Abstract

Combining near-infrared spectroscopy (NIRS) and diffuse correlation spectroscopy (DCS) allows for quantifying cerebral blood volume, flow, and oxygenation changes continuously and non-invasively. As recently shown, the DCS pulsatile cerebral blood flow index () can be used to quantify critical closing pressure (CrCP) and cerebrovascular resistance (). Although current DCS technology allows for reliable monitoring of the slow hemodynamic changes, resolving pulsatile blood flow at large source-detector separations, which is needed to ensure cerebral sensitivity, is challenging because of its low signal-to-noise ratio (SNR). Cardiac-gated averaging of several arterial pulse cycles is required to obtain a meaningful waveform. Taking advantage of the high SNR of NIRS, we demonstrate a method that uses the NIRS photoplethysmography (NIRS-PPG) pulsatile signal to model DCS , reducing the coefficient of variation of the recovered pulsatile waveform () and allowing for an unprecedented temporal resolution (266Hz) at a large source-detector separation (). In 10 healthy subjects, we verified the quality of the NIRS-PPG during common tasks, showing high fidelity against ( ). We recovered CrCP and at 0.25Hz, times faster than previously achieved with DCS. NIRS-PPG improves DCS SNR, reducing the number of gate-averaged heartbeats required to recover CrCP and .

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