Analytical Methods Committee, AMCTB No 56
First published on 14th May 2013
In the early 1980s, emerging evidence of poor inter-laboratory precision in routine analysis for trace contaminants led to major changes in the management of analytical chemistry. The adoption of the CODEX and later VAM principles encouraged laboratories to participate regularly in proficiency test (PT) schemes; to adopt validated analytical methods; to rely increasingly on certified reference materials for calibration and validation of their test methods; to implement effective internal QC; and (more recently) to obtain accreditation to standards such as ISO 17025.
There are many possible reasons for this: post-study investigation of individual cases is not the responsibility of the provider; data collection and its analysis are time-consuming; and the burden on participants of providing detailed information is high. Some of these barriers, however, can be overcome by means of a web-based study set up independently of the scheme's normal operation. A recent publication has provided a pilot example. The results, summarised here, suggest that learning to reduce basic human errors may be among the most effective ways of reducing the number of poor scores in PT and, by implication, generally.
Fig. 1 Causes of error in chemical analysis. |
The study in question was a voluntary-response survey in which PT participants in a number of different schemes were invited to give details of the causes of their most recent poor PT score. Most good laboratories have investigated a poor PT result at some time, so could provide useful information. Further, because electronic data collection could be limited to the specific causes, less information was needed per return than for a full survey of analytical methodology. The question of interest was, effectively, ‘What caused your last poor PT score?’
The original paper indicated that within these broad categories, a few detailed causes of error stood out. Equipment failure was the most common single problem reported (8% of responses); dilution to volume in sample preparation the next (7%). Use of incorrect units in reporting, extraction problems, and transcription errors in data entry and reporting each accounted for about 5% of reported causes. ‘Human error’ was the second most important reported cause of poor PT scores.
This last category, however, did not include all of the features that could be attributed to human error. For example, ‘calculation error’ included errors such as incorrect formulae entered in spreadsheets—a human, rather than software, error. The report therefore identified all the detailed responses that could reasonably be regarded as examples of human error, and then counted the respondents who had recorded one or more of these responses. A total of 49 respondents (44% of the total) had reported one or more of these contributory causes. No other broad category was reported by so many respondents.
This finding does not mean that laboratory managers can stop worrying about validation, accreditation, internal QC and traceability for their reference materials. Proper attention to these issues is a large part of the reason for the large number of acceptable results in PT. But the results do suggest that significant improvements could be made with more attention to the reduction of basic human errors.
This Technical Brief was prepared for the Analytical Methods Committee by the Validation Subcommittee.
This journal is © The Royal Society of Chemistry 2013 |