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磁共振成像中首次和重复使用钆基造影剂的急性不良反应评估:一项回顾性研究。

Assessment of first-time and repeated acute adverse reactions to gadolinium-based contrast agents in MRI: A retrospective study.

机构信息

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.

出版信息

Eur J Radiol. 2024 Jul;176:111504. doi: 10.1016/j.ejrad.2024.111504. Epub 2024 May 14.

Abstract

PURPOSE

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

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