A standard to report biological variation data studies – based on an expert opinion

Author:

Bartlett William A.1ORCID,Sandberg Sverre234,Carobene Anna5,Fernandez-Calle Pilar6,Diaz-Garzon Jorge6ORCID,Coskun Abdurrahman78ORCID,Jonker Niels9,Galior Kornelia10,Gonzales-Lao Elisabet11,Moreno-Parro Isabel6,Sufrate-Vergara Berta6,Webster Craig12,Itkonen Outi13,Marques-García Fernando14,Aarsand Aasne K.23

Affiliation:

1. Biomedical Engineering, School of Engineering and Science , University of Dundee , Dundee , Scotland

2. Norwegian Organization for Quality Improvement of Laboratory Examinations (Noklus) , Haraldsplass Deaconess Hospital , Bergen , Norway

3. The Norwegian Porphyria Centre, Department of Medical Biochemistry and Pharmacology , Haukeland University Hospital , Bergen , Norway

4. Department of Public Health and Primary Health Care University of Bergen , Bergen , Norway

5. Laboratory Medicine , IRCCS San Raffaele Scientific Institute , Milan , Italy

6. Laboratory Medicine Department , La Paz University Hospital , Madrid , Spain

7. School of Medicine, Department of Medical Biochemistry , Atasehir , Istanbul , Türkiye

8. Acibadem Mehmet Ali Aydınlar University , Istanbul , Türkiye

9. Carte, Wilhelmina Ziekenhuis Assen , Assen , The Netherlands

10. Department of Pathology and Laboratory Medicine , Emory University , Atlanta , GA , USA

11. Quality and Patient Safety Department, Consorci Sanitari de Terrassa , University Hospital , Barcelona , Spain

12. Department of Biochemistry, Immunology and Toxicology , University Hospitals Birmingham , Birmingham , UK

13. Endocrinology and Metabolism Laboratory , Helsinki University Hospital , Helsinki , Finland

14. Biochemistry Department, Metropolitan North Clinical Laboratory (LCMN) , Germans Trias I Pujol University Hospital , Barcelona , Spain

Abstract

Abstract There is a need for standards for generation and reporting of Biological Variation (BV) reference data. The absence of standards affects the quality and transportability of BV data, compromising important clinical applications. To address this issue, international expert groups under the European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) have developed an online resource (https://tinyurl.com/bvmindmap) in the form of an interactive mind map that serves as a guideline for researchers planning, performing and reporting BV studies. The mind map addresses study design, data analysis, and reporting criteria, providing embedded links to relevant references and resources. It also incorporates a checklist approach, identifying a Minimum Data Set (MDS) to enable the transportability of BV data and incorporates the Biological Variation Data Critical Appraisal Checklist (BIVAC) to assess study quality. The mind map is open to access and is disseminated through the EFLM BV Database website, promoting accessibility and compliance to a reporting standard, thereby providing a tool to be used to ensure data quality, consistency, and comparability of BV data. Thus, comparable to the STARD initiative for diagnostic accuracy studies, the mind map introduces a Standard for Reporting Biological Variation Data Studies (STARBIV), which can enhance the reporting quality of BV studies, foster user confidence, provide better decision support, and be used as a tool for critical appraisal. Ongoing refinement is expected to adapt to emerging methodologies, ensuring a positive trajectory toward improving the validity and applicability of BV data in clinical practice.

Publisher

Walter de Gruyter GmbH

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