School of Rural Health, University of Melbourne, Shepparton, VIC, Australia.
Eur J Clin Microbiol Infect Dis. 2010 Feb;29(2):207-15. doi: 10.1007/s10096-009-0841-2. Epub 2009 Nov 29.
The limulus assay for endotoxin has been studied as a method for the rapid identification of gram-negative (GN) bacteraemia. The chromogenic (C-limulus) version is 100-fold more sensitive to an internal endotoxin standard than the earlier gelation version (G-limulus). The objective of this analysis is to compare the concordance between GN bacteraemia and endotoxaemia as determined in clinical studies using either version of the limulus assay. The summary results for the diagnostic odds ratio (DOR), sensitivity and specificity were derived using a hierarchical summary receiver operating characteristic (HSROC) method of meta-analysis. Fifty-eight studies (25 G-limulus and 33 C-limulus) were included. Surprisingly, the mean DOR (4.9; 3-7.9 versus 10.7; 5.2-21.8) was inferior for studies using the C-limulus versus the original G-limulus version of the assay. Moreover, among studies limited to sepsis syndrome patients, the mean DOR remains poor at 4.2 (1.8-9.5). The proportion of GN bacteraemic patients for whom endotoxaemia is not detectable with either version of the limulus assay is >20% among the 58 studies overall, but >30% after the exclusion of studies with <25 patients and >20% among studies of patients with sepsis syndrome. These findings help to reconcile seemingly disparate study results.
鲎试验检测内毒素已被研究作为一种快速鉴定革兰氏阴性(GN)菌血症的方法。比早期凝胶化版本(G-鲎试验),显色(C-鲎试验)版本对内部内毒素标准的灵敏度高 100 倍。本分析的目的是比较使用鲎试验的两种版本在临床研究中确定的 GN 菌血症与内毒素血症之间的一致性。使用层次汇总受试者工作特征(HSROC)荟萃分析方法得出诊断比值比(DOR)、灵敏度和特异性的汇总结果。共纳入 58 项研究(25 项 G-鲎试验和 33 项 C-鲎试验)。令人惊讶的是,与原始 G-鲎试验版本相比,使用 C-鲎试验的研究的平均 DOR(4.9;3-7.9 与 10.7;5.2-21.8)较差。此外,在仅限于脓毒症综合征患者的研究中,平均 DOR 仍较差,为 4.2(1.8-9.5)。在这 58 项研究中,总体上有超过 20%的 GN 菌血症患者无法用两种鲎试验版本检测到内毒素血症,但在排除了<25 例患者和>20%脓毒症综合征患者的研究后,这一比例>30%。这些发现有助于解释看似不同的研究结果。