Pacesetter, Inc.

Medtronic, Inc.

St. Jude Medical, Inc.

Other

St. Jude Medical, Cardiology Division, Inc.

Pacsetter, Inc.

Paceetter, Inc.

Xiaoyi Min

Gene A Bornzin

Kyungmoo Ryu

Stuart Rosenberg

Jong Gill

Gabriel A Mouchawar

Wenbo Hou

Zoltan Somogyi

John W Poore

Rahul Mehra

Peter Boileau

Rupinder Bharmi

Joseph J Florio

Wenwen Li

Euljoon Park

Edward Karst

Matthew G Fishler

Richard P Williamson

Keith Victorine

Alexander Kent

Bruce A Morley

Fujian Qu

Michael E Benser

Weiqun Yang

Mark T Stewart

Yougandh Chitre

David E Francischelli

William J Flickinger

Virote Indravudh

Melanie Goodman Keiser

Jeffery D Snell

Mary M Morris

Xing Pei

Terrell M Williams

Phong D Doan

David Muller

Allen J Keel

Luc Roland Mongeon

Annapurna Karicherla

Anders Bjorling

David Ligon

Didier Theret

Yun Qiao

Yong D Zhao

Kritika Gupta

Dorin Panescu

Taraneh Ghaffari Farazi

Timothy G Laske

Steve Koh

Laurence S Sloman

Brian Jeffrey Wenzel

Jan O Mangual-Soto

John G Keimel

Gregory A Boser

Martin Cholette

Michael R Hill

Dan E Gutfinger

Jay Snell

Mihir Naware

Avi Fischer

Mark W Kroll

Paul A Levine

Yelena Nabutovsky

Timothy A Fayram

Eric Falkenberg

Kevin L Morgan

Nima Badie

Luke C McSpadden

Kenneth M Anderson

J Christopher Moulder

Michael R Ujhelyi

Fady Dawoud

Ali Dianaty

Benjamin T Persson

Stuart Owen Schecter

Alan B Vogel

Paul J DeGroot

Peter M Mulier

Riddhi Shah

Eliot L Ostrow

Aditya Goil

Neha Malhotra

Ingmar Viohl

Xiangqun Chen

Shiloh Sison

Xi Lin Chen

Michael Xiaoxuan Yang

Li Ping Wang

Nils Holmström

Walter H Olson

Peter M J Mulier

Reza Shahandeh

Karin Järverud

Sheldon Williams

Aaron T Raines

Gary R Dulak

Chunlan Jiang

Thanh Tieu

Scott Salys

Bing Zhu

A system and method for modeling patient-specific spinal cord stimulation (SCS) is disclosed. The system and method acquire impedance and evoked compound action potential (ECAP) signals from a lead positioned proximate to a spinal cord (SC). The lead includes at least one electrode. The system and method determine a patient-specific anatomical model based on the impedance and ECAP signals, and transform a dorsal column (DC) map template based on a DC boundary of the patient-specific anatomical model. Further, the system and method map the transformed DC map template to the patient-specific anatomical model. The system and method may also include the algorithms to solve extracellular and intracellular domain electrical fields and propagation along neurons. The system and method may also include the user interfaces to collect patient responses and compare with the patient-specific anatomical model as well as using the patient-specific anatomical model for guiding SCS programming.

Spinal cord stimulation guidance system and method of use

Methods and systems for dynamically modifying pacing timing and backup pacing delivery in cardiac stimulation devices include applying pacing impulses, measuring corresponding responses, and, based on such responses, automatically modifying timing or operational settings of the stimulation device to improve pacing functionality. Among other things, the approaches described herein reduce unnecessary backup pacing impulses in HIS bundle pacing applications, facilitate fusion in bundle branch block applications, and automatically enable or disable backup pacing in response to achieving QRS complex correction.

Systems and methods for improved his bundle and backup pacing timing

Described herein are methods for use with an implantable system including at least an atrial leadless pacemaker (aLP). Also described herein are specific implementations of an aLP, as well as implantable systems including an aLP. In certain embodiments, the aLP senses a signal from which cardiac activity associated with a ventricular chamber can be detected by the aLP itself based on feature(s) of the sensed signal. The aLP monitors the sensed signal for an intrinsic or paced ventricular activation within a ventricular event monitor window. In response to the aLP detecting an intrinsic or paced ventricular activation itself from the sensed signal within the ventricular event monitor window, the aLP resets an atrial escape interval timer that is used by the aLP to time delivery of an atrial pacing pulse if an intrinsic atrial activation is not detected within an atrial escape interval.

Ventricular far-field sensing to guide atrial leadless pacemaker and beyond

A subcutaneous implantable medical device and method (SIMD) provided. A pulse generator (PG) is configured to be positioned subcutaneously within a lateral region of a chest of a patient. The PG has a housing that includes a PG electrode. The PG has an electronics module. An elongated lead is electrically coupled to the pulse generator. The elongated lead includes a first electrode that is configured to be positioned along a first parasternal region proximate a sternum of the patient and a second electrode that is configured to be positioned at an anterior region of the patient. The first and second electrodes are coupled to be electrically common with one another. The electronics module is configured to provide electrical shocks for antiarrhythmic therapy along at least one shocking vector between the PG electrode and the first and second electrodes.

Implantation medical device with multiple parasternal-anterior electrodes

A computer implemented method and system for monitoring types of capture within a distributed implantable system having a leadless implantable medical device (LIMD) to be implanted entirely within a local chamber of the heart and having a subcutaneous implantable medical device (SIMD) to be located proximate the heart are provided. The method is under control of one or more processors of the SIMD configured with program instructions. The method collects far field (FF) evoked cardiac signals following the pacing pulses delivered by the LIMD for an event and analyzes the FF evoked cardiac signals to identify a type of HIS capture as loss of capture (LOC), selective capture, myocardial tissue-only (MT-only) capture, or a non-selective (NS) capture and records a label for the event based on the type of HIS capture identified.

