[Skip to Content]
[Skip to Content Landing]
Article
October 11, 1976

Thiazide-Induced Immune Hemolytic Anemia

Author Affiliations

From the Division of Hematology (Drs Vila and Dosik) and the Department of Medicine (Dr Blum), Jewish Hospital and Medical Center of Brooklyn; and the departments of microbiology and immunology (Dr Blum) and medicine (Dr Dosik), State University of New York, Downstate Medical Center, Brooklyn, NY.

JAMA. 1976;236(15):1723-1724. doi:10.1001/jama.1976.03270160045029
Abstract

SINCE the first report of drug-induced hemolytic anemia produced by stibophen,1 the list has been expanded to include 16 other drugs and chemical compounds.2

This group of hemolytic anemias has been classified as "immune" because to become antigenic the drug must combine with a macromolecule in the serum, thus forming a drug-antidrug complex.3 This complex attaches to the red blood cell (RBC) membrane by an unknown mechanism and leads to RBC destruction either by activation of complement or by binding of active C3 to the RBC surface, with subsequent recognition by the macrophages and destruction in the reticuloendothelial system.4

Several drugs have been reported to produce hemolysis without binding complement.5-7 In these cases, RBC destruction is probably due to coating of RBCs by immunoglobulins.

In the present case, an oral antihypertensive drug that is a combination of methyldopa and hydrochlorothiazide (Aldoril) produced immune hemolytic anemia

×