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Can red cell distribution width in very low birth weight infants predict bronchopulmonary dysplasia?

Red cell distribution width (RDW) is a useful marker for assessing the severity and prognosis of various diseases in adults. However, whether it is applicable to children, especially in newborns, has not been determined. This study aimed to investigate the RDW values of preterm infants and evaluate...

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Autores principales: Oh, Seong Hee, Do, Hyun-Jeong, Park, Ji Sook, Cho, Jae Young, Park, Chan-Hoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772710/
https://www.ncbi.nlm.nih.gov/pubmed/35060550
http://dx.doi.org/10.1097/MD.0000000000028640
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author Oh, Seong Hee
Do, Hyun-Jeong
Park, Ji Sook
Cho, Jae Young
Park, Chan-Hoo
author_facet Oh, Seong Hee
Do, Hyun-Jeong
Park, Ji Sook
Cho, Jae Young
Park, Chan-Hoo
author_sort Oh, Seong Hee
collection PubMed
description Red cell distribution width (RDW) is a useful marker for assessing the severity and prognosis of various diseases in adults. However, whether it is applicable to children, especially in newborns, has not been determined. This study aimed to investigate the RDW values of preterm infants and evaluate whether RDW values in the early days of life can predict bronchopulmonary dysplasia (BPD) development. One hundred and eight infants born at <30 weeks of gestation with a birth weight of <1500 g participated in this retrospective study. RDW values measured at birth, 7 days (D7), and 28 days (D28) after birth were reviewed. The changes in RDW values in the first month of life were analyzed, and we evaluated the relationship between RDW and BPD. The mean RDW values at birth, D7, D28 and the change from birth to D7 were 16.2 ± 0.1%, 17.5 ± 0.2%, 17.6 ± 0.2% and 1.3 ± 1.8%, respectively. RDW at birth was lower in the infants born at <28 weeks’ gestational age than in those born at ≥28 weeks’ gestational age (15.7 ± 0.3 vs 16.4 ± 0.2, P = .024). RDW values of both groups increased during the first week after birth and did not differ significantly at D7. The levels remained similar at 1 month of age. RDW at birth, D7, and D28 and the changes in RDW from birth to D7 were not correlated with the development of BPD independent of its severity. The usefulness of RDW as a predictor of BPD development remains questionable and requires further study.
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spelling pubmed-87727102022-01-21 Can red cell distribution width in very low birth weight infants predict bronchopulmonary dysplasia? Oh, Seong Hee Do, Hyun-Jeong Park, Ji Sook Cho, Jae Young Park, Chan-Hoo Medicine (Baltimore) 6200 Red cell distribution width (RDW) is a useful marker for assessing the severity and prognosis of various diseases in adults. However, whether it is applicable to children, especially in newborns, has not been determined. This study aimed to investigate the RDW values of preterm infants and evaluate whether RDW values in the early days of life can predict bronchopulmonary dysplasia (BPD) development. One hundred and eight infants born at <30 weeks of gestation with a birth weight of <1500 g participated in this retrospective study. RDW values measured at birth, 7 days (D7), and 28 days (D28) after birth were reviewed. The changes in RDW values in the first month of life were analyzed, and we evaluated the relationship between RDW and BPD. The mean RDW values at birth, D7, D28 and the change from birth to D7 were 16.2 ± 0.1%, 17.5 ± 0.2%, 17.6 ± 0.2% and 1.3 ± 1.8%, respectively. RDW at birth was lower in the infants born at <28 weeks’ gestational age than in those born at ≥28 weeks’ gestational age (15.7 ± 0.3 vs 16.4 ± 0.2, P = .024). RDW values of both groups increased during the first week after birth and did not differ significantly at D7. The levels remained similar at 1 month of age. RDW at birth, D7, and D28 and the changes in RDW from birth to D7 were not correlated with the development of BPD independent of its severity. The usefulness of RDW as a predictor of BPD development remains questionable and requires further study. Lippincott Williams & Wilkins 2022-01-21 /pmc/articles/PMC8772710/ /pubmed/35060550 http://dx.doi.org/10.1097/MD.0000000000028640 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/)
spellingShingle 6200
Oh, Seong Hee
Do, Hyun-Jeong
Park, Ji Sook
Cho, Jae Young
Park, Chan-Hoo
Can red cell distribution width in very low birth weight infants predict bronchopulmonary dysplasia?
title Can red cell distribution width in very low birth weight infants predict bronchopulmonary dysplasia?
title_full Can red cell distribution width in very low birth weight infants predict bronchopulmonary dysplasia?
title_fullStr Can red cell distribution width in very low birth weight infants predict bronchopulmonary dysplasia?
title_full_unstemmed Can red cell distribution width in very low birth weight infants predict bronchopulmonary dysplasia?
title_short Can red cell distribution width in very low birth weight infants predict bronchopulmonary dysplasia?
title_sort can red cell distribution width in very low birth weight infants predict bronchopulmonary dysplasia?
topic 6200
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772710/
https://www.ncbi.nlm.nih.gov/pubmed/35060550
http://dx.doi.org/10.1097/MD.0000000000028640
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