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Osteomalacia as a Complication of Intravenous Iron Infusion: A Systematic Review of Case Reports

Randomized control trials (RCTs) have shown that certain intravenous iron preparations can induce high levels of fibroblast growth factor 23 (FGF‐23) and persistent hypophosphatemia. Repeated iron infusions may lead to prolonged hypophosphatemia and osteomalacia events not captured by RCTs. Several...

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Autores principales: Vilaca, Tatiane, Velmurugan, Nalini, Smith, Christopher, Abrahamsen, Bo, Eastell, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322686/
https://www.ncbi.nlm.nih.gov/pubmed/35426179
http://dx.doi.org/10.1002/jbmr.4558
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author Vilaca, Tatiane
Velmurugan, Nalini
Smith, Christopher
Abrahamsen, Bo
Eastell, Richard
author_facet Vilaca, Tatiane
Velmurugan, Nalini
Smith, Christopher
Abrahamsen, Bo
Eastell, Richard
author_sort Vilaca, Tatiane
collection PubMed
description Randomized control trials (RCTs) have shown that certain intravenous iron preparations can induce high levels of fibroblast growth factor 23 (FGF‐23) and persistent hypophosphatemia. Repeated iron infusions may lead to prolonged hypophosphatemia and osteomalacia events not captured by RCTs. Several previous case reports have described skeletal adverse effects after repeated iron infusions. To characterize these effects, we conducted a systematic review of case reports. MEDLINE, Embase, Web of Science, and Cochrane databases were searched in March 2021. We selected case reports of patients ≥16 years old. Study quality was assessed using the tool from Murad and colleagues. We report the results in a narrative summary. We identified 28 case reports, reporting 30 cases. Ages ranged from 28 to 80 years (median 50 years). Most patients (n = 18) received ferric carboxymaltose (FCM), whereas 8 received saccharated ferric oxide (SFO) and 3 received iron polymaltose (IPM). All but 2 cases had more than five infusions (range 2 to 198, median 17). The lowest phosphate levels ranged from 0.16 to 0.77 mmol/L (median 0.36 mmol/L). Intact FGF‐23 (iFGF‐23) was high when measured. Serum 25OH vitamin D was low in 10 of 21 cases measured and 1,25(OH)(2) vitamin D in 12 of 18. Alkaline phosphatase was high in 18 of 22 cases. Bone or muscle pain was reported in 28 of the 30 cases. Twenty patients had pseudofractures, 9 had fractures, and 6 patients had both. All 15 available bone scans showed focal isotope uptake. Case reports tend to report severe cases, so potential reporting bias should be considered. Osteomalacia is a potential complication of repeated iron infusion, especially in patients with gastrointestinal disorders receiving prolonged therapy. Pain and fractures or pseudofractures are common clinical findings, associated with low phosphate, high iFGF‐23, high alkaline phosphatase, and abnormal isotope bone scan. Discontinuing or switching the iron formulation was an effective intervention in most cases. © 2022 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).
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spelling pubmed-93226862022-07-30 Osteomalacia as a Complication of Intravenous Iron Infusion: A Systematic Review of Case Reports Vilaca, Tatiane Velmurugan, Nalini Smith, Christopher Abrahamsen, Bo Eastell, Richard J Bone Miner Res Original Articles Randomized control trials (RCTs) have shown that certain intravenous iron preparations can induce high levels of fibroblast growth factor 23 (FGF‐23) and persistent hypophosphatemia. Repeated iron infusions may lead to prolonged hypophosphatemia and osteomalacia events not captured by RCTs. Several previous case reports have described skeletal adverse effects after repeated iron infusions. To characterize these effects, we conducted a systematic review of case reports. MEDLINE, Embase, Web of Science, and Cochrane databases were searched in March 2021. We selected case reports of patients ≥16 years old. Study quality was assessed using the tool from Murad and colleagues. We report the results in a narrative summary. We identified 28 case reports, reporting 30 cases. Ages ranged from 28 to 80 years (median 50 years). Most patients (n = 18) received ferric carboxymaltose (FCM), whereas 8 received saccharated ferric oxide (SFO) and 3 received iron polymaltose (IPM). All but 2 cases had more than five infusions (range 2 to 198, median 17). The lowest phosphate levels ranged from 0.16 to 0.77 mmol/L (median 0.36 mmol/L). Intact FGF‐23 (iFGF‐23) was high when measured. Serum 25OH vitamin D was low in 10 of 21 cases measured and 1,25(OH)(2) vitamin D in 12 of 18. Alkaline phosphatase was high in 18 of 22 cases. Bone or muscle pain was reported in 28 of the 30 cases. Twenty patients had pseudofractures, 9 had fractures, and 6 patients had both. All 15 available bone scans showed focal isotope uptake. Case reports tend to report severe cases, so potential reporting bias should be considered. Osteomalacia is a potential complication of repeated iron infusion, especially in patients with gastrointestinal disorders receiving prolonged therapy. Pain and fractures or pseudofractures are common clinical findings, associated with low phosphate, high iFGF‐23, high alkaline phosphatase, and abnormal isotope bone scan. Discontinuing or switching the iron formulation was an effective intervention in most cases. © 2022 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR). John Wiley & Sons, Inc. 2022-05-07 2022-06 /pmc/articles/PMC9322686/ /pubmed/35426179 http://dx.doi.org/10.1002/jbmr.4558 Text en © 2022 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR). https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Vilaca, Tatiane
Velmurugan, Nalini
Smith, Christopher
Abrahamsen, Bo
Eastell, Richard
Osteomalacia as a Complication of Intravenous Iron Infusion: A Systematic Review of Case Reports
title Osteomalacia as a Complication of Intravenous Iron Infusion: A Systematic Review of Case Reports
title_full Osteomalacia as a Complication of Intravenous Iron Infusion: A Systematic Review of Case Reports
title_fullStr Osteomalacia as a Complication of Intravenous Iron Infusion: A Systematic Review of Case Reports
title_full_unstemmed Osteomalacia as a Complication of Intravenous Iron Infusion: A Systematic Review of Case Reports
title_short Osteomalacia as a Complication of Intravenous Iron Infusion: A Systematic Review of Case Reports
title_sort osteomalacia as a complication of intravenous iron infusion: a systematic review of case reports
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322686/
https://www.ncbi.nlm.nih.gov/pubmed/35426179
http://dx.doi.org/10.1002/jbmr.4558
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