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Letters |
a Address correspondence to this author at: Servizio di Medicina di Laboratorio, Azienda Ospedaliera di Padova, Via Giustiniani 2, 35128 Padova, Italy. Fax 39-49-66-32-40; e-mail pad08821@pd.nettuno.it.
Department of Laboratory Medicine, University-Hospital, 35128 Padova, Italy
To the Editor:
Clinical laboratories must improve the preanalytical phase, a phase highly susceptible to mistakes (1). In some reports, hemolyzed specimens, the most common reason for rejection, account for ~60% of rejected specimens, fivefold more than the second most common cause (2). Cellular contents can falsely increase values for some plasma constituents, such as potassium, lactate dehydrogenase, and aspartate aminotransferase (3). Moreover, hemolysis produces spectrophotometric interference with other laboratory methods.
In vitro hemolysis depends mainly on the way in which the blood samples
are drawn and treated, and it may in particular depend on the blood
being forced through too fine a needle (4) or through the
large-bore needle of a syringe into a tube; it may also be caused by
shaking the tube too vigorously and/or centrifuging blood specimens
before clotting is complete. In vivo hemolysis, on the other hand, may
have at least 50 causes. We evaluated the causes of hemolysis in
samples
References
The following articles in journals at HighWire Press have cited this article:
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P. Bonini, M. Plebani, F. Ceriotti, and F. Rubboli Errors in Laboratory Medicine Clin. Chem., May 1, 2002; 48(5): 691 - 698. [Abstract] [Full Text] [PDF] |
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