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Long term effects of antenatal betamethasone on lung function: 30 year follow up of a randomised controlled trial
Background: Antenatal betamethasone is routinely used for the prevention of neonatal respiratory distress syndrome in preterm infants. However, little is known of the long term effects of exposure to antenatal betamethasone on lung function in adulthood. Methods: Five hundred and thirty four 30 year...
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Published in: | Thorax 2006-08, Vol.61 (8), p.678-683 |
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description | Background: Antenatal betamethasone is routinely used for the prevention of neonatal respiratory distress syndrome in preterm infants. However, little is known of the long term effects of exposure to antenatal betamethasone on lung function in adulthood. Methods: Five hundred and thirty four 30 year olds whose mothers had participated in the first and largest randomised controlled trial of antenatal betamethasone were followed. Lung function was assessed by portable spirometric testing. The prevalence of asthma symptoms was assessed using the European Community Respiratory Health Survey questionnaire. Results: Fifty (20%) betamethasone exposed and 53 (19%) placebo exposed participants met the criteria for current asthma (relative risk 0.98 (95% CI 0.74 to 1.30), p = 0.89). 181 betamethasone exposed and 202 placebo exposed participants had acceptable spirometric data. There were no differences in lung function between betamethasone and placebo exposed groups (mean (SD) forced vital capacity in the betamethasone and placebo groups 105.9 (12.0) v 106.6 (12.6)% predicted, difference = −0.7 (95% CI −3.2 to 1.8), p = 0.59; mean (SD) forced expiratory volume in 1 second in the betamethasone and placebo groups 98.9 (13.4) v 98.5 (13.6)% predicted, difference = 0.3 (95% CI −2.4 to 3.1, p = 0.80)). Conclusions: Antenatal exposure to a single course of betamethasone does not alter lung function or the prevalence of wheeze and asthma at age 30. |
doi_str_mv | 10.1136/thx.2005.051763 |
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However, little is known of the long term effects of exposure to antenatal betamethasone on lung function in adulthood. Methods: Five hundred and thirty four 30 year olds whose mothers had participated in the first and largest randomised controlled trial of antenatal betamethasone were followed. Lung function was assessed by portable spirometric testing. The prevalence of asthma symptoms was assessed using the European Community Respiratory Health Survey questionnaire. Results: Fifty (20%) betamethasone exposed and 53 (19%) placebo exposed participants met the criteria for current asthma (relative risk 0.98 (95% CI 0.74 to 1.30), p = 0.89). 181 betamethasone exposed and 202 placebo exposed participants had acceptable spirometric data. There were no differences in lung function between betamethasone and placebo exposed groups (mean (SD) forced vital capacity in the betamethasone and placebo groups 105.9 (12.0) v 106.6 (12.6)% predicted, difference = −0.7 (95% CI −3.2 to 1.8), p = 0.59; mean (SD) forced expiratory volume in 1 second in the betamethasone and placebo groups 98.9 (13.4) v 98.5 (13.6)% predicted, difference = 0.3 (95% CI −2.4 to 3.1, p = 0.80)). Conclusions: Antenatal exposure to a single course of betamethasone does not alter lung function or the prevalence of wheeze and asthma at age 30.</description><identifier>ISSN: 0040-6376</identifier><identifier>EISSN: 1468-3296</identifier><identifier>DOI: 10.1136/thx.2005.051763</identifier><identifier>PMID: 16601084</identifier><identifier>CODEN: THORA7</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and British Thoracic Society</publisher><subject>Age ; antenatal glucocorticoids ; Asthma ; Asthma - chemically induced ; Asthma - physiopathology ; Babies ; betamethasone ; Betamethasone - adverse effects ; Biological and medical sciences ; Births ; Disease prevention ; Epidemiology ; Family medical history ; Female ; FEV1 ; Follow-Up Studies ; forced expiratory volume in 1 second ; forced vital capacity ; FVC ; Glucocorticoids - adverse effects ; Humans ; Infant, Newborn ; Infant, Premature ; Lung diseases ; lung function ; Medical sciences ; neonatal respiratory distress syndrome ; peak expiratory flow ; PEF ; Pneumology ; Pregnancy ; Prenatal Care ; Prenatal Exposure Delayed Effects - chemically induced ; Prenatal Exposure Delayed Effects - physiopathology ; Randomized Controlled Trials as Topic ; RDS ; Respiratory distress syndrome ; Respiratory Distress Syndrome, Newborn - prevention & control ; Respiratory Function Tests</subject><ispartof>Thorax, 2006-08, Vol.61 (8), p.678-683</ispartof><rights>Copyright 2006 Thorax</rights><rights>2006 INIST-CNRS</rights><rights>Copyright: 2006 Copyright 2006 Thorax</rights><rights>Copyright © 2006 BMJ Publishing Group and British Thoracic Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b522t-257af2af50d20c53fe9aac140624d4ae4925a9ad80922999fc7dff306063157b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2104681/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2104681/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17993669$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16601084$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dalziel, S R</creatorcontrib><creatorcontrib>Rea, H H</creatorcontrib><creatorcontrib>Walker, N K</creatorcontrib><creatorcontrib>Parag, V</creatorcontrib><creatorcontrib>Mantell, C</creatorcontrib><creatorcontrib>Rodgers, A</creatorcontrib><creatorcontrib>Harding, J E</creatorcontrib><title>Long term effects of antenatal betamethasone on lung function: 30 year follow up of a randomised controlled trial</title><title>Thorax</title><addtitle>Thorax</addtitle><description>Background: Antenatal betamethasone is routinely used for the prevention of neonatal respiratory distress syndrome in preterm infants. However, little is known of the long term effects of exposure to antenatal betamethasone on lung function in adulthood. Methods: Five hundred and thirty four 30 year olds whose mothers had participated in the first and largest randomised controlled trial of antenatal betamethasone were followed. Lung function was assessed by portable spirometric testing. The prevalence of asthma symptoms was assessed using the European Community Respiratory Health Survey questionnaire. Results: Fifty (20%) betamethasone exposed and 53 (19%) placebo exposed participants met the criteria for current asthma (relative risk 0.98 (95% CI 0.74 to 1.30), p = 0.89). 181 betamethasone exposed and 202 placebo exposed participants had acceptable spirometric data. There were no differences in lung function between betamethasone and placebo exposed groups (mean (SD) forced vital capacity in the betamethasone and placebo groups 105.9 (12.0) v 106.6 (12.6)% predicted, difference = −0.7 (95% CI −3.2 to 1.8), p = 0.59; mean (SD) forced expiratory volume in 1 second in the betamethasone and placebo groups 98.9 (13.4) v 98.5 (13.6)% predicted, difference = 0.3 (95% CI −2.4 to 3.1, p = 0.80)). Conclusions: Antenatal exposure to a single course of betamethasone does not alter lung function or the prevalence of wheeze and asthma at age 30.</description><subject>Age</subject><subject>antenatal glucocorticoids</subject><subject>Asthma</subject><subject>Asthma - chemically induced</subject><subject>Asthma - physiopathology</subject><subject>Babies</subject><subject>betamethasone</subject><subject>Betamethasone - adverse effects</subject><subject>Biological and medical sciences</subject><subject>Births</subject><subject>Disease prevention</subject><subject>Epidemiology</subject><subject>Family medical history</subject><subject>Female</subject><subject>FEV1</subject><subject>Follow-Up Studies</subject><subject>forced expiratory volume in 1 second</subject><subject>forced vital capacity</subject><subject>FVC</subject><subject>Glucocorticoids - adverse effects</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Infant, Premature</subject><subject>Lung diseases</subject><subject>lung function</subject><subject>Medical sciences</subject><subject>neonatal respiratory distress syndrome</subject><subject>peak expiratory flow</subject><subject>PEF</subject><subject>Pneumology</subject><subject>Pregnancy</subject><subject>Prenatal Care</subject><subject>Prenatal Exposure