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用于新型冠状病毒肺炎的快速社区即时检测(RAPTOR-C19):一项平台诊断研究的方案

Rapid community point-of-care testing for COVID-19 (RAPTOR-C19): protocol for a platform diagnostic study.

作者信息

Nicholson Brian D, Hayward Gail, Turner Philip J, Lee Joseph J, Deeks Alexandra, Logan Mary, Moore Abigail, Seeley Anna, Fanshawe Thomas, Oke Jason, Koshiaris Constantinos, Sheppard James P, Hoang Uy, Parimalanathan Vaishnavi, Edwards George, Liyange Harshana, Sherlock Julian, Byford Rachel, Zambon Maria, Ellis Joanna, Bernal Jamie Lopez, Amirthalingam Gayatri, Linley Ezra, Borrow Ray, Howsam Gary, Baines Sophie, Ferreira Filipa, de Lusignan Simon, Perera Rafael, Hobbs F D Richard

机构信息

Nuffield Department of Primary Care Health Sciences, University of Oxford, Radcliffe Observatory Quarter, Woodstock Road, Oxford, OX2 6GG, UK.

National Infection Service, Public Health England, London, UK.

出版信息

Diagn Progn Res. 2021 Feb 8;5(1):4. doi: 10.1186/s41512-021-00093-8.

Abstract

BACKGROUND

The aim of RApid community Point-of-care Testing fOR COVID-19 (RAPTOR-C19) is to assess the diagnostic accuracy of multiple current and emerging point-of-care tests (POCTs) for active and past SARS-CoV2 infection in the community setting. RAPTOR-C19 will provide the community testbed to the COVID-19 National DiagnOstic Research and Evaluation Platform (CONDOR).

METHODS

RAPTOR-C19 incorporates a series of prospective observational parallel diagnostic accuracy studies of SARS-CoV2 POCTs against laboratory and composite reference standards in patients with suspected current or past SARS-CoV2 infection attending community settings. Adults and children with suspected current SARS-CoV2 infection who are having an oropharyngeal/nasopharyngeal (OP/NP) swab for laboratory SARS-CoV2 reverse transcriptase Digital/Real-Time Polymerase Chain Reaction (d/rRT-PCR) as part of clinical care or community-based testing will be invited to participate. Adults (≥ 16 years) with suspected past symptomatic infection will also be recruited. Asymptomatic individuals will not be eligible. At the baseline visit, all participants will be asked to submit samples for at least one candidate point-of-care test (POCT) being evaluated (index test/s) as well as an OP/NP swab for laboratory SARS-CoV2 RT-PCR performed by Public Health England (PHE) (reference standard for current infection). Adults will also be asked for a blood sample for laboratory SARS-CoV-2 antibody testing by PHE (reference standard for past infection), where feasible adults will be invited to attend a second visit at 28 days for repeat antibody testing. Additional study data (e.g. demographics, symptoms, observations, household contacts) will be captured electronically. Sensitivity, specificity, positive, and negative predictive values for each POCT will be calculated with exact 95% confidence intervals when compared to the reference standard. POCTs will also be compared to composite reference standards constructed using paired antibody test results, patient reported outcomes, linked electronic health records for outcomes related to COVID-19 such as hospitalisation or death, and other test results.

DISCUSSION

High-performing POCTs for community use could be transformational. Real-time results could lead to personal and public health impacts such as reducing onward household transmission of SARS-CoV2 infection, improving surveillance of health and social care staff, contributing to accurate prevalence estimates, and understanding of SARS-CoV2 transmission dynamics in the population. In contrast, poorly performing POCTs could have negative effects, so it is necessary to undertake community-based diagnostic accuracy evaluations before rolling these out.

TRIAL REGISTRATION

ISRCTN, ISRCTN14226970.

摘要

背景

新型冠状病毒肺炎社区即时检测快速评估(RAPTOR-C19)的目的是评估多种现有和新兴即时检测(POCT)在社区环境中对当前和既往严重急性呼吸综合征冠状病毒2(SARS-CoV2)感染的诊断准确性。RAPTOR-C19将为新型冠状病毒肺炎国家诊断研究与评估平台(CONDOR)提供社区测试平台。

方法

RAPTOR-C19纳入了一系列前瞻性观察性平行诊断准确性研究,针对在社区环境中就诊的疑似当前或既往SARS-CoV2感染患者,将SARS-CoV2 POCT与实验室及综合参考标准进行对比。作为临床护理或社区检测一部分而接受口咽/鼻咽(OP/NP)拭子以进行实验室SARS-CoV2逆转录数字/实时聚合酶链反应(d/rRT-PCR)检测的疑似当前SARS-CoV2感染的成人和儿童将被邀请参与。疑似既往有症状感染的成人(≥16岁)也将被招募。无症状个体不符合条件。在基线访视时,将要求所有参与者提交样本用于至少一种正在评估的候选即时检测(POCT)(指标检测),以及一份OP/NP拭子用于由英国公共卫生署(PHE)进行的实验室SARS-CoV2 RT-PCR检测(当前感染的参考标准)。还将要求成人提供一份血液样本用于PHE进行的实验室SARS-CoV-2抗体检测(既往感染的参考标准),在可行的情况下,将邀请成人在28天进行第二次访视以进行重复抗体检测。其他研究数据(如人口统计学、症状、观察结果、家庭接触者)将通过电子方式收集。与参考标准相比时,将计算每种POCT的敏感性、特异性、阳性和阴性预测值,并给出精确的95%置信区间。POCT还将与使用配对抗体检测结果、患者报告结局、与新型冠状病毒肺炎相关结局(如住院或死亡)的关联电子健康记录以及其他检测结果构建的综合参考标准进行比较。

讨论

高性能的社区用POCT可能具有变革性。实时结果可能对个人和公共健康产生影响,例如减少SARS-CoV2感染在家庭中的进一步传播、改善对卫生和社会护理人员的监测、有助于准确估计患病率以及了解人群中SARS-CoV2的传播动态。相比之下,性能不佳的POCT可能产生负面影响,因此在推广这些检测之前进行基于社区的诊断准确性评估很有必要。

试验注册

国际标准随机对照试验编号,ISRCTN14226970。

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