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肝移植后患者静脉内钆增强 MRI 的肾脏安全性。

Renal Safety of Intravenous Gadolinium-enhanced MRI in Patients Following Liver Transplantation.

机构信息

Department of Medicine, Emory University School of Medicine, Atlanta, GA.

Department of Surgery, Emory University School of Medicine, Atlanta, GA.

出版信息

Transplantation. 2019 Jun;103(6):e159-e163. doi: 10.1097/TP.0000000000002678.

DOI:10.1097/TP.0000000000002678
PMID:30801544
Abstract

BACKGROUND

Intravenous contrast-enhanced imaging is invaluable in diagnosing pathology following liver transplantation. Given the potential risk of contrast nephropathy associated with iodinated computed tomography contrast, alternate contrast modalities need to be examined, especially in the setting of renal insufficiency. The purpose of this study was to examine the renal safety of MRI with gadolinium following liver transplantation.

METHODS

The study involved a retrospective analysis of 549 cases of abdominal MRI with low-dose gadobenate dimeglumine in liver transplant recipients at a single center. For each case, serum creatinine values before and after the MRI were compared. In addition, cases were analyzed for the development of nephrogenic systemic fibrosis.

RESULTS

Pre-MRI creatinine values ranged from 0.32 to 6.57 mg/dL (median, 1.28 g/dL), with 191 cases having values ≥1.5 mg/dL (median, 1.86 g/dL). A comparison of the pre- and post-MRI creatinine values showed no significant difference, including those patients with pre-MRI values ≥1.5 mg/dL (mean change of -0.04 [95% confidence interval, -0.07 to -0.01; P = 0.004]). No cases of nephrogenic systemic fibrosis were noted.

CONCLUSIONS

Our findings suggest that, irrespective of baseline renal function, MRI with gadobenate dimeglumine is a nonnephrotoxic imaging modality in liver transplant recipients. Importantly, this intravenous contrast-enhanced imaging modality can be considered in those posttransplant patients who have a contraindication to computed tomography contrast due to renal insufficiency.

摘要

背景

静脉内对比增强成像对于诊断肝移植后的病理学具有重要价值。由于与碘造影剂 CT 相关的对比剂肾病的潜在风险,需要检查其他对比剂方式,尤其是在肾功能不全的情况下。本研究旨在检查肝移植后使用钆喷酸葡胺进行 MRI 的肾脏安全性。

方法

该研究对单一中心的 549 例肝移植受者进行了腹部 MRI 低剂量钆贝葡胺检查,回顾性分析了这些病例。对于每例患者,比较了 MRI 前后的血清肌酐值。此外,还对肾源性系统纤维化的发生情况进行了分析。

结果

MRI 前的肌酐值范围为 0.32 至 6.57mg/dL(中位数为 1.28mg/dL),191 例患者的肌酐值≥1.5mg/dL(中位数为 1.86mg/dL)。MRI 前后的肌酐值比较无显著差异,包括 MRI 前肌酐值≥1.5mg/dL 的患者(平均变化值为-0.04[95%置信区间,-0.07 至 -0.01;P = 0.004])。未发现肾源性系统纤维化病例。

结论

我们的研究结果表明,无论基线肾功能如何,钆喷酸葡胺 MRI 都是肝移植受者的一种非肾毒性影像学检查方法。重要的是,对于因肾功能不全而对 CT 造影剂有禁忌证的移植后患者,可以考虑使用这种静脉内对比增强成像方式。

相似文献

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Renal Safety of Intravenous Gadolinium-enhanced MRI in Patients Following Liver Transplantation.肝移植后患者静脉内钆增强 MRI 的肾脏安全性。
Transplantation. 2019 Jun;103(6):e159-e163. doi: 10.1097/TP.0000000000002678.
2
Renal safety of intravenous gadolinium-enhanced magnetic resonance imaging in patients awaiting liver transplantation.等待肝移植患者静脉注射钆增强磁共振成像的肾脏安全性
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Evaluation of the incidence of nephrogenic systemic fibrosis in patients with moderate renal insufficiency administered gadobenate dimeglumine for MRI.对中度肾功能不全患者静脉注射钆贝葡胺进行磁共振成像(MRI)检查时发生肾源性系统性纤维化的发生率评估。
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Nephrogenic systemic fibrosis: change in incidence following a switch in gadolinium agents and adoption of a gadolinium policy--report from two U.S. universities.肾源性系统性纤维化:钆造影剂更换和采用钆造影剂政策后发病率的变化——来自两所美国大学的报告。
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Gadobenate Dimeglumine Administration and Nephrogenic Systemic Fibrosis: Is There a Real Risk in Patients with Impaired Renal Function?钆贝葡胺给药与肾源性系统性纤维化:肾功能受损患者存在真实风险吗?
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引用本文的文献

1
Risk for Nephrogenic Systemic Fibrosis After Exposure to Newer Gadolinium Agents: A Systematic Review.接触新型钆剂后发生肾源性系统性纤维化的风险:一项系统评价
Ann Intern Med. 2020 Jul 21;173(2):110-119. doi: 10.7326/M20-0299. Epub 2020 Jun 23.