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Validation of the DIGIROP-birth model in a Chinese cohort

BACKGROUND: We aimed to validate the predictive performance of the DIGIROP-Birth model for identifying treatment-requiring retinopathy of prematurity (TR-ROP) in Chinese preterm infants to evaluate its generalizability across countries and races. METHODS: We retrospectively reviewed the medical reco...

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Autores principales: Chen, Sizhe, Wu, Rong, Chen, He, Ma, Wenbei, Du, Shaolin, Li, Chao, Lu, Xiaohe, Feng, Songfu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161896/
https://www.ncbi.nlm.nih.gov/pubmed/34044820
http://dx.doi.org/10.1186/s12886-021-01952-0
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author Chen, Sizhe
Wu, Rong
Chen, He
Ma, Wenbei
Du, Shaolin
Li, Chao
Lu, Xiaohe
Feng, Songfu
author_facet Chen, Sizhe
Wu, Rong
Chen, He
Ma, Wenbei
Du, Shaolin
Li, Chao
Lu, Xiaohe
Feng, Songfu
author_sort Chen, Sizhe
collection PubMed
description BACKGROUND: We aimed to validate the predictive performance of the DIGIROP-Birth model for identifying treatment-requiring retinopathy of prematurity (TR-ROP) in Chinese preterm infants to evaluate its generalizability across countries and races. METHODS: We retrospectively reviewed the medical records of preterm infants who were screened for retinopathy of prematurity (ROP) in a single Chinese hospital between June 2015 and August 2020. The predictive performance of the model for TR-ROP was assessed through the construction of a receiver-operating characteristic (ROC) curve and calculating the areas under the ROC curve (AUC), sensitivity, specificity, and positive and negative predictive values. RESULTS: Four hundred and forty-two infants (mean (SD) gestational age = 28.8 (1.3) weeks; mean (SD) birth weight = 1237.0 (236.9) g; 64.7% males) were included in the study. Analyses showed that the DIGIROP-Birth model demonstrated less satisfactory performance than previously reported in identifying infants with TR-ROP, with an area under the receiver-operating characteristic curve of 0.634 (95% confidence interval = 0.564–0.705). With a cutoff value of 0.0084, the DIGIROP-Birth model showed a sensitivity of 48/93 (51.6%), which increased to 89/93 (95.7%) after modification with the addition of postnatal risk factors. In infants with a gestational age < 28 weeks or birth weight < 1000 g, the DIGIROP-Birth model exhibited sensitivities of 36/39 (92.3%) and 20/23 (87.0%), respectively. CONCLUSIONS: Although the predictive performance was less satisfactory in China than in developed countries, modification of the DIGIROP-Birth model with postnatal risk factors shows promise in improving its efficacy for TR-ROP. The model may also be effective in infants with a younger gestational age or with an extremely low birth weight. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12886-021-01952-0.
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spelling pubmed-81618962021-06-01 Validation of the DIGIROP-birth model in a Chinese cohort Chen, Sizhe Wu, Rong Chen, He Ma, Wenbei Du, Shaolin Li, Chao Lu, Xiaohe Feng, Songfu BMC Ophthalmol Research BACKGROUND: We aimed to validate the predictive performance of the DIGIROP-Birth model for identifying treatment-requiring retinopathy of prematurity (TR-ROP) in Chinese preterm infants to evaluate its generalizability across countries and races. METHODS: We retrospectively reviewed the medical records of preterm infants who were screened for retinopathy of prematurity (ROP) in a single Chinese hospital between June 2015 and August 2020. The predictive performance of the model for TR-ROP was assessed through the construction of a receiver-operating characteristic (ROC) curve and calculating the areas under the ROC curve (AUC), sensitivity, specificity, and positive and negative predictive values. RESULTS: Four hundred and forty-two infants (mean (SD) gestational age = 28.8 (1.3) weeks; mean (SD) birth weight = 1237.0 (236.9) g; 64.7% males) were included in the study. Analyses showed that the DIGIROP-Birth model demonstrated less satisfactory performance than previously reported in identifying infants with TR-ROP, with an area under the receiver-operating characteristic curve of 0.634 (95% confidence interval = 0.564–0.705). With a cutoff value of 0.0084, the DIGIROP-Birth model showed a sensitivity of 48/93 (51.6%), which increased to 89/93 (95.7%) after modification with the addition of postnatal risk factors. In infants with a gestational age < 28 weeks or birth weight < 1000 g, the DIGIROP-Birth model exhibited sensitivities of 36/39 (92.3%) and 20/23 (87.0%), respectively. CONCLUSIONS: Although the predictive performance was less satisfactory in China than in developed countries, modification of the DIGIROP-Birth model with postnatal risk factors shows promise in improving its efficacy for TR-ROP. The model may also be effective in infants with a younger gestational age or with an extremely low birth weight. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12886-021-01952-0. BioMed Central 2021-05-27 /pmc/articles/PMC8161896/ /pubmed/34044820 http://dx.doi.org/10.1186/s12886-021-01952-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chen, Sizhe
Wu, Rong
Chen, He
Ma, Wenbei
Du, Shaolin
Li, Chao
Lu, Xiaohe
Feng, Songfu
Validation of the DIGIROP-birth model in a Chinese cohort
title Validation of the DIGIROP-birth model in a Chinese cohort
title_full Validation of the DIGIROP-birth model in a Chinese cohort
title_fullStr Validation of the DIGIROP-birth model in a Chinese cohort
title_full_unstemmed Validation of the DIGIROP-birth model in a Chinese cohort
title_short Validation of the DIGIROP-birth model in a Chinese cohort
title_sort validation of the digirop-birth model in a chinese cohort
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161896/
https://www.ncbi.nlm.nih.gov/pubmed/34044820
http://dx.doi.org/10.1186/s12886-021-01952-0
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