Literature DB >> 25780248

The effect of storage conditions on sample stability in the routine clinical laboratory.

Rebecca L Kift1, Christopher Byrne2, Richard Liversidge2, Fiona Babbington2, Catherine Knox2, Jeff Binns2, Julian H Barth2.   

Abstract

BACKGROUND: 'Add-on' tests are often requested for samples already in the laboratory. This study was carried out to assess the stability of common analytes in uncapped samples stored in different conditions, and therefore their suitability for 'add-on' requests.
METHODS: Storage conditions evaluated included initial storage at room temperature for 16 hours, followed by storage at 4℃ (Group 1: current conditions employed in the laboratory), compared with storage at 4℃ immediately following analysis (Group 2: optimum storage conditions).
RESULTS: Some analytes were not suitable for 'add-ons' when samples were stored in either storage condition, whereas some were suitable for 'add-ons' irrespective of storage condition. Storage conditions influenced the suitability of 'add-on' tests for a proportion of analytes including urea, amylase, total protein, alkaline phosphatase, adjusted calcium, lactate dehydrogenase, triglycerides, HDL cholesterol and total cholesterol; these analytes were stable in optimum conditions (Group 2) but not in current conditions (Group 1).
CONCLUSIONS: 'Add-on' tests can only be safely performed on a proportion of routine analytes. For some analytes, storage conditions affect their suitability for delayed analysis.
© The Author(s) 2015.

Entities:  

Keywords:  Add-on; degradation; delayed analysis; evaporation; stability; storage

Mesh:

Year:  2015        PMID: 25780248     DOI: 10.1177/0004563215580000

Source DB:  PubMed          Journal:  Ann Clin Biochem        ISSN: 0004-5632            Impact factor:   2.057


  3 in total

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3.  The Influence of Serum Sample Storage Conditions on Selected Laboratory Parameters Related to Oxidative Stress: A Preliminary Study.

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Journal:  Diagnostics (Basel)       Date:  2020-01-19
  3 in total

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