| Literature DB >> 29142077 |
Poornima Ramanan1, Alexandra L Bryson1, Matthew J Binnicker1, Bobbi S Pritt1,2, Robin Patel3,2.
Abstract
The recent development of commercial panel-based molecular diagnostics for the rapid detection of pathogens in positive blood culture bottles, respiratory specimens, stool, and cerebrospinal fluid has resulted in a paradigm shift in clinical microbiology and clinical practice. This review focuses on U.S. Food and Drug Administration (FDA)-approved/cleared multiplex molecular panels with more than five targets designed to assist in the diagnosis of bloodstream, respiratory tract, gastrointestinal, or central nervous system infections. While these panel-based assays have the clear advantages of a rapid turnaround time and the detection of a large number of microorganisms and promise to improve health care, they present certain challenges, including cost and the definition of ideal test utilization strategies (i.e., optimal ordering) and test interpretation.Entities:
Keywords: molecular methods; multiplex PCR; syndromic testing
Mesh:
Year: 2017 PMID: 29142077 PMCID: PMC5740973 DOI: 10.1128/CMR.00024-17
Source DB: PubMed Journal: Clin Microbiol Rev ISSN: 0893-8512 Impact factor: 26.132