What is it about?
It is reported an overview on the automation of the preanalytical phase of laboratory testing and a Failure Mode Effects and Criticality Analysis (FMECA) of its various critical steps, correlated not only with the risk of errors but also with the automated versus human controlled management.
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Why is it important?
Preanalytical errors account for most of the mistakes related to laboratory testing. For patient safety the management of the preanalytical phase can benefit from the contribution of automation and computerization. FMECA methodology represents a useful tool for risk assessment in compliance with certification and accreditation requirements. FMECA provides for an objective measure of risks and the basis on which to make strategic decisions on the degree of automation suitable for the organization.
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This page is a summary of: Defining and Managing the Preanalytical Phase With FMECA: Automation and/or “Human” Control, Human Factors The Journal of the Human Factors and Ergonomics Society, September 2019, SAGE Publications,
DOI: 10.1177/0018720819874906.
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