Evidence map›Paper›PMID 39722770›Full record

ArticleFrontiers in pediatrics2024

Reference ranges for complete blood count in children and adolescents with Down syndrome.

Martina Lattuada, Giulia Capitoli, Marco Casati, Alessandra Lazzerotti, Oscar Maglia, Giulia Maria Ferrari, Chiara Fossati, Andrea Biondi, Alessandro Cattoni, Paola Corti

Abstract read
In one paragraph

Article in Frontiers in pediatrics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Martina Lattuada *School of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Giulia Capitoli *Department of Medicine and Surgery, Bicocca Bioinformatics Biostatistics and Bioimaging Research Centre-B4, University of Milano-Bicocca, Monza, Italy.
Marco CasatiClinical Chemistry Laboratory Medicine, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Alessandra LazzerottiPediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Oscar MagliaTettamanti Center, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Giulia Maria FerrariPediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Chiara FossatiPediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Andrea BiondiSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Alessandro CattoniSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Paola CortiPediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Down syndrome (DS) is linked to unique hematopoietic characteristics that affect complete blood count (CBC) parameters. Accurate reference ranges are essential for proper CBC interpretation in this population. Methods: This retrospective study analyzed 2,627 CBCs from 481 DS patients, aged 31 days to 18 years, at a tertiary care center in Italy. Patients with significant comorbidities were excluded to ensure a homogeneous group. Results: CBC parameters were assessed to establish age- and sex-specific reference ranges. Centile charts were developed for each parameter, and an online tool was created to allow clinicians to compare individual CBC results with the new ranges. Comparisons with the general pediatric population revealed significant differences, particularly in hemoglobin, hematocrit, and mean corpuscular volume, which were higher in DS ( Discussion: These newly established DS-specific reference ranges provide clinicians with a crucial tool for evaluating CBC results, potentially reducing unnecessary tests and emphasizing the need for tailored clinical assessment in managing this unique population.

Indexed as

complete blood countDown syndromehematopoiesispediatricreference ranges

Identifiers

PMID39722770
PMCPMC11668587

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.