Healios Limited, London, United Kingdom.
Institute of Health Informatics, University College London, London, United Kingdom.
JMIR Mhealth Uhealth. 2023 Nov 17;11:e52377. doi: 10.2196/52377.
Diagnostic delays in autism are common, with the time to diagnosis being up to 3 years from the onset of symptoms. Such delays have a proven detrimental effect on individuals and families going through the process. Digital health products, such as mobile apps, can help close this gap due to their scalability and ease of access. Further, mobile apps offer the opportunity to make the diagnostic process faster and more accurate by providing additional and timely information to clinicians undergoing autism assessments.
The aim of this scoping review was to synthesize the available evidence about digital biomarker tools to aid clinicians, researchers in the autism field, and end users in making decisions as to their adoption within clinical and research settings.
We conducted a structured literature search on databases and search engines to identify peer-reviewed studies and regulatory submissions that describe app characteristics, validation study details, and accuracy and validity metrics of commercial and research digital biomarker apps aimed at aiding the diagnosis of autism.
We identified 4 studies evaluating 4 products: 1 commercial and 3 research apps. The accuracy of the identified apps varied between 28% and 80.6%. Sensitivity and specificity also varied, ranging from 51.6% to 81.6% and 18.5% to 80.5%, respectively. Positive predictive value ranged from 20.3% to 76.6%, and negative predictive value fluctuated between 48.7% and 97.4%. Further, we found a lack of details around participants' demographics and, where these were reported, important imbalances in sex and ethnicity in the studies evaluating such products. Finally, evaluation methods as well as accuracy and validity metrics of available tools were not clearly reported in some cases and varied greatly across studies. Different comparators were also used, with some studies validating their tools against the Diagnostic and Statistical Manual of Mental Disorders criteria and others through self-reported measures. Further, while in most cases, 2 classes were used for algorithm validation purposes, 1 of the studies reported a third category (indeterminate). These discrepancies substantially impact the comparability and generalizability of the results, thus highlighting the need for standardized validation processes and the reporting of findings.
Despite their popularity, systematic evaluations and syntheses of the current state of the art of digital health products are lacking. Standardized and transparent evaluations of digital health tools in diverse populations are needed to assess their real-world usability and validity, as well as help researchers, clinicians, and end users safely adopt novel tools within clinical and research practices.
自闭症的诊断延误很常见,从症状出现到确诊的时间长达 3 年。这种延误对正在经历这一过程的个人和家庭有不利影响。数字健康产品(如移动应用程序)可以通过其可扩展性和易于访问性帮助缩小这一差距。此外,移动应用程序通过向进行自闭症评估的临床医生提供额外的及时信息,为更快、更准确地进行诊断提供了机会。
本综述的目的是综合现有关于数字生物标志物工具的证据,以帮助临床医生、自闭症领域的研究人员和最终用户在临床和研究环境中决定采用这些工具。
我们在数据库和搜索引擎上进行了结构化文献检索,以确定描述应用程序特征、验证研究细节以及商业和研究数字生物标志物应用程序准确性和有效性指标的同行评议研究和监管报告,这些应用程序旨在辅助自闭症诊断。
我们确定了 4 项评估 4 种产品的研究:1 种商业产品和 3 种研究应用程序。所确定应用程序的准确性在 28%到 80.6%之间变化。灵敏度和特异性也有所不同,范围分别为 51.6%至 81.6%和 18.5%至 80.5%。阳性预测值范围为 20.3%至 76.6%,阴性预测值在 48.7%至 97.4%之间波动。此外,我们发现参与者的人口统计学细节缺乏,并且在评估这些产品的研究中,性别和种族存在重要的不平衡。最后,在某些情况下,评估方法以及现有工具的准确性和有效性指标没有明确报告,并且在研究之间差异很大。不同的比较器也被使用,一些研究使用《精神障碍诊断与统计手册》标准验证其工具,而另一些研究则使用自我报告的测量方法。此外,虽然在大多数情况下,算法验证目的使用了 2 个类别,但有 1 个研究报告了第 3 个类别(不确定)。这些差异极大地影响了结果的可比性和通用性,因此需要标准化的验证过程和报告结果。
尽管数字健康产品很受欢迎,但缺乏对其当前技术状况的系统评估和综合分析。需要对不同人群的数字健康工具进行标准化和透明的评估,以评估其实际可用性和有效性,并帮助研究人员、临床医生和最终用户在临床和研究实践中安全地采用新工具。