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血浆置换联合英夫利昔单抗作为难治性川崎病的三线治疗。

Plasma exchange and infliximab as a third-line therapy for refractory infantile Kawasaki disease.

机构信息

Department of General Pediatrics and Interdisciplinary Medicine, National Center for Child Health and Development, Tokyo, Japan.

Division of Critical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.

出版信息

Pediatr Int. 2022 Jan;64(1):e15226. doi: 10.1111/ped.15226.

DOI:10.1111/ped.15226
PMID:35831245
Abstract

BACKGROUND

The treatment for Kawasaki disease (KD) patients refractory to intravenous immunoglobulin (IVIG) therapy is still controversial, and the efficacy of plasma exchange (PE) and infliximab (IFX) therapy for infantile KD is unknown.

METHODS

A total of 22 infantile KD patients refractory to initial and additional IVIG, who received either PE or IFX as third-line therapy from October 2008 to February 2020 were examined retrospectively. The patients' sex, age, days of first IVIG, days of PE or IFX therapy, laboratory data preceding PE or IFX therapy, coronary artery lesions (CALs), and adverse effects were investigated.

RESULTS

Thirteen patients received PE and nine patients received IFX as the third-line therapy. For the median age at onset, the median days of first IVIG and PE or IFX, and pre-PE or IFX therapy blood test results, there were no significant between-group differences. At admission, and before and after the third-line therapy, there were also no significant differences in occurrence of CALs. The frequency of serious adverse events was significantly higher in the PE group than in the IFX group.

CONCLUSIONS

Although there were no significant differences in patient background, blood test results, or frequency of CALs, the frequency of adverse events was significantly higher in the PE group. With the trend of expansion of IFX therapy for KD patients refractory to IVIG, the role of PE as the additional therapy may become more limited.

摘要

背景

对于静脉注射免疫球蛋白(IVIG)治疗无效的川崎病(KD)患者的治疗仍存在争议,且血浆置换(PE)和英夫利昔单抗(IFX)治疗婴儿 KD 的疗效尚不清楚。

方法

回顾性分析 2008 年 10 月至 2020 年 2 月期间因初始和额外 IVIG 治疗无效而接受 PE 或 IFX 作为三线治疗的 22 例婴儿 KD 患者。研究了患者的性别、年龄、首次 IVIG 治疗的天数、PE 或 IFX 治疗的天数、PE 或 IFX 治疗前的实验室数据、冠状动脉病变(CAL)和不良反应。

结果

13 例患者接受 PE 治疗,9 例患者接受 IFX 作为三线治疗。在发病年龄中位数、首次 IVIG 和 PE 或 IFX 的中位数天数以及 PE 或 IFX 治疗前的血液检查结果方面,两组间无显著差异。在入院时以及三线治疗前后,CAL 的发生率也无显著差异。PE 组严重不良事件的发生率明显高于 IFX 组。

结论

尽管患者背景、血液检查结果或 CAL 发生率无显著差异,但 PE 组的不良事件发生率明显更高。随着 IFX 治疗 KD 患者对 IVIG 治疗无效的趋势扩大,PE 作为附加治疗的作用可能会变得更加有限。

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