Boston Scientific Neuromodulation Corporation

Leland Stanford Junior University

Novonate, Inc.

Boston Scientific Neuromodulation Corporaton

Ross Daniel Venook

Matthew Lee McDonald

Eric Johnson

Gaurav Gupta

Shivani Alexandra Torres

Eric Fayez Chehab

James Kennedy Wall

Eric Anthony Kramer

Joseph M Bocek

Kiran K Gururaj

Marlo Dreissigacker Kohn

Rafael Carbunaru

Tatum Tarin

Bryant Lin

Mizanur Rahman

Venita Chandra

Siddhartha Joshi

Carl Linden Dambkowski

Lauren So Young Wood

Marisa Janelle San Agustin Borja

Cerys Rohann Murray-Scott

Julie Papanek

Richard G Vecchiotti

Jonathan Andrew Fritz

James Wall

Joseph De-Chung Shih

Jordi Parramon

Anne Margaret Pianca

Friedrich B Prinz

Paul J Wang

Salomo Siilas Murtonen

Joel Goldsmith

Jacob Matthew Muhleman

Matthew Lee Mcdonald

Mario Dreissigacker Kohn

Chirag M Patel

Peter Hwang

Richard Goode

Salomo Murtonen

Lauren So Wood

Matthew L Mcdonald

A catheter interface protection device can include a shield. The shield can include an open bottom, a transparent upper surface, sidewalls, and a cavity at least partially defined by the bottom, the upper surface, and the sidewalls. The device can include a vent. The device can include a clip, a tether, and a latch. A non-therapeutic method of protecting a catheter interface can include extending a catheter in the subject through a slot in a catheter interface protection device, wrapping the catheter at least partially around a clip of the catheter interface protection device, and securing a latch of the catheter interface protection device around the clip. A device for positioning a subject in a prone position can include a padded area including an opening configured to accommodate a catheter interface protection device.

Systems and methods for securing catheters

Catheter securing device

A device for protecting an umbilical stump-catheter interface, includes: a shield having a wall that defines a cavity for accommodating an umbilical stump, wherein the shield further includes a base for attachment to a patient; and an opening at the shield for allowing an umbilical catheter to extend therethrough. A method for protecting an umbilical stump-catheter interface, includes: providing a device having a shield with a wall that defines a cavity for accommodating an umbilical stump, wherein the shield further includes a base for attachment to a patient, and wherein the device further includes an opening at the shield; shielding the umbilical stump from an environment using the shield; and accommodating an umbilical catheter using the opening at the shield.

Systems and methods for protecting umbilical stumps

Methods, medical devices, and magnetic resonance imaging (MRI) systems are provided. A patient implanted with a medical device is exposed to a time-varying magnetic field having a signature, thereby inducing mechanical vibrations in at least one component of the medical device. A vibrational characteristic of the mechanical vibrations induced in the component(s) is detected. The vibrational characteristic is analyzed, and the signature of the magnetic field is identified based on the analyzed vibrational characteristic. The medical device is automatically switched from a first operational mode to a second operational mode when the signature is identified.

Systems and method for automatically detecting an MRI environment for patient implanted with medical device

An active implantable medical device (AIMD) for use with a medical lead carrying at least one lead electrode. The AIMD comprises interior electronic circuitry configured for performing a medical function via the medical lead, an electrically conductive case containing the interior electronic circuitry, at least one electrical terminal configured for electrically coupling the electronic circuitry respectively to the lead electrode(s), and an inductive element coupled in series between the electrical terminal(s) and the case. The inductive element is configured for hindering the shunting of electrical current from the at least one electrical terminal to the case that has been induced by electromagnetic interference (EMI) impinging on the medical lead.

Implantable medical device having electromagnetic interference filter device to reduce pocket tissue heating

A neurostimulation device capable of being placed between a stimulation state and an EMI protection state. The neurostimulation device comprises a plurality of electrical terminals configured for being respectively coupled to a plurality of stimulation electrodes, stimulation output circuitry configured for being selectively activated during the stimulation state to output a plurality of stimulation pulses to the plurality of electrical terminals, electromagnetic protection circuitry configured for being selectively activated during the EMI protection state to prevent at least a portion of the electrical current induced on at least one of the electrical terminals by an electromagnetic field entering the stimulation output circuitry, and a controller configured for automatically defaulting the neurostimulation device to the EMI protection state.

Neurostimulation system with default MRI-mode

An implantable electrical stimulation lead includes a lead body having a distal end, a proximal end, and a longitudinal length; a plurality of electrodes disposed along the distal end of the lead body; a plurality of terminals disposed along the proximal end of the lead body; and a plurality of conductors electrically coupling the plurality of electrodes to the plurality of terminals. To reduce or redistribute current induced in the conductors during an MRI procedure, an internal conductive structure, such as a dummy coil or hollow metal tube, or non-therapeutic electrodes may be provided. Alternatively or additionally, a multi-layer region of the conductors may extend beneath the electrodes or terminals or the electrodes or terminals may vary in size or surface area.

Systems and leads for improved RF compatibility and methods of manufacture and use

An implantable electrical stimulation lead includes electrodes and terminals disposed on opposing ends of the lead. A liner extends along a longitudinal length of the lead and has at least two different outer diameters. Conductors are coiled around the liner and electrically-couple the electrodes to the terminals. The conductors include a first conductor and a second conductor. The first conductor includes alternating first and second coiled regions. The first coiled regions have tighter pitches than the second coiled regions. The second conductor includes alternating third and fourth coiled regions. The third coiled regions have tighter pitches than the fourth coiled regions. The conductors are arranged into repeating adjacent winding geometries disposed along the longitudinal length of the lead. The repeating adjacent winding geometries each include one of the first coiled regions and one of the third coiled regions axially disposed adjacent to one another.

Systems and methods for making and using leads for electrical stimulation systems with improved RF compatibility

The present invention relates generally to dynamic support devices, methods of providing dynamic support to target tissues, and kits comprising these devices. These devices may have particular utility in providing support to the urethra. The dynamic support devices generally comprise at least one attachment member for attachment to bodily tissue, and at least one support member, where the device capable of assuming a first configuration and a second configuration. The dynamic support devices may be configured to support a target tissue when the device is in its second configuration. The support member may comprise one or more rotating components, one or more deformable components, one or more sliding components, or a combination thereof.

Methods and devices for supporting, elevating, or compressing internal structures

A method of estimating response of a medical lead to an electromagnetic field includes providing a medical lead having a proximal end, a distal end, a plurality of electrodes disposed along the distal end, a plurality of terminals disposed along the proximal end, and a plurality of conductors extending along the medical lead and electrically coupling the electrodes to the terminals; individually applying a test field at each of a plurality of test positions along the medical lead using at least one excitation probe; for each application of the test field, determining a response to the application of the test field at one or more of the electrodes or terminals; generating a transfer function using a combination of the responses determined for the applications of the test field; and using the transfer function to estimate a response of the medical lead to an electromagnetic field.

Systems and methods for obtaining and using incident field transfer functions of electrical stimulation systems

Growing community of inventors

Millbrae, CA, United States of America

Ross Daniel Venook