Omisión de factores asociados a los no reportes de eventos adversos durante la fase preanalítica, analítica y pos-analítica del laboratorio clínico.

Abstract

The implementation of clinical diagnostic tests contributes to a great extent to the effectiveness of treatments in various pathologies, becoming a great support for medical diagnosis, however, with the increase in the requirement for diagnostic tests, difficulties have been generated in decision-making. samples referring to the identification of patients, the interpretation of results, among others, which generate adverse events in patients, therefore the present review seeks to identify the factors associated with the non-reporting of adverse events during the pre-analytical, analytical and post-analytical phase. -Clinical laboratory analysis, in order to make decisions aimed at providing safe care to users in an optimal way that guarantees compliance with safe practices for the patient, in this way the report of adverse events will be seen as a help tool to maintain this culture in the Healthcare Institutions.