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Pharmacokinetic/Pharmacodynamic Evaluation of Antimicrobial Treatments of Orofacial Odontogenic Infections

 

作者: Arantxa Isla,   Andrés Canut,   Alicia R Gascón,   Alicia Labora,   Bruno Ardanza-Trevijano,   Maria Ángelés Solinís,   Jose Luis Pedraz,  

 

期刊: Clinical Pharmacokinetics  (ADIS Available online 2005)
卷期: Volume 44, issue 3  

页码: 305-316

 

ISSN:0312-5963

 

年代: 2005

 

出版商: ADIS

 

关键词: Antibacterials, pharmacokinetics;Antibacterials, pharmacodynamics;Antibacterials, therapeutic use;Oral infections, treatment

 

数据来源: ADIS

 

摘要:

ObjectiveTo evaluate the efficacy of antimicrobial therapy in oral odontogenic infections using estimated pharmacokinetic/pharmacodynamic parameters or efficacy indices, and to compare pharmacokinetic/pharmacodynamic breakpoints with National Committee for Clinical Laboratory Standards’ (NCCLS) breakpoints.Study designRetrospective literature search to obtain minimum inhibitory concentration (MIC) values, pharmacokinetic parameters of antimicrobials and NCCLS breakpoints. Pharmacokinetic simulations were carried out using WinNonlin software (Pharsight Corporation, Mountain View, CA, USA).MethodsFor antimicrobials with time-dependent activity, the time that the plasma drug concentration exceeds the MIC as the percentage of dose interval at steady state was calculated. For antimicrobials with concentration-dependent activity, the total area under the plasma concentration-time curve over 24 hours at steady state divided by the MIC was calculated. Pharmacokinetic/pharmacodynamic breakpoints were calculated according to these parameters.ResultsOnly amoxicillin/clavulanic acid and clindamycin showed adequate efficacy indices against the most commonly isolated bacteria in odontogenic infections. Metronidazole reached good indices against anaerobes only. Pharmacokinetic/pharmacodynamic susceptibility breakpoints do not coincide exactly with NCCLS breakpoints.ConclusionOwing to the scarcity of double-blind, clinical trials on the use of antimicrobials in endodontics, this study may be useful in determining the best antimicrobial treatment in these infections. However, as we have not used concentration data in infected tissue to determine pharmacokinetic/pharmacodynamic indices, it would be necessary to design clinical trials in order to confirm these results.

 

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