Performance evaluation of automated cell counts compared with reference methods for body fluid analysis
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Michela Seghezzi
, Giulia Previtali
, Valentina Moioli , Maria Grazia Alessio , Giovanni Guerra and Sabrina Buoro
Abstract
Objectives
Cellular analysis of body fluids (BFs) can assist clinicians for the diagnosis of many medical conditions. The aim of this work is the evaluation of the analytical performance of the UF-5000 body fluid mode (UF-BF) analyzer compared to the gold standard method (optical microscopy, OM) and to XN-1000 (XN-BF), another analyzer produced by the same manufacturer (Sysmex) and with a similar technology for BF analysis.
Methods
One hundred BF samples collected in K3EDTA tubes were analyzed by UF-BF, XN-BF and OM. The agreement was evaluated using Passing and Bablok regression and Bland–Altman plot analysis. The receiver operating characteristic (ROC) curves were selected for evaluating the diagnostic agreement between OM classification and UF-BF parameters.
Results
Comparison between UF-BF and OM, in all BF types, showed Passing and Bablok’s slope comprised between 0.99 (polymorphonuclear cells count, PMN-BF) and 1.39 (mononuclear cells count, MN-BF), the intercepts ranged between 26.47 (PMN-BF parameter) and 226.80 (white blood cell count). Bland–Altman bias was comprised between 7.3% (total cell count, TC-BF) and 52.9% (MN-BF). Comparison between UF-BF and XN-BF in all BF showed slopes ranged between 1.07 (TC-BF and PMN-BF) and 1.16 (MN-BF), intercepts ranged between 8.30 (PMN) and 64.78 (WBC-BF). Bland–Altman bias ranged between 5.8 (TC-BF) and 21.1% (MN-BF). The ROC curve analysis showed an area under the curve ranged between 0.9664 and 1.000.
Conclusions
UF-BF shows very good performance for the differential counts of cells in ascitic, pleural and synovial fluids and therefore it is useful to screen and count cells in this type of BF.
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Research funding: None declared.
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Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: Authors state no conflict of interest.
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Informed consent: Not applicable.
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Ethical approval: Following the assessment of the Ethics Committee of ASST Papa Giovanni XXIII, this type of study does not require the approval of the bioethics committee. The sample data were subjected to anonymization procedure.
References
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© 2021 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Review
- Affective influences on clinical reasoning and diagnosis: insights from social psychology and new research opportunities
- Mini Review
- Homocysteine in coronavirus disease (COVID-19): a systematic literature review
- Opinion Paper
- How insight contributes to diagnostic excellence
- Original Articles
- Diagnostic statements: a linguistic analysis of how clinicians communicate diagnosis
- The use of podcasts as a tool to teach clinical reasoning: a pseudorandomized and controlled study
- Diagnostic delays in infectious diseases
- Diagnostic journeys: characterization of patients and diagnostic outcomes from an academic second opinion clinic
- A pause in pediatrics: implementation of a pediatric diagnostic time-out
- Applying a diagnostic excellence framework to assess opportunities to improve recognition of child physical abuse
- Identifying predictors for source culture positivity in children with acute musculoskeletal infections
- Comparison of SARS-CoV-2 antigen electrochemiluminescence immunoassay to RT-PCR assay for laboratory diagnosis of COVID-19 in Peshawar
- Performance evaluation of automated cell counts compared with reference methods for body fluid analysis
- Short Communication
- Impact of subspecialty consultations on diagnosis in the pediatric intensive care unit
- Case Report - Lessons in Clinical Reasoning
- Pharmacists can improve diagnosis and help prevent diagnostic errors
- Letter to the Editors
- The art of diagnostic reasoning
- Improving the physical exam: a new assessment and evaluation tool for physical examination skills
- Performance of the Wondfo 2019-nCoV antigen test using self-collected nasal versus professional-collected nasopharyngeal swabs in symptomatic SARS-CoV-2 infection
Articles in the same Issue
- Frontmatter
- Review
- Affective influences on clinical reasoning and diagnosis: insights from social psychology and new research opportunities
- Mini Review
- Homocysteine in coronavirus disease (COVID-19): a systematic literature review
- Opinion Paper
- How insight contributes to diagnostic excellence
- Original Articles
- Diagnostic statements: a linguistic analysis of how clinicians communicate diagnosis
- The use of podcasts as a tool to teach clinical reasoning: a pseudorandomized and controlled study
- Diagnostic delays in infectious diseases
- Diagnostic journeys: characterization of patients and diagnostic outcomes from an academic second opinion clinic
- A pause in pediatrics: implementation of a pediatric diagnostic time-out
- Applying a diagnostic excellence framework to assess opportunities to improve recognition of child physical abuse
- Identifying predictors for source culture positivity in children with acute musculoskeletal infections
- Comparison of SARS-CoV-2 antigen electrochemiluminescence immunoassay to RT-PCR assay for laboratory diagnosis of COVID-19 in Peshawar
- Performance evaluation of automated cell counts compared with reference methods for body fluid analysis
- Short Communication
- Impact of subspecialty consultations on diagnosis in the pediatric intensive care unit
- Case Report - Lessons in Clinical Reasoning
- Pharmacists can improve diagnosis and help prevent diagnostic errors
- Letter to the Editors
- The art of diagnostic reasoning
- Improving the physical exam: a new assessment and evaluation tool for physical examination skills
- Performance of the Wondfo 2019-nCoV antigen test using self-collected nasal versus professional-collected nasopharyngeal swabs in symptomatic SARS-CoV-2 infection