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Electronic clinical decision support algorithms incorporating point-of-care diagnostic tests in low-resource settings: a target product profile

机译:电子临床决策支持算法在资源匮乏的环境中结合了现场诊断测试:目标产品配置文件

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摘要

Health workers in low-resource settings often lack the support and tools to follow evidence-based clinical recommendations for diagnosing, treating and managing sick patients. Digital technologies, by combining patient health information and point-of-care diagnostics with evidence-based clinical protocols, can help improve the quality of care and the rational use of resources, and save patient lives. A growing number of electronic clinical decision support algorithms (CDSAs) on mobile devices are being developed and piloted without evidence of safety or impact. Here, we present a target product profile (TPP) for CDSAs aimed at guiding preventive or curative consultations in low-resource settings. This document will help align developer and implementer processes and product specifications with the needs of end users, in terms of quality, safety, performance and operational functionality. To identify the characteristics of CDSAs, a multidisciplinary group of experts (academia, industry and policy makers) with expertise in diagnostic and CDSA development and implementation in low-income and middle-income countries were convened to discuss a draft TPP. The TPP was finalised through a Delphi process to facilitate consensus building. An agreement greater than 75% was reached for all 40 TPP characteristics. In general, experts were in overwhelming agreement that, given that CDSAs provide patient management recommendations, the underlying clinical algorithms should be human-interpretable and evidence-based. Whenever possible, the algorithm’s patient management output should take into account pretest disease probabilities and likelihood ratios of clinical and diagnostic predictors. In addition, validation processes should at a minimum show that CDSAs are implementing faithfully the evidence they are based on, and ideally the impact on patient health outcomes. In terms of operational needs, CDSAs should be designed to fit within clinic workflows and function in connectivity-challenged and high-volume settings. Data collected through the tool should conform to local patient privacy regulations and international data standards.
机译:资源贫乏地区的卫生工作者通常缺乏支持和工具,无法遵循基于证据的临床建议来诊断,治疗和管理患病患者。数字技术通过将患者健康信息和即时诊断与基于证据的临床协议相结合,可以帮助提高护理质量和合理使用资源,并挽救患者生命。在没有安全或影响证据的情况下,越来越多的移动设备上的电子临床决策支持算法(CDSA)正在开发和试验中。在这里,我们介绍CDSA的目标产品资料(TPP),旨在指导在资源匮乏的地区进行预防或治疗性咨询。本文档将帮助开发人员和实施人员的流程以及产品规格与最终用户在质量,安全性,性能和操作功能方面的需求保持一致。为了确定CDSA的特征,召集了在低收入和中等收入国家诊断和CDSA开发和实施方面具有专长的多学科专家(学术界,行业和政策制定者)​​,讨论了TPP草案。 TPP通过Delphi流程完成,以促进共识的建立。对于所有40个TPP特性,都达成了大于75%的协议。总体而言,专家们以压倒性多数达成共识,因为CDSA可以提供患者管理建议,因此基础的临床算法应为人类可解释且基于证据的。只要有可能,该算法的患者管理输出应考虑疾病的预测试概率以及临床和诊断预测指标的似然比。此外,验证过程至少应表明CDSA正在忠实地执行其所依据的证据,并且最好是对患者健康结果的影响。就运营需求而言,CDSA的设计应适合临床工作流程,并在连接性受到挑战的大批量设置中起作用。通过该工具收集的数据应符合当地患者隐私法规和国际数据标准。

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