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The Pharmacodynamics of β‐Lactams

Turnidge, J. D.·1998·Clinical Infectious Diseases

Abstract

Considerable information on the pharmacodynamics of beta-lactams has accumulated in the past 20 years. In vitro, beta-lactams demonstrate time-dependent killing and variable postantibiotic effects. Animal models have shown that the time for which drug levels exceed the minimum inhibitory concentration (MIC) correlates best with bacterial eradication, and this is now being borne out in human studies. In investigations on osteomyelitis and endocarditis, trough serum inhibitory titers have generally correlated better with cure than have peak titers, and studies that have analyzed outcomes in relation to the MIC for the infecting pathogen have shown decreasing clinical efficacy with increasing MICs. One prospective study has shown that time above MIC correlated better with time to pathogen eradication than did area under the curve. In some continuous-infusion studies, significantly better outcomes were achieved with continuous infusion against susceptible bacteria or for patients with persistent, profound neutropenia. With use of time above MIC as the predictor of efficacy, it is possible to reexamine current dosing schedules critically.

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Metadata

Authors
Turnidge, J. D.
Venue
Clinical Infectious Diseases
Published
1998-07
Volume
27
Issue
1
Pages
10-22
ISSN
  • 1058-4838 (ISSN-L)
  • 1537-6591
OpenAlex
W2131171455
Cited by
593
References
0
FWCI
7.63
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: The Pharmacodynamics of β‐Lactams. https://app.cochat.ai/papers/10.1086/514622
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Turnidge, J. D. (1998). The Pharmacodynamics of β‐Lactams. Clinical Infectious Diseases. https://doi.org/10.1086/514622

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.