Antimicrobial Resistance: Pharmacokinetics‐Pharmacodynamics of Antimicrobial Therapy: It’s Not Just for Mice Anymore
Антимикробная резистентность: фармакокинетика–фармакодинамика антимикробной терапии: это уже не только для мышей
2006-12-01
SCID: 54.1/cvap5hns
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antimicrobial chemotherapyantimicrobial resistancein vitro resistancepharmacokinetic-pharmacodynamic infection modelssusceptibility breakpoints
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Abstract (AI)
Since the advent of the modern era of antimicrobial chemotherapy in the 1930s, animal infection models have allowed for the in vivo evaluation of antimicrobial agents for the treatment of experimentally induced infection. Today, animal pharmacokinetic-pharmacodynamic (PK-PD) infection models serve as a cornerstone of the preclinical assessment process for antibacterial agents and dose and dosing interval selection, as decision support for setting in vitro susceptibility breakpoints, and, finally, for the evaluation of the meaning of in vitro resistance. Over the past 15 years, considerable PK-PD data have been derived from infected patients for many classes of antimicrobial agents. These data provide the opportunity to confirm knowledge gained from animal PK-PD infection models.
Key Findings
1
Animal PK-PD infection models support decisions on in vitro susceptibility breakpoints and interpretation of in vitro resistance.
2
Animal infection models remain central to preclinical antibacterial assessment, including dose and dosing-interval selection.
3
Over the past 15 years, substantial PK-PD data have been obtained from patients with infections for multiple antimicrobial classes.
4
Patient-derived PK-PD data provide an opportunity to validate and confirm knowledge generated by animal infection models.
5
The title emphasizes extending antimicrobial PK-PD evaluation beyond animal models to human clinical data.
Research Object
Pharmacokinetic-pharmacodynamic (PK-PD) infection models (animal and patient-derived) used in antimicrobial therapy evaluation
Research Subject
The translation and confirmation of PK-PD relationships from animal infection models to human antimicrobial therapy, including dose selection, dosing intervals, susceptibility breakpoints, and the interpretation of in vitro resistance
Publication Details
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2006-12-01
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