Biological variation (BV) data have many applications in laboratory medicine. However, concern has been raised that some LW estimates in use today may be irrelevant or of unacceptable quality. A number of initiatives have been launched by the European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) and other parties to deliver a more harmonized practice in the generation, reporting and application of BV data. Resulting from a necessary focus upon the veracity of historical BV studies, critical appraisal and meta-analysis of published BV studies is possible through application of the Biological Variation Data Critical Appraisal Checklist (BIVAC), published in 2017. The BIVAC compliant large-scale European Biological Variation Study delivers updated high-quality BV data for a wide range of measurands. Other significant developments include the publication of a Medical Subject Heading term for BV and recommendations for common terminology for reporting of BV data. In the near future, global BV estimates derived from meta-analysis of BIVAC appraised publications will be accessible in a Biological Variation Database at the EFLM website. The availability of these high-quality data, which have many applications that impact on the quality and interpretation of clinical laboratory results, will afford improved patient care.

Harmonization initiatives in the generation, reporting and application of biological variation data / A. Aarsand, T. Røraas, W. Bartlett, A. Coşkun, A. Carobene, P. Fernandez-Calle, N. Jonker, J. Díaz-Garzón, F. Braga, S. Sandberg. - In: CLINICAL CHEMISTRY AND LABORATORY MEDICINE. - ISSN 1434-6621. - 56:10(2018 Sep 25), pp. 1629-1636. [10.1515/cclm-2018-0058]

Harmonization initiatives in the generation, reporting and application of biological variation data

F. Braga;
2018

Abstract

Biological variation (BV) data have many applications in laboratory medicine. However, concern has been raised that some LW estimates in use today may be irrelevant or of unacceptable quality. A number of initiatives have been launched by the European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) and other parties to deliver a more harmonized practice in the generation, reporting and application of BV data. Resulting from a necessary focus upon the veracity of historical BV studies, critical appraisal and meta-analysis of published BV studies is possible through application of the Biological Variation Data Critical Appraisal Checklist (BIVAC), published in 2017. The BIVAC compliant large-scale European Biological Variation Study delivers updated high-quality BV data for a wide range of measurands. Other significant developments include the publication of a Medical Subject Heading term for BV and recommendations for common terminology for reporting of BV data. In the near future, global BV estimates derived from meta-analysis of BIVAC appraised publications will be accessible in a Biological Variation Database at the EFLM website. The availability of these high-quality data, which have many applications that impact on the quality and interpretation of clinical laboratory results, will afford improved patient care.
English
analytical performance specification; biological variation; evidence-based medicine; meta-analysis; reference change values
Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica
Review essay
Esperti anonimi
Pubblicazione scientifica
25-set-2018
Walter de Gruyter
56
10
1629
1636
8
Pubblicato
Periodico con rilevanza internazionale
Aderisco
info:eu-repo/semantics/article
Harmonization initiatives in the generation, reporting and application of biological variation data / A. Aarsand, T. Røraas, W. Bartlett, A. Coşkun, A. Carobene, P. Fernandez-Calle, N. Jonker, J. Díaz-Garzón, F. Braga, S. Sandberg. - In: CLINICAL CHEMISTRY AND LABORATORY MEDICINE. - ISSN 1434-6621. - 56:10(2018 Sep 25), pp. 1629-1636. [10.1515/cclm-2018-0058]
open
Prodotti della ricerca::01 - Articolo su periodico
10
262
Article (author)
no
A. Aarsand, T. Røraas, W. Bartlett, A. Coşkun, A. Carobene, P. Fernandez-Calle, N. Jonker, J. Díaz-Garzón, F. Braga, S. Sandberg
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/610027
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