Recomendaciones para el diseño e implementación de un programa de aseguramiento de la calidad de la fase preanalítica
- Itziar Marzana Sanz
- Mercedes Ibarz Escuer
- María Antonia Llopis Díaz
- Nuria Barba Meseguer
- María Jesús Alsina Kirchner
- Débora Martínez Espartosa 1
- Montserrat Ventura Alemany 2
- Isabel García del Pino Castro 1
- Marta Segovia Amaro 1
- Juan José Puente Lanzarote
- Josep Miquel Bauça 1
- Andrea Caballero Garralda
- Carolina Gómez Gómez 1
- Ana García Álvarez 1
- Virtudes Álvarez Funes
- Rubén Gómez Rioja
- 1 Comisión de Calidad Extraanalítica de la Sociedad Española de Medicina de Laboratorio (SEQCML), Barcelona, España
- 2 Comisión de Calidad Extraanalítica, Sociedad Española de Medicina de Laboratorio
ISSN: 1888-4008
Year of publication: 2019
Volume: 12
Issue: 4
Pages: 54-65
Type: Article
More publications in: Revista del laboratorio clínico
Abstract
The quality assurance of the pre-analytical phase is oriented towards two key aspects; the management of pre-analytical errors from the perspective of patient safety, and the improvement and harmonisation of procedures, based on the application of regulations and professional recommendations. Like the rest of the phases, it should include an internal quality assurance program, as well as the participation in external quality assurance programs. The internal quality control should mainly be based on the identification of risks, systematic detection of errors, and establishment of indicators. The selection of indicators prioritising the impact on the patient, the way to detect and record errors in a systematic and easily exploitable manner, and also the variables used in the calculations, are important aspects to measure the effectiveness of improvement actions and to allow comparability between laboratories. In this sense, the external quality assurance programs of the pre-analytical phase based on the comparison of indicators are a useful tool for the design and implementation of a quality assurance program. This document is intended as a support for each laboratory to select, implement, and evaluate its own indicators, according to the individual characteristics of its pre-analytical procedures, but without losing sight of the harmonisation between laboratories.