Medtronic, Inc.

Other

Michael F Hess

H Toby Markowitz

Yong Kyun Cho

Todd Jon Sheldon

Wade M Demmer

Robert S Kieval

Eduardo N Warman

Rahul Mehra

Michael R S Hill

Nirav Vijay Sheth

James W Busacker

Edward Chinchoy

Kenneth M Riff

Carleen J Juran

Michael A Reinert

Subham Ghosh

Jeffrey M Gillberg

Saul E Greenhut

Mark L Brown

Troy Edward Jackson

Vincent E Splett

John Charles Stroebel

Mark K Erickson

Michael D Eggen

Michael R Ujhelyi

Kathryn Hilpisch

John C Rueter

Nancy Perry Pool

Michael R Hill

Michael B Shelton

Michael C Brown

Donald N Jensen

David E Ritscher

John T Meador

Ursula Gebhardt

Kathleen A Prieve

Weimin Sun

R Hardwin Mead

Christopher M Manrodt

Raylene Pitschneider

Daniel C Warner

Eric Olson

Henry L Weiner

Michael E Eggen

Patrick M Mahoney

Clifton W Owens

David Ritscher

A controller for an implantable blood pump, includes an accelerometer configured to measure at least one from the group consisting of position and movement of the controller. Processing circuitry is configured to control operation of the implantable blood pump, the processing circuitry being in communication with the accelerometer, the processing circuitry being configured to adjust a speed of the implantable blood pump if the measured at least one from the group consisting of position and movement deviates from a respective predetermined threshold.

Body position and activity based flow control for ventricular assist device (VAD) with fully implantable controller

Various embodiments of a transcutaneous energy transfer system are disclosed. The system includes an internal component adapted to be disposed within a body of a patient and an external component adapted to be disposed outside the body of the patient. The external component includes an external controller that is adapted to determine whether an internal coil of the internal component is electromagnetically disconnected from an external coil of the external component. If electromagnetically disconnected, then the external controller is adapted to determine a reconnection time threshold based upon at least one of a power transfer efficiency value between the internal coil and the external coil, a charge state of an internal power source, or a power consumption value of an implantable device, and output a charging alarm if a time interval when the internal coil is electromagnetically disconnected from the external coil exceeds the reconnection time threshold.

Transcutaneous energy transfer system including alarm

Techniques for minimizing rate of depletion of a non-rechargeable power source, to extend the operational lifetime of an implantable medical device that includes the non-rechargeable power source, by enforcing operational-mode-specific communication protocols whereby inter-device communication between the implantable medical device and another implantable medical device is such that level of power draw from the non-rechargeable power source by the implantable medical device is less than level of power draw from the rechargeable power source by the another implantable medical device for the implantable medical devices to engage in communication with each other.

Power management for implantable medical device systems

Systems and methods are described herein for evaluation and adjustment of a left ventricular assist device (LVAD). The systems and methods may utilize at least a plurality of external electrodes to monitor cardiac electrical activity before and during LVAD therapy. The cardiac electrical activity as well as other information such cardiac sound information may be used to determine and adjust one or more LVAD output parameters such as pump speed.

Left ventricular assist device adjustment and evaluation

An intracardiac ventricular pacemaker having a motion sensor is configured to produce a motion signal including an atrial systolic event and at least one ventricular diastolic event. The pacemaker is configured to set an atrial refractory period, detect a change in a ventricular diastolic event metric and adjust the atrial refractory period in response to detecting the change. The pacemaker sets set an atrioventricular pacing interval in response to detecting the atrial systolic event from the motion signal after expiration of the atrial refractory period.

Atrial tracking in an intracardiac ventricular pacemaker

A medical device system including at least a first implantable medical device and a second implantable medical device is configured to establish by a control module of the first implantable medical device whether the second implantable medical device is present in a patient and self-configure an operating mode of the control module in response to establishing that the second implantable medical device is present.

Multi-chamber intracardiac pacing system

A medical device is provided that includes an input/output, at least one sensor, a memory, a controller and at least one delivery member. The input/output is configured to provide a communication path to and from the medical device. The at least one sensor is used to monitor at least one patient function. The memory is used to store patient specific data from the at least one sensor and operating parameters of the medical device. The controller is used to control operations of the medical device. The controller is in communication with the at least one sensor, the memory and the input/output. The controller is configured to deny device operational change requests received via the input/output based at least in part on the patient specific data sensed by the at least one sensor. The at least one delivery member is under the control of the controller and is configured to provide a therapeutic function of the medical device.

