Suen K, Keeka M, Ailabouni R, Tran P
Western Health, 160 Gordon St, Footscray, Victoria 3011, Australia.
Western Health, 160 Gordon St, Footscray, Victoria 3011, Australia and Australian Institute for Musculoskeletal Science (AIMSS), The University of Melbourne and Western Health, Victoria, PO Box 294, 176 Furlong Road, St Albans, Victoria 3021, Australia.
Bone Joint J. 2018 Jan;100-B(1):66-72. doi: 10.1302/0301-620X.100B1.BJJ-2017-0630.R1.
α-defensin is a biomarker which has been described as having a high degree of accuracy in the diagnosis of periprosthetic joint infection (PJI). Current meta-analyses are based on the α-defensin laboratory-based immunoassay rather than the quick on-table lateral flow test kit. This study is the first meta-analysis to compare the accuracy of the α-defensin laboratory-based immunoassay and the lateral flow test kit for the diagnosis of PJI.
A systematic review was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Inclusion criteria were all clinical studies where the diagnosis of PJI was uncertain. All studies selected used the Musculoskeletal Infection Society (MSIS) or modified MSIS criteria. Two independent reviewers reviewed the studies and extracted data. A meta-analysis of results was carried out: pooled sensitivity, specificity, positive and negative likelihood ratio, heterogeneity and areas under curves are reported.
Ten studies (759 patients) were included. Of these, seven studies (640 patients) evaluated the laboratory-based α-defensin immunoassay and three (119 patients) the lateral flow test. The pooled sensitivity and specificity of the qualitative α-defensin laboratory immunoassay was 0.953 (95% confidence interval (CI) 0.87 to 0.984) and 0.965 (95% CI 0.943 to 0.979) respectively. The pooled positive likelihood ratio (PLR) and negative likelihood ratio (NLR) were 34.86 (95% CI 19.34 to 62.85) and 0.02 (95% CI 0.00 to 0.11). The pooled sensitivity and specificity of the lateral flow test were 0.774 (95% CI 0.637 to 0.870) and 0.913 (95% CI 0.828 to 0.958), respectively. The pooled PLR and NLR were 8.675 (95% CI 4.229 to 17.794) and 0.248 (95% CI 0.147 to 0.418), respectively.
The pooled sensitivity and specificity of the lateral flow test were lower than those of the α-defensin laboratory-based immunoassay test. Hence, care must be taken with interpretation of the lateral flow test when relying on its results for the intra-operative diagnosis of PJI. Cite this article: 2018;100-B:66-72.
α-防御素是一种生物标志物,在假体周围关节感染(PJI)的诊断中具有高度准确性。目前的荟萃分析基于基于实验室的α-防御素免疫测定法,而非快速床旁侧向流动检测试剂盒。本研究是第一项比较基于实验室的α-防御素免疫测定法和侧向流动检测试剂盒诊断PJI准确性的荟萃分析。
根据系统评价和荟萃分析的首选报告项目指南进行系统评价。纳入标准为所有PJI诊断不确定的临床研究。所有入选研究均采用肌肉骨骼感染学会(MSIS)或改良的MSIS标准。两名独立的审阅者对研究进行审阅并提取数据。对结果进行荟萃分析:报告合并敏感性、特异性、阳性和阴性似然比、异质性和曲线下面积。
纳入10项研究(759例患者)。其中,7项研究(640例患者)评估了基于实验室的α-防御素免疫测定法,3项研究(119例患者)评估了侧向流动检测。基于实验室的定性α-防御素免疫测定法的合并敏感性和特异性分别为0.953(95%置信区间(CI)0.87至0.984)和0.965(95%CI 0.943至0.979)。合并阳性似然比(PLR)和阴性似然比(NLR)分别为34.86(95%CI 19.34至62.85)和0.02(95%CI 0.00至0.11)。侧向流动检测法的合并敏感性和特异性分别为0.774(95%CI 0.637至0.870)和0.913(95%CI 0.828至0.958)。合并PLR和NLR分别为8.675(95%CI 4.229至17.794)和0.248(95%CI 0.147至0.418)。
侧向流动检测法的合并敏感性和特异性低于基于实验室的α-防御素免疫测定法。因此,在依靠侧向流动检测结果进行PJI术中诊断时,必须谨慎解读检测结果。引用本文:2018;100-B:66-72。