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Performance Assessment of Sysmex DI-60: Is Digital Morphology Analyzer Reliable for White Blood Cell Differentials in Body Fluids?
Shin, Eunju; Hur, Mina; Kim, Hanah; Lee, Gun-Hyuk; Hong, Mi-Hyun; Nam, Minjeong; Lee, Seungho.
Afiliación
  • Shin E; Department of Laboratory Medicine, Konkuk University School of Medicine, Seoul 05030, Republic of Korea.
  • Hur M; Department of Laboratory Medicine, Konkuk University School of Medicine, Seoul 05030, Republic of Korea.
  • Kim H; Department of Laboratory Medicine, Konkuk University School of Medicine, Seoul 05030, Republic of Korea.
  • Lee GH; Department of Laboratory Medicine, Konkuk University School of Medicine, Seoul 05030, Republic of Korea.
  • Hong MH; Department of Laboratory Medicine, Konkuk University School of Medicine, Seoul 05030, Republic of Korea.
  • Nam M; Department of Laboratory Medicine, Korea University Anam Hospital, Seoul 02841, Republic of Korea.
  • Lee S; Department of Preventive Medicine, Dong-A University College of Medicine, Busan 49315, Republic of Korea.
Diagnostics (Basel) ; 14(6)2024 Mar 11.
Article en En | MEDLINE | ID: mdl-38535013
ABSTRACT

BACKGROUND:

Few studies have evaluated digital morphology (DM) analyzers on body fluids (BF). We evaluated the performance of a DM analyzer, Sysmex DI-60 (Sysmex, Kobe, Japan) for white blood cell (WBC) differentials in BF samples.

METHODS:

In five BF samples (two pleural fluids and three ascites) containing a single, dominant cell type (>80%, neutrophils, lymphocytes, macrophages, abnormal lymphocytes, and malignant cells in each sample), we evaluated the precision of the DI-60 and compared the WBC differentials and turnaround times (TAT) between DI-60 and manual counting.

RESULTS:

The precision of the DI-60 pre-classification and verification was excellent (%CV, 0.01-3.16%). After verification, the DI-60 showed high sensitivity, specificity, and efficiency (ranges 90.8-98.1%, 96.8-97.9%, and 92.5-98.0%, respectively) for the dominant cell types in neutrophil- and lymphocyte-dominant samples. For all samples, the DI-60 and manual counting showed high correlations for major cell types (neutrophils, lymphocytes, macrophages, and others, r = 0.72 to 0.94) after verification. The agreement between the pre-classification and verification of the DI-60 was strong in the neutrophil-dominant sample (κ = 0.81). The DI-60 showed a significantly longer TAT (min s) than manual counting for all samples (median TAT/slide 628 vs. 153, p < 0.0001), with remarkable differences in abnormal lymphocyte- and malignant cell-dominant samples (2105 vs. 206; 1234 vs. 225).

CONCLUSIONS:

The DI-60 may provide reliable data in neutrophil- and lymphocyte-dominant BF samples. However, it may require longer times and higher workloads for WBC differentials especially in BF samples containing atypical cells. Further improvement would be needed before applying DM analyzers for routine clinical practice in BF analysis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Diagnostics (Basel) Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Diagnostics (Basel) Año: 2024 Tipo del documento: Article
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