Km. Khan et al., INSTRUMENT PERFORMANCE IN BONE-DENSITY TESTING AT 5 AUSTRALIAN CENTERS, Australian and New Zealand Journal of Medicine, 27(5), 1997, pp. 526-530
Aims: To assess the in vitro precision and accuracy of bone mineral de
nsitometry (BMD) within and between locations at five Australian centr
es. Methods: Using a multicentre reliability study the accuracy and sh
ort-and long-term precision of dual-energy X-ray absorptiometry (DXA)
in vitro was compared on five instruments. Measures were performed usi
ng pencil beam mode on four Hologic QDR-2000 densitometers and one Hol
ogic QDR-1000/W (Hologic Inc, Waltham, MA). Results: Short-term precis
ion of bone mineral density measurement was less than 0.5% for spine p
hantoms (n=10 for each centre, mean intrasite coefficient of variation
[CV] 0.39+/-0.09% [SD]) and for hip phantoms (n=10 for each centre, m
ean intrasite coefficient of variation [CV] 0.34+/-0.10% [SD]). Betwee
n-centre measurement (n=10 for each phantom) of a single spine phantom
and a single hip phantom (specified mineral contents - 58.5 g and 38.
6 g, respectively) revealed ranges of bone mineral content of 57.7-58.
1 g (all-point CV=0.52%) and 37.1-37.8 g (all-point CV=0.70%), respect
ively. When results from pairs of machines were compared there were st
atistically different mean BMD results for the majority of the ten pos
sible pairings for both spine and hip measurements. Each study centre
measured in vitro stability of phantom BMD measurements over a one yea
r period (n=45-283 median 157 for spine; and n=0-262, median 38, for h
ip); CVs ranged from 0.38 to 0.53% for the spine measurements and from
0.38 to 0.54% for the hip measurements. The mean all-point accuracy o
f the spine phantom measurements was 99.1% and the hip phantom measure
ments was 96.7%. Conclusions: Across a number of instruments DXA demon
strates in vitro all-point precision of 0.5% for the spine phantom and
0.7% for the hip phantom. The instrument demonstrates accuracy of gre
ater than 99% at the spine and 96% at the hip. This finding has clinic
al, research and quality control implications.