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The Alara Metriscan phalangeal densitometer: evaluation and triage thresholds.

机译:Alara Metriscan指骨密度仪:评估和分类阈值。

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摘要

The Metriscan (Alara Inc, CA) is a compact digital radiographic absorptiometry device capable of determining phalangeal bone mineral density in arbitrary units (BMD(au)) from the second phalanges of the middle three digits. We have examined the utility and the in vitro and in vivo performances of the Metriscan, and established triage thresholds based on the UK's National Osteoporosis Society guidelines on peripheral densitometry. 170 white female participants (70 osteoporotic and 100 non-osteoporotic at the hip or spine) aged between 55 years and 70 years were recruited from patients attending for routine dual X-ray absorptiometry (DXA) examination. All participants underwent two scans of the non-dominant hand (with repositioning) and one of the dominant hand. An additional 10 participants were excluded owing to finger or hand deformities. Radiation exposure to the patient per scan was <0.1 microSv, and a controlled area of 1 m was established around the device. Phantom-based in vitro short-term precision (%CV) was 0.17% without, and 0.22% with, repositioning. Long-term in vitro precision was 0.31% over a 6-month period. In vivo short-term precision was 1.42% for the group as a whole, and 1.30% and 2.23% for the non-osteoporotic and osteoporotic groups, respectively. Triage thresholds for reassurance/referral or referral/treatment were 54.30 BMD(au) and 46.89 BMD(au), respectively, for the non-dominant hand, and 55.02 BMD(au) and 48.73 BMD(au) for the dominant hand. The dominant side proved superior for triage purposes, with a triage referral rate of 44%, compared with 48% for the non-dominant hand. The Metriscan is suitable for use on post-menopausal women in a community-based setting preferably in a triage role as an adjunct to axial BMD.
机译:Metriscan(Alara Inc,CA)是一款紧凑的数字放射吸收仪,能够从中三位数的第二个指骨以任意单位(BMD(au))确定指骨的骨密度。我们已经检查了Metriscan的效用以及体外和体内性能,并根据英国国家骨质疏松学会外周密度测定法指南建立了分类阈值。招募了年龄在55岁至70岁之间的170名白人女性参与者(70例骨质疏松症患者和100例髋部或脊椎非骨质疏松症患者)进行常规双X线骨密度仪(DXA)检查的患者。所有参与者均接受了非优势手的两次扫描(重新定位)和优势手的其中之一。由于手指或手畸形,另外有10名参与者被排除在外。每次扫描对患者的辐射暴露小于0.1 microSv,并且在设备周围建立了1 m的受控区域。基于幻影的体外短期精度(%CV)在未重新定位的情况下为0.17%,在重新定位的情况下为0.22%。六个月内的长期体外精密度为0.31%。整个组的体内短期精确度分别为1.42%和非骨质疏松组和骨质疏松组的1.30%和2.23%。保证/转诊或转诊/治疗的分流阈值对于非优势手分别为54.30 BMD(au)和46.89 BMD(au),对于优势手为55.02 BMD(au)和48.73 BMD(au)。占优势的一面在分流方面被证明是优越的,其分流推荐率为44%,而非占优手为48%。 Metriscan适用于以社区为基础的绝经后妇女,最好以分流的方式作为轴向BMD的辅助手段使用。

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