Serology of antibodies to second- and third-generation cephalosporins associated with immune hemolytic anemia and/or positive direct antiglobulin tests

BACKGROUND: First‐generation cephalosporins rarely caused immune hemolytic anemia (IHA). Second‐ and third‐generation cephalosporins, especially cefotetan and ceftriaxone, are increasingly associated with severe, sometimes fatal IHA. STUDY DESIGN AND METHODS: Samples from 53 patients with drug‐induc...

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Published inTransfusion (Philadelphia, Pa.) Vol. 39; no. 11; pp. 1239 - 1246
Main Authors Arndt, P.A., Leger, R.M., Garratty, G.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Science Inc 01.11.1999
Blackwell Publishing
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Summary:BACKGROUND: First‐generation cephalosporins rarely caused immune hemolytic anemia (IHA). Second‐ and third‐generation cephalosporins, especially cefotetan and ceftriaxone, are increasingly associated with severe, sometimes fatal IHA. STUDY DESIGN AND METHODS: Samples from 53 patients with drug‐induced IHA and/or positive direct antiglobulin test (DAT) were tested. Patients' sera were tested against drug‐treated red cells (RBCs) and untreated or enzyme‐treated RBCs, with and without the addition of drug solution. Eluates from patients' RBCs were tested against drug‐treated and untreated RBCs. RESULTS: Forty‐three patients had antibodies to cefotetan, 8 to ceftriaxone, 1 to cefoxitin, and 1 to cefotaxime. All patients had a positive DAT; only anti‐cefoxitin and anti‐cefotetan were demonstrable in RBC eluates. Sera containing anti‐cefoxitin, anti‐cefotaxime, and anti‐cefotetan reacted with drug‐treated RBCs (100%) and untreated or enzyme‐treated RBCs in the presence of drug (98% or 100%, respectively). All of the ceftriaxone antibodies reacted with untreated or enzyme‐treated RBCs in the presence of drug, but those tested did not react with ceftriaxone‐treated RBCs. In addition to cefotetan‐dependent antibodies, 19 (44%) and 14 (33%) of 43 sera contained drug‐independent antibodies when tested with and without the presence of a polyethylene glycol potentiator, respectively. CONCLUSION: Cefotetan is by far the most common cause of drug‐induced IHA. All cefotetan antibodies and the single examples of cefoxitin and cefotaxime antibodies reacted with drug‐coated RBCs, and most, in contrast to the reactions of antibodies to first‐generation cephalosporins (e.g., cephalothin), also reacted with RBCs (not treated with drug) in the presence of the drug. Ceftriaxone antibodies reacted only by the latter mechanism. Drug‐independent antibodies (i.e., those reacting without any drug being present) were detected in 33 to 44 percent of patients' sera containing cefotetan antibodies, depending on the sensitivity of the method used.
Bibliography:ark:/67375/WNG-K42Z62DW-7
ArticleID:TRF39111239
istex:33A2868AF4346D2EED18E9125F5E5978C98824CC
George Garratty, PhD, FRCPath, Scientific Director, American Red Cross Blood Services, 1130 South Vermont Avenue, Los Angeles, CA 90006; e‐mail
garratty@usa.redcross.org
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ISSN:0041-1132
1537-2995
DOI:10.1046/j.1537-2995.1999.39111239.x