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Systematic Review and Meta-Analysis of a Urine-Based Pneumococcal Antigen Test for Diagnosis of Community-Acquired Pneumonia Caused by Streptococcus pneumoniae

机译:基于尿液的肺炎球菌抗原检测对肺炎链球菌引起的社区获得性肺炎的诊断的系统评价和荟萃分析

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摘要

Standard culture methods for diagnosis of Streptococcus pneumoniae pneumonia take at least 24 h. The BinaxNOW urine-based test for S. pneumoniae (BinaxNOW-SP) takes only 15 min to conduct, potentially enabling earlier diagnosis and targeted treatment. This study was conducted to assess whether the use of BinaxNOW-SP at the time of hospital admission would provide adequate sensitivity and specificity for diagnosis of community-acquired pneumonia (CAP) in adult patients. We searched PubMed, EMBASE/OVID, Cochrane Collaboration, Centre for Reviews and Dissemination, INAHTA, and CADTH for diagnostic or etiologic studies of hospitalized predominately adult patients with clinically defined CAP that reported the diagnostic performance of BinaxNOW-SP versus cultures. Two authors independently extracted study details and diagnostic two-by-two tables. We found that 27 studies met our inclusion criteria, and three different reference standards were used between them. A bivariate meta-analysis of 12 studies using a composite of culture tests as the reference standard estimated the sensitivity of BinaxNOW-SP as 68.5% (95% credibility interval [CrI], 62.6% to 74.2%) and specificity as 84.2% (95% CrI, 77.5% to 89.3%). A meta-analysis of all 27 studies, adjusting for the imperfect and variable nature of the reference standard, gave a higher sensitivity of 74.0% (CrI, 66.6% to 82·3%) and specificity of 97.2% (CrI, 92.7% to 99.8%). The analysis showed substantial heterogeneity across studies, which did not decrease with adjustment for covariates. We concluded that the higher pooled sensitivity (compared to culture) and high specificity of BinaxNOW-SP suggest it would be a useful addition to the diagnostic workup for community-acquired pneumonia. More research is needed regarding the impact of BinaxNOW-SP on clinical practice.
机译:诊断肺炎链球菌肺炎的标准培养方法至少需要24小时。 BinaxNOW基于尿液的肺炎链球菌检测(BinaxNOW-SP)仅需15分钟即可进行,有可能实现早期诊断和针对性治疗。进行这项研究的目的是评估在住院时使用BinaxNOW-SP是否能为诊断成人患者的社区获得性肺炎(CAP)提供足够的敏感性和特异性。我们搜索了PubMed,EMBASE / OVID,Cochrane合作,评论与传播中心,INAHTA和CADTH,以对临床诊断为CAP的住院为主的成年患者进行诊断或病因研究,这些患者报告了BinaxNOW-SP与培养物的诊断性能。两位作者分别提取了研究细节和诊断表格,每两张表格一张。我们发现27项研究符合我们的纳入标准,并且在它们之间使用了三种不同的参考标准。使用培养试验组合作为参考标准的12项研究的双变量荟萃分析估计BinaxNOW-SP的敏感性为68.5%(可信度区间为[95%[CrI]为62.6%至74.2%),特异性为84.2%(95%) %CrI,77.5%至89.3%)。对所有27项研究进行的荟萃分析,对参考标准品的不完善和可变性质进行了调整,得出的灵敏度更高,为74.0%(CrI,从66.6%到82·3%),特异性为97.2%(CrI,从92.7%到92.7%)。 99.8%)。分析表明,各研究之间存在很大的异质性,但随着协变量的调整,异质性并未降低。我们得出的结论是,BinaxNOW-SP的更高的合并敏感性(与培养相比)和高特异性表明,它将为社区获得性肺炎的诊断检查提供有用的补充。关于BinaxNOW-SP对临床实践的影响,需要进行更多研究。

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