A Systematic Review and Meta-Analysis on the Safety and Efficacy of Second Dose Immunoglobulin Versus High Dose Pulse Methylprednisolone in Refractory Kawasaki Disease

Catherine Uy-Cano, Teldy Ley-Chua, Robert Garcia
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Abstract

Background: There is limited information available regarding the management of IVIG-refractory Kawasaki Disease (KD). Objective: This study aimed to evaluate the safety and efficacy of a second intravenous immunoglobulin (IVIG) infusion versus intravenous methylprednisolone (IVMP) in patients with IVIG-refractory KD. Methodology: Cochrane Library, PubMed, Medline, Elsevier (Science Direct), Springer Link and BMJ databases were searched from May 1, 2020 to December 31, 2020. We included randomized controlled trials (RCTs) and high-quality prospective and retrospective studies, with population restricted to children 0 months to 18 years, with KD refractory to initial IVIG at 2g/kg, who remained febrile for 24-48 hours after completion of initial IVIG, and who received second-line monotherapy with either a second dose IVIG or IVMP. We conducted a meta-analysis using Review Manager [RevMan] 5.4.1 software. Results: A total of six studies (n=188 patients) were analyzed. The incidence of coronary artery lesions was comparable between a second dose of IVIG and IVMP (RR 0.82, 0.34-1.96, P=0.66) in patients with IVIG-refractory KD. The rate of fever resolution to a second IVIG, compared to IVMP, was not significantly different between groups (RR 0.97, 0.84-1.13, P=0.72). There was a significantly higher incidence of adverse events in the IVMP group (RR 0.42, 0.26-0.57, P=0.0002), but these were all transient and resolved without further treatment. Conclusion: There is no significant difference in the incidence of coronary artery lesions and rate of fever resolution post-retreatment with a second dose of IVIG versus IVMP in IVIG-refractory KD. More adverse events were reported in the IVMP group. Keywords: Mucocutaneous Lymph Node Syndrome, Kawasaki Disease, Refractory Kawasaki Disease, Immunosuppressant, Intravenous Immunoglobulin, Methylprednisolone, Second IVIG Infusion
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第二剂免疫球蛋白与高剂量脉冲甲基强的松龙治疗难治性川崎病的安全性和有效性的系统评价和荟萃分析
背景:关于ivig难治性川崎病(KD)治疗的信息有限。目的:本研究旨在评估第二次静脉注射免疫球蛋白(IVIG)与静脉注射甲基强的松龙(IVMP)在IVIG难治性KD患者中的安全性和有效性。方法:检索Cochrane Library、PubMed、Medline、Elsevier (Science Direct)、Springer Link和BMJ数据库,检索时间为2020年5月1日至2020年12月31日。我们纳入了随机对照试验(RCTs)和高质量的前瞻性和回顾性研究,研究对象限于0个月至18岁的儿童,患者KD对初始IVIG (2g/kg)难治性,完成初始IVIG后24-48小时仍处于发热状态,接受二线单药治疗,使用第二剂量IVIG或IVMP。我们使用Review Manager [RevMan] 5.4.1软件进行meta分析。结果:共分析了6项研究(n=188例)。在IVIG难治性KD患者中,第二剂量IVIG和IVMP的冠状动脉病变发生率相当(RR 0.82, 0.34-1.96, P=0.66)。与IVMP相比,第二次IVIG的发热消退率在两组之间无显著差异(RR 0.97, 0.84-1.13, P=0.72)。IVMP组不良事件发生率显著高于IVMP组(RR 0.42, 0.26-0.57, P=0.0002),但这些不良事件都是短暂的,无需进一步治疗即可解决。结论:在IVIG难治性KD患者中,第二次注射IVIG与IVMP治疗后冠状动脉病变发生率和发热消退率无显著差异。IVMP组报告了更多的不良事件。关键词:粘膜皮肤淋巴结综合征,川崎病,难治性川崎病,免疫抑制剂,静脉注射免疫球蛋白,甲基强的松龙,第二次IVIG输注
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