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Hemolytic anemia

Last reviewed: 21 Oct 2024
Last updated: 09 Nov 2022

Summary

Definition

History and exam

Key diagnostic factors

  • pallor
  • jaundice
Full details

Other diagnostic factors

  • fatigue
  • shortness of breath
  • dizziness
  • splenomegaly
  • active infections
  • episodic dark urine (hemoglobinuria)
  • triggered by exposure to cold
Full details

Risk factors

  • autoimmune disorders
  • lymphoproliferative disorders
  • prosthetic heart valve
  • family origin in Mediterranean, Middle East, Africa, or Southeast Asia
  • family history of hemoglobinopathy or red blood cell membrane defects
  • paroxysmal nocturnal hemoglobinuria
  • recent exposure to cephalosporins, penicillins, quinine derivatives, or nonsteroidal anti-inflammatory drugs
  • recent exposure to naphthalene or fava beans
  • thermal injury
  • exceptional exertion
  • recent exposure to nitrites, dapsone, ribavirin, or phenazopyridine
  • recent paraquat ingestion
  • malaria
  • babesiosis
  • bartonellosis
  • leishmaniasis
  • Clostridium perfringens infection
  • Haemophilus influenzae type B infection
  • liver disease
Full details

Diagnostic tests

1st tests to order

  • CBC
  • MCHC
  • reticulocyte count
  • peripheral smear
  • unconjugated (indirect) bilirubin
  • LDH
  • haptoglobin
  • urinalysis
Full details

Tests to consider

  • direct antiglobulin test (Coombs)
  • creatinine, BUN
  • LFTs
  • Donath-Landsteiner antibody
  • Hb electrophoresis
  • flow cytometry for CD55/CD59
  • glucose-6-phosphate dehydrogenase (G6PD) fluorescent spot test and spectrophotometry
  • antinuclear antibody
Full details

Treatment algorithm

ACUTE

acquired: direct antiglobulin test (Coombs) positive

acquired: direct antiglobulin test (Coombs) negative

inherited disorders

Contributors

Authors

John Densmore, MD, PhD

Associate Professor of Clinical Medicine

Department of Medicine

University of Virginia

Charlottesville

VA

Disclosures

JD declares that he has no competing interests.

Acknowledgements

Dr John Densmore would like to gratefully acknowledge Dr Michelle Loch, a previous contributor to this monograph. ML declares that she has no competing interests.

Peer reviewers

Pasquale Niscola, MD

Hematology Unit

Sant'Eugenio Hospital

Rome

Italy

Disclosures

PN declares that he has no competing interests.

Alan Lichtin, MD

Staff Hematologist-Oncologist

Hematologic Oncology and Blood Disorders

Cleveland Clinic

Associate Professor

Internal Medicine

Cleveland Clinic Lerner College of Medicine

Cleveland

OH

Disclosures

AL declares that he has no competing interests.

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  • Guidelines

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    • Recommendations regarding splenectomy in hereditary hemolytic anemias
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