英文摘要 |
In modern clinical laboratory, chemical random-access analyzers that employ dedicated probes, might have various degree of carryover, either in the sample probes or reagent probes. Sample carryover involving analytes from one sample being carried to the subsequent samples, can often be detected due to the abnormal testing results. In contrast, reagent carryover that occurs only in certain specific testing procedure, is more difficult to detect. Our laboratory had once noted that the ratio of abnormal results with elevated fasting blood sugar (>100 mg/dL) in the routine chemical profile analysis among the samples from health-check patients increased from 12.2 % to 32.1 %. However, the glucose levels might become normal if the test rechecked separately. On evaluation for reagent carryover by designing various different testing profiles, we found a significant increase of 15.9% and 9.6% in glucose levels if the glucose testing was concomitantly analyzed with alkaline phosphatase (ALP) and gamma-glutamyl transpeptidase (GGT), respectively. The carryover disappeared when an additional reagent probe washing was applied before the glucose testing. The insidious nature of reagent carryover is caused by the high photometric absorption at 340 nm produced by reagents used in ALP and GGT testing would interfere the glucose detection. In conclusion, the laboratorians should be alert and aware of the potential of reagent carryover in random access chemical analyzers, and should be mindful of appropriate troubleshooting techniques. |