Thoracic imaging tests for the diagnosis of COVID-19.

Nayaar Islam, Jean-Paul Salameh, Mariska Mg Leeflang, Lotty Hooft, Trevor A McGrath, Christian B van der Pol, Robert A Frank, Sakib Kazi, Ross Prager, Samanjit S Hare, Carole Dennie, René Spijker, Jonathan J Deeks, Jacqueline Dinnes, Kevin Jenniskens, Daniël A Korevaar, Jérémie F Cohen, Ann Van den Bruel, Yemisi Takwoingi, Janneke van de Wijgert, Junfeng Wang, Matthew Df McInnes
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However, this is a rapidly developing field and these findings need to be re-evaluated in the light of new research. This is the first update of this 'living systematic review'. This update focuses on people suspected of having COVID-19 and excludes studies with only confirmed COVID-19 participants.</p><p><strong>Objectives: </strong>To evaluate the diagnostic accuracy of thoracic imaging (computed tomography (CT), X-ray and ultrasound) in people with suspected COVID-19.</p><p><strong>Search methods: </strong>We searched the COVID-19 Living Evidence Database from the University of Bern, the Cochrane COVID-19 Study Register, The Stephen B. Thacker CDC Library, and repositories of COVID-19 publications through to 22 June 2020. 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引用次数: 192

Abstract

Background: The respiratory illness caused by SARS-CoV-2 infection continues to present diagnostic challenges. Early research showed thoracic (chest) imaging to be sensitive but not specific in the diagnosis of coronavirus disease 2019 (COVID-19). However, this is a rapidly developing field and these findings need to be re-evaluated in the light of new research. This is the first update of this 'living systematic review'. This update focuses on people suspected of having COVID-19 and excludes studies with only confirmed COVID-19 participants.

Objectives: To evaluate the diagnostic accuracy of thoracic imaging (computed tomography (CT), X-ray and ultrasound) in people with suspected COVID-19.

Search methods: We searched the COVID-19 Living Evidence Database from the University of Bern, the Cochrane COVID-19 Study Register, The Stephen B. Thacker CDC Library, and repositories of COVID-19 publications through to 22 June 2020. We did not apply any language restrictions.

Selection criteria: We included studies of all designs that recruited participants of any age group suspected to have COVID-19, and which reported estimates of test accuracy, or provided data from which estimates could be computed. When studies used a variety of reference standards, we retained the classification of participants as COVID-19 positive or negative as used in the study.

Data collection and analysis: We screened studies, extracted data, and assessed the risk of bias and applicability concerns using the QUADAS-2 domain-list independently, in duplicate. We categorised included studies into three groups based on classification of index test results: studies that reported specific criteria for index test positivity (group 1); studies that did not report specific criteria, but had the test reader(s) explicitly classify the imaging test result as either COVID-19 positive or negative (group 2); and studies that reported an overview of index test findings, without explicitly classifying the imaging test as either COVID-19 positive or negative (group 3). We presented the results of estimated sensitivity and specificity using paired forest plots, and summarised in tables. We used a bivariate meta-analysis model where appropriate. We presented uncertainty of the accuracy estimates using 95% confidence intervals (CIs).

Main results: We included 34 studies: 30 were cross-sectional studies with 8491 participants suspected of COVID-19, of which 4575 (54%) had a final diagnosis of COVID-19; four were case-control studies with 848 cases and controls in total, of which 464 (55%) had a final diagnosis of COVID-19. Chest CT was evaluated in 31 studies (8014 participants, 4224 (53%) cases), chest X-ray in three studies (1243 participants, 784 (63%) cases), and ultrasound of the lungs in one study (100 participants, 31 (31%) cases). Twenty-six per cent (9/34) of all studies were available only as preprints. Nineteen studies were conducted in Asia, 10 in Europe, four in North America and one in Australia. Sixteen studies included only adults, 15 studies included both adults and children and one included only children. Two studies did not report the ages of participants. Twenty-four studies included inpatients, four studies included outpatients, while the remaining six studies were conducted in unclear settings. The majority of included studies had a high or unclear risk of bias with respect to participant selection, index test, reference standard, and participant flow. For chest CT in suspected COVID-19 participants (31 studies, 8014 participants, 4224 (53%) cases) the sensitivity ranged from 57.4% to 100%, and specificity ranged from 0% to 96.0%. The pooled sensitivity of chest CT in suspected COVID-19 participants was 89.9% (95% CI 85.7 to 92.9) and the pooled specificity was 61.1% (95% CI 42.3 to 77.1). Sensitivity analyses showed that when the studies from China were excluded, the studies from other countries demonstrated higher specificity compared to the overall included studies. When studies that did not classify index tests as positive or negative for COVID-19 (group 3) were excluded, the remaining studies (groups 1 and 2) demonstrated higher specificity compared to the overall included studies. Sensitivity analyses limited to cross-sectional studies, or studies where at least two reverse transcriptase polymerase chain reaction (RT-PCR) tests were conducted if the first was negative, did not substantively alter the accuracy estimates. We did not identify publication status as a source of heterogeneity. For chest X-ray in suspected COVID-19 participants (3 studies, 1243 participants, 784 (63%) cases) the sensitivity ranged from 56.9% to 89.0% and specificity from 11.1% to 88.9%. The sensitivity and specificity of ultrasound of the lungs in suspected COVID-19 participants (1 study, 100 participants, 31 (31%) cases) were 96.8% and 62.3%, respectively. We could not perform a meta-analysis for chest X-ray or ultrasound due to the limited number of included studies.

