tocilizumab治疗系统性特发性关节炎患者后,成功应用体外膜氧合治疗危及生命的巨噬细胞激活综合征

Xi Yang, Yingfu Chen, Rongxin Dai, Yunfei An, Xin Yan, Xiaodong Zhao, Xuemei Tang
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摘要

巨噬细胞激活综合征(MAS)是风湿病中一种罕见的、可能危及生命的疾病。主要治疗包括高剂量皮质类固醇和免疫抑制药物,尽管最近有报道称,细胞因子抑制剂如阿那真拉或托珠单抗(TCZ)。我们提出一个病例与系统性青少年特发性关节炎(sJIA)的儿童。在接受单次TCZ输注后,儿童出现进行性缺氧,随后在4天后转移到儿科重症监护病房(PICU)。插管后立即胸部X光片显示弥漫性渗出病灶。尽管不断努力提供机械通气和呼吸支持,患者的血氧饱和度继续下降。此外,患者血流动力学受损,需要给予去甲肾上腺素。最后加入抗利尿激素和多巴胺以维持血流动力学稳定。经过激烈但无效的治疗后,16 h后在PICU开始体外膜氧合(ECMO)。患者成功恢复,并在60 h后断开ECMO支持。出院后,考虑到重症难治性临床特征,我们尝试重新进行TCZ治疗。然而,在TCZ输注半小时内,患者出现了以心悸和胸闷为特征的过敏反应,导致TCZ停药。TCZ作为一种生物制剂,常用于sJIA的治疗。尽管如此,服用TCZ治疗sJIA后MAS和过敏反应的发生可能比以前认识到的更为普遍。小儿风湿病学家在为活动性sJIA启动TCZ时应谨慎行事。此外,我们想强调在紧急情况下,ECMO等挽救生命技术对sJIA患者的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful use of extracorporeal membrane oxygenation for life‐threatening macrophage activation syndrome after treatment with tocilizumab in an systemic juvenile idiopathic arthritis patient
Abstract Macrophage activation syndrome (MAS) is a rare, potentially life‐threatening condition in rheumatic diseases. The primary treatments consist of high‐dose corticosteroids and immunosuppressive drugs, although more recently, cytokine inhibitors like anakinra or tocilizumab (TCZ) have been reported. We present a case of a child with systemic juvenile idiopathic arthritis (sJIA). After receiving a single infusion of TCZ, the child developed progressive hypoxia and was subsequently transferred to the pediatric intensive care unit (PICU) after 4 days. An immediate postintubation chest X‐ray revealed a diffuse exudative lesion. Despite continuous efforts to provide mechanical ventilation and respiratory support, the patient's oxygen saturation continued to decline. Moreover, the patient developed hemodynamic compromise, necessitating the administration of norepinephrine. Eventually, vasopressin and dopamine were added to maintain stable hemodynamics. After an intensive but ineffective treatment, extracorporeal membrane oxygenation (ECMO) was initiated in the PICU after 16 h. The patient successfully recovered and was weaned off ECMO support after 60 h. Following discharge from the PICU, given the severe refractory clinical features, we made an attempt to readminister TCZ treatment. However, within half an hour of TCZ infusion, the patient experienced anaphylaxis characterized by palpitations and chest tightness, leading to the discontinuation of TCZ. TCZ, as a biological agent, is commonly used in the treatment of sJIA. Nonetheless, the occurrence of MAS and anaphylaxis following TCZ administration for sJIA may be more prevalent than previously recognized. Pediatric rheumatologists should exercise caution when initiating TCZ for active sJIA. Furthermore, we want to underscore the importance of life‐saving techniques such as ECMO for sJIA patients in emergency situations.
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