Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2019 Mar;33(3):e22822.
doi: 10.1002/jcla.22822. Epub 2018 Nov 28.

Use of the Sysmex XT-4000i hematology analyzer in the differentiation of cerebrospinal fluid cells in children

Affiliations

Use of the Sysmex XT-4000i hematology analyzer in the differentiation of cerebrospinal fluid cells in children

Beata Zelazowska-Rutkowska et al. J Clin Lab Anal. 2019 Mar.

Abstract

Background: Routine analysis of pleocytosis and cellular composition of cerebrospinal fluid (CSF) is carried out with a phase-contrast microscope. The use of hematological analyzers seems to be an alternative to the manual method. The aim of the study was to assess the usefulness of the automated technique for counting and differentiating CSF cells in children.

Methods: The study group consisted of 59 children (28 girls and 31 boys) aged from 4 to 17 years suffering from viral and bacterial meningitis. Children were divided into three subgroups according to CSF cell count: 1st group had a pleocytosis of 6-50 cells/µL, 2nd group-51-100 cells/µL, and 3rd group->100 cells/µL. A reference group involved 32 children (17 girls and 15 boys) aged from 2 to 18 years with a normal range of 0-5 cells/µL. Examination of CSF was performed in parallel by two different method, manual and automated.

Results: The analysis of pleocytosis revealed that the values obtained by the manual method were statistically significantly lower in relation to the values obtained by automated technique in subgroups I and II. The number of mononuclear and polymorphonuclear cells in subgroups I, II, and III determined by both manual and automated methods was comparable.

Conclusion: We conclude that automated method cannot fully replace the previously used manual method and some of the dubious cases, such as samples with low pleocytosis rates or abnormal cells indicated by the analyzer, will still require microscopic examination.

Keywords: automated method; cerebrospinal fluid; manual method; mononuclear cells; pleocytosis; polymorphonuclear cells.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Linearity of XT‐4000i counts in cerebrospinal fluid for pleocytosis, mononuclear cells, and polymorphonuclear cells counts. The identity line is drawn
Figure 2
Figure 2
Passing‐Bablok regression analysis showing the comparison of pleocytosis, mononuclear cells, and polymorphonuclear cells cells obtained with manual and automated methods in the study whole group and subgroups. The regression equation is given in bottom right corner. The solid line represents the fitted regression line. The dotted line represents the line of identity. The dashed lines represent the regression line confidence interval (95% CI for the regression line)
Figure 3
Figure 3
Bland‐Altman difference plots for pleocytosis, mononuclear cells, and polymorphonuclear cells cells obtained with manual and automated methods in the study whole group and subgroups. The solid line shows average of the differences obtained and corresponds to the bias between cells results obtained with two methods. The dashed lines correspond to the lower and upper limits of the confidence interval at 95% (mean ± 1.96 SD) of the difference between results obtained with two methods

Similar articles

Cited by

References

    1. Fouad R, Khairy M, Fathalah W, Gad T, El‐Kholy B, Yosry A. Role of clinical presentations and routine CSF analysis in the rapid diagnosis of acute bacterial meningitis in cases of negative gram stained smears. J Trop Med. 2014;2014:213762. - PMC - PubMed
    1. Weston CL. Detection of cancer cells in the cerebrospinal fluid: current methods and future directions. Fluids Barriers CNS. 2011;8:14‐19. - PMC - PubMed
    1. Bottini PV, Pompeo DB, Souza MI, Garlipp CR. Comparison between automated and microscopic analysis in body fluids cytology. Int J Lab Hematol. 2015;37:16‐18. - PubMed
    1. Adam P, Sobek O, Taborsky L, Prucha M, Zacek P. Cerebrospinal fluid cytology. Riv Med Lab. 2002;32:22‐32.
    1. Deisenhammer F, Bartos A, Egg R, et al. Guidelines on routine cerebrospinal fluid analysis. Report from an EFNS task force. Eur J Neurol. 2006;13:913‐922. - PubMed

LinkOut - more resources