Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12887-017-0921-x
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dc.titleComparing very low birth weight versus very low gestation cohort methods for outcome analysis of high risk preterm infants
dc.contributor.authorKoller-Smith, L.I.M
dc.contributor.authorShah, P.S
dc.contributor.authorYe, X.Y
dc.date.accessioned2020-10-27T10:23:03Z
dc.date.available2020-10-27T10:23:03Z
dc.date.issued2017
dc.identifier.citationKoller-Smith, L.I.M, Shah, P.S, Ye, X.Y (2017). Comparing very low birth weight versus very low gestation cohort methods for outcome analysis of high risk preterm infants. BMC Pediatrics 17 (1) : 166. ScholarBank@NUS Repository. https://doi.org/10.1186/s12887-017-0921-x
dc.identifier.issn14712431
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181261
dc.description.abstractBackground: Compared to very low gestational age (<32 weeks, VLGA) cohorts, very low birth weight (<1500 g; VLBW) cohorts are more prone to selection bias toward small-for-gestational age (SGA) infants, which may impact upon the validity of data for benchmarking purposes. Method: Data from all VLGA or VLBW infants admitted in the 3 Networks between 2008 and 2011 were used. Two-thirds of each network cohort was randomly selected to develop prediction models for mortality and composite adverse outcome (CAO: mortality or cerebral injuries, chronic lung disease, severe retinopathy or necrotizing enterocolitis) and the remaining for internal validation. Areas under the ROC curves (AUC) of the models were compared. Results: VLBW cohort (24,335 infants) had twice more SGA infants (20.4% vs. 9.3%) than the VLGA cohort (29,180 infants) and had a higher rate of CAO (36.5% vs. 32.6%). The two models had equal prediction power for mortality and CAO (AUC 0.83), and similarly for all other cross-cohort validations (AUC 0.81-0.85). Neither model performed well for the extremes of birth weight for gestation (<1500 g and ≥32 weeks, AUC 0.50-0.65; ≥1500 g and <32 weeks, AUC 0.60-0.62). Conclusion: There was no difference in prediction power for adverse outcome between cohorting VLGA or VLBW despite substantial bias in SGA population. Either cohorting practises are suitable for international benchmarking. © 2017 The Author(s).
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectadult
dc.subjectadverse outcome
dc.subjectarea under the curve
dc.subjectArticle
dc.subjectbrain injury
dc.subjectchronic lung disease
dc.subjectcohort analysis
dc.subjectcontrolled study
dc.subjectfemale
dc.subjectgestational age
dc.subjecthuman
dc.subjectmale
dc.subjectmortality
dc.subjectnecrotizing enterocolitis
dc.subjectpopulation research
dc.subjectprematurity
dc.subjectretinopathy
dc.subjectrisk factor
dc.subjectsmall for date infant
dc.subjectvalidation study
dc.subjectvery low birth weight
dc.subjectAustralia
dc.subjectbenchmarking
dc.subjectCanada
dc.subjectcomparative study
dc.subjectdecision support system
dc.subjectepidemiology
dc.subjecthospital mortality
dc.subjectinfant
dc.subjectinfant mortality
dc.subjectNew Zealand
dc.subjectnewborn
dc.subjectnewborn intensive care
dc.subjectprognosis
dc.subjectreceiver operating characteristic
dc.subjectretrospective study
dc.subjectselection bias
dc.subjectstatistical model
dc.subjectSweden
dc.subjectArea Under Curve
dc.subjectAustralia
dc.subjectBenchmarking
dc.subjectCanada
dc.subjectDecision Support Techniques
dc.subjectFemale
dc.subjectGestational Age
dc.subjectHospital Mortality
dc.subjectHumans
dc.subjectInfant
dc.subjectInfant Mortality
dc.subjectInfant, Extremely Premature
dc.subjectInfant, Newborn
dc.subjectInfant, Premature
dc.subjectInfant, Premature, Diseases
dc.subjectInfant, Small for Gestational Age
dc.subjectInfant, Very Low Birth Weight
dc.subjectIntensive Care, Neonatal
dc.subjectMale
dc.subjectModels, Statistical
dc.subjectNew Zealand
dc.subjectPrognosis
dc.subjectRetrospective Studies
dc.subjectRisk Factors
dc.subjectROC Curve
dc.subjectSelection Bias
dc.subjectSweden
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1186/s12887-017-0921-x
dc.description.sourcetitleBMC Pediatrics
dc.description.volume17
dc.description.issue1
dc.description.page166
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