{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,7,27]],"date-time":"2023-07-27T17:42:42Z","timestamp":1690479762564},"reference-count":49,"publisher":"Georg Thieme Verlag KG","issue":"01","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Zentralbl Chir"],"published-print":{"date-parts":[[2022,2]]},"abstract":"<jats:title>Zusammenfassung<\/jats:title><jats:p>Die \u00d6sophagusatresie (\u00d6A) ist mit einer Inzidenz von 1\u00a0:\u00a03000 bis 1\u00a0:\u00a04000\n                    Neugeborenen eine seltene, angeborene Erkrankung. Die Therapie beinhaltet\n                    obligatorisch die operative Korrektur. Behandlungskonzepte sind abh\u00e4ngig von der\n                    Variabilit\u00e4t der \u00f6sophagotrachealen Fistelm\u00f6glichkeiten, der variablen Distanz\n                    der \u00d6sophagussegmente und der prognostischen Relevanz assoziierter\n                    Fehlbildungen. Die postoperativen Resultate werden entscheidend durch\n                    krankheitsspezifische Symptome und Komplikationen beeinflusst. Ein\n                    interdisziplin\u00e4res Betreuungskonzept von der pr\u00e4natalen Diagnostik \u00fcber die\n                    Geburt, die neonatalogische Intensivpflege und kinderchirurgische Versorgung mit\n                    hochspezialisierter Kinderan\u00e4sthesie bietet in einem spezialisierten\n                    Kinderzentrum mit Logop\u00e4die, Gastroenterologie und Pulmologie die besten\n                    Voraussetzungen f\u00fcr eine optimale Lebensqualit\u00e4t. Systematische Nachsorge- und\n                    Transitionsprogramme sind f\u00fcr betroffene Kinder essenziell.<\/jats:p>","DOI":"10.1055\/a-1657-0661","type":"journal-article","created":{"date-parts":[[2021,12,7]],"date-time":"2021-12-07T00:13:10Z","timestamp":1638835990000},"page":"83-89","source":"Crossref","is-referenced-by-count":1,"title":["Aktuelle Behandlungsstrategien der \u00d6sophagusatresie"],"prefix":"10.1055","volume":"147","author":[{"given":"Karin","family":"Rothe","sequence":"additional","affiliation":[{"name":"Klinik f\u00fcr Kinderchirurgie, Charite Universitatsmedizin\n                    Berlin, Berlin, Deutschland"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"194","published-online":{"date-parts":[[2021,12,6]]},"reference":[{"key":"ref1","first-page":"463","article-title":"Congenital esophageal atresia","volume":"22","author":"EC Vogt","year":"1929","journal-title":"AJR Am J Roentgenol"},{"key":"ref2","first-page":"369","article-title":"Atresia of the esophagus","volume":"74","author":"RE Gross","year":"1947","journal-title":"Am J Dis Child"},{"issue":"01","key":"ref3","doi-asserted-by":"publisher","first-page":"14","DOI":"10.1097\/ANC.0000000000000464","article-title":"Basic Knowledge of Tracheoesophageal Fistula and Esophageal Atresia","author":"S Lee","year":"2018","journal-title":"Adv Neonatal Care"},{"key":"ref4","volume-title":"Smith\u2019s recognizable Patterns of human Malformation","author":"KL Jones","year":"1997","edition":"5"},{"key":"ref5","doi-asserted-by":"publisher","first-page":"888","DOI":"10.1002\/pd.4630","article-title":"Performance of prenatal diagnosis in esophageal atresia","volume":"35","author":"E Spaggiari","year":"2015","journal-title":"Prenat Diagn"},{"key":"ref6","doi-asserted-by":"publisher","first-page":"1268","DOI":"10.1016\/j.jpedsurg.2016.02.001","article-title":"Accuracy of prenatal detection of tracheoesophageal fistula and oesophageal\n                    atresia","volume":"51","author":"CJ Bradshaw","year":"2016","journal-title":"J Pediatr Surg"},{"key":"ref7","first-page":"296","article-title":"Esophageal atresia: plustic sump catheter for drainage of the proximal\n                    pouch","volume":"54","author":"RL Replogle","year":"1963","journal-title":"Surgery"},{"key":"ref8","first-page":"1635","article-title":"Esophageal atresia. 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