The association of perinatal and clinical factors with outcomes in infants with gastroschisis-a retrospective multicenter study in Finland

dc.contributor.authorTauriainen Asta
dc.contributor.authorSankilampi Ulla
dc.contributor.authorRaitio Arimatias
dc.contributor.authorTauriainen Tuomas
dc.contributor.authorHelenius Ilkka
dc.contributor.authorVanamo Kari
dc.contributor.authorHyvärinen Anna
dc.contributor.organizationfi=kirurgia|en=Surgery|
dc.contributor.organizationfi=lastentautioppi|en=Paediatrics and Adolescent Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.40612039509
dc.contributor.organization-code1.2.246.10.2458963.20.97295082107
dc.converis.publication-id53304319
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/53304319
dc.date.accessioned2022-10-28T13:52:00Z
dc.date.available2022-10-28T13:52:00Z
dc.description.abstractThe aim of the present study was to assess the prognostic factors for the outcome of gastroschisis in Finland. A retrospective multicenter study of gastroschisis patients born between 1993 and 2015 in four Finnish university hospitals was undertaken, collecting perinatal, surgical, and clinical data of neonates for uni- and multifactorial modeling analysis. The aim of the present study was to identify risk factors for mortality and the composite adverse outcome (death and/or short bowel syndrome or hospital stay > 60 days). Of the 154 infants with gastroschisis, the overall survival rate was 90.9%. In Cox regression analysis, independent risk factors for mortality included liver herniation, pulmonary hypoplasia, relaparotomy for perforation or necrosis, abdominal compartment syndrome, and central line sepsis. Furthermore, a logistic regression analysis identified central line sepsis, abdominal compartment syndrome, complex gastroschisis, and a younger gestational age as independent predictors of the composite adverse outcome.<div><i><br /></i></div><div><i>Conclusion:</i> The risk of death is increased in newborns with gastroschisis who have liver herniation, pulmonary hypoplasia, abdominal compartment syndrome, relaparotomy for perforation or necrosis, or central line-associated sepsis. Special care should be taken to minimize the risk of central line sepsis in the clinical setting.</div><div><br /></div><div><b>What is known:</b></div><div><ul><li>Gastroschisis is a relatively rare congenital anomaly of the abdominal wall and its incidence is increasing.</li><li>Complex gastroschisis has been reported to increase risk of mortality and complications. </li></ul></div><div><b>What is new:</b></div><div><ul><li>Central line sepsis was found to be independently associated with mortality in gastroschisis patients.</li><li>Liver herniation was also significantly associated with mortality.</li></ul></div>
dc.identifier.jour-issn0340-6199
dc.identifier.olddbid184837
dc.identifier.oldhandle10024/167931
dc.identifier.urihttps://www.utupub.fi/handle/11111/51710
dc.identifier.urlhttps://link.springer.com/article/10.1007/s00431-021-03964-w
dc.identifier.urnURN:NBN:fi-fe2021042823957
dc.language.isoen
dc.okm.affiliatedauthorRaitio, Arimatias
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3123 Gynaecology and paediatricsen_GB
dc.okm.discipline3126 Surgery, anesthesiology, intensive care, radiologyen_GB
dc.okm.discipline3123 Naisten- ja lastentauditfi_FI
dc.okm.discipline3126 Kirurgia, anestesiologia, tehohoito, radiologiafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSPRINGER
dc.publisher.countryGermanyen_GB
dc.publisher.countrySaksafi_FI
dc.publisher.country-codeDE
dc.relation.doi10.1007/s00431-021-03964-w
dc.relation.ispartofjournalEuropean Journal of Pediatrics
dc.source.identifierhttps://www.utupub.fi/handle/10024/167931
dc.titleThe association of perinatal and clinical factors with outcomes in infants with gastroschisis-a retrospective multicenter study in Finland
dc.year.issued2021

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