Robustness assessment of an automated AI‐based white blood cell morphometric analysis system using different smear preparation methods

Author:

Ravzanaadii Mendamar1ORCID,Horiuchi Yuki12ORCID,Iwasaki Yosuke3,Matsuzaki Akihiko2,Kaniyu Kimiko2,Bai Jing2,Konishi Aya4,Ando Jun56,Ando Miki6,Tabe Yoko12

Affiliation:

1. Department of Clinical Laboratory Medicine Juntendo University Graduate School of Medicine Tokyo Japan

2. Department of Advanced Research Institute for Health Science Juntendo University Graduate School of Medicine Tokyo Japan

3. Scientific Affairs Sysmex Corporation Kobe Japan

4. Sysmex Corporation Kobe Japan

5. Division of Cell Therapy & Blood Transfusion Medicine Juntendo University School of Medicine Tokyo Japan

6. Department of Hematology Juntendo University Graduate School of Medicine Tokyo Japan

Abstract

AbstractIntroductionNumerous AI‐based systems are being developed to evaluate peripheral blood (PB) smears, but the feasibility of these systems on different smear preparation methods has not been fully understood. In this study, we assessed the impact of different smear preparation methods on the robustness of the deep learning system (DLS).MethodsWe collected 193 PB samples from patients, preparing a pair of smears for each sample using two systems: (1) SP50 smears, prepared by the DLS recommended fully automated slide preparation with double fan drying and staining (May–Grunwald Giemsa, M–G) system using SP50 (Sysmex) and (2) SP1000i smears, prepared by automated smear preparation with single fan drying by SP1000i (Sysmex) and manually stained with M–G. Digital images of PB cells were captured using DI‐60 (Sysmex), and the DLS performed cell classification. Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were used to evaluate the performance of the DLS.ResultsThe specificity and NPV for all cell types were 97.4%–100% in both smear sets. The average sensitivity and PPV were 88.9% and 90.1% on SP50 smears, and 87.0% and 83.2% on SP1000i smears, respectively. The lower performance on SP1000i smears was attributed to the intra‐lineage misclassification of neutrophil precursors and inter‐lineage misclassification of lymphocytes.ConclusionThe DLS demonstrated consistent performance in specificity and NPV for smears prepared by a system different from the recommended method. Our results suggest that applying an automated smear preparation system optimized for the DLS system may be important.

Publisher

Wiley

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