Hanson Kimberly E, Caliendo Angela M, Arias Cesar A, Hayden Mary K, Englund Janet A, Lee Mark J, Loeb Mark, Patel Robin, El Alayli Abdallah, Altayar Osama, Patel Payal, Falck-Ytter Yngve, Lavergne Valery, Morgan Rebecca L, Murad M Hassan, Sultan Shahnaz, Bhimraj Adarsh, Mustafa Reem A
Department of Internal Medicine and Pathology, University of Utah, Salt Lake City, Utah.
Department of Medicine, Warren Alpert Medical School of Brown University, Providence, Rhode Island.
Clin Infect Dis. 2021 Jan 22. doi: 10.1093/cid/ciab048.
Accurate molecular diagnostic tests are necessary for confirming a diagnosis of coronavirus disease 2019 (COVID-19). Direct detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) nucleic acids in respiratory tract specimens informs patient, healthcare institution and public health level decision-making. The numbers of available SARS-CoV-2 nucleic acid detection tests are rapidly increasing, as is the COVID-19 diagnostic literature. Thus, the Infectious Diseases Society of America (IDSA) recognized a significant need for frequently updated systematic reviews of the literature to inform evidence-based best practice guidance.
The IDSA's goal was to develop an evidence-based diagnostic guideline to assist clinicians, clinical laboratorians, patients and policymakers in decisions related to the optimal use of SARS-CoV-2 nucleic acid amplification tests. In addition, we provide a conceptual framework for understanding molecular diagnostic test performance, discuss the nuance of test result interpretation in a variety of practice settings and highlight important unmet research needs in the COVID-19 diagnostic testing space.
IDSA convened a multidisciplinary panel of infectious diseases clinicians, clinical microbiologists, and experts in systematic literature review to identify and prioritize clinical questions and outcomes related to the use of SARS-CoV-2 molecular diagnostics. Grading of Recommendations Assessment, Development and Evaluation (GRADE) methodology was used to assess the certainty of evidence and make testing recommendations.
The panel agreed on 17 diagnostic recommendations.
Universal access to accurate SARS-CoV-2 nucleic acid testing is critical for patient care, hospital infection prevention and the public response to the COVID-19 pandemic. Information on the clinical performance of available tests is rapidly emerging, but the quality of evidence of the current literature is considered moderate to very low. Recognizing these limitations, the IDSA panel weighed available diagnostic evidence and recommends nucleic acid testing for all symptomatic individuals suspected of having COVID-19. In addition, testing is recommended for asymptomatic individuals with known or suspected contact with a COVID-19 case. Testing asymptomatic individuals without known exposure is suggested when the results will impact isolation/quarantine/personal protective equipment (PPE) usage decisions, dictate eligibility for surgery, or inform solid organ or hematopoietic stem cell transplantation timing. Ultimately, prioritization of testing will depend on institutional-specific resources and the needs of different patient populations.
准确的分子诊断检测对于确诊2019冠状病毒病(COVID-19)至关重要。直接检测呼吸道标本中的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)核酸有助于患者、医疗机构和公共卫生层面的决策制定。可用的SARS-CoV-2核酸检测试验数量正在迅速增加,COVID-19诊断文献亦是如此。因此,美国传染病学会(IDSA)认识到迫切需要对文献进行频繁更新的系统评价,以为循证最佳实践指南提供依据。
IDSA的目标是制定一项循证诊断指南,以协助临床医生、临床检验师、患者和政策制定者做出与SARS-CoV-2核酸扩增试验的最佳使用相关的决策。此外,我们提供了一个理解分子诊断检测性能的概念框架,讨论了在各种实际环境中检测结果解释的细微差别,并强调了COVID-19诊断检测领域重要的未满足的研究需求。
IDSA召集了一个由传染病临床医生、临床微生物学家和系统文献综述专家组成的多学科小组,以确定与SARS-CoV-2分子诊断使用相关的临床问题和结果,并对其进行优先排序。采用推荐分级评估、制定与评价(GRADE)方法来评估证据的确定性并提出检测建议。
该小组就17项诊断建议达成了一致。
普遍获得准确的SARS-CoV-2核酸检测对于患者护理、医院感染预防以及公众应对COVID-19大流行至关重要。关于现有检测临床性能的信息正在迅速涌现,但当前文献证据的质量被认为是中等至非常低。认识到这些局限性,IDSA小组权衡了现有的诊断证据,并建议对所有疑似患有COVID-19的有症状个体进行核酸检测。此外,建议对已知或疑似与COVID-19病例有接触的无症状个体进行检测。当结果将影响隔离/检疫/个人防护装备(PPE)使用决策、决定手术资格或为实体器官或造血干细胞移植时机提供依据时,建议对无已知暴露的无症状个体进行检测。最终,检测的优先级将取决于机构特定资源和不同患者群体的需求。