US 20070123947 A1
A system, comprising a sterilizable package; an implantable medical device placed inside the sterilizable package; and an electrical interface electrically coupled to the implantable medical device and extending from inside the sterilizable package to outside the sterilizable package. In various embodiments, the interface may include package contacts electrically coupled to electrode terminals on the implantable medical device, patient terminals and conductors extending between the package contacts and the patient terminals.
1. A system, comprising:
a sterilizable package;
an implantable medical device placed inside the sterilizable package; and
means for conveying a physiological signal to the implantable medical device within the sterilizable package without breaching the implantable medical device sterility.
2. The system of
3. The system of
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8. The system of
9. The system of
a computerized database;
a communication network coupled to the database;
means for transmitting data from the implantable medical device to the database via the communication network.
10. The system of
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23. An electrical interface that allows electrical coupling to an implantable medical device placed inside a sterilizable package without breaching the sterility of the sterilizable package, comprising:
package contacts in electrical contact with the implantable medical device;
patient terminals positioned outside the sterilizable package; and
a conductor circuit extending between the package contacts and the patient terminals.
The invention relates generally to implantable medical devices, and, in particular, to configurations of implantable medical device packaging systems.
Implantable medical devices (IMDs) such as cardiac pacemakers, implantable cardiovertor defibrillators (ICDs), implantable loop recorders (ILRs), implantable drug pumps, neurostimulators, etc. are generally provided by manufactures in a sterilized package. The package commonly includes an external carton or container for holding a sterilized inner tray or pouch containing the IMD. The IMD is sterilized within the inner tray or pouch using appropriate sterilization methods such as steam, gas or ultrasonic sterilization. The inner tray or pouch is generally provided with a peelable or tearable seal that can be opened to drop the sterile IMD contained therein into a sterile field without compromising the sterility of the IMD or the sterile field. For example, an IMD packaging tray having an open top may be sealed closed with a paper lid that is peeled back at the time of an implant procedure to allow the IMD to be dropped out of the tray into the sterile field.
Some packaging systems may include within the external carton or container an outer tray or pouch for carrying the sterilized inner tray or pouch. The inner tray or pouch and device contained therein may be sterilized within the outer tray or pouch. The outer tray or pouch may then be peeled open to drop the inner tray or pouch into the sterile field at the time of implant. An implanting physician or assistant may then open the inner tray or pouch within the sterile field.
Pre-implant testing, electrophysiological mapping, or system testing is commonly performed at the beginning of an implantation procedure to ensure that a patient meets implantation criteria and/or to determine an optimal implant location for the IMD and/or associated electrodes. Such testing may be performed using the IMD since using the IMD itself would generally provide the most reliable test results. However, during pre-implant testing, considerable care must be taken to ensure that the IMD and associated leads remain sterile for implantation. Once the IMD is removed from the sterile packaging, the IMD cannot be re-shelved should the patient not meet implantation criteria. As such, external equipment is often substituted for making physiological measurements or performing electrophysiological mapping. Use of external equipment for performing testing or mapping includes certain limitations, however, since the electronics of the external equipment will generally be different than the electronics of the IMD. Signals measured by external equipment may not be the same as signals measured at the same location by the IMD. Even minor signal differences can limit the usefulness or reliability of such measurements for the purposes of pre-implant tests.
Since IMDs tend to be costly devices, it is undesirable to open the IMD sterile packaging prior to knowing with reasonable certainty that the IMD is appropriate for the patient and that an acceptable implantation site for the device and/or leads can be identified. Furthermore, external equipment needed for performing pre-implant testing may not be readily available and requires extra space within the operating theater, which is often already crowded with equipment and personnel. Often a programmer that supports surface ECG recording in addition to receiving telemetry signals from the IMD is needed to perform pre-implant testing. Such full-function programmers can be bulky and costly to provide to all clinical centers.
