Cargando…
Recurrent severe hypophosphatemia following intravenous iron administration
Hypophosphatemia postintravenous iron is frequent but under‐recognized. If prolonged or recurrent, it can cause osteomalacia. The likely mechanisms are direct toxicity to proximal tubular cells causing phosphate wasting, elevated Fibroblast growth factor‐23 (FGF‐23), and reduced 1,25‐dihydroxyvitami...
Autores principales: | , |
---|---|
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/PMC7044372/ https://www.ncbi.nlm.nih.gov/pubmed/32128165 http://dx.doi.org/10.1002/ccr3.2595 |
_version_ | 1783501556777222144 |
---|---|
author | Nataatmadja, Melissa Stephanie Francis, Ross |
author_facet | Nataatmadja, Melissa Stephanie Francis, Ross |
author_sort | Nataatmadja, Melissa Stephanie |
collection | PubMed |
description | Hypophosphatemia postintravenous iron is frequent but under‐recognized. If prolonged or recurrent, it can cause osteomalacia. The likely mechanisms are direct toxicity to proximal tubular cells causing phosphate wasting, elevated Fibroblast growth factor‐23 (FGF‐23), and reduced 1,25‐dihydroxyvitamin D (1,25(OH)(2)D). Hypophosphatemia may be severe and persist for months, necessitating phosphate replacement until normalization of serum levels occurs. |
format | Online Article Text |
id | pubmed-7044372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70443722020-03-03 Recurrent severe hypophosphatemia following intravenous iron administration Nataatmadja, Melissa Stephanie Francis, Ross Clin Case Rep Case Reports Hypophosphatemia postintravenous iron is frequent but under‐recognized. If prolonged or recurrent, it can cause osteomalacia. The likely mechanisms are direct toxicity to proximal tubular cells causing phosphate wasting, elevated Fibroblast growth factor‐23 (FGF‐23), and reduced 1,25‐dihydroxyvitamin D (1,25(OH)(2)D). Hypophosphatemia may be severe and persist for months, necessitating phosphate replacement until normalization of serum levels occurs. John Wiley and Sons Inc. 2020-01-09 /pmc/articles/PMC7044372/ /pubmed/32128165 http://dx.doi.org/10.1002/ccr3.2595 Text en © 2019 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Nataatmadja, Melissa Stephanie Francis, Ross Recurrent severe hypophosphatemia following intravenous iron administration |
title | Recurrent severe hypophosphatemia following intravenous iron administration |
title_full | Recurrent severe hypophosphatemia following intravenous iron administration |
title_fullStr | Recurrent severe hypophosphatemia following intravenous iron administration |
title_full_unstemmed | Recurrent severe hypophosphatemia following intravenous iron administration |
title_short | Recurrent severe hypophosphatemia following intravenous iron administration |
title_sort | recurrent severe hypophosphatemia following intravenous iron administration |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044372/ https://www.ncbi.nlm.nih.gov/pubmed/32128165 http://dx.doi.org/10.1002/ccr3.2595 |
work_keys_str_mv | AT nataatmadjamelissastephanie recurrentseverehypophosphatemiafollowingintravenousironadministration AT francisross recurrentseverehypophosphatemiafollowingintravenousironadministration |