Antiasthmatic prescriptions in children with and without congenital anomalies: a population-based study

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Antiasthmatic prescriptions in children with and without congenital anomalies : a population-based study. / Divin, Natalie; Given, Joanne Emma; Tan, Joachim; Astolfi, Gianni; Ballardini, Elisa; Barrachina-Bonet, Laia; Cavero-Carbonell, Clara; Coi, Alessio; Garne, Ester; Gissler, Mika; Heino, Anna; Jordan, Susan; Pierini, Anna; Scanlon, Ieuan; Urhøj, Stine Kjær; Morris, Joan K; Loane, Maria.

In: BMJ Open, Vol. 13, No. 10, e068885, 2023.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Divin, N, Given, JE, Tan, J, Astolfi, G, Ballardini, E, Barrachina-Bonet, L, Cavero-Carbonell, C, Coi, A, Garne, E, Gissler, M, Heino, A, Jordan, S, Pierini, A, Scanlon, I, Urhøj, SK, Morris, JK & Loane, M 2023, 'Antiasthmatic prescriptions in children with and without congenital anomalies: a population-based study', BMJ Open, vol. 13, no. 10, e068885. https://doi.org/10.1136/bmjopen-2022-068885

APA

Divin, N., Given, J. E., Tan, J., Astolfi, G., Ballardini, E., Barrachina-Bonet, L., Cavero-Carbonell, C., Coi, A., Garne, E., Gissler, M., Heino, A., Jordan, S., Pierini, A., Scanlon, I., Urhøj, S. K., Morris, J. K., & Loane, M. (2023). Antiasthmatic prescriptions in children with and without congenital anomalies: a population-based study. BMJ Open, 13(10), [e068885]. https://doi.org/10.1136/bmjopen-2022-068885

Vancouver

Divin N, Given JE, Tan J, Astolfi G, Ballardini E, Barrachina-Bonet L et al. Antiasthmatic prescriptions in children with and without congenital anomalies: a population-based study. BMJ Open. 2023;13(10). e068885. https://doi.org/10.1136/bmjopen-2022-068885

Author

Divin, Natalie ; Given, Joanne Emma ; Tan, Joachim ; Astolfi, Gianni ; Ballardini, Elisa ; Barrachina-Bonet, Laia ; Cavero-Carbonell, Clara ; Coi, Alessio ; Garne, Ester ; Gissler, Mika ; Heino, Anna ; Jordan, Susan ; Pierini, Anna ; Scanlon, Ieuan ; Urhøj, Stine Kjær ; Morris, Joan K ; Loane, Maria. / Antiasthmatic prescriptions in children with and without congenital anomalies : a population-based study. In: BMJ Open. 2023 ; Vol. 13, No. 10.

Bibtex

@article{38ea0756d5464ce6a83b873844d1999d,
title = "Antiasthmatic prescriptions in children with and without congenital anomalies: a population-based study",
abstract = "OBJECTIVES: To explore the risk of being prescribed/dispensed medications for respiratory symptoms and breathing difficulties in children with and without congenital anomalies.DESIGN: A EUROlinkCAT population-based data linkage cohort study. Data on children with and without congenital anomalies were linked to prescription databases to identify children who did/did not receive antiasthmatic prescriptions. Data were analysed by age, European region, class of antiasthmatic, anomaly, sex, gestational age and birth cohort.SETTING: Children born 2000-2014 in six regions within five European countries.PARTICIPANTS: 60 662 children with congenital anomalies and 1 722 912 reference children up to age 10 years.PRIMARY OUTCOME MEASURE: Relative risks (RR) of >1 antiasthmatic prescription in a year, identified using Anatomical Therapeutic Chemical classification codes beginning with R03.RESULTS: There were significant differences in the prescribing of antiasthmatics in the six regions. Children with congenital anomalies had a significantly higher risk of being prescribed antiasthmatics (RR 1.41, 95% CI 1.35 to 1.48) compared with reference children. The increased risk was consistent across all regions and all age groups. Children with congenital anomalies were more likely to be prescribed beta-2 agonists (RR 1.71, 95% CI 1.60 to 1.83) and inhaled corticosteroids (RR 1.74, 95% CI 1.61 to 1.87). Children with oesophageal atresia, genetic syndromes and chromosomal anomalies had over twice the risk of being prescribed antiasthmatics compared with reference children. Children with congenital anomalies born <32 weeks gestational age were over twice as likely to be prescribed antiasthmatics than those born at term (RR 2.20, 95% CI 2.10 to 2.30).CONCLUSION: This study documents the additional burden of respiratory symptoms and breathing difficulties for children with congenital anomalies, particularly those born preterm, compared with children without congenital anomalies in the first 10 years of life. These findings are beneficial to clinicians and healthcare providers as they identify children with greater morbidity associated with respiratory symptoms, as indicated by antiasthmatic prescriptions.",
author = "Natalie Divin and Given, {Joanne Emma} and Joachim Tan and Gianni Astolfi and Elisa Ballardini and Laia Barrachina-Bonet and Clara Cavero-Carbonell and Alessio Coi and Ester Garne and Mika Gissler and Anna Heino and Susan Jordan and Anna Pierini and Ieuan Scanlon and Urh{\o}j, {Stine Kj{\ae}r} and Morris, {Joan K} and Maria Loane",
note = "{\textcopyright} Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.",
year = "2023",
doi = "10.1136/bmjopen-2022-068885",
language = "English",
volume = "13",
journal = "BMJ Open",
issn = "2044-6055",
publisher = "BMJ Publishing Group",
number = "10",

