A patient monitoring system may include a first-fluid-housing, and a drain in communication with the first-fluid-housing that pulls a first non-serosanguinous fluid from a patient into the first-fluid-housing. The system may also include a sensor that measures the first non-serosanguinous fluid entering the first-fluid-housing. The system may further include a computer-controller in communication with the sensor and drain, the computer-controller includes a profile that identifies the patient, the first-fluid-housing, and records the sensor's first non-serosanguinous fluid measurements that any user can retrieve based upon permissions granted to each user.

The test lab set-up includes a test flow bench for mounting one or more test devices, an adjustable nozzle for simulating urine flow, and a sensor for collecting data associated with the simulated urine flowing through the test device(s). A computing device for measuring and/or calculating various parameters associated with the simulated urine flow may also be included. The test device may have a shape corresponding to a handheld uroflowmeter subject to testing. The angle of the adjustable nozzle may be adjusted to test for various angles of urine flow. Similarly, the angle, pitch, and roll of the test device may be adjusted to test for various angles at which a uroflowmeter is held. As fluid flows through the test device, the sensor collects information such as, for example, flow rate, duration, volume, and the like. The sensor transmits the data collected to a computing device for additional processing.

The present disclosure generally relates to uroflowmeters and methods for processing data generated therefrom. In one aspect, the uroflowmeter is a handheld device. The uroflowmeter includes a handle, a flow chamber coupled to the handle, and a sensor associated with the flow chamber that detects a parameter of urine received in the flow chamber. The uroflowmeter may include both reusable and disposable components. As a uroflowmeter it can identify and record data corresponding to the rate of flow over the measured duration of a void of urine, but may also timestamp the voiding act and communicate the data to an external data collection center for additional analysis and incorporation into a comprehensive voiding report or voiding diary.

The present disclosure generally relates to methods and systems for generating a void profile for user void events. The method includes receiving by a processing element a plurality of outputs from a fluid level sensor corresponding to a plurality of levels of fluid flowing through a voiding device during a flow event; determining by the processing element a beginning and an end time of the fluid flow into the voiding device during the flow event; analyzing the plurality of outputs of the fluid level sensor over a time interval defined by the beginning and end time of the fluid flow to determine at least one of a fluid flow rate data and an accumulated volume data for the fluid flowing through the voiding device; and storing the fluid flow rate data and the accumulated flow volume data in a memory.

A bladder monitoring system includes a scanning system and a wearable bladder monitoring device (or patch). The scanning system obtains scan data that shows a bladder in a patient and identifies, based on the scan data, a placement location on the patient for the wearable bladder monitoring device. The scanning system indicates the placement location to a user; and identifies customization settings for one or more sensors of the wearable bladder monitoring device to enable the one or more sensors to detect extents of the bladder when the wearable bladder monitoring device is attached at the placement location.

According to one aspect of the inventive concept there is provided a system for monitoring incontinence comprising: a urine sensitive circuit arranged to present a changed electrical characteristic when exposed to urine; a measurement circuit arranged to perform a measurement on a urine bladder of a wearer to determine at least one parameter which varies with a fill level of the urine bladder; and a processing circuit arranged to: determine whether the urine sensitive circuit has been exposed to urine, and in response to determining that the urine sensitive circuit has been exposed to urine, record data representing the at least one parameter determined by the measurement circuit.

A method performed by a computer correlates vesicoelastic pressure data (10, 12, 14) with volume data and calculates vesicoelastic work performed by the bladder (20), wherein the amount of vesicoelastic work performed by the bladder (20) is determined by calculating an area under said vesicoelastic pressure data (10, 12, 14) when said vesicoelastic pressure data (10, 12, 14) is correlated against the volume data.

The present disclosure generally relates to methods and systems for generating a void profile for user void events. The method includes receiving by a processing element a plurality of outputs from a fluid level sensor corresponding to a plurality of levels of fluid flowing through a voiding device during a flow event; determining by the processing element a beginning and an end time of the fluid flow into the voiding device during the flow event; analyzing the plurality of outputs of the fluid level sensor over a time interval defined by the beginning and end time of the fluid flow to determine at least one of a fluid flow rate data and an accumulated volume data for the fluid flowing through the voiding device; and storing the fluid flow rate data and the accumulated flow volume data in a memory.

This disclosure describes methods, systems, and devices configured to determine a timing of a future bladder related event of a patient. For example, a system includes processing circuitry configured to identify a timing of a plurality of bladder related events of a patient, determine, based on the timing of the plurality of bladder related events of the patient, a probability to experience a bladder related event function for the patient, the probability to experience a bladder related event function indicating a probability that the patient will experience a bladder related event at an elapsed time after a previous bladder related event, predict, based on the probability to experience a bladder related event function, a timing of a future bladder related event, and control delivery of a therapy to the patient based on the predicted timing of the future bladder related event.

Devices, systems, and methods may manage therapy delivery to a patient based on one or more physiological markers. In some examples, a method includes detecting a physiological marker that occurs prior in time to a dysfunctional phase of a physiological cycle, wherein a dysfunctional state of the physiological cycle occurs during the dysfunctional phase without treatment, responsive to detecting the physiological marker, initiating a first phase of the physiological cycle having a duration of time. The method may also include, responsive to the first phase elapsing, controlling a therapy delivery module to deliver neurostimulation therapy during a second phase that begins prior to the dysfunctional phase, wherein the neurostimulation therapy is configured to treat the dysfunctional state.