Electrical Impedance and Colorimetric Measurements Joanna Ellis, MLS(ASCP)

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Electrical Impedance and Colorimetric Measurements Joanna Ellis, MLS(ASCP)

Transcript of Electrical Impedance and Colorimetric Measurements Joanna Ellis, MLS(ASCP)

Page 1: Electrical Impedance and Colorimetric Measurements Joanna Ellis, MLS(ASCP)

Electrical Impedanceand

Colorimetric Measurements

Joanna Ellis, MLS(ASCP)

Page 2: Electrical Impedance and Colorimetric Measurements Joanna Ellis, MLS(ASCP)

Objectives

• Cite the electrical impedance principle of cell counting.

• Identify and interpret microcytic and macrocytic RBC histograms

• Define coincidence• Identify the cell populations represented on a

3-part differential WBC histogram

Page 3: Electrical Impedance and Colorimetric Measurements Joanna Ellis, MLS(ASCP)

HistoryYou CAN patent a hole

• Prior to the 1950s blood cell counts were performed by manual methods:– Hemacytometer blood counts– Spun hematocrits– Spectrophotometrically determined hemoglobins– Peripheral blood cell evaluation for all differentials

• In 1953, Wallace Coulter patented the Coulter Principle in which particles are counted in fluid passed through a hole. The incredulous attorneys who had told him “You can’t patent a hole” were proven wrong.

• Hematology automation has since grown to include additional principles such as optical light scatter and flow cytometry.

Page 4: Electrical Impedance and Colorimetric Measurements Joanna Ellis, MLS(ASCP)

The Coulter Principle

• The poorly conductive blood cells are suspended in a conductive diluent (liquid).

• The diluent is passed through an electric field created between two electrodes.

• The liquid passes through a small aperture (hole).• The passage of each particle through the aperture

momentarily increases the impedance (resistance) of the electrical path between the electrodes.

• The increase in impedance creates a pulse that can be measured.

• The number of pulses = blood cell count• The amplitude (height) of the pulse = Volume of cell

Page 5: Electrical Impedance and Colorimetric Measurements Joanna Ellis, MLS(ASCP)

Electrical Impedance (The Coulter Principle)

Sweep Flow: Steady stream of diluent that flows behind each aperture to prevent cells from re-entering the aperture

Page 6: Electrical Impedance and Colorimetric Measurements Joanna Ellis, MLS(ASCP)

Counting Chambers

• Most common chambers using impedance:RBC/Platelet chamber WBC chamber

RBC/Platelet Chamber

WBC Chamber

Differential ChamberReticulocyte Channel

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RBC/Platelet Chamber

Particle Size Cell the instrument Counts

2-20 femtoliters (fL) Platelet

36-360 fL Red Blood Cell

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RBC and Platelet Histograms

The black line represents normal cell distribution. The red line on the RBC histogram graphically represents a microcytic red cell population.

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Bimodal Histogram

Bimodal peak can be seen in situations such •Cold agglutinin disease•Post-transfusion•Post-treatment of IDA

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Coincidence

Coincidence: Multiple cells passed through the aperture at once.

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WBC Chamber

Lysing agent

In some analyzers the WBC count is directly measured by electric impedance after the red cells have been destroyed by a lysing agent. The lysing agent also shrinks the leukocyte cell membrane and cytoplasm; therefore, the WBC count represents the measure of the cell volume not native cell size. Colorimetric measurements are used to determine hemoglobin.

Aperture in electric field

WBCs

Hgb released

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Colorimetric Measurements• Hemoglobin is often determined by a colorimetric method.

– Imidazole • Non-cyanide reagent with color change and read at 540nm• Instruments

– Abbott CELL-DYN Sapphire– Sodium Lauryl Sulfate

• Non-cyanide reagent with color change and read spectrophotometrically

• Instruments– Sysmex XT and XE

– Lysing agent converts free hemoglobin to cyanmethemoglobin and read spectrophotometrically at 540nm.• Instruments

– Advia 120– Some Beckman Coulters

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Three-part Differential WBC Histogram

Lymphocytes: 35-92LMononuclear Cells: 92-152 fLGranulocytes: 152-450 fL

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References• "Abaxis Veterinary Diagnostics - VetScan HM2 Technology." Abaxis Medical

Diagnostics - Redirect. Abaxis Medical Diagnostics, 2006. Web. 12 Sept. 2010. <http://www.abaxis.com/veterinary/vetscan_hm2_technology.html>.

• Graham, Marshall Don. "The Coulter Principle: Foundation of an Industry." The Association for Laboratory Automation :: Home. JALA Volume 8, Issue 6, Dec. 2003. Web. 12 Sept. 2010. <http://labautomation.org>.

• Kelly, Kathleen. "Modules :: CLIA :: CME." Hematology in the Physician Office Laboratory Section I. University of Iowa Carver College of Medicine, 2008. Web. 12 Sept. 2010. <http://www.medicine.uiowa.edu/cme/clia/modules.asp?testID=4#02>.

• Krantz, Alexander. "Residency & Fellowship Programs | Education." Department of Pathology & Cell Biology | CUMC. Columbia University of Physicians and Surgeons. Web. 12 Sept. 2010. <http://pathology.columbia.edu/education/residency>.

• Harmening., Denise, Clinical Hematology and Fundamentals of Hemostasis, 3rd edition, pp. 593-599.

• Turgeon, Mary Louise, Clinical Hematology - Theories and Procedures, 3rd edition, pp373, 376-382.

• Rodak, Bernadette, Diagnostic Hematology, 1st edition, p.605-606.• Coulter STKS Operating Manual• McKenzie, Shirlyn, Clinical Laboratory Hematology, 2nd edition,pp 813-829.