The invention is directed to devices and methods for brain stimulation including deep brain stimulation. In addition, the invention is directed to devices and method for brain stimulation using a lead with at least one recording electrode and at least one stimulating electrode.
Deep brain stimulation can be useful for treating a variety of conditions including, for example, Parkinson's disease, dystonia, essential tremor, chronic pain, Huntington's Disease, levodopa-induced dyskinesias and rigidity, bradykinesia, epilepsy and seizures, eating disorders, and mood disorders. Typically, a lead with a stimulating electrode at or near a tip of the lead provides the stimulation to target neurons in the brain. Magnetic resonance imaging (MRI) or computerized tomography (CT) scans can provide a starting point for determining where the stimulating electrode should be positioned to provide the desired stimulus to the target neurons. To further refine the position, a recording lead with a recording electrode at or near the tip of the recording lead can be inserted into the brain of the patient to determine a more precise location. Typically, the recording lead is guided to the target location within the brain using a stereotactic frame and microdrive motor system.
As the recording lead is moved through the brain, the recording electrode is observed to determine when the recording electrode is near the target neurons. This observation may include activating the target neurons to generate electrical signals that can be received by the recording electrode. Once the position of the target neurons is determined, the recording lead can be removed and the stimulating lead inserted. The object of this removal of the recording lead and insertion of the stimulating lead is to attempt to precisely locate the target neurons. The precise insertion of the stimulating lead and positioning of the stimulating lead in the precise location indicated by the recording lead can be particularly difficult. In some instances, multiple insertions of the recording lead and stimulating lead may need to occur to properly position the stimulating electrode.
One embodiment is a device for brain stimulation that includes a lead having a longitudinal surface; at least one stimulation electrode disposed along the longitudinal surface of the lead; and at least one recording electrode, separate from the at least one stimulation electrode, disposed along the longitudinal surface of the lead.
Another embodiment is a device for brain stimulation that includes a lead having a circumference; and a set of recording electrodes disposed at intervals around the circumference of the lead.
Yet another embodiment is a device for brain stimulation that includes a lead defining a lumen having a non-circular lateral cross-section; and at least one electrode disposed on the lead.
A further embodiment is a method for brain stimulation. A lead is inserted into a cranium of a patient. The lead includes at least one stimulation electrode disposed along a longitudinal surface of the lead; and at least one recording electrode, separate from the at least one stimulation electrode, disposed along the longitudinal surface of the lead. Target neurons are identified using the at least one recording electrode. The target neurons are stimulated using the at least one stimulation electrode.
Non-limiting and non-exhaustive embodiments of the present invention are described with reference to the following drawings. In the drawings, like reference numerals refer to like parts throughout the various figures unless otherwise specified.
For a better understanding of the present invention, reference will be made to the following Detailed Description, which is to be read in association with the accompanying drawings, wherein:
The present invention is directed to the area of devices and methods for brain stimulation including deep brain stimulation. In addition, the invention is directed to devices and method for brain stimulation using a lead with at least one recording electrode and at least one stimulating electrode.
A lead for deep brain stimulation can include both recording and stimulation electrodes. This allows a practitioner to determine the position of the target neurons using the recording electrode(s) and then position the stimulation electrode(s) accordingly without removal of a recording lead and insertion of a stimulation lead. A lead can also include recording electrodes spaced around the circumference of the lead to more precisely determine the position of the target neurons. In at least some embodiments, the lead is rotatable so that the stimulation electrodes can be aligned with the target neurons after the neurons have been located using the recording electrodes.
The lead 102 can be formed of a non-conducting material such as, for example, a polymeric material. Suitable polymeric materials include, for example, silicone rubber and polyethylene. Preferably, the lead is made using a biocompatible material. In at least some instances, the lead may be in contact, with body tissue for extended periods of time.
The lead often has a cross-sectional diameter of no more than 1.5 mm and may be in the range of 1 to 1.2 mm. The lead often has a length of at least 10 cm and the length of the lead may be in the range of 30 to 70 cm.
