Effectiveness of the complex use of antiseptic agents based on alcohols and iodophors in veterinary surgery
DOI:
https://doi.org/10.31073/onehealthjournal2026-IV-04Keywords:
antiseptics, veterinary surgery, surgical infection, iodophors, alcohol-based preparations, disinfectants, synergism, postoperative complicationsAbstract
The aim of this study was to conduct a laboratory and clinical evaluation of the efficacy of the combined use of an alcohol-based antiseptic and an iodophore-based disinfectant in veterinary surgical practice, as well as to determine their synergistic antimicrobial activity against clinical veterinary isolates. Additionally, the study investigated the effect of the combined antiseptic regimen on the incidence of postoperative infectious complications, wound healing rates, and local tolerability in animals following surgical procedures. The study was conducted in two phases—laboratory and clinical. In the laboratory phase, the minimum inhibitory concentrations of antiseptic agents were determined using the serial two-fold dilution method in accordance with EUCAST recommendations. Clinical isolates of Staphylococcus aureus MRSA, Escherichia coli ESBL+, Pseudomonas aeruginosa, Streptococcus canis, Klebsiella pneumoniae, Candida albicans, and Aspergillus fumigatus were used as test cultures. Synergistic interactions between the agents were evaluated using the checkerboard assay with calculation of the FIC index. Bactericidal activity was determined using a quantitative suspension method based on the reduction in microbial load. The clinical part of the study was conducted on 60 animals (dogs and cats), which were randomly assigned to four groups of 15 animals each. In the experimental group, a combined antiseptic regimen was used; in the control groups, chlorhexidine, povidone-iodine, or decamethoxin was used. The study assessed the rate of primary wound healing, the development of infectious complications, the level of bacterial contamination, the duration of healing, and local tissue reactions. Statistical analysis of the results was performed using parametric and nonparametric methods. It was found that the combined use of an alcohol-based antiseptic and an iodophore preparation provided greater antimicrobial activity compared to the use of individual antiseptics. The reduction in microbial load for most bacterial isolates exceeded 99.97%. The FIC values for the combinations studied ranged from 0.33 to 0.44, indicating a synergistic effect. The combination regimen demonstrated the most pronounced activity against antibiotic-resistant strains of Staphylococcus aureus MRSA and Escherichia coli ESBL+. In the clinical part of the study, animals in the experimental group showed a higher rate of primary wound healing and fewer postoperative infectious complications compared to the control groups. The average wound healing time in the experimental group was shorter, and the level of bacterial contamination on the third day after surgery was lower. Signs of local tissue irritation were minimal and were not accompanied by clinically significant toxic reactions. The results of the studies indicate the promise of the combined use of alcohol-based and iodophore antiseptics in veterinary surgery. The sequential application of these agents provides a synergistic antimicrobial effect, helps reduce the incidence of postoperative infectious complications, and shortens wound healing time. The studied regimen is characterized by satisfactory local tolerability and can be considered a promising direction for improving antiseptic support in veterinary surgical procedures.
References
Abbood H. M., Hijazi K., Gould I. M. (2023). Chlorhexidine resistance or cross-resistance, that is the question. Antibiotics; 12(5), Article 798. https://doi.org/10.3390/antibiotics12050798
Augustin M., Herberger K., Wille A., Twarock S. (2023). Impact of human wound exudate on the bactericidal efficacy of commercial antiseptic products. Journal of Wound Care; 32(7), 422–427. https://doi.org/10.12968/jowc.2023.32.7.422
Bartoli S., Cortese F., Sartelli M., Sganga G. (Eds.). (2025). Infections in surgery: Prevention and management; Springer. https://doi.org/10.1007/978-3-031-60462-1
Bodega-Azuara J., Bellés-Medall M. D., Edo-Peñarrocha J., Ferrando-Piqueres R., Perez-Alba A., Reque-Santivañez J. (2023). Vancomycin and daptomycin stability in heparin or sodium citrate lock solutions. The Journal of Vascular Access; 24(6), 1452–1458. https://doi.org/10.1177/11297298211045893
Buonavoglia C., Martella V. (2007). Canine respiratory viruses. Veterinary Research; 38(2), 355–373. https://doi.org/10.1051/vetres:2006058
European Committee for Standardization. (2021). EN 12353:2021 Chemical disinfectants and antiseptics — Preservation of test organisms used for the determination of bactericidal (including Legionella), mycobactericidal, sporicidal, fungicidal and virucidal (including bacteriophages) activity. CEN.
European Committee for Standardization. (2019). EN 1040:2019 Chemical disinfectants and antiseptics — Quantitative suspension test for the evaluation of basic bactericidal activity of chemical disinfectants and antiseptics — Test method and requirements (phase 1). CEN.
