Teraguchi Masayuki, Ogino Hirotaro, Yoshimura Ken, Taniuchi Shoichiro, Kino Minoru, Okazaki Hitoshi, Kaneko Kazunari
Department of Pediatrics, Kansai Medical University, 2-3-1 Shin-machi, Hirakatashi, Osaka, 573-1191, Japan.
Pediatr Cardiol. 2013 Apr;34(4):959-63. doi: 10.1007/s00246-012-0589-9. Epub 2012 Nov 27.
Patients with Kawasaki disease (KD) who did not respond to the initial IVIG are known to have higher risk for developing coronary arterial lesions (CALs). Our aim is to clarify whether patients with initial IVIG resistant KD may benefit from methylprednisolone pulse therapy (MPT) in comparison with re- treatment of IVIG (2nd IVIG). A total of 237 patients (median age: 2 years 2 months; range 1 months-10 years) with KD were initially treated with IVIG (2 g/kg). Among them, 41 patients (22 %) were assessed as IVIG resistance: these patients were allocated to either group A receiving MPT (n = 14) or group B receiving the 2nd IVIG (n = 27). Patients with resistant to the additional therapy (MPT or 2nd IVIG) were received second IVIG (group A) or MPT (group B). Changes in leukocyte count, C-reactive protein and albumin before and after an additional therapy were significantly greater in group A than those in group B. However, the prevalence of CALs did not differ between the groups (36 % in group A and 26 % in group B, p > 0.05). There was no significant difference in the medical cost between the groups (median cost: 92,032 JPY in group A and 97,331 JPY in group B). MPT does not reduce the risk of development to CAL and does not seem to be beneficial as single agent therapy for IVIG resistant KD.
已知对初始静脉注射免疫球蛋白(IVIG)无反应的川崎病(KD)患者发生冠状动脉病变(CALs)的风险更高。我们的目的是阐明与再次静脉注射免疫球蛋白(第二次IVIG)相比,初始IVIG抵抗性KD患者是否能从甲泼尼龙冲击疗法(MPT)中获益。共有237例KD患者(中位年龄:2岁2个月;范围1个月至10岁)最初接受了IVIG(2 g/kg)治疗。其中,41例患者(22%)被评估为IVIG抵抗:这些患者被分配到接受MPT的A组(n = 14)或接受第二次IVIG的B组(n = 27)。对额外治疗(MPT或第二次IVIG)有抵抗的患者接受了第二次IVIG(A组)或MPT(B组)。A组额外治疗前后白细胞计数、C反应蛋白和白蛋白的变化明显大于B组。然而,两组之间CALs的患病率没有差异(A组为36%,B组为26%,p>0.05)。两组之间的医疗费用没有显著差异(中位费用:A组为92,032日元,B组为97,331日元)。MPT并不能降低发生CAL的风险,似乎作为IVIG抵抗性KD的单一药物治疗并无益处。
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