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川崎病合并冠状动脉瘤患儿的强化治疗。

Treatment Intensification in Patients With Kawasaki Disease and Coronary Aneurysm at Diagnosis.

机构信息

Department of Cardiology and.

Department of Pediatrics, Harvard Medical School, Harvard University, Boston, Massachusetts.

出版信息

Pediatrics. 2019 Jun;143(6). doi: 10.1542/peds.2018-3341. Epub 2019 May 2.

Abstract

BACKGROUND

Coronary artery aneurysms (CAA) are a serious complication of Kawasaki disease. Treatment with intravenous immunoglobulin (IVIg) within 10 days of fever onset reduces the risk of CAA from 25% to <5%. Corticosteroids and infliximab are often used in high-risk patients or those with CAA at diagnosis, but there are no data on their longer-term impact on CAA.

METHODS

Retrospective multicenter study including children who had CAA with a score ≥2.5 and <10 at time of diagnosis and who received primary therapy with IVIg alone or in combination with either corticosteroids or infliximab within 10 days of onset of fever.

RESULTS

Of 121 children, with a median age of 2.8 (range 0.1-15.5) years, 30 (25%) received primary therapy with corticosteroids and IVIg, 58 (48%) received primary therapy with infliximab and IVIg, and 33 (27%) received primary therapy with IVIg only. Median coronary scores at the time of diagnosis did not differ among treatment groups ( = .39). Primary treatment intensification with either corticosteroids or infliximab were independent protective factors against progression of coronary size on follow-up (coefficient: -1.31 [95% confidence interval: -2.33 to -0.29]; coefficient: -1.07 [95% confidence interval: -1.95 to -0.19], respectively).

CONCLUSIONS

Among a high-risk group of patients with Kawasaki disease with CAA on baseline echocardiography, those treated with corticosteroids or infliximab in addition to IVIg had less progression in CAA size compared with those treated with IVIg alone. Prospective randomized trials are needed to determine the best adjunctive treatment of patients who present with CAA.

摘要

背景

冠状动脉瘤(CAA)是川崎病的严重并发症。在发热发病后 10 天内使用静脉注射免疫球蛋白(IVIg)治疗可将 CAA 的风险从 25%降低至<5%。对于高危患者或在诊断时即存在 CAA 的患者,通常会使用皮质类固醇和英夫利昔单抗,但尚无关于这些药物对 CAA 长期影响的数据。

方法

这是一项回顾性多中心研究,纳入了在诊断时 CAA 超声心动图 评分≥2.5 且<10 的儿童,这些儿童在发热发病后 10 天内接受了以 IVIg 为基础的初始治疗,单独使用或联合使用皮质类固醇或英夫利昔单抗。

结果

在 121 名年龄中位数为 2.8(范围 0.1-15.5)岁的儿童中,30 名(25%)接受了以皮质类固醇和 IVIg 为基础的初始治疗,58 名(48%)接受了以英夫利昔单抗和 IVIg 为基础的初始治疗,33 名(27%)接受了仅以 IVIg 为基础的初始治疗。在诊断时,各组的冠状动脉 评分中位数没有差异( =.39)。在随访中,以皮质类固醇或英夫利昔单抗进行初始治疗强化是冠状动脉大小进展的独立保护因素(系数:-1.31[95%置信区间:-2.33 至-0.29];系数:-1.07[95%置信区间:-1.95 至-0.19])。

结论

在基线超声心动图存在 CAA 的川崎病高危患儿中,与仅接受 IVIg 治疗的患儿相比,接受 IVIg 联合皮质类固醇或英夫利昔单抗治疗的患儿的 CAA 大小进展较少。需要进行前瞻性随机试验来确定治疗伴有 CAA 的患者的最佳辅助治疗方法。

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