GE Healthcare Prodigy User Manual
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1
Prodigy required no user intervention 86% of the time, compared with only 53% for Hologic QDR. Steinberg DM. Comparison
of spine scan autoanalysis using Hologic and GE Lunar fan-beam bone densitometers. ISCD Abstract, 2003.
2
Simonelli C, Del Rio L, Binkley N. Comparison of spine BMD measurements from DXA with and without leg elevation. Abstract
published J Bone Miner Res, 2004.
3
InSite may not be available in all markets.
4
Comparison of patient dose using typical modes at most common skeletal sites. GE Prodigy and Hologic measurements
are in micro-Grays (µGy) to be directly comparable. Information collected from Hologic Discovery™ Series and Explorer™
Technical Specifications Manual, December 2003, and GE Lunar Safety Information and Technical Specifications, October 2008.
Compared to other X-ray procedures, the radiation dose from DXA procedures is relatively very low. DXA technology requires
minimal radiation to generate measurements of bone health.
5
Hunt SM, et al. Changing Bone Densitometers in Clinical Practice: Effect on Precision Error. Presented at the American Society
for Bone and Mineral Research Annual Meeting, September 23 to 27, 2005, Nashville, TN, USA.
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Lunar Product Division Americas
GE Healthcare Lunar
Global Headquarters
P.O. Box 7550
Madison, WI 53707-7550
T: +1-800-535-7339
F: +1-608-223-2482
Lunar Product Division
Europe, Middle-East & Africa
GE Healthcare Lunar
Kouterveldstraat 20
B-1831 Diegem, Belgium
T: +32-2-7197217
F: +32-2-7197359
Lunar Densitometry
Asia & Pacific Headquarters
GE Healthcare Lunar
3/F GE China Technology Park
No. 1 Hua Tuo Road
Shanghai 201203, China
T: +86-21-38777888 (Ext. 60128 or 60480)
F: +86-21-38777451