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儿童和青年成人使用血池造影剂的安全性。

Safety of Blood Pool Contrast Agent Administration in Children and Young Adults.

作者信息

Rigsby Cynthia K, Popescu Andrada R, Nelson Paige, Orr R Jason, Boylan Emma E, Schoeneman Samantha, deFreitas R Andrew

机构信息

1 Department of Medical Imaging, Ann & Robert H. Lurie Children's Hospital of Chicago, 225 E Chicago Ave, Chicago, IL 60611.

2 Department of Radiology, Northwestern University Feinberg School of Medicine, Chicago, IL.

出版信息

AJR Am J Roentgenol. 2015 Nov;205(5):1114-20. doi: 10.2214/AJR.14.13991.

Abstract

OBJECTIVE

The objective of our study was to determine the adverse reaction rate associated with the administration of blood pool contrast material in children and young adults.

MATERIALS AND METHODS

A review of the MRI and pharmacy databases identified all patients who received gadofosveset trisodium from October 1, 2011, to June 30, 2014. Patients were classified as having been anesthetized or not anesthetized for the MRI examinations. A review of the electronic medical records identified adverse reactions recorded within 24 hours of contrast administration. The adverse reactions were graded as mild, moderate, or severe. Risk ratios were calculated between the adverse reaction rate experienced by anesthetized patients and that experience by nonanesthetized patients.

RESULTS

During the study period, 626 patients (mean age, 11.7 years) received 711 doses of gadofosveset trisodium; 137 adverse reactions were recorded, which yields a 19.3% (137/711) adverse reaction rate. There were 115 adverse reactions experienced by 367 anesthetized patients (31.3%): 93.0% (107/115) were mild and 7.0% (8/115) were moderate. The remaining 22 adverse reactions were experienced by 344 (6.4%) nonanesthetized patients, and 90.9% (20/22) were mild. Three nonanesthetized patients had allergiclike reactions; of these allergiclike reactions, one was mild and two were severe for a severe allergiclike reaction rate of 0.28% (2/711). Severe allergiclike reactions were treated without any adverse outcomes. Anesthetized patients were 5.7 times more likely to experience an adverse event than nonanesthetized patients; most reactions in anesthetized patients were seen after the administration of anesthesia alone.

CONCLUSION

Most reactions after gadofosveset trisodium administration in children and young adults are mild; however, severe allergiclike reactions occur, so policies must be in place to treat patients with adverse reactions when using this contrast agent. These data may be useful to centers considering administering gadofosveset trisodium to pediatric patients.

摘要

目的

我们研究的目的是确定儿童和青年使用血池造影剂后的不良反应发生率。

材料与方法

回顾MRI和药房数据库,确定2011年10月1日至2014年6月30日期间所有接受过钆布醇三钠的患者。患者被分类为在MRI检查时接受了麻醉或未接受麻醉。回顾电子病历,确定造影剂给药后24小时内记录的不良反应。不良反应分为轻度、中度或重度。计算麻醉患者和未麻醉患者的不良反应发生率之间的风险比。

结果

在研究期间,626例患者(平均年龄11.7岁)接受了711剂钆布醇三钠;记录了137例不良反应,不良反应发生率为19.3%(137/711)。367例麻醉患者发生115例不良反应(31.3%):93.0%(107/115)为轻度,7.0%(8/115)为中度。其余22例不良反应发生在344例(6.4%)未麻醉患者中,90.9%(20/22)为轻度。3例未麻醉患者出现类过敏反应;在这些类过敏反应中,1例为轻度,2例为重度,重度类过敏反应发生率为0.28%(2/711)。重度类过敏反应经治疗后未出现任何不良后果。麻醉患者发生不良事件的可能性是未麻醉患者的5.7倍;麻醉患者的大多数反应仅在麻醉给药后出现。

结论

儿童和青年使用钆布醇三钠后的大多数反应为轻度;然而,会发生重度类过敏反应,因此在使用这种造影剂时必须制定处理不良反应患者的政策。这些数据可能对考虑给儿科患者使用钆布醇三钠的中心有用。

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