Optical coherence tomography angiography measures blood pulsatile waveforms at variable tissue depths.

backgroundPhotoplethysmography (PPG) is routinely used to detect the blood pulse signal from skin tissue beds in clinics. However, the origin of the PPG signal remains controversial. The purpose of this study is to explore optical coherence tomography angiography (OCTA) to indicate pulsatile waveforms in the papillary plexus and dermal plexus separately under different hand elevations.

methodOptical microangiography (OMAG) algorithm was used to obtain a 3D OCTA signals, from which the depth-resolved pulsatile blood flow signals were extracted from different skin vascular plexus. The systolic amplitude, crest time, and delta T were measured from the OCTA pulsatile signals when the hand was placed at the positions of 50 cm below, 0 cm, and 50 cm above the heart level.

resultsThe pulse signal integrated from all the depths has a similar waveform to that of the PPG and showed the same morphological change at different hand elevations. The pulsatile patterns from the papillary plexus and dermal plexus showed distinct morphological changes at different local blood pressure. Less amplitude difference was found from papillary plexus comparing to that of the dermal plexus. Crest time was found in an increasing trend in the OCTA pulsatile waveform from both plexuses when the arm was raised from the position below to above the heart level. In contrast, a decreasing trend of Delta T was detected in the dermal pulsatile but was not observed from that of the papillary plexus, indicating that vascular resistance associated with the arm elevations does not necessarily have the same effect on the two plexuses.

conclusionsOCTA can provide depth-resolved pulsatile waveforms within different microvascular plexus within tissue skin beds. This technique could open doors to understanding the mechanisms of how blood flow changes at different skin circulatory plexus.