A method of assessing bladder storage anomalies via utilization of an indwelling urinary drainage catheter is provided. A urodynamic assessment assembly is provided, the assembly characterized by a pressure sensor for vesical pressure measurement, a processor/controller for receiving, processing and/or displaying select urodynamic patient parameters comprising sensed/monitored pressure data, and a catheter balloon adaptor for operably uniting the pressure sensor of the urodynamic assessment assembly to a balloon inflation valve of the indwelling urinary drainage catheter, the indwelling urinary drainage catheter operably linked with the urodynamic assessment assembly. Vesical pressure is sensed via the vesical pressure sensor during a bladder emptying event, the bladder emptying event characterized by an application of variable resistance to fluid flow from the bladder via the indwelling urinary drainage catheter with vesical pressure/outlet resistance/flow rate relationships established based upon sensed vesical pressure values.

Urodynamic assessment systems, intravesical devices, and methods of their use are provided. In one embodiment, an intravesical device includes an elastic body including an elongated tube defining a reservoir lumen, and a sensor disposed at least partially in the reservoir lumen and configured to measure or detect one or more parameters. The intravesical device is deformable between a deployment shape for passage of the intravesical device through the urethra into the bladder and a retention shape for preventing voiding of the intravesical device through the urethra.

A sensing device can be used for ambulatory urodynamics. The sensing device can include an elongated outer housing constructed of flexible material that can curve within a patients bladder. At least a portion of the outer housing can be filled with a non-compressible fluid. A flexible printed circuit board can be disposed within the outer housing to curve with the outer housing. The printed circuit board can include a pressure sensor, comprising a diaphragm, to collect pressure data; a microcontroller miming control software; and a wireless transmitter to transmit the pressure data. A battery can be disposed within the outer housing and coupled to the printed circuit board. The flexible material of the outer housing is configured to be displaced by a pressure within the patients bladder, the displacement is transmitted through the non-compressible fluid to the pressure sensor that provides the pressure data based on the displacement.

Systems and methods for are disclosed for determining whether to output an indication of a urinary tract infection (UTI) in a patient, based on sensor data indicative of one or more common symptoms of UTIs, including, but not limited to, nocturia, fatigue or tremors; fever or chills; agitation or restlessness; lower back pain; painful urination; and presyncope or syncope.

A bladder urine volume monitoring system and a bladder urine volume monitoring method are provided. The bladder urine volume monitoring system includes at least one ultrasound patch, at least one muscle stimulation patch, and a control circuit. The ultrasound patch is configured to be attached to a surface of an organism to detect a urine volume in a bladder. The muscle stimulation patch is configured to be attached to the surface of the organism to stimulate a muscle of the bladder. The control circuit is coupled to the ultrasound patch and the muscle stimulation patch. The control circuit drives the ultrasound patch to detect the urine volume in the bladder in a first period. The control circuit drives the muscle stimulation patch to stimulate the muscle of the bladder in a second period.

In some examples, a device includes a catheter insert elongated body defining a body lumen, the catheter insert elongated body being configured to be at least partially inserted to a catheter lumen defined by a catheter without covering a first fluid opening of the catheter and to form a fluidically tight coupling with the catheter, and one or more sensors positioned on the elongated body. At least one of the one or more sensors are configured to sense a substance of interest. The catheter insert elongated body includes a material that is a substantially non-permeable to the substance of interest.

In some examples, a medical device includes an elongated body defining an inner lumen. The medical device further includes an anchoring member and a first sensor at a proximal portion of the elongated body, and a second sensor at a distal portion of the elongated body or distal to a distal end of the elongated body. The second sensor is configured to sense a substance of interest and the elongated body comprises a material that is a substantially non-permeable to the substance of interest.

The present disclosure relates generally to estimating an interior diameter of a hollow organ. As such, one aspect of the present disclosure relates to a system that can include a light-based distance sensor and a device housing the light-based distance sensor located within the hollow organ. The light-based distance sensor can include an emitter and a detector. The emitter can transmit a conical beam of light to an inner surface of a hollow organ. The detector can receive a portion of the light back-reflected from the inner surface of the hollow organ. The device can determine a volume of the hollow organ based on a signal related to the back-reflected portion of the light, which can be based on a distance between the light-based distance sensor and the inner surface of the hollow organ.

Provided herein are systems and methods for monitoring and treatment of an injury. The system includes a control device, an implantable device and/or a wearable device, the implantable device configured to be implanted into a body, the implantable device having a sensing device for sensing a condition of the injury and a treatment device configured to apply a treatment to the injury based on the sensed conditions of the injury. Signals of the sensed condition are sent to the control device, and the control device controls the treatment device of the implantable device to apply treatment for the injury. When a wearable device is included, the wearable device may be configured to sense another condition related to the injury and send signal indicative thereof to the control device.

An exemplary catheter can be provided which can include, for example, a first inflation arrangement configured, in operation, to substantially seal and/or anchor the catheter inside the bladder when inflated, a second inflation arrangement configured, in operation, to substantially float in urine when inflated, wherein the second arrangement can be located at a predetermined distance from the first inflation arrangement, and an aperture provided between the first inflation arrangement and the second inflation arrangement, where the first and second arrangements can cause the aperture to be (i) open when the second inflation arrangement can be located at a first position relative to the first inflation arrangement, and (ii) closed when the second inflation arrangement can be located at a second position relative to the first inflation arrangement, and where the second position can be different than the first position.