Severe Hypophosphatemia Occurring After Repeated Exposure to a Parenteral Iron Formulation

Hypophosphatemia is a less known complication of parenteral iron use, particularly after the use of certain iron formulations. We report the case of a young male with inflammatory bowel disease and iron deficiency anemia, who developed severe symptomatic hypophosphatemia after his third exposure to...

Full description

Saved in:
Bibliographic Details
Main Authors: Keerthana Haridas, Alice Yau
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Case Reports in Endocrinology
Online Access:http://dx.doi.org/10.1155/2022/1011401
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850169990851854336
author Keerthana Haridas
Alice Yau
author_facet Keerthana Haridas
Alice Yau
author_sort Keerthana Haridas
collection DOAJ
description Hypophosphatemia is a less known complication of parenteral iron use, particularly after the use of certain iron formulations. We report the case of a young male with inflammatory bowel disease and iron deficiency anemia, who developed severe symptomatic hypophosphatemia after his third exposure to iron carboxymaltose with no evidence of the same occurring upon prior exposures to the compound. Investigations revealed serum phosphorous levels of 0.7 mg/dl, corrected serum calcium of 8–9.5 mg/dl, alkaline phosphatase of 50 U/L (38–126), 25 hydroxy vitamin D level of 40.2 ng/ml, and intact PTH elevated to 207 pg/ml. Urine studies indicated renal phosphate wasting. Presentation was not in keeping with refeeding syndrome. Intact fibroblast growth factor 23 level, measured after the initiation of treatment was within the normal range at 179 RU/mL (44–215). 1,25 dihydroxy vitamin D level, also measured after the initiation of treatment, was normal at 26.3 pg/ml (19.9–79.3). The patient was treated with calcitriol and aggressive oral and intravenous phosphorous repletion. Symptoms then resolved and the patient was discharged on an oral regimen. This phenomenon is postulated to occur due to an increase in the level and activity of FGF23 and decreased cleavage of the same, due to anemia as well as use of specific iron formulations. This is the first instance, in our literature review, of this complication known to occur, not after initial exposure to an implicated iron formulation but occurring on subsequent exposure.
format Article
id doaj-art-ad140af8b3ea4694a5de6d8bc695db44
institution OA Journals
issn 2090-651X
language English
publishDate 2022-01-01
publisher Wiley
record_format Article
series Case Reports in Endocrinology
spelling doaj-art-ad140af8b3ea4694a5de6d8bc695db442025-08-20T02:20:36ZengWileyCase Reports in Endocrinology2090-651X2022-01-01202210.1155/2022/1011401Severe Hypophosphatemia Occurring After Repeated Exposure to a Parenteral Iron FormulationKeerthana Haridas0Alice Yau1Internal Medicine Icahn School of MedicineEndocrinology Icahn School of MedicineHypophosphatemia is a less known complication of parenteral iron use, particularly after the use of certain iron formulations. We report the case of a young male with inflammatory bowel disease and iron deficiency anemia, who developed severe symptomatic hypophosphatemia after his third exposure to iron carboxymaltose with no evidence of the same occurring upon prior exposures to the compound. Investigations revealed serum phosphorous levels of 0.7 mg/dl, corrected serum calcium of 8–9.5 mg/dl, alkaline phosphatase of 50 U/L (38–126), 25 hydroxy vitamin D level of 40.2 ng/ml, and intact PTH elevated to 207 pg/ml. Urine studies indicated renal phosphate wasting. Presentation was not in keeping with refeeding syndrome. Intact fibroblast growth factor 23 level, measured after the initiation of treatment was within the normal range at 179 RU/mL (44–215). 1,25 dihydroxy vitamin D level, also measured after the initiation of treatment, was normal at 26.3 pg/ml (19.9–79.3). The patient was treated with calcitriol and aggressive oral and intravenous phosphorous repletion. Symptoms then resolved and the patient was discharged on an oral regimen. This phenomenon is postulated to occur due to an increase in the level and activity of FGF23 and decreased cleavage of the same, due to anemia as well as use of specific iron formulations. This is the first instance, in our literature review, of this complication known to occur, not after initial exposure to an implicated iron formulation but occurring on subsequent exposure.http://dx.doi.org/10.1155/2022/1011401
spellingShingle Keerthana Haridas
Alice Yau
Severe Hypophosphatemia Occurring After Repeated Exposure to a Parenteral Iron Formulation
Case Reports in Endocrinology
title Severe Hypophosphatemia Occurring After Repeated Exposure to a Parenteral Iron Formulation
title_full Severe Hypophosphatemia Occurring After Repeated Exposure to a Parenteral Iron Formulation
title_fullStr Severe Hypophosphatemia Occurring After Repeated Exposure to a Parenteral Iron Formulation
title_full_unstemmed Severe Hypophosphatemia Occurring After Repeated Exposure to a Parenteral Iron Formulation
title_short Severe Hypophosphatemia Occurring After Repeated Exposure to a Parenteral Iron Formulation
title_sort severe hypophosphatemia occurring after repeated exposure to a parenteral iron formulation
url http://dx.doi.org/10.1155/2022/1011401
work_keys_str_mv AT keerthanaharidas severehypophosphatemiaoccurringafterrepeatedexposuretoaparenteralironformulation
AT aliceyau severehypophosphatemiaoccurringafterrepeatedexposuretoaparenteralironformulation