。