Patent application number | Description | Published |
20130023948 | DYNAMIC REPRESENTATION OF MULTIPOLAR LEADS IN A PROGRAMMER INTERFACE - An external programming system for programming an implantable medical device includes a user display and a memory storing multiple intracardiac lead images. The intracardiac lead images correspond to lead types and includes electrodes spaced according to the spacing of electrodes of a particular lead type. The programmer selects one of the lead images for display based on an indication of which type of lead has been implanted in a patient. The selected image is displayed to a user as part of a graphical user interface for programming cardiac pacing therapy for the patient. | 01-24-2013 |
20130046378 | Stented Prosthetic Heart Valves - A surgical sutureless valve that is attached to a stent frame for delivery to a location in a patient using percutaneous implantation devices and methods. | 02-21-2013 |
20130055941 | Methods and Apparatuses for Assembly of a Pericardial Prosthetic Heart Valve - A method of assembling a prosthetic valve using sheets of material, such as pericardium material, polymer or bioengineered film, or other material. The method provides an accurate and repeatable system of making pericardial valves in which sheets or pieces of material are held securely in place relative to each other throughout the steps of assembling the valve. In addition, methods of the present invention include maintaining consistent alignment of the fixtures and pericardium material throughout the valve assembly process and utilize features that make the tooling components easy to assemble and handle. Certain aspects of the invention can be used to help establish a repeatable sewing and cutting technique for creating a pattern shape for valve leaflets, establishing stitch lengths, and determining the exact placement of stitches. | 03-07-2013 |
20130060117 | Method and Apparatus for Identifying Oversensing Using Far-Field Intracardiac Electrograms and Marker Channels - A method for identifying oversensing in implantable medical devices (IMDs), such as implantable cardioverter defibrillators (ICDs), is described. A near-field electrogram signal and a far-field electrogram signal are obtained via a near-field electrode pair and a far-field electrode pair. The near-field electrogram signal is compared to the far-field electrogram signal and a determination of whether oversensing exists is made based on the comparison. In some instances, a scheduled therapy is withheld in response to determining that oversensing exists. | 03-07-2013 |
20130060303 | GENERATION OF PROPORTIONAL POSTURE INFORMATION OVER MULTIPLE TIME INTERVALS - The disclosure describes techniques for generation of proportional posture information over multiple time intervals. The techniques may include obtaining posture state data sensed by a medical device for a patient during delivery of therapy by the medical device, determining durations for which the patient occupied each of a plurality of posture states based on the posture state data, generating proportional posture information for a plurality of different time intervals based on the durations, wherein the proportional posture information for each of the time intervals indicates proportional amounts of the respective time interval in which the patient occupied the posture states, and presenting the proportional posture information to a user via a user interface. | 03-07-2013 |
20130090702 | BI-VENTRICULAR VENTRICULAR CAPTURE MANAGEMENT IN CARDIAC RESYNCHRONIZIATION THERAPY DELIVERY DEVICES - The present invention provides a technique for verifying pacing capture of a ventricular chamber, particularly to ensure desired delivery of a ventricular pacing regime (e.g., “CRT”). The invention also provides ventricular capture management by delivering a single ventricular pacing stimulus and checking inter-ventricular conduction during a temporal window to determine if the stimulus captured. If a loss-of-capture LOC) signal results from the capture management testing, then the applied pacing pulses are modified and the conduction test repeated. If LOC, an alert message can issue. Other aspects include: use of a trend of A-RV/LV and LV-RV timing intervals to monitor changes in the patient's heart conduction properties; bi-ventricular verification test and search—while still pacing BiV by detecting latent sense; single-V pacing threshold search, use of timing of sense in other V chamber to establish capture and LOC windows; (iv) use of a premature V pace rather than short AV interval if VV cannot be discriminated from AV; (v) option to run a threshold search only if the Bi-ventricular verification test fails. | 04-11-2013 |
20130096673 | Prosthetic Heart Valve Devices And Methods Of Valve Replacement - A stented valve having at least one leaflet made of pericardium or other material having a relatively thin profile at the annulus. The leaflets are attached via chords to a stent frame, where the chords are positioned to mimic the native valve anatomy and functionality. In particular, the valves of one exemplary embodiment of the invention are sized to replace a mitral valve and therefore the chords are arranged to prevent prolapse of the leaflets into the atrium. The stented valve has a relatively short height at its annulus due to the positioning of the chords. In addition, the stented valve is capable of being crimped to a small enough size that it can be delivered to the implantation site via transcatheter delivery systems and methods. | 04-18-2013 |
