S4838 Iron Tablet Gastropathy: When Iron Supplementation for GI Bleeding Leads to More GI Bleeding

Introduction: Iron deficiency anemia is the most common cause of anemia, and its supplementation is typically done via oral tablets. Exposure of iron to the GI tract can produce many side effects, including stomach upset, pyrosis, and constipation, along with darker stools. Pill-induced gastropathy is another adverse symptom of iron exposure, but not well described at therapeutic iron levels. Medication-associated inflammatory changes occur in about 0.7% of patients and are due to the oxidative stress of iron. Even less described is severe iron tablet gastropathy leading to bleeding unable to be managed via endoscopic methods, eventually requiring partial gastrectomy. Case Description/Methods: A 67-year-old woman with a history of CLL on darbepoetin alfa and iron deficiency anemia, presented to the emergency department for evaluation of hematemesis and melena. She reported multiple bouts of melenic stools over the previous 24 hours, beginning after an episode of hematemesis. She denied recent alcohol, nonsteroidal anti-inflammatory drug, aspirin, or anticoagulant use. She reported the use of tirzepatide and daily iron tablets. She was hemodynamically stable and saturated well on room air. Examination was remarkable for conjunctival pallor and melena on digital rectal exam. Labwork was notable for chronic leukocytosis to 23.9 K/mcL, hemoglobin 6.8 g/dL (baseline 8.0), and acute kidney injury. She was transfused blood and given intravenous pantoprazole. Endoscopy noted a large gastric antral mass to which hemostatic spray was applied. Biopsy revealed foveolar hyperplasia, likely related to iron tablet use. Despite intervention, her hemoglobin continued to decline, requiring further transfusion. General surgery took the patient for anterior gastrotomy, resulting in partial gastrectomy with antral mass removal and surrounding serosal repair. Counts stabilized, and she was discharged on intravenous iron infusions. Discussion: Iron tablet-induced gastropathy is a relatively underdiagnosed phenomenon that is the result of oxidative stress to the mucosal lining of the stomach. In our patient, chronic iron supplementation produced a milieu of inflammation that led to gastric mass formation. Her concurrent use of a dual glucagon-like peptide-1 and glucose-dependent insulinotropic polypeptide agonist potentiated this, leading to slower gut transit and extended iron tablet exposure to the stomach, likely worsening the degree of inflammation. Given the prevalence of iron deficiency anemia and use of oral iron supplementation, the generalist and gastroenterologist should be familiar with this risk.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001146812.82541.9e
Primary Topic
Potassium and Related Disorders
Type
article
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article

S4838 Iron Tablet Gastropathy: When Iron Supplementation for GI Bleeding Leads to More GI Bleeding

Nahren Asado, Eli D. Ehrenpreis, Jennifer Kang, Yannis S. Lafazanos et al.
The American Journal of Gastroenterology
Potassium and Related Disorders
article

S4838 Iron Tablet Gastropathy: When Iron Supplementation for GI Bleeding Leads to More GI Bleeding

Nahren Asado, Eli D. Ehrenpreis, Jennifer Kang, Yannis S. Lafazanos, Robin David
article en

Abstract

Introduction: Iron deficiency anemia is the most common cause of anemia, and its supplementation is typically done via oral tablets. Exposure of iron to the GI tract can produce many side effects, including stomach upset, pyrosis, and constipation, along with darker stools. Pill-induced gastropathy is another adverse symptom of iron exposure, but not well described at therapeutic iron levels. Medication-associated inflammatory changes occur in about 0.7% of patients and are due to the oxidative stress of iron. Even less described is severe iron tablet gastropathy leading to bleeding unable to be managed via endoscopic methods, eventually requiring partial gastrectomy. Case Description/Methods: A 67-year-old woman with a history of CLL on darbepoetin alfa and iron deficiency anemia, presented to the emergency department for evaluation of hematemesis and melena. She reported multiple bouts of melenic stools over the previous 24 hours, beginning after an episode of hematemesis. She denied recent alcohol, nonsteroidal anti-inflammatory drug, aspirin, or anticoagulant use. She reported the use of tirzepatide and daily iron tablets. She was hemodynamically stable and saturated well on room air. Examination was remarkable for conjunctival pallor and melena on digital rectal exam. Labwork was notable for chronic leukocytosis to 23.9 K/mcL, hemoglobin 6.8 g/dL (baseline 8.0), and acute kidney injury. She was transfused blood and given intravenous pantoprazole. Endoscopy noted a large gastric antral mass to which hemostatic spray was applied. Biopsy revealed foveolar hyperplasia, likely related to iron tablet use. Despite intervention, her hemoglobin continued to decline, requiring further transfusion. General surgery took the patient for anterior gastrotomy, resulting in partial gastrectomy with antral mass removal and surrounding serosal repair. Counts stabilized, and she was discharged on intravenous iron infusions. Discussion: Iron tablet-induced gastropathy is a relatively underdiagnosed phenomenon that is the result of oxidative stress to the mucosal lining of the stomach. In our patient, chronic iron supplementation produced a milieu of inflammation that led to gastric mass formation. Her concurrent use of a dual glucagon-like peptide-1 and glucose-dependent insulinotropic polypeptide agonist potentiated this, leading to slower gut transit and extended iron tablet exposure to the stomach, likely worsening the degree of inflammation. Given the prevalence of iron deficiency anemia and use of oral iron supplementation, the generalist and gastroenterologist should be familiar with this risk.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 42%
Potassium and Related Disorders
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