Reference Interval Harmonization: Harnessing the Power of Big Data Analytics to Derive Common Reference Intervals across Populations and Testing Platforms

Author:

Bohn Mary Kathryn12,Bailey Dana3,Balion Cynthia4,Cembrowski George5ORCID,Collier Christine6,De Guire Vincent7,Higgins Victoria8,Jung Benjamin12,Ali Zahraa Mohammed9,Seccombe David10,Taher Jennifer211,Tsui Albert K Y512,Venner Allison1213,Adeli Khosrow12

Affiliation:

1. Department of Clinical Biochemistry, Pediatric Laboratory Medicine, The Hospital for Sick Children , Toronto, ON , Canada

2. Department of Laboratory Medicine and Pathobiology, University of Toronto , Toronto, ON , Canada

3. Dynacare , Brampton, ON , Canada

4. Department of Pathology & Molecular Medicine, McMaster University , Hamilton, ON , Canada

5. Department of Laboratory Medicine and Pathology, University of Alberta , Edmonton, AB , Canada

6. Department of Laboratory Medicine, Fraser Health Authority , New Westminster, BC , Canada

7. Department of Clinical Biochemistry, Hospital Maisonneuve-Rosemont , Montreal, QC , Canada

8. DynaLIFE Medical Labs , Edmonton, AB , Canada

9. Department of Laboratory Medicine, Scaraborough Health Network , Toronto, ON , Canada

10. Department of Pathology and Laboratory Medicine, University of British Columbia , Vancouver, BC , Canada

11. Department of Pathology & Laboratory Medicine, Mount Sinai Hospital , Toronto, ON , Canada

12. Alberta Precision Laboratories , Calgary, AB , Canada

13. Department of Pathology & Laboratory Medicine, University of Calgary , Calgary, AB , Canada

Abstract

Abstract Background Harmonization in laboratory medicine is essential for consistent and accurate clinical decision-making. There is significant and unwarranted variation in reference intervals (RIs) used by laboratories for assays with established analytical traceability. The Canadian Society of Clinical Chemists (CSCC) Working Group on Reference Interval Harmonization (hRI-WG) aims to establish harmonized RIs (hRIs) for laboratory tests and support implementation. Methods Harnessing the power of big data, laboratory results were collected across populations and testing platforms to derive common adult RIs for 16 biochemical markers. A novel comprehensive approach was established, including: (a) analysis of big data from community laboratories across Canada; (b) statistical evaluation of age, sex, and analytical differences; (c) derivation of hRIs using the refineR method; and (d) verification of proposed hRIs across 9 laboratories with different instrumentation using serum and plasma samples collected from healthy Canadian adults. Results Harmonized RIs were calculated for all assays using the refineR method, except free thyroxine. Derived hRIs met proposed verification criterion across 9 laboratories and 5 manufacturers for alkaline phosphatase, albumin (bromocresol green), chloride, lactate dehydrogenase, magnesium, phosphate, potassium (serum), and total protein (serum). Further investigation is needed for some analytes due to failure to meet verification criteria in one or more laboratories (albumin [bromocresol purple], calcium, total carbon dioxide, total bilirubin, and sodium) or concern regarding excessively wide hRIs (alanine aminotransferase, creatinine, and thyroid stimulating hormone). Conclusions We report a novel data-driven approach for RI harmonization. Findings support feasibility of RI harmonization for several analytes; however, some presented challenges, highlighting limitations that need to be considered in harmonization and big data analytics.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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