| Literature DB >> 31383269 |
Henrietta Abodakpi1, Audrey Wanger2, Vincent H Tam3.
Abstract
As a class, β-lactamase inhibitors have proved successful in extending the clinical utility of β-lactam antibiotics by circumventing β-lactamase-mediated resistance. However, the rapid evolution of these β-lactamases calls for a critical reevaluation of the relationships between susceptibility, drug exposures, and bacterial response. The existing paradigm for in vitro susceptibility testing and development of β-lactam/β-lactamase inhibitor combinations may not optimally facilitate clinical use. Thus, alternative approaches for pairing these combinations and evaluating in vitro susceptibility are needed to provide better guidance to clinicians.Entities:
Keywords: Combination therapy; Gram-negative bacteria; Optimal dosing; Pharmacokinetics/pharmacodynamics; Susceptibility testing
Year: 2019 PMID: 31383269 PMCID: PMC6686870 DOI: 10.1016/j.cll.2019.05.006
Source DB: PubMed Journal: Clin Lab Med ISSN: 0272-2712 Impact factor: 1.935