摘要
目的探讨利用关节液中细菌16s rRNA与23s rRNA诊断全膝关节置换术后感染的效率及两种基因诊断方法的差异。方法对33例无菌性松动及19例假体周围感染行人工膝关节翻修的患者,通过RT-PCR检测关节液中细菌16s rRNA、23s rRNA保守基因片段诊断假体周围感染。比较两种诊断策略的敏感性、特异性、阳性预测值、阴性预测值及准确性。结果以国外关于假体周围感染诊断方法的文献判定假体周围感染,利用16s rRNA进行诊断的敏感性78.8%,特异性93.9%,阳性预测值88.2%,阴性预测值为88.6%,准确性为88.5%;而采用23s rRNA扩增方法诊断的敏感性、特异性、阳性预测值、阴性预测值及准确性分别为68.4%、78.8%、65.0%、81.2%和75.0%。两种基因诊断的各指标比较差异均无统计学意义(P>0.05)。结论通过检测关节液中细菌16s rRNA或23s rRNA诊断人工膝关节置换术后感染,具有较高的诊断效率,且两者差异无统计学意义。
Objective To explore the power of detecting bacteria 16 s rRNA and 23 srRNA to diagnose periprosthetic joint infection(PJI)after total knee arthroplasty(TKA).Methods A prospective study of 52 patients who had a TKA and were undergoing a reoperation because of infection(19patients)or aseptic loosening(33patients)was conducted.The 16 S rRNA and 23 S rRNA in joint fluid were detected by RT-PCR as a marker to diagnose PJI.The sensitivity,specificity,positive predictive value,negative predictive value,and accuracy were compared.Results The diagnose power of 16 srRNA was higher than 23s rRNA:sensitivity(78.8% vs 68.4%),specificity(93.9% vs 78.8%),positive predictive value(88.2% vs65.0%),negative predictive value(88.6% vs 81.2%)and accuracy(88.5% vs 75.0%).However,all of those difference was not statistically significant(P>0.05).Conclusion Both 16 srRNA and 23 srRNA have satisfactory diagnosis power of to detect PJI,and there was no difference.
引文
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