Department of Diagnostic Radiology, Lasarettet Trelleborg, University of Lund, Trelleborg, Sweden.
Eur Radiol. 2011 Feb;21(2):326-36. doi: 10.1007/s00330-010-1924-2. Epub 2010 Aug 29.
To establish iodine (I) contrast medium (CM) doses iso-attenuating with gadolinium (Gd) CM doses regarded diagnostic in CTA and percutaneous catheter-angiography/vascular interventions (PCA/PVI) in azotemic patients.
CT Hounsfield units (HU) were measured in 20-mL syringes containing 0.01/0.02,/0.05/0.1 mmol/mL of iodine or gadolinium atoms and placed in phantoms. Relative contrast were measured in 20-mL syringes filled with iohexol at 35/50/70/90/110/140 mg I/mL and 0.5 M gadodiamide using radiofluoroscopy (RF), digital radiography (DX) and x-ray angiography (XA) systems. Clinical doses of Gd-CM at CTA/PCA/PVI were reviewed.
At CT 91-116 and 104-125 mg I/mL in the chest and abdominal phantoms, respectively, were iso-attenuating with 0.5 M Gd at 80-140 kVp. At RF/DX/XA systems 35-90 mg I/mL were iso-attenuating with 0.5 M gadodiamide at 60-115 kVp. Clinically, 60 mL 91-125 mg I/mL (5.5-7.5 gram-iodine) at 80-140 kVp CTA and 60 mL of 35-90 mg I/mL (2.1-5.4 gram-iodine) at 60-115 kVp PCA/PVI would be iso-attenuating with 60 mL 0.5 M Gd-CM (=0.4 mmol Gd/kg in a 75-kg person).
Meticulous examination technique and judicious use of ultra-low I-CM doses iso-attenuating with diagnostic Gd-CM doses in CTA and PCA/PVI may minimise the risk of nephrotoxicity in azotemic patients, while there is no risk of NSF.
确定在肾功能不全患者的 CTA 和经皮导管血管造影/血管介入(PCA/PVI)中,与钆对比剂(Gd)剂量诊断等效的碘(I)对比剂(CM)剂量。
在含有 0.01/0.02/0.05/0.1 毫摩尔/毫升碘或钆原子的 20 毫升注射器中测量 CT 亨氏单位(HU),并将其放置在体模中。使用放射性荧光透视(RF)、数字射线照相(DX)和 X 射线血管造影(XA)系统,在充满碘海醇的 20 毫升注射器中测量相对对比度,浓度分别为 35/50/70/90/110/140 毫克 I/mL 和 0.5 M 钆喷替酸。回顾了 CTA/PCA/PVI 时的临床 Gd-CM 剂量。
在胸部和腹部体模中,分别在 CT 上的 91-116 和 104-125 毫克 I/mL 时,与 80-140 kVp 下的 0.5 M Gd 等密度。在 RF/DX/XA 系统中,35-90 毫克 I/mL 与 60-115 kVp 下的 0.5 M 钆喷替酸等密度。临床上,在 80-140 kVp 的 CTA 中,60 毫升 91-125 毫克 I/mL(5.5-7.5 克碘)和 60-115 kVp 的 PCA/PVI 中,60 毫升 35-90 毫克 I/mL(2.1-5.4 克碘)与 60 毫升 0.5 M Gd-CM(=75 公斤人 0.4 毫摩尔 Gd/kg)等效。
在 CTA 和 PCA/PVI 中,对肾功能不全患者进行精细的检查技术和明智地使用与诊断性 Gd-CM 剂量等密度的超低 I-CM 剂量,可能会最大限度地降低肾毒性的风险,而不会有 NSF 的风险。