20130100597 | ELECTRONIC DEVICE WITH ADJUSTABLE KICKSTAND - A programmer for an implantable medical device includes an adjustable kickstand. In one example, the kickstand is configured to combine with the base to support the programmer in an upright position when the kickstand is fully-collapsed to support the programmer in a reclined position when the kickstand is fully-extended. Further, the programmer housing may include a fan grate that allows airflow from a cooling fan to pass through the programmer housing. The fan grate is positioned behind the kickstand when the kickstand is in the fully-collapsed position. The kickstand includes an aperture adjacent the fan grate when the kickstand is in the fully-collapsed position, the aperture allowing airflow from the cooling fan to pass through the fan grate when the kickstand is in the fully-collapsed position. | 04-25-2013 |
20130103049 | Methods, Tools, and Assemblies for Implantation of Medical Leads Having Distal Tip Anchors - Medical leads include distal tip anchors that are retained by fixation mechanisms of implantation tools. The fixation mechanism may include a fixed body that has features retaining the distal tip anchor. The fixation mechanism may include a movable body that can apply tension to the distal tip anchor to force the distal tip anchor to be released from the features of the fixed body. The movable body may include an axial portion that is received by an axial hole of the fixed body to allow for axial movement of the movable body to release the distal tip anchor. The fixation mechanism may instead include an elongated flexible body that passes through the distal tip anchor and is attached to the fixed body. Tension applied to the elongated body creates a releasing motion of the distal tip anchor to free the distal tip anchor from the features of the fixed body. | 04-25-2013 |
20130103141 | Pharmacological Delivery Implement for Use with Cardiac Repair Devices - A pharmacological delivery implement for use with cardiac repair devices. The pharmacological delivery implement comprises a porous member defining an outer surface, an internal channel configured to selectively house a pharmacological agent, and a plurality of release holes each extending from the outer surface to the internal channel. Following implantation of the pharmacological delivery implement, at least a portion of the pharmacological agent exits the internal channel through the plurality of release holes. | 04-25-2013 |
20130116743 | METHOD AND APPARATUS FOR THERAPIES OF THE CARDIOVASCULAR AND CARDIORENAL SYSTEM - A system and method for controlling respiration depth or respiration rate is provided. A bipolar pair of a plurality of electrodes is selected in a location for stimulating a phrenic nerve. Electrical stimulation is delivered through a medical electrical lead electrode proximate phrenic nerve tissue. Modulating respiration is elicited in response to electrical stimulation of the phrenic nerve. | 05-09-2013 |
20130123748 | TOOLS AND METHODS RELATED TO CATHETER DELIVERY - A syringe adapter tool facilitates inline connection of a syringe with a catheter lumen, as well as torque transfer between the syringe and catheter. The adapter tool may further facilitate passage of an instrument through a seal zone portion of the catheter lumen, which seal zone portion is located in a proximal section of the catheter. | 05-16-2013 |
20130123753 | CATHETER APPARATUS - A proximal terminal end of a proximal section of a catheter, preferably tapered, defines a perimeter of an opening into a lumen of the catheter and includes an exposed sealing area. A sealing assembly, that may be removed from the catheter, includes a relatively soft part and a relatively rigid part, wherein the exposed sealing area is formed by the soft part, and the relatively rigid part may include an attachment feature for removable connection of the assembly to the catheter. The lumen of the catheter, within the proximal section, may include a seal zone portion, which preferably includes a slit segment intersecting a funnel-like segment of a bore. The catheter proximal section may further include a feature for interlocking engagement with an accessory tool. | 05-16-2013 |
20130123913 | Catheter-Based Annuloplasty System and Method - A catheter-based annuloplasty system for use in repairing a heart valve having leaflets and a valve annulus, includes a delivery catheter having a proximal end and a distal end, and an expandable stent disposed on the distal end of the catheter. An adjustable annuloplasty ring is disposed on the expandable stent and is configured to expand and contract in response to expansion and contraction of the stent. | 05-16-2013 |
20130131745 | ELECTROCHEMICAL CELL WITH ADJACENT CATHODES - The disclosure includes an electrochemical cell comprising a first cathode and a second cathodes are adjacent one another in a stacked arrangement to form a cathode stack in the electrochemical cell. The first cathode includes a first current collector and a first cathode form of active material covering the first current collector, and the second cathode includes a second current collector and a second cathode form of active material covering the second current collector. The second current collector is in electrical contact with the first current collector. The electrochemical cell further comprises an anode adjacent to the cathode stack, and a separator located between the cathode stack and the anode. | 05-23-2013 |
