Nyman Ulf, Elmståhl Barbara, Leander Peter, Nilsson Mats, Golman Klaes, Almén Torsten
Department of Radiology, University of Lund, Malmö University Hospital, Sweden.
Radiology. 2002 May;223(2):311-8; discussion 328-9. doi: 10.1148/radiol.2232010221.
Gadolinium chelates, intended as intravenous contrast media for magnetic resonance imaging, have been regarded as nonnephrotoxic and recommended to replace iodinated contrast media in patients with azotemia who are undergoing digital subtraction angiography (DSA). High intraarterial doses (up to 220 mmol of gadodiamide) have been used, with a 40% incidence of nephropathy. The authors discourage the use of gadolinium for DSA for several reasons. (a) There exist no randomized studies comparing the nephrotoxic effects of gadolinium-based and iodinated media at equal-attenuating concentrations and doses. (b) Gadolinium-based media are hypertonic, a pathogenetic factor in contrast medium-induced nephropathy after renal angiography, with an osmolality two to seven times that of plasma. Iodinated media in concentrations that are equally attenuating with gadolinium-based media can be made isotonic. (c) In vitro measurements indicate that 0.5 mol/L gadolinium chelates are equally attenuating with 60-80 mg iodine per milliliter at the commonly used 70-90-kV range used for DSA. Thus, 50 mL of 0.5 mol/L gadolinium chelate ( approximately 0.3 mmol/kg in an 80-kg person) would be equally attenuating with a dose of 3-4 g of iodine in an iodinated medium (eg, 50 mL iohexol at 60-80 mg I/mL or 10-13 mL at 300 mg I/mL). (d) By combining these data on attenuation and results of toxicity studies in mice, the general toxicity of gadolinium chelates may be six to 25 times higher than that of equal-attenuating doses of iodinated media at 70-kV DSA. Thus, the authors believe that at equal-attenuating doses for DSA, modern iodinated contrast media should result in a lower toxic load on the body than with presently available gadolinium chelates.
钆螯合物,用作磁共振成像的静脉造影剂,一直被认为无肾毒性,并被推荐用于替代接受数字减影血管造影(DSA)的氮质血症患者的碘化造影剂。已使用高动脉内剂量(高达220 mmol的钆双胺),肾病发生率为40%。作者出于几个原因不鼓励在DSA中使用钆。(a) 不存在比较等衰减浓度和剂量下基于钆的造影剂和碘化造影剂肾毒性作用的随机研究。(b) 基于钆的造影剂是高渗的,这是肾血管造影后造影剂诱导的肾病的致病因素,其渗透压是血浆的两到七倍。与基于钆的造影剂等衰减的碘化造影剂浓度可制成等渗的。(c) 体外测量表明,在DSA常用的70 - 90 kV范围内,0.5 mol/L的钆螯合物与每毫升60 - 80 mg碘的衰减程度相同。因此,50 mL 0.5 mol/L的钆螯合物(在80 kg的人中约为0.3 mmol/kg)与碘化造影剂中3 - 4 g碘的剂量衰减程度相同(例如,60 - 80 mg I/mL的50 mL碘海醇或300 mg I/mL的10 - 13 mL)。(d) 通过结合这些关于衰减的数据和小鼠毒性研究的结果,在70 kV DSA时,钆螯合物的一般毒性可能比等衰减剂量的碘化造影剂高6至25倍。因此,作者认为,在DSA的等衰减剂量下,现代碘化造影剂对身体的毒性负荷应低于目前可用的钆螯合物。