Liu Ville, Koskela Tuomas H, Kaila Minna
Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
JMIR Res Protoc. 2023 Jul 19;12:e41423. doi: 10.2196/41423.
The national Omaolo digital social welfare and health care service of Finland provides a symptom checker, Omaolo, which is a medical device (based on Duodecim Clinical Decision Support EBMEDS software) with a CE marking (risk class IIa), manufactured by the government-owned DigiFinland Oy. Users of this service can perform their triage by using the questions in the symptom checker. By completing the symptom checker, the user receives a recommendation for action and a service assessment with appropriate guidance regarding their health problems on the basis of a selected specific symptom in the symptom checker. This allows users to be provided with appropriate health care services, regardless of time and place.
This study describes the protocol for the mixed methods validation process of the symptom checker available in Omaolo digital services.
This is a mixed methods study using quantitative and qualitative methods, which will be part of the clinical validation process that takes place in primary health care centers in Finland. Each organization provides a space where the study and the nurse triage can be done in order to include an unscreened target population of users. The primary health care units provide walk-in model services, where no prior phone call or contact is required. For the validation of the Omaolo symptom checker, case vignettes will be incorporated to supplement the triage accuracy of rare and acute cases that cannot be tested extensively in real-life settings. Vignettes are produced from a variety of clinical sources, and they test the symptom checker in different triage levels by using 1 standardized patient case example.
This study plan underwent an ethics review by the regional permission, which was requested from each organization participating in the research, and an ethics committee statement was requested and granted from Pirkanmaa hospital district's ethics committee, which is in accordance with the University of Tampere's regulations. Of 964 clinical user-filled symptom checker assessments, 877 cases were fully completed with a triage result, and therefore, they met the requirements for clinical validation studies. The goal for sufficient data has been reached for most of the chief symptoms. Data collection was completed in September 2019, and the first feasibility and patient experience results were published by the end of 2020. Case vignettes have been identified and are to be completed before further testing the symptom checker. The analysis and reporting are estimated to be finalized in 2024.
The primary goals of this multimethod electronic symptom checker study are to assess safety and to provide crucial information regarding the accuracy and usability of the Omaolo electronic symptom checker. To our knowledge, this will be the first study to include real-life clinical cases along with case vignettes.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/41423.
芬兰国家Omaolo数字社会福利与医疗保健服务提供了一款症状检查器Omaolo,它是一种带有CE标志(风险等级IIa)的医疗设备(基于Duodecim临床决策支持EBMEDS软件),由国有公司DigiFinland Oy制造。该服务的用户可以通过使用症状检查器中的问题进行自我分诊。完成症状检查后,用户会收到一份行动建议以及基于症状检查器中所选特定症状对其健康问题的服务评估,并获得适当指导。这使得用户无论何时何地都能获得合适的医疗保健服务。
本研究描述了Omaolo数字服务中症状检查器混合方法验证过程的方案。
这是一项采用定量和定性方法的混合方法研究,将作为芬兰初级卫生保健中心临床验证过程的一部分。每个机构都提供了一个可进行研究和护士分诊的空间,以纳入未经过筛选的目标用户群体。初级卫生保健单位提供即到即看模式服务,无需提前打电话或进行联系。为了验证Omaolo症状检查器,将纳入病例 vignettes 以补充在现实生活场景中无法广泛测试的罕见和急性病例的分诊准确性。vignettes 来自各种临床来源,它们通过使用1个标准化患者病例示例在不同分诊级别测试症状检查器。
本研究计划经过了地区许可的伦理审查,向参与研究的每个机构都提出了申请,并获得了皮尔卡马医院区伦理委员会的伦理委员会声明,这符合坦佩雷大学的规定。在964份临床用户填写的症状检查器评估中,877例病例完全完成并给出了分诊结果,因此符合临床验证研究的要求。大多数主要症状已达到足够数据的目标。数据收集于2019年9月完成,2020年底公布了首批可行性和患者体验结果。病例 vignettes 已确定,在进一步测试症状检查器之前将完成。分析和报告预计于2024年完成。
这项多方法电子症状检查器研究的主要目标是评估安全性,并提供有关Omaolo电子症状检查器准确性和可用性的关键信息。据我们所知,这将是第一项纳入现实生活临床病例以及病例 vignettes 的研究。
国际注册报告识别号(IRRID):DERR1-10.2196/41423。