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Investigating optical path and differential pathlength factor in reflectance photoplethysmography for the assessment of perfusion

机译:研究反射光体积描记法中的光路和微分光程长因子以评估灌注

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Photoplethysmography (PPG) is an optical noninvasive technique with the potential for assessing tissue perfusion. The relative time-change in the concentration of oxyhemoglobin and deoxyhemoglobin in the blood can be derived from DC part of the PPG signal. However, the absolute concentration cannot be determined due to the inadequate data on PPG optical paths. The optical path and differential pathlength factor (DPF) for PPG at red (660 nm) and infrared (880 nm) wavelengths were investigated using a heterogeneous Monte Carlo model of the human forearm. Using the simulated DPFs, the absolute time-change in concentrations were determined from PPG signals recorded from the same tissue site. Results were compared with three conditions of approximated DPFs. Results showed the variation of the optical-path and DPF with different wavelengths and source-detector separations. Approximations resulted in significant errors, for example, using NIRS DPF in PPG led to "cross talk" of -0.4297 and 0.060 and an error of 15.16% to 25.18%. Results confirmed the feasibility of using the PPG (DC) for the assessment of tissue perfusion. The study also identified the inappropriateness of the assumption that DPF is independent of wavelength or source-detector separations and set the platform for further studies on investigating optical pathlengths and DPF in PPG.
机译:光电容积描记术(PPG)是一种光学无创技术,具有评估组织灌注的潜力。血液中氧合血红蛋白和脱氧血红蛋白浓度的相对时间变化可以从PPG信号的DC部分得出。然而,由于PPG光路上的数据不足,无法确定绝对浓度。使用人类前臂的异质蒙特卡洛模型研究了PPG在红色(660 nm)和红外(880 nm)波长下的光路和差分光程长度因子(DPF)。使用模拟的DPF,从相同组织部位记录的PPG信号确定浓度的绝对时间变化。将结果与三种近似DPF的条件进行比较。结果表明,光程和DPF随波长和源-探测器间隔的变化而变化。逼近会导致重大错误,例如,在PPG中使用NIRS DPF会导致-0.4297和0.060的“串扰”,以及15.16%至25.18%的错误。结果证实了使用PPG(DC)评估组织灌注的可行性。该研究还确定了DPF与波长或源-检测器分离无关的假设的不恰当性,并为进一步研究PPG中的光程和DPF奠定了平台。

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