Implantable neurostimulator with refractory stimulation

Information

  • Patent Grant
  • 7869867
  • Patent Number
    7,869,867
  • Date Filed
    Friday, October 27, 2006
    17 years ago
  • Date Issued
    Tuesday, January 11, 2011
    13 years ago
Abstract
In some embodiments, a method comprises providing an electrical signal to a nerve to evoke an action potential. The nerve thereby enters a refractory period in which the nerve is in a refractory state. The method further comprises, during the refractory period, providing an electrical signal to the nerve thereby altering the refractory period of the nerve or non-target tissues.
Description
BACKGROUND

Implantable neurostimulators are effective at treating various disorders such as epilepsy and depression. A neurostimulator is implanted in the patient and connected via one or more electrodes to a target nerve, such as the vagus nerve. Current from the electrical signal provided by the neurostimulator or action potentials evoked by the stimulated target nerve can propagate to a non-target nerve (including nerves nearby the target nerve as well as specific non-target fibers within the target nerve) and non-target muscle tissue adjacent to the electrodes. As a result, such nearby tissues may be stimulated thereby resulting in wasted energy that is non-therapeutic and which may in addition cause undesired side effects such as contractions of the muscle tissue. For example, it is possible for vagus nerve stimulation to excite the muscles at or near the patient's vocal cords thereby potentially causing hoarseness. While generally regarded as benign, the excitation of muscle tissue and the resultant hoarseness may be uncomfortable to the patient and is at any rate undesired, wasteful and non-therapeutic. Ameliorating the foregoing problems while improving the efficacy of the underlying therapy provided by the neurostimulator is desirable.


BRIEF SUMMARY

In accordance with at least one embodiment of the invention, an implantable medical device comprises a neurostimulator that provides a first electrical signal to a nerve (e.g., the vagus nerve) in a first, non-refractory period. The first electrical signal is adapted to induce action potentials in one or more target axons (fibers) of the nerve. The neurostimulator also provides a second electrical signal to the nerve during a second period in which one or more of the non-target tissues (e.g. adjacent muscles or non-target nerve fibers) are refractory. The second period may comprise at least a portion of one or both of an absolute refractory period and a relative refractory period for the non-target tissue. The second signal provided to the nerve during the refractory period causes the refractory period of the non-target tissue to be altered, i.e., extended or shortened, depending on the attributes of the second signal. Extending the refractory period ameliorates various side effects that might otherwise occur. Shortening the relative refractory period facilitates additional therapies to be implemented.


In accordance with some embodiments, a method comprises applying a first electrical signal to a nerve to evoke an action potential. As a result, the nerve enters a refractory period in which the nerve is refractory to further induction of action potentials. During the refractory period, the method also comprises providing a second electrical signal to the nerve thereby altering the refractory period.


In accordance with another embodiment, a method comprises applying a first electrical signal to a nerve to evoke an action potential. The first electrical signal or action potential evokes action potentials in non-target tissue. The non-target tissue thereafter enters a refractory period in which the non-target tissue is refractory to further induction of action potentials. During the refractory period, the method further comprises applying a second electrical signal to the nerve thereby altering the refractory period of the non-target tissue.


In accordance with another embodiment, an implantable neurostimulator comprises an electrical signal generator and an electrode coupled to the electrical signal generator. The electrode is adapted to couple to a nerve. The electrical signal generator applies a first electrical signal to a nerve to evoke an action potential. As a result, the nerve enters a refractory period in which the nerve is in a refractory state. During the refractory period, the electrical signal generator provides a second electrical signal to the nerve thereby altering the refractory period of the nerve.


In accordance with yet another embodiment, an implantable neurostimulator comprises an electrical signal generator and an electrode. The electrode is adapted to be coupled to the electrical signal generator and to a nerve to thereby provide therapy to a target nerve fiber. The electrical signal generator applies a first electrical signal to a nerve to evoke an action potential in the target nerve which causes an action potential to be evoked in a non-target nerve fiber or tissue. The non-target nerve fiber or tissue thereby enters a refractory period in which the non-target nerve fiber or tissue is in a refractory state. During the refractory period, the electrical signal generator applies a second electrical signal to the nerve fiber or tissue thereby altering the refractory period of the non-target nerve fiber or tissue.





BRIEF DESCRIPTION OF THE DRAWINGS

For a detailed description of exemplary embodiments of the invention, reference will now be made to the accompanying drawings in which:



FIG. 1 depicts, in schematic form, an implantable neurostimulator, in accordance with a preferred embodiment of the invention, implanted within a patient and programmable by an external programming system;



FIG. 2 shows an illustrative embodiment of the implantable neurostimulator of FIG. 1;



FIG. 3 illustrates a refractory period of an electrically-excitable tissue as comprising an absolute refractory period and a relative refractory period;



FIG. 4 illustrates an embodiment in which the relative refractory period is extended by providing an electrical signal during the relative refractory period;



FIG. 5 illustrates an embodiment in which particular types of nerve fibers are targeted for refractory period adjustment;



FIG. 6 illustrates an embodiment in which the refractory period is shortened via the application of an electrical signal with a different polarity than the polarity used to stimulate the nerve initially; and



FIG. 7 illustrates a method of adjusting a refractory period of a nerve or other non-target tissue in accordance with a preferred embodiment of the invention.





DETAILED DESCRIPTION

The following discussion is directed to various embodiments of the invention. Although one or more of these embodiments may be preferred, the embodiments disclosed should not be interpreted, or otherwise used, as limiting the scope of the disclosure, including the claims. In addition, one skilled in the art will understand that the following description has broad application, and the discussion of any embodiment is meant only to be exemplary of that embodiment, and is not intended to limit the scope of the disclosure, including the claims, to that embodiment.



FIG. 1 illustrates an implantable medical device (“IMD”) 10 implanted in a patient. The IMD 10 may be representative of any of a variety of medical devices. At least one preferred embodiment of the IMD 10 comprises a neurostimulator for stimulating a neural structure in a patient, particularly a neurostimulator for stimulating a patient's cranial nerve such as a vagus nerve 13. Although the IMD 10 is described below in terms of a vagus nerve stimulation (“VNS”) embodiment, the disclosure and claims that follow are not limited to VNS unless expressly noted, and may be applied to the stimulation of other tissues such as the trigeminal and/or glossopharyngeal nerves, or to other neural tissue such as one or more brain structures of the patient, spinal nerves, and other spinal structures, as well as various non-neural tissues and organs.


Referring still to FIG. 1, a lead assembly 16 comprising one or more leads is coupled to the IMD 10. The lead assembly 16 includes one or more electrodes, such as electrodes 12 and 14. Each lead assembly 16 has a proximal end that connects to the IMD 10. The electrodes 12, 14 are coupled to a distal end of the lead assembly. At least one electrode 12 or 14, and preferably an electrode pair (12 and 14), is used as a therapeutic electrode to deliver an electrical signal to target tissues such as the patient's vagus nerve 13. At least one electrode 12, 14 (preferably an electrode pair 12 and 14) may in some embodiments be used as a sensing electrode to detect electrical activity of target tissue (e.g., the vagus nerve 13). In alternative embodiments, separate sensing electrode(s) may be used. The housing (or “can”) of the IMD 10 may also be used as a stimulating or sensing electrode. Sensing electrodes may alternatively be omitted entirely.



