A variety of medical and non-medical devices are exploited by users to address a wide range of conditions. However, in the vast majority of instances, the device has a limited number of options with respect to its fit for the user and its performance. Further, the determination of target performance and fit are established on a qualitative basis rather than a quantitative basis. In many instances, these combinations lead to low user acceptance of the device due to the resulting performance and fit issues. Accordingly, it would enhance performance and user acceptance if a quantitative determination provided a recommended type where options exist, and this determination provided the basis of a custom designed device to the user's specific anatomical and/or performance requirements.

A method of using a magnetometer system to analyse the magnetic field of a region of a subject's body is disclosed. The method comprises using one or more detectors to detect the time varying magnetic field of a region of a subject's body, filtering a signal or signals from the one or more detectors using a filter or filters, and using the filtered signal or signals to analyse the magnetic field generated by the region of a subject's body. The filter or filters is configured to attenuate noise in the signal or signals that is synchronised with motion of the region of the subject's body such as ballistocardiographic noise.

Use of the peritoneal space provides a more direct tracking of blood glucose, capturing faster glucose kinetics, avoiding membrane/encapsulation effects, having less lag time and lag time variability, and eliminating the effect of variations in skin temperature, cardiac output, and body position during sleep. A peritoneal sensor system may be implanted within the peritoneal space and may generally include a sensor/sampler portion, which is implanted in the peritoneal space, and a control portion/controller, which may be implanted elsewhere, such as subcutaneously, or may be external to the patient.

The various embodiments disclosed here relate to systems, methods, and devices for monitoring bladder health. Certain implementations are directed to patients who require daily catheterization. The various embodiments have at least one tube coupled to a catheter, a pressure sensor, a pump, and a processor. Certain embodiments include a digital device with a software application capable of displaying the monitored readings.

Embodiments of the invention provide devices and systems to monitor fullness of a patient's bladder. One embodiment of a bladder fullness (BF) measure system comprises a sensor device (SD) and a controller. The SD generates an output signal (OS) based on the force exerted by the bladder against SD the wherein the OS corresponds to a degree of BF. The SD may be attached to the bladder wall or adjoining tissue and positioned between the bladder and the pubic bone such that the SD is not affected by tissues force other than that from the bladder. The controller connects to the SD and causes an associated implant to perform a function when the SD output signal exceeds a predetermined threshold. Embodiments are particularly useful for providing information on BF to patients suffering from spinal injury or other conditions whereby they have lost the ability to sense BF and/or voluntarily urinate.

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.

The present disclosure provides diagnostic methods for evaluating a urinary bladder and methods of enhancing the visibility of the bladder from outside of a patient. The method includes introducing urinary catheter having a proximal end and a distal end into a patient's urinary bladder by way of the urethra, the urinary catheter including an outer tubular member including an inflatable balloon disposed thereon, and a visualization stylet that is slidably disposable within a passage defined in the outer tubular member. The method further includes inflating the inflatable member inside of the bladder, inflating the bladder with a liquid to enhance visualization of an inner surface of the bladder, illuminating a light source through the inflatable member to illuminate the inner surface of the bladder, and visualizing an inner portion of the bladder using the visualization stylet.

The various embodiments disclosed here relate to systems, methods, and devices for monitoring bladder health. Certain implementations are directed to patients who require daily catheterization. The various embodiments have at least one tube coupled to a catheter, a pressure sensor, a pump, and a processor. Certain embodiments include a digital device with a software application capable of displaying the monitored readings.

A vesical pressure measurement system is provided. One or more elements of the system are operably combinable with a previously deployed urinary drainage catheter. The system includes a urodynamic data system and a urinary drainage catheter balloon adaptor. The data system is characterized by a pressure sensor for vesical pressure measurement, and a processor/controller for receiving, processing and/or displaying select urodynamic patient parameters comprising sensed/monitored pressure data. The adaptor operably unites the pressure sensor of the data system to a balloon inflation valve of the catheter. The adaptor includes an adaptor valve for connection to the balloon inflation valve, and a housing, the housing including a balloon inflation valve portion and an adaptor valve portion, the portions urgingly uniteable in furtherance of establishing and maintaining a secure interface between the balloon inflation valve and the adaptor valve.

The present disclosure relates generally to using detected bladder events for the diagnosis of urinary incontinence or the treatment of lower urinary tract dysfunction. A system includes a sensing device comprising a pressure sensor to directly detect a pressure within a bladder. The sensing device is adapted to be located within the bladder. The system also includes a signal processing device to: receive a signal indicating the detected pressure within the bladder; detect a bladder event based the detected pressure within the signal; and characterize the bladder event as a bladder contraction event or a non-contraction event. The characterization of the bladder event can be used in the diagnosis of urinary incontinence or the treatment of lower urinary tract dysfunction.