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一项前瞻性随机试验,旨在确定在心脏导管插入术中使用碘帕醇340(尼奥普明)和碘比醇350(泽尼特克斯)后的早期和晚期反应。

A prospective, randomized trial to determine the early and late reactions after the use of iopamidol 340 (Niopam) and iobitridol 350 (Xenetix) in cardiac catheterization.

作者信息

Vijayalakshmi Kunadian, Williams David, Wright Robert A, Hall James A, Harcombe Alun A, Linker Nicholas J, Stewart Michael J, Davies Adrian, de Belder Mark A

机构信息

Department of Cardiology, The James Cook University Hospital, Marton Road, Middlesbrough, TS4 3BW, United Kingdom.

出版信息

J Invasive Cardiol. 2004 Dec;16(12):707-11.

Abstract

BACKGROUND

Intravascular contrast agents presently used in modern digital catheter laboratories during cardiac catheterization are superior to older agents as regards patient tolerance. There are, however, significant differences between these agents.

PURPOSE

The aim of this study was to determine the incidence of early (< 24 hours) and late (> 24 hours to 7 days) reactions to 2 contrast agents currently used during cardiac catheterization: iopamidol 340 (Niopam) and iobitridol 350 (Xenetix).

METHODS

This was a prospective, randomized, double-blinded trial. Two thousand and nineteen patients undergoing cardiac catheterization received one of the following contrast agents: iopamidol 340 (Niopam) and iobitridol 350 (Xenetix). Reactions that were possibly related to the contrast agents were recorded during hospital admission (early reaction) and after discharge (late reaction) by means of a questionnaire.

RESULTS

The baseline characteristics were matched in both the groups. There was no significant difference in the incidence of heat sensation experienced between the 2 groups, (p = 0.1). Early non-heat reactions occurred in 3.2% of patients receiving iopamidol 340 (Niopam) and 3.6% of those receiving iobitridol 350 (Xenetix), (p = 0.65). Electrocardiographic changes were recorded in 0.7% of patients who received iopamidol 340 (Niopam), and 2.6% of those who received iobitridol 350 (Xenetix), (p = < 0.01). Seven patients (0.8%) receiving iobitridol 350 suffered ventricular fibrillation requiring DC cardioversion compared with none in the iopamidol 340 group (p = < 0.01). Late reactions (post discharge symptoms) occurred in 13.9% of those receiving iopamidol 340 (Niopam) and 18.5% of those receiving iobitridol 350 (Xenetix) (p = 0.02).

CONCLUSIONS

Iobitridol 350 (Xenetix) was associated with more ECG changes and, importantly, ventricular fibrillation, than iopamidol (Niopam). There were no features to suggest other benefits from iobitridol 350. These results suggest that iopamidol 340 is a preferable contrast agent in cardiac catheterization.

摘要

背景

现代数字心导管实验室在心脏导管插入术中目前使用的血管内造影剂在患者耐受性方面优于旧的造影剂。然而,这些造影剂之间存在显著差异。

目的

本研究的目的是确定心脏导管插入术中目前使用的两种造影剂碘帕醇340(尼奥普兰)和碘克沙醇350(泽尼克)的早期(<24小时)和晚期(>24小时至7天)反应的发生率。

方法

这是一项前瞻性、随机、双盲试验。2019例接受心脏导管插入术的患者接受以下造影剂之一:碘帕醇340(尼奥普兰)和碘克沙醇350(泽尼克)。通过问卷调查在入院期间(早期反应)和出院后(晚期反应)记录可能与造影剂相关的反应。

结果

两组的基线特征相匹配。两组之间经历热感的发生率没有显著差异(p=0.1)。接受碘帕醇340(尼奥普兰)的患者中有3.2%发生早期非热反应,接受碘克沙醇350(泽尼克)的患者中有3.6%发生早期非热反应(p=0.65)。接受碘帕醇340(尼奥普兰)的患者中有0.7%记录到心电图改变,接受碘克沙醇350(泽尼克)的患者中有2.6%记录到心电图改变(p<0.01)。接受碘克沙醇350的7例患者(0.8%)发生心室颤动,需要直流电复律,而碘帕醇340组无1例发生(p<0.01)。接受碘帕醇340(尼奥普兰)的患者中有13.9%发生晚期反应(出院后症状),接受碘克沙醇350(泽尼克)的患者中有18.5%发生晚期反应(p=0.02)。

结论

与碘帕醇(尼奥普兰)相比,碘克沙醇350(泽尼克)与更多心电图改变相关,重要的是与心室颤动相关。没有特征表明碘克沙醇350有其他益处。这些结果表明碘帕醇340是心脏导管插入术中更可取的造影剂。

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