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Color Atlas of Hematology - Practical Microscopic and Clinical ...

Color Atlas of Hematology - Practical Microscopic and Clinical ...

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Procedures, Assays, <strong>and</strong> Normal Values17In sum, a healthy distrust for the single data point is the most importantbasis for the interpretation <strong>of</strong> all data, including those outside the referencerange. For every sample <strong>of</strong> drawn blood, <strong>and</strong> every countingmethod, at least two or three values should be available before conclusionscan be drawn, unless the clinical findings reflect the cytological data.In addition to this, every laboratory has its own set <strong>of</strong> reference data tosome extent.After this account <strong>of</strong> the problems <strong>and</strong> wide variations between differentgroups, the data in Table 2 are presented in a simplified form, with valuesrounded up or down for ease <strong>of</strong> comparison <strong>and</strong> memorization. Absolutevalues <strong>and</strong> the new SI units are given where they are clinically relevant.The Blood Smear <strong>and</strong> Its Interpretation(Differential Blood Count, DBC)A blood smear uses capillary or venous EDTA-blood, preferably no morethan three hours old. The slides must be grease-free, otherwise cell aggregation<strong>and</strong> stain precipitation may occur. Unless commercially availablegrease-free slides are used, the slides should be soaked for several hours ina solution <strong>of</strong> equal parts <strong>of</strong> ethanol <strong>and</strong> ether <strong>and</strong> then allowed to dry. Adroplet <strong>of</strong> the blood sample is placed close to the edge <strong>of</strong> the slide. Aground cover glass (spreader slide) is placed in front <strong>of</strong> the droplet ontothe slide at an angle <strong>of</strong> about 30. The cover slide is then slowly backed intothe blood droplet. Upon contact, the blood droplet spreads along the edge<strong>of</strong> the slide (Fig. 4). Without pressure, the cover glass is now lightly movedover the slide. The faster the cover glass is moved, <strong>and</strong> the steeper angle atwhich it is held, the thinner the smear will be.The quality <strong>of</strong> the smear technique is crucial for the assessment, becausethe cell density at the end <strong>of</strong> the smear is <strong>of</strong>ten twice that at the beginning.In a well-prepared smear the blood sample will show a “feathered” edgewhere the cover glass left the surface <strong>of</strong> the slide. The smear must bethoroughly air-dried; for good staining, at least two hours’ drying time isneeded. The quality <strong>of</strong> the preparation will be increased by 10 minutes’fixation with methanol, <strong>and</strong> it will then also keep better. After drying,name <strong>and</strong> date are pencilled in on the slide.

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