Abstract

IntroductionDifferent immunoglobulin manufacturing processes may influence its effectiveness for Kawasaki disease. However, nationwide studies with longitudinal follow-up are still lacking. The aim of this study was to evaluate the comparative effectiveness of immunoglobulin preparations from a nationwide perspective.Materials and MethodsThis is a nationwide retrospective cohort study with a new user design. Data came from the National Health Insurance Research Database of Taiwan. From 1997 to 2008, children under 2 years old who received immunoglobulin therapy for the first time under the main diagnosis of Kawasaki disease were enrolled. The manufacturing processes were divided into β-propiolactonation, acidification and those containing IgA. The endpoints were immunoglobulin non-responsiveness, acute aneurysm, prolonged use of anti-platelets or anti-coagulants, and recurrence.ResultsIn total, 3830 children were enrolled. β-propiolactonation had a relative risk of 1.45 (95% CI 1.08∼1.94) of immunoglobulin non-responsiveness, however, the relative risks for acidification and containing IgA were non-significant. For acute aneurysms, acidification had a relative risk of 1.49 (95% CI 1.17∼1.90), however the relative risks for β-propiolactonation and containing IgA were non-significant. For prolonged use of anti-platelets or anti-coagulants, β-propiolactonation had a relative risk of 1.44 (95% CI 1.18∼1.76), and acidification protected against them both with a relative risk of 0.82 (95% CI 0.69∼0.97), whereas the relative risk for containing IgA was non-significant. For recurrence, all three factors were non-significant.ConclusionsThe effectiveness of immunoglobulin may differ among different manufacturing processes. β-propiolactonation had a higher risk of treatment failure and prolonged use of anti-platelets or anti-coagulants. Acidification may increase the risk of acute coronary aneurysms.

Highlights

  • Different immunoglobulin manufacturing processes may influence its effectiveness for Kawasaki disease

  • The effectiveness of immunoglobulin may differ among different manufacturing processes. b-propiolactonation had a higher risk of treatment failure and prolonged use of anti-platelets or anti-coagulants

  • Acidification may increase the risk of acute coronary aneurysms

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Summary

Introduction

Different immunoglobulin manufacturing processes may influence its effectiveness for Kawasaki disease. Kawasaki disease is the most common form of acquired heart disease among children in most industrialized countries [1,2,3,4,5,6,7,8,9]. It is a systemic vasculitis, and predominantly involves the coronary arteries [10,11,12,13,14,15]. Intravenous immunoglobulin (IVIG) is the most effective therapy for acute Kawasaki disease. IVIG therapy has been shown to decrease the rate of coronary aneurysms from 20,25% to less than 5% [18,20,22]

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