FIG. 1 also illustrates an external device implemented as a programming system 20 for the IMD 10. The programming system 20 may comprise a personal computer, a handheld computer such as a personal digital assistant (PDA) device, or other suitable computing device consistent with the description contained herein, as well as a wand 28 used for transmitting and receiving signals to and from the IMD 10. In systems where the programming system 20 uses one or more channels in the Medical Implant Communications Service (MICS) bandwidths, the wand 28 may be omitted to permit more convenient communication between the programming system and the IMD 10. Methods and apparatus for communication between the IMD 10 and an external programming system 20 are known in the art, including telemetry via an RF communication link. Representative techniques for such communication are disclosed in U.S. Pat. No. 5,304,206, and U.S. Pat. No. 5,235,980, both incorporated herein by reference. The IMD 10 includes a transceiver (such as a coil) that permits signals to be communicated wirelessly between the programming system 20 and/or wand 28 and the IMD 10. The programming system 20 monitors the performance of the IMD 10 and downloads new executable operational programming (i.e., software) and/or therapy parameters into the IMD 10 to alter its operation as desired. In accordance with preferred embodiments of the invention and as further explained below, the programming system 20 downloads configuration parameters that cause the IMD 10 to extend or shorten the refractory period of either the nerve 13 being stimulated or non-target tissue in or near the nerve.



FIG. 2 shows a block diagram of a preferred embodiment of the IMD 10. As shown, the IMD 10 includes a power supply 30 (e.g., a battery), a stimulation and communication unit (“SCU”) 32, and a controller 34. The illustrative SCU 32 of FIG. 2 comprises a current generator 37 and a communication system 38. Under the control of controller 34, the current generator 37 of the SCU 32 generates an electrical signal (e.g., a programmable, constant current pulsed signal) to stimulate a target neural tissue in a patient. Further, under the control of controller 34, the communication system 38 of the SCU 32 telemeters data (e.g., therapy parameters) or operational programming (e.g., executable software) to/from the programming system 20. In the embodiment of FIG. 2, the battery 30 provides power for both the SCU 32 and the controller 34.


The controller 34 generally assists, controls, and/or programs the SCU 32. Controller 34 preferably comprises a processor 36 such as a low-power, mixed-signal microcontroller. One suitable processor is available from Texas Instruments, Inc., selected from the MSP430F family of processors. Other suitable processors from the PIC1xF family of processors are available from MicroChip Technology. Other suitable processors may be used and/or integrated into the controller 34, although the processor 36 preferably is capable of processing a variety of sensor inputs, uses low power, and operates at a high speed. In general, however, any suitable processor 36 can be used in the controller 34 to implement the functionality performed by the controller 34 as explained herein. It will be appreciated that some features of the controller 34 may also be provided in whole or in part by the SCU 32, and vice versa. Thus, while certain features of preferred embodiments of the present invention may be described as comprising part of the SCU 32, it is not intended thereby to preclude embodiments in which the features are provided by the controller 34. Likewise, certain features described herein as comprising part of the controller 34 are not intended to preclude embodiments in which the features comprise part of the SCU 32.


In the embodiment of FIG. 2, the controller 34 additionally comprises a memory 40 integrated into the controller. In some embodiments, the processor 36 of the controller 34 directly executes programs from the integrated memory 40. That is, executable instructions (i.e., operational programming) can be fetched directly from memory 40 for execution by the processor 36 without first copying the instructions to another memory (e.g., a RAM). The integrated memory 40 may be upgraded by erasing one or more segments of the integrated memory 40 and, via the programmer 20, writing a new program to the integrated memory 40.


The external programming system 20 can wirelessly transmit programs and configuration data to the IMD 10 for storage in the IMD's memory 40, registers internal to the processor 36, or other storage of the IMD 10.


Like all electrically-excitable tissue, neural tissue, such as the vagus nerve, has an intrinsic property called the “refractory period.” Once a nerve is excited (i.e., an action potential is generated), the nerve enters the refractory period during which time the nerve is resistant to further induction of action potentials, even if another or additional electrical current is applied to the nerve. During this time period, the nerve is said to be “refractory” to an applied electrical signal. In general, action potentials can again be induced in the nerve with an applied electrical signal once the refractory period is over.


As illustrated by FIG. 3, the refractory period comprises an “absolute” refractory period followed by a “relative” refractory period. The absolute refractory period begins upon the stimulation of a nerve at 50. During the absolute refractory period, the nerve cannot be induced to generate an action potential regardless of the strength of the applied electrical signal. During the relative refractory period, which immediately follows the absolute refractory period, it is possible to induce an action potential in the nerve with a sufficiently strong applied electrical signal. A stronger electrical signal is required to generate an action potential during the relative refractory period than to initially stimulate the nerve during a non-refractory period. The lengths of the absolute and relative refractory periods may be altered by applying an electrical signal to the nerve during one or both of the absolute and relative refractory periods. The duration of the absolute and relative refractory periods without an externally applied signal are relatively constant for a particular tissue, and are referred to herein as the “intrinsic” absolute and relative refractory periods. The nerve's intrinsic relative refractory period ends at reference numeral 53 in FIG. 3.


Muscle tissue (e.g., the heart) is also characterized by a refractory period. Different types of muscular and neural tissues have different refractory periods. The refractory period of cardiac tissue tends to be substantially longer than the refractory period of neural tissue. Further, the vagus nerve comprises different types of nerve fibers, e.g., A fibers, B fibers and C fibers, with many subtypes. A and B vagus nerve fibers have larger diameters than C fibers. C fibers tend to have substantially longer refractory periods than A and B fibers, and B fibers have slightly longer refractory periods than A fibers.


Without limiting the scope of this disclosure, Table I below provides exemplary values for the absolute and relative refractory periods of various types of nerves and tissues. In general muscle tissues have substantially longer refractory periods than nerve tissues.











TABLE I






Absolute Refractory
Relative Refractory


Tissue type
(mS)
(mS)

















Large diameter nerve
0.4
 Up to 1.6


(e.g., A and B fiber types)




Small diameter nerve
4
Up to 16


(e.g., C fiber type)




Cardiac muscle
100
 Up to 400









In accordance with various embodiments of the invention, the IMD 10 alters the length of the refractory period and, in some embodiments, specifically the relative refractory period. In some embodiments, the IMD 10 extends the relative refractory period, while in other embodiments, the IMD 10 shortens the relative refractory period. Further still, in some embodiments, the IMD 10 extends the relative refractory period in accordance with some therapies or situations, while shortening the relative refractory in accordance with other therapies or situations. Extending a relative refractory period can be accomplished by providing an electrical signal to the nerve during the relative refractory period at a level low enough so as not to re-stimulate the nerve. Shortening the relative refractory period can be accomplished by providing a signal during the relative refractory period with a polarity opposite to that of the first electrical signal that induced the action potential.



