Standard Practice for Collection and Preparation of Blood for Dynamic in vitro Evaluation of Hemolysis in Blood Pumps


Importancia y uso:

5.1 In vitro hemolysis test results for blood pumps may be substantially affected by donor species, sex, age, fasting, the method of harvesting, the anticoagulant properties, the period of storage, the biochemical state of the blood, and the hemoglobin and hematocrit level of blood.3,4 Therefore, standardization of proper whole blood collection and preparation for the dynamic in vitro evaluation of blood pumps is essential, and this recommended practice will allow an acceptable comparison of test results among hemolysis tests involving similar testing methods.

Subcomité:

F04.30

Referida por:

F1841-19E01

Volúmen:

13.01

Número ICS:

11.100 (Laboratory medicine)

Palabras clave:

blood trauma; condition of test blood; hemolysis; source of blood donor;

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Norma
F1830

Versión
19(2024)

Estatus
Active

Clasificación
Practice

Fecha aprobación
2024-12-01