What does the medical acronym HI stand for?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: January 12, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

What Does the Medical Acronym HI Stand For?

In the context of myelodysplastic syndromes (MDS) and hematologic disorders, HI stands for "Hematologic Improvement," which refers to measurable improvements in blood cell counts (erythroid, platelet, or neutrophil lineages) that persist for at least 2 months. 1

However, in a completely different medical context, HI also stands for "Hyperinsulinism" (or Congenital Hyperinsulinism), a disorder of inappropriate insulin secretion causing hypoglycemia. 2, 3, 4

Context Matters: Two Distinct Meanings

HI as Hematologic Improvement (MDS Context)

The International Working Group defines HI as a response criterion specifically for evaluating treatments in myelodysplastic syndromes that improve cytopenias without necessarily modifying disease course. 1

HI is categorized by affected cell lineage:

  • HI-E (Erythroid response): Major response requires hemoglobin increase >2 g/dL for patients with baseline <11 g/dL, or achieving transfusion independence in transfusion-dependent patients 1, 5

  • HI-P (Platelet response): Major response requires absolute platelet increase ≥30,000/mm³ for patients with baseline <100,000/mm³, or achieving platelet transfusion independence 1, 5

  • HI-N (Neutrophil response): Major response requires at least 100% increase in absolute neutrophil count (ANC) or absolute increase >500/mm³ (whichever is greater) for patients with baseline ANC <1500/mm³ 1, 5

All improvements must be sustained for at least 2 months in the absence of ongoing cytotoxic therapy and confirmed on at least 2 successive determinations at least 1 week apart. 1, 5

The ESMO guidelines clarify that HI responses are particularly adapted to treatments like growth factors that improve cytopenias but have no obvious effect on disease course, distinguishing them from complete remission (CR) or partial remission (PR). 1

HI as Hyperinsulinism (Endocrine Context)

In pediatric endocrinology, HI refers to congenital hyperinsulinism, a disorder of inappropriate insulin secretion by pancreatic β-cells causing recurrent hypoglycemia, with incidence of 1/50,000 live births (or 1/2,500 in consanguineous populations). 2, 3

This condition presents with:

  • Recurrent hypoglycemic episodes requiring high glucose administration rates to maintain normoglycemia 3, 4
  • Responsiveness to exogenous glucagon 3
  • Risk of irreversible brain damage if untreated 2, 3, 6

The most severe forms are caused by recessive ABCC8 or KCNJ11 mutations affecting pancreatic potassium channels and are typically diazoxide-unresponsive. 2, 3, 4

Clinical Pitfall to Avoid

When encountering "HI" in medical documentation, always verify the clinical context—hematology/oncology versus endocrinology—as the meanings are completely unrelated and management implications are entirely different. The acronym appears in completely different specialties with no overlap in meaning or treatment approach.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Congenital hyperinsulinism: current trends in diagnosis and therapy.

Orphanet journal of rare diseases, 2011

Research

Congenital hyperinsulinism.

Early human development, 2010

Research

Hyperinsulinism of the newborn.

Seminars in perinatology, 2000

Guideline

Response Criteria for Megaloblastic 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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.