Non-invasive Intracranial Pressure Measurement

To assess various aspects of dynamic visual and visuomotor function including peripheral attention, spatial localization, perceptual motion processing, and oculomotor responsiveness, NASA developed a simple five-minute clinically relevant test that measures and computes more than a dozen largely independent eye-movement-based (oculometric) measures of human neural performance. This set of oculomotor metrics provide valid and reliable measures of dynamic visual performance and may prove to be a useful assessment tool for mild functional neural impairments across a wide range of etiologies and brain regions. The technology may be useful to clinicians to localize affected brain regions following trauma, degenerative disease, or aging, to characterize and quantify clinical deficits, to monitor recovery of function after injury, and to detect operationally-relevant altered or impaired visual performance at subclinical levels. This novel system can be used as a sensitive screening tool by comparing the oculometric measures of an individual to a normal baseline population, or from the same individual before and after exposure to a potentially harmful event (e.g., a boxing match, football game, combat tour, extended work schedule with sleep disruption, blast or toxic exposure, space mission), or on an ongoing basis to monitor performance for recovery to baseline. The technology provides set of largely independent metrics of visual and visuomotor function that are sensitive and reliable within and across observers, yielding a signature multidimensional impairment vector that can be used to characterize the nature of a mild deficit, not just simply detect it. Initial results from peer-reviewed studies of Traumatic Brain Injury, sleep deprivation with and without caffeine, and low-dose alcohol consumption have shown that this NASA technology can be used to assess subtle deficits in brain function before overt clinical symptoms become obvious, as well as the efficacy of countermeasures.

The technology utilizes four cutting-edge sensor technologies to enable minimally- or non-invasive analysis of various biological samples, including saliva, breath, and blood. The combination of technologies and sample pathways have unique advantages that collectively provides a powerful analytical capability. The four key technology components include the following: (1) the carbon nanotube (CNT) array designed for the detection of volatile molecules in exhaled breath; (2) a breath condenser surface to isolate nonvolatile breath compounds in exhaled breath; (3) the miniaturized differential mobility spectrometer (DMS) -like device for the detection of volatile and non-volatile molecules in condensed breath and saliva; and (4) the miniaturized circular disk (CD)-based centrifugal microfluidics device that can detect analytes in any liquid sample as well as perform blood cell counts. As an integrated system, the device has two ports for sample entry a mouthpiece for sampling of breath and a port for CD insertion. The breath analysis pathway consists of a CNT array followed by a condenser surface separating liquid and gas phase breath. The exhaled breath condensate is then analyzed via a DMS-like device and the separated gas breath can be analyzed by both CNT sensor array again and by DMS detectors.

Microphones and stethoscopes are regularly used by physicians to detect sounds when monitoring physiological conditions. These monitors are coupled directly to a person's body and measure in certain bandwidths either by listening or by recording the signals. The physiological processes such as respiration and cardiac activity are reflected in a different frequency bandwidth from 0.01 Hz to 500 Hz. This technology can monitor physiological conditions in the entire bandwidth range. Signals can also be wirelessly transmitted, using Bluetooth, to other recording devices at any other location.

Check valves are traditionally designed as a simple poppet/spring system where the spring is designed to equal the force created from the sealing area of the valve seat multiplied by the cracking pressure. Since the valve seat diameter in these types of valves are relatively small, less than 0.5 inches diameter, a low cracking pressure required for back pressure relief devices results in a low spring preload. When sealing in the reverse direction, the typical 20 psid storage pressure of the cryogenic fluid is not enough pressure force to provide adequate sealing stress. To better control the cracking pressure and sealing force, a bellows mechanism was added to a poppet check valve (see Figure 2). The bellows serves as a reference pressure gauge; once the targeted pressure differential is reached, the bellows compresses and snaps the valve open. Prior to reaching the desired crack pressure differential, the bellows diaphragm is fully expanded, providing sufficient seal forces to prevent valve flow (including reverse flow) and undesired internal leakage. Room temperature testing of cracking pressure, full flow pressure, and flow capacity all showed improvements. The overall results of the test proved to be 10-20 times greater than conventional check valves with no internal leakage at three different pressure differentials.

The crimping innovations are based on traditional ultrasonic nondestructive evaluation methods. The quality of the contact between the connector and wire is determined by sending an acoustic wave through the crimp assembly. As the applied pressure increases and the crimp terminal deforms around the wire, the ultrasonic signature passing through the crimp is altered. The system analyzes the changes in the signal, including the amplitude and frequency content, as an indication of the quality of both the electrical and mechanical connection between the wire and terminal. Various crimp quality issues such as undercrimping, missing wire strands, incomplete wire insertion, partial insulation removal, and incorrect wire gauge have been tested using this technique, and results show that the instrumented crimp tool consistently discriminates between good and poor crimps for all of these potential quality issues. This information can be used to provide a pass or fail indication for instant verification of the crimp quality and to give a better prediction for the service life of the crimp.