FIG. 4 depicts a timeline in which a second electrical signal 55 to alter the refractory period of the nerve is applied to the nerve beginning at a time in the relative refractory period of the nerve. The end of the nerve's intrinsic relative refractory period (53) is extended due to the application of the signal at 55. The relative refractory period can be extended almost indefinitely as long as the signal continues to be or is repetitively applied. However, the tissue will eventually either exit a refractory state or become permanently damaged or impaired, even with an applied current. Once the application of the signal is removed, the relative refractory period of the nerve will subsequently end, after which the nerve returns to a non-refractory state in which action potentials can again be induced with a first electrical signal.


Extending the relative refractory is useful to ameliorate side effects that might otherwise be caused by the IMD 10. For example, action potentials generated by applying a first electrical signal to a vagus nerve of a patient may propagate to adjacent muscle tissues. Such muscle tissues may include muscles adjacent to, or that directly control, the patient's vocal cords. As a result of stimulating the patient's vagus nerve, the patient's vocal cords, or controlling muscles, may be affected possibly resulting in hoarseness or changes to the patient's voice during delivery of a first electrical signal. All tissues stimulated by the first electrical signal, including both target nerve fibers and non-target nerve fibers or muscles, will begin their respective intrinsic refractory periods approximately synchronous with the first electrical signal. However, the difference between intrinsic refractory periods of different tissues may be exploited to ameliorate undesired side effects.


In accordance with at least some embodiments, the current generator 37 of the IMD 10 provides a second electrical signal during the relative refractory period of at least one non-target tissue, such as a particular nerve fiber type, or muscle tissue. The magnitude of the second electrical signal is small enough to prevent additional action potentials from being generated. Instead, the second electrical signal provided to the nerve causes the non-target tissue, which is in a refractory state, to remain in a refractory state, thereby extending the duration of the relative refractory period. By extending the relative refractory period of the non-target tissue, no additional action potentials will be induced that otherwise would propagate to, and stimulate, adjacent tissues. In at least some such embodiments, the relative refractory period is extended as long as the second electrical signal continues to be applied to the nerve.


The magnitude of the second electrical signal used to extend the relative refractory period depends, at least in part, on the point in time during the relative refractory period at which the second electrical signal is first applied to the nerve. The earlier in the relative refractory period that the second electrical signal is applied, the larger the magnitude the second electrical signal needs to be to cause the relative refractory period to be extended. By contrast, the later in the relative refractory period that the current is applied, the smaller the magnitude of the current needs to be to cause the relative refractory period to be extended.



FIG. 5 illustrates refractory periods for two different types of nerve fibers—large diameter fibers (e.g., A and B fibers) and small diameter fibers (e.g., C fibers). The refractory period for the small fiber type is longer than the refractory period of the large fiber type. In FIG. 5, it can be seen that it is possible to apply a second electrical signal to the nerve (comprising both fiber types) at a point in time (e.g., 60) that falls within the relative refractory period of the small diameter fibers, and yet falls outside the relative refractory period of the large diameter fibers. A second electrical signal applied at point 60 of an appropriate magnitude will extend the relative refractory period of the small diameter fibers. Because the second electrical signal occurs after the end of the relative refractory period of the large diameter fibers, it may still be used for stimulation of the large fibers. That is, the second electrical signal does not extend the relative refractory period of the large fibers (thereby allowing action potentials to occur) and does extend the relative refractory period in the small fibers (thereby precluding action potentials from occurring). As a result, the relative refractory period of selected fiber types can be extended. To the extent the fiber types whose relative refractory periods are selectively extended would otherwise cause various side effects, such side effects can be reduced or eliminated by keeping the selected fiber types in a relative refractory state.



FIG. 6 illustrates the shortening of the intrinsic relative refractory period of a nerve via the application of a reverse polarity second electrical signal during the nerve's relative refractory period. A reverse polarity second electrical signal means that the current flows in the opposite direction than the direction of current flow in the first, therapeutic electrical signal applied at 50. As illustrated in FIG. 6, the end 53 of the nerve's intrinsic relative refractory period is shortened to 62 via the application of a reverse polarity current beginning at time 64 during the relative refractory period. The amount of time 65 by which the refractory period is shortened is a function of the magnitude and time duration of the reverse polarity second electrical signal.


Shortening the relative refractory period of a nerve causes the nerve to be available to be re-stimulated sooner than otherwise would be possible. As a result, therapies are possible in which the nerve can be stimulated a faster rate than without the use of the second electrical signal. Further, as illustrated in FIG. 5, some fiber types have longer refractory periods than other fiber types. By applying a reverse polarity current during the refractory period of the fiber types having the longer refractory periods (e.g., the small fiber types), the refractory periods of such fibers can be shortened and made substantially the same as, or at least closer to, the refractory periods of the fiber types having the intrinsically smaller relative refractory periods.



FIG. 7 shows a method 80 of altering the refractory period of a nerve in accordance with an embodiment of the invention. At 82, method 80 comprises applying a first electrical signal in a nerve during a non-refractory period. The first electrical signal is selected to induce an action potential in the nerve, as shown at 84. Following the induced action potential, the method further comprises applying (step 86) a second electrical signal to the nerve during a refractory period of the non-target nerve/nerve fibers or non-target tissue. The second electrical signal alters the length of the refractory period (step 88). As discussed above, the alteration to the nerve's or non-target tissue's relative refractory period can be to extend or shorten the relative refractory period.


In accordance with at least some embodiments of the invention, the external programming system 20 (FIG. 1) can be used to program the IMD 10 to shorten or extend the nerve's or non-target tissue's relative refractory period. Via the programming system 20, one or more parameters are transmitted to the IMD 10 that cause the current generator 37 of the IMD 10 to provide an appropriate current to the nerve during the nerve's or non-target tissue's relative refractory period so as to shorten or lengthen the refractory period as desired.


The above discussion is meant to be illustrative of the principles and various embodiments of the present invention. Numerous variations and modifications will become apparent to those skilled in the art once the above disclosure is fully appreciated. It is intended that the following claims be interpreted to embrace all such variations and modifications.

