Bahrainwala Jehan Z, Leonberg-Yoo Amanda K, Rudnick Michael R
Renal-Electrolyte and Hypertension Division, Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Semin Dial. 2017 Jul;30(4):290-304. doi: 10.1111/sdi.12593. Epub 2017 Apr 5.
Contrast exposure in a population with chronic kidney disease (CKD) requires additional consideration given the risk of contrast-induced nephropathy (CIN) after exposure to iodinated contrast as well as systemic injury with exposure to gadolinium-based contrast agents (GBCA). Strategies to avoid CIN, and manage patients after exposure, including extracorporeal removal of contrast media, may differ among an advanced CKD population as compared to a general population. There is strong evidence to support the use of isotonic volume expansion and the lowest dose of low-osmolar or iso-osmolar contrast media possible to decrease CIN. The current literature on other newer prophylactic strategies such as statins, remote ischemic preconditioning, discontinuation of renin angiotensin aldosterone system (RAAS) blockade, and RenalGuard is limited thus these strategies cannot currently be recommended as routine prophylaxis for CIN. The use of extracorporeal removal of contrast agents as prophylaxis to reduce CIN has been the subject of multiple studies; however, data do not support a beneficial effect in reduction in CIN. Immediate removal of contrast by dialysis in a maintenance dialysis population is also not recommended, unless an individual's cardiopulmonary status is dependent on strict volume management. In patients with reduced renal function, GCBA exposure increases the risk of NSF. In patients with AKI, CKD stage 3 or greater (eGFR <30 ml/minute/1.73 m ), or patients on dialysis, we do not recommend the use of GBCA and alternative imaging modalities should be considered. If patients absolutely need magnetic resonance imaging with GBCA, we recommend the use of the lowest dose possible of the newer macrocylic, ionic agents (gadoterate meglumine) as well as immediate postprocedural HD in patients already on HD or peritoneal dialysis or with stage 5 CKD and with a functioning dialysis access already in place.
鉴于暴露于碘化造影剂后发生造影剂肾病(CIN)的风险以及暴露于钆基造影剂(GBCA)后的全身损伤风险,在慢性肾脏病(CKD)人群中进行造影剂暴露需要额外考虑。与普通人群相比,晚期CKD人群中避免CIN以及暴露后管理患者的策略(包括体外清除造影剂)可能有所不同。有强有力的证据支持使用等渗容量扩张以及尽可能低剂量的低渗或等渗造影剂来降低CIN。关于其他较新的预防策略(如他汀类药物、远程缺血预处理、停用肾素血管紧张素醛固酮系统(RAAS)阻滞剂和RenalGuard)的现有文献有限,因此目前这些策略不能作为CIN的常规预防措施推荐。使用体外清除造影剂作为预防措施以降低CIN已成为多项研究的主题;然而,数据并不支持其在降低CIN方面有有益效果。除非个体的心肺状态依赖于严格的容量管理,否则也不建议在维持性透析人群中通过透析立即清除造影剂。在肾功能减退的患者中,接触GBCA会增加发生 NSF 的风险。对于急性肾损伤(AKI)患者、CKD 3期及以上(估算肾小球滤过率(eGFR)<30 ml/分钟/1.73 m²)患者或透析患者,我们不建议使用GBCA,应考虑使用替代成像方式。如果患者绝对需要使用GBCA进行磁共振成像,我们建议在已经进行血液透析(HD)或腹膜透析的患者、5期CKD且已有功能良好的透析通路的患者中,尽可能使用最低剂量的新型大环离子型制剂(钆喷酸葡胺),并在检查后立即进行HD。