Validation of pleural fluid group A Streptococcus and Staphylococcus aureus PCR assays and their potential clinical impact in children with complicated pneumonia
Erin C. Ho , Molly Butler , Kaitlin E. Olson , Dennis Simmons , Colsen Beveridge , Kristen Miller , Meghan Birkholz , Sarah A. Jung , Samuel R. Dominguez
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引用次数: 0
Abstract
Background
Better diagnostic tools are needed to increase the yield and speed of pathogen identification in pediatric complicated community-acquired pneumonia (cCAP), and thereby, improve patient care through optimization of antibiotic therapy.
Methods
We performed analytical and clinical validations of a laboratory-developed group A Streptococcus (GAS) PCR and a commercially available Staphylococcus aureus (S. aureus), including methicillin-resistant S. aureus (MRSA), PCR for pleural fluid specimens and studied the potential clinical impact of pleural fluid GAS and S. aureus PCR testing in children with cCAP.
Results
Both assays demonstrated high analytical sensitivity, specificity, reproducibility, and accuracy in detection of their target pathogens in pleural fluid. In potential clinical impact analysis for 62 children with cCAP requiring pleural fluid drainage, the addition of GAS and S. aureus PCR testing to existing diagnostic testing increased pathogen yield from 71.0 % to 83.2 % (p = 0.023), decreased theoretical median time from hospitalization to optimal therapy from 5.1 days (95 % CI: 2.4–7.2) to 3.7 days (95 % CI: 1.9–6.9, p = 0.001) and theoretical median time from start to stop of unwarranted MRSA therapy from 1.5 days (95 % CI: 1.0–3.7) to 0.8 days (95 % CI: 0.5–1.2, p < 0.001).
Conclusion
PCR testing is a sensitive and specific method for detecting GAS and S. aureus in pleural fluid. Clinical implementation of these targeted pleural fluid PCR assays has the potential to significantly increase pathogen yield, facilitate faster de-escalation of MRSA therapy and transition to narrow, targeted antibiotics, suggesting their utility for pediatric complicated pneumonia.
期刊介绍:
The Journal of Microbiological Methods publishes scholarly and original articles, notes and review articles. These articles must include novel and/or state-of-the-art methods, or significant improvements to existing methods. Novel and innovative applications of current methods that are validated and useful will also be published. JMM strives for scholarship, innovation and excellence. This demands scientific rigour, the best available methods and technologies, correctly replicated experiments/tests, the inclusion of proper controls, calibrations, and the correct statistical analysis. The presentation of the data must support the interpretation of the method/approach.
All aspects of microbiology are covered, except virology. These include agricultural microbiology, applied and environmental microbiology, bioassays, bioinformatics, biotechnology, biochemical microbiology, clinical microbiology, diagnostics, food monitoring and quality control microbiology, microbial genetics and genomics, geomicrobiology, microbiome methods regardless of habitat, high through-put sequencing methods and analysis, microbial pathogenesis and host responses, metabolomics, metagenomics, metaproteomics, microbial ecology and diversity, microbial physiology, microbial ultra-structure, microscopic and imaging methods, molecular microbiology, mycology, novel mathematical microbiology and modelling, parasitology, plant-microbe interactions, protein markers/profiles, proteomics, pyrosequencing, public health microbiology, radioisotopes applied to microbiology, robotics applied to microbiological methods,rumen microbiology, microbiological methods for space missions and extreme environments, sampling methods and samplers, soil and sediment microbiology, transcriptomics, veterinary microbiology, sero-diagnostics and typing/identification.