Bone Densitometry Equipment

The Dept of Nuclear Medicine & Bone Densitometry provides a range of equipment for determining bone density. We now operate:

Reporting of all DXA scans uses the same report format, giving an indication of fracture risk, peer relationship, change since previous scan, and recommendations for followup and therapy. Reports are sent for upload to the hospital database, and from there to the statewide patient database. Reports are also available electronically to physicians via the IMVS.

Dual Energy X-Ray Absorptiometers (DXA)
The principle underlying DXA relies on measurement of the absorption of two different photon energies. By knowing how many photons are transmitted with respect to the number generated, the amount of bone mineral and soft tissue can be determined.

GE-LUNAR DPX-IQ

  • This pencil beam densitometer is used primarily for research and some routine scanning.
    This older generation was installed in October 2000, to supplement the DPX-L. The primary difference between this scanner and the new instruments is the software platform.
DPX-IQ and DPX-Pro in the DXA scanning suite
GE-LUNAR Prodigy Vision
  • The replacement for the GE-LUNAR Expert provides the same functionality, but utilises a mini-fan beam and high sensitivity Cadmium-Zinc-Telluride detectors, giving much lower radiation doses
  • The high throughput of this scanner ensures patient waiting times are kept to a minimum
GE-LUNAR Prodigy vision performing a lumbar spine scan
GE-LUNAR DPX-PRO
  • This is the next generation pencil beam densitometer, and the evolution of the DPX-IQ. It uses the same software as the Prodigy Vision, allowing excellent compatibility for all scans performed by the service.
    Two scanners are in operation:
    • at the RAH campus. This instrument replaced our original DPX-L (installed in 1990) scanner in mid 2005. The DPX-L and DPX-IQ databases have been imported into this system. Correlation studies of the two scanners show almost perfect agreement in the results, with minor discrepancies at the extremes of bone density.
    • in our Mobile Bone Densitometry caravan providing rural South Australia with modern DXA facilities for most of the year. The improved scan times, and full calibration compatibility with the RAH campus bone densitometers ensures all patients, regardless of location, have continuity of care.
      Patients previously scanned on the Hologic QDR-1000+ have had their scan results converted and added to the DPX-Pro database. All mobile scan data is available at the RAH.
Scanning in the mobile bone density unit
Hologic QDR-2000
  • This fan beam densitometer is used for research studies and replaces the QDR-1000+ (originally from the Mobile Bone Densitometry service) for routine animal research
 

 

Our DXA scanners capability and performance times are listed below:
Scanner
Scan type
DPX-IQ
DPX-Pro
DPX-Pro (mobile)
Prodigy Vision
Hologic
QDR-2000
Posterior/Anterior lumbar spine

3-4 minutes

1-2 minutes

1-2 minutes

1 minute

2-3 minutes
Femur (including Dual femur mode)

1 minute

2-3 minutes
Forearm

4-5 minutes

4-5 minutes

4-5 minutes

20 seconds

3-4 minutes
Lateral decubitus lumbar spine

6 minutes

6 minutes

6 minutes

90 seconds
lateral vertebral assessment (morphometry)

3-4 minutes
Orthopaedic (prosthesis monitoring)
Paediatric bone assessment
Hand for monitoring rheumatoid arthritis
Total body & body composition

20-30 minutes

15 minutes


4 minutes


5-7 minutes
Small animal/research mode
 

Ultrasound Absorptiometers
The principle underlying this method relies on the transmission of sound. The more dense and contiguous a material, the more sound will be transmitted. In addition, the speed at which the sound traverses the material is proportional to the contiguous nature of the material. These two properties can be used to assess the quality of bone. It is not a measurement of bone mineral.
Ultrasound measures of bone are poorly correlated to bone density, however, a number of research studies have shown that it may be a good predictor of fracture.
The limitation with this method is its poor reproducibility compared to DXA, making it unsuitable for monitoring therapy.

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