The lead typically defines a lumen 120 (see
The lumen can have any shape. In one embodiment, the lateral cross-sectional shape of the lumen is non-circular. For example, the lateral cross-sectional shape of the lumen can have an oval, square, rectangular, or, as illustrated in
The stylet 110 can be made of a rigid material. Examples of suitable materials include tungsten, stainless steel, or plastic. The stylet 110 may have a handle 111 to assist insertion into the lead, as well as rotation of the stylet and lead.
Conductors 122 (e.g., wires) that attach to or form the recording electrode(s) 106 and stimulation electrode(s) 104 also pass through the lead 102. These conductors may pass through the material of the lead as illustrated, for example, in one configuration for
The lead 102 includes one or more recording electrodes 106 disposed along the longitudinal axis of the lead near a distal end of the lead. In at least some embodiments, the lead includes a plurality of recording electrodes. The recording electrodes can be made using a metal, alloy, conductive oxide, or other conductive material. Examples of suitable materials include platinum, iridium, platinum iridium alloy, stainless steel, titanium, or tungsten.
Any type of recording electrode can be used including monopolar recording electrodes, bipolar recording electrodes (as illustrated in
Any type of recording electrode can be used including electrode pads or plates. A preferred recording electrode for at least some embodiments is a tip of a wire. This type of electrode can assist in more precise location of the target neurons because of the small surface area for detection of electrical signals. Such recording electrodes often have a diameter of no more than 100 μm or no more than 50 μm. The diameter may be in the range from, for example, 25 μm to 100 μm. In one embodiment, the recording electrodes 106 correspond to wire conductors 122 that extend out of the lead 102 and are then trimmed or ground down flush with the lead surface.
The lead 102 also includes one or more stimulation electrodes 104 arranged along the longitudinal axis of the lead near a distal end of the lead. In at least some embodiments, the lead includes a plurality of stimulation electrodes. A conductor 122 is attached to each stimulation electrode 104. The stimulation electrodes often have a surface area of at least 1 mm2 or at least 5 mm2. The surface area may be in the range from, for example, 1 mm2 to 6 mm2. A variety of shapes can be used for the stimulation electrodes including, for example, rings, circles, ovals, squares, rectangles, triangles, etc. In some embodiments, a stimulation electrode 104 forms a ring that fully or substantially encircles the lead 102. Preferably, however, the stimulation electrodes are not rings, but are instead discrete shapes disposed on one side of the lead. Ring electrodes typically stimulate neurons on all sides of the lead instead, of focusing on the target neurons that may face only a portion of the lead circumference.
The stimulation electrodes can be made using a metal, alloy, conductive oxide or other conductive material Examples of suitable materials include platinum, iridium, platinum iridium alloy, stainless steel, titanium, or tungsten. Preferably, the stimulation electrodes axe made of a material that is biocompatible and does not substantially corrode under expected operating conditions in the operating environment for the expected duration of use.
The arrangement of recording electrodes 106 and stimulation electrodes 104 on the lead 102 can facilitate detection and stimulation of target neurons. Some embodiments include a single recording electrode and a single stimulation electrode. Other embodiments, however, include two or more recording electrodes, two or more stimulation electrodes, or both.
In other embodiments, one or more recording electrodes 106 may be provided within one or more of the stimulation electrodes 104. One example of such an arrangement is illustrated in
In at least some embodiments, recording electrodes 106 axe arranged at various positions around the lateral circumference of the lead 102. Examples of such arrangements are illustrated in the cross-sectional views of
Positioning the recording electrodes 106 around the lead 102 in this manner can assist in determining the position of the target neurons because the recording electrodes can sample the brain tissue around the lead without rotating the lead.
