Efficacy of immunoglobulin plus prednisolone for prevention of coronary artery abnormalities in severe Kawasaki disease (RAISE study): a randomised, open-label, blinded-endpoints trial
- PMID: 22405251
- DOI: 10.1016/S0140-6736(11)61930-2
Efficacy of immunoglobulin plus prednisolone for prevention of coronary artery abnormalities in severe Kawasaki disease (RAISE study): a randomised, open-label, blinded-endpoints trial
Abstract
Background: Evidence indicates that corticosteroid therapy might be beneficial for the primary treatment of severe Kawasaki disease. We assessed whether addition of prednisolone to intravenous immunoglobulin with aspirin would reduce the incidence of coronary artery abnormalities in patients with severe Kawasaki disease.
Methods: We did a multicentre, prospective, randomised, open-label, blinded-endpoints trial at 74 hospitals in Japan between Sept 29, 2008, and Dec 2, 2010. Patients with severe Kawasaki disease were randomly assigned by a minimisation method to receive either intravenous immunoglobulin (2 g/kg for 24 h and aspirin 30 mg/kg per day) or intravenous immunoglobulin plus prednisolone (the same intravenous immunoglobulin regimen as the intravenous immunoglobulin group plus prednisolone 2 mg/kg per day given over 15 days after concentrations of C-reactive protein normalised). Patients and treating physicians were unmasked to group allocation. The primary endpoint was incidence of coronary artery abnormalities during the study period. Analysis was by intention to treat. This trial is registered with the University Hospital Medical Information Network clinical trials registry, number UMIN000000940.
Findings: We randomly assigned 125 patients to the intravenous immunoglobulin plus prednisolone group and 123 to the intravenous immunoglobulin group. Incidence of coronary artery abnormalities was significantly lower in the intravenous immunoglobulin plus prednisolone group than in the intravenous immunoglobulin group during the study period (four patients [3%] vs 28 patients [23%]; risk difference 0·20, 95% CI 0·12-0·28, p<0·0001). Serious adverse events were similar between both groups: two patients had high total cholesterol and one neutropenia in the intravenous immunoglobulin plus prednisolone group, and one had high total cholesterol and another non-occlusive thrombus in the intravenous immunoglobulin group.
Interpretation: Addition of prednisolone to the standard regimen of intravenous immunoglobulin improves coronary artery outcomes in patients with severe Kawasaki disease in Japan. Further study of intensified primary treatment for this disease in a mixed ethnic population is warranted.
Funding: Japanese Ministry of Health, Labour and Welfare.
Copyright © 2012 Elsevier Ltd. All rights reserved.
Comment in
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Management of Kawasaki disease: corticosteroids revisited.Lancet. 2012 Apr 28;379(9826):1571-2. doi: 10.1016/S0140-6736(12)60196-2. Epub 2012 Mar 8. Lancet. 2012. PMID: 22405252 No abstract available.
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Vascular disease. Corticosteroid therapy improves outcomes for Japanese children with Kawasaki disease.Nat Rev Cardiol. 2012 Mar 27;9(5):255. doi: 10.1038/nrcardio.2012.43. Nat Rev Cardiol. 2012. PMID: 22450125 No abstract available.
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Adding prednisolone to standard immunoglobulin therapy is beneficial for patients with severe Kawasaki disease.J Pediatr. 2012 Nov;161(5):967. doi: 10.1016/j.jpeds.2012.08.049. J Pediatr. 2012. PMID: 23095696 No abstract available.
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Prednisolone added to intravenous immunoglobulin treatment improves outcome in children with severe Kawasaki disease.Arch Dis Child Educ Pract Ed. 2013 Apr;98(2):77-8. doi: 10.1136/archdischild-2012-303413. Arch Dis Child Educ Pract Ed. 2013. PMID: 23492399 No abstract available.
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Critical review of: Efficacy of immunoglobulin plus prednisone for prevention of coronary artery prednisolone for prevention of coronary abnormalities in severe Kawasaki disease (RAISE study): a randomized, open-label, blinded-endpoints trial.J Popul Ther Clin Pharmacol. 2013;20(2):e91-4. Epub 2013 Apr 22. J Popul Ther Clin Pharmacol. 2013. PMID: 23648367 No abstract available.
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