In the following description, references are made to illustrative embodiments for carrying out the invention. It is understood that other embodiments may be utilized without departing from the scope of the invention. For the purposes of illustration, various embodiments of the invention are described herein in the context of IMDs used to monitor cardiac function. Such IMDs may or may not include cardiac stimulation therapy delivery capabilities. Such devices include, for example, cardiac pacemakers, which may be used for delivering a wide variety of cardiac stimulation therapies including, for example, bradycardia pacing, cardiac resynchronization therapy, extra systolic stimulation, and anti-tachycardia pacing. Such devices further include cardiovertor/defibrillators, implantable ECG recorders, and implantable hemodynamic monitors.
The scope of the invention is not limited, however, to devices configured to monitor cardiac signals. Aspects of the invention may be implemented in any IMD system in which electrical connection to the IMD electronics, prior to removing the IMD from sterilized packaging, is desired. Access to the IMD electronics may be desired for demonstration purposes, for verifying device functionality, or for performing pre-implant testing. Among the other types of IMDs in which aspects of the invention may be implemented are implantable drug pumps and neurostimulators, which are used for stimulating any portion of the central or peripheral nervous system. For example, neurostimulators may be used for controlling pain, reducing tremor, restoring muscle function, controlling incontinence, treating sleep apnea, treating digestive disorders or for vagal nerve stimulation for controlling cardiac function.
It can be appreciated that the selection of an implant site for IMD 10 is important in ensuring that the ECG signal strength is adequate. Typically, pre-implant mapping is performed using an external ECG monitor connected to electrodes placed on the surface of the patient's skin to localize a site corresponding to the strongest ECG signal strength. Since the electrodes 14 incorporated on the IMD housing 12 are relatively small compared to typical surface ECG electrodes, neonatal or pediatric-sized surface electrodes are commonly used to mimic the size and separation of the subcutaneous electrodes 14 on IMD housing 12. However, even when the subcutaneous electrode size and spacing is closely represented by the surface electrodes used for pre-implant mapping, the electronics of the external ECG monitor may bear different mapping results than when the ECG measurements are taken directly using the IMD electronics module 16.
Leads 26 are each provided with a proximal connector assembly having connectors corresponding to each of the electrodes/sensors carried by the individual lead. Connector header 24 includes electrical contacts which become electrically coupled to the lead connectors when the lead connector assembly is fully inserted in the connector header 24. Electrical contacts included in connector header 24 provide electrical connection between the lead connector assembly and the internal IMD electronics 16. Connection methods for connecting leads to an IMD are known in the art. An IMD may alternatively be provided with any combination of electrodes or sensors adapted for subcutaneous or non-subcutaneous implantation, either on the device housing as shown in
Terminals 15 may also be used for coupling electrodes used for sensing electrical signals within the body to the electronics module 16. With regard to the cardiac monitoring IMD 10 shown in
Electrodes used for sensing and electrodes used for stimulation may be selected via switch matrix 36. When used for sensing, electrode terminals 15 are coupled to signal processing circuitry 38 via switch matrix 36. Signal processor 38 includes sense amplifiers and may include other signal conditioning circuitry and an analog to digital converter. Electrical signals may then be used by microprocessor 30 for detecting physiological events, such as detecting and discriminating cardiac arrhythmias. In other embodiments, electrical signals sensed at electrode terminals 15 may be used for measuring impedance signals for monitoring edema, respiration or heart chamber volume.
One or more physiological sensors 41 may optionally be included. Such sensors may include pressure sensors, accelerometers, impedance sensors, flow sensors, blood chemistry sensors, activity sensors or other physiological sensors known for use with IMDs. Sensors 41 are coupled to electronics module 16 via a sensor interface 40 which provides sensor signals to signal processing circuitry 38. Sensor signals are used by microprocessor 30 for detecting physiological events or conditions. For example, an IMD may monitor heart wall motion, blood pressure, blood chemistry, respiration, or patient activity. Monitored signals may be used for sensing the need for delivering a therapy under control of the operating system.
