Evidence map›Paper›PMID 41938297›Full record

ArticleAACE endocrinology and diabetes

Two Cases of Iron-Induced Hypophosphatemia.

Sarah Haroon, Robert D Blank, Joseph L Shaker, Denise A Teves Qualler

Abstract readCase Reports
In one paragraph

Article in AACE endocrinology and diabetes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Sarah HaroonDivision of Endocrinology and Mineral Metabolism, University of Texas Southwestern Medical Center, Dallas, Texas.
Robert D BlankDepartment of Bone Biology, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
Joseph L ShakerDivision of Endocrinology and Molecular Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Denise A Teves QuallerDivision of Endocrinology and Molecular Medicine, Medical College of Wisconsin and Zablocki VA Medical Center, Milwaukee, Wisconsin.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Objective: Present 2 cases of severe hypophosphatemia related to ferric carboxymaltose infusions with a brief overview of the pathophysiology and factors that predispose certain patients to this phenomenon. Case Report: A 46-year-old male with history of hereditary hemorrhagic telangiectasias presented with severe progressive bilateral foot and leg pain as well as insufficiency fractures after initiating on ferric carboxymaltose infusions. Biochemical evaluation demonstrated severe hypophosphatemia and renal phosphate wasting. Discontinuation of further iron infusions led to resolution of symptoms and improvement in phosphate levels.Similarly, a 61-year-old male with history of Crohn disease and prior bowel resections was identified to have consistent hypophosphatemia after ferric carboxymaltose infusions. Discussion: Hypophosphatemic disorders due to renal phosphate wasting present a diagnostic challenge and morbidity to patients further exacerbated by delays in diagnosis and treatment. Intravenous iron infusions are commonly used to treat a variety of medical conditions. These treatments, especially ferric carboxymaltose, can cause severe FGF23 mediated renal phosphate wasting and osteomalacia. Conclusion: It is crucial for clinicians to recognize FGF23 mediated renal phosphate wasting in the setting of intravenous iron infusions. Patients with gastrointestinal malabsorption and secondary hyperparathyroidism can have sustained hypophosphatemia as a result of ferric carboxymaltose infusions.

Indexed as

FGF23hypophosphatemiaintravenous ironosteomalacia

Identifiers

PMID41938297
PMCPMC13043461

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.