{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,26]],"date-time":"2026-09-26T01:36:07Z","timestamp":1790386567563,"version":"4.1.0"},"reference-count":25,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2021,3,18]],"date-time":"2021-03-18T00:00:00Z","timestamp":1616025600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100004837","name":"Ministerio de Ciencia e Innovaci\u00f3n","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100004837","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100003243","name":"Ministerstvo Zdravotnictv\u00ed Cesk\u00e9 Republiky","doi-asserted-by":"publisher","award":["AZV 17\u201029622A"],"award-info":[{"award-number":["AZV 17\u201029622A"]}],"id":[{"id":"10.13039\/501100003243","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Birth Defects Research"],"published-print":{"date-parts":[[2021,7,15]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Esophageal atresia (EA) affects around 2.3\u20132.6 per 10,000 births world\u2010wide. Infants born with this condition require surgical correction soon after birth. Most survival studies of infants with EA are locally or regionally based. We aimed to describe survival across multiple world regions.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>We included infants diagnosed with EA between 1980 and 2015 from 24 birth defects surveillance programs that are members of the International Clearinghouse for Birth Defects Surveillance and Research. We calculated survival as the proportion of liveborn infants alive at 1\u2009month, 1\u2010 and 5\u2010years, among all infants with EA, those with isolated EA, those with EA and additional anomalies or EA and a chromosomal anomaly or genetic syndrome. We also investigated trends in survival over the decades, 1980s\u20132010s.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>We included 6,466 liveborn infants with EA. Survival was 89.4% (95% CI 88.1\u201390.5) at 1\u2010month, 84.5% (95% CI 83.0\u201385.9) at 1\u2010year and 82.7% (95% CI 81.2\u201384.2) at 5\u2010years. One\u2010month survival for infants with isolated EA (97.1%) was higher than for infants with additional anomalies (89.7%) or infants with chromosomal or genetic syndrome diagnoses (57.3%) with little change at 1\u2010 and 5\u2010years. Survival at 1\u2009month improved from the 1980s to the 2010s, by 6.5% for infants with isolated EA and by 21.5% for infants with EA and additional anomalies.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Almost all infants with isolated EA survived to 5\u2009years. Mortality was higher for infants with EA and an additional anomaly, including chromosomal or genetic syndromes. Survival improved from the 1980s, particularly for those with additional anomalies.<\/jats:p><\/jats:sec>","DOI":"10.1002\/bdr2.1891","type":"journal-article","created":{"date-parts":[[2021,3,18]],"date-time":"2021-03-18T12:03:08Z","timestamp":1616068988000},"page":"945-957","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":29,"title":["Survival of infants born with esophageal atresia among 24 international birth defects surveillance programs"],"prefix":"10.1002","volume":"113","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6940-6517","authenticated-orcid":false,"given":"Jane C.","family":"Bell","sequence":"first","affiliation":[{"name":"Child Population and Translational Health Research, Children's Hospital at Westmead Clinical School University of Sydney  Sydney Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gareth","family":"Baynam","sequence":"additional","affiliation":[{"name":"The Western Australian Register of Developmental Anomalies, Department of Health Government of Western Australia  Subiaco Australia"},{"name":"School of Medicine, Division of Pediatrics; and Telethon Kids Institute University of Western Australia  Perth Western Australia Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3929-3619","authenticated-orcid":false,"given":"Jorieke E. H.","family":"Bergman","sequence":"additional","affiliation":[{"name":"University of Groningen, University Medical Center Groningen Department of Genetics  Groningen The Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Eva","family":"Bermejo\u2010S\u00e1nchez","sequence":"additional","affiliation":[{"name":"ECEMC, Research Unit on Congenital Anomalies Institute of Rare Diseases Research (IIER), Instituto de Salud Carlos III  Madrid Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lorenzo D.","family":"Botto","sequence":"additional","affiliation":[{"name":"International Center on Birth Defects (ICBD) of the International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR), Division of Medical Genetics University of Utah School of Medicine  Salt Lake City Utah USA"},{"name":"Division of Medical Genetics, Department of Pediatrics University of Utah School of Medicine  Salt Lake City Utah USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mark A.","family":"Canfield","sequence":"additional","affiliation":[{"name":"Birth Defects Epidemiology and Surveillance Branch Texas Department of State Health Services  Austin Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Saeed","family":"Dastgiri","sequence":"additional","affiliation":[{"name":"Tabriz Health Services Management Research Center, School of Medicine Tabriz University of Medical Sciences  Tabriz Iran"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Miriam","family":"Gatt","sequence":"additional","affiliation":[{"name":"Malta Congenital Anomalies Registry Directorate for Health Information and Research  Guardamangia Malta"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6263-2562","authenticated-orcid":false,"given":"Boris","family":"Groisman","sequence":"additional","affiliation":[{"name":"National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics National Administration of Laboratories and Health Institutes (ANLIS), National Ministry of Health  Buenos Aires Argentina"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Paula","family":"Hurtado\u2010Villa","sequence":"additional","affiliation":[{"name":"Pontificia Universidad Javeriana Cali Centro M\u00e9dico Imbanaco  Cali Colombia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Karin","family":"Kallen","sequence":"additional","affiliation":[{"name":"Swedish National Board of Health and Welfare and Institution of Clinical Sciences, Lund University of Lund  Stockholm Sweden"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Babak","family":"Khoshnood","sequence":"additional","affiliation":[{"name":"Universit\u00e9 de Paris, Center of Research in Epidemiology and Statistics\/CRESS\/Obstetrical Perinatal and Pediatric Epidemiology Research Team (EPOP\u00e9) INSERM, INRA  Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Victoria","family":"Konrad","sequence":"additional","affiliation":[{"name":"National Center on Birth Defects and Developmental Disabilities US Centers for Disease Control and Prevention  Atlanta Georgia USA"},{"name":"National Center on Birth Defects and Developmental Disabilities Carter Consulting, Incorporated  Atlanta Georgia USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Danielle","family":"Landau","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynecology Soroka University Medical Center  Beersheva Israel"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jorge S.","family":"Lopez\u2010Camelo","sequence":"additional","affiliation":[{"name":"ECLAMC Latin American Collaborative Study of Congenital Malformations  Buenos Aires Argentina"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Laura","family":"Martinez","sequence":"additional","affiliation":[{"name":"Registro DAN (Registro de Defectos al Nacimiento), Departamento de Gen\u00e9tica Hospital Universitario Dr. Jos\u00e9 E. 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