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Sökning: WFRF:(Mutchinick Osvaldo M.) > Survival of infants...

  • Bell, Jane C.University of Sydney,Children's Hospital At Westmead (författare)

Survival of infants born with esophageal atresia among 24 international birth defects surveillance programs

  • Artikel/kapitelEngelska2021

Förlag, utgivningsår, omfång ...

  • 2021-03-18
  • Wiley,2021

Nummerbeteckningar

  • LIBRIS-ID:oai:lup.lub.lu.se:8b586616-5c4c-42ff-8143-ecd0fbec2744
  • https://lup.lub.lu.se/record/8b586616-5c4c-42ff-8143-ecd0fbec2744URI
  • https://doi.org/10.1002/bdr2.1891DOI

Kompletterande språkuppgifter

  • Språk:engelska
  • Sammanfattning på:engelska

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Klassifikation

  • Ämneskategori:art swepub-publicationtype
  • Ämneskategori:ref swepub-contenttype

Anmärkningar

  • Background: Esophageal atresia (EA) affects around 2.3–2.6 per 10,000 births world-wide. 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. Methods: 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 month, 1- and 5-years, 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–2010s. Results: We included 6,466 liveborn infants with EA. Survival was 89.4% (95% CI 88.1–90.5) at 1-month, 84.5% (95% CI 83.0–85.9) at 1-year and 82.7% (95% CI 81.2–84.2) at 5-years. One-month 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- and 5-years. Survival at 1 month 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. Conclusions: Almost all infants with isolated EA survived to 5 years. 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.

Ämnesord och genrebeteckningar

Biuppslag (personer, institutioner, konferenser, titlar ...)

  • Baynam, GarethGovernment of Western Australia,University of Western Australia, Perth (författare)
  • Bergman, Jorieke E.H.University of Groningen,University Medical Center Groningen (författare)
  • Bermejo-Sánchez, EvaCarlos III Health Institute (författare)
  • Botto, Lorenzo D.University of Utah (författare)
  • Canfield, Mark A.Texas Department of State Health Services (författare)
  • Dastgiri, SaeedTabriz University of Medical Sciences (författare)
  • Gatt, MiriamDirectorate for Health Information and Research (författare)
  • Groisman, BorisNational Center of Medical Genetics (CENAGEM) (författare)
  • Hurtado-Villa, PaulaPontificia Universidad Javeriana, Cali (författare)
  • Kallen, KarinLund University,Lunds universitet,Miljöepidemiologi,Forskargrupper vid Lunds universitet,Environmental Epidemiology,Lund University Research Groups(Swepub:lu)anat-kka (författare)
  • Khoshnood, BabakCentre of Epidemiology And Biostatistics Sorbonne Paris Cité Center (CRESS) (författare)
  • Konrad, VictoriaCenters For Disease Control And Prevention (författare)
  • Landau, DanielleSoroka Medical Center (författare)
  • Lopez-Camelo, Jorge S.Centro De Educacion Medica e Investigaciones Clinicas Norberto Quirno Escuela de Medicina (ECLAMC) (författare)
  • Martinez, LauraUniversidad Autonoma de Nuevo Leon (författare)
  • Morgan, MargerySingleton Hospital (författare)
  • Mutchinick, Osvaldo M.Instituto Nacional de Ciencias Médicas y Nutrición (författare)
  • Nance, Amy E.Utah Department of Health (författare)
  • Nembhard, WendyUniversity of Arkansas for Medical Sciences (författare)
  • Pierini, AnnaGabriele Monasterio Foundation,CNR Institute of Clinical Physiology (IFC-CNR) (författare)
  • Rissmann, AnkeUniversity Hospital Magdeburg (författare)
  • Shan, XiaoyiArkansas Children's Hospital (författare)
  • Sipek, AntoninThomayer Hospital (författare)
  • Szabova, ElenaSlovak Medical University (författare)
  • Tagliabue, GiovannaIstituto Nazionale dei Tumori (författare)
  • Yevtushok, Lyubov S.Rivne Regional Medical Diagnostic Center,Omni-Net for Children International Charitable Fund Rivne (författare)
  • Zarante, IgnacioPontificia Universidad Javeriana (författare)
  • Nassar, NatashaUniversity of Sydney (författare)
  • University of SydneyChildren's Hospital At Westmead (creator_code:org_t)

Sammanhörande titlar

  • Ingår i:Birth Defects Research: Wiley113:12, s. 945-9572472-1727

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