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Erythropoietin prevents necrotizing enterocolitis in very preterm infants: a randomized controlled trial

BACKGROUND: Necrotizing enterocolitis (NEC) is one of the most severe complications in very preterm infants, but there are currently no accepted methods to prevent NEC. Studies have shown that erythropoietin (EPO) has the potential to prevent NEC or improve outcomes of preterm NEC. This study aimed...

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Autores principales: Wang, Yong, Song, Juan, Sun, Huiqing, Xu, Falin, Li, Kenan, Nie, Chunxia, Zhang, Xiaoli, Peng, Xirui, Xia, Lei, Shen, Ziyun, Yuan, Xiao, Zhang, Shan, Ding, Xue, Zhang, Yaodong, Kang, Wenqing, Qian, Liling, Zhou, Wenhao, Wang, Xiaoyang, Cheng, Xiuyong, Zhu, Changlian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7414749/
https://www.ncbi.nlm.nih.gov/pubmed/32771013
http://dx.doi.org/10.1186/s12967-020-02459-w
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author Wang, Yong
Song, Juan
Sun, Huiqing
Xu, Falin
Li, Kenan
Nie, Chunxia
Zhang, Xiaoli
Peng, Xirui
Xia, Lei
Shen, Ziyun
Yuan, Xiao
Zhang, Shan
Ding, Xue
Zhang, Yaodong
Kang, Wenqing
Qian, Liling
Zhou, Wenhao
Wang, Xiaoyang
Cheng, Xiuyong
Zhu, Changlian
author_facet Wang, Yong
Song, Juan
Sun, Huiqing
Xu, Falin
Li, Kenan
Nie, Chunxia
Zhang, Xiaoli
Peng, Xirui
Xia, Lei
Shen, Ziyun
Yuan, Xiao
Zhang, Shan
Ding, Xue
Zhang, Yaodong
Kang, Wenqing
Qian, Liling
Zhou, Wenhao
Wang, Xiaoyang
Cheng, Xiuyong
Zhu, Changlian
author_sort Wang, Yong
collection PubMed
description BACKGROUND: Necrotizing enterocolitis (NEC) is one of the most severe complications in very preterm infants, but there are currently no accepted methods to prevent NEC. Studies have shown that erythropoietin (EPO) has the potential to prevent NEC or improve outcomes of preterm NEC. This study aimed to determine whether recombinant human EPO (rhEPO) could protect against NEC in very preterm infants. METHODS: The study was a prospective randomized clinical trial performed among four NICU centers. A total of 1327 preterm infants with gestational age ≤ 32 weeks were admitted to the centers, and 42 infants were excluded leaving 1285 eligible infants to be randomized to the rhEPO or control group. Infants in the rhEPO group were given 500 IU/kg rhEPO intravenously every other day for 2 weeks, while the control group was given the same volume of saline. The primary outcome was the incidence of NEC in very preterm infants at 36 weeks of corrected gestational age. RESULTS: A total of 1285 infants were analyzed at 36 weeks of corrected age for the incidence of NEC. rhEPO treatment significantly decreased the incidence of NEC (stage I, II and III) (12.0% vs. 17.1%, p = 0.010), especially confirmed NEC (stage II and III) (3.0% vs. 5.4%, p = 0.027). Meanwhile, rhEPO treatment significantly reduced the number of red blood cells transfusion in the confirmed NEC cases (1.2 ± 0.4 vs. 2.7 ± 1.0, p = 0.004). Subgroup analyses showed that rhEPO treatment significantly decreased the incidence of confirmed NEC at gestational age < 28 weeks (p = 0.019), and the incidence of all stages NEC in preterm infants with hemoglobin < 90 g/l (p = 0.000) and 5 min Apgar score > 5 (p = 0.028). CONCLUSION: Repeated low-dose rhEPO treatment is beneficial against NEC in very preterm infants. Trial registration The protocol was registered retrospectively at ClinicalTrials.gov (NCT03919500) on April 18, 2019. https://clinicaltrials.gov/ct2/show/NCT03919500
