Comparing very low birth weight versus very low gestation cohort methods for outcome analysis of high risk preterm infants
Koller-Smith, LIM
Shah, PS
Ye, XY
Sjörs, G
Wang, YA
Chow, SSW
Darlow, BA
Lee, SK
Håkanson, S
Lui, K
Marshall, P
Craven, P
Simmer, K
Stack, J
Knight, D
Watkins, A
Ramsden, A
Tan, K
Bawden, K
Downe, L
Singde, V
Stewart, M
Berry, A
Hunt, R
Kilburn, C
Dargaville, P
Paradisis, M
Evans, N
Reid, S
Cartwright, D
Kuschel, C
Doyle, L
Numa, A
Kecskes, Z
Badawi, N
Koh, G
Resnick, S
Tracy, M
Tarnow-Mordi, W
Andersen, C
Austin, N
Darlow, B
Broadbent, R
Corban, J
Mildenhall, L
Battin, M
Bourchier, D
Richardson, V
Haslam, R
Rajadurai, VS
Kajetanowicz, A
Synnes, A
Rouvinez-Bouali, N
Piedboeuf, B
Bertelle, V
Bulleid, B
Yee, W
Shivananda, S
Lee, KS
Seshia, M
Barrington, K
Lefebvre, F
McMillan, D
Andrews, W
Kovacs, L
Dow, K
da Silva, O
Riley, P
Peliowski, A
Aziz, K
Cieslak, Z
Kalapesi, Z
Sankaran, K
Faucher, D
Alvaro, R
Canning, R
Ojah, C
Monterrosa, L
Dunn, M
Sorokan, T
Harrison, A
Nwaesei, C
Adie, M
Håkansson, S
Segerdahl, N
Morad, T
Morén, S
Stenberg, Å
Simonsson, C
Stigsson, L
Christensen, JL
Åmasn, L
Ingemanson, F
österdal, L
Ellström, KG
Abrahamsson, T
Heimdahl, I
Hägg, T
Hedlund, A
Lund, EE
- Publication Type:
- Journal Article
- Citation:
- BMC Pediatrics, 2017, 17 (1)
- Issue Date:
- 2017-07-14
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Koller-Smith, LIM | en_US |
dc.contributor.author | Shah, PS | en_US |
dc.contributor.author | Ye, XY | en_US |
dc.contributor.author | Sjörs, G | en_US |
dc.contributor.author |
Wang, YA https://orcid.org/0000-0002-3656-4284 |
en_US |
dc.contributor.author | Chow, SSW | en_US |
dc.contributor.author | Darlow, BA | en_US |
dc.contributor.author | Lee, SK | en_US |
dc.contributor.author | Håkanson, S | en_US |
dc.contributor.author | Lui, K | en_US |
dc.contributor.author | Marshall, P | en_US |
dc.contributor.author | Craven, P | en_US |
dc.contributor.author | Simmer, K | en_US |
dc.contributor.author | Stack, J | en_US |
dc.contributor.author | Knight, D | en_US |
dc.contributor.author | Watkins, A | en_US |
dc.contributor.author | Ramsden, A | en_US |
dc.contributor.author | Tan, K | en_US |
dc.contributor.author | Bawden, K | en_US |
dc.contributor.author | Downe, L | en_US |
dc.contributor.author | Singde, V | en_US |
dc.contributor.author | Stewart, M | en_US |
dc.contributor.author | Berry, A | en_US |
dc.contributor.author | Hunt, R | en_US |
dc.contributor.author | Kilburn, C | en_US |
dc.contributor.author | Dargaville, P | en_US |
dc.contributor.author | Paradisis, M | en_US |
dc.contributor.author | Evans, N | en_US |
dc.contributor.author | Reid, S | en_US |
dc.contributor.author | Cartwright, D | en_US |
dc.contributor.author | Kuschel, C | en_US |
dc.contributor.author | Doyle, L | en_US |
dc.contributor.author | Numa, A | en_US |
dc.contributor.author | Kecskes, Z | en_US |
dc.contributor.author | Badawi, N | en_US |
dc.contributor.author | Koh, G | en_US |
dc.contributor.author | Resnick, S | en_US |
dc.contributor.author | Tracy, M | en_US |
dc.contributor.author | Tarnow-Mordi, W | en_US |
dc.contributor.author | Andersen, C | en_US |
dc.contributor.author | Austin, N | en_US |
dc.contributor.author | Darlow, B | en_US |
dc.contributor.author | Broadbent, R | en_US |
dc.contributor.author | Corban, J | en_US |
dc.contributor.author | Mildenhall, L | en_US |
dc.contributor.author | Battin, M | en_US |
dc.contributor.author | Bourchier, D | en_US |
dc.contributor.author | Richardson, V | en_US |
dc.contributor.author | Haslam, R | en_US |
dc.contributor.author | Rajadurai, VS | en_US |
dc.contributor.author | Kajetanowicz, A | en_US |
dc.contributor.author | Synnes, A | en_US |
dc.contributor.author | Rouvinez-Bouali, N | en_US |
dc.contributor.author | Piedboeuf, B | en_US |
dc.contributor.author | Bertelle, V | en_US |
dc.contributor.author | Bulleid, B | en_US |
dc.contributor.author | Yee, W | en_US |
dc.contributor.author | Shivananda, S | en_US |
dc.contributor.author | Lee, KS | en_US |
dc.contributor.author | Seshia, M | en_US |
dc.contributor.author | Barrington, K | en_US |
dc.contributor.author | Lefebvre, F | en_US |
