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Continuous non-invasive measurement of bladder voiding pressure using an experimental constant low-flow test
Becky Clarkson1, Clive Griffiths, Frank McArdle
1Department of Medical Physics, Newcastle University, Newcastle upon Tyne, UK.
Neurourology and Urodynamics
|December 23, 2011
Summary
A new penile cuff device offers promising non-invasive measurement of bladder voiding pressure in men. Validation against invasive methods showed potential for continuous monitoring, with improvements planned for future clinical use.
Area of Science:
- Urology
- Biomedical Engineering
- Medical Devices
Background:
- Accurate measurement of bladder voiding pressure is crucial for diagnosing and managing lower urinary tract conditions in men.
- Current invasive methods for measuring bladder pressure can be uncomfortable and carry risks.
- There is a need for non-invasive, continuous monitoring techniques.
Purpose of the Study:
- To validate a prototype device using an automatically controlled inflatable penile cuff for continuous, non-invasive measurement of bladder voiding pressure in men.
- To compare the device's pressure measurements against simultaneous invasive pressure measurements (PFS).
Main Methods:
- A prototype device was developed to modulate flow rate by controlling penile cuff pressure.
- Forty men undergoing urodynamics studies participated, using the device during an additional fill-void cycle.
- Pressure measurements from the penile cuff (p(cuff)) were compared with simultaneous vesical pressure (p(ves)) using maximum pressure and root mean square (RMS) difference.
Main Results:
- The mean difference between maximum cuff and vesical pressures was not significant (1.3 (15.6) cmH2O).
- Moderate to good agreement (RMS difference <20 cmH2O) between cuff and vesical pressures was observed in 50% of participants.
- Factors leading to unsuccessful measurements were identified.
Conclusions:
- The penile cuff device shows promise as a prototype for continuous, non-invasive bladder pressure measurement.
- Recommended improvements have been implemented for the next generation of the device.
- Further development aims to enable clinical application assessment.
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