Claims
  • 1. A method, comprising: applying a first electrical signal to a nerve to evoke an action potential, said nerve thereafter entering a refractory period in which said nerve is refractory to further induction of action potentials; andafter applying said first electrical signal, altering said refractory period by applying a second electrical signal to said nerve during said refractory period, wherein said second electrical signal is effective to alter said refractory period and is unable to stimulate said nerve to evoke an action potential.
  • 2. The method of claim 1 wherein applying said second electrical signal during said refractory period comprises providing current during a relative refractory period.
  • 3. The method of claim 1 wherein applying said second electrical signal during said refractory period comprises providing current for a period of time that extends past said nerve's intrinsic refractory period.
  • 4. The method of claim 1 wherein said refractory period comprises an absolute refractory period and a relative refractory period, and wherein applying said second electrical signal to said nerve during said refractory period comprises beginning to apply said second electrical signal to said nerve during said relative refractory period.
  • 5. The method of claim 1 wherein altering said refractory period comprises shortening said refractory period by applying said second electrical signal having a polarity opposite that of a polarity of the first electrical signal.
  • 6. The method of claim 1 wherein altering said refractory period comprises extending said refractory period by applying said second electrical signal having a polarity that is the same as a polarity of the first electrical signal.
  • 7. The method of claim 1 wherein applying said second electrical signal to said nerve comprises applying said second electrical signal during a relative refractory period of a select nerve fiber type while not applying said second electrical signal during the refractory period of another nerve fiber type.
  • 8. A method, comprising: applying a first electrical signal to a nerve to evoke an action potential;wherein said first electrical signal or said action potential evokes action potentials in non-target tissue;said non-target tissue thereafter entering a refractory period in which the nontarget tissue is refractory to further induction of action potentials; andafter applying said first electrical signal, altering said refractory period of the non-target tissue by applying a second electrical signal to said nerve during said refractory period, wherein said second electrical signal is effective to alter said refractory period and has an insufficient magnitude to trigger an action potential in said non-target tissue.
  • 9. The method of claim 8 wherein applying said second electrical signal during said refractory period comprises providing current during a relative refractory period.
  • 10. The method of claim 8 wherein applying said second electrical signal during said refractory period comprises providing current for a period of time that extends past the non-target tissue's intrinsic refractory period.
  • 11. The method of claim 8 wherein said refractory period comprises an absolute refractory period and a relative refractory period, and wherein applying said second electrical signal to said nerve during said refractory period comprises beginning to apply said second electrical signal to said nerve during said relative refractory period.
  • 12. The method of claim 8 wherein altering said refractory period of the non-target tissue comprises shortening said refractory period by applying said second electrical signal having a polarity opposite that of a polarity of the first electrical signal.
  • 13. The method of claim 8 wherein altering said refractory period of the non-target tissue comprises extending said refractory period by applying said second electrical signal having a polarity that is the same as a polarity of the first electrical signal.
  • 14. The method of claim 8 wherein applying said second electrical signal to said nerve comprises applying said second electrical signal during a relative refractory period of a select nerve fiber type while not applying said second electrical signal during the refractory period of another nerve fiber type.
  • 15. An implantable neurostimulator, comprising: an electrical signal generator; andan electrode coupled to said electrical signal generator and adapted to couple to a nerve;wherein said electrical signal generator applies a first electrical signal to said nerve to evoke an action potential, said nerve thereby entering a refractory period in which said nerve is in a refractory state, and during said refractory period after applying said first electrical signal, said electrical signal generator alters said refractory period by applying a second electrical signal to said nerve, said second electrical signal being effective to alter said refractory period and unable to stimulate said nerve to evoke an action potential.
  • 16. The implantable neurostimulator of claim 15 wherein said electrical signal generator extends said refractory period of said nerve.
  • 17. The implantable neurostimulator of claim 15 wherein said electrical signal generator extends a relative refractory period of said nerve.
  • 18. The implantable neurostimulator of claim 15 wherein said electrical signal generator shortens said refractory period of said nerve.
