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多重呼吸道病原体检测 panel 对流感或呼吸道合胞病毒感染的诊断准确性:系统评价和荟萃分析。

Diagnostic accuracy of multiplex respiratory pathogen panels for influenza or respiratory syncytial virus infections: systematic review and meta-analysis.

机构信息

Barcelona Institute for Global Health (ISGlobal), Hospital Clínic - Universitat de Barcelona, Carrer Rosselló 132, 08036, Barcelona, Spain.

Imperial College London, London, UK.

出版信息

BMC Infect Dis. 2022 Oct 13;22(1):785. doi: 10.1186/s12879-022-07766-9.

Abstract

Respiratory syncytial virus (RSV) and influenza viruses are important global causes of morbidity and mortality. We evaluated the diagnostic accuracy of the Luminex NxTAG respiratory pathogen panels (RPPs)™ (index) against other RPPs (comparator) for detection of RSV and influenza viruses. Studies comparing human clinical respiratory samples tested with the index and at least one comparator test were included. A random-effect latent class meta-analysis was performed to assess the specificity and sensitivity of the index test for RSV and influenza. Risk of bias was assessed using the QUADAS-2 tool and certainty of evidence using GRADE. Ten studies were included. For RSV, predicted sensitivity was 99% (95% credible interval [CrI] 96-100%) and specificity 100% (95% CrI 98-100%). For influenza A and B, predicted sensitivity was 97% (95% CrI 89-100) and 98% (95% CrI 88-100) respectively; specificity 100% (95% CrI 99-100) and 100% (95% CrI 99-100), respectively. Evidence was low certainty. Although index sensitivity and specificity were excellent, comparators' performance varied. Further research with clear patient recruitment strategies could ascertain performance across different populations.Protocol Registration: Prospero CRD42021272062.

摘要

呼吸道合胞病毒(RSV)和流感病毒是造成全球发病率和死亡率的重要原因。我们评估了 Luminex NxTAG 呼吸道病原体检测试剂盒(RPPs)(指标)与其他 RPPs(对照)检测 RSV 和流感病毒的诊断准确性。纳入了比较用指标和至少一种对照检测试剂盒检测人类临床呼吸道样本的研究。采用随机效应潜在类别荟萃分析评估指标检测 RSV 和流感的特异性和敏感性。使用 QUADAS-2 工具评估偏倚风险,使用 GRADE 评估证据确定性。纳入了 10 项研究。对于 RSV,预测敏感性为 99%(95%可信区间[CrI]96-100%),特异性为 100%(95% CrI 98-100%)。对于流感 A 和 B,预测敏感性分别为 97%(95% CrI 89-100)和 98%(95% CrI 88-100);特异性分别为 100%(95% CrI 99-100)和 100%(95% CrI 99-100)。证据确定性为低。尽管指标的敏感性和特异性很好,但对照的性能有所不同。进一步的研究应采用明确的患者招募策略,以确定不同人群中的性能。注册协议:Prospéro CRD42021272062。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/086d/9563105/5952920fa5b4/12879_2022_7766_Fig1_HTML.jpg

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