Embodiments related to implantable medical leads that include electrode segments where one or more segments of the electrode segments are different sizes than other segments.
Implantable medical systems that include an implantable medical device and an implantable medical lead provide therapy to and/or monitoring of physiological conditions. Typically, the implantable medical device is implanted at a location of convenience which may be some distance from the target area to be stimulated or sensed. The implantable medical lead is implanted by being routed to the target area so that a position on the implantable medical lead has electrodes at the target area to deliver stimulation signals and/or sense physiological signals.
Conductors within the implantable medical lead carry electrical signals between a set of electrical connectors on a proximal end of the lead body and the electrodes located on the lead body and distal of the set of connectors. The proximal end is connected to the implantable medical device. Where the lead is not long enough to extend from the target area to the implantable medical device, a lead extension may be used where the proximal end of the lead connects to the distal end of the lead extension and the proximal end of the lead extension connects to the implantable medical device.
The distal electrodes are often rings that surround the entire circumference of the lead body. While such rings are effective in many cases, some situations call for a more precise location of the electrodes so as to steer stimulation current to and/or to capture physiological signals from a more precise location. In such a case, electrode segments may be used instead of a continuous ring. Conventionally, the electrode segments are electrically isolated and are uniformly positioned about the circumference of the lead and are uniformly sized. A given row of electrode segments are uniformly spaced about the circumference of the lead in the position where a ring would otherwise be.
These uniformly positioned and sized electrode segments provide a degree of additional precision about the circumference of the lead. However, even with the uniformly positioned and sized electrode segments, blind spots can occur at the intersections between segments of a given row and between segments of axially adjacent rows. At these blind spots, sensing of physiological signals and/or delivery of stimulation signals may be hindered. Furthermore, such uniformly positioned and sized electrodes may limit the ability to craft a desirable volume of neural activation (VNA).
Embodiments address issues such as these and others by providing leads having distal electrode segments where the segments have different sizes. For instance, within a given row, the size of the electrode segments may differ and/or the size of electrode segments in adjacent rows may differ. Furthermore, the rows of segments may be immediately adjacent, and the electrode segments may be arranged to minimize the blind spots that otherwise occur at intersections of the segments and/or to better craft the VNA.
Embodiments provide an implantable medical lead that includes a lead body having a proximal end and a distal end and a set of connectors on the proximal end. The implantable medical lead also includes a set of electrode segments on the lead body and distal of the set of connectors, the set of electrode segments being provided in at least two rows separated along a length of the lead body. A first of the at least two rows has at least two electrode segments that have a different size than each other. A second of the at least two rows is immediately adjacent to the first of the at least two rows and has at least two electrode segments that have a different size than each other. The implantable medical lead further includes a plurality of conductors with each conductor electrically connecting a corresponding connector on the proximal end to a corresponding electrode segment.
Embodiments provide an implantable medical system that includes an implantable medical device having electrical circuitry connected to electrical contacts and also includes an implantable medical lead. The implantable medical lead includes a lead body having a proximal end and a distal end, the proximal end being coupled to the implantable medical device. The implantable medical lead also includes a set of connectors on the proximal end that are coupled to corresponding electrical contacts of the implantable medical device. The implantable medical lead further includes a set of electrode segments on the lead body and distal of the set of connectors, the set of electrode segments being provided in at least two rows separated along a length of the lead body. A first of the at least two rows has at least two electrode segments that have a different size than each other. A second of the at least two rows is immediately adjacent to the first of the at least two rows and has at least two electrode segments that have a different size than each other. The implantable medical lead additionally includes a plurality of conductors with each conductor electrically connecting a corresponding connector on the proximal end to a corresponding electrode segment.
Embodiments provide a method of providing therapy to a patient that involves providing an implantable medical device having electrical circuitry connected to electrical contacts. The method further involves providing an implantable medical lead. The implantable medical lead comprises a lead body having a proximal end and a distal end, the proximal end being coupled to the implantable medical device. The implantable medical lead also includes a set of connectors on the proximal end that are coupled to corresponding electrical contacts of the implantable medical device. The implantable medical lead further includes a set of electrode segments on the lead body and distal of the set of connectors, the set of electrode segments being provided in at least two rows separated along a length of the lead body. A first of the at least two rows has at least two electrode segments that have a different size than each other. A second of the at least two rows is immediately adjacent to the first of the at least two rows and has at least two electrode segments that have a different size than each other. The implantable medical lead additionally includes a plurality of conductors with each conductor electrically connecting a corresponding connector on the proximal end to a corresponding electrode segment. The method also involves passing electrical signals between at least one of the electrode segments of the first row and at least one of the electrode segments of the second row and the electrical circuitry.