20130131755 | PATIENT DIRECTED THERAPY CONTROL - A patient controls the delivery of therapy through volitional inputs that are detected by a biosignal within the brain. The volitional patient input may be directed towards performing a specific physical or mental activity, such as moving a muscle or performing a mathematical calculation. In one embodiment, a biosignal detection module monitors an electroencephalogram (EEG) signal from within the brain of the patient and determines whether the EEG signal includes the biosignal. In one embodiment, the biosignal detection module analyzes one or more frequency components of the EEG signal. In this manner, the patient may adjust therapy delivery by providing a volitional input that is detected by brain signals, wherein the volitional input may not require the interaction with another device, thereby eliminating the need for an external programmer to adjust therapy delivery. Example therapies include electrical stimulation, drug delivery, and delivery of sensory cues. | 05-23-2013 |
20130138176 | BRAIN STIMULATION PROGRAMMING - A programming system allows a user to program therapy parameter values for therapy delivered by a medical device by specifying a desired therapeutic outcome. In an example, the programming system presents a model of a brain network associated with a patient condition to the user. The model may be a graphical representation of a network of anatomical structures of the brain associated with the patient condition and may indicate the functional relationship between the anatomical structures. Using the model, the user may define a desired therapeutic outcome associated with the condition, and adjust excitatory and/or inhibitory effects of the stimulation on the anatomical structures. The system may determine therapy parameter values for therapy delivered to the patient based on the user input. | 05-30-2013 |
20130138991 | CLOCK SYNCHRONIZATION IN AN IMPLANTABLE MEDICAL DEVICE SYSTEM - This disclosure is directed to the synchronization of clocks of a secondary implantable medical device (IMD) to a clock of a primary IMD. The secondary IMD includes a communications clock. The communications clock may be synchronized based on at least one received communications pulse. The secondary IMD further includes a general purpose clock different than the communications clock. The general purpose clock may be synchronized based on at least one received power pulse. The communications clock may also be synchronized based on the at least one received power pulse. | 05-30-2013 |
20130139090 | Display of Target Cardiac Flow Based on Cardiac Index Calculation - User interfaces for medical perfusion systems that provide oxygenation, filleting, and recirculation of blood in connection with various medical procedures are provided. In particular, methods of displaying and communicating a desired target flow rate and cardiac index during cardiopulmonary bypass surgeries are provided. | 05-30-2013 |
20130144538 | Clot Protection and Detection Algorithm for Activated Clotting Time Testing - Activated clotting time (ACT) tests detect blood clotting time based on the viscosity changes of a test sample, using a ferromagnetic washer lifted to the top of a test chamber and then dropped from the top via gravity; a drop time greater than a preset threshold value indicates clotting of the test sample. Blood samples which have high levels of heparin usually produce very weak clots that may easily be destroyed by the lifting movement of the washer. But if the clot threshold is set low to detect the weak clots, false detections occur during early testing cycles when activators are not fully suspended during the mixing cycle. Improved algorithms for lifting the washer and adjusting over time enable accurate detection of weak clots. | 06-06-2013 |
20130148260 | HIGH DENSITY CAPACITOR ARRAY PATTERNS - A thin-film device system includes a substrate and a plurality of pillars. The plurality of pillars project from a surface of the substrate. Each of the plurality of pillars have a perimeter that includes at least four protrusions that define at least four recessed regions between the at least four protrusions. Each of the at least four recessed regions of each of the plurality of pillars receives one protrusion from an adjacent one of the plurality of pillars. A thin-film device is fabricated over the plurality of pillars. | 06-13-2013 |
20130150921 | AUTOMATIC THERAPY ADJUSTMENTS - A medical device detects a previously defined event, and controls delivery of therapy to a patient according to therapy information associated with the previously defined event. In exemplary embodiments, the medical device enters a learning mode in response to a command received from a user, e.g., the patient or a clinician. In such embodiments, the medical device defines the event, collects the therapy information, and associates the therapy information with the defined event while operating in the learning mode. In some embodiments, the medical device defines the event based on the output of a sensor that indicates a physiological parameter of the patient during the learning mode. The sensor may be an accelerometer, which generates an output that reflects motion and/or posture of the patient. The medical device may collect therapy information by recording therapy changes made by the user during the learning mode. | 06-13-2013 |
