Cefazolin-induced hemolytic anemia: a case report and systematic review of literature

Elizabeth Mause1, Mohammad Selim2, Manasa Velagapudi3

  • 1Creighton University School of Medicine, Omaha, NE, USA. eam19739@creighton.edu.

Abstract

Insights

Cefazolin-induced hemolytic anemia (CIHA) is rare but requires prompt recognition. Early diagnosis and cefazolin discontinuation are crucial, especially with long-term use, to manage this drug-induced anemia.

Area of Science:

  • Pharmacology
  • Hematology
  • Immunology

Background:

  • Cefazolin, a first-generation cephalosporin, is widely used for infections and surgical prophylaxis.
  • Cephalosporins can induce hemolytic anemia, typically autoimmune, with cefazolin being a less common cause.
  • Methicillin-sensitive Staphylococcus aureus (MSSA) infections are a common indication for cefazolin therapy.

Observation:

  • A rare case of cefazolin-induced hemolytic anemia (CIHA) and eosinophilia occurred in an elderly female with MSSA endocarditis.
  • Hemoglobin levels improved and eosinophilia resolved after switching from intravenous cefazolin to vancomycin.
  • Analysis of five case reports focused on direct antiglobulin test (DAT) results, penicillin sensitivity, and exclusion of other anemia causes.

Findings:

  • Cefazolin-induced hemolytic anemia (CIHA) is a rare but clinically significant condition.
  • Diagnosis of drug-induced anemia is achieved through exclusion.
  • Direct antiglobulin test (DAT) results and prior penicillin sensitivity are important considerations in diagnosing CIHA.

Implications:

  • Prompt recognition and cefazolin discontinuation are vital for managing CIHA, particularly in long-term treatment scenarios.
  • Clinicians should consider CIHA in patients developing anemia during cefazolin therapy.
  • Understanding the diagnostic factors, including DAT and penicillin sensitivity, aids in identifying cefazolin-induced anemia.