Rr. Romero et al., USEFULNESS OF CRYOHEMOLYSIS TEST IN THE DIAGNOSIS OF HEREDITARY SPHEROCYTOSIS, Archives of medical research, 28(2), 1997, pp. 247-251
The clinical suspicion of hereditary spherocytosis (HS) must be confir
med at the clinical laboratory. The osmotic fragility test (OFT) and t
he autohemolysis test(AHT) are the worldwide accepted assays to establ
ish a definite diagnosis of HS; however, they have some disadvantages.
We describe herein our experience with the cryohemolysis test (CHT) a
s a tool to confirm the HS diagnosis. We included four groups of subje
cts, namely, patients with clinical HS, patients with mechanical heart
valve prosthesis, malignant hematological diseases and healthy blood
donors. CHT was carried out in all the groups, while OFT and AHT only
in the HS patients and healthy individuals. OFT and AHT were performed
according to previously described techniques. CHT was performed using
red blood cells incubated in a hypertonic solution, preheated for 10
min and then transferred to an ice bath for an additional 10 min. The
resulting cryohemolysis was determined measuring the free hemoglobin i
n the sample. There were no differences among the groups in terms of g
eneral characteristics. All HS suspicious patients had a positive OFT
and AHT. CHT was positive in all patients from the HS group but in non
e of the subjects from the control groups (p < 0.001). We found that C
HT is a faster and easier-to-perform assay compared with OFT and AHT.
Moreover, using CBT, the zone between normal and abnormal results is w
ider than OFT or AHT. We propose 0.7 to 11% hemolysis as reference val
ues for CHT.