NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

Recentrifugation of Lithium Heparin Gel Separator Tubes up to 8 h after Blood Collection Has No Relevant Influence on the Stability of 30 Routine Biochemical Analytes.

Author(s): van Balveren JA, Gemen EFA, Kusters R

Publication: J Appl Lab Med, 2019, Vol. 3, Page 864-869

PubMed ID: 31639761 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to investigate the effects of storing blood and plasma in lithium heparin gel tubes at room temperature before centrifugation/recentrifugation using two different protocols on the levels of 30 clinical chemistry analytes.

Conclusion of Paper

Storage of blood in lithium heparin tubes resulted in deviations in levels of glucose, phosphate, and calcium that exceeded the predefined total allowable error (TEa) depending on the storage duration and centrifugation protocol. The variation in calcium levels exceeded the TEa when plasma was stored in the tube after centrifugation and recentrifuged at 1650 x g for 10 min after 8 h of storage but remained within the acceptable range when specimens were centrifuged at 3000 x g for 8 min. The variation in all other analytes was within the TEa when blood or plasma was stored in the lithium heparin tubes before centrifugation/recentrifugation.

Studies

  1. Study Purpose

    The purpose of this study was to investigate the effects of storing blood and plasma in lithium heparin gel tubes at room temperature before centrifugation/recentrifugation using two different protocols on the levels of 30 clinical chemistry analytes. Blood from 10 healthy volunteers was collected into lithium heparin gel tubes. Blood was centrifuged immediately after collection with or without a second centrifugation step 4 or 8 h later and 4 h after collection with or without a second centrifugation step 8 h after collection. Centrifugation was performed for each of the different timepoints using two different protocols: at 1650 x g for 10 min (BD settings) or at 3000 x g for 8 min. Levels of alanine aminotransferase (ALT), albumin, alkaline phosphatase, amylase, aspartate aminotransferase (AST), bicarbonate, bilirubin direct, bilirubin total, calcium, chloride, cholesterol, creatinine, C-reactive protein (CRP), ferritin, folic acid, free thyroxine 4, gamma-glutamyl transferase, glucose, lactate dehydrogenase, lipase, magnesium, phosphate, potassium, sodium, triglycerides, troponin I, thyroid stimulating hormone (TSH), urea nitrogen, uric acid, and vitamin B12 were analyzed by a Dimension VISTA 1500 clinical chemistry analyzer.

    Summary of Findings:

    When blood was stored for 4 or 8 h before centrifugation using either protocol, the deviation in glucose levels exceeded the TEa from those in the immediately centrifuged specimen. The deviation in phosphate levels exceeded the TEa when blood was stored for 4 h and centrifuged at 1650 x g for 10 min or stored for 8 h and centrifuged using either protocol. The deviation in calcium levels exceeded the TEa compared to immediately centrifuged specimens when blood was stored for 8 h and centrifuged at 1650 x g for 10 min. When plasma was stored in the tube after immediate centrifugation and centrifuged again at 1650 x g for 10 min  after 8 h after of storage, the mean deviation in the calcium levels from specimens analyzed after the first centrifugation exceeded the TEa (2.55%), but the variation in calcium levels was within the acceptable range when specimens centrifuged at 3000 x g for 8 min were recentrifuged after 4 or 8 h. The variation in all other analytes was within previously determined TEa when recentrifuged and analyzed 4 or 8 h after the initial centrifugation, regardless of centrifugation protocol.

    Biospecimens
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Normal
    Platform:
    AnalyteTechnology Platform
    Carbohydrate Clinical chemistry/auto analyzer
    Electrolyte/Metal Clinical chemistry/auto analyzer
    Glycoprotein Clinical chemistry/auto analyzer
    Small molecule Clinical chemistry/auto analyzer
    Peptide Clinical chemistry/auto analyzer
    Protein Clinical chemistry/auto analyzer
    Lipoprotein Clinical chemistry/auto analyzer
    Lipid Clinical chemistry/auto analyzer
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Biospecimen Aliquots and Components Centrifugation Centrifugation delays investigated
    Multiple durations compared
    Multiple speeds compared
    Storage Storage conditions Uncentrifuged (blood)
    Centrifuged (plasma)
    Storage Storage duration 0 h
    4 h
    8 h

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