Question 1 · Hard
During an analyzer breakdown at a small clinic laboratory, a CBC on a 34-year-old woman is done by manual methods: cyanmethemoglobin Hb 128 g/L (12.8 g/dL), spun microhematocrit 0.33 L/L and hemocytometer RBC 4.20 × 10^12/L. Reference ranges: MCV 80-100 fL, MCH 27-33 pg, MCHC 320-360 g/L. The stained film shows normocytic, normochromic red cells with no spherocytes, target cells or agglutination, and the plasma in the hematocrit tube is clear. Before releasing the results, the technologist calculates the red cell indices. The best action is:
- ARepeat the hemoglobin on a fresh dilution
- BRepeat the hemocytometer red cell count
- CReport the indices with a spherocyte comment
- DRepeat the microhematocrit before reporting
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Answer: D · Repeat the microhematocrit before reporting
The indices are MCV 0.33 ÷ 4.20 × 1,000 = 79 fL, MCH 128 ÷ 4.20 = 30.5 pg and MCHC 128 ÷ 0.33 = 388 g/L. The MCH, which uses only the Hb and the RBC count, is normal, while both indices that use the hematocrit (MCV and MCHC) disagree with the normocytic, normochromic film. A falsely low hematocrit explains both: a value of about 0.38 L/L would give an MCV near 90 fL and an MCHC near 337 g/L. The microhematocrit should be repeated and read at the top of the red cell column, below the buffy coat, before any result is released. An MCHC above 360 g/L with no spherocytes on the film signals a measurement error, not a red cell disorder.
- A: The normal MCH shows the Hb agrees with the RBC count; the error is in the hematocrit.
- B: The MCHC does not use the RBC count, and the normal MCH shows the count agrees with the Hb.
- C: There are no spherocytes, so an MCHC of 388 g/L means a measurement error.