Abstract: A cryoablation catheter assembly includes a catheter that defines at least one coolant outtake region and receives a rotatable guide tube and a coolant transfer tube. The coolant transfer tube receives and transfers coolant from a coolant source to a distal end of the coolant transfer tube. An expansion element is coupled to a distal portion of the catheter and defines an inner expansion-element space. The inner expansion-element space is in fluid communication with the at least one coolant outtake region and the distal end of the coolant transfer tube. A distal end of the expansion element couples to the guide tube. A rotation system is coupleable to, or coupled to, a proximal end of the guide tube and rotates the distal end of the expansion element relative to the proximal end of the expansion element by rotating the guide tube relative to the catheter.

Abstract: A therapeutic illumination assembly includes a catheter and a point source treatment fiber. The catheter comprises a catheter wall encircling a luminal fluid pathway. The point source treatment fiber is positioned within the luminal fluid pathway of the catheter. Further, the point source treatment fiber comprises a plurality of light emitting point sources intermittently positioned along a treatment length of the point source treatment fiber such that the plurality of light emitting point sources irradiate the catheter when the plurality of light emitting point sources emit light.

Abstract: Systems and methods for generating notifications based on bladder volume signals and bladder muscle signals are disclosed. A system includes a processor, a plurality of bladder electrical signal application electrodes, a plurality of bladder volume measurement electrodes, a plurality of bladder muscle measurement electrodes, a memory module communicatively coupled to the processor, and machine readable instructions stored in the memory module. When executed by the processor, the machine readable instructions cause the system to output a first electrical output signal with the plurality of bladder electrical signal application electrodes, receive the bladder volume signal at the plurality of bladder volume measurement electrodes in response to the first electrical output signal, receive the bladder muscle signal at the plurality of bladder muscle measurement electrodes, and generate the notification based on the bladder volume signal and the bladder muscle signal.

Abstract: A medical device may include a tool body and a handle. The handle may include a first body having a first coupling feature extending axially along the first body and a second body including a second coupling feature positioned within the first coupling feature. In a first orientation, the first body and second body may be rotatable and axially translatable relative to each other as a function of the first and second coupling features.

Abstract: An implantable medical device includes an activity sensor, a pulse generator, and a control module. The control module is configured to determine activity metrics from the activity signal and determine an activity metric value at a predetermined percentile of the activity metrics. The control module sets a lower pacing rate set point based on the activity metric value at the predetermined percentile.

Abstract: A system is provided for monitoring physiological parameter(s) and providing a context under which the physiological parameter is measured. The system may include a data processing device. The data processing device may be configured to receive data corresponding to physiological parameter(s) measured from a body. The data processing device may be further configured to receive data that enables determination of one or more of orientation of the body and determination of movements of the body. The data processing device may be additionally configured to correlate and present the correlation between the measured physiological parameter(s) and one or more of orientation a body and activity the body is indulged in, which is derived based on the movements of the body.

Abstract: A system to measure sweat vapor may include a skin contact sensor, a sweat vapor sensor, and a processor. The skin contact sensor may be configured to measure one or more aspects indicative of whether the measuring device is in contact with skin of a user of the measuring device. The sweat vapor sensor may be configured to measure one or more properties of sweat vapor of the user; and the processor may be communicatively coupled to the skin contact sensor and the sweat vapor sensor. The processor may be configured to confirm operation of the measuring device based on the one or more aspects measured by the skin contact sensor, and the sweat vapor sensor receiving the sweat vapor.

Abstract: A multi-point light-delivering device, comprising a waveguide carrying light along a longitudinal axis and including multiple optical windows, through which the carried light is out-coupled from the waveguide. The waveguide comprises a tapered region along which the optical windows are distributed, wherein each optical window out-couples a specific subset of propagating modes of the carried light, to which the optical window is matched.

Abstract: A patch-type module includes a substrate provided with one surface and another surface that is a sticky surface; an air cell mounted to the substrate; a seal that blocks air from entering the air cell whose first surface is attached to the air cell; an electronic component mounted on the substrate; and a protection sheet that is attached to the sticky surface of the substrate through an adhesion layer, wherein a second surface of the seal is attached to the protection sheet through the adhesion layer, wherein when the protection sheet is peeled, the adhesion layer and the seal are peeled together to expose the sticky surface of the substrate and start introduction of air inside the air cell so that electric power is capable of being power supplied to the electronic component from the air cell.

Abstract: A minimally invasive pre-cardiogenic heart assist device has been developed. A method of increasing myocardial blood flow using a Subclavian Diastolic Augmentation Device (SDAD) includes grafting a subclavian vein to a first synthetic chamber, the first synthetic chamber located inside of a body of the patient; grafting a subclavian artery to a second synthetic chamber, the second synthetic chamber located inside of the body of the patient; and pumping blood from the first synthetic chamber to the second synthetic chamber with a pump located inside of the body of the patient.

Abstract: Embodiments of this disclosure disclose an imaging system, including an eye interface device, a scanning assembly, a beam source, a free-floating mechanism, and a detection assembly. The beam source generates an electromagnetic radiation beam. The detection assembly generates a signal indicative of an intensity of a portion of the electromagnetic radiation beam reflected from the focal point location. A subsequent focal point of the electromagnetic radiation beam may be adjusted per the measured intensity signal. In some embodiments, an intensity signal below a lower threshold value may suggest a depth increase for a subsequent focal point. An intensity signal above an upper threshold value may suggest a depth decrease for a subsequent focal point. And, an intensity signal between the lower and upper thresholds may suggest a depth be maintained for a subsequent focal point. The focal point may be adjusted after each pulse or after a plurality of pulses.

Abstract: A computerized pain visualization system and method. A web-based application and interface allows individuals to anonymously share information about where they hurt or specific regions of the body that are most worrisome to them. The web-based application comprises a visual interface that supports selection of parts or regions on an image of a human body. The data becomes viewable and filterable by geographic location, age, sex, or a variety of other data sets collected from the anonymous users. In an example embodiment, Users register and sign in at a web site. A selectable body interface is presented and the user is prompted to select one or more pain locations on the virtual body. The user's selections are recorded in a database. Another page of the application presents a search option that facilitates searching and visualizing the data, filterable by users' registration information.

Abstract: An example of a system may include an arrangement of electrodes configured to be operationally positioned for use in modulating targeted neural tissue, a neural modulator, a communication module, and a controller. The neural modulator may be configured to use at least some electrodes within the arrangement of electrodes to generate a modulation field. The communication module may be configured to receive user-provided selections. The controller may be configured to use the communication module to receive a user-provided selection of a desired electrode list where the electrode list identifies electrodes within the arrangement of electrodes that are available for use in modulating the targeted neural tissue, control the neural stimulation modulator to generate the modulation field, and use the electrodes identified in the electrode list to modulate the targeted neural tissue.

Abstract: A system and method for automatically producing and monitoring a cryotherapy session within a chamber includes a plumbing system coupled to the chamber for cooling the chamber. A central controller may be coupled to the plumbing system. The central controller may be operable for: initiating the cryotherapy session within the chamber with a cryogenic gas flowing through the plumbing system for cooling the chamber to a first temperature; determining if the first temperature has been reached within the chamber; determining if a check-in command has been received for the cryotherapy session; and stopping the cryotherapy session after a predetermined period of time. The central controller may initiate a pre-cooling session for cooling the chamber to a second temperature which is different than the first temperature; and determine if the second temperature has been reached in the chamber. The pre-cooling session generally occurs prior to the cryotherapy session for removing ambient heat.