2020 · AGA · Iron-deficiency anemia (GI evaluation)

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Summary

AGA 2020 guideline on the gastrointestinal evaluation of iron deficiency anemia (IDA), developed using GRADE. Covers ferritin cutoff for diagnosis, endoscopic evaluation strategy by sex/menopausal status, and workup for H. pylori, celiac disease, atrophic gastritis, and small-bowel sources after negative bidirectional endoscopy. Does not address refractory/recurrent IDA, obscure GI bleeding, or iron replacement regimens.

Key Recommendations

  • Use ferritin cutoff of 45 ng/mL (not 15 ng/mL) to diagnose iron deficiency in patients with anemia (strong, high quality).
  • In patients with chronic inflammation or CKD, add CRP, transferrin saturation, or soluble transferrin receptor to ferritin to diagnose iron deficiency.
  • Perform bidirectional endoscopy (EGD + colonoscopy) in asymptomatic postmenopausal women and men with IDA, done at the same setting (strong, moderate quality).
  • Suggest bidirectional endoscopy over iron replacement alone in asymptomatic premenopausal women with IDA, with shared decision-making given low malignancy yield (conditional, moderate quality).
  • After negative bidirectional endoscopy without an identified etiology, perform noninvasive H. pylori testing (stool antigen, urea breath, or serology) and treat if positive (conditional, low quality).
  • Do not perform routine gastric biopsies to diagnose autoimmune atrophic gastritis in IDA patients (conditional, very low quality).
  • In asymptomatic adults with IDA and plausible celiac disease, obtain celiac serology first and pursue small-bowel biopsy only if positive, rather than routine duodenal biopsy (conditional, very low quality).
  • Consider routine duodenal biopsies if celiac prevalence in the population is >5%, if duodenum appears abnormal endoscopically, or in higher-risk patients (family history, type 1 DM, symptoms).
  • In uncomplicated asymptomatic IDA with negative bidirectional endoscopy, trial iron supplementation rather than routine video capsule endoscopy (conditional, very low quality).
  • Start oral iron as initial therapy in most patients; reserve IV iron for malabsorption, prior gastric surgery, IBD, CKD, or blood loss exceeding oral repletion capacity.
  • Reassess for nonadherence, malabsorption, ongoing blood loss, or missed celiac disease if hemoglobin does not improve within ~1 month of oral iron.

Thresholds & Doses

  • Ferritin <45 ng/mL: diagnostic threshold for iron deficiency in anemic patients (preferred over <15 ng/mL).
  • Anemia definition: hemoglobin <13 g/dL in men, <12 g/dL in nonpregnant women.
  • Diagnostic yield in postmenopausal women/men with IDA: lower GI malignancy 8.9% (95% CI 8.3–9.5%), upper GI malignancy 2.0% (95% CI 1.7–2.3%).
  • Diagnostic yield in premenopausal women with IDA: lower GI malignancy 0.9% (95% CI 0.3–1.9%), upper GI malignancy 0.2% (95% CI 0–0.9%).
  • Celiac disease prevalence threshold favoring routine duodenal biopsy over serology-first: >5%.
  • Historical oral iron dose: 150–200 mg elemental iron daily; lower or alternate-day dosing may improve tolerability/absorption.
  • Expected hemoglobin response to oral iron: within ~1 month.

Citations

  • Table 3 (Executive Summary of Recommendations) — all 7 recommendations and strength/quality grades.
  • Recommendation 1 (ferritin cutoff) — 45 ng/mL over 15 ng/mL, strong/high quality.
  • Recommendation 2 (bidirectional endoscopy in postmenopausal women and men) — strong/moderate quality, with pooled malignancy yields.
  • Recommendation 3 (premenopausal women) — conditional recommendation for bidirectional endoscopy with shared decision-making.
  • Recommendations 4–5 (H. pylori testing and against routine gastric biopsies for atrophic gastritis) — post-endoscopy workup.
  • Recommendation 6 (celiac serology first vs routine small-bowel biopsy) — including >5% prevalence caveat.
  • Recommendation 7 (iron trial over video capsule endoscopy after negative bidirectional endoscopy).
  • Section ‘How should iron supplementation be managed?’ — oral vs IV iron, dosing, response timing.