dc.contributor.author | McMillan, D | en_US |
dc.contributor.author | Andrews, W | en_US |
dc.contributor.author | Kovacs, L | en_US |
dc.contributor.author | Dow, K | en_US |
dc.contributor.author | da Silva, O | en_US |
dc.contributor.author | Riley, P | en_US |
dc.contributor.author | Peliowski, A | en_US |
dc.contributor.author | Aziz, K | en_US |
dc.contributor.author | Cieslak, Z | en_US |
dc.contributor.author | Kalapesi, Z | en_US |
dc.contributor.author | Sankaran, K | en_US |
dc.contributor.author | Faucher, D | en_US |
dc.contributor.author | Alvaro, R | en_US |
dc.contributor.author | Canning, R | en_US |
dc.contributor.author | Ojah, C | en_US |
dc.contributor.author | Monterrosa, L | en_US |
dc.contributor.author | Dunn, M | en_US |
dc.contributor.author | Sorokan, T | en_US |
dc.contributor.author | Harrison, A | en_US |
dc.contributor.author | Nwaesei, C | en_US |
dc.contributor.author | Adie, M | en_US |
dc.contributor.author | Håkansson, S | en_US |
dc.contributor.author | Segerdahl, N | en_US |
dc.contributor.author | Morad, T | en_US |
dc.contributor.author | Morén, S | en_US |
dc.contributor.author | Stenberg, Å | en_US |
dc.contributor.author | Simonsson, C | en_US |
dc.contributor.author | Stigsson, L | en_US |
dc.contributor.author | Christensen, JL | en_US |
dc.contributor.author | Åmasn, L | en_US |
dc.contributor.author | Ingemanson, F | en_US |
dc.contributor.author | österdal, L | en_US |
dc.contributor.author | Ellström, KG | en_US |
dc.contributor.author | Abrahamsson, T | en_US |
dc.contributor.author | Heimdahl, I | en_US |
dc.contributor.author | Hägg, T | en_US |
dc.contributor.author | Hedlund, A | en_US |
dc.contributor.author | Lund, EE | en_US |
dc.date.available | 2017-07-05 | en_US |
dc.date.issued | 2017-07-14 | en_US |
dc.identifier.citation | BMC Pediatrics, 2017, 17 (1) | en_US |
dc.identifier.uri | http://hdl.handle.net/10453/123936 | |
dc.description.abstract | © 2017 The Author(s). 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. | en_US |
dc.relation.ispartof | BMC Pediatrics | en_US |
dc.relation.isbasedon | 10.1186/s12887-017-0921-x | en_US |
dc.subject.classification | Pediatrics | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Infant, Premature, Diseases | en_US |
dc.subject.mesh | Prognosis | en_US |
dc.subject.mesh | Intensive Care, Neonatal | en_US |
dc.subject.mesh | Hospital Mortality | en_US |
dc.subject.mesh | Infant Mortality | en_US |
dc.subject.mesh | Area Under Curve | en_US |
dc.subject.mesh | Models, Statistical | en_US |
dc.subject.mesh | Risk Factors | en_US |
dc.subject.mesh | Retrospective Studies | en_US |
dc.subject.mesh | ROC Curve | en_US |
dc.subject.mesh | Selection Bias | en_US |
dc.subject.mesh | Gestational Age | en_US |
dc.subject.mesh | Decision Support Techniques | en_US |
dc.subject.mesh | Infant | en_US |
dc.subject.mesh | Infant, Newborn | en_US |
dc.subject.mesh | Infant, Small for Gestational Age | en_US |
dc.subject.mesh | Infant, Very Low Birth Weight | en_US |
dc.subject.mesh | Infant, Premature | en_US |
dc.subject.mesh | Benchmarking | en_US |
dc.subject.mesh | Canada | en_US |
dc.subject.mesh | Australia | en_US |
dc.subject.mesh | Sweden | en_US |
dc.subject.mesh | New Zealand | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Infant, Extremely Premature | en_US |
dc.title | Comparing very low birth weight versus very low gestation cohort methods for outcome analysis of high risk preterm infants | en_US |
dc.type | Journal Article | |
utslib.citation.volume | 1 | en_US |
utslib.citation.volume | 17 | en_US |
utslib.for | 1114 Paediatrics and Reproductive Medicine | en_US |
pubs.embargo.period | Not known | en_US |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Health | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Health/Public Health | |
pubs.organisational-group | /University of Technology Sydney/Strength - CHSP - Health Services and Practice | |
utslib.copyright.status | open_access | |
pubs.issue | 1 | en_US |
pubs.publication-status | Published | en_US |
pubs.volume | 17 | en_US |
Abstract:
© 2017 The Author(s). 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.
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