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spelling pubmed-74147492020-08-10 Erythropoietin prevents necrotizing enterocolitis in very preterm infants: a randomized controlled trial Wang, Yong Song, Juan Sun, Huiqing Xu, Falin Li, Kenan Nie, Chunxia Zhang, Xiaoli Peng, Xirui Xia, Lei Shen, Ziyun Yuan, Xiao Zhang, Shan Ding, Xue Zhang, Yaodong Kang, Wenqing Qian, Liling Zhou, Wenhao Wang, Xiaoyang Cheng, Xiuyong Zhu, Changlian J Transl Med Research BACKGROUND: Necrotizing enterocolitis (NEC) is one of the most severe complications in very preterm infants, but there are currently no accepted methods to prevent NEC. Studies have shown that erythropoietin (EPO) has the potential to prevent NEC or improve outcomes of preterm NEC. This study aimed to determine whether recombinant human EPO (rhEPO) could protect against NEC in very preterm infants. METHODS: The study was a prospective randomized clinical trial performed among four NICU centers. A total of 1327 preterm infants with gestational age ≤ 32 weeks were admitted to the centers, and 42 infants were excluded leaving 1285 eligible infants to be randomized to the rhEPO or control group. Infants in the rhEPO group were given 500 IU/kg rhEPO intravenously every other day for 2 weeks, while the control group was given the same volume of saline. The primary outcome was the incidence of NEC in very preterm infants at 36 weeks of corrected gestational age. RESULTS: A total of 1285 infants were analyzed at 36 weeks of corrected age for the incidence of NEC. rhEPO treatment significantly decreased the incidence of NEC (stage I, II and III) (12.0% vs. 17.1%, p = 0.010), especially confirmed NEC (stage II and III) (3.0% vs. 5.4%, p = 0.027). Meanwhile, rhEPO treatment significantly reduced the number of red blood cells transfusion in the confirmed NEC cases (1.2 ± 0.4 vs. 2.7 ± 1.0, p = 0.004). Subgroup analyses showed that rhEPO treatment significantly decreased the incidence of confirmed NEC at gestational age < 28 weeks (p = 0.019), and the incidence of all stages NEC in preterm infants with hemoglobin < 90 g/l (p = 0.000) and 5 min Apgar score > 5 (p = 0.028). CONCLUSION: Repeated low-dose rhEPO treatment is beneficial against NEC in very preterm infants. Trial registration The protocol was registered retrospectively at ClinicalTrials.gov (NCT03919500) on April 18, 2019. https://clinicaltrials.gov/ct2/show/NCT03919500 BioMed Central 2020-08-08 /pmc/articles/PMC7414749/ /pubmed/32771013 http://dx.doi.org/10.1186/s12967-020-02459-w Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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
Wang, Yong
Song, Juan
Sun, Huiqing
Xu, Falin
Li, Kenan
Nie, Chunxia
Zhang, Xiaoli
Peng, Xirui
Xia, Lei
Shen, Ziyun
Yuan, Xiao
Zhang, Shan
Ding, Xue
Zhang, Yaodong
Kang, Wenqing
Qian, Liling
Zhou, Wenhao
Wang, Xiaoyang
Cheng, Xiuyong
Zhu, Changlian
Erythropoietin prevents necrotizing enterocolitis in very preterm infants: a randomized controlled trial
title Erythropoietin prevents necrotizing enterocolitis in very preterm infants: a randomized controlled trial
title_full Erythropoietin prevents necrotizing enterocolitis in very preterm infants: a randomized controlled trial
title_fullStr Erythropoietin prevents necrotizing enterocolitis in very preterm infants: a randomized controlled trial
title_full_unstemmed Erythropoietin prevents necrotizing enterocolitis in very preterm infants: a randomized controlled trial
title_short Erythropoietin prevents necrotizing enterocolitis in very preterm infants: a randomized controlled trial
title_sort erythropoietin prevents necrotizing enterocolitis in very preterm infants: a randomized controlled trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7414749/
https://www.ncbi.nlm.nih.gov/pubmed/32771013
http://dx.doi.org/10.1186/s12967-020-02459-w
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