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Harmonization protocols for TSH immunoassays: A multicenter study in Italy

  • Aldo Clerico
  • , Andrea Ripoli
  • , Antonio Fortunato
  • , Antonio Alfano
  • , Cinzia Carrozza
  • , Mario Correale
  • , Ruggero Dittadi
  • , Gianluca Gessoni
  • , Marco Migliardi
  • , Sara Rizzardi
  • , Concetta Prontera
  • , Silvia Masotti
  • , Giancarlo Zucchelli
  • , Cristina Guiotto
  • , Palma Aurelia Iacovazzi
  • , Giorgio Iervasi
  • National Research Council of Italy
  • Sant'Anna School of Advanced Studies
  • Azienda Sanitaria Ulss 6 Vicenza
  • Hospital ASL TO4
  • IRCCS Ente Ospedaliero specializzato in gastroenterologia Saverio De Bellis - Castellana Grotte (BA)
  • Ospedale dell'Angelo
  • Ospedale Madonna della Navicella
  • A.O. Ordine Mauriziano di Torino
  • Azienda Socio-Sanitaria Territoriale di Cremona
  • QualiMedLab and CNR Clinical Physiology Institute Pisa
  • CNR Clinical Physiology Institute Pisa

Risultato della ricerca: Contributo in rivistaArticolo

Abstract

Background: Systematic difference between thyroid-stimulating hormone (TSH) immunoassays may produce misleading interpretation when samples of the same patients are measured with different methods. The study aims were to evaluate whether systematic differences are present among TSH immunoassays, and whether it is possible to obtain a better harmonization among TSH methods using results obtained in external quality assessment (EQA) schemes. Methods: Seven Italian clinical laboratories measured TSH in 745 serum samples of healthy subjects and patients with thyroid disorders. These samples were also re-measured by two reference laboratories of the study with the six TSH immunoassays most popular in Italy after 2 months of storage at -80 degrees C. Moreover, these data were compared to 53,823 TSH measurements, obtained by laboratories participant to 2012-2015 EQA annual cycles in 72 quality control samples (TSH concentrations from about 0.1 mIU/L to 18.0mIU/L). TSH concentrations were recalibrated using a mathematical approach based on the principal component analysis (PCA). Results: Systematic differences were found between the most popular commercially available TSH immunoassays. TSH concentrations measured by the clinical laboratories were very closely correlated to those measured with the same method by reference laboratories after 2 months of storage at -80 degrees C. After recalibration using the PCA approach the variation of TSH values significantly decreased from a median pre-calibration value of 13.53% (10.79%-16.53%) to 9.63% (6.90%-13.21%) after recalibration. Conclusions: Our data suggest that EQA schemes are useful to improve harmonization among TSH immunoassays and also to produce some mathematical formulas, which can be used by clinicians to better compare TSH values measured with different methods.
Lingua originaleInglese
pagine (da-a)1722-1733
Numero di pagine12
RivistaClinical Chemistry and Laboratory Medicine
Volume55
DOI
Stato di pubblicazionePubblicato - 2017

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Keywords

  • Humans
  • Immunoassay
  • Italy
  • Laboratories
  • Linear Models
  • Principal Component Analysis
  • Quality Control
  • Reagent Kits, Diagnostic
  • Thyroid Diseases
  • Thyrotropin
  • blood
  • blood sampling
  • calibration
  • circannual rhythm
  • clinical laboratory
  • clinical protocol
  • controlled clinical trial
  • controlled study
  • diagnostic kit
  • harmonization
  • human
  • immunoassay
  • immunoassay methods
  • intermethod comparison
  • laboratory
  • major clinical study
  • mathematical analysis
  • multicenter study
  • principal component analysis
  • priority journal
  • procedures
  • quality control
  • quality specification
  • reference value
  • standardization
  • standards
  • statistical model
  • storage
  • storage temperature
  • thyroid disease
  • thyroid disease, Calibration
  • thyroid-stimulating hormone (TSH)
  • thyrotropin
  • thyrotropin blood level
  • thyrotropin, Article

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