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Neonatal Refeeding Syndrome and Clinical Outcome in Extremely Low‐Birth‐Weight Babies: Secondary Cohort Analysis From the ProVIDe Trial

BACKGROUND: Refeeding syndrome (RS) following preterm birth has been linked to high intravenous (IV) protein intake in the presence of low electrolyte supply. In extremely low‐birth‐weight (ELBW) babies, we aimed to determine the incidence of RS and associations with birth characteristics and clinic...

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Autores principales: Cormack, Barbara E., Jiang, Yannan, Harding, Jane E., Crowther, Caroline A., Bloomfield, Frank H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891336/
https://www.ncbi.nlm.nih.gov/pubmed/32458478
http://dx.doi.org/10.1002/jpen.1934
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author Cormack, Barbara E.
Jiang, Yannan
Harding, Jane E.
Crowther, Caroline A.
Bloomfield, Frank H.
author_facet Cormack, Barbara E.
Jiang, Yannan
Harding, Jane E.
Crowther, Caroline A.
Bloomfield, Frank H.
author_sort Cormack, Barbara E.
collection PubMed
description BACKGROUND: Refeeding syndrome (RS) following preterm birth has been linked to high intravenous (IV) protein intake in the presence of low electrolyte supply. In extremely low‐birth‐weight (ELBW) babies, we aimed to determine the incidence of RS and associations with birth characteristics and clinical outcomes. METHOD: Prospective cohort study of ELBW ProVIDe Trial participants in 6 New Zealand neonatal intensive care units. RS was defined as serum phosphate < 1.4 mmol.L(−1) and total calcium > 2.8 mmol.L(−1). Relationships between RS and other factors were explored using 2‐sample tests and logistic regression adjusted for sex, gestation, and birth‐weight z‐score. RESULTS: Of 338 babies (mean [SD] birth‐weight, 780 (134) g, gestational age, 25.9 [1.7] weeks), 68 (20%) had RS. Mortality was greater in babies with RS (32% vs 11%; P < .0001). More small‐ than appropriate‐for‐gestational‐age babies developed RS (22% vs 8%; P = .001). Growth from birth to 36 weeks’ corrected age was not different between babies who did and did not have RS. In logistic regression, the odds of RS decreased by 70% for each 1 mmol per kg(−1).d(−1) IV phosphate intake (odds ratio [OR], 0.3; CI, 0.1–0.6; P = .002) and increased by 80% for each 1 g.kg(−1).d(−1) IV protein intake (OR, 1.8; CI, 1.3–2.7; P = .002). CONCLUSIONS: Neonatal RS is common in this cohort of ELBW babies and is associated with increased morbidity and mortality. Optimizing phosphate and calcium intakes in IV nutrition solutions may reduce RS and its consequences.
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spelling pubmed-78913362021-03-02 Neonatal Refeeding Syndrome and Clinical Outcome in Extremely Low‐Birth‐Weight Babies: Secondary Cohort Analysis From the ProVIDe Trial Cormack, Barbara E. Jiang, Yannan Harding, Jane E. Crowther, Caroline A. Bloomfield, Frank H. JPEN J Parenter Enteral Nutr Original Communications BACKGROUND: Refeeding syndrome (RS) following preterm birth has been linked to high intravenous (IV) protein intake in the presence of low electrolyte supply. In extremely low‐birth‐weight (ELBW) babies, we aimed to determine the incidence of RS and associations with birth characteristics and clinical outcomes. METHOD: Prospective cohort study of ELBW ProVIDe Trial participants in 6 New Zealand neonatal intensive care units. RS was defined as serum phosphate < 1.4 mmol.L(−1) and total calcium > 2.8 mmol.L(−1). Relationships between RS and other factors were explored using 2‐sample tests and logistic regression adjusted for sex, gestation, and birth‐weight z‐score. RESULTS: Of 338 babies (mean [SD] birth‐weight, 780 (134) g, gestational age, 25.9 [1.7] weeks), 68 (20%) had RS. Mortality was greater in babies with RS (32% vs 11%; P < .0001). More small‐ than appropriate‐for‐gestational‐age babies developed RS (22% vs 8%; P = .001). Growth from birth to 36 weeks’ corrected age was not different between babies who did and did not have RS. In logistic regression, the odds of RS decreased by 70% for each 1 mmol per kg(−1).d(−1) IV phosphate intake (odds ratio [OR], 0.3; CI, 0.1–0.6; P = .002) and increased by 80% for each 1 g.kg(−1).d(−1) IV protein intake (OR, 1.8; CI, 1.3–2.7; P = .002). CONCLUSIONS: Neonatal RS is common in this cohort of ELBW babies and is associated with increased morbidity and mortality. Optimizing phosphate and calcium intakes in IV nutrition solutions may reduce RS and its consequences. John Wiley and Sons Inc. 2020-07-04 2021-01 /pmc/articles/PMC7891336/ /pubmed/32458478 http://dx.doi.org/10.1002/jpen.1934 Text en © 2020 The Authors. Journal of Parenteral and Enteral Nutrition published by Wiley Periodicals, Inc. on behalf of American Society for Parenteral and Enteral Nutrition. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Communications
Cormack, Barbara E.
Jiang, Yannan
Harding, Jane E.
Crowther, Caroline A.
Bloomfield, Frank H.
Neonatal Refeeding Syndrome and Clinical Outcome in Extremely Low‐Birth‐Weight Babies: Secondary Cohort Analysis From the ProVIDe Trial
title Neonatal Refeeding Syndrome and Clinical Outcome in Extremely Low‐Birth‐Weight Babies: Secondary Cohort Analysis From the ProVIDe Trial
title_full Neonatal Refeeding Syndrome and Clinical Outcome in Extremely Low‐Birth‐Weight Babies: Secondary Cohort Analysis From the ProVIDe Trial
title_fullStr Neonatal Refeeding Syndrome and Clinical Outcome in Extremely Low‐Birth‐Weight Babies: Secondary Cohort Analysis From the ProVIDe Trial
title_full_unstemmed Neonatal Refeeding Syndrome and Clinical Outcome in Extremely Low‐Birth‐Weight Babies: Secondary Cohort Analysis From the ProVIDe Trial
title_short Neonatal Refeeding Syndrome and Clinical Outcome in Extremely Low‐Birth‐Weight Babies: Secondary Cohort Analysis From the ProVIDe Trial
title_sort neonatal refeeding syndrome and clinical outcome in extremely low‐birth‐weight babies: secondary cohort analysis from the provide trial
topic Original Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891336/
https://www.ncbi.nlm.nih.gov/pubmed/32458478
http://dx.doi.org/10.1002/jpen.1934
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