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Serum creatinine concentration in very-low-birth-weight infants from birth to 34–36 wk postmenstrual age

BACKGROUND: Serum creatinine (s[Cr]) reference ranges for very-low-birth-weight (VLBW) infants must account for physiologic changes in the first months of life. METHODS: We retrospectively identified a sample of 218 appropriate-for-gestational age (GA) VLBW infants without risk factors for renal imp...

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Autores principales: Bateman, David A., Thomas, William, Parravicini, Elvira, Polesana, Elena, Locatelli, Chiara, Lorenz, John M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407015/
https://www.ncbi.nlm.nih.gov/pubmed/25675426
http://dx.doi.org/10.1038/pr.2015.25
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author Bateman, David A.
Thomas, William
Parravicini, Elvira
Polesana, Elena
Locatelli, Chiara
Lorenz, John M.
author_facet Bateman, David A.
Thomas, William
Parravicini, Elvira
Polesana, Elena
Locatelli, Chiara
Lorenz, John M.
author_sort Bateman, David A.
collection PubMed
description BACKGROUND: Serum creatinine (s[Cr]) reference ranges for very-low-birth-weight (VLBW) infants must account for physiologic changes in the first months of life. METHODS: We retrospectively identified a sample of 218 appropriate-for-gestational age (GA) VLBW infants without risk factors for renal impairment, and classified into one of three GA groups: 25–27, 28–29, and 30–33 wk. We observed three phases of s[Cr] change (initial, decline, and equilibrium), whose characteristics varied by GA group. We used mixed-effects regression models to estimate mean and upper 95th prediction interval of s[Cr] for each GA group from birth to 34–36 wk post menstrual age (PMA). RESULTS: In phase I, s[Cr] increased after birth, then returned slowly to baseline. The duration of phase I and the magnitude of s[Cr] rise decreased with increasing GA. In phase II, s[Cr] declined abruptly at a rate that increased with GA. A gradual transition to phase III, a steady-state equilibrium with similar s[Cr] among GA groups, began at approximately 34–36 wk PMA. We constructed GA group-specific nomograms depicting s[Cr] behaviour across the three phases. CONCLUSION: The reference ranges derived from a sample of infants without risk factors for renal impairment provide a context for quantitative interpretation of s[Cr] trends in VLBW infants.
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spelling pubmed-44070152015-05-07 Serum creatinine concentration in very-low-birth-weight infants from birth to 34–36 wk postmenstrual age Bateman, David A. Thomas, William Parravicini, Elvira Polesana, Elena Locatelli, Chiara Lorenz, John M. Pediatr Res Clinical Investigation BACKGROUND: Serum creatinine (s[Cr]) reference ranges for very-low-birth-weight (VLBW) infants must account for physiologic changes in the first months of life. METHODS: We retrospectively identified a sample of 218 appropriate-for-gestational age (GA) VLBW infants without risk factors for renal impairment, and classified into one of three GA groups: 25–27, 28–29, and 30–33 wk. We observed three phases of s[Cr] change (initial, decline, and equilibrium), whose characteristics varied by GA group. We used mixed-effects regression models to estimate mean and upper 95th prediction interval of s[Cr] for each GA group from birth to 34–36 wk post menstrual age (PMA). RESULTS: In phase I, s[Cr] increased after birth, then returned slowly to baseline. The duration of phase I and the magnitude of s[Cr] rise decreased with increasing GA. In phase II, s[Cr] declined abruptly at a rate that increased with GA. A gradual transition to phase III, a steady-state equilibrium with similar s[Cr] among GA groups, began at approximately 34–36 wk PMA. We constructed GA group-specific nomograms depicting s[Cr] behaviour across the three phases. CONCLUSION: The reference ranges derived from a sample of infants without risk factors for renal impairment provide a context for quantitative interpretation of s[Cr] trends in VLBW infants. Nature Publishing Group 2015-05 2015-03-11 /pmc/articles/PMC4407015/ /pubmed/25675426 http://dx.doi.org/10.1038/pr.2015.25 Text en Copyright © 2015 International Pediatric Research Foundation, Inc. http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed. under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Clinical Investigation
Bateman, David A.
Thomas, William
Parravicini, Elvira
Polesana, Elena
Locatelli, Chiara
Lorenz, John M.
Serum creatinine concentration in very-low-birth-weight infants from birth to 34–36 wk postmenstrual age
title Serum creatinine concentration in very-low-birth-weight infants from birth to 34–36 wk postmenstrual age
title_full Serum creatinine concentration in very-low-birth-weight infants from birth to 34–36 wk postmenstrual age
title_fullStr Serum creatinine concentration in very-low-birth-weight infants from birth to 34–36 wk postmenstrual age
title_full_unstemmed Serum creatinine concentration in very-low-birth-weight infants from birth to 34–36 wk postmenstrual age
title_short Serum creatinine concentration in very-low-birth-weight infants from birth to 34–36 wk postmenstrual age
title_sort serum creatinine concentration in very-low-birth-weight infants from birth to 34–36 wk postmenstrual age
topic Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407015/
https://www.ncbi.nlm.nih.gov/pubmed/25675426
http://dx.doi.org/10.1038/pr.2015.25
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