Pregledni rad

https://doi.org/10.11613/BM.2014.013

How to conduct External Quality Assessment Schemes for the pre-analytical phase?

Gunn B.B. Kristensen ; The Norwegian EQA Program (NKK), Bergen, Norway
Kristin Moberg Aakre ; The Norwegian EQA Program (NKK), Bergen, Norway; Laboratory of Clinical Biochemistry, Haukeland University Hospital, Bergen, Norway
Ann Helen Kristoffersen ; Laboratory of Clinical Biochemistry, Haukeland University Hospital, Bergen, Norway; Noklus (Norwegian Centre for Quality Improvement of Primary Care Laboratories), University of Bergen, Bergen, Norway
Sverre Sandberg ; Laboratory of Clinical Biochemistry, Haukeland University Hospital, Bergen, Norway; Noklus (Norwegian Centre for Quality Improvement of Primary Care Laboratories), University of Bergen, Bergen, Norway

Sažetak

In laboratory medicine, several studies have described the most frequent errors in the different phases of the total testing process, and a large proportion of these errors occur in the pre-analytical phase. Schemes for registration of errors and subsequent feedback to the participants have been conducted for decades concerning the analyticalphase by External Quality Assessment (EQA) organizations operating in most countries. The aim of the paper is to present an overview of different types of EQA schemes for the pre-analytical phase, and give examples of some existing schemes. So far, very few EQA organizations have focused on the pre-analytical phase, and most EQA organizations do not offer pre-analytical EQA schemes (EQAS). It is more difficult to perform and standardize pre-analytical EQAS and also, accreditation bodies do not ask the laboratories for results from such schemes. However, some ongoing EQA programs for the pre-analytical phase do exist, and some examples are given in this paper. The methods used can be divided into three different types; collecting information about pre-analytical laboratory procedures, circulating real samples to collect information about interferences that might affect the measurement procedure, or register actual laboratory errors and relate these to quality indicators. These three types have different focus and different challenges regarding implementation, and a combination of the three is probably necessary to be able to detect and monitor the wide range of errors occurring in the pre-analytical phase.

Ključne riječi

quality assurance, health care; pre-analytical; quality indicators, health care; external quality assessment

Hrčak ID:

115752

URI

https://hrcak.srce.hr/115752

Datum izdavanja:

15.2.2014.

Posjeta: 2.381 *