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Case report: hemolytic anemia produced by tolmetin
Immunohematology
|March 1, 1992
Summary
Tolmetin, a nonsteroidal anti-inflammatory drug, caused acute hemolytic anemia in a patient through an immune complex mechanism. The drug-induced hemolytic anemia resolved spontaneously after tolmetin discontinuation.
Area of Science:
- Pharmacology
- Hematology
- Immunology
Background:
- Nonsteroidal anti-inflammatory drugs (NSAIDs) can rarely cause adverse hematologic reactions.
- Drug-induced hemolytic anemia (DIHA) is a serious condition requiring prompt diagnosis and management.
Purpose of the Study:
- To identify the etiologic agent in a case of drug-induced hemolytic anemia.
- To elucidate the immunoserologic mechanism of tolmetin-induced hemolysis.
Main Methods:
- Case report of a 35-year-old female presenting with acute hemolysis after tolmetin ingestion.
- Laboratory investigations including complete blood count, liver function tests, reticulocyte count, and direct antiglobulin test (DAT).
- In vitro testing of patient's serum with tolmetin and reagent red blood cells.
Main Results:
- The patient developed severe anemia (hemoglobin 7.0 g/dL) with signs of hemolysis.
- Direct antiglobulin test was weakly positive for IgG and complement.
- Patient's serum demonstrated tolmetin-dependent agglutination of red blood cells, indicating an immune complex mechanism.
Conclusions:
- Tolmetin was identified as the causative agent of drug-induced hemolytic anemia in this patient.
- The mechanism of hemolysis involved the formation of immune complexes with tolmetin.
- Spontaneous resolution of hemolysis and anemia occurred upon cessation of tolmetin.