Division of Hematology and Oncology, Department of Pediatrics.
Bioethics Research Center, Department of Medicine, Washington University School of Medicine, St Louis, Missouri.
Pediatrics. 2023 Jun 1;151(6). doi: 10.1542/peds.2023-061213.
After enactment of the 21st Century Cures Act, many health care systems offer adolescents and parents access to electronic health information through online portals. Few studies have evaluated adolescent portal access policies since the implementation of the Cures Act.
We performed structured interviews with informatics administrators in US hospitals with ≥50 dedicated pediatric beds. We performed thematic analysis of challenges to developing and implementing adolescent portal policies.
We interviewed 65 informatics leaders representing 63 pediatric hospitals, 58 health care systems, 29 states, and 14 379 pediatric hospital beds. Most hospitals provided portal access to adolescents (86%) and parents (95%). Filtering of results sent to parental portals ranged widely, with 14% providing unfiltered access, 31% performing minimal filtering for sensitive information, and 43% offering limited access. Portal access policies also varied widely within states. Challenges to developing policies included legislation and compliance issues, tension between confidentiality and usefulness, clinicians' preferences and concerns, limited understanding and investment of institutions in pediatric issues, and limited focus of vendors on pediatric issues. Challenges to implementing policies included technical challenges, educating end-users, potential for parental coercion, harms of bad news, complex enrollment processes, and informatics workforce limitations.
Adolescent portal access policies vary widely across and within states. Informatics administrators identified multiple challenges related to developing and implementing adolescent portal policies. Future efforts should strive to develop intrastate consensus on portal policies and to engage parents and adolescent patients to better understand preferences and needs.
《21 世纪治愈法案》颁布后,许多医疗保健系统通过在线门户为青少年及其家长提供电子健康信息。自《治愈法案》实施以来,很少有研究评估青少年门户访问政策。
我们对美国拥有 50 张以上专用儿科病床的医院的信息管理员进行了结构化访谈。我们对制定和实施青少年门户政策所面临的挑战进行了主题分析。
我们采访了 65 名信息学主管,他们代表了 63 家儿科医院、58 家医疗保健系统、29 个州和 14379 张儿科病床。大多数医院为青少年(86%)和家长(95%)提供门户访问。发送到家长门户的结果过滤范围很广,14%提供无过滤访问,31%对敏感信息进行最小过滤,43%提供有限访问。各州内的门户访问政策也存在很大差异。制定政策的挑战包括立法和合规问题、保密性和有用性之间的紧张关系、临床医生的偏好和担忧、机构对儿科问题的理解和投资有限,以及供应商对儿科问题的关注有限。实施政策的挑战包括技术挑战、教育最终用户、父母胁迫的可能性、坏消息的危害、复杂的注册流程以及信息学劳动力的限制。
青少年门户访问政策在各州之间和内部差异很大。信息管理员确定了与制定和实施青少年门户政策相关的多个挑战。未来的努力应致力于在州内就门户政策达成共识,并让家长和青少年患者参与进来,以更好地了解他们的偏好和需求。