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Cranial MR imaging with Gd-DTPA in neonates and young infants: preliminary experience
1Department of Radiology, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, NC 27103.
Insights
Gadolinium diethylenetriaminepentaacetic acid (DTPA) contrast is safe and effective for infant MRI, revealing abnormalities in 27% of cases. Enhanced imaging in newborns may offer a prolonged diagnostic window due to slower clearance.
Area of Science:
- Neuroradiology
- Pediatric Imaging
- Pharmacology
Background:
- Gadopentetate dimeglumine (Gd-DTPA) is a contrast agent used in magnetic resonance (MR) imaging.
- Its use in neonates and young infants (less than 6 weeks old) requires safety and efficacy evaluation.
- Understanding contrast enhancement patterns in this age group is crucial for accurate diagnosis.
Purpose of the Study:
- To assess the preliminary safety and efficacy of gadopentetate dimeglumine in neonates and young infants.
- To compare contrast enhancement patterns and time courses in infants with those in older children and adults.
- To determine the diagnostic utility of Gd-DTPA in routine cranial MR imaging for this population.
Main Methods:
- Prospective administration of gadopentetate dimeglumine (0.1 mmol/kg) to 15 neonates and young infants.
- Routine cranial MR imaging performed before and after contrast administration.
- Evaluation of image quality, enhancement patterns, and time course of contrast material.
Main Results:
- Gd-DTPA enhanced MR images revealed significant abnormalities in 4 out of 15 patients (27%) not visible on pre-contrast scans.
- The standard adult dose provided bright enhancement of normal intracranial structures.
- Vivid contrast enhancement persisted for several hours due to reduced glomerular filtration and renal clearance rates in newborns.
Conclusions:
- Gadopentetate dimeglumine administration is safe and effective for cranial MR imaging in neonates and young infants.
- Gd-DTPA enhances diagnostic yield by revealing abnormalities missed on non-contrast imaging.
- The prolonged enhancement in infants suggests a potentially extended imaging window for diagnosis.
Abstract:
Gadopentetate dimeglumine (gadolinium diethylenetriaminepentaacetic acid [DTPA]) was prospectively administered to 15 consecutive neonates and young infants (less than 6 weeks old) referred for routine cranial magnetic resonance (MR) imaging. The goals of the study were (a) to provide preliminary safety and efficacy data concerning the use of this drug in neonates and (b) to determine whether the patterns and time course of normal contrast material enhancement were similar to those seen in older children and adults. Gd-DTPA-enhanced MR images revealed significant abnormalities not seen on the MR images obtained before administration of contrast material in four (27%) of 15 patients. The adult dose (0.1 mmol/kg) provided bright enhancement of normal intracranial structures. Because of significantly reduced glomerular filtration and renal clearance rates in newborns, vivid contrast enhancement of normal structures was seen to persist for several hours after injection. A prolonged window of time for imaging may therefore exist for neonates and young infants.
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