Departments of Pathology, Microbiology and Immunology, and Medicine, Dalhousie University, Halifax, Nova Scotia.
Departments of Pathology, Microbiology and Immunology, and Medicine, Dalhousie University, Halifax, Nova Scotia ; Division of Microbiology, Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia.
Can J Infect Dis Med Microbiol. 2013 Summer;24(2):85-8. doi: 10.1155/2013/747145.
Amplification of the 16S ribosomal RNA gene by polymerase chain reaction (PCR) followed by analysis of generated sequences can be an important adjunct to conventional cultures.
To determine how the results of this approach influence physicians' decisions regarding the management of bone and joint infections.
Clinical and laboratory findings of patients seen at the Queen Elizabeth II Health Sciences Centre (Halifax, Nova Scotia) between December 2005 and September 2009 were reviewed. Patients who had negative cultures but likely or possible bone and joint infections were further evaluated using 16S rRNA PCR. The impact of the 16S rRNA PCR result on antibiotic management was evaluated and it was assessed whether untreated patients with negative 16S rRNA PCR subsequently presented with infections, suggesting a false-negative result.
A total of 36 patients (mean age 62 years) were reviewed. Thirty-two patients were evaluated by infectious disease consultants; of these, 20 were considered likely to have infections. Seventeen patients were admitted with suspected prosthetic joint infections. Twenty-nine patients received antimicrobial treatment before the sample for the 16S rRNA PCR assay was obtained. Of the 36 patients, 26 (72.2%) were treated appropriately with modifications to their antibiotic regimen in response to the 16S rRNA PCR assay results. Antimicrobials were discontinued for 19 patients based on negative PCR assay and, in seven patients, antibiotics were changed based on a positive result. There were no relapses among patients with negative PCR assay in whom antibiotics were discontinued.
16S ribosomal RNA gene PCR and sequencing is a valuable tool in the guidance of antimicrobial therapy for bone and joint infections.
聚合酶链反应(PCR)扩增 16S 核糖体 RNA 基因,然后分析生成的序列,这可能是辅助常规培养的重要方法。
确定这种方法的结果如何影响医生对骨和关节感染的治疗决策。
回顾 2005 年 12 月至 2009 年 9 月在伊丽莎白女王二世健康科学中心(新斯科舍省哈利法克斯)就诊的患者的临床和实验室检查结果。对培养结果阴性但可能或可能患有骨和关节感染的患者进一步使用 16S rRNA PCR 进行评估。评估 16S rRNA PCR 结果对抗生素管理的影响,并评估未接受治疗且 16S rRNA PCR 结果为阴性的患者随后是否出现感染,提示存在假阴性结果。
共回顾 36 例患者(平均年龄 62 岁)。32 例患者由传染病顾问评估;其中 20 例被认为有感染的可能。17 例患者因疑似人工关节感染入院。在获得 16S rRNA PCR 检测样本之前,29 例患者接受了抗菌治疗。在 36 例患者中,26 例(72.2%)根据 16S rRNA PCR 检测结果对其抗生素方案进行了适当调整。根据 PCR 检测结果为阴性,19 例患者停止使用抗生素,在 7 例患者中,根据阳性结果改变了抗生素。停止使用抗生素后,PCR 检测结果为阴性的患者中无复发。
16S 核糖体 RNA 基因 PCR 和测序是指导骨和关节感染抗菌治疗的有价值的工具。