Patent classifications
A61B5/4277
METHODS FOR MITIGATING BIOFOULING EFFECTS OF BIOFLUID INTERFERENTS TO DETECT IN VIVO BIOCHEMICAL AND WEARABLE DEVICE THEREFOR
Example implementations include a device with an electrode electrically responsive to presence of a biochemical present within a biofluid, and one or more biofouling and interferent mitigation layers disposed on the electrode to block transmission of biofouling agents to the electrode and the reaction of interferents on the electrode. Example implementations also include a method of obtaining a biofluid sample, mitigating a biofouling characteristic associated with the biofluid sample, and obtaining a biochemical characteristic associated with the biofluid sample.
Predictive use of quantitative imaging
The present disclosure provides systems and methods for predicting a disease state of a subject using ultrasound imaging and ancillary information to the ultrasound imaging. At least two quantitative measurements of a subject, including at least one measurement taken using ultrasound imaging, as part of quantified information can be identified. One of the quantitative measurements can be compared to a first predetermined standard, included as part of ancillary information to the quantified information, in order to identify a first initial value. Further, another of the quantitative measurements can be compared to a second predetermined standard, included as part of the ancillary information, in order to identify a second initial value. Subsequently, the quantitative information can be correlated with the ancillary information using the first initial value and the second initial value to determine a final value that is predictive of a disease state of the subject.
Portable biomarker reader
A portable imaging apparatus and system. A sample processing device has a reaction chamber configured to receive a sample and react the sample with a fluorescent compound that emits a specified wavelength of light when excited by light within an excitation band. An illumination source can be positioned to illuminate the reaction chamber when the sample processing device is positioned for imaging. A light guide can be positioned to face the reaction chamber and transfer the emitted light to an imaging detector. The light guide has a filter that blocks the wavelength of light from the illumination source and passes the fluorescent emitted light. The light guide unit defines an angular light acceptance range and is configured to constrain angular spreading of light.
MEASURING DEVICE
A measuring device is provided with an improved contact property of a measuring surface of a sensor with respect to a surface of a target object. The measuring device includes a main body and a probe that has a head section at the distal end thereof and an arm section connecting the head section to the main body. The head section has a support portion, a measuring portion, and a coupling portion. The support portion is connected to the distal end of the arm section. The measuring portion has a first surface at which a measuring surface of a sensor is exposed and a thickness with the first surface as a datum plane. The coupling portion is disposed between and couples the measuring portion and the support portion. The coupling portion has a first connection portion connected to the measuring portion and a through hole.
SYSTEM FOR INTRAORAL MONITORING AND RELATED METHODS THEREOF
An intraoral monitoring device includes a flexible substrate, a plurality of sensors, a rechargeable battery, a device module and a communication module. The plurality of sensors senses a plurality of health parameters from an associated user, in real time, to generate a plurality of sensed signals. The device module includes a memory, a controller and a segregation module. The memory stores various health parameters and their respective ranges, various health reports of the user, and basic details of all users. A controller is configured to generate sensed data and the segregation module is configured to segregate the data corresponding to the plurality of health parameters associated with the users. A communication module is configured to enable data communication to and from the intraoral device.
Long-term, continual, wireless, intraoral monitor
This disclosure relates to wireless electronics designed for use within the oral cavity to measure biological or chemical variables, including pH or analyte concentrations, and transmit the measurements. More particularly, the disclosure relates to a wearable intraoral sensor comprising sensing electronics arranged within a flexible circuit mounted onto a molar band, a wireless transmission unit coupled to the sensing electronics and configured to wirelessly transmit electrical data signals to a receiver outside of the oral cavity, and a power source operably coupled to the sensing electronics and wireless transmission unit. The wearable intraoral sensor can be installed around a tooth and continually measure and wirelessly transmit measurement data for extended periods of time without user action.
Method and device of detecting and/or blocking reflux
A naso/orogastric device having backflow blocking means and comprises a naso/orogastric tube sized and shaped for being disposed within the esophagus so that at least a distal end thereof being placed in the stomach lumen of a patient, at least one elastic esophageal body, positioned along the naso/orogastric tube, having a pressure dependent volume, at least one esophageal sensor that detects fluid around at least one segment of the naso/orogastric tube, and a pressure regulator that regulates a pressure within the elastic esophageal body according to the detection.
Predictive use of quantitative imaging
The present disclosure provides systems and methods for predicting a disease state of a subject using ultrasound imaging. The method includes identifying at least one quantitative measurement of a subject using ultrasound imaging, the at least one quantitative measurement included as part of quantitative information of the subject gathered based on the ultrasound imaging, comparing the at least one quantitative measurement to a first predetermined standard to determine a first initial value, the first predetermined standard falling within a first range of quantities, identifying at least one qualitative measurement of the subject using the ultrasound imaging, the at least one qualitative measurement included as part of qualitative information of the subject gathered based on the ultrasound imaging, comparing the at least one qualitative measurement to a second predetermined standard to determine a second initial value, the second predetermined standard falling within a second range of quantities; and correlating at least the quantitative information and the qualitative information using the first initial value and the second initial value to determine a final value that is used in predicting a disease state of the subject.
Method and apparatus for health condition of a person based on bodily fluid
In one embodiment, a hydration sensor or sensing element is configured to measure the hydration level of a user. The sensing element can include a water-permeable material positioned in between two water-impermeable material. The sensing element can be coupled to a bottle of fluid, or a carrier with a timer. The sensing element can be incorporated into a handheld device. The sensing element can be a disposable element, an element applicable for more than one-time use, or a re-usable element. The sensing element or sensor can be calibrated for a specific user or a group of users. One or more additional sensors that do not measure hydration level of the user can be coupled to a hydration sensing element to determine the amount of fluid consumption for the user in different conditions.
SPECIMEN COLLECTION DEVICE
This specification discloses devices and apparatus for collecting a material specimen, including a sheath; and an inner assembly. The inner assembly can include a handling element; one or more fluid chamber elements; and a swab element. The handling element, the one or more fluid chamber elements, and the swab element are connected and arranged along a first axis; and the inner assembly is operable to slide within the sheath between (i) a first position in which the swab element is in a non-retracted position outside of the sheath while at least a portion of the inner assembly remains within the sheath, and (ii) a second position in which the swab element is in a retracted position within the sheath.