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Volume 13, Issue 3, Pages 292-300 (July 2010)


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Clinical Evaluation of a Phalangeal Bone Mineral Density Assessment System

Rajesh PatelCorresponding Author Information1email address, Glen M. Blake2, Elleny Panayiotou2, Ignac Fogelman2

Received 21 December 2009; received in revised form 11 March 2010; accepted 3 April 2010. published online 31 May 2010.

Abstract 

Because osteoporosis is common and usually managed in primary care, there is a requirement for cheap and convenient methods of measuring bone mineral density (BMD). AccuDEXA (Lone Oak Medical Technologies, Doylestown, PA) is a tabletop dual-energy X-ray absorptiometry (DXA) device that performs BMD measurements of the hand in the middle phalanges of the third finger. The aims of this study were to (1) evaluate the use of AccuDEXA in UK women; (2) investigate the concordance between AccuDEXA T-scores and DXA T-scores for central (spine and hip) sites; (3) investigate the comparative response of AccuDEXA measurements to clinical risk factors for osteoporosis. Measurements of phalangeal and central BMD were performed in 620 women referred by their family doctors for bone densitometry (group 1) and 159 healthy female volunteers (group 2). For 65 women in group 2, aged 39yr or younger, the mean Z-scores for AccuDEXA and the central sites calculated from US reference ranges were consistent with the expected value of 0, whereas for the 62 group 2 women, aged 50yr or older, the mean Z-scores for AccuDEXA and the central sites were in the range 0.4–0.7 and were statistically significantly different from 0. In both group 1 and group 2, the AccuDEXA T-scores in older and younger women were systematically higher than those in the central sites by up to 1 unit. Of the 157 women aged 50yr or older, with osteoporosis, based on their central DXA results, only 34 (22%) had an AccuDEXA T-score less than or equal to −2.5, whereas 76 (48%) had osteopenia and 47 (30%) were normal based on their AccuDEXA T-scores. When assessed by the effect of clinical risk factors on Z-scores, both AccuDEXA and central BMD were affected to a similar extent. We conclude that the conventional World Health Organisation T-score criteria for the diagnosis of osteoporosis should not be applied to AccuDEXA measurements in UK women. Clinical risk factors for low BMD were found to affect AccuDEXA measurements to a similar extent as central BMD measurements. AccuDEXA measurements could, therefore, provide an alternative method for identifying individuals with low bone mass, provided care is taken in interpreting T-scores, perhaps, through the use of device-specific thresholds.

1 Department of Biosurgery and Surgical Technology, Division of Surgery, Academic Bone Densitometry Unit, Imperial College London, London, UK

2 Osteoporosis Screening and Research Unit, King's College London, Guy's Campus, London, UK

Corresponding Author InformationAddress correspondence to: Rajesh Patel, PhD, Department of Biosurgery and Surgical Technology, Division of Surgery, Academic Bone Densitometry Unit, Imperial College Faculty of Medicine, Charing Cross Hospital, Fulham Palace Road, London W6 8RF, United Kingdom.

PII: S1094-6950(10)00161-7

doi:10.1016/j.jocd.2010.04.001


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