The invention relates to the field of magnetic stimulation. Specifically, the invention relates to cooling a magnetic stimulation device. In addition, the invention relates to acoustically insulating such a magnetic stimulation device.
Magnetic devices are used in many applications, such as in magnetic stimulation devices, speakers and so forth. Magnetic devices tend to generate heat because of resistive losses in the coil(s) that generate magnetic fields(s), and the amount of heat generated is proportional to the amount of power consumed by the device. Thus, high-voltage magnetic devices that consume large amounts of power, such as those used in magnetic stimulation therapy, can become very hot when in operation. The environment in which the magnetic device operates—or the operating characteristics of the device itself—may dictate that the device operate under a certain temperature threshold. For example, in magnetic stimulation therapy, the temperature of a magnetic stimulation device used to generate a therapeutic magnetic field should be kept below approximately 41.5° C. to stay within certain regulatory requirements (e.g., FDA guidelines). If a magnetic stimulation device is to be operated at temperatures exceeding 41.5° C., such regulatory requirements dictate that the device manufacturer and/or health practitioner must meet additional guidelines to prove that operation of the device is safe. These additional requirements increase complexity of operation and overall cost, and are best avoided when possible.
Conventionally, a magnetic stimulation device used for such therapy is used until it reaches a threshold temperature, and then the therapy is temporarily halted until the stimulation device cools. Such an arrangement therefore adds to the time required to perform a treatment, which is undesirable for both the patient and the health practitioner. Alternatively, a second magnetic stimulation device may need to be used (i.e., swapped with the first device when the first device reaches the threshold temperature) so as to continue the therapy without interruption while the first, overheated stimulation device cools. This arrangement is also undesirable because of the added expense associated with the purchase and maintenance of an additional magnetic stimulation device. Furthermore, additional time is required of the patient and health practitioner, as the second magnetic device will need to be set-up and/or calibrated to perform magnetic stimulation therapy on the patient. Because the set-up and/or calibration steps provide opportunities for operator error, requiring the operator to perform such steps multiple times may decrease the overall safety level of the treatment.
Conventional cooling solutions typically involve the use of air or fluid cooling mechanisms. An air cooling mechanism may involve a fan that rapidly circulates cooled or room temperature air past the magnetic device. A fluid cooling mechanism may involve the circulation of a cool fluid past the magnetic device, where the fluid cools the device and is heated in the process, and then to a cooling mechanism, after which the fluid is returned to the magnetic device. Both mechanisms have several drawbacks. For example, both mechanisms require additional moving parts (e.g., fans, cooling mechanisms such as a refrigeration or heat exchange unit, etc.), which add to the cost and complexity of the magnetic device. Furthermore, the additional moving parts add to the potential for a device malfunction.
An additional consideration of magnetic devices is acoustical noise generated by the magnetic coil of a magnetic device as the coil is energized. For example, when the coil is energized, it creates a strong magnetic field that, in many applications, rapidly changes in intensity. The changing magnetic field causes windings of the coil to experience hoop stresses that intermittently stress the windings, which causes a sharp acoustic click.
Such noise is especially pronounced in magnetic stimulation devices, as the therapeutic magnetic fields are created by pulsing the stimulation device's coil. Such noise is problematic for patients, as the stimulation device is typically located in close proximity to the patient's head, and therefore the noise from the stimulation device may be uncomfortable. In addition, a health practitioner who is repeatedly exposed to such noise may be adversely affected. A conventional solution, placing earplugs in the patient's ears, is undesirable because it is an additional step to perform in the therapeutic process and does not solve the problem of the noise caused by the device in the treatment facility (e.g., physician's office, hospital, etc.). In addition, the use of earplugs is undesirable because some psychiatric or young patients may be uncooperative, and therefore the use of earplugs unnecessarily complicates the procedure.
Thus, a conventional solution for the reduction of acoustical noise is the placement of noise reduction material around all or part of a magnetic device. Alternatively, a chamber containing a partial vacuum may be formed around the magnetic device, because a partial vacuum contains very few particles that may propagate a mechanical (sound) wave. However, such noise reduction techniques have the disadvantage of adversely affecting heat transfer for cooling. For example, the best noise reduction materials are fabricated to contain air pockets that do not transfer noise well. However, such air pockets also have the characteristic being poor conductors of heat. The same is true to an even greater extent in the case of a vacuum. Thus, if such a noise reduction technique is used, the magnetic stimulation device cannot be adequately cooled. Attempting to mitigate such a dilemma by placing acoustical material, or forming a partial vacuum, around a cooling system that is itself arranged around a magnetic device is undesirable because of the added size, cost and complexity of the resulting device.
