Department of Applied Medical Imaging, Gunma University Graduate School of Medicine, 3-39-22 Showa, Maebashi, Gunma 371-8511, Japan.
Department of Radiology, Gunma University Hospital, 3-39-15 Showa, Maebashi, Gunma 371-8511, Japan.
Eur J Radiol. 2024 Jul;176:111504. doi: 10.1016/j.ejrad.2024.111504. Epub 2024 May 14.
To identify gadolinium-based contrast agents (GBCAs)-related and patient-related risk factors for acute adverse reactions (AARs), and to examine the incidence and severity of repeated AARs.
This study retrospectively evaluated all intravenous GBCA injections in MRI studies at a single institution from January 2012 to September 2019. First-time AARs in patients without a past history of AARs and risk factors were assessed using multivariable regression models with generalized estimating equations. For patients with a past history of AAR(s), we evaluated the incidence of repeated AARs using the Fisher's exact test, as well as the severity of these repeated AARs.
First-time AARs occurred in 129 of 41,827 GBCA injections (0.31 %; 0.70 % of 18,431 patients). With gadoterate meglumine as the reference, the odds ratio (OR) for allergic-like reactions to three GBCAs ranged from 3.27 to 8.03 (p = 0.012 to <0.001). For chemotoxic reactions, the OR was 3.75 (p = 0.001) for gadoteridol. Outpatients had a lower OR for chemotoxic reactions, while higher ORs were observed in head/neck and breast MRI (p < 0.05). The OR for age was 0.99 (p < 0.05). Patients with a past history of AAR(s) had a 3.6 % incidence of mild repeated AARs for all GBCA, significantly higher than the 0.31 % in first-time AARs (p < 0.001). No effectiveness was found for steroid premedication.
The occurrence of first-time AARs was related to the GBCA used and other factors. The incidence of repeated AARs was higher than first-time AARs, though all were mild in severity.
确定钆基对比剂(GBCA)相关和患者相关的急性不良反应(AAR)危险因素,并检查重复 AAR 的发生率和严重程度。
本研究回顾性评估了 2012 年 1 月至 2019 年 9 月在一家机构进行的所有 MRI 研究中的静脉内 GBCA 注射。使用广义估计方程的多变量回归模型评估无 AAR 病史和危险因素的患者的首次 AAR。对于有 AAR 病史的患者,我们使用 Fisher 精确检验评估重复 AAR 的发生率,并评估这些重复 AAR 的严重程度。
在 41827 次 GBCA 注射(0.31%;18431 例患者的 0.70%)中发生了 129 次首次 AAR。与钆喷酸葡胺相比,三种 GBCA 的过敏样反应的比值比(OR)范围为 3.27 至 8.03(p=0.012 至<0.001)。对于化学毒性反应,OR 为 3.75(p=0.001),用于 gadoteridol。门诊患者的化学毒性反应的 OR 较低,而头部/颈部和乳房 MRI 则观察到更高的 OR(p<0.05)。OR 与年龄呈负相关(p<0.05)。有 AAR 病史的患者使用所有 GBCA 的轻度重复 AAR 的发生率为 3.6%,明显高于首次 AAR 的 0.31%(p<0.001)。皮质类固醇预用药无效。
首次 AAR 的发生与 GBCA 的使用和其他因素有关。重复 AAR 的发生率高于首次 AAR,但严重程度均较轻。