Delayed Effects - chemically induced</subject><subject>Prenatal Exposure Delayed Effects - physiopathology</subject><subject>Randomized Controlled Trials as Topic</subject><subject>RDS</subject><subject>Respiratory distress syndrome</subject><subject>Respiratory Distress Syndrome, Newborn - prevention & control</subject><subject>Respiratory Function Tests</subject><issn>0040-6376</issn><issn>1468-3296</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkc1v1DAQxSMEotvCmRuyhLggZTu2E3vNoRJaPsUKRAWImzWb2N0sib21ndL-93jJqoUTJ480v3l-eq8onlCYU8rFadpczxlAPYeaSsHvFTNaiUXJmRL3ixlABaXgUhwVxzFuAWBBqXxYHFEhgMKimhWXK-8uSDJhIMZa06RIvCXoknGYsCdrk3AwaYPRO0O8I_2YeTu6JnXevSQcyI3BQKzve_-LjLs_5ySga_3QRdOSxrsU8jaPKXTYPyoeWOyjeXx4T4pvb998Xb4vV5_ffVi-WpXrmrFUslqiZWhraBk0NbdGITa0AsGqtkJTKVajwnYBijGllG1kay0HAYLTWq75SXE26e7G9WDaxmQb2Otd6AYMN9pjp__duG6jL_yVZhRyhjQLPDsIBH85mpj01o_BZc-aysU-bip5pk4nqgk-xmDs7Q8U9L4jnTvS-4701FG-ePq3sTv-UEoGnh8AjA32NofZdPGOk0pxIVTmyonrYjLXt3sMP7WQXNb60_el_lG_ruD84xd9nvkXE78etv91-RsJw7e6</recordid><startdate>20060801</startdate><enddate>20060801</enddate><creator>Dalziel, S R</creator><creator>Rea, H H</creator><creator>Walker, N K</creator><creator>Parag, V</creator><creator>Mantell, C</creator><creator>Rodgers, A</creator><creator>Harding, J E</creator><general>BMJ Publishing Group Ltd and British Thoracic Society</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><general>BMJ Group</general><scope>BSCLL</scope><scope>IQODW</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20060801</creationdate><title>Long term effects of antenatal betamethasone on lung function: 30 year follow up of a randomised controlled trial</title><author>Dalziel, S R ; 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However, little is known of the long term effects of exposure to antenatal betamethasone on lung function in adulthood. Methods: Five hundred and thirty four 30 year olds whose mothers had participated in the first and largest randomised controlled trial of antenatal betamethasone were followed. Lung function was assessed by portable spirometric testing. The prevalence of asthma symptoms was assessed using the European Community Respiratory Health Survey questionnaire. Results: Fifty (20%) betamethasone exposed and 53 (19%) placebo exposed participants met the criteria for current asthma (relative risk 0.98 (95% CI 0.74 to 1.30), p = 0.89). 181 betamethasone exposed and 202 placebo exposed participants had acceptable spirometric data. There were no differences in lung function between betamethasone and placebo exposed groups (mean (SD) forced vital capacity in the betamethasone and placebo groups 105.9 (12.0) v 106.6 (12.6)% predicted, difference = −0.7 (95% CI −3.2 to 1.8), p = 0.59; mean (SD) forced expiratory volume in 1 second in the betamethasone and placebo groups 98.9 (13.4) v 98.5 (13.6)% predicted, difference = 0.3 (95% CI −2.4 to 3.1, p = 0.80)). Conclusions: Antenatal exposure to a single course of betamethasone does not alter lung function or the prevalence of wheeze and asthma at age 30.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and British Thoracic Society</pub><pmid>16601084</pmid><doi>10.1136/thx.2005.051763</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Age antenatal glucocorticoids Asthma Asthma - chemically induced Asthma - physiopathology Babies betamethasone Betamethasone - adverse effects Biological and medical sciences Births Disease prevention Epidemiology Family medical history Female FEV1 Follow-Up Studies forced expiratory volume in 1 second forced vital capacity FVC Glucocorticoids - adverse effects Humans Infant, Newborn Infant, Premature Lung diseases lung function Medical sciences neonatal respiratory distress syndrome peak expiratory flow PEF Pneumology Pregnancy Prenatal Care Prenatal Exposure Delayed Effects - chemically induced Prenatal Exposure Delayed Effects - physiopathology Randomized Controlled Trials as Topic RDS Respiratory distress syndrome Respiratory Distress Syndrome, Newborn - prevention & control Respiratory Function Tests |
title | Long term effects of antenatal betamethasone on lung function: 30 year follow up of a randomised controlled trial |
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