Publication:
Outcome in neonates with necrotizing enterocolitis and patent ductus arteriosus.

cris.virtual.author-orcid0000-0002-9310-3548
cris.virtualsource.author-orcidba98568d-9b6b-4035-baa6-72c0908c56c4
cris.virtualsource.author-orcidfe777fde-e05c-4eef-a2b6-bff3878a3acf
cris.virtualsource.author-orcid121fac7f-b6a1-45a2-a0d8-6918eddae070
cris.virtualsource.author-orcid3e46d252-d8ef-40a6-b4b7-86aefceb0a62
cris.virtualsource.author-orcid6027a6d3-1e9b-48d2-adf4-b4f9ae89310d
cris.virtualsource.author-orcid497bbedd-1298-4b95-b700-41411cdbeeb1
datacite.rightsopen.access
dc.contributor.authorKessler, Ulf
dc.contributor.authorSchulte, Franzisca
dc.contributor.authorCholewa, Dietmar
dc.contributor.authorNelle, Mathias
dc.contributor.authorSchaefer, Stephan C
dc.contributor.authorKlimek, Peter Michael
dc.contributor.authorBerger, Steffen Michael
dc.date.accessioned2024-10-24T16:18:46Z
dc.date.available2024-10-24T16:18:46Z
dc.date.issued2016
dc.description.abstractBACKGROUND There is no agreement of the influence of patent ductus arteriosus (PDA) on outcomes in patients with necrotizing enterocolitis (NEC). In this study, we assessed the influence of PDA on NEC outcomes. METHODS A retrospective study of 131 infants with established NEC was performed. Outcomes (death, disease severity, need for surgery, hospitalization duration), as well as multiple clinical parameters were compared between NEC patients with no congenital heart disease (n=102) and those with isolated PDA (n=29). Univariate, multivariate and stepwise logistic regression analyses were performed. RESULTS Birth weight and gestational age were significantly lower in patients with PDA [median (95% CI): 1120 g (1009-1562 g), 28.4 wk (27.8-30.5 wk)] than in those without PDA [median (95% CI): 1580 g (1593-1905 g), 32.4 wk (31.8-33.5 wk); P<0.05]. The risk of NEC-attributable fatality was higher in NEC patients with PDA (35%) than in NEC patients without PDA (14%)[univariate odds ratio (OR)=3.3, 95% CI: 1.8-8.6, P<0.05; multivariate OR=2.4, 95% CI: 0.82-2.39, P=0.111]. Significant independent predictors for nonsurvival within the entire cohort were advanced disease severity stage III (OR=27.9, 95% CI: 7.4-105, P<0.001) and birth weight below 1100 g (OR=5.7, 95% CI: 1.7-19.4, P<0.01). CONCLUSIONS In patients with NEC, the presence of PDA is associated with an increased risk of death. However, when important differences between the two study groups are controlled, only birth weight and disease severity may independently predict mortality.
dc.description.numberOfPages5
dc.description.sponsorshipUniversitätsklinik für Kinderchirurgie
dc.description.sponsorshipUniversitätsklinik für Neurochirurgie
dc.description.sponsorshipDepartement Klinische Forschung, Kinderchirurgie
dc.description.sponsorshipUniversitätsklinik für Kinderheilkunde
dc.description.sponsorshipLehrkörper, Medizinische Fakultät
dc.identifier.doi10.7892/boris.75066
dc.identifier.pmid26684305
dc.identifier.publisherDOI10.1007/s12519-015-0059-6
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/137529
dc.language.isoen
dc.publisherInstitute of Pediatrics
dc.relation.ispartofWorld journal of pediatrics WJP
dc.relation.issn1708-8569
dc.relation.organizationDCD5A442BADBE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BADAE17DE0405C82790C4DE2
dc.relation.organization192C24A47FAA1137E053960C5C82B94B
dc.relation.organizationDCD5A442C057E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BDBCE17DE0405C82790C4DE2
dc.subjectcongenital heart disease
dc.subjectnecrotizing enterocolitis
dc.subjectneonatal mortality
dc.subjectpatent ductus arteriosus
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleOutcome in neonates with necrotizing enterocolitis and patent ductus arteriosus.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage59
oaire.citation.issue1
oaire.citation.startPage55
oaire.citation.volume12
oairecerif.author.affiliationLehrkörper, Medizinische Fakultät
oairecerif.author.affiliationUniversitätsklinik für Neurochirurgie
oairecerif.author.affiliationDepartement Klinische Forschung, Kinderchirurgie
oairecerif.author.affiliationUniversitätsklinik für Kinderheilkunde
oairecerif.author.affiliationUniversitätsklinik für Kinderchirurgie
oairecerif.author.affiliationUniversitätsklinik für Kinderchirurgie
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unibe.description.ispublishedpub
unibe.eprints.legacyId75066
unibe.journal.abbrevTitleWORLD J PEDIATR
unibe.refereedtrue
unibe.subtype.articlejournal

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