Stimulation electrodes 104 can be positioned around the circumference of the lead 102 in a similar manner as that described for the recording electrodes. In at least some embodiments, however, stimulation electrode(s) 104 are positioned only along one side of the lead 102 and one or more sets of recording electrodes 106 are arrayed around the lateral circumference of the lead. Sets of recording electrodes can be displaced from each other longitudinally along the lead (e.g., the arrangement illustrated in
The recording electrodes 106 can be used to determine the site of the target neurons and then the lead can then be rotated, if necessary when the recording electrode is not one of those aligned with the stimulation electrode(s), and advanced or retreated, if necessary or desired, to align the stimulation electrode(s) with the target neurons. Rotation of the lead can be facilitated using a stylet and lead with non-circular lumen such as, for example, those illustrated in
In one example of operation of the lead illustrated in
In some embodiments, the microdrive motor system 202 can be fully or partially automatic. For example, the microdrive motor system 202 can perform one or more actions on the lead 102 in response to the signals from the recording electrode(s) 106, stimulation electrode(s) 104, or both. The microdrive motor system may be configured to perform one or more the following actions (alone or in combination): rotate the lead, insert the lead, or retract the lead. In one embodiment, the microdrive motor system, can rotate the lead to position the stimulation electrode(s) in the position of the recording electrode(s) that detect the target neurons. In another embodiment, the microdrive motor system can rotate the bad partially and the recording electrode(s) can then be observed, in the new position to iteratively determine the best position for the stimulation electrode(s). For example, if recording electrodes are positioned every 90° around the lead, the initial rotation of the lead can be less than 90° (e.g., 30° or 45°) and the recording electrodes can again be observed to more accurately identify the location of the target neurons.
In some embodiments, measurement devices coupled to the muscles or other tissues stimulated by the target neurons or a unit responsive to the patient or clinician can be coupled to the control unit or microdrive motor system. The measurement device, user, or clinician can indicate a response by the target muscles or other tissues to the stimulation or recording electrode(s) to further identify the target neurons and facilitate positioning of the stimulation electrode(s). For example, if the target neurons are directed to a muscle experiencing tremors, a measurement device can he used to observe the muscle and indicate changes in tremor frequency or amplitude in response to stimulation of neurons. Alternatively, the patient or clinician may observe the muscle and provide feedback.
The above specification, examples and data provide a description of the manufacture and use of the composition of the invention. Since many embodiments of the invention can be made without departing from the spirit and scope of the invention, the invention also resides in the claims hereinafter appended.
This patent application is a continuation of allowed U.S. application Ser. No. 13/943,175 filed Jul. 16, 2013 which is a continuation of U.S. patent application Ser. No. 12/881,000 filed on Sep. 13, 2010, now U.S. Pat. No. 8,498,718, which is a continuation of U.S. patent application Ser. No. 11/030,546 tiled on Jan. 5, 2005, now U.S. Pat. No. 7,809,446, which is incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
4350159 | Gouda | Sep 1982 | A |
4471777 | McCorkle, Jr. | Sep 1984 | A |
4565200 | Cosman | Jan 1986 | A |
4668221 | Luther | May 1987 | A |
4886065 | Collins, Jr. | Dec 1989 | A |
4931056 | Ghajar et al. | Jun 1990 | A |
4955891 | Carol | Sep 1990 | A |
5006122 | Wyatt et al. | Apr 1991 | A |
5114424 | Hagen et al. | May 1992 | A |
