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Clinical Use of a 16S Ribosomal RNA Gene-Based Sanger and/or Next Generation Sequencing Assay to Test Preoperative Synovial Fluid for Periprosthetic Joint Infection Diagnosis.基于 16S 核糖体 RNA 基因的 Sanger 和/或下一代测序检测技术在术前关节滑液中用于诊断假体周围关节感染的临床应用。
mBio. 2022 Dec 20;13(6):e0132222. doi: 10.1128/mbio.01322-22. Epub 2022 Nov 10.
2
Targeted Versus Shotgun Metagenomic Sequencing-based Detection of Microorganisms in Sonicate Fluid for Periprosthetic Joint Infection Diagnosis.靶向与 shotgun 宏基因组测序法检测超声冲洗液中的微生物对假体周围关节感染的诊断价值。
Clin Infect Dis. 2023 Feb 8;76(3):e1456-e1462. doi: 10.1093/cid/ciac646.
3
Targeted Metagenomic Sequencing-based Approach Applied to 2146 Tissue and Body Fluid Samples in Routine Clinical Practice.基于靶向宏基因组测序的方法在常规临床实践中应用于 2146 份组织和体液样本。
Clin Infect Dis. 2022 Nov 14;75(10):1800-1808. doi: 10.1093/cid/ciac247.
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Diagnostic accuracy of multiplex polymerase chain reaction on tissue biopsies in periprosthetic joint infections.组织活检中多重聚合酶链反应在假体周围关节感染中的诊断准确性。
Sci Rep. 2021 Sep 30;11(1):19487. doi: 10.1038/s41598-021-99076-4.
5
Targeted next generation sequencing for elbow periprosthetic joint infection diagnosis.针对肘假体关节感染的靶向下一代测序诊断。
Diagn Microbiol Infect Dis. 2021 Oct;101(2):115448. doi: 10.1016/j.diagmicrobio.2021.115448. Epub 2021 Jun 5.
6
Microbiology of hip and knee periprosthetic joint infections: a database study.髋关节和膝关节假体周围关节感染的微生物学:数据库研究。
Clin Microbiol Infect. 2022 Feb;28(2):255-259. doi: 10.1016/j.cmi.2021.06.006. Epub 2021 Jun 12.
7
Development of antibiotic resistance in periprosthetic joint infection after total knee arthroplasty.全膝关节置换术后假体周围关节感染中抗生素耐药性的发展。
Bone Joint J. 2021 Jun;103-B(6 Supple A):171-176. doi: 10.1302/0301-620X.103B6.BJJ-2020-1923.R1.
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Emergence of Antibiotic Resistance Across Two-Stage Revision for Periprosthetic Joint Infection.两阶段翻修治疗假体周围关节感染中抗生素耐药性的出现。
J Arthroplasty. 2021 Aug;36(8):2946-2950. doi: 10.1016/j.arth.2021.04.007. Epub 2021 Apr 15.
9
Projected Economic Burden of Periprosthetic Joint Infection of the Hip and Knee in the United States.美国人工髋关节和膝关节置换术后假体周围感染的预期经济负担。
J Arthroplasty. 2021 May;36(5):1484-1489.e3. doi: 10.1016/j.arth.2020.12.005. Epub 2020 Dec 9.
10
Culture-Negative Periprosthetic Joint Infection: An Update on What to Expect.培养阴性假体周围关节感染:最新情况及预期
JB JS Open Access. 2018 Jul 12;3(3):e0060. doi: 10.2106/JBJS.OA.17.00060. eCollection 2018 Sep 25.

比较 BioFire 联合感染面板与基于 16S 核糖体 RNA 基因的靶向宏基因组测序,用于检测膝关节置换失败患者的关节液。

Comparison of the BioFire Joint Infection Panel to 16S Ribosomal RNA Gene-Based Targeted Metagenomic Sequencing for Testing Synovial Fluid from Patients with Knee Arthroplasty Failure.

机构信息

Division of Public Health, Infectious Diseases, and Occupational Medicine, Department of Medicine, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.

Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.

出版信息

J Clin Microbiol. 2022 Dec 21;60(12):e0112622. doi: 10.1128/jcm.01126-22. Epub 2022 Nov 21.

DOI:10.1128/jcm.01126-22
PMID:36409108
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9769560/
Abstract

The diagnosis of periprosthetic joint infection (PJI) is challenging, often requiring multiple clinical specimens and diagnostic techniques, some with prolonged result turnaround times. Here, the diagnostic performance of the Investigational Use Only (IUO) BioFire Joint Infection (JI) Panel was compared to 16S rRNA gene-based targeted metagenomic sequencing (tMGS) applied to synovial fluid for PJI diagnosis. Sixty synovial fluid samples from knee arthroplasty failure archived at -80°C were tested. Infectious Diseases Society of America (IDSA) diagnostic criteria were used to classify PJI. For culture-positive PJI with pathogens targeted by the JI panel, JI panel sensitivity was 91% (21/23; 95% confidence interval [CI], 73 to 98%), and tMGS sensitivity was 96% (23/24; 95% CI, 80 to 99%) ( = 0.56). Overall sensitivities of the JI panel and tMGS for PJI diagnosis were 56% (24/43; 95% CI, 41 to 70%) and 93% (41/44; 95% CI, 82 to 98%), respectively ( < 0.001). JI panel and tMGS overall specificities were 100% (16/16; 95% CI, 81 to 100%) and 94% (15/16; 95% CI, 72 to 99%), respectively. While the clinical sensitivity of the JI panel was excellent for on-panel microorganisms, overall sensitivity for PJI diagnosis was low due to the absence of Staphylococcus epidermidis, a common causative pathogen of PJI, on the panel. A PJI diagnostic algorithm for the use of both molecular tests is proposed.

摘要

假体周围关节感染(PJI)的诊断具有挑战性,通常需要多个临床标本和诊断技术,其中一些需要较长的检测周转时间。在此,比较了仅限研究使用(IUO)的 BioFire 关节感染(JI)面板与针对滑液的基于 16S rRNA 基因的靶向宏基因组测序(tMGS)在 PJI 诊断中的诊断性能。测试了 60 份保存在-80°C 的膝关节置换失败的关节滑液存档样本。使用感染病学会(IDSA)诊断标准对 PJI 进行分类。对于 JI 面板靶向病原体的培养阳性 PJI,JI 面板的敏感性为 91%(21/23;95%置信区间 [CI],73 至 98%),tMGS 敏感性为 96%(23/24;95%CI,80 至 99%)(=0.56)。JI 面板和 tMGS 用于 PJI 诊断的总体敏感性分别为 56%(24/43;95%CI,41 至 70%)和 93%(41/44;95%CI,82 至 98%)(<0.001)。JI 面板和 tMGS 的总体特异性分别为 100%(16/16;95%CI,81 至 100%)和 94%(15/16;95%CI,72 至 99%)。虽然 JI 面板针对面板上的微生物具有出色的临床敏感性,但由于面板上缺少表皮葡萄球菌(一种常见的 PJI 病原体),因此整体 PJI 诊断敏感性较低。提出了一种用于两种分子检测的 PJI 诊断算法。