Literature DB >> 20121916

Monitoring bacterial contamination in equine platelet concentrates obtained by the tube method in a clean laboratory environment under three different technical conditions.

M E Alvarez1, C E Giraldo, J U Carmona.   

Abstract

REASONS FOR PERFORMING STUDY: There is a growing interest in the use of autologous platelet concentrates (PCs) as treatment for chronic musculoskeletal diseases in horses. However, there is no information on the risk of bacterial contamination during their preparation.
OBJECTIVES: To: 1) assess the risk of bacterial contamination in equine PCs obtained by the tube method under 3 technical conditions: a) in a laminar flow cabinet, in a clean laboratory environment both with (b) and without (c) Bunsen burner; 2) identify the critical points of the process of PCs preparation with risk of bacterial contamination; and 3) identify the potential bacterial contaminants in the process and their antibiotic susceptibility.
METHODS: Bacteriological samples were taken from: the skin (shaved or unshaved) of the venipuncture site in 15 horses, both before and after being disinfected; hands and throat of the operator; caps of the tubes where the blood was processed; environment where the equine blood samples were collected; laboratory environment; laminar flow cabinet; bacteriological stove; and PCs obtained under 3 technical conditions.
RESULTS: Bacteria were isolated from nonaseptically prepared equine skin, hands and throat of the operator, and the place where the blood samples were taken. Bacteria were not isolated from tube caps, laboratory environment, laminar flow cabinet or PCs. The isolated bacteria were normal biota from equine skin, human skin and throat, and environmental contaminants. Of the isolated bacteria, 23% were resistant to penicillin, 19% to ampicillin, 2.12% to ceftiofur, 3.2% to sulphamethoxazole/trimethoprim and 1.1% to enrofloxacin. Resistance to amikacin and gentamicin was not seen. CONCLUSIONS AND POTENTIAL RELEVANCE: Uncontaminated PCs can be obtained by the tube method in a clean laboratory environment without the need for either a laminar flow cabinet or a Bunsen burner. It is mandatory to perform the procedure following strict aseptic technique.

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Year:  2010        PMID: 20121916     DOI: 10.2746/042516409X455221

Source DB:  PubMed          Journal:  Equine Vet J        ISSN: 0425-1644            Impact factor:   2.888


  5 in total

1.  Simple tube centrifugation for processing platelet-rich plasma in the horse.

Authors:  Robin L Fontenot; Carolyn A Sink; Stephen R Werre; Nicole M Weinstein; Linda A Dahlgren
Journal:  Can Vet J       Date:  2012-12       Impact factor: 1.008

2.  Temporal Bacteriostatic Effect and Growth Factor Loss in Equine Platelet Components and Plasma Cultured with Methicillin-Sensitive and Methicillin-Resistant Staphylococcus aureus: A Comparative In Vitro Study.

Authors:  Catalina López; María E Alvarez; Jorge U Carmona
Journal:  Vet Med Int       Date:  2014-11-24

3.  Effects of sodium citrate and acid citrate dextrose solutions on cell counts and growth factor release from equine pure-platelet rich plasma and pure-platelet rich gel.

Authors:  Carlos E Giraldo; María E Álvarez; Jorge U Carmona
Journal:  BMC Vet Res       Date:  2015-03-14       Impact factor: 2.741

Review 4.  A Critical Overview of the Use of Platelet-Rich Plasma in Equine Medicine Over the Last Decade.

Authors:  Livia Camargo Garbin; Catalina Lopez; Jorge U Carmona
Journal:  Front Vet Sci       Date:  2021-03-31

5.  Temporal Release and Denature of Several Mediators in Pure Platelet-Rich Plasma and Temperature-Induced Platelet Lysates Derived from a Similar Bovine Platelet Concentrate.

Authors:  Jorge U Carmona; Catalina López; Alejandro Ceballos-Márquez
Journal:  Vet Med Int       Date:  2022-09-23
  5 in total

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