Patient specific data driven safety interlocks for medical devices

A system and method for monitoring at least one chamber of a heart (e.g., a left ventricular chamber) during delivery of extrasystolic stimulation to determine if the desired extra-systole (i.e., ventricular mechanical capture following refractory period expiration) occurs. The system includes an implantable or external cardiac stimulation device in association with a set of leads such as epicardial, endocardial, and/or coronary sinus leads equipped with motion sensor(s). The device receives and processes acceleration sensor signals to determine a signal characteristic indicative of chamber capture resulting from one or more pacing stimulus delivered closely following expiration of the refractory period. A threshold optimization method optionally evaluates capture and at least one of: runs an iterative routine to establish or re-establish chamber capture for the PESP therapy, sets a logical flag relating to chamber capture status and stores parameter(s) relating to successful chamber capture for one or more subsequent cardiac cycles.

Mechanical ventricular pacing capture detection for a post extrasystolic potentiation (PESP) pacing therapy using at least one lead-based accelerometer

A system for accessing implantable medical device (IMD) data is provided including an interrogation appliance to retrieve data from an IMD and transfer the data to a processor. The processor converts the device data to a viewable form that is transferred by the processor to a data destination. The data destination may be an electronic mail address, a secure web site, a facsimile number or the interrogation appliance. The data is presented in a viewable form at the data destination either on a display or by printing. Any number of interrogation appliances may be communicatively coupled to the processor for converting IMD data and providing the IMD data back to a data destination in a viewable form for use by a clinician.

Clinic based instrument system for remote processing and access to implanted systems information

An implantable medical device used for thoracic fluid monitoring by detection of changes in impedance in a patient. The device measures impedances of the patient in a supine position and in an upright position. The device determines impedance differences between the supine and upright positions which correspond to a diurnal delta value, which may in turn be employed as a diagnostic parameter.

Advanced thoracic fluid monitoring capability with impedance

A device for delivering pacing therapy includes an atrial and ventricular leads, sensing circuitry connected to the leads for detecting depolarizations, and pulse generation circuitry for delivering ventricular pacing pulses based on sensed atrial depolarizations. The device includes control circuitry for controlling the pulse generation circuitry in a first mode in which the pulse generation circuitry delivers atrial synchronized pulses to both the right and left ventricular leads in response to each atrial depolarization sensed. In response to a detected atrial arrhythmia, the control circuitry causes the pulse generation circuitry to deliver atrial synchronized ventricular pacing pulses in response only to selected atrial depolarizations.

Device and method for providing atrial-synchronized ventricular pacing with selective atrial tracking

In some embodiments, a method for operating a cardiac rhythm management device may include one or more of the following steps: (a) sensing atrial depolarizations through an implanted atrial electrode, (b) administering a sequential CRT pacing therapy in a sequential CRT pacing mode to a left and right ventricle of a heart of a patient via implanted ventricular electrodes in a sequential bi-ventricular fashion, (c) switching from the sequential CRT pacing mode to a simultaneous CRT pacing mode, (d) administering a simultaneous CRT pacing therapy in the simultaneous CRT pacing mode to the left and right ventricle in a simultaneous bi-ventricular fashion, (e) analyzing the sensed atrial depolarizations to detect the presence of an atrial arrhythmia, (f) analyzing the sensed atrial depolarizations while in the sequential CRT pacing mode to detect the presence of atrial arrhythmia, and (g) sensing ventricular depolarizations of the left and the right ventricle.

Delivery of CRT therapy during AT/AF termination

A system and method for monitoring at least one chamber of a heart (e.g., a left ventricular chamber) during delivery of a refractory period stimulation (RPS) therapy to determine if the desired non-capture (i.e., lack of ventricular mechanical capture due to refractory period stimulation) occurs. The system includes an implantable or external cardiac stimulation device in association with a set of leads such as epicardial, endocardial, and/or coronary sinus leads equipped with motion sensor(s). The device receives and processes acceleration sensor signals to determine a signal characteristic indicative of chamber capture due to pacing stimulus delivery, non-capture due to RPS therapy delivery, and/or contractile status based on the qualities of evoked response to pacing stimulation.

Mechanical ventricular pacing non-capture detection for a refractory period stimulation (RPS) pacing therapy using at least one lead-based accelerometer

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Minneapolis, MN, United States of America

Michael F Hess