5116345 | Jewell et al. | May 1992 | A |
5300080 | Clayman et al. | Apr 1994 | A |
5303704 | Molacek et al. | Apr 1994 | A |
5318041 | DuBois et al. | Jun 1994 | A |
5330485 | Clayman et al. | Jul 1994 | A |
5450846 | Goldreyer | Sep 1995 | A |
5579764 | Goldreyer | Dec 1996 | A |
5618287 | Fogarty et al. | Apr 1997 | A |
5728148 | Bostrom et al. | Mar 1998 | A |
5752937 | Otten et al. | May 1998 | A |
5843148 | Gijsbers et al. | Dec 1998 | A |
5913882 | King | Jun 1999 | A |
5925073 | Chastain et al. | Jul 1999 | A |
5978713 | Prutchi et al. | Nov 1999 | A |
6011996 | Gielen et al. | Jan 2000 | A |
6026567 | Swoyer et al. | Feb 2000 | A |
6066165 | Racz | May 2000 | A |
6181971 | Doan | Jan 2001 | B1 |
6261300 | Carol et al. | Jul 2001 | B1 |
6301492 | Zonenshayn | Oct 2001 | B1 |
6343226 | Sunde et al. | Jan 2002 | B1 |
6413263 | Lobdill et al. | Jul 2002 | B1 |
6416520 | Kynast et al. | Jul 2002 | B1 |
6456869 | Raylman et al. | Sep 2002 | B1 |
6456889 | Pianca et al. | Sep 2002 | B2 |
6510347 | Borkan | Jan 2003 | B2 |
6529774 | Greene | Mar 2003 | B1 |
6572624 | U et al. | Jun 2003 | B2 |
6597954 | Pless et al. | Jul 2003 | B1 |
6687549 | Helland et al. | Feb 2004 | B1 |
6782292 | Whitehurst | Aug 2004 | B2 |
6849062 | Kantor | Feb 2005 | B2 |
7033326 | Pianca et al. | Apr 2006 | B1 |
7177701 | Pianca | Feb 2007 | B1 |
7212867 | Van Venrooij et al. | May 2007 | B2 |
7783359 | Meadows | Aug 2010 | B2 |
7809446 | Meadows | Oct 2010 | B2 |
8498718 | Meadows | Jul 2013 | B2 |
8571665 | Moffitt et al. | Oct 2013 | B2 |
20010027336 | Gielen et al. | Oct 2001 | A1 |
20020151924 | Shiber | Oct 2002 | A1 |
20040199235 | Younis | Oct 2004 | A1 |
20050004637 | Singhal et al. | Jan 2005 | A1 |
20050015130 | Gill | Jan 2005 | A1 |
20080103572 | Gerber | May 2008 | A1 |
Number | Date | Country |
---|---|---|
1062973 | Dec 2000 | EP |
9936122 | Jul 1999 | WO |
Entry |
---|
“System and Method for Selective Multi-Site Microeloectrode Recording,” IP.com, IPCOM000016587D, Jul. 1, 2003. |
“Universaly Instrument Guide and Surgical Insertion Tool for Stereotactic Frames,” IP.com, IPCOM00011023D, Feb. 7, 2003. |
Official Communication for U.S. Appl. No. 11/030,546 mailed Sep. 26, 2007. |
Official Communication for U.S. Appl. No. 11/030,546 mailed Mar. 20, 2008. |
Official Communication for U.S. Appl. No. 11/030,546 mailed May 21, 2008. |
Official Communication for U.S. Appl. No. 11/030,546 mailed Jan. 21, 2009. |
Official Communication for U.S. Appl. No. 11/030,546 mailed May 22, 2009. |
Official Communication for U.S. Appl. No. 11/030,546 mailed Dec. 7, 2009. |
Official Communication for U.S. Appl. No. 11/030,546 mailed Dec. 28, 2009. |
Official Communication for U.S. Appl. No. 11/030,546 mailed Jun. 17, 2010. |
Official Communication for U.S. Appl. No. 11/230,052 mailed Sep. 26, 2007. |
Official Communication for U.S. Appl. No. 11/230,052 mailed Mar. 18, 2008. |
Official Communication for U.S. Appl. No. 11/230,052 mailed May 27, 2008. |
Official Communication for U.S. Appl. No. 11/230,052 mailed Sep. 30, 2008. |
Official Communication for U.S. Appl. No. 11/230,052 mailed Jan. 29, 2009. |
Official Communication for U.S. Appl. No. 11/230,052 mailed Jun. 1, 2009. |
Official Communication for U.S. Appl. No. 11/230,052 mailed Aug. 12, 2009. |
Official Communication for U.S. Appl. No. 11/230,052 mailed Dec. 28, 2009. |
Official Communication for U.S. Appl. No. 11/230,052 mailed May 7, 2010. |
Official Communication for U.S. Appl. No. 12/881,000 mailed Nov. 6, 2012. |
Official Communication for U.S. Appl. No. 12/881,000 mailed Feb. 20, 2013. |
Official Communication for U.S. Appl. No. 13/943,175 mailed Nov. 26, 2013. |
Number | Date | Country | |
---|---|---|---|
20140249598 A1 | Sep 2014 | US |
Number | Date | Country | |
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Parent | 13943175 | Jul 2013 | US |
Child | 14274606 | US | |
Parent | 12881000 | Sep 2010 | US |
Child | 13943175 | US | |
Parent | 11030546 | Jan 2005 | US |
Child | 12881000 | US |