Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Feb 24;17(3):278.
doi: 10.3390/ijms17030278.

Critical Overview of the Risk Scoring Systems to Predict Non-Responsiveness to Intravenous Immunoglobulin in Kawasaki Syndrome

Affiliations
Review

Critical Overview of the Risk Scoring Systems to Predict Non-Responsiveness to Intravenous Immunoglobulin in Kawasaki Syndrome

Donato Rigante et al. Int J Mol Sci. .

Abstract

Kawasaki syndrome (KS) is the most relevant cause of heart disease in children living in developed countries. Intravenous immunoglobulin (IVIG) has a preventive function in the formation of coronary artery abnormalities and a poor strictly-curative action in established coronary damage. More than two decades ago, the Harada score was set to assess which children with KS should be subject to administration of IVIG, evaluating retrospectively a large cohort of patients with regard to age, sex and laboratory data. Nowadays, high dose IVIG is administered to all children with a confirmed diagnosis of KS, but a tool for predicting non-responsiveness to the initial infusion of IVIG has not been found. The prediction of IVIG resistance is a crucial issue, as recognising these high-risk patients should consent the administration of an intensified initial treatment in combination with IVIG in order to prevent coronary injuries. Few reports have focused on factors, referring to both clinical parameters and laboratory data at the onset of KS, in order to predict which patients might be IVIG non-responsive. We have analysed three different risk scores which were formulated to predict IVIG resistance in Japanese children with typical KS, but their application in non-Japanese patients or in those with incomplete and atypical patterns of the disease has been studied in a fragmentary way. Overall, our analysis showed that early and definite ascertainment of likely IVIG non-responders who require additional therapies reducing the development of coronary artery involvement in children with KS is still a challenge.

Keywords: Kawasaki syndrome; coronary artery abnormalities; intravenous immunoglobulin.

PubMed Disclaimer

References

    1. Newburger J.W., Takahashi M., Gerber M.A., Gewitz M.H., Tani L.Y., Burns J.C., Shulman S.T., Bolger A.F., Ferrieri P., Baltimore R.S., et al. Committee on Rheumatic Fever, Endocarditis and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association, American Academy of Pediatrics. Diagnosis, treatment, and long-term management in Kawasaki disease: A statement for health professionals from the committee on rheumatic fever, endocarditis and Kawasaki disease, council on cardiovascular disease in the young, American Heart Association. Circulation. 2004;110:2747–2771. - PubMed
    1. Alexoudi I., Kanakis M., Kapsimali V., Vaiopoulos G. Kawasaki disease: Current aspects on aetiopathogenesis and therapeutic management. Autoimmun. Rev. 2011;10:544–547. doi: 10.1016/j.autrev.2011.04.005. - DOI - PubMed
    1. Principi N., Rigante D., Esposito S. The role of infection in Kawasaki syndrome. J. Infect. 2013;67:1–10. doi: 10.1016/j.jinf.2013.04.004. - DOI - PMC - PubMed
    1. Rigante D., Tarantino G., Valentini P. Non-infectious makers of Kawasaki syndrome: Tangible or elusive triggers? Immunol. Res. 2015 doi: 10.1007/s12026-015-8679-4. - DOI - PubMed
    1. Furusho K., Kamiya T., Nakano H., Kiyosawa N., Shinomiya K., Hayashidera T., Tamura T., Hirose O., Manabe Y., Yokoyama T., et al. High-dose intravenous γ globulin for Kawasaki disease. Lancet. 1984;2:1055–1058. doi: 10.1016/S0140-6736(84)91504-6. - DOI - PubMed

MeSH terms