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静脉注射免疫球蛋白联合皮质类固醇治疗难治性川崎病。

Intravenous immune globulin plus corticosteroids in refractory Kawasaki disease.

作者信息

Jibiki Toshiaki, Kato Izumi, Shiohama Tadashi, Abe Katsuaki, Anzai Satoshi, Takeda Nobue, Yamaguchi Ken-Ichi, Kanazawa Masaki, Kurosaki Tomomichi

机构信息

Department of Pediatrics, Chiba Kaihin Municipal Hospital, Chiba, Japan.

出版信息

Pediatr Int. 2011 Oct;53(5):729-735. doi: 10.1111/j.1442-200X.2011.03338.x.

Abstract

BACKGROUND

The aim of the present study was to investigate the efficacy of i.v. immune globulin (IVIG) therapy combined with corticosteroids for additional treatment of acute Kawasaki disease (KD) unresponsive to initial IVIG treatment.

METHODS

In 50 prospective KD patients, six IVIG non-responders without clinical improvement within 24-48 h after completion of initial IVIG, received 2 g/kg IVIG concurrently with 2 mg/kg i.v. prednisolone sodium succinate (PSL) until normalization of C-reactive protein level. Treatment was then changed to oral PSL, which was tapered over time. Clinical and coronary artery lesion (CAL) outcomes were compared with those of 13 IVIG non-responders who received additional heterogeneous therapies in 125 retrospective KD patients. In addition, the scoring system of Kobayashi et al. for prediction of non-responsiveness to initial IVIG treatment was retrospectively verified in 175 KD subjects, consisting of 50 prospective and 125 retrospective patients in order to evaluate the efficacy of the re-treatment regimen.

RESULTS

Incidence of CAL in the study patients was lower than in the control patients, although differences were not significant both in the acute stage (within 1 month: 1/6, 16.7% vs 7/13, 53.8%; P= 0.177) and in the convalescent stage (after 1 month: 0/6, 0.0% vs 4/13, 30.8%; P= 0.255). According to the non-responder prediction system, the scores of six study and 13 control patients before initial IVIG treatment were similar (7.2 ± 1.9 vs 5.3 ± 3.1; P= 0.200). No serious adverse effects related to each treatment were noted in patients of either group.

CONCLUSIONS

Additional IVIG combined with concurrent PSL appears to be safe and worth evaluation for the treatment of acute KD unresponsive to initial IVIG treatment.

摘要

背景

本研究旨在探讨静脉注射免疫球蛋白(IVIG)联合皮质类固醇对初始IVIG治疗无反应的急性川崎病(KD)进行辅助治疗的疗效。

方法

在50例前瞻性KD患者中,6例在初始IVIG治疗结束后24 - 48小时内无临床改善的IVIG无反应者,接受2 g/kg IVIG同时联合2 mg/kg静脉注射琥珀酸钠泼尼松龙(PSL),直至C反应蛋白水平恢复正常。随后治疗改为口服PSL,并逐渐减量。将临床和冠状动脉病变(CAL)结果与125例回顾性KD患者中接受其他不同治疗的13例IVIG无反应者进行比较。此外,在175例KD受试者(包括50例前瞻性患者和125例回顾性患者)中对Kobayashi等人用于预测初始IVIG治疗无反应性的评分系统进行回顾性验证,以评估再治疗方案的疗效。

结果

研究患者中CAL的发生率低于对照患者,尽管在急性期(1个月内:1/6,16.7% 对7/13,53.8%;P = 0.177)和恢复期(1个月后:0/6,0.0% 对4/13,30.8%;P = 0.255)差异均无统计学意义。根据无反应者预测系统,6例研究患者和13例对照患者在初始IVIG治疗前的评分相似(7.2 ± 1.9对5.3 ± 3.1;P = 0.200)。两组患者均未观察到与各治疗相关的严重不良反应。

结论

额外的IVIG联合同时使用PSL似乎是安全的,对于初始IVIG治疗无反应的急性KD治疗值得评估。

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