Embodiments provide an implantable medical lead that includes a lead body having a proximal end and a distal end and a set of connectors on the proximal end. The implantable medical lead also includes a set of electrode segments on the lead body and distal of the set of connectors, the set of electrode segments being provided in at least two rows separated along a length of the lead body, the set of electrode segments having at least two electrode segments that have a same shape type and different proportions than each other. The implantable medical lead further includes a plurality of conductors with each conductor electrically connecting a corresponding connector on the proximal end to a corresponding electrode segment.
Embodiments provide implantable medical leads that have one or more rows of electrode segments where the electrode segments have a different size. Electrode segments within a given row at a particular axial position may have different sizes than one another. Electrodes segments within adjacent rows at different axial positions may have different sizes than one another. Embodiments may further provide that the electrode segments of a given row and/or in adjacent rows have a same shape type but different proportions to achieve the difference in size.
As shown in subsequent figures and discussed below, the proximal end of the lead 104 and/or lead extension has electrical connectors attached to a lead body 111 of the lead 104 which may be constructed of a non-conductive biocompatible material such as polyurethane. These electrical connectors engage electrical contacts within the header 108 that are electrically coupled through a feedthrough assembly from the header 108 and to the electrical circuitry 107. Conductors within the lead body 111 of the lead 104 then carry the electrical signals between the circuitry 107 of the housing 106 and electrodes 114, including rows of electrode segments, on a distal end 112 of the lead body 111 of the lead 104. The distal end 112 is positioned at the target stimulation and/or sensing site within the body of the patient. It will be appreciated that the electrodes and electrode segments may be positioned along the lead body at any point distal of the set of proximal connectors and the positioning of the electrodes and electrode segments are shown at the distal end of the lead in the various figures herein for purposes of example.
The distal end 112 is positioned at the target area within the body of the patient so that electrodes 302, 304, 306 and so on located on the distal end 112 can engage body tissue to either deliver electrical stimulation therapy pulses through the tissue or to sense electrical physiological signals emanating from the tissue. Each of the distal electrodes 302, 312 and electrode segments 303, 304, 305, 306, 308, and 310 have an associated electrical conductor attached thereto electrically interconnect the proximal connectors to distal electrodes. The electrical conductors are shown in dashed line format to preserve clarity of the electrodes and electrode segments. It will be appreciated that conductor 224 is connected to electrode segment 303 present on the back side of the lead 104 while conductor 232 is connected to electrode segment 305 also present on the backside of the lead 104.
The conductors may be constructed of electrically conductive material used in conventional leads such as various metals such as platinum, platinum-iridium alloys, carbon, and the like. The proximal connectors, distal electrodes, and distal electrode segments may be constructed of conductive materials used in conventional leads such as those listed above for the conductors. These conductors may be individually insulated such as by having a non-conductive coating or other insulator on the conductors 210, 212, 216 to avoid short circuits between conductors. The insulative coating or insulation may be of materials used in conventional leads such as polytetrafluoroethylene based materials. Because these conductors are individually insulated, they may co-exist within the lead 104, such as within a stylet lumen where contact between the conductors may occur. Furthermore, while the conductors of
Additionally, it can be seen that due to the differences in size in one or both of the rows of electrode segments, the space between adjacent electrode segments of a given row do not align with the space between adjacent electrode segments of the immediately adjacent row. The lack of alignment occurs because the space between electrode segments of one row is located at a different circumferential position than the space between electrode segments of the immediately adjacent row. For instance, the space between electrode segment 304 and electrode segment 305 does not align with the space between electrode segment 308 and electrode segment 310. Similarly, the space between electrode segment 303 and electrode segment 304 does not align with the space between electrode segment 306 and electrode segment 308.
