Systems and methods for physiological signal enhancement and biometric extraction using non-invasive optical sensors

A system and method for signal processing to remove unwanted noise components including: (i) wavelength-independent motion artifacts such as tissue, bone and skin effects, and (ii) wavelength-dependent motion artifact/noise components such as venous blood pulsation and movement due to various sources including muscle pump, respiratory pump and physical perturbation. Disclosed are methods, analytics, and their uses for reliable perfusion monitoring, arterial oxygen saturation monitoring, heart rate monitoring during daily activities and in hospital settings and for extraction of physiological parameters such as respiration information, hemodynamic parameters, venous capacity, and fluid responsiveness. The system and methods disclosed are extendable to include monitoring platforms for perfusion, hypoxia, arrhythmia detection, airway obstruction detection and sleep disorders including apnea.Board of Regents, University of Texas Syste

Methods and systems for extracting venous pulsation and respiratory information from photoplethysmographs

A system and method for separating a venous component and an arterial component from a red signal and an infrared signal of a PPG sensor is provided. The method uses the second order statistics of venous and arterial signals to separate the venous andarterial signals. After reliable separation of the venous and thearterial component signals,the component signals can be used for different purposes. In a preferred embodiment, the respiratory signal, pattern, and rate are extracted from the separated venous component and a reliable ?ratio of ratios? is extracted for SpO, using only the arterial component of the PPG signals. The disclosed embodiments enable real-time continuous monitoring of respiration pattern/rate and site-independentarterial oxygen saturation.Board of Regents, University of Texas Syste

Pulmonary Embolism

There have been a number of approaches taken to image the pulmonary vasculature. This unit presents basic protocols based on black blood spin echo and/or gradient echo techniques for detection of pulmonary embolisms and deep vein thrombosis. Bright blood magnetic resonance angiography (MRA), 2‐D time‐of‐flight (TOF), and 3‐D contrast‐enhanced MRA is also presented for visualizing the entire vascular tree. The parameters provided in this unit are acquired from Siemens 1.5T Vision Scanner. These parameters may need to be altered depending on the field strength and equipment manufacturer.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/145381/1/cpmia1301.pd

NASA contributions to - Cardiovascular monitoring

NASA contributions to cardiovasular monitorin

Aortic Aneurysm and Pseudoaneurysm Assessment

Although contrast angiography is still considered the “gold standard” for evaluation of the aorta and its major branches, Magnetic Resonance Angiography (MRA) has quickly gained popularity as an imaging tool for the assessment of the entire aorta. MRA serves as an alternative imaging modality that can be utilized in patients with impaired renal function and with allergies to iodinated contrast medium (iodinated contrast medium is required in contrast angiography and computed tomography, CT). The purpose of this unit is to present fundamental MRA techniques useful in the evaluation of the thoracic and abdominal aorta based on experience on a 1.5 T GE LX scanner.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/145258/1/cpmia1202.pd

Contrast‐Enhanced Renal MRA

The rapid growth of magnetic resonance imaging systems with enhanced gradient systems together with improved pulse sequences has improved the ability to image blood vessels with a spatial and temporal resolution similar to conventional X‐ray angiography. With patients who cannot undergo X‐ray angiography because they are contraindicated for iodinated contrast agents (having a creatinine level > 2.0), MRA (magnetic resonance angiography) has proven to be the modality of choice. Since the first demonstration of such contrast‐enhanced studies in the abdominal aorta, there have been continual improvements in methods due to improved hardware/software capabilities. This unit presents the MR protocols to image vascular morphology using contrast‐enhanced 3‐D‐MRA techniques. The pulse sequences described herein are based on the authors’ experience with a Siemens 1.5 T Vision and 1.5 T Sonata scanners, but are expected to be equally applicable to machines from other manufacturers.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/145369/1/cpmia2801.pd

Development of a novel diffuse correlation spectroscopy platform for monitoring cerebral blood flow and oxygen metabolism: from novel concepts and devices to preclinical live animal studies