State Committee of Ukraine for Technical Regulation and Consumer Policy. (2004). DSTU EN 1040:2004. Chemical disinfectants and antiseptics — Basic bactericidal activity — Test method and requirements (phase 1) (EN 1040:1997, IDT). Derzhspozhyvstandart of Ukraine.
Centers for Disease Control and Prevention. (2026). National Healthcare Safety Network (NHSN). Patient Safety Component Manual. Chapter 9: Surgical Site Infection (SSI) Event; https://www.cdc.gov/nhsn/pdfs/pscmanual/9pscssicurrent.pdf
Chen S., Chen J. W., Guo B., Xu C. C. (2020). Preoperative antisepsis with chlorhexidine versus povidone-iodine for the prevention of surgical site infection: A systematic review and meta-analysis. World Journal of Surgery; 44(5), 1412–1424. https://doi.org/10.1007/s00268-020-05384-7
Doyle A. J., Saab M. E., McClure J. T. (2022). Comparison of chlorhexidine and alcohol-based antisepsis on the paralumbar fossa in cattle. Veterinary Surgery; 51(7), 1191–1195. https://doi.org/10.1111/vsu.13878
European Committee on Antimicrobial Susceptibility Testing. (2022). EUCAST guidelines for detection of resistance mechanisms and specific resistances of clinical and/or epidemiological importance; (Version 2.0).
Fink K., Örgel M., Baier C., Brauckmann V., Giannoudis V., Liodakis E. (2023). Quality of lower limb preoperative skin preparation using colorless versus colored disinfectants–Results of an experimental, randomized study in a close to reality setting. PLOS ONE; 18(3), Article e0282662. https://doi.org/10.1371/journal.pone.0282662
Kovalenko V. L. (Ed.). (2014). Metody kontroliu dezinfikuiuchykh zasobiv [Methods for control of disinfectants]. VSP “IPO KNUBA”.
Kovalenko V. L., Kovalenko P. L., Ponomarenko G. V., Kukhtyn M. D., Midyk S. V., Horiuk Yu. V., Garkavenko V. M. (2018). Changes in lipid composition of Escherichia coli and Staphylococcus aureus cells under the influence of disinfectants Barez, Biochlor and Geocide. Ukrainian Journal of Ecology; 8(1), 547–550. https://doi.org/10.15421/2018_248
Marchionatti E., Constant C., Steiner A. (2024). Preoperative skin asepsis in bovine surgery: An outcome-blinded 3-arm randomized clinical trial under non-sterile operating room conditions. Frontiers in Veterinary Science; 11, Article 1446649. https://doi.org/10.3389/fvets.2024.1446649
Mönch E., Bolten A., Niesalla H., Senges C. (2024). Alcohol-based hand rubs can fulfil efficacy requirements of EN 1500 in 15 seconds. GMS Hygiene and Infection Control; 19, Doc41. https://doi.org/10.3205/dgkh000496
Odds F. C. (2003). Synergy, antagonism, and what the chequerboard puts between them. Journal of Antimicrobial Chemotherapy; 52(1), 1. https://doi.org/10.1093/jac/dkg301
Ortega-Llamas L., Quiñones-Vico M. I., García-Valdivia M., et al. (2022). Cytotoxicity and wound closure evaluation in skin cell lines after treatment with common antiseptics for clinical use. Cells; 11(9), Article 1395. https://doi.org/10.3390/cells11091395
Sørensen T. M., Scahill K., Espinel Rupérez J., Oleniuk M., Swinbourne F., Verwilghen D., et al. (2024). Antimicrobial prophylaxis in companion animal surgery: A scoping review for European Network for Optimization of Antimicrobial Therapy (ENOVAT) guidelines. The Veterinary Journal; 304, Article 106101. https://doi.org/10.1016/j.tvjl.2024.106101
Spettel K., Bumberger D., Camp I., Kriz R., Willinger B. (2022). Efficacy of octenidine against emerging echinocandin-, azole- and multidrug-resistant Candida albicans and Candida glabrata. Journal of Global Antimicrobial Resistance; 29, 23–28. https://doi.org/10.1016/j.jgar.2022.01.028
Välkki K. J., Thomson K. H., Grönthal T. S. C., Junnila J. J. T., Rantala M. H. J., Laitinen-Vapaavuori O. M., Mölsä S. H. (2020). Antimicrobial prophylaxis is considered sufficient to preserve an acceptable surgical site infection rate in clean orthopaedic and neurosurgeries in dogs. Acta Veterinaria Scandinavica; 62(1), Article 53. https://doi.org/10.1186/s13028-020-00545-z
Verwilghen D. R., Pelosi A., Abbas M., Allerton F., Archer D., Baxter G., et al. (2026). Surgical site infection definitions consensus: A first step toward improving prevention in veterinary medicine. American Journal of Veterinary Research; 87(3), 1–14. https://doi.org/10.2460/ajvr.25.03.0099
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