Allen Brian S, Kidd Mehgan, Sue Paul K, Filkins Laura M
Department of Pediatrics, Division of Infectious Diseases, University of Missouri School of Medicine, Columbia, MO, United States.
Department of Pediatrics, Division of Infectious Diseases, University of Texas Southwestern Medical Center, Dallas, TX, United States.
J Appl Lab Med. 2025 Jan 3;10(1):59-65. doi: 10.1093/jalm/jfae084.
Metagenomic next-generation sequencing (mNGS) for pathogen detection offers the potential for broad pathogen detection directly from clinical specimens. However, the yield and impact of testing is variable, financial cost is high, and questions surrounding its optimal use remain. Our pediatric institution used a clinical committee-based approach to discuss and approve or deny mNGS test requests. In this study, we evaluate the patient characteristics for which mNGS testing was considered, test yield, and clinical impact of mNGS results when employing this model of diagnostic stewardship.
Patients for which plasma cell-free DNA mNGS testing was requested and assessed by the clinical committee between August 1, 2018, and April 30, 2021, were included. The committee discussion emails were used to evaluate reasons for making the test request and treatment plans. Patient characteristics and additional clinical information were gathered by chart review. For approved cases, the clinical impact of the mNGS results were retrospectively adjudicated by infectious disease and clinical microbiology experts.
Twelve requests for plasma cell-free DNA mNGS were evaluated and 9 were approved. mNGS results led to a positive clinical management change in 55% of approved requests. Negative clinical impact of mNGS testing did not occur during the study. The patients for which testing requests were denied had resolution of symptoms without further intervention.
This committee-based test request approval diagnostic stewardship model has the potential to support high-yield mNGS testing while using healthcare resources responsibly.
用于病原体检测的宏基因组下一代测序(mNGS)为直接从临床标本中进行广泛的病原体检测提供了可能。然而,检测的产量和影响各不相同,财务成本高昂,围绕其最佳使用的问题仍然存在。我们的儿科机构采用基于临床委员会的方法来讨论并批准或拒绝mNGS检测请求。在本研究中,我们评估了考虑进行mNGS检测的患者特征、检测产量以及采用这种诊断管理模式时mNGS结果的临床影响。
纳入2018年8月1日至2021年4月30日期间临床委员会请求并评估了游离血浆DNA mNGS检测的患者。委员会讨论邮件用于评估提出检测请求的原因和治疗计划。通过病历审查收集患者特征和其他临床信息。对于获批病例,由传染病和临床微生物学专家对mNGS结果的临床影响进行回顾性判定。
评估了12项游离血浆DNA mNGS检测请求,其中9项获批。mNGS结果使55%的获批请求在临床管理上产生了积极变化。研究期间未出现mNGS检测的负面临床影响。检测请求被拒绝的患者症状自行缓解,无需进一步干预。
这种基于委员会的检测请求批准诊断管理模式有潜力支持高产的mNGS检测,同时合理利用医疗资源。