Conventionally, ferrofluids have been used to cool audio speaker systems, which is a lower voltage application when compared to a magnetic stimulation device or other high voltage magnetic device. A ferrofluid is a fluid with suspended ferromagnetic particles. The ferromagnetic particles can be influenced by the magnetic field created by the speaker so as to enhance fluid convection between the speaker and a heat sink to cool the speaker. An additional benefit of ferrofluids is that they can be used to cool a device while still performing noise reduction, because a ferrofluid typically does not support shear waves. Furthermore, a mismatch in sound velocity may also cause the reflection of some of the sound waves.
Unfortunately, even the ferrofluid solution used in connection with speakers has disadvantages that may render it unsuitable for use with high voltage magnetic devices, such as a magnetic stimulation device. For example, the ferrofluid used in connection with speaker cooling, while a dielectric when exposed to normal speaker-level voltages, may be unable to maintain dielectric isolation at the higher voltage levels used in connection with a magnetic stimulation device. As a result, arcing or other problems may occur.
Therefore, what is needed is a ferrofluidic cooling apparatus, system and method for high voltage applications. More particularly, what is needed is an apparatus, system and method for convectively circulating a ferrofluid to cool a high voltage magnetic device. Even more particularly, what is needed is an apparatus, system and method of using a ferrofluid to cool such a high voltage magnetic device while also mitigating acoustical noise.
In view of the foregoing shortcomings and drawbacks, an apparatus, system and method for cooling a magnetic device using a ferrofluid is described. According to an embodiment, a ferrofluid chamber has a housing that is adapted to be coupled to a component that generates a magnetic field of sufficient strength to stimulate anatomical tissue. In addition, a ferrofluid is disposed within the housing for cooling the component.
The subject matter of the present invention is described with specificity to meet statutory requirements. However, the description itself is not intended to limit the scope of this patent. Rather, the inventors have contemplated that the claimed subject matter might also be embodied in other ways, to include different steps or elements similar to the ones described in this document, in conjunction with other present or future technologies. Moreover, although the term “step” may be used herein to connote different aspects of methods employed, the term should not be interpreted as implying any particular order among or between various steps herein disclosed unless and except when the order of individual steps is explicitly described.
Magnetic Device Overview
As is well known to those skilled in the art, the magnitude of an electric field induced on a conductor is proportional to the rate of change of magnetic flux density across the conductor. When an electric field is induced in a conductor, the electric field creates a corresponding current flow in the conductor. The current flow is in the same direction of the electric field vector at a given point. The peak electric field occurs when the time rate of change of the magnetic flux density is the greatest and diminishes at other times. During a magnetic pulse, the current flows in a direction that tends to preserve the magnetic field (i.e., Lenz's Law).
As may be appreciated, various devices may take advantage of the above principles to induce an electric field, and such devices may be used in a variety of applications. For example, magnetic devices may be used for electrical stimulation of the anatomy, and the like. While the discussion herein focuses on magnetic devices that are used in connection with magnetic stimulation of anatomical tissue, it will be appreciated that such discussion is so limited solely for purposes of explanation and clarity. Thus, it will be understood that an embodiment is equally applicable to any application of a magnetic device in any field of endeavor. Thus, the present discussion of magnetic devices should not be construed as limiting embodiments of the invention to medical or other applications.
Therefore, and turning now to the context of electrical stimulation of the anatomy, certain parts of the anatomy (e.g., nerves, tissue, muscle, brain) act as a conductor and carry electric current when an electric field is applied. The electric field may be applied to these parts of the anatomy transcutaneously by applying a time varying (e.g., pulsed) magnetic field to the portion of the body. For example, in the context of TMS, a time-varying magnetic field may be applied across the skull to create an electric field in the brain tissue, which produces a current. If the induced current is of sufficient density, neuron action potential may be reduced to the extent that the membrane sodium channels open and an action potential response is created. An impulse of current is then propagated along the axon membrane that transmits information to other neurons via modulation of neurotransmitters. Such magnetic stimulation has been shown to acutely affect glucose metabolism and local blood flow in cortical tissue. In the case of major depressive disorder, neurotransmitter dysregulation and abnormal glucose metabolism in the prefrontal cortex and the connected limbic structures may be a likely pathophysiology. Repeated application of magnetic stimulation to the prefrontal cortex may produce chronic changes in neurotransmitter concentrations and metabolism so that depression is alleviated.
In a similar fashion, non-cortical neurons (e.g., cranial nerves, peripheral nerves, sensory nerves) may also be stimulated by an induced electric field. Techniques have been developed to intentionally stimulate peripheral nerves to diagnose neuropathologies by observing response times and conduction velocities in response to a pulsed magnetic field induced stimulus. Discomfort and/or pain may result if the induced electric field applied to a peripheral or cranial nerve is very intense or focused on a small area of such a nerve. This discomfort may be diminished by intentionally over-stimulating the sensory nerves in the affected nerve bundle so that they can no longer respond to external pain stimuli, or by reducing the intensity and focus of the induced electric field that is causing the pain sensation.
