Hojreh Azadeh, Mulabdic Amra, Heilos Andreas, Peyrl Andreas, Lampichler Katharina, Raudner Marcus, Tamandl Dietmar, Ba-Ssalamah Ahmed, Szepfalusi Zsolt
Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Division of Pediatric Nephrology and Gastroenterology Department of Pediatrics and Adolescent Medicine, Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria.
PLoS One. 2024 Dec 3;19(12):e0313495. doi: 10.1371/journal.pone.0313495. eCollection 2024.
Repeated gadolinium-based contrast agent (GBCA)-enhanced MRIs are crucial in the diagnosis and follow-up of oncologic and chronic disorders in pediatric patients. The aim of the study was to evaluate the frequency and severity of adverse reactions to GBCAs in children after a single vs. multiple GBCA-enhanced abdomen MRIs.
All pediatric patients with at least one GBCA-enhanced abdominal MRI between 2009 and 2020 were retrospectively evaluated based on adverse reactions reports, according to the classification system of the American College of Radiology and guidelines on contrast agents of the European Society of Urogenital Radiology. A Student´s t-test analysis, a spearman ρ-correlation and a Chi-square test between the reported adverse reactions and the total number of GBCA applications, and the number of each applied GBCA was calculated. A p-value <0.05 was considered significant.
Of 623 patients with 964 GBCA-enhanced abdomen MRIs, there were 464 patients with only one and 159 patients with multiple GBCA administrations. Of 964 GBCA doses administrated, two cases with urticaria (mild allergy-like adverse reaction) and one case with vomiting (mild chemotoxic adverse reaction) were recorded (3/964 = 0.31%), but all the reports were in patients with multiple GBCA administration (3/159 = 1.89%). No adverse reactions in patients with a single GBCA administration were observed. The reported adverse reactions correlated significantly with the total number of GBCAs (p<0.001) and the number of each GBCA (p<0.001 or p = 0.002). The independent two-tailed t-tests, and the chi-square test were significant (p<0.001, p = 0.003).
GBCA-associated adverse reactions are rare and mostly mild, but initially well-tolerated GBCA could cause adverse reactions due to the increase likelihood of drug hypersensitivity upon repeated GBCA exposure.
重复使用基于钆的造影剂(GBCA)增强的磁共振成像(MRI)对于儿科患者肿瘤和慢性疾病的诊断及随访至关重要。本研究的目的是评估儿童在单次与多次GBCA增强腹部MRI后对GBCA不良反应的频率和严重程度。
根据美国放射学会的分类系统和欧洲泌尿生殖放射学会的造影剂指南,基于不良反应报告对2009年至2020年间至少进行过一次GBCA增强腹部MRI的所有儿科患者进行回顾性评估。计算报告的不良反应与GBCA应用总数以及每种应用的GBCA数量之间的学生t检验分析、斯皮尔曼ρ相关性和卡方检验。p值<0.05被认为具有统计学意义。
在623例患者的964次GBCA增强腹部MRI中,464例患者仅接受过一次GBCA,159例患者接受过多次GBCA。在964剂GBCA给药中,记录到2例荨麻疹(轻度过敏样不良反应)和1例呕吐(轻度化学毒性不良反应)(3/964 = 0.31%),但所有报告均来自多次GBCA给药的患者(3/159 = 1.89%)。未观察到单次GBCA给药患者出现不良反应。报告的不良反应与GBCA总数(p<0.001)和每种GBCA的数量(p<0.001或p = 0.002)显著相关。独立双尾t检验和卡方检验具有统计学意义(p<0.001,p = 0.003)。
GBCA相关的不良反应罕见且大多为轻度,但最初耐受性良好的GBCA可能因重复接触GBCA后药物超敏反应可能性增加而导致不良反应。