A medical device system and method for detecting dislodgement of a ventricular lead determines one or more characteristics of a cardiac signal received via the ventricular lead that are associated with dislodgement of the ventricular lead during atrial fibrillation, and detects dislodgement of the ventricular lead based on the determined characteristics. The medical device and system provides a lead dislodgment alert in response to detecting dislodgement. In some examples, an implantable medical device withholds delivery of a ventricular defibrillation therapy based on detecting dislodgement of the ventricular lead.

Methods and systems for seamless adjustment of treatment are disclosed. A determination is made as to whether to intervene with a patient's treatment. Implanted device memory data is acquired over a pre-specified time period. Risk status is determined from the device memory data. Another external device memory data is acquired over a pre-specified time period. A determination is made as to whether to adjust treatment of the patient in response to the risk status, the data acquired from the implanted device memory and the external device memory data.

An apparatus for emitting a field comprising a core, a conductive winding with a first end, a second end, and an intermediate portion, where the conductive winding surrounds a portion of the core and is wound about a winding axis, a protrusion for aligning the apparatus where the protrusion is parallel with the winding axis, and a conductive connector extending from the conductive winding, wherein the conductive connector is electrically coupled with the conductive winding at the intermediate portion.

An apparatus includes a sensing circuit configured to generate a sensed physiological signal that includes physiological information of a subject, a detection circuit, and a control circuit. The detection circuit detects a physiological condition of a subject using the physiological signal. The control circuit stores sampled values of a segment of the physiological signal in temporary memory storage; and stores the sampled values in non-temporary storage in response to receiving an indication of continued detection of the physiological condition.

A method of displaying electrophysiology information includes obtaining a three-dimensional medical image of an anatomical region, registering a localization system to the model; localizing an electrophysiology catheter within the anatomical region; displaying a representation of the localization of the electrophysiology catheter on the model; and displaying image slices of the model. The image slices are selected based upon the localization of the electrophysiology catheter. For example, the image slices can pass through a user-selected localization element carried by the electrophysiology catheter. Rigid and/or non-rigid transforms can be used to register the localization system to the model. Electrophysiology data collected by the catheter can be displayed on the model and/or the image slices thereof. The three-dimensional medical image and/or the electrophysiology data can also be time-varying. In embodiments, scalar maps can also be displayed on the model.

A method and apparatus for implementing scar tissue identification using a processor coupled to a memory is disclosed. The method and apparatus receive a first modality and a second modality. The first modality is of a first type. The second modality is of a second type, which is different from the first type. Each of the first modality and the second modality respectively describe organic tissue of a patient according to the first and second types. The method and apparatus cross reference the first modality and the second modality and generates improved image data for the first modality based on the cross referencing. The image data includes enhanced accuracy over or higher resolution than original data of the first modality.

A medical device system may include a structure including a first elongate member, a line including a plurality of flexible members, and an actuator coupled to the line to selectively transmit force to at least the first elongate member. The structure may include a delivery configuration in which at least a portion of the structure is arranged to be percutaneously delivered to a bodily cavity. Respective portions of the flexible members may be intertwined together to form a braided portion of the line, and the line may include an unbraided portion secured at least to the first elongate member. The braided portion of the line may be located between the actuator and the first elongate member.

An implantable medical device performs a method that includes detecting a cardiac event interval that is greater than a P-wave oversensing threshold interval. In response to detecting the cardiac event interval greater than the P-wave oversensing threshold interval, the device determines the amplitude of the sensed cardiac signal and withholds restarting a pacing interval in response to the amplitude satisfying P-wave oversensing criteria. A pacing pulse may be generated in response to the pacing interval expiring without sensing an intrinsic cardiac electrical event that is not detected as a P-wave oversensing event.

Cardiac electrical activity is monitored from tissue of the patient using the plurality of external electrodes. One or more cardiac metrics of the patient are generated based on the monitored electrical activity. It is determined whether the patient is a candidate for a cardiac resynchronization therapy (CRT) device based on a first global dyssynchrony metric using the one or more cardiac metrics if the patient has a right bundle branch block. It is determined whether the patient is a candidate for a cardiac resynchronization therapy (CRT) device based on a second global dyssynchrony metric using the one or more cardiac metrics if the patient does not have a right bundle branch block.

Systems and methods are described herein for determining whether or not each of a plurality of cardiac signals monitored from a plurality of electrodes is stable. A dispersion signal may be generated based on the plurality of cardiac signals, and low dispersion time period may be selected within which the cardiac signals may be analyzed for stability.