20130150939 | TECHNIQUES FOR PLACING MEDICAL LEADS FOR ELECTRICAL STIMULATION OF NERVE TISSUE - This disclosure is directed to extra, intra, and transvascular medical lead placement techniques for arranging medical leads and electrical stimulation and/or sensing electrodes proximate nerve tissue within a patient. | 06-13-2013 |
20130158564 | PERCUTANEOUS FLAT LEAD INTRODUCER - In general, the invention is directed to a technique for percutaneously introducing a stimulation lead into a target stimulation site via the epidural region proximate the spine of a patient. The process of introducing the stimulation lead may include the use of a hollow stimulation lead introducer, which comprises an elongated sheath and an elongated dilator. The dilator fits within the sheath and serves to widen a path through the epidural region for the introduction of a stimulation lead. At least a portion of the stimulation lead introducer has an oblong cross-section, allowing passage of stimulation leads such as paddle leads. The stimulation lead introducer may enter the epidural region proximate a spine of a patient via a guidewire. The stimulation lead introducer provides a path through the epidural region of a patient to a target stimulation site. A stimulation lead may travel through the path to reach the target stimulation site where it may provide therapy to the patient. | 06-20-2013 |
20130164584 | NEGATIVE-LIMITED LITHIUM-ION BATTERY - A rechargeable lithium-ion battery includes a housing including a titanium or a titanium alloy, a positive electrode having a first capacity and at least one positive active material selected from the group consisting of LiCoO | 06-27-2013 |
20130165983 | MONITORING ACTIVATION TIMES FOR USE IN DETERMINING PACING EFFECTIVNESS - Methods and/or devices may be configured to track effectiveness of pacing therapy by monitoring activation times over time, e.g., between pacing stimulus and electrical activity resulting from the pacing stimulus. Generally, the methods and/or devices may determine whether the delivered pacing therapy was effective based on the measured activation times. | 06-27-2013 |
20130165987 | FAULT TOLERANT PACING - Methods and/or devices may be configured to monitor the performance of pacing therapy and provide fault-tolerant operation to provide therapy in the event of certain failure modes occurring in the pacing delivery circuits, leads, and/or lead/tissue interfaces. Generally, the methods and/or devices may provide fault-detection, fault-recovery and fault-handling to, e.g., handle potential faults. | 06-27-2013 |
20130165988 | EFFECTIVENESS OF VENTRICULAR SENSE RESPONSE IN CRT - A method for monitoring the effectiveness of VSR and for taking action to improve the effectiveness of VSRs, if they are determined to be ineffective, includes comparing the a VSR evoked electrogram to a template electrogram of a pure biventricular paced CRT beat. If the electrograms, or features thereof, are similar, the VSR is determined to be effective. If the VSR is determined to be ineffective, the AV delay of biventricular CRT is shortened in a step-wise fashion in an incremental manner. | 06-27-2013 |
20130170287 | STABLE MEMORY SOURCE BIAS OVER TEMPERATURE AND METHOD - Random access memory having a plurality of memory cells, each of the plurality of memory cells having a memory element and a first electrical characteristic being variable based, at least in part, on temperature and a bias circuit operatively coupled to at least one of the plurality of memory cells, the bias circuit being configured to generate a bias voltage for the at least one of the plurality of memory cells. The bias circuit has a second electrical characteristic being variable based, at least in part, on temperature. The first electrical characteristic is approximately proportional to the second electrical characteristic over a predetermined range of temperatures, the predetermined range of temperatures being greater than zero. The bias voltage on each of the plurality of memory cells is approximately proportional with variations in the first electrical characteristic over the predetermined range of temperatures. | 07-04-2013 |
20130184654 | MEDICAL DELIVERY SYSTEMS AND APPARATUS - A catheter proximal section is preferably formed from a relatively soft part and a relatively rigid part, and includes a proximal terminal end that defines a perimeter of an opening into a lumen of the catheter. The proximal section may further include a feature for interlocking engagement with an accessory tool. An inner surface of each of the relatively soft and rigid parts may be located opposite one another, on either side of the catheter lumen. The relatively soft and rigid parts may be included in a sealing assembly that further includes an attachment feature for removable connection of the assembly to the proximal section catheter. | 07-18-2013 |
20130184786 | IMPLANTABLE MEDICAL DEVICES STORING GRAPHICS PROCESSING DATA - In one example, a device includes a telemetry module configured to retrieve graphics processing data from a device that is not configured to perform a rendering process using the graphics processing data and that is associated with delivering therapy to a therapy target of a patient, and a control unit configured to apply the graphics processing data while performing the rendering process to generate an image of an anatomical feature of the patient, wherein the anatomical feature comprises the therapy target for an implantable medical device, and to cause a display unit of a user interface to display the image, wherein the image of the anatomical feature is specific to the patient. The graphics processing data may include a list of vertices or a transform to be applied to a non-patient-specific anatomical atlas. The data may also include a location of a therapy element of the implantable medical device. | 07-18-2013 |