The operating system includes associated memory 18 for storing a variety of programmed-in operating mode and parameter values that are used by microprocessor 30. The memory 18 may also be used for storing data compiled from sensed physiological signals and/or relating to device operating history for telemetry transmission upon receipt of a retrieval or interrogation instruction. These functions and operations are known in the art, and are generally employed to store operating commands and data for controlling device operation and for later retrieval to diagnose device function or patient condition.
Telemetry circuitry 42 is typically provided to enable bidirectional communication between the IMD and an external programmer, home monitor, patient activator, or other external device, according to methods and apparatus known in the art. Programming commands or data are transmitted during uplink or downlink telemetry between IMD telemetry circuitry 42 and external telemetry circuitry included in a programmer or monitoring unit. According to one embodiment of the invention, pre-implant test data is obtained using a packaging system that enables connection to electronics module 16 through a sterile IMD package. Pre-implant test data so obtained can be transmitted in real time, or at a delayed time, to an external monitor/programmer using telemetry circuitry 42. Telemetry circuitry 42 may correspond to telemetry systems known in the art, and may be configured for long-range telemetry communication with a monitor/programmer. Long-range telemetry systems are generally disclosed in U.S. Pat. No. 6,482,154 issued to Haubrich et al., incorporated herein by reference in its entirety.
In some embodiments, an alert unit 44 is provided for generating an audible tone or sound. As will be described in greater detail below, electronics module 16 may be used to perform pre-implant testing using a flexible circuit or other coupling appliance for connecting external electrodes to terminals 15 without compromising the sterility of IMD within a sterile package. Microprocessor 30 may process signals received at terminals 15 for determining if implantation criteria are met or for identifying an optimal implantation location or orientation. Alert unit 44 may be used to generate an audible tone or sound to indicate to a clinician that a particular test location or orientation meets or does not meet implant criteria or acceptable signal quality.
It is recognized that the overall complexity of electronics module 16 and other IMD components may vary depending on the functionality provided by the IMD. Functional units may be added or removed from the block diagram represented in
Electrical interface 50 includes patient terminals 54, signal/conduction transmission 56, and package contacts 52. Patient terminals 54 may be in the form of electrodes adapted for placement directly on or in patient 66. Alternatively, patient terminals 54 may be provided as connectors, such as snaps or clips, onto which electrodes or sensors placed on or in patient 66 may be attached using a cable, extension or lead. One or more package contacts 52 are electrically coupled to IMD electrode terminals 15 (or sensor terminals 41) included in IMD 10 and thereby electrically coupled to electronics module 16. As described previously, IMD electrode terminals 15 may be embodied as electrodes formed in or on the housing of IMD 10. IMD electrode terminals 15 may alternatively be embodied as contacts used for electrically coupling lead-based electrodes and/or sensors to IMD 10. The number of package contacts and corresponding patient terminals provided will depend on the application and may correspond to the total number of electrodes and sensors used by the IMD or a subset of electrodes and sensors used by the IMD.
Electrical interface 50 includes signal conduction/transmission 56 which acts to convey signals received from the patient at patient terminals 54 to package contacts 52, across a sterile barrier 61 of package 60. Signal conduction/transmission 53, generally referred to as “conductor circuit” hereafter, may include conductors in the form of wires, foils, conductive tape, film or ink. However, it is recognized that conductor circuit 53 is not limited to include only conductive elements. In various embodiments, conductor circuit 53 may include inductive elements, capacitive elements, antennas, optical fibers, or any other elements appropriate for conducting or transmitting a physiological signal received at patient terminals 54 to package contacts 52. Alternatively, signals may be transmitted from IMD electronics module 16 to patient 66 using electrical interface 50. Depending on the type of sensors used by IMD 10, electrical excitation signals may be required and transmitted to a sensor operatively positioned in patient 66 via electrical interface 50. During some pre-implant testing, system tests or demonstration procedures, electrical pulses, for example stimulation pulses, may be transmitted from electronics module 16 to patient terminals 54.
