Preterm birth and prescriptions for cardiovascular, antiseizure, antibiotics and antiasthmatic medication in children up to 10 years of age: a population-based data linkage cohort study across six European regions.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
17 10 2022
Historique:
entrez: 17 10 2022
pubmed: 18 10 2022
medline: 20 10 2022
Statut: epublish

Résumé

Preterm children are exposed to many medications in neonatal intensive care units, but little is known about the effect of prematurity on medication use throughout infancy and childhood. We examined prescriptions of cardiovascular medication (CVM), antiseizure medication (ASM), antiasthmatic medication and antibiotics issued/dispensed in the first 10 years of life for very and moderately preterm children compared with term. Population-based data linkage cohort study linking information from birth records to prescription records. Six registries from five countries in the EUROlinkCAT study. The study population included 1 722 912 children, of whom 10 820 (0.6%) were very preterm (<32 weeks gestational age (GA)), 92 814 (5.4%) were moderately preterm (32-36 weeks GA), 1 606 643 (93.3%) were born at term (≥37 weeks GA) and 0.7% had missing GA. Children with major or minor congenital anomalies were excluded (including patent ductus arteriosus). Relative risk (RR) of receiving a prescription for CVM, ASM, antiasthmatic and antibiotics. Very preterm children had a higher RR of receiving a prescription for CVM and ASM than preterm children. For all preterm children, the RR of having a CVM prescription was 3.58 (95% CI 2.06 to 6.23); 2.06 (95% CI 1.73 to 2.41) for ASM; 1.13 (95% CI 0.99 to 1.29) for antiasthmatics and 0.96 (95% CI 0.93 to 0.99) for antibiotics in the first year of life. Increased prescription of CVM, ASM and antiasthmatics persisted for all 10 years of follow-up. Although the RR was highest for CVM and ASM, in absolute numbers more children received prescriptions for antibiotics (42.34%, 95% CI 38.81% to 45.91%) and antiasthmatics (28.40%, 95% CI 16.07% to 42.649%) than for CVM (0.18%, 95% CI 0.12% to 0.25%) and ASM (0.16%, 95% CI 0.13% to 0.20%) in the first year of life. Preterm children had a higher risk of being prescribed/dispensed CVM, ASM and antiasthmatics up to age 10. This study highlights a need for further research into morbidity beyond age 10.

Identifiants

pubmed: 36253045
pii: bmjopen-2022-061746
doi: 10.1136/bmjopen-2022-061746
pmc: PMC9577906
doi:

Substances chimiques

Anti-Asthmatic Agents 0
Anti-Bacterial Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e061746

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Mads Damkjaer (M)

Paediatrics, Lillebaelt Hospital - University Hospital of Southern, Vejle, Denmark mads.damkjaer2@rsyd.dk.

Maria Loane (M)

Centre for Maternal, Fetal and Infant Research, University of Ulster, Newtownabbey, UK.

Stine Kjær Urhøj (SK)

Department of Public Health, University of Copenhagen, Copenhagen K, Denmark.
Paediatric Department, Hospital Lillebaelt Kolding, Kolding, Denmark.

Elisa Ballardini (E)

Neonatal Intensive Care Unit, Paediatric Section, University of Ferrara, Ferrara, Italy.

Clara Cavero-Carbonell (C)

Rare Diseases Research Unit, Fundacio per al Foment de la Investigacio Sanitaria i Biomedica, Valencia, Spain.

Alessio Coi (A)

National Research Council Pisa Research Area, Institute of Clinical Physiology, Pisa, Italy.

Laura García-Villodre (L)

Center for Biomedical Research in Network on Rare Diseases, Valencia, Spain.

Joanne Emma Given (JE)

Faculty of Life & Health Sciences, Ulster University, Newtownabbey, UK.

Mika Gissler (M)

Information, THL National Institute for Health and Welfare, Helsinki, Finland.

Anna Heino (A)

Finnish Institute for Health and Welfare, Helsinki, Finland.

Susan Jordan (S)

Nursing, University of Swansea, Swansea, UK.

Amanda Neville (A)

IMER, University de Ferrara, Florence, Italy.

Anna Pierini (A)

National Research Council, Institute of Clinical Physiology, Pisa, Italy.

Joachim Tan (J)

Population Health Research Institute, St George's, University of London, London, UK.

Ieuan Scanlon (I)

Faculty of Medicine, Health and Life Sciences, Swansea University, Swansea, UK.

Ester Garne (E)

Department of Paediatrics and Adolescent Medicinene, Hospital Lillebaelt Kolding, Kolding, Denmark.

Joan K Morris (JK)

Population Health Research Institute, St George's, University of London, London, UK.

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