#VisualAbstract: Risk of Nephrogenic Systemic Fibrosis in Patients With Stage 4 or 5 Chronic Kidney Disease Receiving a Group II Gadolinium-Based Contrast Agent

1. In a systematic review and meta-analysis of the use of group II (low risk) gadolinium-based contrast agents (GBCA) for MRI in patients with stage 4 and 5 chronic kidney disease (CKD), there were no reported cases of nephrogenic systemic fibrosis (NSF).

2. The use of gadobenate dimeglumine, which is partially eliminated through hepatic metabolism, had the greatest number of reported patients and therefore the best estimated safety profile.

Evidence Rating Level: 2 (Good)    

Study Rundown: Nephrogenic systemic fibrosis is a rare complication of gadolinium exposure and risk is linked to decreased gadolinium renal clearance. Original guidelines recommended against exposure to GBCA if the creatinine clearance is less than 30 ml/min/1.73m2. However, the use of newer formulations of (group II) GBCA has reduced the risk of NSF and the avoidance of contrast in patients with renal insufficiency may lead to indirect harms of delayed or missed diagnosis. The current study is a systematic review and meta-analysis which evaluated the incidence and risk of NSF in patients with stage 4 and 5 CKD receiving group II GBCA. The study found that in a pooled sample of 4931 patients there was no reported cases of NSF and the upper 95% confidence interval limit for incidence was 0.07%. Gadobenate dimeglumine, an agent with some hepatic clearance, had the largest number of patients studied and therefore the greatest safety margin.

The main strengths of the meta-analysis include the large sample size, and low estimated bias in most domains. The main limitations of the study include the reliance on predominantly retrospective data with unblinded assessments, and the lack of universal standard for the diagnosis of NSF.

Click to read the study in JAMA Internal Medicine

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