Department of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
Br J Radiol. 2014 Feb;87(1034):20130325. doi: 10.1259/bjr.20130325. Epub 2013 Dec 19.
To determine the incidence of immediate and delayed adverse drug reactions (ADRs), and to assess patient discomfort following administration of iodixanol during imaging examinations in routine clinical practice.
A total of 20 185 patients across 95 clinical centres were enrolled in a prospective post-marketing surveillance registry with iodixanol. Patients were monitored for occurrence of ADRs immediately following iodixanol administration and for up to 7 days after administration.
The overall rate of ADRs was 1.52%, of which 0.58% was immediate and 0.97% was delayed onset. Two patients had non-fatal serious ADRs (0.01%). The ADRs were significantly more common in patients who underwent contrast-enhanced CT/coronary CT angiography vs others (p < 0.001), in those receiving pre-heated iodixanol vs non-heating (p < 0.001), in those aged 70 years or younger (p < 0.001), in those in whom a power injector was used for contrast delivery (p < 0.001) and in those with a history of an allergic reaction to contrast (p = 0.024). Multivariate analysis showed that female gender, intravenous route of contrast injection, body weight ≥ 80 kg, age less than 65 years, contrast flow rate ≥ 4 ml s⁻¹ and prior reaction to iodinated contrast medium were all significant and independent contributors to ADRs. Pre-treatment contrast volume and history of cardiac disease, gout, hypertension, diabetes mellitus or asthma did not affect the rate of ADRs. Discomfort was generally mild, with 94.8% of patients reporting a composite score of 0-3.
The safety of iodixanol in routine clinical practice was shown to be similar to the published safety profiles of other non-ionic iodinated contrast agents. Patient discomfort during administration was mild or absent in most patients.
The major strength of this study is that it included 20 185 patients enrolled in various types of imaging examinations. The safety profile of iodixanol was comparable to previously published work.
在常规临床实践中,评估碘克沙醇成像检查后即刻和延迟不良药物反应(ADR)的发生率,并评估患者的不适程度。
共有 20185 名患者在 95 个临床中心参与了碘克沙醇的前瞻性上市后监测登记。患者在碘克沙醇给药后即刻及给药后 7 天内监测 ADR 的发生情况。
ADR 的总发生率为 1.52%,其中 0.58%为即刻发生,0.97%为延迟发生。两名患者发生非致命性严重 ADR(0.01%)。与其他患者相比,接受增强 CT/冠状动脉 CT 血管造影的患者 ADR 更常见(p < 0.001),接受预热碘克沙醇的患者比未加热的患者更常见(p < 0.001),年龄 70 岁或以下的患者更常见(p < 0.001),使用高压注射器进行对比剂输送的患者更常见(p < 0.001),以及有对比剂过敏史的患者更常见(p = 0.024)。多变量分析显示,女性、静脉内对比注射途径、体重≥80 kg、年龄<65 岁、对比剂流速≥4 ml/s 和既往对碘化对比剂的反应均为 ADR 的显著独立危险因素。预处理对比剂体积和心脏病、痛风、高血压、糖尿病或哮喘史均不影响 ADR 发生率。不适通常较轻,94.8%的患者报告综合评分 0-3。
在常规临床实践中,碘克沙醇的安全性与其他非离子型碘造影剂的已发表安全性概况相似。大多数患者在给药过程中仅有轻度或无不适。
本研究的主要优势在于纳入了 20185 名接受各种类型成像检查的患者。碘克沙醇的安全性与之前的研究结果相似。