As noted above, it should be appreciated that transcutaneous magnetic stimulation is not limited to treatment of depression. In addition to depression, the transcutaneous magnetic stimulation methods and apparatus of the invention may be used to treat a patient such as a human suffering from epilepsy, schizophrenia, Parkinson's disease, Tourette's syndrome, amyotrophic lateral sclerosis (ALS), multiple sclerosis (MS), Alzheimer's disease, attention deficit/hyperactivity disorder, obesity, bipolar disorder/mania, anxiety disorders (e.g., panic disorder with and without agoraphobia, social phobia also known as social anxiety disorder, acute stress disorder and generalized anxiety disorder), post-traumatic stress disorder (one of the anxiety disorders in DSM), obsessive compulsive disorder (also one of the anxiety disorders in DSM), pain (such as, for example, migraine and trigeminal neuralgia, as well as chronic pain disorders, including neuropathic pain, e.g., pain due to diabetic neuropathy, post-herpetic neuralgia, and idiopathic pain disorders, e.g., fibromyalgia, regional myofascial pain syndromes), rehabilitation following stroke (neuro plasticity induction), tinnitus, stimulation of implanted neurons to facilitate integration, substance-related disorders (e.g., dependence, abuse and withdrawal diagnoses for alcohol, cocaine, amphetamine, caffeine, nicotine, cannabis and the like), spinal cord injury and regeneration/rehabilitation, stroke, head injury, sleep deprivation reversal, primary sleep disorders (primary insomnia, primary hypersomnia, circadian rhythm sleep disorder), cognitive enhancements, dementias, premenstrual dysphoric disorder (PMS), drug delivery systems (changing the cell membrane permeability to a drug), induction of protein synthesis (induction of transcription and translation), stuttering, aphasia, dysphagia, essential tremor, and/or eating disorders (such as bulimia, anorexia and binge eating).
Example Magnetic Stimulation Device
A ferromagnetic core may be used in connection with a magnetic device to produce a magnetic field. In some embodiments, such a magnetic field may be for purposes of carrying out transcutaneous magnetic stimulation such as, for example, Transcranial Magnetic Stimulation (TMS), Repetitive TMS (rTMS), Magnetic Seizure Therapy (MST), reduction of peripheral nerve discomfort and so forth. Again, although some of the examples that follow may be discussed in connection with TMS and rTMS embodiments for the purposes of explanation and clarity, any type of transcutaneous magnetic stimulation, including all of those listed above, may be performed according to an embodiment of the invention. In addition, and as noted above, embodiments of the invention are not limited to transcutaneous magnetic stimulation, as an embodiment may be used in connection with magnetic devices that generate a magnetic field for any purpose.
Furthermore, embodiments of the invention are not limited to the use of ferromagnetic core magnetic stimulation devices, as other core materials may be used such as, for example, air. The discussion herein therefore describes a ferromagnetic core magnetic stimulation device solely for purposes of explanation and clarity. In an embodiment, a ferromagnetic core may be approximately hemispherical, and in another embodiment the ferromagnetic core may include a highly saturable magnetic material having a magnetic saturation of at least 0.5 Tesla. In some embodiments, a ferromagnetic core may be shaped to optimize the magnetic field distribution in the treatment area. Treatment areas for other forms of treatment (e.g., reduction of discomfort in peripheral nerves, etc.) may be more or less deep than is the case for TMS.
Ferromagnetic core 12 can be fabricated from various ferromagnetic materials such as, for example, 3% grain oriented silicon steel or vanadium permendur (also known as supermendur). The material is chosen to have, for example, a high saturation level, a sharp-knee B-H curve (i.e., quickly switches from saturated to non-saturated states), low eddy current losses, and a practical cost. The core material may be fabricated into many electrically isolated layers to minimize eddy current losses. The orientation of the lamination may be such as to disrupt the eddy currents (i.e., perpendicular to the direction of induced current flow whenever possible). Also, if the material has a grain orientation, it may be directed parallel to the induced magnetic flux. In one embodiment, the ferromagnetic core is according to U.S. Pat. Nos. 6,132,361 and 5,725,471, each of which is hereby incorporated by reference in their entireties.
In one embodiment, patient treatment typically includes applying a magnetic field to the patient using a coil constructed with an approximately hemispherical ferromagnetic core. The strength of the field and switching rate is sufficient to produce stimulation of the target area in a manner that is appropriate to the type of treatment being administered. As noted above, the generation of a magnetic field having the approximate strength for therapeutic treatment or other purposes also generates heat and noise. Therefore, an embodiment that provides an apparatus, system and method for mitigating such heat and/or noise using a ferrofluid is discussed below.