20130189789 | High Range Activated Clotting Time Assay Formulation - High range activated clotting time (HR-ACT) tests detect blood clotting time in blood samples which have high levels of heparin. Reagents such as calcium chloride and kaolin within the test apparatus trigger clotting. Physical separation of the reagents from each other prevents interaction between them before the test sample introduction. In one embodiment, to improve dry kaolin re-suspension, kaolin may be suspended in water rather than buffered saline before being dispensed into the test chamber. The combination of removing the buffered saline and the calcium chloride from the kaolin suspension enables clot detection in blood samples containing 5-6 u/ml of heparin. | 07-25-2013 |
20130190834 | MODIFYING ATRIOVENTRICULAR DELAY BASED ON ACTIVATION TIMES - Methods and/or devices may be configured to monitor ventricular activation times and modify an atrioventricular delay (AV delay) based on the monitored ventricular activation times. Further, the methods and/or devices may determine whether the AV delay should be modified based on the measured activation times before modifying the AV delay. | 07-25-2013 |
20130193914 | ADAPTIVE RATE RECHARGING SYSTEM - Devices, systems, and techniques for selecting a period for charging an implantable rechargeable power source are disclosed. Implantable medical devices may include a rechargeable power source that can be transcutaneously charged. A system may control a charging module to begin charging the rechargeable power source of the implantable medical device with a high power level. The system may then determine an estimated heat loss based on power initially delivered to the rechargeable power source when beginning the charging. Based on this estimated heat loss during the initial period of recharging, the system may select a boost period that includes a duration of time that the rechargeable power source is charged with the high power level. | 08-01-2013 |
20130193990 | SERVO TECHNIQUES FOR APPROXIMATION OF DIFFERENTIAL CAPACITANCE OF A SENSOR - Techniques and circuits are described for approximation of the differential capacitance of a capacitive sensor to, among other things, optimize device operation and power consumption. In particular, feedback techniques are utilized for measurement and approximation of the differential capacitance of the capacitive sensor. In accordance with the disclosure, the capacitance approximation value for a test cycle preceding a given test cycle is utilized to reduce the number of iterations to be performed in a continuous series of test cycles. The capacitance approximation value for the given test cycle is reported as being equivalent to that of the preceding test cycle if the variance between the selected capacitance and the unselected capacitance is less than or equal to a first predefined value. | 08-01-2013 |
20130197373 | IMPLANTABLE MEDICAL DEVICE HAVING OPTICAL FIBER FOR SENSING ELECTRICAL ACTIVITY - An implantable medical device for optically sensing action potential signals in excitable body tissue. The device includes an elongated tubular lead body carrying an optical fiber extending from a proximal lead end to a distal lead end to position the optical fiber at a target site. The lead body additionally carries a conduit for dispensing a voltage-sensitive fluorescent dye into tissue surrounding the target site. The optical fiber transmits excitation light to the fluorescent dye to cause the dye to fluoresce with varying intensity as the transmembrane potentials of local tissue cells vary due to passing depolarization wavefronts. The optical fiber transmits the fluorescence signal to the device to generate an action potential signal or fiducial points of an action potential signal for use in accurately measuring and characterizing electrical activity of excitable tissue. | 08-01-2013 |
20130197381 | AUTOMATIC SELECTION OF ELECTRODE VECTORS FOR ASSESSING RISK OF HEART FAILURE DECOMPENSATION EVENTS - An implantable medical device (IMD) is implanted in a patient. The IMD uses a plurality of electrode vectors to generate intrathoracic impedance measurements. The intrathoracic impedance measurements can be indicative of amounts of intrathoracic fluid in the patient. An accumulation of intrathoracic fluid may indicate that the patient is at an increased risk of experiencing a heart failure event in the near future. The IMD performs a vector selection operation on a recurring basis. When the IMD performs the vector selection operation, the IMD uses impedance measurements to select one of the electrode vectors. The IMD can perform a risk assessment operation on another recurring basis. During performance of the risk assessment operation, the IMD uses impedance measurements of the selected electrode vector and/or other patient characteristics stored within the IMD to determine whether the patient is at an increased risk of experiencing a heart failure event. | 08-01-2013 |
