Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan
J Am Heart Assoc. 2017 Jul 6;6(7):e005370. doi: 10.1161/JAHA.116.005370.
We previously reported that biofilms and innate immunity contribute to the pathogenesis of Kawasaki disease. Therefore, we aimed to assess the efficacy of clarithromycin, an antibiofilm agent, in patients with Kawasaki disease.
We conducted an open-label, multicenter, randomized, phase 2 trial at 8 hospitals in Japan. Eligible patients included children aged between 4 months and 5 years who were enrolled between days 4 and 8 of illness. Participants were randomly allocated to receive either intravenous immunoglobulin (IVIG) or IVIG plus clarithromycin. The primary end point was the duration of fever after the initiation of IVIG treatment. Eighty-one eligible patients were randomized. The duration of the fever did not differ between the 2 groups (mean±SD, 34.3±32.4 and 31.1±31.1 hours in the IVIG plus clarithromycin group and the IVIG group, respectively [=0.66]). The relapse rate of patients in the IVIG plus clarithromycin group was significantly lower than that in the IVIG group (12.5% versus 30.8%, =0.046). No serious adverse events occurred during the study period. In a post hoc analysis, the patients in the IVIG plus clarithromycin group required significantly shorter mean lengths of hospital stays than those in the IVIG group (8.9 days versus 10.3 days, =0.049).
Although IVIG plus clarithromycin therapy failed to shorten the duration of fever, it reduced the relapse rate and shortened the duration of hospitalization in patients with Kawasaki disease.
URL: http://www.umin.ac.jp/ctr/index.htm. Unique identifier: UMIN000015437.
我们之前报道过生物膜和固有免疫与川崎病的发病机制有关。因此,我们旨在评估抗生物膜药物克拉霉素治疗川崎病患者的疗效。
我们在日本的 8 家医院进行了一项开放标签、多中心、随机、2 期临床试验。符合条件的患者包括年龄在 4 个月至 5 岁之间、在发病第 4 天至第 8 天入组的儿童。参与者被随机分配接受静脉注射免疫球蛋白(IVIG)或 IVIG 加克拉霉素。主要终点是 IVIG 治疗开始后发热的持续时间。81 名符合条件的患者被随机分组。两组患者的发热持续时间无差异(IVIG 加克拉霉素组和 IVIG 组分别为 34.3±32.4 小时和 31.1±31.1 小时[=0.66])。IVIG 加克拉霉素组患者的复发率明显低于 IVIG 组(12.5%对 30.8%,=0.046)。研究期间未发生严重不良事件。在事后分析中,IVIG 加克拉霉素组患者的平均住院时间明显短于 IVIG 组(8.9 天对 10.3 天,=0.049)。
虽然 IVIG 加克拉霉素治疗未能缩短发热持续时间,但降低了川崎病患者的复发率并缩短了住院时间。