Ferrofluidic Convection and Cooling
Generally, a ferrofluid is a suspension of small magnetic particles that may be, for example, approximately 10 nm in size. Such a small particle size may be selected to assure that settling of the particles does not occur during a time period that is appropriate for an application in which the ferrofluid is used. In addition, one or more surfactants may be used to ensure continued suspension of the magnetic particles in the fluid, which may be, for example, oil, water, etc. Each particle may have a permanent magnetic moment, and may be comprised from magnetic materials such as, for example, iron oxide compounds or the like. In the absence of an external magnetic field, the magnetic moments of the individual particles within the ferrofluid are not aligned with each other. When a magnetic field is applied, the magnetic moments align with the applied magnetic field. This alignment often is called “superparamagnetic” as the fluid behaves as a paramagnet with magnetic moments that are the size of the individual magnetic particles.
It will be appreciated that an increase in temperature of a ferrofluid decreases its magnetization in an applied field. For example, at higher temperatures, the saturation moment of a ferrofluid, as well as its initial susceptibility, are reduced. The relationship between the magnetization of a ferrofluid and an applied magnetic field is called the Langevin function, which is known to those of skill in the art.
Natural convection is a phenomenon caused by the change in volume of liquid with temperature. Hot fluids are less dense, and therefore a fluid exposed to a heat source will expand and rise. Cool fluid distant from a heat source will move to replace the hot fluid. In this way, heat is mechanically transported away from a heat source.
In the case of ferrofluid convection, a ferrofluid is placed in a magnetic field gradient where the magnetic field is greatest. As noted above, a cool ferrofluid has a higher magnetic susceptibility than a hot ferrofluid and therefore is preferentially drawn to the areas of greatest magnetic field. In an embodiment, the area of the cool ferrofluid greatest magnetic field may be proximate a magnetic device (e.g., a magnetic stimulation device, or the like) when such a magnetic device is in operation. Therefore, ferrofluid that is proximate the magnetic device may be heated, which reduces the ferrofluid's magnetic susceptibility and also causes the ferrofluid to expand in volume. As a result, cool ferrofluid (e.g., ferrofluid that is further away from the magnetic device), which has a higher magnetic susceptibility and is more dense, is drawn to the magnetic device. Thus, it will be appreciated that magnetic and thermal convection of the ferrofluid may be established by the increasing and decreasing of the magnetic susceptibility and volume of the ferrofluid. Details relating to the fabrication of ferrofluid-filled chambers is assumed to be known to those of skill in the art, and such details are therefore omitted herein for clarity.
In addition, ferrofluids may be used to reduce unwanted noise in solenoids and other devices. This is because a ferrofluid is not a good supporter of transverse sound waves. Also, an interface between a ferrofluid and an adjacent object (e.g., a magnetic device or the like) may reduce noise produced by the magnetic device. This is because of the difference of sound velocities at such an interface, as is known to one of skill in the art. Furthermore, the ferrofluid may provide vibrational damping. Thus, it will be appreciated that a ferrofluid that is being used to cool a magnetic device may also reduce noise produced by such a magnetic device. It will be further appreciated that a ferrofluid that is being used to cool a magnetic device may, for example, be used in connection with other methods of sound absorption. For example, sound absorbing material may be used to augment the sound-reducing abilities of the ferrofluid.
An embodiment provides a chamber containing a ferrofluid. The ferrofluid within the chamber may be used to cool a magnetic device substantially around which the chamber may be disposed. For example, a magnetic field created by the magnetic device may induce magnetic convection of the ferrofluid as discussed above. In addition, the heat generated by the magnetic device may induce thermal convection.
In one embodiment, a heat exchanger may be coupled to the chamber to cool the ferrofuid, thereby further enabling cooling of the magnetic device as the ferrofluid circulates between the device, where the ferrofluid is heated, and the heat exchanger, where the ferrofluid is cooled. Sound reduction may also be affected by the ferrofluid, as in one embodiment the chamber may be disposed around the magnetic stimulation device to substantially enclose a sound-producing region of the device. In an embodiment, properties of the ferrofluid may be selected so as to enhance its magnetic, thermal and/or sound-mitigating properties.
While an embodiment discussed herein relates to Magnetic Seizure Therapy (MST) and Transcranial Magnetic Stimulation (TMS) for purposes of explanation and clarity, it will be appreciated that an embodiment may be employed in connection with any type of high-voltage magnetic device that is used for any purpose.