In the embodiment shown, package contact 52 is disposed over a subcutaneous electrode 14 located on IMD housing 12 while the IMD remains in package 60. Package contact 52 makes electrical connection with electrode 14 thereby allowing electrical connection to the electronics contained in IMD 10 using patient terminal 54, located outside of sterilizable package 60. In various embodiments, package contact 52 may be adapted for electrical coupling to any electrode or any electrode/sensor terminal or contact incorporated in or on IMD 10.
Sterilizable package 60 is provided as a tray, pouch or other container for enclosing and maintaining sterility of IMD 10. Sterilizable package 60 is typically sealed closed after receiving IMD 10 to form sterile barrier 61 and submitted to a sterilization method appropriate for the particular IMD contained therein, e.g., steam, gas, or ultrasonic sterilization. Electrical interface 50 conveys electrical signals received at patient terminals 54 across sterile barrier 61 without compromising the integrity of the sealed package 60 or the sterility of the IMD 10.
Electrical interface 50 may be fabricated as a flexible circuit using conductive ink (e.g., silver-silver chloride ink or a carbon-based ink) printed on a flexible, insulative substrate 55 to form conductors 56, package contacts 52 and patient contacts 54. Alternatively, any of conductors 56, package contacts 52 and patient contacts 54 may be formed by laminating or adhering electrically conductive materials in the form of wires, foils, film, or tape, onto flexible substrate 55. As will be described in greater detail below, in some embodiments flexible substrate 55 includes a portion of sterilizable package 60 wherein electrical interface 50 is formed on a surface of package 60.
Patient terminals 54 may be provided for direct placement on a patient's skin. Electrical body signals may then be provided to IMD 10 via electrical interface 50. Electrical interface 50 is provided with a “neck” 64 along which conductors 56 extend. Neck 64 may be provided with any length to facilitate unencumbered placement of patient terminals 54 on a patient. Alternatively, patient terminals 54 may be embodied as coupling terminals or contacts to which electrode cables or extensions 80 may be attached to thereby allow greater maneuverability and flexibility during pre-implant testing, without patient-to-IMD distance limitations. Electrode extensions 80 may be standard surface electrode cables carrying surface electrodes 82, which may be standard “off-the shelf” electrodes, adapted for placement on a patient's skin.
Patient terminals 54 may alternatively be adapted for electrical coupling to patient leads or lead extensions. For example, extensions 80 may be provided with snaps, alligator clips, manufacturer-provided connectors, or other electrical connectors for facilitating electrical connection to patient terminals 54 at one end of an extension 80 and to a connector assembly of an implanted lead at the other end of an extension 80. Extensions 80 may be provided in a sterile condition to allow connection to implanted sterile leads. It is recognized that numerous configurations may be used for connecting patient terminals 54 to a patient, either directly or indirectly using extensions and/or leads, and such embodiments may include any number of electrodes and/or sensors positioned on or in the patient.
A template 84 may be provided for guiding placement of surface electrodes 82 to correspond to the separation distance of IMD electrodes 14. Alternatively, electrode extensions 80 and surface electrodes 82 may be custom components, provided with template 84 for mimicking the size and separation of IMD electrodes 14. Patient terminals 54 may be provided as snaps, clips, or any other mechanism for mechanically and electrically coupling electrode extensions 80. Template 84 may include labeling to indicate which patient terminals 54 correspond to which IMD electrode terminals 15 and/or sensor terminals 41.
During pre-implant testing, signals obtained during placement of patient terminals 54 at different body locations and orientations may be stored and analyzed by IMD 10 for determining an optimal implant location. Alternatively or additionally, IMD 10 may transmit signals received using electrical interface 50 to an external programmer/monitor 70 via a telemetry connection 71.
External programmer/monitor 70 may correspond generally to programmer/monitors known in the art and typically includes telemetry circuitry 72, a microprocessor-based control system 74, a display 76, and a user-interface 78, which may be embodied as a graphical user interface. Display 76 may be in the form of an LCD screen or other graphical or video display that allows a clinician to observe displayed signal data, for example ECG signals, while patient terminals 54 are positioned at different body locations or orientations. The clinician may manually select an optimal implant location based on observed data.