}

RIS

TY - JOUR

T1 - Antiasthmatic prescriptions in children with and without congenital anomalies

T2 - a population-based study

AU - Divin, Natalie

AU - Given, Joanne Emma

AU - Tan, Joachim

AU - Astolfi, Gianni

AU - Ballardini, Elisa

AU - Barrachina-Bonet, Laia

AU - Cavero-Carbonell, Clara

AU - Coi, Alessio

AU - Garne, Ester

AU - Gissler, Mika

AU - Heino, Anna

AU - Jordan, Susan

AU - Pierini, Anna

AU - Scanlon, Ieuan

AU - Urhøj, Stine Kjær

AU - Morris, Joan K

AU - Loane, Maria

N1 - © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

PY - 2023

Y1 - 2023

N2 - OBJECTIVES: To explore the risk of being prescribed/dispensed medications for respiratory symptoms and breathing difficulties in children with and without congenital anomalies.DESIGN: A EUROlinkCAT population-based data linkage cohort study. Data on children with and without congenital anomalies were linked to prescription databases to identify children who did/did not receive antiasthmatic prescriptions. Data were analysed by age, European region, class of antiasthmatic, anomaly, sex, gestational age and birth cohort.SETTING: Children born 2000-2014 in six regions within five European countries.PARTICIPANTS: 60 662 children with congenital anomalies and 1 722 912 reference children up to age 10 years.PRIMARY OUTCOME MEASURE: Relative risks (RR) of >1 antiasthmatic prescription in a year, identified using Anatomical Therapeutic Chemical classification codes beginning with R03.RESULTS: There were significant differences in the prescribing of antiasthmatics in the six regions. Children with congenital anomalies had a significantly higher risk of being prescribed antiasthmatics (RR 1.41, 95% CI 1.35 to 1.48) compared with reference children. The increased risk was consistent across all regions and all age groups. Children with congenital anomalies were more likely to be prescribed beta-2 agonists (RR 1.71, 95% CI 1.60 to 1.83) and inhaled corticosteroids (RR 1.74, 95% CI 1.61 to 1.87). Children with oesophageal atresia, genetic syndromes and chromosomal anomalies had over twice the risk of being prescribed antiasthmatics compared with reference children. Children with congenital anomalies born <32 weeks gestational age were over twice as likely to be prescribed antiasthmatics than those born at term (RR 2.20, 95% CI 2.10 to 2.30).CONCLUSION: This study documents the additional burden of respiratory symptoms and breathing difficulties for children with congenital anomalies, particularly those born preterm, compared with children without congenital anomalies in the first 10 years of life. These findings are beneficial to clinicians and healthcare providers as they identify children with greater morbidity associated with respiratory symptoms, as indicated by antiasthmatic prescriptions.

AB - OBJECTIVES: To explore the risk of being prescribed/dispensed medications for respiratory symptoms and breathing difficulties in children with and without congenital anomalies.DESIGN: A EUROlinkCAT population-based data linkage cohort study. Data on children with and without congenital anomalies were linked to prescription databases to identify children who did/did not receive antiasthmatic prescriptions. Data were analysed by age, European region, class of antiasthmatic, anomaly, sex, gestational age and birth cohort.SETTING: Children born 2000-2014 in six regions within five European countries.PARTICIPANTS: 60 662 children with congenital anomalies and 1 722 912 reference children up to age 10 years.PRIMARY OUTCOME MEASURE: Relative risks (RR) of >1 antiasthmatic prescription in a year, identified using Anatomical Therapeutic Chemical classification codes beginning with R03.RESULTS: There were significant differences in the prescribing of antiasthmatics in the six regions. Children with congenital anomalies had a significantly higher risk of being prescribed antiasthmatics (RR 1.41, 95% CI 1.35 to 1.48) compared with reference children. The increased risk was consistent across all regions and all age groups. Children with congenital anomalies were more likely to be prescribed beta-2 agonists (RR 1.71, 95% CI 1.60 to 1.83) and inhaled corticosteroids (RR 1.74, 95% CI 1.61 to 1.87). Children with oesophageal atresia, genetic syndromes and chromosomal anomalies had over twice the risk of being prescribed antiasthmatics compared with reference children. Children with congenital anomalies born <32 weeks gestational age were over twice as likely to be prescribed antiasthmatics than those born at term (RR 2.20, 95% CI 2.10 to 2.30).CONCLUSION: This study documents the additional burden of respiratory symptoms and breathing difficulties for children with congenital anomalies, particularly those born preterm, compared with children without congenital anomalies in the first 10 years of life. These findings are beneficial to clinicians and healthcare providers as they identify children with greater morbidity associated with respiratory symptoms, as indicated by antiasthmatic prescriptions.

U2 - 10.1136/bmjopen-2022-068885

DO - 10.1136/bmjopen-2022-068885

M3 - Journal article

C2 - 37832979

VL - 13

JO - BMJ Open

JF - BMJ Open

SN - 2044-6055

IS - 10

M1 - e068885

ER -

ID: 369782919