The potential of molecular diagnostics and serum procalcitonin levels to change the antibiotic management of community-acquired pneumonia
- PMID: 27377675
- PMCID: PMC7126930
- DOI: 10.1016/j.diagmicrobio.2016.06.008
The potential of molecular diagnostics and serum procalcitonin levels to change the antibiotic management of community-acquired pneumonia
Abstract
Two diagnostic bundles were compared in 127 evaluable patients admitted with community-acquired pneumonia (CAP). Diagnostic modalities in all patients included cultures of sputum (if obtainable) and blood, urine for detection of the antigens of Streptococcus pneumoniae and Legionella pneumophila, and nasal swabs for PCR probes for S. pneumoniae and Staphylococcus aureus. At least one procalcitonin level was measured in all patients. For virus detection, patients were randomized to either a 5-virus, lab-generated PCR panel or the broader and faster FilmArray PCR panel. Overall, an etiologic diagnosis was established in 71% of the patients. A respiratory virus was detected in 39%. The potential for improved antibiotic stewardship was evident in 25 patients with only detectable respiratory virus and normal levels of PCT.
Keywords: Community-acquired pneumonia; Diagnostic bundles; FilmArray; Molecular diagnostics; Procalcitonin.
Copyright © 2016 Elsevier Inc. All rights reserved.
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References
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- Andrews A.L., Simpson A.N., Heine D., Teufel R.J. A cost-effectiveness analysis of obtaining blood cultures in children hospitalized for community-acquired pneumonia. J Pediatrics. 2015;167:1280–1286. - PubMed
-
- Becker K.L., Snider R., Nylen E.S. Procalcitonin assay in systemic inflammation, infection and sepsis: clinical utility and limitatons. Crit Care Med. 2008;36:941–952. - PubMed
-
- Collins A.M., Johnstone C.M.K., Gritzfeld J.F., Banyard A., Hancock C.A. wright AD et al. Pneumococcal colonization rates in patients admitted to a United kingdom Hospital with Lower Respiratory Tract Infection: a Prospective Case-Control study. J. Clinical Microbiology. 2016;54:944–949. - PMC - PubMed
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