20130197385 | RESPIRATORY FUNCTION DETECTION - A method and system for monitoring respiratory function that includes an impedance sensor configured to sense a first thoracic impedance waveform for at least one breath of a patient, a memory configured to store a first threshold slope value, and a processor configured to determine an first breath slope value in response to the impedance waveform, compare the first breath slope value to a first threshold slope value, and determine an indication of respiratory function of the patient in response to the comparing. | 08-01-2013 |
20130197386 | RESPIRATORY FUNCTION DETECTION - A system and method for monitoring respiratory function that includes an acoustic sensing device sensing an acoustic waveform ocurring during one of an inspiration phase associated with at least one breath of a patient and an expiration phase associated with at least one breath of a patient, and a processor configured to determine changes in high frequency acoustic amplitude associated with the sensed acoustic waveform and, in response to the determined changes in high frequency acoustic amplitude, determine an indication of respiratory function. | 08-01-2013 |
20130197472 | Low Profile Instrument Immobilizer - This document discusses, among other things, examples of a low profile instrument immobilizer and means for positioning the same. In one example, the low profile instrument immobilizer grasps, secures, and immobilizes an electrode or other instrument that extends through a burr hole in a skull to a target location in a patient's brain. | 08-01-2013 |
20130197562 | Gastric Stretch Devices, and Methods for Treatment of Obesity - Medical devices, systems and methods are provided and are designed to stretch the stomach wall of a patient to treat obesity. Stretch devices attached to the stomach wall may trigger stretch receptors to expand the stomach into a state of apparent stretching, causing early onset of satiety thereby causing the patient to consume less food. Stretching of the stomach can be achieved by the attachment of stretch devices to the wall of the stomach. The devices may be expandable and contractible and, in some embodiments, may take the form of a device that expands following attachment to a wall of the stomach. | 08-01-2013 |
20130197605 | STIMULATION ELECTRODE SELECTION - Bioelectrical signals may be sensed within a brain of a patient with a plurality of sense electrode combinations. A stimulation electrode combination for delivering stimulation to the patient to manage a patient condition may be selected based on the frequency band characteristics of the sensed signals. In some examples, a stimulation electrode combination associated with the sense electrode combination that sensed a bioelectrical brain signal having a relatively highest relative beta band power level may be selected to deliver stimulation therapy to the patient. Other frequency bands characteristics may also be used to select the stimulation electrode combination. | 08-01-2013 |
20130197616 | MEDICAL ELECTRICAL LEAD - An improved medical electrical lead is disclosed herein. The lead may include a longitudinally extending body having a distal end, a proximal end, a conductive element extending between the distal and proximal ends, and an electrode coupled to the conductive element utilizing a reflow process. The conductive element and electrode may comprise materials that are incompatible. | 08-01-2013 |
20130197944 | Techniques for Data Reporting in an Implantable Medical Device - Methods and apparatus for storing data records associated with a medical monitoring event in a data structure. An implanted device obtains data and stores the data in the data record in a first data structure that is age-based. Before an oldest data record is lost, the oldest data record may be stored in a second data structure that is priority index-based. The priority index may be determined by a severity level and may be further determined by associated factors. The implanted device may organize, off-load, report, and/or display a plurality of data records based on an associated priority index. Additionally, the implanted device may select a subset or composite of physiologic channels from the available physiologic channels based on a selection criterion. | 08-01-2013 |
20130204337 | MRI-Safe Implantable Medical Device - A medical lead is provided for use in a pulse stimulation system of the type which includes a pulse generator for producing electrical stimulation therapy. The lead comprises an elongate insulating body and at least one electrical conductor within the insulating body. The conductor has a proximal end configured to be electrically coupled to the pulse generator and has a DC resistance in the range of 375-2000 ohms. At least one distal electrode is coupled to the conductor. | 08-08-2013 |
20130204356 | Transcatheter Valve Delivery Systems and Methods - Delivery devices and methods for percutaneously delivering a prosthetic valve to the heart of a patient. These prosthetic valves may be configured to provide complimentary features that promote optimal placement of the prosthetic valve in a native heart valve, such as the aortic valve, mitral valve, pulmonic valve, and/or tricuspid valve. The delivery device includes a release sheath assembly housed within an outer delivery sheath. A release sheath component of the assembly captures a portion of the prosthetic valve to the delivery device, and effectuates complete release of the prosthetic valve with retraction of the outer sheath. | 08-08-2013 |