Patient- and parent-reported diagnostic delay in children with central nervous system tumors in Denmark.

adolescents central nervous system children diagnostic delay symptoms tumors

Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
30 May 2024
Historique:
revised: 01 05 2024
received: 27 03 2024
accepted: 18 05 2024
medline: 30 5 2024
pubmed: 30 5 2024
entrez: 30 5 2024
Statut: aheadofprint

Résumé

Diagnostic delays in childhood tumors of the central nervous system (CNS) pose a significant challenge. The aim of this study was to map diagnostic delay and presenting symptoms in Denmark. The study was a retrospective questionnaire study, mapping delay and symptoms in pediatric patients (0-17 years), diagnosed with a CNS tumor from 2015 to 2019. Descriptive analysis was performed to measure delay in days, reported as total diagnostic interval (TDI), patient interval (PI), and diagnostic interval (DI). Analysis of symptoms, contacts to healthcare professionals, and socioeconomic status was also performed. We included 89 patients (median age 7.0 years, 54% male). The TDI was median of 106 days (range: 0-2694 days). Low-grade tumors had longer TDI than high-grade tumors (125 vs. 43 days; p ≤ .02). Patients aged 15-17 displayed the longest TDI (median 665 days). Number of symptoms at onset were inversely associated with longer TDI in patients presenting one symptom (247 days) and patients presenting two to three (110 days) or greater than three complaints (66 days). PI was not associated with sex (p = .14), tumor grade (p = .63), location (p = .32), or socioeconomic status (p = .82). Most frequent single complaint at onset was headache (19%), most frequent combination of symptoms was headache and vomiting (60%). We found TDIs longer than reported in contemporary publications. TDI was longer in patients with low-grade tumors and only few symptoms at the time of onset. The findings support the crucial need of awareness and improved diagnostic tools to recognize and interpret symptoms to promote timely diagnosis.

Sections du résumé

BACKGROUND BACKGROUND
Diagnostic delays in childhood tumors of the central nervous system (CNS) pose a significant challenge. The aim of this study was to map diagnostic delay and presenting symptoms in Denmark.
METHODS METHODS
The study was a retrospective questionnaire study, mapping delay and symptoms in pediatric patients (0-17 years), diagnosed with a CNS tumor from 2015 to 2019. Descriptive analysis was performed to measure delay in days, reported as total diagnostic interval (TDI), patient interval (PI), and diagnostic interval (DI). Analysis of symptoms, contacts to healthcare professionals, and socioeconomic status was also performed.
RESULTS RESULTS
We included 89 patients (median age 7.0 years, 54% male). The TDI was median of 106 days (range: 0-2694 days). Low-grade tumors had longer TDI than high-grade tumors (125 vs. 43 days; p ≤ .02). Patients aged 15-17 displayed the longest TDI (median 665 days). Number of symptoms at onset were inversely associated with longer TDI in patients presenting one symptom (247 days) and patients presenting two to three (110 days) or greater than three complaints (66 days). PI was not associated with sex (p = .14), tumor grade (p = .63), location (p = .32), or socioeconomic status (p = .82). Most frequent single complaint at onset was headache (19%), most frequent combination of symptoms was headache and vomiting (60%).
CONCLUSION CONCLUSIONS
We found TDIs longer than reported in contemporary publications. TDI was longer in patients with low-grade tumors and only few symptoms at the time of onset. The findings support the crucial need of awareness and improved diagnostic tools to recognize and interpret symptoms to promote timely diagnosis.

Identifiants

pubmed: 38814259
doi: 10.1002/pbc.31128
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e31128

Subventions

Organisme : Danish Childhood Cancer Foundation
Organisme : CONTROL - National Research Center for Childhood Cancer
Organisme : Helsefonden
Organisme : Dagmar Marshalls Fond
Organisme : BørneHjerneCancerFonden

Informations de copyright

© 2024 The Author(s). Pediatric Blood & Cancer published by Wiley Periodicals LLC.

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Auteurs

Kathrine Synne Weile (KS)

Department of Pediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, HEALTH, Aarhus University, Aarhus, Denmark.

Anne Sophie Lind Helligsoe (ASL)

Department of Pediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, HEALTH, Aarhus University, Aarhus, Denmark.

Sarah Linea von Holstein (SL)

Department of Ophthalmology, Copenhagen University Hospital, Copenhagen, Denmark.
Department of Clinical Medicine, Faculty of Medicine, University of Copenhagen, Copenhagen, Denmark.

Jeanette Falck Winther (JF)

Department of Clinical Medicine, HEALTH, Aarhus University, Aarhus, Denmark.
Danish Cancer Institute, Copenhagen, Denmark.

René Mathiasen (R)

Department of Clinical Medicine, Faculty of Medicine, University of Copenhagen, Copenhagen, Denmark.
Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Copenhagen, Denmark.

Henrik Hasle (H)

Department of Pediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, HEALTH, Aarhus University, Aarhus, Denmark.

Louise Tram Henriksen (LT)

Department of Pediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, HEALTH, Aarhus University, Aarhus, Denmark.

Classifications MeSH