Schmid Isabelle, Didier Dominique, Pfammatter Thomas, Garachemani Ali, Fleisch Martin, Kirchin Miles A, Meier Bernhard
University Hospital, Freiburgstrasse 4, 3010, Bern, Switzerland.
Int J Cardiol. 2007 Jun 12;118(3):389-96. doi: 10.1016/j.ijcard.2006.12.011. Epub 2007 Mar 21.
To compare the effects on heart rate (HR), on left ventricular (LV) or arterial pressures, and the general safety of a non-ionic low-osmolar contrast medium (CM) and a non-ionic iso-osmolar CM in patients undergoing cardiac angiography (CA) or peripheral intra-arterial digital subtraction angiography (IA-DSA).
Two double-blind, randomized studies were conducted in 216 patients who underwent CA (n=120) or peripheral IA-DSA (n=96). Patients referred for CA received a low-osmolar monomeric CM (iomeprol-350, n=60) or an iso-osmolar dimeric CM (iodixanol-320; n=60). HR and LV peak systolic and end-diastolic pressures were determined before and after the first injection during left and right coronary arteriography and left ventriculography. Monitoring for all types of adverse event (AE) was performed for 24 h following the procedure. t-tests were performed to compare CM for effects on HR. Patients referred for IA-DSA received iomeprol-300 (n=49) or iodixanol-320 (n=47). HR and arterial blood pressure (BP) were evaluated before and after the first 4 injections. Monitoring for AE was performed for 4 h following the procedure. Repeated-measures ANOVA was used to compare mean HR changes across the first 4 injections, whereas changes after the first injection were compared using t-tests.
No significant differences were noted between iomeprol and iodixanol in terms of mean changes in HR during left coronary arteriography (p=0.8), right coronary arteriography (p=0.9), and left ventriculography (p=0.8). In patients undergoing IA-DSA, no differences between CM were noted for effects on mean HR after the first injection (p=0.6) or across the first 4 injections (p=0.2). No significant differences (p>0.05) were noted in terms of effects on arterial BP in either study or on LV pressures in patients undergoing CA. Non-serious AE considered possibly CM-related (primarily headache and events affecting the cardiovascular and digestive systems) were reported more frequently by patients undergoing CA and more frequently after iodixanol (14/60 [23.3%] and 2/47 [4.3%]; CA and IA-DSA, respectively) than iomeprol (10/60 [16.7%] and 1/49 [2%], respectively).
Iomeprol and iodixanol are safe and have equally negligible effects on HR and LV pressures or arterial BP during and after selective intra-cardiac injection and peripheral IA-DSA.
Iomeprol and iodixanol are safe and equally well tolerated with regard to cardiac rhythm and clinical preference should be based on diagnostic image quality alone.
比较非离子低渗造影剂(CM)和非离子等渗造影剂对接受心脏血管造影(CA)或外周动脉数字减影血管造影(IA-DSA)患者的心率(HR)、左心室(LV)或动脉压力的影响以及总体安全性。
对216例接受CA(n = 120)或外周IA-DSA(n = 96)的患者进行了两项双盲随机研究。接受CA的患者接受低渗单体造影剂(碘美普尔-350,n = 60)或等渗二聚体造影剂(碘克沙醇-320;n = 60)。在左右冠状动脉造影和左心室造影的首次注射前后测定HR以及LV收缩压峰值和舒张压末期压力。术后24小时对所有类型的不良事件(AE)进行监测。采用t检验比较造影剂对HR的影响。接受IA-DSA的患者接受碘美普尔-300(n = 49)或碘克沙醇-320(n = 47)。在首次4次注射前后评估HR和动脉血压(BP)。术后4小时对AE进行监测。采用重复测量方差分析比较前4次注射期间HR的平均变化,而首次注射后的变化采用t检验进行比较。
在左冠状动脉造影(p = 0.8)、右冠状动脉造影(p = 0.9)和左心室造影(p = 0.8)期间,碘美普尔和碘克沙醇在HR平均变化方面无显著差异。在接受IA-DSA的患者中,造影剂对首次注射后(p = 0.6)或前4次注射期间(p = 0.2)的平均HR影响无差异。在两项研究中,造影剂对动脉BP的影响以及对接受CA患者的LV压力影响均未发现显著差异(p>0.05)。接受CA的患者报告的被认为可能与造影剂相关的非严重AE(主要是头痛以及影响心血管和消化系统的事件)比接受碘美普尔的患者更频繁(分别为14/60 [23.3%]和2/47 [4.3%];分别为CA和IA-DSA)(分别为10/60 [16.7%]和1/49 [2%])。
碘美普尔和碘克沙醇是安全的,在选择性心内注射和外周IA-DSA期间及之后对HR、LV压力或动脉BP的影响同样可忽略不计。
碘美普尔和碘克沙醇在心律方面是安全的且耐受性相当,临床选择应仅基于诊断图像质量。