Abciximab, on Fab monoclonal antibody fragment that blocks the platelet gly
coprotein IIb/IIIa receptor, is increasingly used as an adjunct to coronary
intervention. Little is known, however, about the efficacy and safely of r
eadministration of abciximab. This study examined and characterized outcome
s of patients receiving abciximab for a second time. From April 1995 to Jun
e 1997, 164 consecutive patients were readministered abciximab at our 3 ins
titutions. We retrospectively examined and analyzed in-hospital outcomes in
this cohort. The median time to readministration was 95 days. The angiogra
phic success rate of percutaneous intervention was 99.5%. Rates and 95% con
fidence intervals of in-hospital events were death 2% (0.7% to 6.1%), myoca
rdial infarction 3% (1% to 7%), coronary bypass surgery 0% (0% to 2.2%), an
d intracranial hemorrhage 2% (0.4% to 5.3%). Severe thrombocytopenia was ob
served in 4% of patients (1.4% to 7.8%) after readministration. Allergic or
anaphylactic reactions were not observed. Major bleeding was associated wi
th excessive concomitant antithrombotic therapy. patients undergoing readmi
nistration of abciximab within 2 weeks of first administration experienced
a higher incidence of severe thrombocytopenia (12% vs 2%, p = 0.046). Thus,
abciximab remains clinically efficacious when readministered as an adjunct
to percutaneous coronary intervention. However, concomitant heparin admini
stration must be carefully monitored and warfarin therapy should be avoided
. Vigilant surveillance for thrombocytopenia should be employed. Reduced do
sing may be necessary when abciximab is readministered within days of the i
nitial administration. (C) 2000 by Excerpta Medica, Inc.