  • 19. The implantable neurostimulator of claim 15 wherein said electrical signal generator shortens a relative refractory period of said nerve.
  • 20. The implantable neurostimulator of claim 15 wherein said electrical signal generator applies said second electrical signal during a refractory period of a select nerve fiber type while not applying said second electrical signal during the refractory period of another nerve fiber type.
  • 21. An implantable neurostimulator, comprising: an electrical signal generator; andan electrode coupled to said electrical signal generator and adapted to couple to a nerve to thereby provide therapy to a target nerve fiber;wherein said electrical signal generator applies a first electrical signal to a nerve to evoke an action potential in the target nerve which causes an action potential to be evoked in a non-target nerve fiber or tissue, said non-target nerve fiber or tissue thereby entering a refractory period in which the non-target nerve fiber or tissue is in a refractory state, and during said refractory period after applying said first electrical signal, said electrical signal generator alters said refractory period of said non-target nerve fiber or tissue by applying a second electrical signal to said target nerve, said second electrical signal being effective to alter said refractory period and unable to trigger an action potential in said non-target nerve fiber or tissue.
  • 22. The implantable neurostimulator of claim 21 wherein said first and second electrical signals have opposite polarities to each other and said refractory period is thereby shortened.
  • 23. The implantable neurostimulator of claim 21 wherein said first and second electrical signals have a common polarity to each other and said refractory period is thereby extended.
US Referenced Citations (551)
Number Name Date Kind
3760812 Timm et al. Sep 1973 A
3796221 Hagfors Mar 1974 A
4107469 Jenkins Aug 1978 A
4305402 Katims Dec 1981 A
4338945 Kosugi et al. Jul 1982 A
4424812 Lesnick Jan 1984 A
4431000 Butler et al. Feb 1984 A
4459989 Borkan Jul 1984 A
4503863 Katims Mar 1985 A
4541432 Molina-Negro et al. Sep 1985 A
4573481 Bullara Mar 1986 A
4577316 Schiff Mar 1986 A
4590946 Loeb May 1986 A
4592339 Kuzmak et al. Jun 1986 A
4606349 Livingston et al. Aug 1986 A
4608985 Crish et al. Sep 1986 A
4612934 Borkan Sep 1986 A
4625308 Kim et al. Nov 1986 A
4628942 Sweeney et al. Dec 1986 A
4640286 Thomson Feb 1987 A
4649936 Ungar et al. Mar 1987 A
4702254 Zabara Oct 1987 A
4793353 Borkan Dec 1988 A
4867164 Zabara Sep 1989 A
4920979 Bullara May 1990 A
4949721 Toriu et al. Aug 1990 A
4977895 Tannenbaum Dec 1990 A
5025807 Zabara Jun 1991 A
5081987 Nigam Jan 1992 A
5154172 Terry, Jr. et al. Oct 1992 A
5179950 Stanislaw Jan 1993 A
5186170 Varrichio et al. Feb 1993 A
5188104 Wernicke et al. Feb 1993 A
5205285 Baker, Jr. Apr 1993 A
5215086 Terry, Jr. et al. Jun 1993 A
5222494 Baker, Jr. Jun 1993 A
5231988 Wernicke et al. Aug 1993 A
5235980 Varrichio et al. Aug 1993 A
5263480 Wernicke et al. Nov 1993 A
5269303 Wernicke et al. Dec 1993 A
5299569 Wernicke et al. Apr 1994 A
5330507 Schwartz Jul 1994 A
5330515 Rutecki et al. Jul 1994 A
5334221 Bardy Aug 1994 A
5354320 Schaldach et al. Oct 1994 A
5411531 Hill et al. May 1995 A
5411540 Edell et al. May 1995 A
5423872 Cigaina Jun 1995 A
5507784 Hill et al. Apr 1996 A
5522862 Testerman et al. Jun 1996 A
5522865 Schulman et al. Jun 1996 A
5540730 Terry, Jr. et al. Jul 1996 A
5540734 Zabara Jul 1996 A
5571150 Wernicke et al. Nov 1996 A
5601617 Loeb et al. Feb 1997 A
5611350 John Mar 1997 A
5620468 Mongeon et al. Apr 1997 A
5645570 Corbucci Jul 1997 A
5651378 Matheny et al. Jul 1997 A
5658318 Stroetmann et al. Aug 1997 A
5690681 Geddes et al. Nov 1997 A
5690688 Noren et al. Nov 1997 A
5690691 Chen et al. Nov 1997 A
5700282 Zabara Dec 1997 A
5702428 Tippey et al. Dec 1997 A
5702429 King Dec 1997 A
5707400 Terry, Jr. et al. Jan 1998 A
5755750 Petruska et al. May 1998 A
5792212 Weijand Aug 1998 A
5800474 Benabid et al. Sep 1998 A
5814092 King Sep 1998 A
5836994 Bourgeois Nov 1998 A
5861014 Familoni Jan 1999 A
5871505 Adams et al. Feb 1999 A
5913882 King Jun 1999 A
5916239 Geddes et al. Jun 1999 A
5928272 Adkins et al. Jul 1999 A
5941906 Barreras, Sr. et al. Aug 1999 A
5995868 Osorio et al. Nov 1999 A
6002966 Loeb et al. Dec 1999 A
6016449 Fischell et al. Jan 2000 A
6041258 Cigaina et al. Mar 2000 A
6083249 Familoni Jul 2000 A
6101412 Duhaylongsod Aug 2000 A
6104955 Bourgeois Aug 2000 A
6104956 Naritoku et al. Aug 2000 A
6115628 Stadler et al. Sep 2000 A
6132361 Epstein et al. Oct 2000 A
6141590 Renirie et al. Oct 2000 A
6161044 Silverstone Dec 2000 A
6167311 Rezai Dec 2000 A
6175764 Loeb et al. Jan 2001 B1
6188929 Giordano Feb 2001 B1
6219580 Faltys et al. Apr 2001 B1
6221908 Kilgard et al. Apr 2001 B1
6238423 Bardy May 2001 B1
6249704 Maltan et al. Jun 2001 B1
6253109 Gielen Jun 2001 B1
6266564 Hill et al. Jul 2001 B1
6269270 Boveja Jul 2001 B1
6295472 Rubinstein et al. Sep 2001 B1
6304775 Iasemidis et al. Oct 2001 B1
6308102 Sieracki Oct 2001 B1
6324421 Stadler et al. Nov 2001 B1
6327503 Familoni Dec 2001 B1
6339725 Naritoku et al. Jan 2002 B1
6341236 Osorio et al. Jan 2002 B1
6353762 Baudino et al. Mar 2002 B1
6356788 Boveja Mar 2002 B2
6358203 Bardy Mar 2002 B2
6366813 DiLorenzo Apr 2002 B1
6366814 Boveja Apr 2002 B1
6374140 Rise Apr 2002 B1
6381493 Stadler et al. Apr 2002 B1
6381496 Meadows et al. Apr 2002 B1
6381499 Taylor et al. Apr 2002 B1
6418344 Rezai et al. Jul 2002 B1
6425852 Epstein et al. Jul 2002 B1
