Department of Pediatrics, Taichung Veterans General Hospital, Taichung, Taiwan.
PLoS One. 2013 May 1;8(5):e63399. doi: 10.1371/journal.pone.0063399. Print 2013.
Different 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.
This 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.
In total, 3830 children were enrolled. β-propiolactonation had a relative risk of 1.45 (95% CI 1.081.94) 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 1.171.90), 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 1.181.76), and acidification protected against them both with a relative risk of 0.82 (95% CI 0.690.97), whereas the relative risk for containing IgA was non-significant. For recurrence, all three factors were non-significant.
The 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.
不同的免疫球蛋白制造工艺可能会影响其在川崎病中的疗效。然而,目前仍缺乏全国性的、具有纵向随访的研究。本研究旨在从全国范围评估免疫球蛋白制剂的比较效果。
这是一项全国性的回顾性队列研究,采用新用户设计。数据来自台湾全民健康保险研究数据库。1997 年至 2008 年间,2 岁以下经主要诊断为川崎病首次接受免疫球蛋白治疗的患儿纳入研究。制造工艺分为β-丙内酯处理、酸化处理和含有 IgA 的处理。终点为免疫球蛋白无反应、急性动脉瘤、抗血小板或抗凝剂延长使用以及复发。
共纳入 3830 例患儿。β-丙内酯处理的免疫球蛋白无反应风险比为 1.45(95%可信区间 1.081.94),但酸化处理和含有 IgA 的处理风险比均无统计学意义。对于急性动脉瘤,酸化处理的风险比为 1.49(95%可信区间 1.171.90),β-丙内酯处理和含有 IgA 的处理风险比均无统计学意义。对于抗血小板或抗凝剂延长使用,β-丙内酯处理的风险比为 1.44(95%可信区间 1.181.76),酸化处理则具有保护作用,风险比为 0.82(95%可信区间 0.690.97),而含有 IgA 的处理风险比无统计学意义。对于复发,这三个因素均无统计学意义。
免疫球蛋白的疗效可能因制造工艺不同而有所差异。β-丙内酯处理的治疗失败和抗血小板或抗凝剂延长使用风险较高。酸化处理可能会增加急性冠状动脉动脉瘤的风险。