New optical technologies were developed to continuously measure cerebral blood flow (CBF) and oxygen metabolism (CMRO2) non-invasively through the skull. Methods and devices were created to improve the performance of near-infrared spectroscopy (NIRS) and diffuse correlation spectroscopy (DCS) for use in experimental animals and humans. These were employed to investigate cerebral metabolism and cerebrovascular reactivity under different states of anesthesia and during models of pathological states. Burst suppression is a brain state arising naturally in pathological conditions or under deep general anesthesia, but its mechanism and consequences are not well understood. Electroencephalography (EEG) and cortical hemodynamics were simultaneously measured in rats to evaluate the coupling between cerebral oxygen metabolism and neuronal activity in the burst suppressed state. EEG bursts were used to deconvolve NIRS and DCS signals into the hemodynamic and metabolic response function for an individual burst. This response was found to be similar to the stereotypical functional hyperemia evoked by normal brain activation. Thus, spontaneous burst activity does not cause metabolic or hemodynamic dysfunction in the cortex. Furthermore, cortical metabolic activity was not associated with the initiation or termination of a burst. A novel technique, time-domain DCS (TD-DCS), was introduced to significantly increase the sensitivity of transcranial CBF measurements to the brain. A new time-correlated single photon counting (TCSPC) instrument with a custom high coherence pulsed laser source was engineered for the first-ever simultaneous measurement of photon time of flight and DCS autocorrelation decays. In this new approach, photon time tags are exploited to determine path-length-dependent autocorrelation functions. By correlating photons according to time of flight, CBF is distinguished from superficial blood flow. Experiments in phantoms and animals demonstrate TD-DCS has significantly greater sensitivity to the brain than existing transcranial techniques. Intracranial pressure (ICP) modulates both steady-state and pulsatile CBF, making CBF a potential marker for ICP. In particular, the critical closing pressure (CrCP) has been proposed as a surrogate measure of ICP. A new DCS device was developed to measure pulsatile CBF non-invasively. A novel method for estimating CrCP and ICP from DCS measurement of pulsatile microvascular blood flow in the cerebral cortex was demonstrated in rats.2018-03-08T00:00:00

Magnetic Resonance Imaging of Neural and Pulmonary Vascular Function: A Dissertation

Magnetic resonance imaging (MRI) has emerged as the imaging modality of choice in a wide variety experimental and clinical applications. In this dissertation, I will describe novel MRI techniques for the characterization of neural and pulmonary vascular function in preclinical models of disease. In the first part of this dissertation, experimental results will be presented comparing the identification of ischemic lesions in experimental stroke using dynamic susceptibility contrast (DSC) and a well validated arterial spin labeling (ASL). We show that DSC measurements of an index of cerebral blood flow are sensitive to ischemia, treatment, and stroke subregions. Further, we derived a threshold of cerebral blood flow for ischemia as measured by DSC. Finally, we show that ischemic lesion volumes as defined by DSC are comparable to those defined by ASL. In the second part of this dissertation, a methodology of visualizing clots in experimental animal models of stroke is presented. Clots were rendered visible by MRI through the addition of a gadolinium based contrast agent during formation. Modified clots were used to induce an experimental embolic middle cerebral artery occlusion. Clots in the cerebral vasculature were visualized in vivousing MRI. Further, the efficacy of recombinant tissue plasminogen activator (r-tPA) and the combination of r-tPA and recombinant annexin-2 (rA2) was characterized by clot visualization during lysis. In the third part of this dissertation, we present results of the application of hyperpolarized helium (HP-He) in the characterization of new model of experimental pulmonary ischemia. The longitudinal relaxation time of HP-He is sensitive to the presence of paramagnetic oxygen. During ischemia, oxygen exchange from the airspaces of the lungs to the capillaries is hindered resulting in increased alveolar oxygen content which resulted in the shortening of the HP-He longitudinal relaxation time. Results of measurements of the HP-He relaxation time in both normal and ischemic animals are presented. In the final part of this dissertation, I will present results of a new method to measure pulmonary blood volume (PBV) using proton based MRI. A T1 weighted, inversion recovery spin echo sequence with cardiac and respiratory gating was developed to measure the changes in signal intensity of lung parenchyma before and after the injection of a long acting intravascular contrast agent. PBV is related to the signal change in the lung parenchyma and blood before and after contrast agent. We validate our method using a model of hypoxic pulmonary vasoconstriction in rats

Cardiovascular Magnetic Resonance Imaging in Experimental Models

Cardiovascular magnetic resonance (CMR) imaging is the modality of choice for clinical studies of the heart and vasculature, offering detailed images of both structure and function with high temporal resolution