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Rapid Molecular Diagnostics to Inform Empiric Use of Ceftazidime/Avibactam and Ceftolozane/Tazobactam Against Pseudomonas aeruginosa: PRIMERS IV
Author(s) -
Scott Evans,
Thuy Tien T. Tran,
Andrea M. Hujer,
Carol Hill,
Kristine M. Hujer,
José R. Mediavilla,
Claudia Manca,
Tatiana Domitrovic,
Federico Pérez,
Michael Farmer,
Kelsey Pitzer,
Brigid Wilson,
Barry N. Kreiswirth,
Robin Patel,
Michael R. Jacobs,
Liang Chen,
Vance G. Fowler,
Henry F. Chambers,
Robert A. Bonomo
Publication year - 2018
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1093/cid/ciy801
Subject(s) - ceftazidime/avibactam , pseudomonas aeruginosa , ceftazidime , medicine , tazobactam , empiric therapy , microbiology and biotechnology , cephalosporin , resistome , intensive care medicine , antibiotic resistance , antibiotics , piperacillin , biology , bacteria , genetics , integron
Background Overcoming β-lactam resistance in pathogens such as Pseudomonas aeruginosa is a major clinical challenge. Rapid molecular diagnostics (RMDs) have the potential to inform selection of empiric therapy in patients infected by P. aeruginosa. Methods In this study, we used a heterogeneous collection of 197 P. aeruginosa that included multidrug-resistant isolates to determine whether 2 representative RMDs (Acuitas Resistome test and VERIGENE gram-negative blood culture test) could identify susceptibility to 2 newer β-lactam/β-lactamase inhibitor (BL-BLI) combinations, ceftazidime/avibactam (CZA) and ceftolozane/tazobactam (TOL/TAZO). Results We found that the studied RMD platforms were able to correctly identify BL-BLI susceptibility (susceptibility sensitivity, 100%; 95% confidence interval [CI], 97%, 100%) for both BLs-BLIs. However, their ability to detect resistance to these BLs-BLIs was lower (resistance sensitivity, 66%; 95% CI, 52%, 78% for TOL/TAZO and 33%; 95% CI, 20%, 49% for CZA). Conclusions The diagnostic platforms studied showed the most potential in scenarios where a resistance gene was detected or in scenarios where a resistance gene was not detected and the prevalence of resistance to TOL/TAZO or CZA is known to be low. Clinicians need to be mindful of the benefits and risks that result from empiric treatment decisions that are based on resistance gene detection in P. aeruginosa, acknowledging that such decisions are impacted by the prevalence of resistance, which varies temporally and geographically.

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