Method and system for monitoring types of capture of a leadless implantable medical device

Disclosed herein is a screw-in lead implantable in the pericardium of a patient heart and a system for delivering such leads to an implantation location. The leads include a helical tip electrode and a curvate body including a defibrillator coil with improved contact between the defibrillator coil and the patient heart. The delivery system includes a delivery catheter and lead receiving sheath disposed within the catheter. A fixation tine is disposed on one of the delivery catheter and the lead receiving sheath such that the delivery system may be anchored into the pericardium during fixation of the screw-in lead. In certain implementations, an implantable sleeve receives the leads to bias the defibrillator coil against the patient heart.

Screw-in pericardial leads and systems for delivering screw-in pericardial leads

Embodiments described herein relate to implantable medical devices (IMDs) and methods for use therewith. Such a method includes using an accelerometer of an IMD (e.g., a leadless pacemaker) to produce one or more accelerometer outputs indicative of the orientation of the IMD. The method can also include the IMD using an accelerometer to identify when the orientation of the IMD is such that the IMD will likely be able to successfully communicate with another IMD via one or more communication pulses sent from the IMD to the other IMD. The method also includes the IMD sending of the one or more communication pulses, that are used to communicate with the other IMD, when the orientation of the IMD is such that the IMD will likely be able to successfully communicate with the other IMD via one or more communication pulses sent from the IMD to the other IMD.

Enhanced implant-to-implant communications using accelerometer

Implantable medical devices (IMDs), systems, and methods for use therewith are disclosed. One such method is for use by a leadless pacemaker (LP) configured to perform conductive communication with another implantable medical device (IMD). The method includes the LP storing information that specifies when, within a cardiac cycle, the LP and the other IMD implanted in a patient are likely oriented relative to one another such that conductive communication therebetween should be successful. The method also includes the LP sensing a signal indicative of cardiac activity of the patient over a plurality of cardiac cycles, and outputting one or more conductive communication pulses, during a portion of at least one of the cardiac cycles, wherein the portion of the at least one of the cardiac cycles is identified based on the signal that is sensed and the information that is stored.

Enhanced implant-to-implant communications

The present disclosure provides systems and methods for applying anti-tachycardia pacing (ATP) using subcutaneous implantable cardioverter-defibrillators (SICDs). An SICD implantable in a subject includes a case including a controller, and at least one conductive lead extending from the case. The at least one conductive lead includes a plurality of coil electrodes, wherein the SICD is configured, via the controller, to apply anti-tachycardia pacing (ATP) to the subject using the at least one conductive lead.

Systems and methods for applying anti-tachycardia pacing using subcutaneous implantable cardioverter-defibrillators

Subcutaneous implantation medical device with multiple parasternal-anterior electrodes

System and methods are provided herein and include a HIS electrode configured to be located proximate to a HIS bundle and to at least partially define a HIS sensing vector. They system includes memory to store program instructions and cardiac activity (CA) signals for a series of beats utilizing a candidate sensing configuration. The candidate sensing configuration is defined by i) the HIS sensing vector and ii) a sensing channel that utilizes sensing circuitry configured to operate based on one or more sensing settings to detect near field and far field activity. The system includes one or more processors that, when executing the program instructions, are configured to analyze the CA signals to obtain an atrial (A) feature of interest (FOI) and a ventricular (V) FOI for the corresponding beats within the series of beats and identify a V-A FOI relation between the A FOIs and the V FOIs across the series of beats. The system adjusts the candidate sensing configuration and repeat the obtain, analyze and identify operations to obtain a collection of V-A FOI relations for a corresponding collection of candidate sensing configurations and selects a resultant sensing configuration from the collection of candidate sensing configurations based on one or more criteria, the resultant sensing configuration to be utilized to manage HIS bundle pacing during an atrial arrhythmia.

Method and device for managing his bundle pacing in a non-tracking mode during AF/AT

An implantable system includes a first leadless pacemaker (LP1) implanted in or on a first chamber of a heart and a second leadless pacemaker (LP2) implanted in or on a second chamber of the heart. The LP1 is configured to time delivery of one or more pacing pulses delivered to the first chamber of the heart based on timing of cardiac activity associated with the second chamber of the heart detected by the LP1 itself. The LP1 is also configured to transmit implant-to-implant (i2i) messages to the LP2. The LP2 is configured to time delivery of one or more pacing pulses delivered to the second chamber of the heart based on timing of cardiac activity associated with the second chamber of the heart as determined based on one or more i2i messages received by the LP2 from the LP1.

Systems and methods for performing pacing using multiple leadless pacemakers

Systems and methods for implanting a lead. The system includes an active guidewire having proximal and distal ends. The distal end includes a guidewire anchor that is configured to be attached to a target SOL. The active guidewire is configured to be utilized to electrically map the target SOI by at least one of delivering stimulation energy through the active guide wire to the target SOI or sensing an evoked response at the target SOI from the guidewire. The system also includes a lead having a lead body with proximal and distal ends and with a lumen extending between the proximal and distal ends. The distal end of the lead body is configured to receive the proximal end of the active guidewire. The lumen is configured to permit the lead body to be advanced over the active guidewire.

Systems and methods for implanting a medical device using an active guidewire

Growing community of inventors

Thousand Oaks, CA, United States of America

Xiaoyi Min