According to one aspect of the invention, there is provided a method for calculating information on urination. The method includes the steps of acquiring a sound signal related to urination of a user, calculating a urination parameter related to an effective value (or urination parameters related to an effective value and a spectral centroid) from the acquired sound signal, and estimating a urine flow rate of the user with reference to the calculated urination parameter.

A ureteral catheter is provided, including a drainage lumen including a proximal portion and a distal portion configured to be positioned in a patient's kidney, renal pelvis, and/or in the ureter adjacent to the renal pelvis, the distal portion including a retention portion for maintaining positioning of the distal portion of the drainage lumen, the retention portion including at least two openings on a sidewall of the retention portion for permitting fluid flow into the drainage lumen wherein a total area of a proximal most opening of the at least two openings is less than a total area of more distal opening(s) nearer to the distal end of the drainage lumen, and wherein when negative pressure is applied through the ureteral catheter, fluid is drawn into the ureteral catheter through the at least two openings.

An analytical toilet, comprising: a bowl adapted to receive excreta; one or more conduits for transporting a sample from the bowl; one or more fluid sources in fluid connection with the one or more conduits; and one or more microfluidic chips, comprising: at least one microfluidic fluid inlet channel; and a sensor configured to detect at least one property of an excreta sample is disclosed.

A ureteral catheter includes a drainage lumen including a proximal portion configured to be positioned in at least a portion of a patient's urethra and/or bladder and a distal portion configured to be positioned in a patient's kidney, renal pelvis, and/or in the ureter adjacent to the renal pelvis, the distal portion including a retention portion for maintaining positioning of the distal portion of the drainage lumen, the retention portion including two or more openings on a sidewall of the retention portion for permitting fluid flow into the drainage lumen, wherein a number of the openings nearer to a distal end of the retention portion is greater than a number of the opening(s) nearer to a proximal end of the retention portion.

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 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.

The invention relates to methods, systems and computer program products for monitoring the biosignals of a test subject, in particular electrocardiograms, wherein a plurality of reference biosignals are recorded along with a respective assigned reference parameter value, a control biosignal is measured, a reference parameter value to be assigned to the control biosignal is determined and, on the basis of the reference parameter value assigned to the control biosignal and on the basis of the plurality of reference parameter values assigned to the plurality of reference biosignals, at least one comparative biosignal is selected from the plurality of stored reference biosignals for comparison, and wherein values of the reference parameter at least partially describe a physiological state of the test subject and/or general conditions of an environment.