6438423 Rezai et al. Aug 2002 B1
6449512 Boveja Sep 2002 B1
6453199 Kobozev Sep 2002 B1
6459936 Fischell et al. Oct 2002 B2
6463328 John Oct 2002 B1
6466822 Pless Oct 2002 B1
6473639 Fischell et al. Oct 2002 B1
6473644 Terry, Jr. et al. Oct 2002 B1
6477417 Levine Nov 2002 B1
6477418 Plicchi et al. Nov 2002 B2
6480743 Kirkpatrick et al. Nov 2002 B1
6484132 Hively et al. Nov 2002 B1
6487446 Hill et al. Nov 2002 B1
6505074 Boveja et al. Jan 2003 B2
6522928 Whitehurst et al. Feb 2003 B2
6532388 Hill et al. Mar 2003 B1
6549804 Osorio et al. Apr 2003 B1
6556868 Naritoku et al. Apr 2003 B2
6564102 Boveja May 2003 B1
6565503 Leysieffer et al. May 2003 B2
6579280 Kovach et al. Jun 2003 B1
6587719 Barrett et al. Jul 2003 B1
6587724 Mann Jul 2003 B2
6587726 Lurie et al. Jul 2003 B2
6587727 Osorio et al. Jul 2003 B2
6591138 Fischell et al. Jul 2003 B1
6594524 Esteller et al. Jul 2003 B2
6600953 Flesler et al. Jul 2003 B2
6609025 Barrett et al. Aug 2003 B2
6609030 Rezai et al. Aug 2003 B1
6609031 Law et al. Aug 2003 B1
6610713 Tracey Aug 2003 B2
6611715 Boveja Aug 2003 B1
6612983 Marchal Sep 2003 B1
6615081 Boveja Sep 2003 B1
6615084 Cigaina Sep 2003 B1
6615085 Boveja Sep 2003 B1
6622038 Barrett et al. Sep 2003 B2
6622041 Terry, Jr. et al. Sep 2003 B2
6622047 Barrett et al. Sep 2003 B2
6628987 Hill et al. Sep 2003 B1
6656960 Puskas Dec 2003 B2
6662053 Borkan Dec 2003 B2
6668191 Boveja Dec 2003 B1
6671547 Lyster et al. Dec 2003 B2
6671555 Gielen et al. Dec 2003 B2
6671556 Osorio et al. Dec 2003 B2
6684104 Gordon et al. Jan 2004 B2
6684105 Cohen et al. Jan 2004 B2
6690973 Hill et al. Feb 2004 B2
6690974 Archer et al. Feb 2004 B2
6701187 Bornzin et al. Mar 2004 B1
6708064 Rezai Mar 2004 B2
6721603 Zabara et al. Apr 2004 B2
6731979 MacDonald May 2004 B2
6731986 Mann May 2004 B2
6754536 Swoyer et al. Jun 2004 B2
6760626 Boveja Jul 2004 B1
6764498 Mische Jul 2004 B2
6768969 Nikitin et al. Jul 2004 B1
6775573 Schuler et al. Aug 2004 B2
6793670 Osorio et al. Sep 2004 B2
6819956 DiLorenzo Nov 2004 B2
6826428 Chen et al. Nov 2004 B1
6832114 Whitehurst et al. Dec 2004 B1
6853862 Marchal et al. Feb 2005 B1
6885888 Rezai Apr 2005 B2
6895278 Gordon May 2005 B1
6904390 Nikitin et al. Jun 2005 B2
6907295 Gross et al. Jun 2005 B2
6920357 Osorio et al. Jul 2005 B2
6934580 Osorio et al. Aug 2005 B1
6944501 Pless Sep 2005 B1
6944503 Crowe et al. Sep 2005 B2
6961618 Osorio et al. Nov 2005 B2
7006859 Osorio et al. Feb 2006 B1
7006872 Gielen et al. Feb 2006 B2
7050856 Stypulkowski May 2006 B2
7054686 MacDonald May 2006 B2
7146217 Firlik et al. Dec 2006 B2
7167750 Knudson et al. Jan 2007 B2
7177678 Osorio et al. Feb 2007 B1
7188053 Nikitin et al. Mar 2007 B2
7204833 Osorio et al. Apr 2007 B1
7209787 DiLorenzo Apr 2007 B2
7231254 DiLorenzo Jun 2007 B2
7236830 Gliner Jun 2007 B2
7236831 Firlik et al. Jun 2007 B2
7242983 Frei et al. Jul 2007 B2
7242984 DiLorenzo Jul 2007 B2
7340302 Falkenberg et al. Mar 2008 B1
20010034541 Lyden Oct 2001 A1
20010037220 Merry et al. Nov 2001 A1
20020052539 Haller et al. May 2002 A1
20020065509 Lebel et al. May 2002 A1
20020072782 Osorio et al. Jun 2002 A1
20020082480 Riff et al. Jun 2002 A1
20020099412 Fischell et al. Jul 2002 A1
20020099417 Naritoku et al. Jul 2002 A1
20020116030 Rezai Aug 2002 A1
20020120310 Linden et al. Aug 2002 A1
20020133204 Hrdlicka Sep 2002 A1
20020143368 Bakels et al. Oct 2002 A1
20020151939 Rezai Oct 2002 A1
20020153901 Davis et al. Oct 2002 A1
20020188214 Misczynski et al. Dec 2002 A1
20030028226 Thompson et al. Feb 2003 A1
20030055457 MacDonald Mar 2003 A1
20030074032 Gliner Apr 2003 A1
20030083716 Nicolelis et al. May 2003 A1
20030083727 Casavant et al. May 2003 A1
20030088274 Gliner et al. May 2003 A1
20030095648 Kaib et al. May 2003 A1
20030097161 Firlik et al. May 2003 A1
20030109903 Berrang et al. Jun 2003 A1
20030125786 Gliner et al. Jul 2003 A1
20030130706 Sheffield et al. Jul 2003 A1
20030144711 Pless et al. Jul 2003 A1
20030144829 Geatz et al. Jul 2003 A1
20030181954 Rezai Sep 2003 A1
20030181958 Dobak Sep 2003 A1
20030181959 Dobak Sep 2003 A1
20030208212 Cigaina Nov 2003 A1
20030210147 Humbard Nov 2003 A1
20030212440 Boveja Nov 2003 A1
20030236558 Whitehurst et al. Dec 2003 A1
20040006278 Webb et al. Jan 2004 A1
20040015205 Whitehurst et al. Jan 2004 A1
20040036377 Mezinis Feb 2004 A1
20040039424 Merritt et al. Feb 2004 A1
20040088024 Firlik et al. May 2004 A1
20040102811 Schwartz et al. May 2004 A1
20040111139 McCreery Jun 2004 A1
20040112894 Varma Jun 2004 A1
20040122484 Hatlestad et al. Jun 2004 A1
20040122485 Stahmann et al. Jun 2004 A1
20040122489 Mazar et al. Jun 2004 A1
20040133119 Osorio et al. Jul 2004 A1
20040138516 Osorio et al. Jul 2004 A1
20040138517 Osorio et al. Jul 2004 A1
20040138518 Rise et al. Jul 2004 A1
20040138647 Osorio et al. Jul 2004 A1
20040138711 Osorio et al. Jul 2004 A1
20040147969 Mann et al. Jul 2004 A1
20040147992 Bluger et al. Jul 2004 A1
20040153129 Pless et al. Aug 2004 A1
20040158119 Osorio et al. Aug 2004 A1
20040158165 Yonce et al. Aug 2004 A1
20040167583 Knudson et al. Aug 2004 A1
20040167587 Thompson Aug 2004 A1
20040172085 Knudson et al. Sep 2004 A1
20040172088 Knudson et al. Sep 2004 A1
20040172089 Whitehurst et al. Sep 2004 A1
20040172091 Rezai Sep 2004 A1
20040172094 Cohen et al. Sep 2004 A1
20040176812 Knudson et al. Sep 2004 A1
20040176831 Gliner et al. Sep 2004 A1
20040193231 David et al. Sep 2004 A1
20040199146 Rogers et al. Oct 2004 A1
20040199187 Loughran Oct 2004 A1
20040199212 Fischell et al. Oct 2004 A1
20040210270 Erickson Oct 2004 A1
