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基于数字频域漫反射光学光谱的实时手持式探头跟踪与图像形成。

Real-Time Handheld Probe Tracking and Image Formation Using Digital Frequency-Domain Diffuse Optical Spectroscopy.

出版信息

IEEE Trans Biomed Eng. 2021 Nov;68(11):3399-3409. doi: 10.1109/TBME.2021.3072036. Epub 2021 Oct 19.

Abstract

OBJECTIVE

Frequency-domain diffuse optical spectroscopic imaging (FD-DOS) is a non-invasive method for measuring absolute concentrations of tissue chromophores such as oxy- and deoxy-hemoglobin in vivo. The utility of FD-DOS for clinical applications such as monitoring chemotherapy response in breast cancer has previously been demonstrated, but challenges for further clinical translation, such as slow acquisition speed and lack of user feedback, remain. Here, we propose a new high speed FD-DOS instrument that allows users to freely acquire measurements over the tissue surface, and is capable of rapidly imaging large volumes of tissue.

METHODS

We utilize 3D monocular probe tracking combined with custom digital FD-DOS hardware and a high-speed data processing pipeline for the instrument. Results are displayed during scanning over the surface of the sample using a probabilistic Monte Carlo light propagation model.

RESULTS

We show this instrument can measure absorption and scattering coefficients with an error of 7% and 1% respectively, with 0.7 mm positional accuracy. We demonstrate the equivalence of our visualization methodology with a standard interpolation approach, and demonstrate two proof-of-concept in vivo results showing superficial vasculature in the human forearm and surface contrast in a healthy human breast.

CONCLUSION

Our new FD-DOS system is able to compute chromophore concentrations in real-time (1.5 Hz) in vivo.

SIGNIFICANCE

This method has the potential to improve the quality of FD-DOS image scans while reducing measurement times for a variety of clinical applications.

摘要

目的

频域漫射光学光谱成像(FD-DOS)是一种非侵入性方法,可测量组织色团(如氧合和脱氧血红蛋白)在体内的绝对浓度。FD-DOS 已在乳腺癌化疗反应监测等临床应用中得到验证,但仍存在一些挑战,如采集速度慢和缺乏用户反馈。在这里,我们提出了一种新的高速 FD-DOS 仪器,允许用户在组织表面自由采集测量,并能够快速成像大面积组织。

方法

我们利用 3D 单目探头跟踪技术,结合定制的数字 FD-DOS 硬件和高速数据处理管道来实现该仪器。在对样品表面进行扫描时,使用概率蒙特卡罗光传播模型显示结果。

结果

我们表明,该仪器可以以 7%和 1%的误差分别测量吸收和散射系数,具有 0.7 毫米的位置精度。我们证明了我们的可视化方法与标准插值方法具有等效性,并展示了两个体内初步结果,显示了人类前臂的浅表血管和健康人类乳房的表面对比度。

结论

我们的新型 FD-DOS 系统能够实时(1.5 Hz)计算体内色团浓度。

意义

该方法有可能在各种临床应用中提高 FD-DOS 图像扫描的质量,同时减少测量时间。

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