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Clinical prediction models for bronchopulmonary dysplasia: a systematic review and external validation study

BACKGROUND: Bronchopulmonary dysplasia (BPD) is a common complication of preterm birth. Very different models using clinical parameters at an early postnatal age to predict BPD have been developed with little extensive quantitative validation. The objective of this study is to review and validate cl...

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Autores principales: Onland, Wes, Debray, Thomas P, Laughon, Matthew M, Miedema, Martijn, Cools, Filip, Askie, Lisa M, Asselin, Jeanette M, Calvert, Sandra A, Courtney, Sherry E, Dani, Carlo, Durand, David J, Marlow, Neil, Peacock, Janet L, Pillow, J Jane, Soll, Roger F, Thome, Ulrich H, Truffert, Patrick, Schreiber, Michael D, Van Reempts, Patrick, Vendettuoli, Valentina, Vento, Giovanni, van Kaam, Anton H, Moons, Karel G, Offringa, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878731/
https://www.ncbi.nlm.nih.gov/pubmed/24345305
http://dx.doi.org/10.1186/1471-2431-13-207
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author Onland, Wes
Debray, Thomas P
Laughon, Matthew M
Miedema, Martijn
Cools, Filip
Askie, Lisa M
Asselin, Jeanette M
Calvert, Sandra A
Courtney, Sherry E
Dani, Carlo
Durand, David J
Marlow, Neil
Peacock, Janet L
Pillow, J Jane
Soll, Roger F
Thome, Ulrich H
Truffert, Patrick
Schreiber, Michael D
Van Reempts, Patrick
Vendettuoli, Valentina
Vento, Giovanni
van Kaam, Anton H
Moons, Karel G
Offringa, Martin
author_facet Onland, Wes
Debray, Thomas P
Laughon, Matthew M
Miedema, Martijn
Cools, Filip
Askie, Lisa M
Asselin, Jeanette M
Calvert, Sandra A
Courtney, Sherry E
Dani, Carlo
Durand, David J
Marlow, Neil
Peacock, Janet L
Pillow, J Jane
Soll, Roger F
Thome, Ulrich H
Truffert, Patrick
Schreiber, Michael D
Van Reempts, Patrick
Vendettuoli, Valentina
Vento, Giovanni
van Kaam, Anton H
Moons, Karel G
Offringa, Martin
author_sort Onland, Wes
collection PubMed
description BACKGROUND: Bronchopulmonary dysplasia (BPD) is a common complication of preterm birth. Very different models using clinical parameters at an early postnatal age to predict BPD have been developed with little extensive quantitative validation. The objective of this study is to review and validate clinical prediction models for BPD. METHODS: We searched the main electronic databases and abstracts from annual meetings. The STROBE instrument was used to assess the methodological quality. External validation of the retrieved models was performed using an individual patient dataset of 3229 patients at risk for BPD. Receiver operating characteristic curves were used to assess discrimination for each model by calculating the area under the curve (AUC). Calibration was assessed for the best discriminating models by visually comparing predicted and observed BPD probabilities. RESULTS: We identified 26 clinical prediction models for BPD. Although the STROBE instrument judged the quality from moderate to excellent, only four models utilised external validation and none presented calibration of the predictive value. For 19 prediction models with variables matched to our dataset, the AUCs ranged from 0.50 to 0.76 for the outcome BPD. Only two of the five best discriminating models showed good calibration. CONCLUSIONS: External validation demonstrates that, except for two promising models, most existing clinical prediction models are poor to moderate predictors for BPD. To improve the predictive accuracy and identify preterm infants for future intervention studies aiming to reduce the risk of BPD, additional variables are required. Subsequently, that model should be externally validated using a proper impact analysis before its clinical implementation.
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spelling pubmed-38787312014-01-03 Clinical prediction models for bronchopulmonary dysplasia: a systematic review and external validation study Onland, Wes Debray, Thomas P Laughon, Matthew M Miedema, Martijn Cools, Filip Askie, Lisa M Asselin, Jeanette M Calvert, Sandra A Courtney, Sherry E Dani, Carlo Durand, David J Marlow, Neil Peacock, Janet L Pillow, J Jane Soll, Roger F Thome, Ulrich H Truffert, Patrick Schreiber, Michael D Van Reempts, Patrick Vendettuoli, Valentina Vento, Giovanni van Kaam, Anton H Moons, Karel G Offringa, Martin BMC Pediatr Research Article BACKGROUND: Bronchopulmonary dysplasia (BPD) is a common complication of preterm birth. Very different models using clinical parameters at an early postnatal age to predict BPD have been developed with little extensive quantitative validation. The objective of this study is to review and validate clinical prediction models for BPD. METHODS: We searched the main electronic databases and abstracts from annual meetings. The STROBE instrument was used to assess the methodological quality. External validation of the retrieved models was performed using an individual patient dataset of 3229 patients at risk for BPD. Receiver operating characteristic curves were used to assess discrimination for each model by calculating the area under the curve (AUC). Calibration was assessed for the best discriminating models by visually comparing predicted and observed BPD probabilities. RESULTS: We identified 26 clinical prediction models for BPD. Although the STROBE instrument judged the quality from moderate to excellent, only four models utilised external validation and none presented calibration of the predictive value. For 19 prediction models with variables matched to our dataset, the AUCs ranged from 0.50 to 0.76 for the outcome BPD. Only two of the five best discriminating models showed good calibration. CONCLUSIONS: External validation demonstrates that, except for two promising models, most existing clinical prediction models are poor to moderate predictors for BPD. To improve the predictive accuracy and identify preterm infants for future intervention studies aiming to reduce the risk of BPD, additional variables are required. Subsequently, that model should be externally validated using a proper impact analysis before its clinical implementation. BioMed Central 2013-12-17 /pmc/articles/PMC3878731/ /pubmed/24345305 http://dx.doi.org/10.1186/1471-2431-13-207 Text en Copyright © 2013 Onland et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Onland, Wes
Debray, Thomas P
Laughon, Matthew M
Miedema, Martijn
Cools, Filip
Askie, Lisa M
Asselin, Jeanette M
Calvert, Sandra A
Courtney, Sherry E
Dani, Carlo
Durand, David J
Marlow, Neil
Peacock, Janet L
Pillow, J Jane
Soll, Roger F
Thome, Ulrich H
Truffert, Patrick
Schreiber, Michael D
Van Reempts, Patrick
Vendettuoli, Valentina
Vento, Giovanni
van Kaam, Anton H
Moons, Karel G
Offringa, Martin
Clinical prediction models for bronchopulmonary dysplasia: a systematic review and external validation study
title Clinical prediction models for bronchopulmonary dysplasia: a systematic review and external validation study
title_full Clinical prediction models for bronchopulmonary dysplasia: a systematic review and external validation study
title_fullStr Clinical prediction models for bronchopulmonary dysplasia: a systematic review and external validation study
title_full_unstemmed Clinical prediction models for bronchopulmonary dysplasia: a systematic review and external validation study
title_short Clinical prediction models for bronchopulmonary dysplasia: a systematic review and external validation study
title_sort clinical prediction models for bronchopulmonary dysplasia: a systematic review and external validation study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878731/
https://www.ncbi.nlm.nih.gov/pubmed/24345305
http://dx.doi.org/10.1186/1471-2431-13-207
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