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Detectors can reduce doses by up to 40 percent.
February 19, 2015
By: Michael Barbella
Managing Editor
The U.S. Food and Drug Administration (FDA) has cleared Agfa Healthcare’s DXD Imaging package, which includes cesium bromide needle-based image plates for computed radiography (CR) devices and cesium iodide detectors for digital radiography (DR) units.
Already, Cesium-based detectors have been used in examinations for over 60 million people worldwide, Agfa claims. With the launch of Agfa HealthCare’s Fast Forward program, hospitals can upgrade from traditional CR to Cesium-based CR or DR, extending the potential for dose reduction to more than 100,000 patients each month. Zwanger-Pesiri, currently one of the largest non-hospital based radiology practices in the United States, conducted its own study to verify the dose reduction capabilities of Agfa HealthCare’s solution. The study aimed to determine whether Agfa HealthCare’s DX-D 300 DR system required less exposure and patient dose compared to two other systems in use at Zwanger-Pesiri. The results showed that, while the amount of dose reduction varied depending on the type of exam, the average dose in most cases was more than 40 percent lower with the Agfa HealthCare system, while still providing high quality. “We want to ensure that any hospital or private practice that is focused on image quality can benefit from the advantages of the NIP plates,” said Kuitenbrouwer. “With our Fast Forward program, hospitals can add CR with NIP to DR rooms as a backup that provides the same image quality and dose settings, and/or use a cassette-based system for special exams such as sunrise X-rays.”
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