Wireless Bladder Pressure Monitor for Closed-Loop Bladder Neuromodulation

I. Introduction

Conditional neuromodulation for bladder control relies on a feedback signal indicating bladder status [1]. For a chronic therapy, real-time feedback of bladder pressure is required, and existing catheters are not suitable for long-term use due to infection risk and their impractical and stigmatized nature. There is presently no option for ambulatory, catheter-free real-time bladder pressure feedback, other than relying on patient sensation (which may not be intact for all individuals).

Existing implantable bladder pressure sensors have mainly targeted acute diagnosis applications. Some wireless pressure sensors [2] [3] use primary cell batteries or transmit pressure data at millihertz rates to save energy; this data rate cannot provide real-time feedback for neuromodulation. A chronic bladder pressure sensor should include wireless energy transfer to maintain device operation over years of operation. Because the bladder is located in the pelvis and can be surrounded by more than 20 cm of tissue in obese patients, continuous RF-powering—which has been very successful in shallow-depth wireless sensors—is not feasible without reducing patient mobility.

We developed a wireless pressure sensor specifically for cystoscopic implantation within the bladder wall [4] (Fig. 1). The sensor uses a rechargeable battery which may be recharged while the user sleeps or sits atop a cushion with embedded RF induction coil. This scheme does not limit patient mobility and can provide continuous real-time bladder pressure telemetry.

Several details of this work have been previously published in various formats [4], [5]. Here, we present a cohesive overview of our approach to designing the wireless pressure monitor, specifically details on sensor encapsulation and chronic implant testing. We also are presenting new data gathered during large-animal implantation testing.

II. Wireless Pressure Monitor Microsystem

Achieving a small implant size in a chronic medical device requires ultra-low-power circuitry to reduce battery capacity. To maintain a small power budget while providing real-time transmission of pressure data, we created an ultra-low-power, fully-integrated pressure sensor ASIC. The ASIC was combined with a MEMS pressure sensor (Sensonor SW415 [7]), discrete capacitors, radio antennas, and a rechargeable battery to form a complete implantable microsystem.

Details on the ASIC and microsystem design have been previously discussed [6] and are summarized here (Fig. 2). The ASIC achieves ultra-low-power draw through switched-bias power control and adaptive transmission rate based on bladder pressure activity. Long-term pressure sensor drift is a known concern—especially in implanted sensors interfacing with tissue—so a novel DC offset removal feedback loop based on discrete-time computation was included [8].

III. Nonhermetic Pressure Sensor Encapsulation

We developed a nonhermetic polymer sensor package over a period of iteration using interdigitated electrodes soaked in hot saline to determine failure modes. Our key finding in these studies was that any inclusions of foreign particles provides water condensation points, leading to layer delamination and package failure. Our packaging process was performed in a Class-100 clean room to minimize contamination (Fig 3).

Full details of the packaging process were published [9], and are only briefly summarized here. Devices were cleaned and the MEMS pressure sensor protected by a convex drop of PDMS gel (Sylgard 527, Dow Corning). Two 5-μm layers of Parylene-C (Specialty Coating Systems) were deposited (PDS 2010 reactor) as vapor barriers and to create a flexible pressure-sensitive diaphragm (Fig. 4c,d). PDMS molds were cast from 3D-printed parts; the pressure diaphragm was fixed to the inner mold wall by PDMS (MDX-4210, Dow Corning) to prevent ingress of molding epoxy. Epoxy (EB-107LP, Epoxyset, Inc) was injected into the mold under vacuum and cured. A final 100-μm layer of PDMS was applied by a roller to the exterior of the device to enhance biocompatibility.

IV. In Vivo Wireless Bladder Pressure Sensing

Sterilized wireless pressure monitors (n=6) were implanted with conventional urologic instruments in large animal models (female Jersey calves) weighing 60–75 kg (n=5). Device position was confirmed by X-ray, and the wireless recharge antenna alignment was determined (Fig. 6). Animals carried the implanted wireless sensors for 2–4 weeks. We recorded wireless data and performed conscious wireless battery charging every other day. Animals were anesthetized weekly to assess the bladder healing response, bladder capacity, and device position.

During anesthetized checkups, data were collected from the pressure monitor and a reference catheter. A loss of device sensitivity was apparent after implantation. During manual bladder compressions, for example, the wireless sensor detected attenuated pressure changes (Fig. 7a,b). Correlation coefficients (Table 2) during compressions were high (mean $\overline{r}=0.90$) and correlation during 300-s recordings was moderate (r=0.68–0.77).

After the device was explanted, the static pressure sensor response was linear (Fig. 7c). Therefore, we hypothesize that a biomechanical effect may have caused the sensitivity loss when the sensor was implanted within the bladder muscle.

The outcomes from in vivo tests of the pressure monitor showed that the pressure sensor circuits functioned in large mammals. Pressure accuracy was affected by implant location, but correlation with compressions was noted, which is still useful for conditional bladder neuromodulation. No device failures due to moisture ingress were observed, confirming efficacy of the nonhermetic package. Device retention within the bladder was poor, with erosion into the bladder occurring at 2–4 weeks. Improvements to device anchoring may mitigate this effect.

V. Conclusion

We designed and tested a wireless pressure sensor intended for chronic implantation in the bladder wall. A nonhermetic polymer encapsulation package was tested to be chronically viable over 6 months of implantation in rodents. Pressure monitors were implanted in large animals using conventional urologic instruments and minimally-invasive methods. Wireless pressure measurements and battery recharge were performed in freely moving animals. Simultaneous pressure recordings from the pressure monitor and a reference catheter showed a damping effect caused by sensor measurement from within the bladder muscle—wireless data were attenuated but correlated with bladder compressions. Ultimately, the implant location was found to be unsuitable due to the damping effect and poor device retention rates at one month. By addressing these effects, a chronic pressure monitor capable of providing real-time pressure feedback for conditional neuromodulation may be realized.