A Progress Report of the IFCC Committee for Standardization of Thyroid Function Tests

被引:54
作者
Thienpont, Linda M. [1 ]
Van Uytfanghe, Katleen [1 ]
Van Houcke, Sofie [1 ]
Das, Barnali [3 ]
Faix, James D. [4 ]
MacKenzie, Finlay [6 ]
Quinn, Frank A. [5 ]
Rottmann, Michael [7 ]
Van den Brue, Annick [2 ]
机构
[1] Univ Ghent, Fac Pharmaceut Sci, Analyt Chem Lab, Harelbekestraat 72, B-9000 Ghent, Belgium
[2] Gen Hosp Sint Jan, Dept Endocrinol, Brugge, Belgium
[3] Kokilaben Dhirubhai Ambani Hosp, Med Res Inst, Biochem & Immunol Lab, Mumbai, Maharashtra, India
[4] Stanford Univ, Sch Med, Palo Alto, CA USA
[5] Med & Sci Affairs, Abbott Diagnost, Abbott Labs, Abbott Pk, IL USA
[6] Univ Hosp Birmingham NHS Fdn Trust, Birmingham Quality UK NEQAS, Birmingham, W Midlands, England
[7] Roche Diagnost GmbH, Penzberg, Germany
关键词
Free thyroxine; Thyrotropin; Standardization; Harmonization; Method comparison; Traceability;
D O I
10.1159/000358270
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The IFCC Committee for Standardization of Thyroid Function Tests aims at equivalence of laboratory test results for free thyroxine (FT4) and thyrotropin (TSH). Objectives: This report describes the phase III method comparison study with clinical samples representing a broad spectrum of thyroid disease. The objective was to expand the feasibility work and explore the impact of standardization/harmonization in the clinically relevant concentration range. Methods: Two sets of serum samples (74 for FT4, 94 for TSH) were obtained in a clinical setting. Eight manufacturers participated in the study (with 13 FT4 and 14 TSH assays). Targets for FT4 were set by the international conventional reference measurement procedure of the IFCC; those for TSH were based on the all-procedure trimmed mean. The manufacturers recalibrated their assays against these targets. Results: All FT4 assays were negatively biased in the mid-to high concentration range, with a maximum interassay discrepancy of approximately 30%. However, in the low range, the maximum deviation was approximately 90%. For TSH, interassay comparability was reasonable in the mid-concentration range, but worse in the pathophysiological ranges. Recalibration was able to eliminate the interassay differences, so that the remaining dispersion of the data was nearly entirely due to within-assay random error components. The impact of recalibration on the numerical results was particularly high for FT4. Conclusions: Standardization and harmonization of FT4 and TSH measurements is feasible from a technical point of view. Because of the impact on the numerical values, the implementation needs careful preparation with the stakeholders. (C) 2014 European Thyroid Association Published by S. Karger AG, Basel
引用
收藏
页码:109 / 116
页数:8
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