Paediatric Personalized Research Network Switzerland (SwissPedHealth): A Joint Paediatric National Data Stream

Rebeca Mozun, Fabiën N. Belle, Andrea Agostini, Matthias R. Baumgartner, Jacques Fellay, Christopher B. Forrest, D Sean Froese, Eric Giannoni, Sandra Goetze, Katrin Hofmann, Philipp Latzin, Roger Lauener, Aurelie Martin Necker, Kelly E. Ormond, Jana Pachlopnik, Patrick G. A. Pedrioli, Klara M. Posfay Barbe, Anita Rauch, Sven Schulzke, Martin Stocker, Ben D. Spycher, Effy Vayena, Tatjana Welzel, Nicola Zamboni, Julia E. Vogt, Luregn J. Schlapbach, Julia A. Bielicki, Claudia E. Kuehni
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Abstract

Introduction: Children represent a large and vulnerable patient group. However, the evidence-base for most paediatric diagnostic and therapeutic procedures remains limited or is often inferred from adults. There is urgency to improve paediatric health care provision based on real-world evidence generation. The digital transformation is a unique opportunity to shape a data-driven, agile, learning health care system and deliver more efficient and personalized care to children and their families. The goal of SwissPedHealth is to build a sustainable and scalable infrastructure to make routine clinical data from paediatric hospitals in Switzerland interoperable, standardized, quality-controlled, and ready for observational research, quality assurance, trials, and health-policy creation. This paper describes the design, aims, and current achievements of SwissPedHealth. Methods and analysis: SwissPedHealth started in September 2022 as one of four National Data Streams co-funded by the Swiss Personalized Health Network (SPHN) and the Personalized Health and Related Technologies (PHRT). SwissPedHealth develops modular governance and regulatory strategies, and harnesses SPHN automatization procedures, in collaboration with clinical data warehouses, the Data Coordination Center, Biomedical Information Technology Network, and other SPHN institutions and funded projects. The SwissPedHealth consortium is led by a multi-site, multi-disciplinary Steering Committee incorporating patient and family representatives. The data stream contains work packages focusing on: 1) governance and implementation of standardized data collection, 2) nested projects to test the feasibility of the data stream, 3) a lighthouse project that enriches the data stream by integrating multi-omics data, aiming to improve diagnoses of rare diseases, and 4) engagement with families through patient and public involvement activities and bioethics interviews. Ethics and dissemination: The health database regulation of SwissPedHealth was approved by the ethics committee (AO_2022-00018). Research findings will be disseminated through national and international conferences, publications in peer-reviewed journals and in lay language via online media and podcasts.
瑞士儿科个性化研究网络(SwissPedHealth):全国儿科联合数据流
导言儿童是一个庞大而脆弱的患者群体。然而,大多数儿科诊断和治疗程序的证据基础仍然有限,或者往往是从成人那里推断出来的。根据真实世界的证据来改善儿科医疗服务已迫在眉睫。数字化转型是一个独特的机会,可借以打造一个数据驱动、灵活、学习型的医疗保健系统,为儿童及其家庭提供更高效、更个性化的医疗保健服务。SwissPedHealth 的目标是建立一个可持续、可扩展的基础设施,使瑞士儿科医院的常规临床数据具有互操作性、标准化、质量可控,并为观察研究、质量保证、试验和卫生政策制定做好准备。本文介绍了 SwissPedHealth 的设计、目标和目前取得的成就。方法与分析:SwissPedHealth 于 2022 年 9 月启动,是由瑞士个性化健康网络 (SPHN) 和个性化健康及相关技术 (PHRT) 共同资助的四个国家数据流之一。SwissPedHealth 与临床数据仓库、数据协调中心、生物医学信息技术网络以及其他 SPHN 机构和资助项目合作,制定模块化治理和监管策略,并利用 SPHN 自动化程序。SwissPedHealth 联合体由一个多站点、多学科的指导委员会领导,其中包括患者和家庭代表。数据流包含以下工作包1)标准化数据收集的管理和实施;2)测试数据流可行性的嵌套项目;3)通过整合多组学数据丰富数据流的灯塔项目,旨在改善罕见病的诊断;4)通过患者和公众参与活动及生物伦理学访谈让家庭参与进来。伦理和传播:SwissPedHealth 的健康数据库条例已获得伦理委员会批准(AO_2022-00018)。研究成果将通过国内和国际会议、在同行评审期刊上发表以及通过网络媒体和播客以通俗语言传播。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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