CHU Nantes, Laboratoire de Bactériologie, Nantes, France.
Inserm, CIC 1415, Tours, France.
Clin Microbiol Infect. 2018 Jan;24(1):83.e1-83.e6. doi: 10.1016/j.cmi.2017.05.017. Epub 2017 May 27.
Prosthetic joint infections (PJI) are responsible for significant morbidity and mortality and their number continues to rise. Their management remains complex, especially the microbiological diagnosis. Besides 'homemade' tests developed by several teams, new molecular biology methods are now available with different analytical performance and usability.
We studied the performances of one of these tests: ITI multiplex PCR (mPCR) by the Curetis company and compared it to either 'optimized' culture or 16S rRNA PCR. We performed a retrospective multicentre study to assess the contributions of mPCR in the diagnosis of PJI. We randomly selected 484 intraoperative specimens among 1252 of various types (biopsy, bone, tissue around the prosthesis, synovial fluid) from 251 patients in seven different hospitals. Each sample was treated according to the recommendations of the manufacturer.
In all, 154 out of 164 (93.9%) samples negative in culture were negative with the mPCR. Among the 276 positive samples in culture, 251 (90.9%) were monomicrobial, of which 119 (47.4%) were positive with the mPCR, and 25 (9.1%) were polymicrobial, of which 12 (48%) were positive with the mPCR. The concordance rate of mPCR with culture was 58.1% (53.6%-62.7%) and the concordance rate with 16S rRNA PCR was 70.1% (65.5%-74.6%).
This new standardized molecular test showed a lack of detection when the bacterial inoculum was low (number of positive media per sample and number of colonies per media) but can be useful when patients have received antibiotic therapy previously.
人工关节感染(PJI)可导致严重的发病率和死亡率,其数量仍在不断增加。其治疗仍然很复杂,特别是微生物学诊断。除了几个团队开发的“自制”检测方法外,现在还可以使用新的分子生物学方法,这些方法具有不同的分析性能和可用性。
我们研究了 Curetis 公司开发的一种检测方法 ITI 多重 PCR(mPCR)的性能,并将其与“优化”培养或 16S rRNA PCR 进行了比较。我们进行了一项回顾性多中心研究,以评估 mPCR 在 PJI 诊断中的作用。我们从 7 家不同医院的 251 名患者的 1252 种不同类型(活检、骨、假体周围组织、滑膜液)的术中标本中随机选择了 484 个。每个样本均按照制造商的建议进行处理。
在所有培养阴性的 164 个样本中,有 154 个(93.9%)mPCR 检测也为阴性。在培养阳性的 276 个样本中,251 个(90.9%)为单一微生物感染,其中 119 个(47.4%)mPCR 检测阳性,25 个(9.1%)为多微生物感染,其中 12 个(48%)mPCR 检测阳性。mPCR 与培养的一致性率为 58.1%(53.6%-62.7%),与 16S rRNA PCR 的一致性率为 70.1%(65.5%-74.6%)。
这种新的标准化分子检测方法在细菌接种量低时(每个样本的阳性培养基数量和每个培养基的菌落数量)显示出检测不足,但在患者先前接受抗生素治疗时可能有用。