Turning now to
At step 203, a ferrofluid is circulated. It will be appreciated that a ferrofluid may be contained within a chamber, as will be discussed below in connection with
At step 205, the ferrofluid is heated. Such heating may take place, for example, proximate magnetic device 10. Such heating may occur due to the heating of such device 10 while device 10 is in operation, as was discussed above. At step 207, the ferrofluid is cooled. Such cooling may take place due to, for example, heat loss facilitated by a heat exchanger such as a heat sink, refrigeration unit or the like. Alternatively, such cooling may take place without the assistance of a heat exchanger. It will be appreciated that the heating of step 205 and the cooling of step 207 may facilitate thermal convection of the ferrofluid, as was discussed above. Such thermal convection may, in an embodiment, assist the magnetic convection of the ferrofluid discussed above in connection with step 203.
As can be seen in
It can be seen in
Convection (i.e., magnetic and/or thermal convection) of ferrofluid 30 is enabled as discussed above, and is represented by direction arrow A. Thus, it can be appreciated that, in an embodiment, ferrofluid 30 that is proximate device 10 while device 10 is in operation and therefore generating heat is also heated. In addition, ferrofluid 30 may be attracted to device 10 because of a magnetic field generated by device 10 (not shown in
It should be appreciated that the example configuration depicted in
In
Turning now to
In addition, one-way valves 60A-B may be present to facilitate enhanced circulation of ferrofluid 30. For example, magnetic material 62 may cause ferrofluid 30 to flow in the direction indicated by arrow D when attracted to winding 54, but may case ferrofluid 30 to flow in an opposite direction when repelled from winding 54. Thus, one or more one-way valves 60A-B may be operatively coupled to chamber 36 to ensure that ferrofluid 30 only flows in the direction indicated by arrow D. It should be appreciated that any technique may be used to ensure such directional flow of ferrofluid 30, if any is used at all, and any such apparatus is equally consistent with an embodiment.
Therefore, it will be appreciated that magnetic material 62 acts as a pumping mechanism for driving the circulation of ferrofluid 30. Alternate embodiments may use other such pumping mechanisms, and such embodiments are in no way limited to the use of magnetic material 62, which is presented herein merely as an illustrative example. For example, a fluid pump may be operatively coupled to chamber 36 to circulate ferrofluid 30, and such a configuration would remain consistent with an embodiment. In addition, such a fluid pump (or a second fluid pump) may also circulate an additional, non-ferrofluid for additional cooling or other purposes. Thus, any type of pumping mechanism may be employed to circulate ferrofluid 30, and any such pumping mechanism may operate to augment or replace the aforementioned magnetic and/or thermal convection of ferrofluid 30.
It is to be understood that the foregoing illustrative embodiments have been provided merely for the purpose of explanation and are in no way to be construed as limiting of the invention. Words used herein are words of description and illustration, rather than words of limitation. In addition, the advantages and objectives described herein may not be realized by each and every embodiment practicing the present invention. Further, although the invention has been described herein with reference to particular structure, materials and/or embodiments, the invention is not intended to be limited to the particulars disclosed herein. Rather, the invention extends to all functionally equivalent structures, methods and uses, such as are within the scope of the appended claims. Those skilled in the art, having the benefit of the teachings of this specification, may affect numerous modifications thereto and changes may be made without departing from the scope and spirit of the invention.
