Hôpital Necker Enfants Malades, Paris, France.
Université de Paris, Paris, France.
J Clin Apher. 2021 Dec;36(6):823-830. doi: 10.1002/jca.21934. Epub 2021 Sep 1.
Therapeutic plasma exchange (TPE) is acknowledged to be an effective treatment in life-threatening pediatric disorders. Apheresis for pediatric diseases has been poorly investigated, and most studies to date featured small numbers of patients and lacked control groups. The objective of the present study was to evaluate the tolerance of TPE in pediatric patients.
A retrospective cohort study via a web-based electronic case report form including pediatric patients referred for TPE between January 2005 and December 2014.
A total of 78 patients (median [range] age: 9.8 [0.53-17.93]) and 731 TPE procedures were analyzed. The indications were antibody-mediated rejection (n = 33; 42%) and desensitization therapy (n = 5; 6%) after solid organ or hematopoietic stem cell transplantation, thrombotic microangiopathy (n = 17; 22%), pediatric inflammatory diseases (n = 16; 21%), kidney diseases (n = 6; 8%), and hyperviscosity syndrome (n = 1; 1%). On average, each patient underwent six procedures during the first session [range: 1-19]. In the 2 weeks following the start of a session, 72 patients (92%) presented a total of 311 adverse events (AEs) potentially related to TPE. The risk of AEs was not related to the indication for TPE, the intensity of care, venous access, plasma substitute use, or body weight. None of the deaths was related to the TPE.
We studied one of the largest retrospective pediatric cohorts described to date. Our experience of TPE children's TPE feasibility concerned specific, life-threatening conditions and otherwise treatment-refractory diseases.
治疗性血浆置换(TPE)已被确认为治疗危及生命的儿科疾病的有效方法。儿科疾病的体外血液治疗研究甚少,迄今为止的大多数研究都纳入了少量患者,且缺乏对照组。本研究的目的是评估 TPE 在儿科患者中的耐受性。
这是一项通过基于网络的电子病例报告表进行的回顾性队列研究,纳入了 2005 年 1 月至 2014 年 12 月期间因 TPE 而转诊的儿科患者。
共分析了 78 例患者(中位数[范围]年龄:9.8[0.53-17.93])和 731 次 TPE 操作。适应证为实体器官或造血干细胞移植后抗体介导的排斥反应(n=33;42%)和脱敏治疗(n=5;6%)、血栓性微血管病(n=17;22%)、儿科炎症性疾病(n=16;21%)、肾脏疾病(n=6;8%)和高粘滞血症综合征(n=1;1%)。平均每位患者在首次治疗中接受了 6 次治疗[范围:1-19]。在开始治疗后的 2 周内,72 例患者(92%)共出现了 311 次与 TPE 相关的不良事件(AE)。AE 的风险与 TPE 的适应证、护理强度、静脉通路、血浆替代物使用或体重无关。无一例死亡与 TPE 有关。
我们研究了迄今为止描述的最大的儿科回顾性队列之一。我们对 TPE 儿科患者的经验涉及危及生命的特定情况和其他治疗抵抗性疾病。