Multicentre comparison of free thyroid hormones immunoassays: the Immunocheck study

Stefania Giovannini1, Gian Carlo Zucchelli, Giorgio Iervasi

  • 1QualiMedLab Srl, Scuola Superiore Sant'Anna, Fondazione CNR-Regione Toscana G. Monasterio, Istituto di Fisiologia Clinica del CNR, Pisa, Italy.

Insights

Significant variability persists in free thyroid hormone immunoassays, impacting analytical performance. Clinicians should be aware of assay differences and avoid switching methods during patient follow-up.

Area of Science:

  • Clinical Chemistry
  • Immunoassay Technology
  • Endocrinology

Background:

  • External Quality Assessment (EQA) schemes are crucial for evaluating analytical performance.
  • Previous assessments indicated variability in free thyroid hormone (FT) immunoassays.
  • The Immunocheck EQA scheme was utilized to assess current FT immunoassay performance.

Purpose of the Study:

  • To evaluate the extent of variability in measured values and analytical performance among different free thyroid hormone immunoassays.
  • To assess assay imprecision and agreement between methods used in clinical laboratories.

Main Methods:

  • Utilized data from the Immunocheck EQA scheme, involving approximately 1000 laboratories.
  • Analyzed results from 54 quality control samples across three annual cycles (2007-2009).
  • Estimated assay imprecision (within-method and between-laboratories variability) and percent bias.

Main Results:

  • A significant variability in measured values among different free thyroid hormone immunoassays was confirmed.
  • Higher imprecision (CV%) was observed for samples with lower free triiodothyronine (FT3) and free thyroxine (FT4) concentrations.
  • Some immunoassays exhibited percent bias values exceeding 20% compared to the consensus mean for FT3 and FT4.

Conclusions:

  • Substantial analytical variability persists in current free thyroid hormone immunoassays.
  • Laboratories must communicate assay performance and reference limits to clinicians.
  • Clinicians are advised against using different immunoassay methods for serial patient monitoring to ensure result consistency.
Abstract

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