This application is a divisional of application Ser. No. 11/130,657, filed May 17, 2005, the entirety of which is incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
2651258 | Pierce | Sep 1953 | A |
3658051 | MacLean | Apr 1972 | A |
3683923 | Anderson | Aug 1972 | A |
4078392 | Kestner | Mar 1978 | A |
4473074 | Vassiliadis | Sep 1984 | A |
4601753 | Soileau et al. | Jul 1986 | A |
4638798 | Shelden et al. | Jan 1987 | A |
4712558 | Kidd et al. | Dec 1987 | A |
4808079 | Crowley et al. | Feb 1989 | A |
4940453 | Cadwell | Jul 1990 | A |
4994015 | Cadwell | Feb 1991 | A |
4995395 | Ilmoniemi et al. | Feb 1991 | A |
5047005 | Cadwell | Sep 1991 | A |
5061234 | Chaney | Oct 1991 | A |
5066272 | Eaton et al. | Nov 1991 | A |
5078674 | Cadwell | Jan 1992 | A |
5097833 | Campos | Mar 1992 | A |
5116304 | Cadwell | May 1992 | A |
5254123 | Bushey | Oct 1993 | A |
5299569 | Wernicke et al. | Apr 1994 | A |
5462685 | Raj et al. | Oct 1995 | A |
5655534 | Ilmoniemi | Aug 1997 | A |
5707334 | Young | Jan 1998 | A |
5725471 | Davey et al. | Mar 1998 | A |
5766124 | Polson | Jun 1998 | A |
5769778 | Abrams et al. | Jun 1998 | A |
5812301 | Nakamura | Sep 1998 | A |
5813970 | Abrams et al. | Sep 1998 | A |
5820623 | Ng | Oct 1998 | A |
5871517 | Abrams et al. | Feb 1999 | A |
6057373 | Fogel | May 2000 | A |
6066084 | Edrich et al. | May 2000 | A |
6074385 | Klopotek | Jun 2000 | A |
6086525 | Davey et al. | Jul 2000 | A |
6117066 | Abrams et al. | Sep 2000 | A |
6155966 | Parker | Dec 2000 | A |
6169963 | Markov | Jan 2001 | B1 |
6179769 | Ishikawa et al. | Jan 2001 | B1 |
6179770 | Mould | Jan 2001 | B1 |
6179771 | Mueller | Jan 2001 | B1 |
6198958 | Ives et al. | Mar 2001 | B1 |
6210317 | Bonlie | Apr 2001 | B1 |
6253109 | Gielen | Jun 2001 | B1 |
6256531 | Ilmoniemi et al. | Jul 2001 | B1 |
6266556 | Ives et al. | Jul 2001 | B1 |
6279579 | Riaziat et al. | Aug 2001 | B1 |
6366814 | Boveja et al. | Apr 2002 | B1 |
6389318 | Zarinetchi et al. | May 2002 | B1 |
6402678 | Fischell et al. | Jun 2002 | B1 |
6425852 | Epstein et al. | Jul 2002 | B1 |
6434410 | Cordero et al. | Aug 2002 | B1 |
6463328 | John | Oct 2002 | B1 |
6480743 | Kirkpatrick et al. | Nov 2002 | B1 |
6484059 | Gielen | Nov 2002 | B2 |
6488617 | Katz | Dec 2002 | B1 |
6497648 | Rey | Dec 2002 | B1 |
6503187 | Ilmoniemi et al. | Jan 2003 | B1 |
6516288 | Bagne | Feb 2003 | B2 |
6537197 | Ruohonen et al. | Mar 2003 | B1 |
6551233 | Perreault et al. | Apr 2003 | B2 |
6560490 | Grill et al. | May 2003 | B2 |
6567702 | Nekhendzy et al. | May 2003 | B1 |
6571123 | Ives et al. | May 2003 | B2 |
6572528 | Rohan et al. | Jun 2003 | B2 |
6591138 | Fischell et al. | Jul 2003 | B1 |
6629935 | Miller et al. | Oct 2003 | B1 |
6641520 | Bailey et al. | Nov 2003 | B2 |
6663556 | Barker | Dec 2003 | B2 |
6671555 | Gielen et al. | Dec 2003 | B2 |
6827681 | Tanner et al. | Dec 2004 | B2 |
6849040 | Ruohonen et al. | Feb 2005 | B2 |
6927510 | Beitelman et al. | Aug 2005 | B1 |
6978179 | Flagg et al. | Dec 2005 | B1 |
6982501 | Kotha et al. | Jan 2006 | B1 |
7367936 | Myers et al. | May 2008 | B2 |
7396326 | Ghiron et al. | Jul 2008 | B2 |
7745962 | Morgenstein | Jun 2010 | B2 |
20010031906 | Ishikawa et al. | Oct 2001 | A1 |
20020013612 | Whitehurst | Jan 2002 | A1 |
20020087201 | Firlik et al. | Jul 2002 | A1 |
20020091419 | Firlik et al. | Jul 2002 | A1 |
20020103515 | Davey et al. | Aug 2002 | A1 |
20020123780 | Grill et al. | Sep 2002 | A1 |
20020160436 | Markov et al. | Oct 2002 | A1 |
20020169355 | Rohan et al. | Nov 2002 | A1 |
20030004392 | Tanner et al. | Jan 2003 | A1 |
20030023159 | Tanner | Jan 2003 | A1 |
20030028072 | Fischell et al. | Feb 2003 | A1 |
20030050527 | Fox et al. | Mar 2003 | A1 |