Alternatively, external programmer/monitor 70 or IMD 10 may analyze received signals using a programmed signal evaluation routine and automatically recommend an implant site or at least indicate when a location or orientation meets signal quality or other implant criteria. Such information can be displayed graphically or using text messages on display 76. Alternatively, display 76 may be embodied as an LED display which indicates through color or number of LEDs illuminated acceptable on unacceptable signal quality. In yet another embodiment, display 76 may include a speaker for broadcasting sound messages indicating acceptable or unacceptable signal quality. As described previously, alert circuitry 44 may generate a signal indicating acceptable or unacceptable signal quality. A signal evaluation routine may determine signal features, signal-to-noise ratio, or other signal characteristics for determining if the signal quality meets predefined acceptance criteria.
Display 76 may further be used to prompt a clinician or other user to move patient terminals 54 to a number of body locations or orientations while IMD 10 and/or external monitor/programmer 70 collects signal data corresponding to each location. The clinician or other user may use user interface 78 to indicate to IMD 10 or external monitor/programmer 70 when patient terminals 54 are being moved to a new location and thereby indicate when IMD 10 or external monitor/programmer 70 should begin a new signal evaluation routine. When multiple electrodes or sensors are available and coupled simultaneously to IMD 10 using patient terminals 54, the IMD 10 may select different sensing vectors using switching circuitry 36 (shown in
External programmer/monitor 70 may vary in functionality and complexity in different embodiments. For example, in some embodiments, external programmer/monitor 70 may receive signal data using telemetry circuit 72, process signal data using microprocessor 74, and display pre-implant test results on display 76. External programmer/monitor 70 may include a data storage module for printing or storing received data and/or test results electronically. In other embodiments, external programmer/monitor 70 may be interfaced with a monitoring device 94 used for displaying and/or storing signal data obtained using electrical interface 50.
In still other embodiments, external programmer/monitor 70 may serve as a communication conduit between IMD 10 and a computerized database 90. Database 90 may be a web-based patient management system or implemented on a personal computer. Database 90 is coupled to a communication network 92, which may be a wireless network, enabling communication between database 90 and external programmer/monitor 70. Signal data received by external programmer/monitor 70 is transmitted to database 90 via communication network 92. As such, signals obtained using electrical interface 50, or test results based on such signals, may be transmitted directly to database 90 for further analysis and/or viewing by a user. Database 90 may be accessible on a local or remote computer, allowing pre-implant testing to be performed in a time and place independent manner. Database 90 and external programmer/monitor 70 may be provided according to known patient management systems, such as those generally disclosed in U.S. Pat. No. 6,250,309 (Krichen, et al.) and U.S. Pat. No. 6,622,045 (Snell et al.), both of which patents are incorporated herein by reference in their entirety.
Tray 104 includes a seal area 108 along inner surface 110 onto which a tray lid 102 is sealed after the IMD and any other package contents are placed in tray 104. Tray lid 102 includes an outer surface 105 and an inner surface 103 and is commonly fabricated from coated paper or a high-density woven or non-woven polymer material. Tray lid 102 and tray 104 are typically sealed together along seal area 108 using an appropriate adhesive for forming a reliable sterile barrier. After undergoing sterilization, package 60 is placed in any desired outer packaging, which is typically a box or carton provided with appropriate labeling. In some embodiments, the packaging system may include an outer tray and outer tray lid for containing inner tray 104 sealed with inner tray lid 102. Inner tray 104 may be sterilized within the outer tray, and the outer tray is placed in the desired outer packaging.
The depth of IMD cavity 106 in inner tray 104 is dimensioned appropriately to cause electrode 14 to come into contact with package contact 52 when the packaging system 62 is assembled. To promote reliable coupling between package contact 52 and IMD electrode 14, the thickness 115 of substrate 55, at least in the area of package contact 52, is provided to create pressure between contact 52 and IMD electrode 14. Package contacts 52 may be formed as blisters or buttons, having a generally hemispherical shape, for example, which protrudes from flexible circuit substrate 55 to thereby promote reliable electrical contact with IMD electrodes 14.
