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Risk of congenital anomalies after exposure to asthma medication in the first trimester of pregnancy – a cohort linkage study

Objective To examine the effect of maternal exposure to asthma medications on the risk of congenital anomalies. Design Meta‐analysis of aggregated data from three cohort studies. Setting Linkage between healthcare databases and EUROCAT congenital anomaly registries. Population 519 242 pregnancies in...

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Published in:BJOG : an international journal of obstetrics and gynaecology 2016-09, Vol.123 (10), p.1609-1618
Main Authors: Garne, E, Vinkel Hansen, A, Morris, J, Jordan, S, Klungsøyr, K, Engeland, A, Tucker, D, Thayer, DS, Davies, GI, Nybo Andersen, A‐M, Dolk, H
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cited_by cdi_FETCH-LOGICAL-c5706-74a50f8d5e388ffda01c4541f6fae5a31edb1ed46a21ca49239ed94862796f9e3
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container_title BJOG : an international journal of obstetrics and gynaecology
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creator Garne, E
Vinkel Hansen, A
Morris, J
Jordan, S
Klungsøyr, K
Engeland, A
Tucker, D
Thayer, DS
Davies, GI
Nybo Andersen, A‐M
Dolk, H
description Objective To examine the effect of maternal exposure to asthma medications on the risk of congenital anomalies. Design Meta‐analysis of aggregated data from three cohort studies. Setting Linkage between healthcare databases and EUROCAT congenital anomaly registries. Population 519 242 pregnancies in Norway (2004–2010), Wales (2000–2010) and Funen, Denmark (2000–2010). Methods Exposure defined as having at least one prescription for asthma medications issued (Wales) or dispensed (Norway, Denmark) from 91 days before to 91 days after the pregnancy start date. Odds ratios (ORs) were estimated separately for each register and combined in meta‐analyses. Main outcome measures ORs for all congenital anomalies and specific congenital anomalies. Results Overall exposure prevalence was 3.76%. For exposure to asthma medication in general, the adjusted OR (adjOR) for a major congenital anomaly was 1.21 (99% CI 1.09–1.34) after adjustment for maternal age and socioeconomic position. The OR of anal atresia was significantly increased in pregnancies exposed to inhaled corticosteroids (3.40; 99% CI 1.15–10.04). For severe congenital heart defects, an increased OR (1.97; 1.12–3.49) was associated with exposure to combination treatment with inhaled corticosteroids and long‐acting beta‐2‐agonists. Associations with renal dysplasia were driven by exposure to short‐acting beta‐2‐agonists (2.37; 1.20–4.67). Conclusion The increased risk of congenital anomalies for women taking asthma medication is small with little confounding by maternal age or socioeconomic status. The study confirmed the association of inhaled corticosteroids with anal atresia found in earlier research and found potential new associations with combination treatment. The potential new associations should be interpreted with caution due to the large number of comparisons undertaken. Tweetable This cohort study found a small increased risk of congenital anomalies for women taking asthma medication. Tweetable This cohort study found a small increased risk of congenital anomalies for women taking asthma medication.