20040210274 Bauhahn et al. Oct 2004 A1
20040249302 Donoghue et al. Dec 2004 A1
20040249416 Yun et al. Dec 2004 A1
20040260346 Overall et al. Dec 2004 A1
20040263172 Gray et al. Dec 2004 A1
20050004615 Sanders Jan 2005 A1
20050004621 Boveja et al. Jan 2005 A1
20050010262 Rezai et al. Jan 2005 A1
20050015128 Rezai et al. Jan 2005 A1
20050016657 Bluger Jan 2005 A1
20050020887 Goldberg Jan 2005 A1
20050021092 Yun et al. Jan 2005 A1
20050021103 DiLorenzo Jan 2005 A1
20050021104 DiLorenzo Jan 2005 A1
20050021105 Firlik et al. Jan 2005 A1
20050021106 Firlik et al. Jan 2005 A1
20050021107 Firlik et al. Jan 2005 A1
20050021118 Genau et al. Jan 2005 A1
20050027284 Lozano et al. Feb 2005 A1
20050028026 Shirley et al. Feb 2005 A1
20050033378 Sheffield et al. Feb 2005 A1
20050033379 Lozano et al. Feb 2005 A1
20050038326 Mathur Feb 2005 A1
20050038484 Knudson et al. Feb 2005 A1
20050049515 Misczynski et al. Mar 2005 A1
20050049655 Boveja et al. Mar 2005 A1
20050060007 Goetz Mar 2005 A1
20050060008 Goetz Mar 2005 A1
20050060009 Goetz Mar 2005 A1
20050060010 Goetz Mar 2005 A1
20050065562 Rezai Mar 2005 A1
20050065573 Rezai Mar 2005 A1
20050065574 Rezai Mar 2005 A1
20050065575 Dobak Mar 2005 A1
20050070971 Fowler et al. Mar 2005 A1
20050075679 Gliner et al. Apr 2005 A1
20050075680 Lowry et al. Apr 2005 A1
20050075681 Rezai et al. Apr 2005 A1
20050075691 Phillips et al. Apr 2005 A1
20050075701 Shafer Apr 2005 A1
20050075702 Shafer Apr 2005 A1
20050088145 Loch Apr 2005 A1
20050101873 Misczynski et al. May 2005 A1
20050102002 Salo et al. May 2005 A1
20050107753 Rezai et al. May 2005 A1
20050107842 Rezai May 2005 A1
20050107858 Bulger May 2005 A1
20050113705 Fischell et al. May 2005 A1
20050113744 Donoghue et al. May 2005 A1
20050119703 DiLorenzo Jun 2005 A1
20050124901 Misczynski et al. Jun 2005 A1
20050131467 Boveja et al. Jun 2005 A1
20050131485 Knudson et al. Jun 2005 A1
20050131486 Boveja et al. Jun 2005 A1
20050131493 Boveja et al. Jun 2005 A1
20050131506 Rezai et al. Jun 2005 A1
20050137480 Alt et al. Jun 2005 A1
20050143781 Carbunaru et al. Jun 2005 A1
20050143786 Boveja et al. Jun 2005 A1
20050148893 Misczynski et al. Jul 2005 A1
20050148894 Misczynski et al. Jul 2005 A1
20050148895 Misczynski et al. Jul 2005 A1
20050153885 Yun et al. Jul 2005 A1
20050154425 Boveja et al. Jul 2005 A1
20050154435 Stern et al. Jul 2005 A1
20050159789 Brockway et al. Jul 2005 A1
20050161052 Rezai et al. Jul 2005 A1
20050165458 Boveja et al. Jul 2005 A1
20050177192 Rezai et al. Aug 2005 A1
20050177200 George et al. Aug 2005 A1
20050177206 North et al. Aug 2005 A1
20050182389 LaPorte et al. Aug 2005 A1
20050187590 Boveja et al. Aug 2005 A1
20050187593 Housworth et al. Aug 2005 A1
20050187796 Rosenfeld et al. Aug 2005 A1
20050192644 Boveja et al. Sep 2005 A1
20050197590 Osorio et al. Sep 2005 A1
20050222631 Dalal et al. Oct 2005 A1
20050228693 Webb et al. Oct 2005 A1
20050240246 Lee et al. Oct 2005 A1
20050245944 Rezai Nov 2005 A1
20050245971 Brockway et al. Nov 2005 A1
20050245990 Roberson Nov 2005 A1
20050261542 Riehl Nov 2005 A1
20050267550 Hess et al. Dec 2005 A1
20050272280 Osypka Dec 2005 A1
20050277872 Colby et al. Dec 2005 A1
20050277998 Tracey et al. Dec 2005 A1
20050283200 Rezai et al. Dec 2005 A1
20050283201 Machado et al. Dec 2005 A1
20050283208 Von Arx et al. Dec 2005 A1
20050288600 Zhang et al. Dec 2005 A1
20050288736 Persen et al. Dec 2005 A1
20050288760 Machado et al. Dec 2005 A1
20060009815 Boveja Jan 2006 A1
20060020292 Goetz et al. Jan 2006 A1
20060020491 Mongeon et al. Jan 2006 A1
20060041222 Dewing et al. Feb 2006 A1
20060041223 Dewing et al. Feb 2006 A1
20060041287 Dewing et al. Feb 2006 A1
20060047205 Ludomirsky et al. Mar 2006 A1
20060052843 Elsner et al. Mar 2006 A1
20060058597 Machado et al. Mar 2006 A1
20060064133 Von Arx et al. Mar 2006 A1
20060064134 Mazar et al. Mar 2006 A1
20060064143 Von Arx et al. Mar 2006 A1
20060069322 Zhang et al. Mar 2006 A1
20060074450 Boveja Apr 2006 A1
20060079936 Boveja Apr 2006 A1
20060079942 Deno et al. Apr 2006 A1
20060079945 Libbus Apr 2006 A1
20060085046 Rezai et al. Apr 2006 A1
20060094971 Drew May 2006 A1
20060095081 Zhou et al. May 2006 A1
20060100667 Machado et al. May 2006 A1
20060106430 Fowler et al. May 2006 A1
20060106431 Wyler et al. May 2006 A1
20060111644 Guttag et al. May 2006 A1
20060122525 Shusterman Jun 2006 A1
20060122667 Chavan et al. Jun 2006 A1
20060122864 Gottesman et al. Jun 2006 A1
20060135877 Giftakis et al. Jun 2006 A1
20060135881 Giftakis et al. Jun 2006 A1
20060155495 Osorio et al. Jul 2006 A1
20060161459 Rosenfeld et al. Jul 2006 A9
20060167497 Armstrong et al. Jul 2006 A1
20060173493 Armstrong et al. Aug 2006 A1
20060173522 Osorio Aug 2006 A1
20060190056 Fowler et al. Aug 2006 A1
20060195155 Firlik et al. Aug 2006 A1
20060195163 KenKnight et al. Aug 2006 A1
20060200206 Firlik et al. Sep 2006 A1
20060212091 Lozano et al. Sep 2006 A1
20060217780 Gliner et al. Sep 2006 A1
20060220839 Fifolt et al. Oct 2006 A1
20060224067 Giftakis et al. Oct 2006 A1
20060224191 DiLorenzo Oct 2006 A1
20060241697 Libbus et al. Oct 2006 A1
20060241725 Libbus et al. Oct 2006 A1
20060247698 Burnes et al. Nov 2006 A1
20060253164 Zhang et al. Nov 2006 A1
20060253168 Wyler et al. Nov 2006 A1
20060253169 Wyler et al. Nov 2006 A1
20060253170 Wyler et al. Nov 2006 A1
20060253171 Wyler et al. Nov 2006 A1
20060259095 Wyler et al. Nov 2006 A1
20060264730 Stivoric et al. Nov 2006 A1
20060265018 Smith et al. Nov 2006 A1
20060271409 Rosenfeld et al. Nov 2006 A1
20060293720 DiLorenzo Dec 2006 A1
