Comparison of five automated urine sediment analyzers with manual microscopy for accurate identification of urine sediment
Abstract
Background
While the introduction of automated urine analyzers is expected to reduce the labor involved, turnaround time and potential assay variations, microscopic examination remains the “gold standard” for the analysis of urine sediments. In this study, we evaluated the analytical and diagnostic performance of five recently introduced automated urine sediment analyzers.
Methods
A total of 1016 samples were examined using five automated urine sediment analyzers and manual microscopy. Concordance of results from each automated analyzer and manual microscopy were evaluated. In addition, image and microscopic review rates of each system were investigated.
Results
The proportional bias for red blood cells (RBCs), white blood cells (WBCs) and squamous epithelial cells in the automated urine sediment analyzers were within ±20% of values obtained using the manual microscope, except in the cases of RBCs and WBCs analyzed using URiSCAN PlusScope and Iris iQ200SPRINT, respectively. The sensitivities of Roche Cobas® u 701 and Siemens UAS800 for pathologic casts (73.6% and 81.1%, respectively) and crystals (62.2% and 49.5%, respectively) were high, along with high image review rates (24.6% and 25.2%, respectively). The detection rates for crystals, casts and review rates can be changed for the Sysmex UF-5000 platform according to cut-off thresholds.
Conclusions
Each automated urine sediment analyzer has certain distinct features, in addition to the common advantages of reducing the burden of manual processing. Therefore, laboratory physicians are encouraged to understand these features, and to utilize each system in appropriate ways, considering clinical algorithms and laboratory workflow.
Author contributions: All authors have accepted responsibility for the entire content of this manuscript and have approved its submission.
Research funding: This work was supported by five companies – Sysmex Corporation (Kobe, Japan), Roche Diagnostics International (Rotkreuz, Switzerland), Siemens Healthineers (Erlangen, Germany), Beckman Coulter (Brea, CA, USA), and YD diagnostics (Yongin, Korea).
Employment or leadership: None declared.
Honorarium: None declared.
Competing interests: The funding organizations played no role in designing the study, collection, analysis and interpretation of data, writing of the report, or in the decision to submit the findings for publication.
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Supplementary Material
The online version of this article offers supplementary material (https://doi.org/10.1515/cclm-2019-0211).
©2019 Walter de Gruyter GmbH, Berlin/Boston
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Artikel in diesem Heft
- Frontmatter
- Editorial
- Identification and management of spurious hemolysis: controversies, concerns and criticisms
- Reviews
- CYP24A1 and SLC34A1 genetic defects associated with idiopathic infantile hypercalcemia: from genotype to phenotype
- Meta-analysis: compared with anti-CCP and rheumatoid factor, could anti-MCV be the next biomarker in the rheumatoid arthritis classification criteria?
- Opinion Paper
- Collection, transport and storage procedures for blood culture specimens in adult patients: recommendations from a board of Italian experts
- General Clinical Chemistry and Laboratory Medicine
- Using the hemoglobin-binding Staphylococcus aureus protein IsdH to enable plasma analysis of hemolyzed blood samples
- Handling of hemolyzed serum samples in clinical chemistry laboratories: the Nordic hemolysis project
- Clinical biomarker innovation: when is it worthwhile?
- Impact of total automation consolidating first-line laboratory tests on diagnostic blood loss
- Diagnostic and prognostic value of the D-dimer test in emergency department patients: secondary analysis of an observational study
- Screening of chemical libraries in pursuit of kallikrein-5 specific inhibitors for the treatment of inflammatory dermatoses
- Comparison of five automated urine sediment analyzers with manual microscopy for accurate identification of urine sediment
- Establishment of an international autoantibody reference standard for human anti-DFS70 antibodies: proof-of-concept study for a novel Megapool strategy by pooling individual specific sera
- Only monospecific anti-DFS70 antibodies aid in the exclusion of antinuclear antibody associated rheumatic diseases: an Italian experience
- Performance evaluation of an Indoxyl Sulfate Assay Kit “NIPRO”
- Variable and inaccurate serum IgG4 levels resulting from lack of standardization in IgG subclass assay calibration
- Hematology and Coagulation
- Influence of hypertriglyceridemia, hyperbilirubinemia and hemolysis on thrombin generation in human plasma
- Reference Values and Biological Variations
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- Cardiovascular Diseases
- Serum concentrations of free fatty acids are associated with 3-month mortality in acute heart failure patients
- Letters to the Editor
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- Unexpected analytical interference in isavuconazole UV determination in a child in therapy with lumacaftor/ivacaftor for cystic fibrosis
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