Mining the Gap: Deriving Pregnancy Reference Intervals for Hematology Parameters Using Clinical Datasets

Author:

Barakauskas Vilte E12,Bohn Mary Kathryn3,Branch Emma4,Boutin Amelie5,Albert Arianne4,Luke Sabrina46,Dittrick Michelle1,Higgins Victoria7,Adeli Khosrow3,Vallance Hilary12,Jung Benjamin3,Dooley Kent8,Dahlgren-Scott Leanne9,Chan Wee-Shian10

Affiliation:

1. Department of Pathology and Laboratory Medicine, BC Children’s and Women’s Hospital , Vancouver, BC , Canada

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

3. Clinical Biochemistry, Pediatric Laboratory Medicine, The Hospital for Sick Children and Department of Laboratory Medicine and Pathobiology, University of Toronto , Toronto, ON , Canada

4. Women’s Health Research Institute, BC Women’s Hospital , Vancouver, BC , Canada

5. Department of Pediatrics, Université Laval, and Reproduction, Mother and Youth Health Unit, CHU de Quebec-Université Laval Research Center , Quebec City, QC , Canada

6. Research and Surveillance Group, Perinatal Services British Columbia , Vancouver, BC , Canada

7. Clinical Biochemistry, DynaLIFE Medical Labs and Department of Laboratory Medicine and Pathology, University of Alberta , Edmonton, AB , Canada

8. Clinical Biochemistry, LifeLabs Medical Laboratories , Victoria, BC , Canada

9. Department of Obstetrics and Gynecology, University of British Columbia , Vancouver, BC , Canada

10. Department of Medicine, BC Women’s Hospital and Division of General Internal Medicine, Department of Medicine, University of British Columbia , Vancouver, BC , Canada

Abstract

Abstract Background Physiological changes during pregnancy invalidate use of general population reference intervals (RIs) for pregnant people. The complete blood count (CBC) is commonly ordered during pregnancy, but few studies have established pregnancy RIs suitable for contemporary Canadian mothers. Prospective RI studies are challenging to perform during pregnancy while retrospective techniques fall short as pregnancy and health status are not readily available in the laboratory information system (LIS). This study derived pregnancy RIs retrospectively using LIS data linked to provincial perinatal registry data. Methods A 5-year healthy pregnancy cohort was defined from the British Columbia Perinatal Data Registry and linked to laboratory data from two laboratories. CBC and differential RIs were calculated using direct and indirect approaches. Impacts of maternal and pregnancy characteristics, such as age, body mass index, and ethnicity, on laboratory values were also assessed. Results The cohort contained 143 106 unique term singleton pregnancies, linked to >972 000 CBC results. RIs were calculated by trimester and gestational week. Result trends throughout gestation aligned with previous reports in the literature, although differences in exact RI limits were seen for many tests. Trimester-specific bins may not be appropriate for several CBC parameters that change rapidly within trimesters, including red blood cells (RBCs), some leukocyte parameters, and platelet counts. Conclusions Combining information from comprehensive clinical databases with LIS data provides a robust and reliable means for deriving pregnancy RIs. The present analysis also illustrates limitations of using conventional trimester bins during pregnancy, supporting use of gestational age or empirically derived bins for defining CBC normal values during pregnancy.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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