Developing an evidence-based approach to quality control
被引:13
作者:
Badrick, Tony
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机构:
RCPA Qual Assurance Programs, Sydney, NSW, Australia
RCPAQAP, 8 Herbert St, St Leonards, NSW 2065, AustraliaRCPA Qual Assurance Programs, Sydney, NSW, Australia
Badrick, Tony
[1
,3
]
Loh, Tze Ping
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机构:
Natl Univ Singapore Hosp, Singapore, SingaporeRCPA Qual Assurance Programs, Sydney, NSW, Australia
Loh, Tze Ping
[2
]
机构:
[1] RCPA Qual Assurance Programs, Sydney, NSW, Australia
Effective Quality Control remains one of the pillars of Clinical Biochemistry. An understanding of the possible analytical errors that may occur, how to detect them efficiently and how to prevent them from causing patient harm are critical components of a Quality System. For some time, there have been questions about the theoretical basis of the models used to describe and detect analytical error. The current theory recognises two types of error, systematic and random and a system based on sampling the analytical process using a synthetic material to detect these errors. However, there are at least two other errors that are present. One is related to the QC material and the other, irregular errors. In this Opinion Piece, some of the underlying assumptions of Quality Control systems are described and analysed.