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]
Affiliations
- 1 Laboratory of Experimental Infection, Infectious Diseases Service, IDIBELL-Hospital Universitari Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain. Electronic address: celhaj@idibell.cat.
- 2 Laboratory of Experimental Infection, Infectious Diseases Service, IDIBELL-Hospital Universitari Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain.
- 3 Nephrology Service and Laboratory of Experimental Nephrology, University of Barcelona, Campus Bellvitge, Pavelló de Govern, L'Hospitalet de Llobregat, Barcelona, Spain.
- 4 Department of Microbiology, IDIBELL-Hospital Universitari Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain; CIBERES ISCIII, Spain.
- 5 Laboratory of Experimental Infection, Infectious Diseases Service, IDIBELL-Hospital Universitari Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain; Spanish Network for the Research in Infectious Diseases (REIPIRD12/0015), Instituto de Salud Carlos III, Madrid, Spain.
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.
Copyright © 2017 Elsevier España, S.L.U. and Sociedad Española de Enfermedades Infecciosas y Microbiología Clínica. All rights reserved.
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