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Error tracking in a clinical biochemistry laboratory.
1Department of Clinical Biochemistry, University of Copenhagen, Roskilde Hospital, Roskilde, Denmark. palsze01@geh.regionh.dk
Clinical Chemistry and Laboratory Medicine
|August 12, 2009
Summary
Clinical laboratory errors were systematically recorded, revealing a high rate of pre-analytical mistakes primarily caused by human error. Structured data recording is recommended to improve laboratory quality and patient safety.
Area of Science:
- Clinical Laboratory Science
- Healthcare Quality Improvement
- Patient Safety
Background:
- Systematic error recording in a standard clinical laboratory was conducted over one year.
- Data collection involved all laboratory personnel using a commercial database program.
Purpose of the Study:
- To systematically record and analyze errors occurring within a clinical laboratory setting.
- To identify the types, sources, and frequency of laboratory errors.
Main Methods:
- Errors were classified by testing process function and type (pre-analytical, analytical, post-analytical, service-related).
- Sample sources included hospital wards, outpatient clinics, general practitioners, and other hospitals.
- Error data was categorized into descriptive subgroups.
Main Results:
- 1189 errors were reported in 1151 reports, with an error rate of 1 per 142 patients or 1 per 1223 tests.
- Human errors constituted the majority (82.6%), with technical errors being infrequent (4.3%).
- Pre-analytical errors were most common (81%), followed by analytical (10%), post-analytical (8%), and service-related (1%).
Conclusions:
- Clinical laboratories should implement structured error recording systems.
- Relational databases are effective tools for managing and analyzing laboratory error data.
- Understanding error patterns can guide quality improvement initiatives.
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