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Quality Control of Compounded Crystalloid Fluids for Intravenous Delivery to Horses.
Magnusson, C B; Poulsen, K P; Budde, J A; Hartmann, F A; Aulik, N A; Raabis, S M; Moreira, A S D; Darien, B J; Peek, S F.
Afiliación
  • Magnusson CB; Department of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
  • Poulsen KP; Department of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
  • Budde JA; Wisconsin Veterinary Diagnostic Laboratory, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
  • Hartmann FA; UW Veterinary Care Pharmacy, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
  • Aulik NA; Clinical Pathology Laboratory, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
  • Raabis SM; Wisconsin Veterinary Diagnostic Laboratory, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
  • Moreira ASD; Department of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
  • Darien BJ; Department of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
  • Peek SF; Department of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
J Vet Intern Med ; 32(1): 469-473, 2018 Jan.
Article en En | MEDLINE | ID: mdl-29114956
ABSTRACT

BACKGROUND:

Periodic lack of availability and high cost of commercially produced isotonic fluids for intravenous (IV) use in horses have increasingly led to use of home-made or commercially compound fluids by veterinarians. Data regarding the quality control and safety of compounded fluids would be of benefit to equine veterinarians.

OBJECTIVES:

To compare electrolyte concentrations, sterility, and endotoxin contamination of commercially available fluids to 2 forms of compounded isotonic crystalloid fluids intended for IV use in horses.

METHODS:

Prospective study. Two methods of preparing compounded crystalloids formulated to replicate commercial Plasma-Lyte A (Abbott, Chicago, IL) were compared. One formulation was prepared by a hand-mixed method involving chlorinated drinking water commonly employed by equine practitioners, and the other was prepared by means of ingredients obtained from a commercial compounding pharmacy. The variables for comparison were electrolyte concentrations, sterility, and presence of endotoxin contamination.

RESULTS:

Electrolyte concentrations were consistent within each product but different between types of fluids (P < 0.0001). Hand-mixed fluids had significantly more bacterial contamination compared to commercial Plasma-Lyte A (P = 0.0014). One of the hand-mixed fluid samples had detectable endotoxin contamination. CONCLUSIONS AND CLINICAL IMPORTANCE Chlorinated drinking water is not an acceptable source of water to compound isotonic fluids for IV administration. Equine practitioners should be aware of this risk and obtain the informed consent of their clients.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Control de Calidad / Infusiones Intravenosas / Composición de Medicamentos / Electrólitos / Caballos / Soluciones Isotónicas Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: J Vet Intern Med Asunto de la revista: MEDICINA INTERNA / MEDICINA VETERINARIA Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Control de Calidad / Infusiones Intravenosas / Composición de Medicamentos / Electrólitos / Caballos / Soluciones Isotónicas Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: J Vet Intern Med Asunto de la revista: MEDICINA INTERNA / MEDICINA VETERINARIA Año: 2018 Tipo del documento: Article