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Published on: January 28, 2020
Does abciximab promote coronary artery remodeling in patients with Kawasaki disease?
Rachel T McCandless1, L Luann Minich, Lloyd Y Tani
1Division of Cardiology, Department of Pediatrics, Primary Children's Medical Center and the University of Utah, Salt Lake City, Utah, USA. rachel.mccandless@hsc.utah.edu
Insights
Standard therapy for Kawasaki disease reduces coronary artery aneurysms (CAAs), but large CAAs may persist. Abciximab, when added to standard therapy, showed greater long-term regression of large CAAs compared to standard therapy alone.
Area of Science:
- Cardiology
- Pediatric Rheumatology
- Vascular Biology
Background:
- Kawasaki disease (KD) is a leading cause of acquired pediatric heart disease.
- Standard therapy (intravenous immunoglobulin and aspirin) reduces but does not eliminate coronary artery aneurysms (CAAs).
- Large CAAs can persist, posing long-term cardiovascular risks.
Purpose of the Study:
- To evaluate the long-term efficacy of abciximab in promoting regression of large CAAs in KD patients.
- To compare the vascular remodeling effects of abciximab plus standard therapy versus standard therapy alone in large CAAs.
Main Methods:
- Retrospective cohort study of KD patients with large CAAs (diameter >5 mm or Z score >10) treated between 1986 and 2007.
- Patients were divided into two groups: abciximab plus standard therapy (n=11) and standard therapy alone (n=7).
- Coronary artery aneurysm Z scores were assessed via echocardiography at baseline, 1 year, and 3-5 years post-treatment.
Main Results:
- Baseline characteristics including age, treatment interval, gender, and initial CAA Z scores were similar between groups.
- No significant difference in CAA Z score change was observed between groups at 1-year follow-up.
- At 3-5 years, the abciximab group demonstrated a significantly greater decrease in CAA Z score compared to the no-abciximab group (p=0.04).
Conclusions:
- Abciximab treatment, in addition to standard therapy, may promote significant long-term vascular remodeling and regression of large coronary artery aneurysms in Kawasaki disease patients.
- These findings suggest a potential role for abciximab in managing persistent large CAAs, warranting further investigation.
Abstract:
Standard therapy, consisting of intravenous immunoglobulin and aspirin, reduces, but does not eliminate, coronary artery aneurysms (CAAs) in patients with Kawasaki disease. Large CAAs can persist or undergo varying degrees of regression. The treatment of large CAAs using abciximab has been associated with short-term regression; however, longer term data are unavailable. We sought to obtain longer term follow-up data regarding the changes in the diameters of large CAAs in patients receiving both abciximab and standard therapy and to compare these changes to those of a similar group receiving standard therapy alone. All patients with Kawasaki disease and large CAAs (diameter >5 mm or Z score >10) treated from 1986 to 2007 were identified and divided into 2 groups. The abciximab group received abciximab plus standard therapy and the no-abciximab group received standard therapy alone. The maximum diameters of the proximal right and left anterior descending CAAs were obtained from echocardiograms. The Z scores were calculated for 3 points: the acute/subacute phase (<8 weeks) and at 1 and 3 to 5 years of follow-up. The patients in the abciximab (n = 11) and no-abciximab (n = 7) groups were similar in age, interval to treatment, gender, and largest CAA Z score at diagnosis (19.6 +/- 6.2 vs 25.8 +/- 9.5, p = 0.11). The change in CAA Z score was similar between the 2 groups at 1 year (p = 0.99). At 3 to 5 years of follow-up, compared to baseline, the abciximab group had a greater decrease in the CAA Z score than did the no-abciximab group (-14.0 +/- 4.0 vs -8.2 +/- 5.9, p = 0.04). In conclusion, abciximab treatment might be associated with vascular remodeling in patients with large CAAs.
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