Ams Research Corporation

Nuvectra Corporation

Medtronic, Inc.

Boston Scientific Scimed, Inc.

Steven Siegel

Kimberly A Anderson

Kevin R Arnal

Brian P Watschke

Robert E Lund

Norbert F Kaula

Yohannes Iyassu

Michele Spinelli

Martin T Gerber

John Matthew Swoyer

Eric H Bonde

Scott F Drees

Giancarlo Barolat

Johann J Neisz

A method of evaluating an implantation of a lead is disclosed. Via a graphical user interface of an electronic device, a visual representation of a sacrum of the patient and a lead that is implanted in the sacrum is displayed. The lead includes a plurality of electrode contacts. An evaluation is made as to how well the lead has been implanted in the sacrum based on the visual representation of the sacrum and the lead. The evaluating comprises: determining whether the lead is inserted in a predetermined region of the sacrum, determining how far a predetermined one of the electrode contacts is located from an edge of the sacrum, and determining a degree of curvature of the lead.

Systems, methods, and devices for evaluating lead placement based on generated visual representations of sacrum and lead

An anal electrode device is configured to measure a response of a patient to a stimulation pulse. The anal electrode device includes an elongated shaft that is configured to be at least partially inserted into an anal canal of the patient. A first sensory electrode is disposed on a first region of the shaft. The first sensory electrode is configured to measure a compound motor action potential (CMAP) from an internal sphincter of the patient while the shaft is partially inserted into the anal canal of the patient. A second sensory electrode is disposed on a second region of the shaft. The second sensory electrode is configured to measure the CMAP from an external sphincter of the patient while the shaft is partially inserted into the anal canal of the patient.

Methods, systems and devices for determining optimal placement for pudendal nerve stimulation lead using patient feedback

In various examples, an apparatus includes a stimulation lead including an elongate body including a distal end and a proximal end. At least one first electrode is disposed proximate the distal end of the elongate body and is configured to stimulate a first target nerve. At least one second electrode is disposed between the at least one first electrode and the proximal end of the elongate body and is configured to stimulate a second target nerve. At least one first fixation structure is disposed between the at least one second electrode and the proximal end of the elongate body. The at least one first fixation structure is configured to anchor the stimulation lead proximate the sacrum, wherein the at least one first fixation structure is located on the elongate body and spaced a first distance proximally along the elongate body from the at least one first electrode.

Implantable medical lead for stimulation of multiple nerves

The present invention includes a method of implanting a urethral prosthesis. The method includes making an incision, positioning arms of the prosthesis in the pelvic region of the patient, and positioning a stem of the prosthesis in the scrotum of the patient.

Male urethral prosthesis with tensioning member

The present disclosure involves a method of measuring a physiological feedback from a patient in response to electrical stimulation. A stimulation parameter of a sacral nerve stimulation therapy is ramped up. The sacral nerve stimulation therapy includes electrical pulses generated by a pulse generator based on programming instructions received from an electronic programmer. The electrical pulses are delivered to a patient via a stimulation lead that is implanted in the patient. Via an anal electrode device that is at least partially inserted inside an anal canal of the patient, a compound motor action potential (CMAP) is measured from an anal sphincter of the patient while the stimulation parameter of the sacral nerve stimulation therapy is being ramped up. A stimulation threshold is determined based on the measured CMAP.

The present invention provides a urethral prosthesis including a first and a second arm that join to form a junction, and a stem that is also joined to the junction. The junction is adapted to exert sufficient pressure on a portion of a patient's urethra to prevent unintentional voiding of the patient's bladder. However, upon exerting a tension force on the stem, the pressure exerted by the junction is reduced such that the patient's bladder may be intentionally voided.

The disclosure is directed to a method and tool for implanting a stimulation lead or other medical device adjacent a pudendal nerve. The tool includes a shaped needle that enters a patient and passes through an obturator foramen passage in a pelvis. A physician places a tip of the tool at the pudendal nerve and performs test stimulation to confirm an effective stimulation location. A shape memory cannula initially covering the needle remains at the pudendal nerve when the physician removes the tool. The cannula deforms to follow the curve of the pudendal nerve once the needle is removed, and a lead is inserted into the cannula and secured at the pudendal nerve placement site. This method may provide an easier and more consistent procedure for implanting the stimulation lead near the pudendal nerve.

Transobturator lead implantation for pelvic floor stimulation

The present invention provides a urethral prosthesis including a substrate, an inflatable pillow attached to the substrate, a pressurized reservoir in fluid communication with the pillow and a restrictor. Upon compression of the inflatable pillow, inflating agent is transferred from the inflatable pillow to the pressurized reservoir. Upon terminating compression, inflating agent returns to the inflatable pillow. The urethral prosthesis may be implanted such that the inflatable pillow prevents unintentional voiding of a patient's bladder.

Growing community of inventors

North Oaks, MN, United States of America

Steven Siegel