Drawbacks of the use of cotrimoxazole in foreign-body infections

Enferm Infecc Microbiol Clin (Engl Ed). 2018 Jun-Jul;36(6):362-365. doi: 10.1016/j.eimc.2017.07.005. Epub 2017 Aug 14.
[Article in English, Spanish]

Abstract

Introduction: The anti-staphylococcal efficacy of cotrimoxazole in the setting of difficult-to-treat infections seems to be compromised by large amounts of pus and devitalized tissue, and, therefore, high levels of thymidine. Our objective was to evaluate the activity of cotrimoxazole against a staphylococcal foreign-body infection experimental model, which also yields significant quantities of thymidine.

Material and methods: We used a rat tissue-cage model of infection (with high inherent thymidine levels) caused by a strain of methicillin-susceptible Staphylococcus aureus (MSSA; ATCC 29213). MIC values were determined (microdilution method) and compared in the presence or absence of tissue-cage fluid samples.

Results: The inefficacy of cotrimoxazole was found to be similar to that of the control group. The MIC of cotrimoxazole was 4-8 fold higher in the presence of rat tissue-cage fluid.

Conclusions: The inefficacy of cotrimoxazole in our foreign-body infection model by MSSA, and the probable negative impact of the presence of thymidine on its efficacy, challenge the use of this drug in acute phases of foreign-body infections. It should be reserved as an alternative treatment when the infection is more controlled.

Keywords: Cotrimoxazol; Cotrimoxazole; Foreign-body infection; Infección por cuerpo extraño; S. aureus; Thymidine; Timidina.

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacokinetics
  • Anti-Bacterial Agents / therapeutic use*
  • Bacterial Load
  • Diffusion Chambers, Culture
  • Dose-Response Relationship, Drug
  • Foreign Bodies / complications*
  • Microbial Sensitivity Tests
  • Rats
  • Staphylococcal Infections / drug therapy*
  • Staphylococcal Infections / microbiology
  • Thymidine / analysis
  • Treatment Failure
  • Trimethoprim, Sulfamethoxazole Drug Combination / pharmacokinetics
  • Trimethoprim, Sulfamethoxazole Drug Combination / therapeutic use*
  • Wound Infection / drug therapy*
  • Wound Infection / etiology
  • Wound Infection / metabolism

Substances

  • Anti-Bacterial Agents
  • Trimethoprim, Sulfamethoxazole Drug Combination
  • Thymidine