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Symptomatic severe hypophosphatemia after intravenous ferric carboxymaltose
Intravenous iron is commonly prescribed for treatment of iron deficiency, with modern formulations demonstrating an acceptable safety profile in the majority of patients. We report the case of a patient who was hospitalised with muscle pain, deteriorating mobility and multiple fractures following re...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Publishing Asia Pty Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788463/ https://www.ncbi.nlm.nih.gov/pubmed/31633052 http://dx.doi.org/10.1002/jgh3.12150 |
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author | Fang, Wendy McMahon, Lawrence P Bloom, Stephen Garg, Mayur |
author_facet | Fang, Wendy McMahon, Lawrence P Bloom, Stephen Garg, Mayur |
author_sort | Fang, Wendy |
collection | PubMed |
description | Intravenous iron is commonly prescribed for treatment of iron deficiency, with modern formulations demonstrating an acceptable safety profile in the majority of patients. We report the case of a patient who was hospitalised with muscle pain, deteriorating mobility and multiple fractures following repeated ferric carboxymaltose infusions. Investigations revealed severe hypophosphatemia with serum phosphate of 0.27 mmol/L, 25‐hydroxyvitamin D (25OHD) level of 32 nmol/L and insufficiency fractures of the sacrum and L5 transverse process. The patient's hypophosphatemia was corrected with several infusions of intravenous phosphate, as well as oral phosphate and calcitriol, with subsequent resolution of her muscle aches, back pain and immobility. The risk of persistent hypophosphatemia and osteomalacia may be higher with iron carboxymaltose than other iron formulations and a transient increase in intact fibroblast growth factor‐23 with reduced renal tubular phosphate absorption has been postulated as the key mechanism. This risk appears increased by repeated iron infusions, underlying malnutrition, hypophosphatemia at baseline, vitamin D deficiency, hyperparathyroidism or anti‐resorptive medication use. The true risk and incidence of hypophosphatemia need to be clarified so that appropriate monitoring, prevention and treatment strategies can be developed. |
format | Online Article Text |
id | pubmed-6788463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wiley Publishing Asia Pty Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-67884632019-10-18 Symptomatic severe hypophosphatemia after intravenous ferric carboxymaltose Fang, Wendy McMahon, Lawrence P Bloom, Stephen Garg, Mayur JGH Open Case Reports Intravenous iron is commonly prescribed for treatment of iron deficiency, with modern formulations demonstrating an acceptable safety profile in the majority of patients. We report the case of a patient who was hospitalised with muscle pain, deteriorating mobility and multiple fractures following repeated ferric carboxymaltose infusions. Investigations revealed severe hypophosphatemia with serum phosphate of 0.27 mmol/L, 25‐hydroxyvitamin D (25OHD) level of 32 nmol/L and insufficiency fractures of the sacrum and L5 transverse process. The patient's hypophosphatemia was corrected with several infusions of intravenous phosphate, as well as oral phosphate and calcitriol, with subsequent resolution of her muscle aches, back pain and immobility. The risk of persistent hypophosphatemia and osteomalacia may be higher with iron carboxymaltose than other iron formulations and a transient increase in intact fibroblast growth factor‐23 with reduced renal tubular phosphate absorption has been postulated as the key mechanism. This risk appears increased by repeated iron infusions, underlying malnutrition, hypophosphatemia at baseline, vitamin D deficiency, hyperparathyroidism or anti‐resorptive medication use. The true risk and incidence of hypophosphatemia need to be clarified so that appropriate monitoring, prevention and treatment strategies can be developed. Wiley Publishing Asia Pty Ltd 2019-03-27 /pmc/articles/PMC6788463/ /pubmed/31633052 http://dx.doi.org/10.1002/jgh3.12150 Text en © 2019 The Authors. JGH Open: An open access journal of gastroenterology and hepatology published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Fang, Wendy McMahon, Lawrence P Bloom, Stephen Garg, Mayur Symptomatic severe hypophosphatemia after intravenous ferric carboxymaltose |
title | Symptomatic severe hypophosphatemia after intravenous ferric carboxymaltose |
title_full | Symptomatic severe hypophosphatemia after intravenous ferric carboxymaltose |
title_fullStr | Symptomatic severe hypophosphatemia after intravenous ferric carboxymaltose |
title_full_unstemmed | Symptomatic severe hypophosphatemia after intravenous ferric carboxymaltose |
title_short | Symptomatic severe hypophosphatemia after intravenous ferric carboxymaltose |
title_sort | symptomatic severe hypophosphatemia after intravenous ferric carboxymaltose |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788463/ https://www.ncbi.nlm.nih.gov/pubmed/31633052 http://dx.doi.org/10.1002/jgh3.12150 |
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