Abstract:
In some embodiments, systems, methods and devices for using passive pressure sensors to measure pressure at an inaccessible location are provided. In some embodiments, a system for determining pressure in a ventriculoperitoneal shunt implanted in a subject is provided, the system comprising: an acoustic source emitting signals over a range of frequencies; the ventriculoperitoneal shunt, comprising: a lumen that provides a conduit for cerebrospinal fluid between; and a passive acoustic element in a wall of the ventriculoperitoneal shunt filled with a gas, wherein the passive acoustic element emits a second signal at a resonant frequency that varies based on the pressure on the passive acoustic element; an acoustic receiver that detects the second signal and outputs an electrical signal that represents at least the resonant frequency; and a processor programmed to: receive the electrical signal; determine the pressure using the resonant frequency; and present the pressure using a display.
Abstract:
A method for detecting a stenosis in a prosthesis includes providing a tubular prosthesis having a sensor coupled to the prosthesis and implanting the tubular prosthesis in a native fluid conduit. The sensor senses the stenosis and captures data that characterizes the stenosis. A spectral analysis of the data may then be performed in order to provide a frequency spectrum of the data. The frequency spectrum may be examined in order to identify a break frequency value in the frequency spectrum. The break frequency may then be translated into a percentage of stenosis in the tubular prosthesis.
Abstract:
Devices, systems, and methods configured to assess the severity of a blockage in a vessel and, in particular, a stenosis in a blood vessel, provide visual depictions of vessel that allow assessment of the vessel and,in particular, any stenosis or lesion of the vessel, simulate one or more treatment options for the vessel, and perform treatment on any stenosis or lesion of the vessel, including guiding placement of one or more treatment devices are provided. The method can include obtaining pressure measurements from first and second instruments positioned within a vessel of a patient during a diagnostic procedure where the second instrument is moved longitudinally through the vessel; identifying a treatment option based on the obtained pressure measurements; and performing the identified treatment option, wherein a user display guides placement of one or more treatment devices associated with the identified treatment option.
Abstract:
A method for implanting a stent includes contracting a self-expanding/forcibly-expanding stent of a shape-memory material set to a given shape to a reduced implantation size with a delivery system having drive wires. The stent has a selectively adjustable assembly with adjustable elements operatively connected to the drive wires such that, when the adjustable elements are adjusted by the drive wires, a configuration change in at least a portion of the self-expanding stent occurs. The contracted stent is inserted into a native annulus in which the stent is to be implanted. The drive wires are rotated with the delivery system to forcibly expand the stent into the native annulus. While rotating the drive wires, a torque applied to the drive wires is determined with the delivery system. Rotation of the drive wires is stopped based upon a value of the determined torque.
Abstract:
Assemblies are provided comprising a stent and a sensor positioned on and/or in the stent. Within certain aspects the sensors are wireless sensors, and include for example one or more fluid pressure sensors, contact sensors, position sensors, accelerometers, pulse pressure sensors, blood volume sensors, blood flow sensors, blood chemistry sensors, blood metabolic sensors, mechanical stress sensors and/or temperature sensors. Within certain aspects these stents may be utilized to assist in stent placement, monitor stent function, identify complications of stent treatment, monitor physiologic parameters and/or medically image a body passageway, e.g., a vascular lumen.
Abstract:
An intravascular device (4) for placement within an animal vessel (6), the intravascular device (4) being adapted to at least one of sense and stimulate activity of neural tissue (54) located outside the vessel (6) proximate the intravascular device (4).
Abstract:
A system for monitoring a body includes a surgical implant configured for implantation within a body, a sensory module coupled to the surgical implant and configured for implantation into the body in conjunction with the surgical implant, and a communication module coupled to the surgical implant and configured for implantation into a body in conjunction with the surgical implant. The sensory module is configured to monitor characteristics of the surgical implant, surrounding tissue and/or adjacent tissue. The communication module is electrically coupled to the sensory module and is configured to communicate a signal derived from said characteristics to an external entity.
Abstract:
Implantable apparatuses or biosensors for facilitating imaging-based diagnoses and methods thereof are disclosed. An implantable apparatus is configured to exhibit a form when subjected to a first physical parameter indicative of a first physiological state, and a second form when subjected to a second physical parameter indicative of a second physiological state.
Abstract:
Various implantable medical device embodiments stimulate an autonomic neural target from within a pulmonary artery, and comprise at least one electrode, a power supply, a neural stimulator connected to the power supply, and an anchor structure. The neural stimulator is configured to generate a neural stimulation signal for delivery to the neural stimulation target through the at least one electrode. The anchor structure is configured to chronically and securely implant the neural stimulator, the power supply and the at least one electrode within the pulmonary artery. The anchor structure, the neural stimulator, the power supply and the at least one electrode are configured to be implanted through a pulmonary valve into the pulmonary artery. In various embodiments, the neural stimulator is configured to be operational to implement a neural stimulation protocol when chronically implanted within the pulmonary artery without a wired connection through the pulmonary valve.