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hemoglobin F in blood (Kleihauer-Betke test)
Clinical significance:
Fetal hemoglobin estimations are sometimes made to determine possible hemorrhage in the newborn, particularly in cases where there are signs of rectal bleeding. Hemoglobin F assay is also applied to adult as an aid in diagnosing certain types of anemia. For example,10-90% fetal hemoglobin is encountered in patients with thalassemia major. Moreover, small increases of fetal blood pigment is usually observed in patients with sickle cell disease.
It is becoming increasingly common in cases of Rh incompatibility to suppress immune reactions to red blood cells entering maternal circulation from the fetus. The amount of specific gamma globulin, containing anti Rh[D] to be administered, is calculated by assessing the magnitude of fetal-maternal hemorrhage.
Distribution of hemoglobin F within red cells. HbF shows 3 distribution patterns: both HbA & HbF are present in strictly separated cell populations; both hemoglobins are present in equal concentrations in all cells; & both hemoglobins are irregularly distributed within the cells, some cells containing only HbA, some only HbF, & some varying amounts of both.
1) HbA & HbF present in strictly separate cell populations:
a) This distribution pattern is seen in feto-maternal hemorrhage if the mother's blood is examined or in maternal-fetal hemorrhage if the infant's blood is examined
b) In cases of anemia of the newborn or when a Rh-negative or Du-negative woman delivers or miscarries (aborts), the mother's blood should be collected immediately after delivery & examined for fetal cells by the Kleihauer method.
c) According to Oski & Naiman, this method is capable of detecting as little as 0.1 mL of fetal blood in maternal circulation
2) Even distribution of HbF & HbA within red cells:
- This picture is seen in hereditary persistence of HbF.
3) Uneven distribution of HbA & HbF in the red cells:
- This pattern is seen in thalassemia (minor & major), hemoglobin SS disease, Fanconi anemia, & hereditary spherocytosis
Below are distribution patterns of HbF & HbA in red cells.
1) Two separate cell populations, HbF containing cells & HbA containing cells.
2) Even distribution of HbA & HbF within cells.
3) Irregular distribution of HbA & HbF within cells, some cells containing more HbF than others & some containing none.
Increases:
- excessive values are observed in:
- Aplastic anemia
- Erythremic myelosis
- Hemoglobin H disease
- Hereditary persistence of hemoglobin F
- Hereditary spherocytic anemia
- Thalassemia major [40-90% fetal hemoglobin]
- Thalassemia minor [5-10% fetal hemoglobin]
- Sickle cell anemia
Principle:
When blood smears are immersed in acid buffer, adult hemoglobin is eluted from the erythrocytes, whereas fetal hemoglobin is not. If blood smears are treated in this manner & subsequently stained, erythrocytes having hemoglobin F will take up the stain, while those containing only adult hemoglobin appear as 'ghosts'.
Specimen:
Patient preparation: No special patient preparations required. Fresh capillary or oxalated blood, a minimum of 1 mL. Specimens allowed to stand overnight may give false positive results.
Related
erythrocytes.fetal in blood
fetal blood in blood
hemoglobin F
Specific
hemoglobin F in blood qualitative
General
hemoglobin F in specimen
References
- Package Insert, Fetal Hemoglobin, Sigma Diagnostics, St. Louis,
M0, 1988.
- Tietz, Norbort W.: Textbook of Clinical Chemistry, W.B.
Saunders Company, Philadelphia, PA, p. 1555, 1986.
- Bauer, John D. M.D.: Clinical Laboratory Methods, The C.U Mosby
Company, St. Louis, MO, pp. 108-109, 1974.
- Oski, F.A., Naiman, J.L.: Histologic Problems in the Newborn,
2nd Ed. W.B. Saunders Company, Philadelphia, PA, pp. 62-63,
1972.
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Component-of
hemoglobin F/hemoglobin total in blood
hemoglobin F/hemoglobin total in blood by HPLC