Cardiac Pacemakers, Inc.

The UAB Research Foundation (The University of Alabama at Birmingham)

Mudit Jain

Qingsheng Zhu

Bruce H KenKnight

Ronald W Heil, Jr

Milton M Morris

Rodney W Salo

Scott A Meyer

Gregory P Walcott

Jeffrey A Hall

David S Wood

Steven L Higgins

An apparatus includes an implantable device, such as a chronically implantable device that has a device body. One or more chemical sensors are coupled with the device body. A drug eluting substance is disposed at a location including at least one of on, directly adjacent, or near the one or more chemical sensors, where the drug eluting substance prevents fibrotic growth on the one or more chemical sensors.

Sensors having protective eluting coating and method therefor

This document describes systems, devices, and methods that measure a distance between ultrasound or other acoustic transducers to provide a contractility or other therapy efficacy indication. In one example, the indication is communicated to a caregiver for assisting in the caregiver's determination of particular therapy settings. In another example, the indication is used in a feedback controller to automatically adjust one or more therapy parameters based at least in part on the indication.

Cardiac rhythm management systems and methods using acoustic contractility indicator

A cardiac management implantable device that has an intravascular device body, and one or more chemical sensors coupled with the intravascular device body. A drug eluting substance is disposed at a location including at least one of on, directly adjacent, or near the one or more chemical sensors, where the drug eluting substance prevents fibrotic growth on the one or more chemical sensors.

A distal segment of a catheter shaft is adapted to be positioned against tissue in a biological organ. The distal segment has a tissue-contacting area intended to contact the tissue. One or more pressure sensors positioned within the tissue-contacting area provide pressure data indicative of the pressure exerted on the distal segment. The distal segment carries one or more electrodes and the pressure sensors are located either on an electrode or on the catheter shaft near an electrode. The pressure sensors provide pressure data to a processor that analyzes the data to determine if the tissue-contacting area of the distal segment is contacting the tissue. The pressure sensors may also provide temperature data indicative of the temperature at the sensor. A flow sensor, located opposite the pressure sensor on the shaft, provides data related to the flow rate of fluid through the organ.

Ablation catheter with transducer for providing one or more of pressure, temperature and fluid flow data for use in controlling ablation therapy

For chronic monitoring of the effects of pacing and/or drug therapy in treating CHF, a strain gauge element is disposed at the distal end of a cardiac lead and is effective to produce a signal relating to the amount of flexure being induced into the lead by the beating action of the heart.

Cardiac lead incorporating strain gauge for assessing cardiac contractility

An ablation catheter stores a platelet inhibitor substance within a plurality of pockets or recesses of its shaft. The substance is adapted to elute upon contact with biological fluid. In the pocket configuration, the platelet inhibitor substance is in a capsule positioned within the pocket. In the recess configuration, the platelet inhibitor substance is in a hydrogel or silicone-based porous/semi-porous matrix positioned within the recess. Elution of the platelet inhibitor substance prevents or at least substantially minimizes the adhesion of blood platelets on the catheter surface during ablation. In another configuration, the catheter includes an internal lumen network having apertures terminating at the surface of the shaft. The lumen communicates with a source of platelet inhibitor fluid that is forced through the lumen by a variable pump.

Platelet inhibitor eluting ablation catheter

An apparatus for delivering energy to a biological site includes a catheter having an ablation electrode and a plurality of backplates distributed at various locations proximal the biological site. The backplates are coupled to a switching device for selecting which backplate to utilize as a return electrode to complete the circuit with the ablation electrode in order to obtain deeper, larger lesions for a given amount of energy. The backplate selection is made by determining which return electrode most closely places the biological site between the ablation electrode and the backplate. Backplate selection may be made automatically based on impedance measurements or conduction time measurements. Alternatively, the backplate selection can be made manually.

Ablation system with selectable current path means

Information indicative of the flow rate of fluid through a biological organ is provided to a processor. Using this information the processor assesses whether the fluid-flow rate is high or low and controls a generator such that the generator provides energy to an electrode positioned within the organ to effect tissue ablation. Energy of a first level is provided during periods of high fluid-flow and energy of a second level, less than the first level, during periods of low fluid-flow. The flow rate information may be provided by an electrocardiograph (ECG) device or a flow sensor. A temperature sensor provides temperature signals to the processor indicative of the electrode temperature. The processor further controls the generator based on the electrode temperature to maintain the temperature at or near a target temperature and below a maximum threshold temperature.

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Woodbury, MN, United States of America

Mudit Jain