Unnikrishnan Greeshma, Singh Abhinav, Purohit Abhishek
All India Institute of Medical Sciences Bhopal India All India Institute of Medical Sciences, Bhopal, India.
Postgraduate Institute of Medical Education and Research Chandigarh India Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Rev Panam Salud Publica. 2024 Dec 4;48:e131. doi: 10.26633/RPSP.2024.131. eCollection 2024.
To evaluate diagnostic accuracy of polymerase chain reaction (PCR) in detecting mpox infection in humans by pooling the estimates of sensitivity and specificity across different study settings.
A systematic search was conducted in PubMed, Cochrane database, Scopus, and Google Scholar. Studies that evaluated the diagnostic accuracy of PCR test for the detection of monkeypox virus providing the sensitivity and specificity values and the total number of samples were included. The sensitivity and specificity values of PCR test were pooled for all the included studies. The meta-analysis was conducted in accordance with PRISMA guidelines using the metadta package in STATA software. A summary receiver operating characteristic (SROC) curve and forest plot were generated. The protocol was registered in PROSPERO (CRD-NIHR) database with Reference ID CRD42024590183.
Twelve studies were included for meta-analysis. The pooled sensitivity and specificity estimate across all the studies using a random effects model was 0.99 (95% CI [0.95, 1.00]) and 1 (95% CI [0.96, 1.00]), respectively. The SROC curve confirmed high diagnostic accuracy of PCR. The quality assessment of diagnostic accuracy studies (QUADAS) tool depicted low risk of bias.
This systematic review and meta-analysis is the first study in the scientific literature to provide a pooling for diagnostic accuracy for PCR test for mpox and confirms it as an accurate tool in detecting the infection in humans.
通过汇总不同研究背景下的敏感性和特异性估计值,评估聚合酶链反应(PCR)检测人类猴痘感染的诊断准确性。
在PubMed、Cochrane数据库、Scopus和谷歌学术中进行了系统检索。纳入评估PCR检测猴痘病毒诊断准确性并提供敏感性和特异性值以及样本总数的研究。对所有纳入研究的PCR检测敏感性和特异性值进行汇总。使用STATA软件中的metadta包按照PRISMA指南进行荟萃分析。生成汇总受试者工作特征(SROC)曲线和森林图。该方案已在PROSPERO(CRD-NIHR)数据库中注册,参考编号为CRD42024590183。
纳入12项研究进行荟萃分析。使用随机效应模型对所有研究汇总的敏感性和特异性估计值分别为0.99(95%CI[0.95,1.00])和1(95%CI[0.96,1.00])。SROC曲线证实了PCR的高诊断准确性。诊断准确性研究的质量评估(QUADAS)工具显示偏倚风险较低。
这项系统评价和荟萃分析是科学文献中第一项对猴痘PCR检测诊断准确性进行汇总的研究,并证实其为检测人类感染的准确工具。