Required section · Section 2 of 6
Measured signals and calculated relationships
On the declared Sysmex XN-series style analyzer, red blood cell and platelet counts use direct-current (DC) electrical impedance with hydrodynamic focusing. White blood cells and the differential use fluorescence flow cytometry. Hemoglobin is measured photometrically after lysis with a cyanide-free sodium lauryl sulfate (SLS) method.
Hematocrit, mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), and mean corpuscular hemoglobin concentration (MCHC) are calculated from measured inputs. MCV (fL) = hematocrit (%) × 10 / RBC count (× 10^12/L); MCH (pg) = hemoglobin (g/dL) × 10 / RBC count (× 10^12/L); MCHC (g/dL) = hemoglobin (g/dL) × 100 / hematocrit (%). A defect in one measured input can therefore distort several calculated values together.
An extreme MCHC is a screening clue, not a diagnosis. Localize the affected measured channel before any intervention: photometric hemoglobin, impedance RBC/hematocrit, or a specimen feature that makes either result unreliable.
Illustrative drawing — this picture was drawn rather than captured.
A bounded investigation sequence for a discordant CBC.
Hold the discordant result
Do not release while the relationship, flags, and specimen evidence are unresolved.
Review relationships and analyzer information
Use formulas, analyzer flags, and method-specific histogram or scattergram information to localize the affected signal.
Inspect specimen and original smear
Compare specimen appearance and direct morphology with the suspected interference before intervention.
Use a validated intervention
Rerun, smear review, warming, dilution, alternate channel, or recollection must follow local procedure.
Verify and reach an endpoint
Release only an evidence-supported result; otherwise document suppression, recollection, consultation, or escalation.
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