doi_str_mv 10.1111/1471-0528.14026
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Design Meta‐analysis of aggregated data from three cohort studies. Setting Linkage between healthcare databases and EUROCAT congenital anomaly registries. Population 519 242 pregnancies in Norway (2004–2010), Wales (2000–2010) and Funen, Denmark (2000–2010). Methods Exposure defined as having at least one prescription for asthma medications issued (Wales) or dispensed (Norway, Denmark) from 91 days before to 91 days after the pregnancy start date. Odds ratios (ORs) were estimated separately for each register and combined in meta‐analyses. Main outcome measures ORs for all congenital anomalies and specific congenital anomalies. Results Overall exposure prevalence was 3.76%. For exposure to asthma medication in general, the adjusted OR (adjOR) for a major congenital anomaly was 1.21 (99% CI 1.09–1.34) after adjustment for maternal age and socioeconomic position. The OR of anal atresia was significantly increased in pregnancies exposed to inhaled corticosteroids (3.40; 99% CI 1.15–10.04). For severe congenital heart defects, an increased OR (1.97; 1.12–3.49) was associated with exposure to combination treatment with inhaled corticosteroids and long‐acting beta‐2‐agonists. Associations with renal dysplasia were driven by exposure to short‐acting beta‐2‐agonists (2.37; 1.20–4.67). Conclusion The increased risk of congenital anomalies for women taking asthma medication is small with little confounding by maternal age or socioeconomic status. The study confirmed the association of inhaled corticosteroids with anal atresia found in earlier research and found potential new associations with combination treatment. The potential new associations should be interpreted with caution due to the large number of comparisons undertaken. Tweetable This cohort study found a small increased risk of congenital anomalies for women taking asthma medication. Tweetable This cohort study found a small increased risk of congenital anomalies for women taking asthma medication.</description><identifier>ISSN: 1470-0328</identifier><identifier>EISSN: 1471-0528</identifier><identifier>DOI: 10.1111/1471-0528.14026</identifier><identifier>PMID: 27172856</identifier><identifier>CODEN: BIOGFQ</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Abnormalities, Drug-Induced - epidemiology ; Acute Kidney Injury - epidemiology ; Adrenal Cortex Hormones - administration &amp; dosage ; Adrenal Cortex Hormones - adverse effects ; Adrenergic beta-2 Receptor Agonists - administration &amp; dosage ; Adrenergic beta-2 Receptor Agonists - adverse effects ; Adult ; Aerosols - adverse effects ; Anti-Asthmatic Agents - administration &amp; dosage ; Anti-Asthmatic Agents - adverse effects ; Anus, Imperforate - epidemiology ; Asthma ; Asthma - drug therapy ; Asthma medication ; Birth defects ; Cohort Studies ; congenital anomalies ; Congenital diseases ; Denmark - epidemiology ; Epidemiology ; Female ; first trimester exposure ; Heart Defects, Congenital - epidemiology ; Humans ; Infant, Newborn ; inhaled beta‐2 agonists ; inhaled corticosteroids ; Norway - epidemiology ; Pregnancy ; Pregnancy Complications - epidemiology ; Pregnancy Trimester, First ; Prenatal Exposure Delayed Effects - epidemiology ; Prescription drugs ; Prevalence ; Registries ; Research Design - statistics &amp; numerical data ; Risk Factors ; Wales - epidemiology</subject><ispartof>BJOG : an international journal of obstetrics and gynaecology, 2016-09, Vol.123 (10), p.1609-1618</ispartof><rights>2016 The Authors. published by John Wiley &amp; Sons Ltd on behalf of Royal College of Obstetricians and Gynaecologists.</rights><rights>2016 The Authors. BJOG An International Journal of Obstetrics and Gynaecology published by John Wiley &amp; Sons Ltd on behalf of Royal College of Obstetricians and Gynaecologists.</rights><rights>Copyright © 2016 Royal College of Obstetricians and Gynaecologists</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5706-74a50f8d5e388ffda01c4541f6fae5a31edb1ed46a21ca49239ed94862796f9e3</citedby><cites>FETCH-LOGICAL-c5706-74a50f8d5e388ffda01c4541f6fae5a31edb1ed46a21ca49239ed94862796f9e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27172856$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Garne, E</creatorcontrib><creatorcontrib>Vinkel Hansen, A</creatorcontrib><creatorcontrib>Morris, J</creatorcontrib><creatorcontrib>Jordan, S</creatorcontrib><creatorcontrib>Klungsøyr, K</creatorcontrib><creatorcontrib>Engeland, A</creatorcontrib><creatorcontrib>Tucker, D</creatorcontrib><creatorcontrib>Thayer, DS</creatorcontrib><creatorcontrib>Davies, GI</creatorcontrib><creatorcontrib>Nybo Andersen, A‐M</creatorcontrib><creatorcontrib>Dolk, H</creatorcontrib><title>Risk of congenital anomalies after exposure to asthma medication in the first trimester of pregnancy – a cohort linkage study</title><title>BJOG : an international journal of obstetrics and gynaecology</title><addtitle>BJOG</addtitle><description>Objective To examine the effect of maternal exposure to asthma