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Hypophosphatemia in a Specialized Intestinal Failure Unit: An Observational Cohort Study

BACKGROUND: Patients with intestinal failure (IF) are prone to hypophosphatemia and shifts in magnesium and potassium levels. Although these shifts are often attributed to refeeding syndrome (RFS), the incidence of electrolyte shifts among patients with IF is unknown. We evaluated the occurrence of...

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Autores principales: Eriksen, Marcel Kjærsgaard, Baunwall, Simon Mark Dahl, Lal, Simon, Dahlerup, Jens Frederik, Hvas, Christian Lodberg
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/PMC8451901/
https://www.ncbi.nlm.nih.gov/pubmed/32841404
http://dx.doi.org/10.1002/jpen.2006
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author Eriksen, Marcel Kjærsgaard
Baunwall, Simon Mark Dahl
Lal, Simon
Dahlerup, Jens Frederik
Hvas, Christian Lodberg
author_facet Eriksen, Marcel Kjærsgaard
Baunwall, Simon Mark Dahl
Lal, Simon
Dahlerup, Jens Frederik
Hvas, Christian Lodberg
author_sort Eriksen, Marcel Kjærsgaard
collection PubMed
description BACKGROUND: Patients with intestinal failure (IF) are prone to hypophosphatemia and shifts in magnesium and potassium levels. Although these shifts are often attributed to refeeding syndrome (RFS), the incidence of electrolyte shifts among patients with IF is unknown. We evaluated the occurrence of hypophosphatemia and other electrolyte shifts according to the functional and pathophysiological IF classifications. METHODS: We consecutively included all patients’ first admission to an IF unit from 2013 to 2017. Electrolyte shifts were defined as severe hypophosphatemia <0.6 mmol/L (mM) or any 2 other shifts below reference range, comprising hypomagnesemia <0.75 mM, hypophosphatemia <0.8 mM, or hypokalemia <3.5 mM. Outcomes included length of stay, central line–associated bloodstream infection, and other infections. Mortality was evaluated 6 months after discharge. RESULTS: Of 236 patients with IF, electrolyte shifts occurred in 99 (42%), and 127 (54%) of these patients received intravenous supplementation with either phosphate, magnesium, or potassium. In patients who started parenteral nutrition, up to 62% of early‐onset shifts (<5 days) related to refeeding, and up to 63% of late‐onset shifts (≥5 days) could be ascribed to infections. Derangements occurred in 7 (18%) with type 1 IF, 53 (43%) with type 2 IF, and 39 (53%) readmitted patients with type 3 IF. Of 133 patients with IF secondary to short‐bowel syndrome, 65 (49%) developed shifts. CONCLUSION: In patients with IF, electrolyte shifts are frequent but not always due to RFS. Electrolyte shifts are common in patients with type 2 and those readmitted with type 3 IF.
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spelling pubmed-84519012021-09-27 Hypophosphatemia in a Specialized Intestinal Failure Unit: An Observational Cohort Study Eriksen, Marcel Kjærsgaard Baunwall, Simon Mark Dahl Lal, Simon Dahlerup, Jens Frederik Hvas, Christian Lodberg JPEN J Parenter Enteral Nutr Original Communications BACKGROUND: Patients with intestinal failure (IF) are prone to hypophosphatemia and shifts in magnesium and potassium levels. Although these shifts are often attributed to refeeding syndrome (RFS), the incidence of electrolyte shifts among patients with IF is unknown. We evaluated the occurrence of hypophosphatemia and other electrolyte shifts according to the functional and pathophysiological IF classifications. METHODS: We consecutively included all patients’ first admission to an IF unit from 2013 to 2017. Electrolyte shifts were defined as severe hypophosphatemia <0.6 mmol/L (mM) or any 2 other shifts below reference range, comprising hypomagnesemia <0.75 mM, hypophosphatemia <0.8 mM, or hypokalemia <3.5 mM. Outcomes included length of stay, central line–associated bloodstream infection, and other infections. Mortality was evaluated 6 months after discharge. RESULTS: Of 236 patients with IF, electrolyte shifts occurred in 99 (42%), and 127 (54%) of these patients received intravenous supplementation with either phosphate, magnesium, or potassium. In patients who started parenteral nutrition, up to 62% of early‐onset shifts (<5 days) related to refeeding, and up to 63% of late‐onset shifts (≥5 days) could be ascribed to infections. Derangements occurred in 7 (18%) with type 1 IF, 53 (43%) with type 2 IF, and 39 (53%) readmitted patients with type 3 IF. Of 133 patients with IF secondary to short‐bowel syndrome, 65 (49%) developed shifts. CONCLUSION: In patients with IF, electrolyte shifts are frequent but not always due to RFS. Electrolyte shifts are common in patients with type 2 and those readmitted with type 3 IF. John Wiley and Sons Inc. 2020-09-10 2021-08 /pmc/articles/PMC8451901/ /pubmed/32841404 http://dx.doi.org/10.1002/jpen.2006 Text en © 2020 American Society for Parenteral and Enteral Nutrition https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://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
Eriksen, Marcel Kjærsgaard
Baunwall, Simon Mark Dahl
Lal, Simon
Dahlerup, Jens Frederik
Hvas, Christian Lodberg
Hypophosphatemia in a Specialized Intestinal Failure Unit: An Observational Cohort Study
title Hypophosphatemia in a Specialized Intestinal Failure Unit: An Observational Cohort Study
title_full Hypophosphatemia in a Specialized Intestinal Failure Unit: An Observational Cohort Study
title_fullStr Hypophosphatemia in a Specialized Intestinal Failure Unit: An Observational Cohort Study
title_full_unstemmed Hypophosphatemia in a Specialized Intestinal Failure Unit: An Observational Cohort Study
title_short Hypophosphatemia in a Specialized Intestinal Failure Unit: An Observational Cohort Study
title_sort hypophosphatemia in a specialized intestinal failure unit: an observational cohort study
topic Original Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8451901/
https://www.ncbi.nlm.nih.gov/pubmed/32841404
http://dx.doi.org/10.1002/jpen.2006
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