Authors' conclusions: Our findings indicate that chest CT is sensitive and moderately specific for the diagnosis of COVID-19 in suspected patients, meaning that CT may have limited capability in differentiating SARS-CoV-2 infection from other causes of respiratory illness. However, we are limited in our confidence in these results due to the poor study quality and the heterogeneity of included studies. Because of limited data, accuracy estimates of chest X-ray and ultrasound of the lungs for the diagnosis of suspected COVID-19 cases should be carefully interpreted. Future diagnostic accuracy studies should pre-define positive imaging findings, include direct comparisons of the various modalities of interest on the same participant population, and implement improved reporting practices. Planned updates of this review will aim to: increase precision around the accuracy estimates for chest CT (ideally with low risk of bias studies); obtain further data to inform accuracy of chest X-rays and ultrasound; and obtain data to further fulfil secondary objectives (e.g. 'threshold' effects, comparing accuracy estimates across different imaging modalities) to inform the utility of imaging along different diagnostic pathways.

胸部影像学检查诊断COVID-19
背景:由SARS-CoV-2感染引起的呼吸道疾病继续呈现诊断挑战。早期研究表明,胸部影像学对2019冠状病毒病(COVID-19)的诊断敏感但不特异性。然而,这是一个快速发展的领域,这些发现需要根据新的研究进行重新评估。这是“活的系统评价”的第一次更新。本更新主要关注疑似感染COVID-19的人,不包括仅确诊COVID-19参与者的研究。目的:评价胸部影像学(CT、x线、超声)对疑似COVID-19患者的诊断准确性。检索方法:我们检索了伯尔尼大学的COVID-19活证据数据库、Cochrane COVID-19研究登记处、Stephen B. Thacker CDC图书馆和COVID-19出版物库,检索时间截止到2020年6月22日。我们没有使用任何语言限制。选择标准:我们纳入了所有设计的研究,这些研究招募了疑似感染COVID-19的任何年龄组的参与者,并报告了测试准确性的估计值,或提供了可以计算估计值的数据。当研究使用各种参考标准时,我们保留了研究中使用的将参与者分类为COVID-19阳性或阴性。数据收集和分析:我们筛选研究,提取数据,并使用QUADAS-2域列表独立评估偏倚风险和适用性问题,一式两份。根据指标检测结果的分类,我们将纳入的研究分为三组:报告了指标检测阳性的具体标准的研究(第一组);没有报告具体标准,但测试阅读者明确将成像测试结果分类为COVID-19阳性或阴性的研究(第2组);以及报告了指数测试结果概述的研究,但没有明确将成像测试分类为COVID-19阳性或阴性(第3组)。我们使用成对森林图给出了估计敏感性和特异性的结果,并在表格中进行了总结。我们在适当的地方使用了双变量元分析模型。我们使用95%置信区间(ci)给出了准确度估计的不确定性。主要结果:我们纳入34项研究:30项为横断面研究,共8491名疑似COVID-19受试者,其中4575名(54%)最终诊断为COVID-19;4项是病例对照研究,共848例病例和对照组,其中464例(55%)最终诊断为COVID-19。31项研究(8014名参与者,4224例(53%))评估了胸部CT, 3项研究(1243名参与者,784例(63%))评估了胸部x线,1项研究(100名参与者,31例(31%))评估了肺部超声。所有研究报告中有26%(9/34)只提供预印本。19项研究在亚洲进行,10项在欧洲,4项在北美,1项在澳大利亚。16项研究只包括成人,15项研究同时包括成人和儿童,还有一项研究只包括儿童。有两项研究没有报告参与者的年龄。24项研究包括住院患者,4项研究包括门诊患者,其余6项研究在不明确的环境中进行。大多数纳入的研究在受试者选择、指标检验、参考标准和受试者流方面存在较高或不明确的偏倚风险。对于疑似COVID-19参与者(31项研究,8014名参与者,4224例(53%)病例)的胸部CT,敏感性为57.4%至100%,特异性为0%至96.0%。疑似COVID-19参与者的胸部CT综合敏感性为89.9% (95% CI 85.7 ~ 92.9),综合特异性为61.1% (95% CI 42.3 ~ 77.1)。敏感性分析显示,当排除来自中国的研究时,来自其他国家的研究比总体纳入的研究具有更高的特异性。当排除未将指标测试分类为COVID-19阳性或阴性的研究(第3组)时,其余研究(第1组和第2组)与纳入的总体研究相比显示出更高的特异性。敏感性分析仅限于横断面研究,或至少进行两次逆转录酶聚合酶链反应(RT-PCR)试验(如果第一次试验为阴性)的研究,并没有实质性地改变准确性估计。我们没有将发表状态确定为异质性的来源。对于疑似COVID-19参与者的胸部x线检查(3项研究,1243名参与者,784例(63%)病例),敏感性为56.9%至89.0%,特异性为11.1%至88.9%。疑似COVID-19患者(1项研究,100例,31例(31%))肺部超声灵敏度和特异性分别为96.8%和62.3%。 由于纳入的研究数量有限,我们无法对胸部x线或超声进行meta分析。作者结论:我们的研究结果表明,胸部CT对疑似患者的COVID-19诊断敏感且具有中等特异性,这意味着CT在区分SARS-CoV-2感染与其他呼吸道疾病原因方面的能力可能有限。然而,由于研究质量差和纳入研究的异质性,我们对这些结果的信心有限。由于数据有限,应仔细解释用于诊断疑似COVID-19病例的胸部x线和肺部超声的准确性估计。未来的诊断准确性研究应预先定义阳性影像学结果,包括在同一参与者人群中直接比较各种感兴趣的模式,并实施改进的报告实践。本综述计划更新的目的是:提高胸部CT准确度估计的准确性(理想情况下是低偏倚风险的研究);获得进一步的数据,以提高胸部x光和超声波的准确性;并获取数据以进一步实现次要目标(例如:“阈值”效应,比较不同成像模式下的准确性估计),以告知不同诊断途径下成像的效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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