Comparative evaluation of blood collection tubes for clinical chemistry analysis.

Anticoagulant Hemolysis Interference Lipemia Stability Tube

Journal

Clinica chimica acta; international journal of clinical chemistry
ISSN: 1873-3492
Titre abrégé: Clin Chim Acta
Pays: Netherlands
ID NLM: 1302422

Informations de publication

Date de publication:
Sep 2021
Historique:
received: 19 02 2021
revised: 27 04 2021
accepted: 21 05 2021
pubmed: 28 5 2021
medline: 21 7 2021
entrez: 27 5 2021
Statut: ppublish

Résumé

Routine chemistry testing is typically performed using serum or plasma to assess a patient's clinical status. At our institution, serum is the specimen type used. To reduce processing times, evaluation of plasma-based and rapid serum gel separator tubes was performed. We compared the results of routine chemistry analytes collected in serum gel separator tubes (SST), plasma gel separator tubes (PST), rapid serum gel separator tubes (RST), and plasma tubes without gel separators (DGT). Result concordance was assessed at baseline (immediate testing after processing) and up to one week of refrigerated storage. Other parameters assessed were the susceptibility to hemolysis and lipemia interference, and changes in results after re-centrifugation. Percent changes were compared against the SST and evaluated according to established bias thresholds. Total protein and potassium results at baseline in plasma-based tubes had percent changes from the SST that exceeded acceptability thresholds. Stability was significantly shortened for glucose, potassium, aspartate aminotransferase (AST) and lactate dehydrogenase (LDH) when collected in the PST as compared to the SST. The RST was the least susceptible to hemolysis and lipemia interferents. Re-centrifugation affected the serum-based analysis of potassium. Plasma may reduce processing time at the expense of shortened sample stability and may require specimen source-specific reference intervals for potassium and total protein. The RST provides an alternate option to reduce processing time, while maintaining storage stability.

Sections du résumé

BACKGROUND BACKGROUND
Routine chemistry testing is typically performed using serum or plasma to assess a patient's clinical status. At our institution, serum is the specimen type used. To reduce processing times, evaluation of plasma-based and rapid serum gel separator tubes was performed.
METHODS METHODS
We compared the results of routine chemistry analytes collected in serum gel separator tubes (SST), plasma gel separator tubes (PST), rapid serum gel separator tubes (RST), and plasma tubes without gel separators (DGT). Result concordance was assessed at baseline (immediate testing after processing) and up to one week of refrigerated storage. Other parameters assessed were the susceptibility to hemolysis and lipemia interference, and changes in results after re-centrifugation. Percent changes were compared against the SST and evaluated according to established bias thresholds.
RESULTS RESULTS
Total protein and potassium results at baseline in plasma-based tubes had percent changes from the SST that exceeded acceptability thresholds. Stability was significantly shortened for glucose, potassium, aspartate aminotransferase (AST) and lactate dehydrogenase (LDH) when collected in the PST as compared to the SST. The RST was the least susceptible to hemolysis and lipemia interferents. Re-centrifugation affected the serum-based analysis of potassium.
CONCLUSIONS CONCLUSIONS
Plasma may reduce processing time at the expense of shortened sample stability and may require specimen source-specific reference intervals for potassium and total protein. The RST provides an alternate option to reduce processing time, while maintaining storage stability.

Identifiants

pubmed: 34043979
pii: S0009-8981(21)00175-3
doi: 10.1016/j.cca.2021.05.019
pii:
doi:

Substances chimiques

Potassium RWP5GA015D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

118-125

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Nadia Ayala-Lopez (N)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Steven E Conklin (SE)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Brandon J Tenney (BJ)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Maryann Ness (M)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Mark A Marzinke (MA)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: mmarzin1@jhmi.edu.

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Classifications MeSH