Additionally or alternatively, a compressible element 120 may be included or incorporated in inner tray 104. Physical contact between package contact 52 and IMD electrode 14 should be adequate to create an electrical connection between contact 52 and electrode 14 without causing mechanical damage to electrode 14. As shown, compressible element 120, which may be embodied as a compressed foam member, is placed between the inner surface 110 of inner tray 104 and IMD 10. Compressible element 120 generates pressure between IMD electrode 14 and package contact 52 to promote reliable electrical contact there between. Compressible element 120 could alternatively be positioned between the inner surface 103 of inner tray lid 102 and electrical interface 50 or along the outer surface 105 of inner tray lid 102, between inner tray lid 102 and outer tray lid 112. Compressible element 120 may alternatively be enclosed in an outer carton containing package 60 and positioned to generate pressure in the area of package contact 52 and IMD electrode 14.
Pressure generating member 121 may be packaged in an outer carton along with sterile package 60 and placed in the position shown in
Pressure generating member 121 may be formed of a relatively rigid polymeric or metal material which may be flexible along closed side 119 to allow open side 117 to be opened wider to enable member 121 to be slid over the outside of sterile package 60 (or inner tray 104 and tray lid 102 or IMD 10 and electrical interface 50). It is recognized that pressure-generating member 121 may be provided in numerous configurations for promoting good contact between electrical interface 50 and IMD 10. For example, pressure generating member 121 may alternatively be formed having a “clam-shell” shape, having a hinged or spring-loaded side or sides, or having latching mechanisms. Pressure generating member 121 may be used alone or in combination with compressible element 120. Pressure generating member 121 and/or compressible element 120 may be designed to create a predetermined, constant pressure at the contact point between IMD 10 and electrical interface 50.
Conductors 56 may be insulated by a dielectric layer 124 formed over conductors 56. Dielectric layer 124 may additionally extend over any portion or all of substrate 55, while leaving package contacts 52 and patient contacts 54 exposed. Dielectric layer 124 may extend over the entire inner tray seal area 108 to promote a uniform, reliable seal. Dielectric layer 124 may be formed from any dielectric polymeric material including polyesters, ethylene-vinyl acetate copolymers, terpolymers such as acrylonitrile-butadiene styrene, or polyvinyl chloride and its copolymers. Alternatively, conductor circuit 53 may include shielded conductors and contacts to protect the IMD and/or patient from electrical noise.
The exterior end of substrate 55 may be formed into a template 84 upon which patient contacts 54 are mounted. Template 84 corresponds to the size and shape of IMD 10 with patient contacts 54 sized and spaced relative to one another to mimic the size and spacing of IMD electrodes 14. Once an optimal implant site is identified through pre-implant testing, the site may be marked or traced using template 84. Template 84 may be provided having stencil openings 122 to facilitate marking a selected implant site on a patient.
After completing pre-implant testing, the outer tray lid may be removed from outer tray 114. Neck 64 of electrical interface 50 may be provided with notches or perforations 126 to facilitate tearing of the electrical interface 50 just outside of inner tray 104. Tearing of electrical interface 50 allows inner tray 104 to be removed from outer tray 114 without hindrance due to attachment of electrical interface 50 to outer tray 114 along outer tray seal area 118.
A removable short circuit element 138 may be provided across conductors 56 so as to prevent unwanted electrical signals from reaching the IMD electronics. Short circuit element 138 may be provided, for example, as a strip of conductive tape extending across conductors 56 which can be removed at the appropriate time to enable pre-implant testing or other use of electrical interface 50. Short circuit element 138 may be provided as a replaceable element such that after testing is completed, short circuit element 138 can be put back in place to create a short across conductors 56.
