Patent Application
20050038476
The present invention generally relates to implantable electro-stimulation devices for use in the human body. More specifically, the present invention relates to the specific configuration and tailoring of non-conducting coatings so that electrical stimulation signals are more carefully controlled through the remaining surfaces of the device.
The human heart normally maintains its own intrinsic rhythm in order to consistently pump a proper supply of blood throughout the body's circulatory system. However, some people are afflicted with irregular cardiac rhythms, or cardiac arrhythmias, resulting in diminished blood circulation. Drug therapy is one mode of treatment for cardiac arrhythmias. Unfortunately, drug therapy is not effective for treating all cardiac arrhythmias. Hence, alternative modes of treatment including an implantable electrotherapy devices, such as pacemakers and defibrillators, are utilized.
Patients with bradyarrythmias, or symptomatic or slow beating of the heart, are often treated with pacemakers. These devices deliver timed sequences of low energy electrical stimuli to the heart via leads having one or more electrodes placed about the heart. With proper timing of the electrical stimuli, heart contractions are regulated such that the heart contracts at a proper rate, greatly improving blood supply throughout the body's circulatory system.
Patients with malignant tachyarrhythmia, or potentially life threatening fast beating of the heart, are often treated with implantable cardioverter defibrillators. These devices deliver high-energy electrical stimuli called defibrillation countershock to the heart. The countershock interrupts the tachyarrhythmia allowing the heart to establish a perfusing rhythm which allows the heart to completely fill with blood before pumping. Other implantable electrotherapy devices include pacer/defibrillators, which combine the functions of pacemakers and defibrillators, drug delivery devices, and other systems designed for diagnosing and treating arrhythmias.
In addition to the above heart conditions that are treated with electrical stimulation signals, various muscle and nerve conditions also benefit from electrical stimulation. For example, electrical signals may be used for pain management, where signals effect nerve system reaction. Further, electrical systems also include muscular stimulation devices, which provide appropriate-signals to the body to aid in injury recovery. In another example, drug delivery is achieved using electrical signals to “drive” certain drugs into the body.
Conventional implantable electrode leads used together with implantable electrotherapy devices are commonly known. An implantable electrode lead is generally comprised of at least one electrode for supplying an electrical stimulation pulse or sensing an electrically evoked response of the heart, an electrical connector for connecting the electrode lead to an implantable electrotherapy device, and a lead body inserted between the electrode and the electrical connector for transmitting an electrical signal between the electrode and the implantable electrotherapy device. In some cases the connector is eliminated as the lead body is directly connected to the therapy device.
When providing electrical signals to the human body, a minimum threshold signal level is often required in order to establish current flow. Once achieved, the same signal flow can be maintained using less overall power. Further, this threshold becomes a major design consideration for the implantable device. The threshold itself generally relates to the electrical characteristics of human tissue. Further, the configuration of the electrodes themselves will affect the amount of power required to overcome this threshold (which is often measured in terms of current density amperes per centimeters squared). Thus, the surface area of the electrodes will have a direct affect on the threshold current achieved, and thus the overall power required for any particular device.
Biocompatible materials have been developed for covering implantable leads with dissolvable coatings for improving initial placement and extraction of leads and electrodes. In addition these coatings help to minimize infection and scar tissue development around leads and electrodes. (See e.g., U.S. Pat. No. 6,584,363 B2).
In addition to the electrodes, the implantable device itself is a source of electrical current. The configuration of the device's surface area will also effect the electrical operation of the device. Hence, there is currently a need to control the surface area of these electrical components that are exposed to patient tissue when the electrical signals are emitted from the implantable electrotherapy device (including pacemaker or defibrillator surfaces and lead and electrode surfaces).
Implantable electrotherapy devices (e.g., pacemakers, defibrillators, etc.) are all specifically configured to provide a desired electrical signal to a patient. Often, these devices include control or signal generation circuitry that is included within a “package” or “can”. Further, these devices often utilize electrodes, which are placed some distance away from the main device body. The “can” is also configured to operate as an electrode in the system, thus creating a current path when combined with the remote electrodes.
At the present time, the entire implantable device package is utilized as one electrode. The present invention utilizes a biologically stable, non-conductive coating material applied to the device package to modify the amount of surface area exposed to human tissue. Additionally, the electrodes cooperating with the device package are similarly coated in order to provide only a limited amount of exposed area. By eliminating the conducting surface area exposed to patient tissue, the current density may be more easily controlled. More specifically, the same amount of current density can be achieved using much lower current levels. Because lower current levels would be required, the efficiency of the overall system is enhanced. Additionally, the longevity of the implantable electrotherapy device is increased because lower power levels are required.
Further details of the preferred embodiment can be seen by reading the following description in conjunction with the drawings in which:
The present invention pertains to a non-conductive, biocompatible coating, such as a polymer, ceramic, Teflon or silicon based material for use in conjunction with an implantable electrotherapy device. More specifically, it pertains to the use of such a coating on specific surfaces of the implantable electrotherapy device and leads in order to selectively enhance and control of the delivery of electrical current to the surrounding human tissue.
Referring to the drawings, a device 10 of the present invention is depicted. Preferably, the device 10 comprises an implantable electrotherapy device 10. It will be understood that electrotherapy device 10 contains electrical circuitry required to generate all electrotherapy signals desired. The bottom surface 12 of the implantable electrotherapy device may be coated with a non-conductive, biocompatible material 14 such that some portion 16 of the surface remains uncoated and electrically active. The remaining surfaces of the implantable electrotherapy device, including the four sides 18 and top 20, may also be coated with a non-conductive, biocompatible material.
The portion 16 of the implantable electrotherapy device that remains uncoated will allow electric current from the device to enter the surrounding human tissue in a specific, localized fashion. In this manner, a predetermined current density may be delivered to a specific area in the body. Allowing this specificity for the delivery of the electrical current will improve the performance of the implantable electrotherapy device for stimulating heart response. In addition, the implantable electrotherapy device 10 will operate more precisely for a longer period of time because less energy will be used.
The size of the exposed area 16 is proportional to the current density that passes therethrough. Thus, one aspect of the present invention provides a coating 14 that can be removed from the device by a physician or technician in order to custom-fit the size of the exposed area to the application.
Referring now to
The foregoing detailed description of the preferred embodiments of the invention has been provided for the purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise embodiments disclosed. Many modifications and variations will be apparent to practitioners skilled in this art. The embodiments were chosen and described in order to best explain the principles of the invention and its practical application, thereby enabling others skilled in the art to understand the invention for various embodiments and with various modifications as are suited to the particular use contemplated. It is intended that the scope of the invention be defined by the following claims and their equivalents.
This application claims priority from provisional application Ser. No. 60/495,235, filed Aug. 14, 2003.
| Number | Date | Country | |
|---|---|---|---|
| 60495235 | Aug 2003 | US |
