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注射用钆喷酸葡胺在儿科患者中的神经影像学安全性和有效性。

The safety and efficacy of neuroimaging with gadoversetamide injection in pediatric patients.

作者信息

Lowe Lisa H, Kearns Gregory L, Wible James H

机构信息

Children's Mercy Hospitals and Clinics and the University of Missouri-Kansas City, Kansas City, MO, USA.

出版信息

Curr Med Res Opin. 2006 Dec;22(12):2515-24. doi: 10.1185/030079906X159452.

Abstract

OBJECTIVE

The safety and efficacy of gadoversetamide injection (OptiMARK) was examined in pediatric patients referred for magnetic resonance imaging (MRI) of the central nervous system (CNS).

RESEARCH AND DESIGN METHODS

This was an open-label, multicenter study in patients aged between 2 and 18 years scheduled for a contrast-enhanced MRI study. Patients received a single injection of gadoversetamide (0.1 mmol/kg). Safety of gadoversetamide was evaluated by physical examinations and monitoring of adverse events, laboratory values, vital signs, and electrocardiogram readings before and after drug administration. Efficacy was assessed by three independent, blinded readers for confidence in diagnosis and level of conspicuity for lesion visualization on precontrast and postcontrast images. The diagnostic accuracy, sensitivity, and specificity of lesion detection were determined for the precontrast images, the postcontrast images, and the precontrast and postcontrast images read together.

RESULTS

No drug-related moderate or serious adverse events were observed in this study, according to site investigators. A total of four adverse events in four of 100 patients (4%) were deemed likely related to gadoversetamide injection by the site investigators. All were mild in severity and not clinically significant. The most common adverse events, regardless of relationship to study drug, were injection-site reactions and a small prolongation of the QT interval. The administration of gadoversetamide significantly increased the level of lesion conspicuity and diagnostic confidence (p < 0.05). Compared with the nonenhanced image, gadoversetamide significantly increased the accuracy and sensitivity of lesion detection (p < 0.05). Limitations of the study included a lack of physiological measurements after sedation and prior to contrast administration, a single dose of gadoversetamide administered (0.1 mmol/kg) and patients younger than 2 years of age were excluded.

CONCLUSION

The administration of gadoversetamide injection (0.1 mmol/kg) was safe, well tolerated and produced clinically appropriate contrast enhancement for MRI of the CNS in the pediatric population.

摘要

目的

在因中枢神经系统(CNS)磁共振成像(MRI)而接受检查的儿科患者中,对钆塞酸二钠注射液(OptiMARK)的安全性和有效性进行研究。

研究与设计方法

这是一项针对年龄在2至18岁、计划进行增强MRI检查的患者的开放标签、多中心研究。患者接受单次钆塞酸二钠注射(0.1 mmol/kg)。通过体格检查以及监测给药前后的不良事件、实验室检查值、生命体征和心电图读数,对钆塞酸二钠的安全性进行评估。由三名独立的、不知情的阅片者对造影前和造影后图像上病变显示的诊断可信度和清晰度进行评估,以确定疗效。分别针对造影前图像、造影后图像以及同时读取的造影前和造影后图像,确定病变检测的诊断准确性、敏感性和特异性。

结果

根据各研究点的调查人员,本研究中未观察到与药物相关的中度或严重不良事件。100名患者中有4名(4%)共发生4起不良事件,各研究点的调查人员认为这些事件可能与钆塞酸二钠注射有关。所有事件严重程度均为轻度,且无临床意义。无论与研究药物有无关联,最常见的不良事件为注射部位反应和QT间期轻度延长。钆塞酸二钠的给药显著提高了病变的清晰度和诊断可信度(p < 0.05)。与未增强图像相比,钆塞酸二钠显著提高了病变检测的准确性和敏感性(p < 0.05)。本研究的局限性包括:未在镇静后和造影剂给药前进行生理指标测量;仅给予单次剂量的钆塞酸二钠(0.1 mmol/kg);排除了年龄小于2岁的患者。

结论

钆塞酸二钠注射液(0.1 mmol/kg)给药安全、耐受性良好,可为儿科人群的中枢神经系统MRI提供临床上合适的造影增强效果。

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