Department of Neurology, Liege University Hospital Center, Liège, Belgium.
Neuromuscular Reference Center, Division of Paediatrics University, Hospital University of Liège, Liège, Belgium.
Orphanet J Rare Dis. 2023 Aug 2;18(1):224. doi: 10.1186/s13023-023-02813-3.
Developing drugs for rare diseases is challenging, and the precision and objectivity of outcome measures is critical to this process. In recent years, a number of technologies have increasingly been used for remote monitoring of patient health. We report a systematic literature review that aims to summarize the current state of progress with regard to the use of digital outcome measures for real-life motor function assessment of patients with rare neurological diseases. Our search of published literature identified 3826 records, of which 139 were included across 27 different diseases. This review shows that use of digital outcome measures for motor function outside a clinical setting is feasible and employed in a broad range of diseases, although we found few outcome measures that have been robustly validated and adopted as endpoints in clinical trials. Future research should focus on validation of devices, variables, and algorithms to allow for regulatory qualification and widespread adoption.
开发罕见病药物具有挑战性,而结局测量的精确性和客观性对这一过程至关重要。近年来,许多技术越来越多地被用于远程监测患者的健康状况。我们报告了一项系统的文献综述,旨在总结使用数字结局测量在罕见神经疾病患者的现实生活中的运动功能评估方面的最新进展。我们对已发表文献的搜索确定了 3826 条记录,其中 139 条记录涵盖了 27 种不同的疾病。这项综述表明,在临床环境之外使用数字结局测量进行运动功能评估是可行的,并且在广泛的疾病中得到了应用,尽管我们发现很少有结局测量已经得到了充分的验证,并被采纳为临床试验的终点。未来的研究应集中于设备、变量和算法的验证,以实现监管资格和广泛采用。