Socioeconomic position and prediagnostic health care contacts in children with cancer in Denmark: a nationwide register study

Line Hjøllund Pedersen, Friederike Erdmann, Gitte Lerche Aalborg, Lisa Lyngsie Hjalgrim, Hanne Bækgaard Larsen, Kjeld Schmiegelow, Jeanette Falck Winther, Susanne Oksbjerg Dalton

Abstract

BACKGROUND: While underlying mechanisms and pathways of social inequalities in cancer survival have been extensively examined in adults, this is less so for children with cancer. Hypothesized mechanisms include prediagnostic utilization of and navigation through the health care system, which may differ by socioeconomic resources of the families. In this nationwide register-based study we investigated the association between measures of family socioeconomic position in relation to prediagnostic health care contacts and stage of disease at diagnosis in children with cancer in Denmark.

METHODS: We identified all children diagnosed with a cancer at ages 0-15 years in 1998-2016 (N = 3043) from the Danish Childhood Cancer Registry. We obtained comprehensive information on measures of socioeconomic position, parental health and prediagnostic contacts to both general practitioners and hospitals 24 months prior to diagnosis from various national registries. We fitted multivariable conditional logistic regression models for the association of family socioeconomic and health-related variables with firstly, frequent health care contacts and secondly, advanced stage.

RESULTS: We found higher odds ratios (OR) of frequent both overall and emergency health care contacts in the last 3 months before diagnosis in children from households with short parental education and mixed affiliation to work market, when compared to children with high family socioeconomic position. Further, children of parents with depression or of non-Western origin, respectively, had higher OR for frequent overall and emergency contacts. We found no association between socioeconomic position, parental health and stage of disease.

CONCLUSION: Families with socioeconomic disadvantage, non-Western origin or depression more frequently utilize prediagnostic health care services, both generally and in the acute setting, indicating that some disadvantaged families may struggle to navigate the health care system when their child is sick. Reassuringly, this was not reflected in disparities in stage at diagnosis. In order to improve the diagnostic process and potentially reduce health care contacts, attention and support should be given to families with a high number of health care contacts over a short period of time.

Original languageEnglish
Article number1104
JournalBMC Cancer
Volume21
Issue number1
Pages (from-to)1104
ISSN1471-2407
DOIs
Publication statusPublished - 14 Oct 2021

Keywords

  • Adolescent
  • Child
  • Child, Preschool
  • Denmark
  • Educational Status
  • Emergency Service, Hospital/statistics & numerical data
  • Fathers
  • Female
  • Health Services Needs and Demand/statistics & numerical data
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Maternal Age
  • Maternal Health
  • Neoplasms/diagnosis
  • Odds Ratio
  • Parents
  • Paternal Age
  • Registries
  • Socioeconomic Factors

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