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https://doi.org/10.1186/s12887-017-0921-x
DC Field | Value | |
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dc.title | Comparing very low birth weight versus very low gestation cohort methods for outcome analysis of high risk preterm infants | |
dc.contributor.author | Koller-Smith, L.I.M | |
dc.contributor.author | Shah, P.S | |
dc.contributor.author | Ye, X.Y | |
dc.date.accessioned | 2020-10-27T10:23:03Z | |
dc.date.available | 2020-10-27T10:23:03Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Koller-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.issn | 14712431 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/181261 | |
dc.description.abstract | Background: 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.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | adult | |
dc.subject | adverse outcome | |
dc.subject | area under the curve | |
dc.subject | Article | |
dc.subject | brain injury | |
dc.subject | chronic lung disease | |
dc.subject | cohort analysis | |
dc.subject | controlled study | |
dc.subject | female | |
dc.subject | gestational age | |
dc.subject | human | |
dc.subject | male | |
dc.subject | mortality | |
dc.subject | necrotizing enterocolitis | |
dc.subject | population research | |
dc.subject | prematurity | |
dc.subject | retinopathy | |
dc.subject | risk factor | |
dc.subject | small for date infant | |
dc.subject | validation study | |
dc.subject | very low birth weight | |
dc.subject | Australia | |
dc.subject | benchmarking | |
dc.subject | Canada | |
dc.subject | comparative study | |
dc.subject | decision support system | |
dc.subject | epidemiology | |
dc.subject | hospital mortality | |
dc.subject | infant | |
dc.subject | infant mortality | |
dc.subject | New Zealand | |
dc.subject | newborn | |
dc.subject | newborn intensive care | |
dc.subject | prognosis | |
dc.subject | receiver operating characteristic | |
dc.subject | retrospective study | |
dc.subject | selection bias | |
dc.subject | statistical model | |
dc.subject | Sweden | |
dc.subject | Area Under Curve | |
dc.subject | Australia | |
dc.subject | Benchmarking | |
dc.subject | Canada | |
dc.subject | Decision Support Techniques | |
dc.subject | Female | |
dc.subject | Gestational Age | |
dc.subject | Hospital Mortality | |
dc.subject | Humans | |
dc.subject | Infant | |
dc.subject | Infant Mortality | |
dc.subject | Infant, Extremely Premature | |
dc.subject | Infant, Newborn | |
dc.subject | Infant, Premature | |
dc.subject | Infant, Premature, Diseases | |
dc.subject | Infant, Small for Gestational Age | |
dc.subject | Infant, Very Low Birth Weight | |
dc.subject | Intensive Care, Neonatal | |
dc.subject | Male | |
dc.subject | Models, Statistical | |
dc.subject | New Zealand | |
dc.subject | Prognosis | |
dc.subject | Retrospective Studies | |
dc.subject | Risk Factors | |
dc.subject | ROC Curve | |
dc.subject | Selection Bias | |
dc.subject | Sweden | |
dc.type | Article | |
dc.contributor.department | DUKE-NUS MEDICAL SCHOOL | |
dc.description.doi | 10.1186/s12887-017-0921-x | |
dc.description.sourcetitle | BMC Pediatrics | |
dc.description.volume | 17 | |
dc.description.issue | 1 | |
dc.description.page | 166 | |
Appears in Collections: | Elements Staff Publications |
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