Desarrollo de un sistema de control de calidad en la preparación de citostáticos
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Carles Iniesta Navalón [1] ; Pilar Llopis Salvià [1]
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[1] Hospital de la Ribera
Hospital de la Ribera
Valencia, España
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- Localización: Atención Farmacéutica, ISSN 1139-7357, Vol. 5, Nº. 6, 2003, págs. 388-396
- Idioma: español
- Títulos paralelos:
- Development of quality control system for the preparation of cytostatic drugs
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Resumen
Objective: To describe a quality control system for the detection of errors in the preparation of cytostatic drugs. Methods: The program of quality control implemented in the intravenous therapy unit is based on a gravimetric control. Results: 26% of the preparations carried out underwent a gravimetric control. From the evaluated preparations, 71.4% presented an absolute difference between the observed and the theoretical weight lower than 1.0 g, a value inferior to the sensitivity limit of the used analytical technique. For the MIVs with absolute differences superior to 1.0 g (n = 273), 89 presented a deviation in absolute value =5% of the nominal dose (9.1% of the controls carried out). Conclusion: A fast, reliable and low cost system has been developed for the detection of errors in the preparation of mixtures with cytostatic drugs
