How do I test stools for iron?

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Last updated: December 16, 2025View editorial policy

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Testing Stools for Iron

You should NOT test stools for iron content directly—instead, use fecal occult blood testing (FOBT) to detect gastrointestinal bleeding as the cause of iron deficiency. The purpose is to identify blood loss, not to measure iron itself in the stool.

Primary Testing Method

A stool guaiac test for occult blood is the recommended approach when investigating iron deficiency to detect gastrointestinal bleeding 1. This test detects the presence of blood in stool, which indicates potential GI blood loss causing iron depletion.

Available Testing Options

  • Guaiac-based FOBT (gFOBT): Traditional chemical test that detects peroxidase activity of hemoglobin 1
  • Fecal Immunochemical Test (FIT): More specific test that detects human hemoglobin directly 1

Critical Limitations and Caveats

When NOT to Use FOBT

FIT should NOT be used in patients with iron deficiency anemia for diagnostic purposes 1. The sensitivity is only 58% (95% CI 0.53-0.63) with specificity of 84% (95% CI 0.75-0.89), meaning 42% of patients with identifiable causes of iron deficiency anemia will have false-negative results 2.

FOBT should be avoided during acute diarrhea episodes, as sensitivities range from only 38% to 87% with variable specificity 1.

Effect of Oral Iron Supplementation

There is contradictory evidence regarding whether oral iron causes false-positive results:

  • Older data (1982): Ferrous sulfate and ferrous gluconate caused 50-65% false-positive Hemoccult reactions and 25-65% false-positive Hematest reactions 3, 4
  • More recent data (1990): A controlled study found oral iron supplementation (ferrous sulfate or ferrous gluconate) did NOT cause false-positive results with Hemoccult II or Hemoccult Sensa methods 5

In clinical practice, the more recent controlled study suggests oral iron does not interfere with modern Hemoccult testing 5.

Proper Clinical Approach to Iron Deficiency

Instead of Relying on Stool Testing

Bidirectional endoscopy (gastroscopy and colonoscopy) should be performed as first-line investigation in adults with newly diagnosed iron deficiency anemia 6. This is far superior to FOBT for identifying bleeding sources:

  • Gastroscopy reveals a cause in 30-50% of patients 6
  • Colonoscopy should be performed even if upper endoscopy finds a lesion, as dual pathology occurs in 10-15% of patients 6
  • FOBT has poor sensitivity (54%) for non-colorectal cancer lesions that commonly cause iron deficiency 2

Complementary Testing

  • Coeliac disease screening should be performed serologically (tissue transglutaminase antibody with IgA level), as it's found in 3-5% of iron deficiency anemia cases 6
  • Urinalysis should be performed to exclude urinary tract bleeding 6
  • H. pylori testing should be considered after negative bidirectional endoscopy 1

Key Clinical Pitfall

Do not use a positive or negative FOBT result to guide decisions about whether to pursue endoscopic evaluation in iron deficiency anemia 2. The test performance is inadequate for this purpose, and endoscopy should be pursued based on clinical criteria, not FOBT results 1.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Reliability of chemical tests for fecal occult blood in hospitalized patients.

The American journal of digestive diseases, 1976

Guideline

Diagnostic Approach to Iron Deficiency Anemia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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