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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 |
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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.
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This cohort study found a small increased risk of congenital anomalies for women taking asthma medication.
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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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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5084768</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1815700033</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5706-74a50f8d5e388ffda01c4541f6fae5a31edb1ed46a21ca49239ed94862796f9e3</originalsourceid><addsrcrecordid>eNqFkc1u1DAUhS0EoqWwZocssWGT1j-J42yQaMWvKlVCsLZuk-sZt4k92A4wK3gH3pAnwemUEbDBkuUr-7vH5-oQ8pizY17WCa9bXrFG6GNeM6HukMP9zd2bmlVMCn1AHqR0xRhXgsn75EC0vBW6UYfk23uXrmmwtA9-hd5lGCn4MMHoMFGwGSPFr5uQ5og0BwopryegEw6uh-yCp87TvEZqXUyZ5ugmTEtTkdxEXHnw_Zb-_P6DQvliHWKmo_PXsEKa8jxsH5J7FsaEj27PI_Lx1csPZ2-q84vXb89enFd90zJVtTU0zOqhQam1tQMw3tdNza2ygA1IjsNl2bUCwXuoOyE7HLpaK9F2ynYoj8jzne5mvizme_Q5wmg2xS_ErQngzN8v3q3NKnw2DdN1q3QReHYrEMOnucxoJpd6HEfwGOZkuObFKWNSFvTpP-hVmKMv4y0UbyXTchE82VF9DClFtHsznJklXLNEaZYozU24pePJnzPs-d9pFqDZAV_ciNv_6ZnTdxc74V_XY7HY</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1811730838</pqid></control><display><type>article</type><title>Risk of congenital anomalies after exposure to asthma medication in the first trimester of pregnancy – a cohort linkage study</title><source>Wiley-Blackwell Read & Publish Collection</source><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</creator><creatorcontrib>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</creatorcontrib><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.
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This cohort study found a small increased risk of congenital anomalies for women taking asthma medication.
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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 & 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</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 & 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 & 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.
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This cohort study found a small increased risk of congenital anomalies for women taking asthma medication.
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This cohort study found a small increased risk of congenital anomalies for women taking asthma medication.</description><subject>Abnormalities, Drug-Induced - epidemiology</subject><subject>Acute Kidney Injury - epidemiology</subject><subject>Adrenal Cortex Hormones - administration & dosage</subject><subject>Adrenal Cortex Hormones - adverse effects</subject><subject>Adrenergic beta-2 Receptor Agonists - administration & dosage</subject><subject>Adrenergic beta-2 Receptor Agonists - adverse effects</subject><subject>Adult</subject><subject>Aerosols - adverse effects</subject><subject>Anti-Asthmatic Agents - administration & dosage</subject><subject>Anti-Asthmatic Agents - adverse effects</subject><subject>Anus, Imperforate - epidemiology</subject><subject>Asthma</subject><subject>Asthma - drug therapy</subject><subject>Asthma medication</subject><subject>Birth defects</subject><subject>Cohort Studies</subject><subject>congenital anomalies</subject><subject>Congenital diseases</subject><subject>Denmark - epidemiology</subject><subject>Epidemiology</subject><subject>Female</subject><subject>first trimester exposure</subject><subject>Heart Defects, Congenital - epidemiology</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>inhaled beta‐2 agonists</subject><subject>inhaled corticosteroids</subject><subject>Norway - epidemiology</subject><subject>Pregnancy</subject><subject>Pregnancy Complications - epidemiology</subject><subject>Pregnancy Trimester, First</subject><subject>Prenatal Exposure Delayed Effects - epidemiology</subject><subject>Prescription drugs</subject><subject>Prevalence</subject><subject>Registries</subject><subject>Research Design - statistics & numerical data</subject><subject>Risk Factors</subject><subject>Wales - epidemiology</subject><issn>1470-0328</issn><issn>1471-0528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkc1u1DAUhS0EoqWwZocssWGT1j-J42yQaMWvKlVCsLZuk-sZt4k92A4wK3gH3pAnwemUEbDBkuUr-7vH5-oQ8pizY17WCa9bXrFG6GNeM6HukMP9zd2bmlVMCn1AHqR0xRhXgsn75EC0vBW6UYfk23uXrmmwtA9-hd5lGCn4MMHoMFGwGSPFr5uQ5og0BwopryegEw6uh-yCp87TvEZqXUyZ5ugmTEtTkdxEXHnw_Zb-_P6DQvliHWKmo_PXsEKa8jxsH5J7FsaEj27PI_Lx1csPZ2-q84vXb89enFd90zJVtTU0zOqhQam1tQMw3tdNza2ygA1IjsNl2bUCwXuoOyE7HLpaK9F2ynYoj8jzne5mvizme_Q5wmg2xS_ErQngzN8v3q3NKnw2DdN1q3QReHYrEMOnucxoJpd6HEfwGOZkuObFKWNSFvTpP-hVmKMv4y0UbyXTchE82VF9DClFtHsznJklXLNEaZYozU24pePJnzPs-d9pFqDZAV_ciNv_6ZnTdxc74V_XY7HY</recordid><startdate>201609</startdate><enddate>201609</enddate><creator>Garne, E</creator><creator>Vinkel Hansen, A</creator><creator>Morris, J</creator><creator>Jordan, S</creator><creator>Klungsøyr, K</creator><creator>Engeland, A</creator><creator>Tucker, D</creator><creator>Thayer, DS</creator><creator>Davies, GI</creator><creator>Nybo Andersen, A‐M</creator><creator>Dolk, H</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>ASE</scope><scope>FPQ</scope><scope>K6X</scope><scope>K9.</scope><scope>5PM</scope></search><sort><creationdate>201609</creationdate><title>Risk of congenital anomalies after exposure to asthma medication in the first trimester of pregnancy – a cohort linkage study</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5706-74a50f8d5e388ffda01c4541f6fae5a31edb1ed46a21ca49239ed94862796f9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Abnormalities, Drug-Induced - epidemiology</topic><topic>Acute Kidney Injury - epidemiology</topic><topic>Adrenal Cortex Hormones - administration & dosage</topic><topic>Adrenal Cortex Hormones - adverse effects</topic><topic>Adrenergic beta-2 Receptor Agonists - administration & dosage</topic><topic>Adrenergic beta-2 Receptor Agonists - adverse effects</topic><topic>Adult</topic><topic>Aerosols - adverse effects</topic><topic>Anti-Asthmatic Agents - administration & dosage</topic><topic>Anti-Asthmatic Agents - adverse effects</topic><topic>Anus, Imperforate - epidemiology</topic><topic>Asthma</topic><topic>Asthma - drug therapy</topic><topic>Asthma medication</topic><topic>Birth defects</topic><topic>Cohort Studies</topic><topic>congenital anomalies</topic><topic>Congenital diseases</topic><topic>Denmark - epidemiology</topic><topic>Epidemiology</topic><topic>Female</topic><topic>first trimester exposure</topic><topic>Heart Defects, Congenital - epidemiology</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>inhaled beta‐2 agonists</topic><topic>inhaled corticosteroids</topic><topic>Norway - epidemiology</topic><topic>Pregnancy</topic><topic>Pregnancy Complications - epidemiology</topic><topic>Pregnancy Trimester, First</topic><topic>Prenatal Exposure Delayed Effects - epidemiology</topic><topic>Prescription drugs</topic><topic>Prevalence</topic><topic>Registries</topic><topic>Research Design - statistics & numerical data</topic><topic>Risk Factors</topic><topic>Wales - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>British Nursing Index</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>British Nursing Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BJOG : an international journal of obstetrics and gynaecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garne, E</au><au>Vinkel Hansen, A</au><au>Morris, J</au><au>Jordan, S</au><au>Klungsøyr, K</au><au>Engeland, A</au><au>Tucker, D</au><au>Thayer, DS</au><au>Davies, GI</au><au>Nybo Andersen, A‐M</au><au>Dolk, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk of congenital anomalies after exposure to asthma medication in the first trimester of pregnancy – a cohort linkage study</atitle><jtitle>BJOG : an international journal of obstetrics and gynaecology</jtitle><addtitle>BJOG</addtitle><date>2016-09</date><risdate>2016</risdate><volume>123</volume><issue>10</issue><spage>1609</spage><epage>1618</epage><pages>1609-1618</pages><issn>1470-0328</issn><eissn>1471-0528</eissn><coden>BIOGFQ</coden><abstract>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.
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This cohort study found a small increased risk of congenital anomalies for women taking asthma medication.
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This cohort study found a small increased risk of congenital anomalies for women taking asthma medication.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>27172856</pmid><doi>10.1111/1471-0528.14026</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | Wiley-Blackwell Read & Publish Collection |
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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