20070027486 Armstrong et al. Feb 2007 A1
20070032734 Najafi et al. Feb 2007 A1
20070032834 Gliner et al. Feb 2007 A1
20070038262 Kieval et al. Feb 2007 A1
20070043392 Gliner et al. Feb 2007 A1
20070055320 Weinand et al. Mar 2007 A1
20070073150 Gopalsami et al. Mar 2007 A1
20070073346 Corbucci et al. Mar 2007 A1
20070073355 DiLorenzo Mar 2007 A1
20070078491 Siejko et al. Apr 2007 A1
20070088403 Wyler et al. Apr 2007 A1
20070088404 Wyler et al. Apr 2007 A1
20070088405 Jacobson et al. Apr 2007 A1
20070100278 Frei et al. May 2007 A1
20070100397 Seeberger et al. May 2007 A1
20070100398 Sloan May 2007 A1
20070112393 Gliner et al. May 2007 A1
20070123946 Masoud May 2007 A1
20070135855 Foshee et al. Jun 2007 A1
20070142862 DiLorenzo Jun 2007 A1
20070142873 Esteller et al. Jun 2007 A1
20070149952 Bland et al. Jun 2007 A1
20070150011 Meyer et al. Jun 2007 A1
20070150014 Kramer et al. Jun 2007 A1
20070150024 Leyde et al. Jun 2007 A1
20070150025 DiLorenzo et al. Jun 2007 A1
20070156179 Karashurov Jul 2007 A1
20070156450 Roehm et al. Jul 2007 A1
20070156626 Roehm et al. Jul 2007 A1
20070161919 DiLorenzo Jul 2007 A1
20070162086 DiLorenzo Jul 2007 A1
20070167991 DiLorenzo Jul 2007 A1
20070173901 Reeve Jul 2007 A1
20070179534 Firlik et al. Aug 2007 A1
20070179558 Gliner et al. Aug 2007 A1
20070179584 Gliner Aug 2007 A1
20070203548 Pawelzik et al. Aug 2007 A1
20070208212 DiLorenzo Sep 2007 A1
20070208390 Von Arx et al. Sep 2007 A1
20070213785 Osorio et al. Sep 2007 A1
20070233192 Craig Oct 2007 A1
20070238939 Giftakis et al. Oct 2007 A1
20070239210 Libbus et al. Oct 2007 A1
20070239211 Lorincz et al. Oct 2007 A1
20070239220 Greenhut et al. Oct 2007 A1
20070244407 Osorio Oct 2007 A1
20070249953 Frei et al. Oct 2007 A1
20070249954 Virag et al. Oct 2007 A1
20070250130 Ball et al. Oct 2007 A1
20070250145 Kraus et al. Oct 2007 A1
20070255147 Drew et al. Nov 2007 A1
20070255155 Drew et al. Nov 2007 A1
20070255330 Lee et al. Nov 2007 A1
20070255337 Lu Nov 2007 A1
20070260147 Giftakis et al. Nov 2007 A1
20070260289 Giftakis et al. Nov 2007 A1
20070265489 Fowler et al. Nov 2007 A1
20070265508 Sheikhzadeh-Nadjar et al. Nov 2007 A1
20070265536 Giftakis et al. Nov 2007 A1
20070272260 Nikitin et al. Nov 2007 A1
20070282177 Pilz Dec 2007 A1
20070287931 DiLorenzo Dec 2007 A1
20070288072 Pascual-Leone et al. Dec 2007 A1
20070299349 Alt et al. Dec 2007 A1
20070299473 Matos Dec 2007 A1
20070299480 Hill Dec 2007 A1
20080015651 Ettori et al. Jan 2008 A1
20080015652 Maile et al. Jan 2008 A1
20080021332 Brainard, III Jan 2008 A1
20080021341 Harris et al. Jan 2008 A1
20080021517 Dietrich Jan 2008 A1
20080021520 Dietrich Jan 2008 A1
20080027347 Harris et al. Jan 2008 A1
20080027348 Harris et al. Jan 2008 A1
20080027515 Harris et al. Jan 2008 A1
20080033502 Harris et al. Feb 2008 A1
20080033503 Fowler et al. Feb 2008 A1
20080033508 Frei et al. Feb 2008 A1
20080039895 Fowler et al. Feb 2008 A1
20080046035 Fowler et al. Feb 2008 A1
20080046037 Haubrich et al. Feb 2008 A1
20080046038 Hill et al. Feb 2008 A1
20080051852 Dietrich et al. Feb 2008 A1
20080058884 Matos Mar 2008 A1
20080064934 Frei et al. Mar 2008 A1
20080071323 Lowry et al. Mar 2008 A1
20080077028 Schaldach et al. Mar 2008 A1
20080081962 Miller et al. Apr 2008 A1
20080082132 Annest et al. Apr 2008 A1
20080103548 Fowler et al. May 2008 A1
20080114417 Leyde May 2008 A1
20080119900 DiLorenzo May 2008 A1
20080125820 Stahmann et al. May 2008 A1
20080139870 Gliner et al. Jun 2008 A1
20080146890 LeBoeuf et al. Jun 2008 A1
20080146959 Sheffield et al. Jun 2008 A1
20080161712 Leyde Jul 2008 A1
20080161713 Leyde et al. Jul 2008 A1
20080161879 Firlik et al. Jul 2008 A1
20080161880 Firlik et al. Jul 2008 A1
20080161881 Firlik et al. Jul 2008 A1
20080161882 Firlik et al. Jul 2008 A1
20080183096 Snyder et al. Jul 2008 A1
20080183097 Leyde et al. Jul 2008 A1
20080183245 Van Oort et al. Jul 2008 A1
20080195175 Balzer et al. Aug 2008 A1
20080200925 Johnson et al. Aug 2008 A1
20080208013 Zhang et al. Aug 2008 A1
20080208074 Snyder et al. Aug 2008 A1
20080208285 Fowler et al. Aug 2008 A1
20080208291 Leyde et al. Aug 2008 A1
20080208781 Snyder Aug 2008 A1
20080215112 Firlik et al. Sep 2008 A1
20080215114 Stuerzinger et al. Sep 2008 A1
20080221644 Vallapureddy et al. Sep 2008 A1
20080234598 Snyder et al. Sep 2008 A1
20080249591 Gaw et al. Oct 2008 A1
20080255582 Harris Oct 2008 A1
20090054795 Misczynski et al. Feb 2009 A1
20090076567 Fowler et al. Mar 2009 A1
20090318779 Tran Dec 2009 A1
Foreign Referenced Citations (43)
Number Date Country
2339971 Jun 2004 CA
0402683 Dec 1990 EP
0713714 May 1996 EP
1139861 Dec 1999 EP
1070518 Jan 2001 EP
0944411 Apr 2001 EP
1145736 Oct 2001 EP
1483020 Dec 2004 EP
1486232 Dec 2004 EP
1595497 Nov 2005 EP
1120130 Dec 2005 EP
1647300 Apr 2006 EP
1202775 Sep 2006 EP
2026870 Feb 1980 GB
2079610 Jan 1982 GB
9302744 Feb 1993 WO
9417771 Aug 1994 WO
0064336 Nov 2000 WO
0108749 Feb 2001 WO
0064336 Jun 2002 WO
03085546 Oct 2003 WO
2004036377 Apr 2004 WO
2004064918 Aug 2004 WO
2004069330 Aug 2004 WO
2004071575 Aug 2004 WO
2004075982 Sep 2004 WO
2004112894 Dec 2004 WO
2005007120 Jan 2005 WO
2005007232 Jan 2005 WO
2005028026 Mar 2005 WO
2005053788 Jun 2005 WO
2005067599 Jul 2005 WO
2005101282 Oct 2005 WO
2006014760 Feb 2006 WO
2006019822 Feb 2006 WO
2006050144 May 2006 WO
2006122148 Nov 2006 WO
2007066343 Jun 2007 WO
2007072425 Jun 2007 WO
2007124126 Nov 2007 WO
2007124190 Nov 2007 WO
2007124192 Nov 2007 WO
2007142523 Dec 2007 WO
Related Publications (1)
Number Date Country
20080103532 A1 May 2008 US