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Lippi, G. and Guidi, G. (2007) Risk Management in Pre-Analytical Phase of Laboratory Testing. Clinical Chemistry and Laboratory Medicine, 45, 720-727.
https://doi.org/10.1515/CCLM.2007.167

has been cited by the following article:

  • TITLE: Errors of Clinical Laboratory and Its Impact on Patient Safety

    AUTHORS: Elisabet González Lao, Ángel Salas García, Marta Buxeda Figuerola, Ester Moreno, Ariadna Hernández Paraire

    KEYWORDS: Patient Safety, Medical Laboratory, Risks, Failure Modes, Processes

    JOURNAL NAME: Open Journal of Social Sciences, Vol.5 No.3, March 31, 2017

    ABSTRACT: The aim of this study is to analyse the potential risks of medical laboratory activities in all processes: Strategic, operational (pre-preanalytical, preanalytical, analytical, postanalytical and post-postanalytical) and support. Also, we value the impact of these risks in the patient safety. The methodology used in this study to identify and estimate the possible failure modes was the Failure Model and Effects Analysis (FMEA). The real failures then were registered in the same processes according to the methodology Failure Reporting Analysis and Corrective Action System (FRACAS). Moreover, it used the basis of available information of the laboratory quality system. The Risk Priority Number (RPN) with FMEA and FRACAS was calculated for every laboratory processes and it was made a comparative of the results obtained with both methodologies. Based on these results, we made the risk map in medical laboratory. These results allowed us identifying critical points in all laboratory processes and prioritize the control of these points. Furthermore, it helped to select preventive or corrective action that should be incorporated in the laboratory improvement planning and risk management.