MRI with Contrast in a Patient with eGFR of 59 mL/min/1.73m²
A patient with an eGFR of 59 mL/min/1.73m² can safely undergo an MRI with gadolinium-based contrast agents, as this level of renal function is not associated with significant risk of nephrogenic systemic fibrosis (NSF). 1
Risk Assessment Based on eGFR
The patient's laboratory values show:
- eGFR: 59 mL/min/1.73m² (mildly reduced)
- Creatinine: 1.27 mg/dL (at upper limit of normal range)
- BUN: 23 mg/dL (normal)
Risk Stratification:
- eGFR > 45 mL/min/1.73m²: Low risk for contrast-related complications 1, 2
- eGFR 30-45 mL/min/1.73m²: Intermediate risk
- eGFR < 30 mL/min/1.73m²: High risk for NSF 1, 2, 3
Recommendations for This Patient
Proceed with contrast-enhanced MRI
Contrast agent selection
Dosing considerations
Important Precautions
Monitor for hypersensitivity reactions: Although rare (less than 0.01% for serious reactions), ensure availability of personnel trained and medications to treat potential reactions 2, 3
Patient education: Inform the patient about potential mild side effects such as nausea, headache, and injection site reactions 3
Hydration status: Ensure the patient is well-hydrated before and after the procedure 4
Alternative Options (If Needed)
If there are additional concerns about using contrast:
Non-contrast MRI techniques: Consider unenhanced MRI protocols if clinically appropriate for the diagnostic question 5
Alternative imaging modalities: Ultrasound with contrast agents can be safely used in patients with kidney disease if MRI is contraindicated for other reasons 4
Clinical Perspective
The historical concern about gadolinium contrast in patients with mild renal impairment has been significantly reduced by newer evidence. The ACR Manual on Contrast Media recognizes eGFR of 30 mL/min/1.73m² as the threshold with the greatest level of evidence for NSF risk 1. With an eGFR of 59 mL/min/1.73m², this patient falls into a low-risk category.
Studies have demonstrated that MRI with gadolinium contrast (at 0.2 mmol/kg) does not cause significant changes in renal function tests or acute kidney injury biomarkers in high-risk patients 6, further supporting the safety of this procedure in a patient with only mildly reduced renal function.