20030073899 | Ruohonen et al. | Apr 2003 | A1 |
20030074032 | Gliner et al. | Apr 2003 | A1 |
20030082507 | Stypulkowski | May 2003 | A1 |
20030087264 | Kaplitt et al. | May 2003 | A1 |
20030088274 | Gliner et al. | May 2003 | A1 |
20030097161 | Firlik et al. | May 2003 | A1 |
20030125786 | Gliner et al. | Jul 2003 | A1 |
20030130706 | Sheffield et al. | Jul 2003 | A1 |
20030195588 | Fischell et al. | Oct 2003 | A1 |
20030204135 | Bystritsky | Oct 2003 | A1 |
20040010177 | Rohan et al. | Jan 2004 | A1 |
20040019370 | Gliner et al. | Jan 2004 | A1 |
20040051279 | Grant et al. | Mar 2004 | A1 |
20040077921 | Becker et al. | Apr 2004 | A1 |
20040077923 | Frimerman et al. | Apr 2004 | A1 |
20040127942 | Yomtov et al. | Jul 2004 | A1 |
20040138524 | Ueda et al. | Jul 2004 | A1 |
20040138550 | Hartlep et al. | Jul 2004 | A1 |
20040138578 | Pineda et al. | Jul 2004 | A1 |
20040143300 | Rogers | Jul 2004 | A1 |
20040153129 | Pless et al. | Aug 2004 | A1 |
20040172012 | Otsuka et al. | Sep 2004 | A1 |
20040193001 | Miller | Sep 2004 | A1 |
20040204625 | Riehl et al. | Oct 2004 | A1 |
20050021104 | DiLorenzo | Jan 2005 | A1 |
20050124848 | Holzner | Jun 2005 | A1 |
20050216071 | Devlin et al. | Sep 2005 | A1 |
20050228209 | Schneider et al. | Oct 2005 | A1 |
20050256539 | George et al. | Nov 2005 | A1 |
20060110260 | Hsu | May 2006 | A1 |
Number | Date | Country |
---|---|---|
0998958 | Dec 2000 | EP |
1 273 320 | Jan 2003 | EP |
1996-52231 | Feb 1996 | JP |
2001-509635 | Jul 2001 | JP |
2006-516480 | Jul 2006 | JP |
WO 96016692 | Jun 1996 | WO |
WO 9902467 | Jan 1999 | WO |
WO 9955421 | Nov 1999 | WO |
WO 9964884 | Dec 1999 | WO |
WO 99064884 | Dec 1999 | WO |
WO 0074777 | Dec 2000 | WO |
WO 0112236 | Feb 2001 | WO |
WO 0128622 | Apr 2001 | WO |
WO 0197906 | Dec 2001 | WO |
WO 0209811 | Feb 2002 | WO |
WO 0231604 | Apr 2002 | WO |
WO 0232504 | Apr 2002 | WO |
WO 02072194 | Sep 2002 | WO |
WO 02085449 | Oct 2002 | WO |
WO 02085454 | Oct 2002 | WO |
WO 02089902 | Nov 2002 | WO |
WO 02094997 | Nov 2002 | WO |
WO 03035163 | May 2003 | WO |
WO 03039468 | May 2003 | WO |
WO 03082405 | Oct 2003 | WO |
WO 03084605 | Oct 2003 | WO |
WO 03085546 | Oct 2003 | WO |
WO 03090604 | Nov 2003 | WO |
WO 03098268 | Nov 2003 | WO |
WO 2004006750 | Jan 2004 | WO |
WO 2004018128 | Mar 2004 | WO |
WO 2004082759 | Sep 2004 | WO |
WO 2004100765 | Nov 2004 | WO |
WO 2005000401 | Jan 2005 | WO |
WO 2005065768 | Jul 2005 | WO |
Entry |
---|
Baudewig, J. et al., “Functional MRI of Cortical Activations Induced by Transcranial Magnetic Stimulation(TMS)”, Brain Imaging-NeuroReport, 2001, 12(16), 3543-3548. |
Bohning, D.E. et al., “A TMS Coil Positioning/Holding System for MR Image-Guided TMS Interleaved with fMRI”, Clinical Neurophysiology, 2003, 114, 2210-2219. |
Bohning, D.E. Ph.D. et al., “A Combined TMS/fMRI Study of Intensity-Dependant TMS over Motor Cortex”, Society of Biological Psychiatry, 1999, 45, 385-394. |
Bohning, D.E. Ph.D. et al., “BOLD-fMRI Response to Single-Pulse Transcranial Magnetic Stimulation (TMS)”, Journal of Magnetic Resonance Imaging, 2000, 11, 569-574. |
Garcia-Toro, M. et al., “Modest Adjunctive Benefit with Transcranial Magnetic Stimulation in Medication-Resistant Depression”, Journal of Affective Disorders, 2001, 64, 271-275. |
George, M.S. et al., “A Controlled Trial of Daily Left Prefrontal Cortex TMS for Treating Depression”, Society of Biological Psychiatry, 2000, 48, 962-970. |
George, M.S. “New Methods of Minimally Invasive Brain Modulation as Therapies in Psychiatry: TMS,MST,VNS and DBS”, Chinese Medical Journal (Taipei), 2002, 65, 349-360. |
Grafman, J. Ph.D., “TMS as a Primary Brain Mapping Tool” Transcranial Magnetic Stimulation in Neuropsychiatry, 2000, 115-140. |
Nahas, Z.et al., “Left Prefrontal Transcranial Magnetic Stimulation(TMS) Treatment of Depression in Bipolar Affective Disorder: A Pilot Study of Acute Safety and Efficacy”, Bipolar Disorders, 2003, 5, 40-47. |
