Systems and methods for deploying a paddle neurostimulation lead within a patient. A delivery tool includes a delivery tube including a first linear segment, a second linear segment, and an arcuate segment coupled between the first and second linear segments, the second linear segment defining an elongated opening. The delivery tool further includes a stylet positioned within an interior of the delivery tube, and a handle coupled to the delivery tube and including a stylet actuation mechanism, the stylet actuation mechanism configured to selectively advance and retract the stylet between a deployed position and a retracted position, wherein the stylet extends across the elongated opening in the deployed position to engage an engagement member of the paddle neurostimulation lead.

Some embodiments include a dipolar antenna system to electrically power an implantable miniature device and/or to stimulate bioelectrically excitable tissue. Other related systems and methods are also disclosed.

An antenna for an implantable medical device, the antenna being configured for inductive wireless power transfer and/or near-field magnetic induction communication, the antenna comprising at least one coil or at least one set of coils, each coil comprising several windings. Furthermore, the present disclosure relates to an implantable medical device (IMD).

Systems and methods for monitoring and treating patients with heart failure (HF) are discussed. The system may sense cardiac signals, and receives information about patient physiological or functional conditions. A stimulation parameter table that includes recommended values of atrioventricular delay (AVD) or other timing parameters maybe created at a multitude of patient physiological or functional conditions. The system may periodically reassess patient physiological or functional conditions. A therapy programmer circuit may dynamically switch between left ventricular-only pacing and biventricular pacing, or switch between single site pacing and multisite pacing based on the patient condition. The therapy programmer circuit may adjust AVD and other timing parameters using the cardiac signal input and the stored stimulation parameter table. A HF therapy may be delivered according to the determined stimulation site, stimulation mode, and the stimulation timing.

A header for an implantable medical device includes at least an antenna and a receptacle for receiving a signal transmission line. Either one or a combination of the antenna and the receptacle are encased in a dielectric material. The dielectric material can be one of or include one of a polymer, a ceramic material, polyoxymethylene, polysulfone, polybutylene terephthalate. A medical device and a method for assembling a medical device are also provided.

A controller implantable within the body of a patient as part of a left ventricular assist device (LVAD) system and a method therefore are provided. According to one aspect, the controller includes processing circuitry configured to receive inputs from at least one of: at least one internal component of the LVAD system, at least one external component of the LVAD system, and at least one clinician's device, and determine a charging rate for charging a battery of the LVAD system internal to the patient based on at least one of the received inputs.

A medical system comprising an internal unit; a transformer core; internal cabling comprising an internal winding around the transformer core; and an external unit comprising power supply circuitry and external cabling coupled to the power supply circuitry for enabling supply of power from the power supply circuitry to the internal unit via the transformer core. The external cabling comprises a connector including a first connector part and a second connector part; a first conductive current path between the power supply circuitry and the first connector part; a second conductive current path between the power supply circuitry and the second connector part; and a third conductive current path between the first connector part and the second connector part, conductively connecting the first connector part and the second connector part.

Examples disclosed herein are relevant to testing capacitors to identify potentially faulty DC blocking capacitors in implantable stimulators. In an example, the test includes selecting an active electrode, a return electrode, and a reference electrode. Short duration monophasic stimulation is used to charge up the DC blocking capacitors of the active and return electrodes. The electrodes are subsequently disconnected from all other nodes except a discharge circuit (e.g., a star circuit) and the tissue. The reference electrode is used to measure the voltage of the DC blocking capacitor of the active electrode during the charging phase and the discharging phase (via the discharge circuit). The characteristics of one or more of the capacitors charging or discharging can be sensed and then analyzed to determine whether the one or more capacitors are functioning properly. Faulty capacitors can be identified by comparing actual and expected characteristics.

Systems and methods for monitoring and treating patients with heart failure (HF) are discussed. The system may sense cardiac signals, and receives information about patient physiological or functional conditions. A stimulation parameter table that includes recommended values of atrioventricular delay (AVD) or other timing parameters may be created at a multitude of patient physiological or functional conditions. The system may periodically reassess patient physiological or functional conditions. A therapy programmer circuit may dynamically switch between left ventricular-only pacing and biventricular pacing, or switch between single site pacing and multisite pacing based on the patient condition. The therapy programmer circuit may adjust AVD and other timing parameters using the cardiac signal input and the stored stimulation parameter table. A HF therapy may be delivered according to the determined stimulation site, stimulation mode, and the stimulation timing.

In some examples, a medical device system includes a first implantable medical device. The first implantable medical device (IMD) may comprise circuitry configured to at least one of deliver a therapy to a patient or sense a physiological signal from the patient; generate stimulation deliverable to a patient; a first rechargeable power source; and a secondary coil coupled to the first rechargeable power source, the secondary coil configured to charge the first rechargeable power source via inductive coupling with a primary coil of an external charging device. The medical device system may comprise processing circuitry configured to control charging of the first rechargeable power source based on a charge state of a second rechargeable power source of a second IMD.