The US Food and Drug Administration has okayed removal of the contraindication for use during CT and MRI under certain conditions.
The US Food and Drug Administration has cleared the Abbott Libre 2 and 3 continuous glucose monitoring sensors for use during most imaging procedures, including MRI under certain specifications.
The sensors may also now be worn during CT or x-ray procedures. Previously, they were contraindicated for use during MRI, CT, and high-frequency electrical heat treatment due to concern that the exposure could potentially damage the sensor and lead to incorrect readings. Those contraindications remain in place for the older FreeStyle Libre 14-day Flash Glucose Monitoring System, and the diathermy contraindication remains for all models.
“MRI protocols are evolving and can vary, so it’s best if people with diabetes speak to their healthcare provider or the radiology department prior to an MRI scan to ensure the conditions meet the safety requirements as stated in the labeling,” Anila Bindal, MD, associate medical director for Abbott Diabetes Care business, toldPatients should also be instructed to leave their phones and the sensor reader outside the exam room.
Continuous Glucose Monitoring (CGM) CGM Computed Tomography CT Ct Scan Scan U.S. Food And Drug Administration United States Food And Drug Administration Fda Deep Heat Diathermy Washington DC Washington - District Of Columbia Washington Pelvis Breastbone X-Ray Xray
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