Oguzhan Zhengi, the sole author of the journal entitled “The Transition from Gel Separatory Serum Tubes to Lithium Heparin Gel Tubes in the Clinical Laboratory”, stated that a specific criteria was adhered to when handling the specimens. Throughout the Methodology, Zhengi explained the Clinical and Laboratory Standards Institute (CLSI) Criteria - GP34-A:2010. What was the content of this specific criteria and how did he utilize this document?
Oguzhan Zhengi utilized the Clinical and Laboratory Standards Institute (CLSI) Criteria - GP34-A:2010 upon handling his specimens for testing. It is a consensus-based medical laboratory standards which is most widely recognized resource for continually improving testing quality, safety, and efficiency. In the Methodology part of the journal, he stated that recommendations of the tube manufacturers were followed concerning tube inversions, clotting time, and centrifugation characteristics while still adhering to the said CLSI criteria. The CLSI Criteria utilized contains specific guidelines on the validation and verification of tubes for venous and capillary blood specimen collections. Through this, the samples were centrifuged for 1800 g for 10 minutes and visual inspection of sample quality indicators which included hemolysis, lipemia, icterus, fibrin, and clots were taken into careful consideration.
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