Lisanby, S.H. MD. et al., “Magnetic Seizure Therapy of Major Depression”, Arch Gen Psychiatry, 2001, 58, 303-307. |
Lisanby, S.H. et al., “Sham TMS: Intracerebral Measurement of the Induced Electrical Field and the Induction of Motor-Evoked Potentials”, Society of Biological Psychiatry, 2001, 49, 460-463. |
Lisanby, S.H., “Safety and Feasibility of Magnetic Seizure Therapy(MST) in Major Depression: Randomized Within-Subject Comparasion with Electroconvulsive Therapy”, Neuropsychopharmacology, New York State Psychiatric Institute, 2003, 28, 1852-1865. |
Lisanby, S.H., “Update on Magnetic Seizure Therapy: A Novel Form of Convulsive Therapy”, The Journal of ECT, 2002, 18, 182-188. |
Lorberbaum, J.P., M.D. et al., “Safety Concerns of TMS”, Transcranial Magnetic Stimulation in Neuropsychiatry, 2000, 141-161. |
Loo, C.K. et al., “Transcranial Magnetic Stimulation (TMS) in Controlled Treatment Studies: Are Some “Sham” Forms Active?”, Society of Biological Psychiatry, 2000, 47, 325-331. |
Nahas, Z. et al., “Unilateral Left Prefrontal Transcranial Magnetic Stimulation(TMS) Produces Intensity-Dependent Bilateral Effects as Measured by Interleaved BOLD fMRI”, Society of Biological Psychiatry, 2001, 50, 712-720. |
Pridmore, S., “Rapid Transcranial Magnetic Stimulation and Normalization of the Dexamethasone Suppression Test”, Psychiatry and Clinical Neurosciences, 1999, 53, 33-37. |
Roth, Y. et al., “A Coil Design for Transcranial Magnetic Stimulation of Deep Brain Regions”, Journal of Clinical Neurophysiology, 2002, 19(4), 361-370. |
Ruohonen, J., “Electroencephalography Combined with TMS”, BioMag Laboratory, Helsinki University Central Hospital, http://www.biomag.helsinki.fi/tms/TMSEEG.html, Oct. 6, 1999, 22 pages. |
Terrace, H.S. et al., “The Cognitive Effects of Electroconvulsive Shock and Magnetic Seizure Therapy in Rhesus Monkeys”, Society for Neuroscience Abstract Viewer and Itinerary Planner, 2002, Abstract Only # 184.14. |
Terrace, H.S. et al., “The Cognitive Effects of Electroconvulsive Shock Stimulation and Magnetic Seizure Therapy in Rhesus Monkeys”, Society for Neuroscience Abstracts, 2001, 27(1), 536.7, p. 1418. |
Trivedi, M.H., MD., “Treatment-Resistant Depression: New Therapies on the Horizon”, Annals of Clinical Psychiatry, 2003, 15(1), 59-70. |
Hess, C.W. et al., “Magnetic Stimulation of the Human Brain: Influence of Size and Shape of the Stimulating Coil”, Motor Disturbances II, 1990, 3, 31-42. |
Wassermann, E.M., “Repetitive Transcranial Magnetic Stimulation: An Introduction and Overview”, CNS Spectrums, The International Journal of Neuropsychiatric Medicine, Jan. 1997, 7 pages. |
Awiszus, F. et al., “Characterization of Paired-Pulse Transcranial Magnetic Stimulation Conditions Yielding Intracortical Inhibition of I-Wave Facilitation using a Threshold Paradigm”, Experimental Brain Research, 1999, 129, 317-324. |
Keiji, I. et al., “Effects of Transcranial Magnetic Stimulation on EEG Activity”, IEEE transactions on Magnetics, 2002, 38(5), 3347-3349, XP 011075410. |
Pascual-Leone, A. et al., “Rapid-Rate Transcranial Magnetic Stimulation of Left Dorsolateral Prefrontal Cortex in Drug-Resistant Depression”, The Lancet, 1996, 18, 233-237. |
Sommer, M. et al., “Increased Transcranial Magnetic Motor Threshold after ECT”, European Archives of Psychiatry and Clinical Neuroscience, 2002, 252, 250-252. |
Pridmore, S., “Substituition of Rapid Transcranial Magnetic Stimulation Treatments for Electroconvulsive Therapy Treatments in a Course of Electroconvulsive Therapy”, Depression and Anxiety, 2000, 12, 118-123. cited by other. |
Number | Date | Country | |
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20080224808 A1 | Sep 2008 | US |
Number | Date | Country | |
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Parent | 11130657 | May 2005 | US |
Child | 12127226 | US |