Volume 69, Issue 12 e30002
HEMATOLOGY: RESEARCH ARTICLE

Blood counts in children with Down syndrome

Susan Harvey

Susan Harvey

Center of Cancer and Blood Disorders, Children's Hospital Colorado, Aurora, Colorado, USA

Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA

Department of Pediatrics, Children's National, Washington, District of Columbia, USA

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Kristine Wolter-Warmerdam

Corresponding Author

Kristine Wolter-Warmerdam

Sie Center for Down Syndrome, Children's Hospital Colorado, Aurora, Colorado, USA

Correspondence

Kristine Wolter-Warmerdam, 13123 East 16th Ave, Box 745, Aurora, CO 80045, USA.

Email: [email protected]

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Francis Hickey

Francis Hickey

Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA

Sie Center for Down Syndrome, Children's Hospital Colorado, Aurora, Colorado, USA

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Dee Daniels

Dee Daniels

Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA

Sie Center for Down Syndrome, Children's Hospital Colorado, Aurora, Colorado, USA

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Melkon DomBourian

Melkon DomBourian

Department of Pathology, Children's Hospital Colorado, Aurora, Colorado, USA

Department of Pathology, University of Colorado School of Medicine, Aurora, Colorado, USA

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Daniel R. Ambruso

Daniel R. Ambruso

Center of Cancer and Blood Disorders, Children's Hospital Colorado, Aurora, Colorado, USA

Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA

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Christopher McKinney

Christopher McKinney

Center of Cancer and Blood Disorders, Children's Hospital Colorado, Aurora, Colorado, USA

Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA

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First published: 24 September 2022
Citations: 1

Abstract

Background

Children with Down syndrome (DS) are more likely to have hematologic and immunologic abnormalities compared to their typically developing peers, but normal ranges have not been defined. The goal of this study was to create references for complete blood counts (CBCs) in patients with DS.

Methods

A retrospective investigation of 355 (male = 196, 55.2%; mean age = 6.49 years, SD = 5.07) healthy pediatric patients with DS who received a CBC between 2011 and 2017 as part of their medical care at a single, large, pediatric teaching hospital. Control data on 770 healthy patients without DS were included. Descriptive statistics were performed on demographic and clinical characteristics. Kruskal–Wallis H tests, nested analysis-of-variance tests, and t-tests were run to determine the significant associations.

Results

Age-related normative curves for healthy children with DS outlining 2.5th, 25th, 50th, 75th, and 97.5th percentiles are provided for total white blood count, hemoglobin concentration, hematocrit, mean corpuscular volume, and platelet, absolute neutrophil, absolute lymphocyte, eosinophil, monocyte, and basophil counts. Statistical differences were found between children with and without DS receiving care at the same hospital based on matched age/sex groups.

Conclusions

This study demonstrates that patients with DS have different reference ranges for multiple blood counts compared to those without DS, creating a new resource for pediatricians to refer to when evaluating CBCs in this population.

CONFLICT OF INTEREST

The authors declare that they have no conflict of interest relevant to this article to disclose.

DATA AVAILABILITY STATEMENT

Per the institutional review board approval, research data are not shared.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.