FDA Approves Glucose Monitoring Device for Children

However, device doesn't perform as well in children as in adults, FDA says.
However, device doesn't perform as well in children as in adults, FDA says.

U.S. Food and Drug Administration approval of the Dexcom G4 Platinum Continuous Monitoring System has been expanded to include children with diabetes aged 2 years to 17 years, the agency said.

Previously approved for adults only, the device constantly monitors the user's blood sugar, checking for dangerously high or low levels, the FDA said in a news release. An estimated 25.8 million people in the United States -- including 215,000 under age 20 -- have diabetes.

The externally-worn device continuously displays an estimate of blood glucose levels and the direction and rate of any changes in levels. It is intended to be worn by a single patient for up to seven days. The device requires a prescription and is meant to be used in addition to standard home glucose monitoring devices, not as a replacement.

The device was evaluated in clinical studies involving 176 people ages 2 to 17. The FDA warned the device's "performance in pediatric subjects was not as accurate as the performance of the same device in adults." Nonetheless, the agency said the device is still "effective for tracking and trending to determine patterns in glucose levels," and for warning users that their blood glucose levels had risen too high or fallen too low.

The system is produced by Dexcom Inc., based in San Diego.

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