A strain relief member 165 is shown in
Outer carton 150 has an inner surface 154 and an outer surface 152 which form a recess 156 in which a carton contact 160 is mounted on a compressible member 162. When carton contact 160 is pressed down, carton contact 160 makes electrical contact with patient terminal 54. Carton contact 160 may be provided with a snap or clip member to facilitate attaching an external electrode extension or cable. Connection to the electronics within IMD 10 is thereby made possible via carton electrode 160 and electrical interface 50 while IMD 10 remains inside sterilized inner tray 104, outer tray 114 and outer carton 150. It is recognized that in various embodiments, other signal conveying elements may be added to or substituted for carton electrode 160, such as capacitive elements, inductive elements, optical fibers, or antennas.
Carton 150 may be formed with a closing member 158, such as a closable flap or resealable tape that can be closed over recess 156 to protect carton electrode 160. It is recognized that numerous configurations may be conceived for incorporating a carton electrode 160 in outer carton 150. For example, in other embodiments, carton electrode 160 may be located along outer surface 152 extending through to inner surface 154 without being positioned in a recess 156. It is further recognized that a removable insulating layer may be provided over carton electrode 160. In some embodiments, compression member 162 may not be provided, and the normal position of carton contact 160 may be in electrical contact with patient terminal 54. An insulating material over carton contact 160 may or may not be used.
Furthermore, the electrical interface 50 may be formed on a substrate extending along any outer or inner surface of the sterilizable IMD package, including an outer or inner surface of any tray, tray lid, pouch or other sterilizable IMD package. Alternatively, electrical interface 50 may be fabricated using a separate substrate 55, which likewise may extend along any outer or inner surface of the sterilizable IMD package. The exact configuration of electrical interface 50 with respect to the IMD package 60 may vary from embodiment to embodiment depending on the orientation of the IMD within the package and the resulting location of IMD electrodes or electrode terminals with which package contact(s) 52 are to be electrically coupled.
To facilitate electrical connection to electrical interface 50, IMD 20 may be packaged within sterilizable package 60 with a connector appliance 210 inserted into connector bore 200. Connector appliance 210 is provided with a connector assembly 212 adapted for insertion into connector bore 200. Connector assembly 212 includes two connectors 214 and 215 separated by an insulating segment 216. Connectors 214 and 215 align with and become electrically coupled to contacts 202 and 204 when connector assembly 212 is fully inserted in connector bore 200. Connector assembly 212 of connector appliance 210 generally corresponds to a connector assembly provided on a lead intended for use with IMD 20. Connector appliance 210 is provided with electrode contacts 220 which are separately coupled to each of connectors 214 and 215 by conductors 217 extending through appliance 210. Package contacts 52 included on electrical interface 50 are positioned over electrode contacts 220 such that patient terminals 54, located outside of package 60, can be coupled to the electronics included in IMD 20 via connector appliance 210. Alternatively, conductors 217 may extend along a substrate to the outside of package 60 directly to patient terminals 54, without the use of package contacts 52.
Patient terminals 54 may be positioned on or in a patient or coupled to electrodes or any other physiological sensors positioned on or in a patient via appropriate leads or extension cables. As such, electrical interface 50 may be used to access IMD electronics included in an IMD having a connector header 24 with the use of a connector appliance 210.
For the sake of illustration, various embodiments described herein have generally related to an electrical interface that allows connection to IMD electronics for pre-implant testing relating to optimizing subcutaneous electrode placement. However, it is recognized that an electrical interface used to access the electronics within an IMD still contained in a sterile package may be designed to mimic electrodes/sensors adapted for other implant locations, e.g., epicardial, endocardial, sub-muscular, or otherwise. As such, embodiments that include using an electrical interface for testing non-subcutaneous implant locations of an IMD or electrodes/sensors are included in the scope of the invention. Pre-implant testing using the interface may be performed to determine if the patient meets implant criteria and/or selecting an optimal implant site.
Various embodiments of the electrical interface 50 shown in
Packaging systems having an interface that allows access to IMD electronics across a sterile barrier have been presented in the foregoing description with reference to specific embodiments. It is appreciated that various modifications to the referenced embodiments may be made without departing from the scope of the invention as set forth in the following claims.