1. Can the 72-hour rule based on "Blast/Abn Lymph" flag on Sysmex XN-10 optimize the workflow in hematology laboratory?
- Author
-
Paridaens H, Sabor L, Simar J, Ronez E, Cornet E, and Defour JP
- Subjects
- Automation, Laboratory instrumentation, Automation, Laboratory methods, Automation, Laboratory standards, Belgium, Blood Specimen Collection standards, Cytodiagnosis instrumentation, Cytodiagnosis methods, Cytodiagnosis standards, False Positive Reactions, France, Hematologic Tests instrumentation, Hematologic Tests methods, Hematologic Tests standards, Hematology methods, Humans, Laboratory Proficiency Testing, Leukocyte Count instrumentation, Leukocyte Count methods, Leukocyte Count standards, Leukocytes cytology, Lymphocytes cytology, Pre-Analytical Phase standards, Retrospective Studies, Sensitivity and Specificity, Time Factors, Blood Cell Count instrumentation, Blood Cell Count methods, Blood Cell Count standards, Hematology instrumentation, Hematology standards, Practice Guidelines as Topic, Workflow
- Abstract
Despite the continuing improvement of automated blood cell counters, confirmation by blood smear examination remains the gold standard in case of anomalies. With a constant goal of standardisation, different experts committees (e.g. the French-speaking cellular hematology group (Groupe francophone d'hématologie cellulaire, GFHC and the ISLH International society for laboratory hematology) recently published criteria for microscopic analysis of blood smears. Cornet et al. evaluated the application of those criteria and propose to suppress any review for 72 hours when a "Blast/Abn lymph" flag is triggered for a sample with no abnormal cell on the microscopic review. The aims of our study were to retrospectively evaluate whether this 72-hour rule adequately operates and whether it is possible to extend the arbitrary 72-hour timeframe to 96h and 144h. To achieve this goal, 40,688 blood samples were collected from three French-speaking hospitals. 1,548 samples presented an isolated "Blast/Abn lymph" flag. Only 221 samples presented the application of the 72-hour rule at least once for our study period. We were able to extend this rule to 144 hours for 10 samples of them. All blood smears for which the rule was applied were verified and there was no abnormal cell on smears at 72 and 144 hours. In conclusion, the 72-hour rule derived from the GFHC's criteria is secure and reduces the slide review rate and thus the production costs and the turnaround time of hemogram results. Further investigations could confirm that its extension to 144 hours is also adequate.
- Published
- 2019
- Full Text
- View/download PDF