medications on the risk of congenital anomalies. Design Meta‐analysis of aggregated data from three cohort studies. Setting Linkage between healthcare databases and EUROCAT congenital anomaly registries. Population 519 242 pregnancies in Norway (2004–2010), Wales (2000–2010) and Funen, Denmark (2000–2010). Methods Exposure defined as having at least one prescription for asthma medications issued (Wales) or dispensed (Norway, Denmark) from 91 days before to 91 days after the pregnancy start date. Odds ratios (ORs) were estimated separately for each register and combined in meta‐analyses. Main outcome measures ORs for all congenital anomalies and specific congenital anomalies. Results Overall exposure prevalence was 3.76%. For exposure to asthma medication in general, the adjusted OR (adjOR) for a major congenital anomaly was 1.21 (99% CI 1.09–1.34) after adjustment for maternal age and socioeconomic position. The OR of anal atresia was significantly increased in pregnancies exposed to inhaled corticosteroids (3.40; 99% CI 1.15–10.04). For severe congenital heart defects, an increased OR (1.97; 1.12–3.49) was associated with exposure to combination treatment with inhaled corticosteroids and long‐acting beta‐2‐agonists. Associations with renal dysplasia were driven by exposure to short‐acting beta‐2‐agonists (2.37; 1.20–4.67). Conclusion The increased risk of congenital anomalies for women taking asthma medication is small with little confounding by maternal age or socioeconomic status. The study confirmed the association of inhaled corticosteroids with anal atresia found in earlier research and found potential new associations with combination treatment. The potential new associations should be interpreted with caution due to the large number of comparisons undertaken. Tweetable This cohort study found a small increased risk of congenital anomalies for women taking asthma medication. 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Design Meta‐analysis of aggregated data from three cohort studies. Setting Linkage between healthcare databases and EUROCAT congenital anomaly registries. Population 519 242 pregnancies in Norway (2004–2010), Wales (2000–2010) and Funen, Denmark (2000–2010). Methods Exposure defined as having at least one prescription for asthma medications issued (Wales) or dispensed (Norway, Denmark) from 91 days before to 91 days after the pregnancy start date. Odds ratios (ORs) were estimated separately for each register and combined in meta‐analyses. Main outcome measures ORs for all congenital anomalies and specific congenital anomalies. Results Overall exposure prevalence was 3.76%. For exposure to asthma medication in general, the adjusted OR (adjOR) for a major congenital anomaly was 1.21 (99% CI 1.09–1.34) after adjustment for maternal age and socioeconomic position. The OR of anal atresia was significantly increased in pregnancies exposed to inhaled corticosteroids (3.40; 99% CI 1.15–10.04). For severe congenital heart defects, an increased OR (1.97; 1.12–3.49) was associated with exposure to combination treatment with inhaled corticosteroids and long‐acting beta‐2‐agonists. Associations with renal dysplasia were driven by exposure to short‐acting beta‐2‐agonists (2.37; 1.20–4.67). Conclusion The increased risk of congenital anomalies for women taking asthma medication is small with little confounding by maternal age or socioeconomic status. The study confirmed the association of inhaled corticosteroids with anal atresia found in earlier research and found potential new associations with combination treatment. The potential new associations should be interpreted with caution due to the large number of comparisons undertaken. Tweetable This cohort study found a small increased risk of congenital anomalies for women taking asthma medication. 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subjects Abnormalities, Drug-Induced - epidemiology
Acute Kidney Injury - epidemiology
Adrenal Cortex Hormones - administration & dosage
Adrenal Cortex Hormones - adverse effects
Adrenergic beta-2 Receptor Agonists - administration & dosage
Adrenergic beta-2 Receptor Agonists - adverse effects
Adult
Aerosols - adverse effects
Anti-Asthmatic Agents - administration & dosage
Anti-Asthmatic Agents - adverse effects
Anus, Imperforate - epidemiology
Asthma
Asthma - drug therapy
Asthma medication
Birth defects
Cohort Studies
congenital anomalies
Congenital diseases
Denmark - epidemiology
Epidemiology
Female
first trimester exposure
Heart Defects, Congenital - epidemiology
Humans
Infant, Newborn
inhaled beta‐2 agonists
inhaled corticosteroids
Norway - epidemiology
Pregnancy
Pregnancy Complications - epidemiology
Pregnancy Trimester, First
Prenatal Exposure Delayed Effects - epidemiology
Prescription drugs
Prevalence
Registries
Research Design - statistics & numerical data
Risk Factors
Wales - epidemiology
title Risk of congenital anomalies after exposure to asthma medication in the first trimester of pregnancy – a cohort linkage study
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