The measurement of osmotic fragility of erythrocytes can be an easy and rapid routine laboratory test. As shown by Danon and co-workers (1, 2 ) , the automatically recorded osmotic fragility curve of blood or of its derivative ("fragiligrams") are quite different in normal fresh blood than in blood which has been stored for several weeks. David, Lustig and Nahas (3) also showed that the fragiligrams of blood sampled from patients with thalassemia major or with spherocytosis have a very abnormal shape.These authors expressed their measurements by correlating the start and the completion of hemolysis to % dilution of an isotonic salt solution with distilled water: in normal blood, Danon reported that hemolysis starts at about 0.55-0.42c/o XaC1 (165 to 126 mOsm) and is completle at 0.34-0.3070 NaCl (102 to 90 mOsm). However, it was also observed that blood from patients with blood dyscrasias presents similar values for the start and the end of hemolysis (3). All of these measurements performed in normal and abnormal cell populations present a considerable standard deviation and were not significantly different. The interpretation of a "fragiligram," in order to be meaningful, requires, therefore, a more precise definition.In the present studies, two types of "fragiligrams" were recorded: one which relates light scattering of the erythrocytes to osmolarity, the second which is a derivative of the first. These curves permitted the calculation of an "osmotic fragility index" of blood which defines numerically normal and abnormal cell populations.Method. The present instrument, which will be described in detail in a separate publication, consists of light emitting diodes which transilluminate a sample of blood contained in a 15 ml test tube. Only carefully matched test tubes are used. The blood is diluted . -150 125 mOsm 3bO 200 -FIG. 1. Fragiligrams ,of normal blood. The upper curve relates light scattering of the erythrocytes (hemolysis) to osmolarity of Ithe suspension medium. The lower curve is a derivative of the ,upper one, and is a display o f the erythrocytes undengoing hemolysis as osmolarity of the solution is decreased.Using these two curves, iit is possible to d&e the 'change in osmolarity ( A mOsm) during which hemolysis proceeds at the hjighest rate in 50% of the cell population (from 25 to 75%). The curvilinear excursion of the recorded pen accounts for the curvdinear shape of the lower curve. "Start" and "end" correspond to the start and end of hemlolysis.
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