AI Article Synopsis

  • Antibiotic treatment for bone and joint infections (BJI) often follows standard dosing, but it's unclear if this provides sufficient concentration at the infection site to effectively kill bacteria.
  • A literature review assessed the concentration of antibiotics in bone and synovial tissues of humans, noting details like patient numbers, dosing, and sampling methods, while comparing findings to epidemiological cutoff values for targeted bacteria.
  • While some antibiotics like ciprofloxacin and vancomycin showed adequate exposure with standard dosing, the overall research is limited and varied, indicating the need for more thorough studies on pharmacokinetics and pharmacodynamics in BJI.

Article Abstract

Introduction: Currently, antibiotic treatment is often a standard dosing regimen in bone and joint infections (BJI). However, it remains unknown if exposure at the target-site is adequate. The aim of this review is to gain more insight in the relationship between the target site concentration of antibiotic and the minimal inhibitory concentration to target the bacteria in bone and joint infections (BJI).

Areas Covered: A literature search was performed by Erasmus MC Medical library. Bone, bone tissue and synovial concentration of antibiotics were covered in humans. In addition, we reported number of patients, dose, sampling method, analytical method and tissue and plasma concentrations. We used the epidemiological cutoff value (ECOFF) values of the targeted micro-organisms. If more than 3 publications were available on the antibiotic, we graphically presented ECOFFS values against reported antibiotic concentrations.

Expert Opinion: For most antibiotics, the literature is sparse. In addition, a lot of variable and total antibiotic concentrations are published. Ciprofloxacin, cefazolin, cefuroxime, vancomycin and linezolid seem to have adequate average exposure if correlating total concentration to ECOFF, when standard dosing is used. With regard to other antibiotics, results are inconclusive. More extensive pharmacokinetic/pharmacodynamic modeling in BJI is needed.

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Source
http://dx.doi.org/10.1080/17425255.2022.2117607DOI Listing

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