This lack of alignment helps to reduce the blind spots that otherwise occur in leads with same sized electrode segments where sensing or stimulation is being performed by an electrode segment of each row, especially relative to conventional leads where the gaps between same sized electrode segments are aligned at the same circumferential position. For instance, electrode segments 303 and 304 of the first row may be electrically connected to the stimulation circuitry to provide a channel of bipolar stimulation to pass electrical stimulation signals between the stimulation circuitry and the electrode segments 303 and 304 providing a desired VNA. Meanwhile in this example, electrode segments 306, 308 and 310 of the second row may be electrically connected to sensing circuitry along with electrode 302 to provide three channels of physiological sensing to detect evoked potentials and the like from the desired VNA and to pass sensed electrical signals between these electrode segments and the sensing circuitry. It will be appreciated that many configurations of stimulation and/or sensing are possible, and since the electrodes and electrode segments are individually wired to the circuitry 107, the circuitry 107 may utilize any given electrode or electrode segment for stimulation, sensing, or both. For instance, a given bipolar stimulation channel may involve electrodes and electrode segments from multiple rows, for instance segment 303 and segment 306, depending upon the desired VNA.
Likewise, differences in size between an electrode of one row and an adjacent electrode of the next row contributes to the lack of alignment of inter-segment spaces to help reduce blind spots in this example. For instance, electrode segment 305 is adjacent to electrode segment 310 and the two have different sizes while having the same shape type but with different proportions. The same is true for electrode segment 304 relative to electrode segment 310 and for electrode segment 303 relative to electrode segment 306.
This example also provides the ability during stimulation to more precisely control the desired VNA. For instance, a more narrow VNA may be achieved than would otherwise be possible without commonly sized electrode segments within the rows.
Additionally, it can be seen that due to the differences in size in the first row of electrode segments, the space between adjacent electrode segments of the first row do not align with the space between adjacent electrode segments of the immediately adjacent row. For instance, the space between electrode segment 504 and electrode segment 505 does not align with the space between electrode segment 508 and electrode segment 510. As another observation, the space between electrode segments 506 and 508 does not align with the space on either side of electrode segment 503. As previously discussed, this helps to reduce the blind spots that otherwise occur in leads with only same sized electrode segments, especially where the gaps between those same sized electrode segments are aligned.
Likewise, differences in size between an electrode of one row and an adjacent electrode of the next row contributes to the lack of alignment of inter-segment spaces to help reduce blind spots in this example, even where one of the rows has same sized electrode segments as in the second row of
This example also provides the ability during stimulation to more precisely control the desired VNA. For instance, as with the previous example a more narrow VNA may be achieved than would otherwise be possible without commonly sized electrode segments within the rows.
Additionally, it can be seen that despite the differences in size among segments in the first row of electrode segments and the differences in size among segments in the second row of electrode segments, the size of axially adjacent electrode segments is the same. Furthermore, the space between adjacent electrode segments of the first row do align with the space between adjacent electrode segments of the immediately adjacent second row. For instance, the space between electrode segment 604 and electrode segment 605 does align with the space between electrode segment 608 and electrode segment 610. The space between electrode segments 603 and 604 does align with the space between electrode segments 606 and 608. While this configuration of electrode segments may have decreased blind spot avoidance relative to the prior examples in
It will be appreciated that many variations may occur from the examples discussed above. For instance, there may be a different number of electrode segments per row than three. There may be a different number of electrode segment rows than two. The position of the rows of electrode segments relative to the ring electrodes may be different. For instance, the rings may be immediately adjacent rather than separated by the two rows of electrode segments so that one row of electrode segments is in the first or last axial position. Through each of these variations, the difference in sizes of electrode segments within the same row and/or in relation to electrode segments of an adjacent row allow for the reduction in blind spots for sensing and/or stimulation.
While embodiments have been particularly shown and described, it will be understood by those skilled in the art that various other changes in the form and details may be made therein without departing from the spirit and scope of the invention.
This application claims priority to U.S. Provisional Application No. 63/214,201, filed Jun. 23, 2021, which is incorporated by reference herein.
Number | Date | Country | |
---|---|---|---|
63214201 | Jun 2021 | US |