Perrin E, Jackson M, Grant R, Lloyd C, Chinaka F, Goh V
Guy's and St Thomas' NHS Foundation Trust, Great Maze Pond, London SE1 9RT, UK; St George's, University of London, Cranmer Terrace, London SW17 0RE, UK.
St George's, University of London, Cranmer Terrace, London SW17 0RE, UK.
Radiography (Lond). 2018 Feb;24(1):22-27. doi: 10.1016/j.radi.2017.08.011. Epub 2017 Oct 14.
In many centres, a fixed method of contrast-media administration is used for CT regardless of patient body habitus. The aim of this trial was to assess contrast enhancement of the aorta, portal vein, liver and spleen during abdomino-pelvic CT imaging using a weight-adapted contrast media protocol compared to the current fixed dose method.
Thirty-nine oncology patients, who had previously undergone CT abdomino-pelvic imaging at the institution using a fixed contrast media dose, were prospectively imaged using a weight-adapted contrast media dose (1.4 ml/kg). The two sets of images were assessed for contrast enhancement levels (HU) at locations in the liver, aorta, portal vein and spleen during portal-venous enhancement phase. The t-test was used to compare the difference in results using a non-inferiority margin of 10 HU.
When the contrast dose was tailored to patient weight, contrast enhancement levels were shown to be non-inferior to the fixed dose method (liver p < 0.001; portal vein p = 0.003; aorta p = 0.001; spleen p = 0.001). As a group, patients received a total contrast dose reduction of 165 ml using the weight-adapted method compared to the fixed dose method, with a mean cost per patient of £6.81 and £7.19 respectively.
Using a weight-adapted method of contrast media administration was shown to be non-inferior to a fixed dose method of contrast media administration. Patients weighing 76 kg, or less, received a lower contrast dose which may have associated cost savings. A weight-adapted contrast media protocol should be implemented for portal-venous phase abdomino-pelvic CT for oncology patients with adequate renal function (>70 ml/min/1.73 m).
在许多中心,无论患者体型如何,CT检查都采用固定的造影剂给药方法。本试验的目的是评估在腹部盆腔CT成像过程中,与当前固定剂量方法相比,采用根据体重调整的造影剂方案时主动脉、门静脉、肝脏和脾脏的造影剂增强效果。
39名肿瘤患者,此前在该机构使用固定造影剂剂量进行过腹部盆腔CT成像,前瞻性地采用根据体重调整的造影剂剂量(1.4毫升/千克)进行成像。在门静脉增强期,对两组图像的肝脏、主动脉、门静脉和脾脏部位的造影剂增强水平(HU)进行评估。采用t检验比较结果差异,非劣效性界值为10HU。
当造影剂剂量根据患者体重调整时,造影剂增强水平显示不劣于固定剂量方法(肝脏p<0.001;门静脉p = 0.003;主动脉p = 0.001;脾脏p = 0.001)。总体而言,与固定剂量方法相比,采用根据体重调整的方法,患者接受的造影剂总剂量减少了165毫升,每位患者的平均费用分别为6.81英镑和7.19英镑。
采用根据体重调整的造影剂给药方法显示不劣于固定剂量造影剂给药方法。体重76千克及以下的患者接受的造影剂剂量较低,可能节省相关费用。对于肾功能正常(>70毫升/分钟/1.73平方米)的肿瘤患者,腹部盆腔CT门静脉期应采用根据体重调整的造影剂方案。