Bacterial multiplex polymerase chain reaction tests for the diagnosis and management of pneumonia: ready for prime time?

医学 肺炎 抗生素耐药性 重症监护医学 多重聚合酶链反应 社区获得性肺炎 观察研究 抗生素 金标准(测试) 抗菌管理 呼吸机相关性肺炎 抗药性 内科学 聚合酶链反应 微生物学 生物 病理 肺结核 基因 生物化学
作者
Lowell Ling,Christopher K.C. Lai,Chanu Rhee
出处
期刊:Thorax [BMJ]
卷期号:: thorax-222297
标识
DOI:10.1136/thorax-2024-222297
摘要

Background The diagnosis and management of pneumonia is often challenging due to its overlapping clinical presentations with other respiratory illnesses, low pathogen identification rates, and slow turnaround time of conventional bacterial cultures. These factors contribute to both inadequate empiric therapy and overuse of broad-spectrum antibiotics, which can negatively impact outcomes. Recently, multiplex polymerase chain reaction (mPCR) assays capable of rapidly detecting multiple bacterial respiratory pathogens and resistance genes have emerged. However, their clinical utility in pneumonia management remains uncertain. Objective To assess the utility of bacterial mPCR assays in pneumonia diagnosis, their impact on antimicrobial usage, and their effect on patient outcomes. Methods A comprehensive literature review was conducted using MEDLINE to identify observational studies and randomised controlled trials (RCTs) evaluating the accuracy and clinical impact of bacterial mPCR tests for pneumonia. Results Bacterial mPCR assays demonstrate high sensitivity for pathogen detection, rapid turnaround compared to conventional cultures, and the ability to identify many common resistance genes. They may also improve pathogen detection in patients who received empirical antibiotics prior to specimen collection. However, mPCRs do not detect all potential pathogens, cannot reliably differentiate colonisation from infection, and may show discordance between genetic and phenotypic resistance. mPCR panels also generally require lower respiratory tract specimens, limiting their utility since many pneumonia patients cannot produce adequate sputum. Observational studies and RCTs suggest that mPCR may help optimise antibiotic selection, but RCTs have not clearly demonstrated reductions in overall antibiotic use or improved clinical outcomes including mortality. Implementation of mPCR without structured antimicrobial stewardship may limit clinical impact. Conclusions Bacterial mPCR assays offer rapid and sensitive pathogen detection, but their integration into pneumonia management requires careful consideration of clinical context and expert antimicrobial stewardship guidance. Future research should focus on optimising their diagnostic and therapeutic applications, evaluating cost-effectiveness, and assessing patient-centered outcomes.

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