The invention relates generally to medical devices and procedures, and more particularly to apparatuses and methods for positioning electrodes on the body.
Surface electrodes can be used in a variety of medical procedures, such as, for example, electromyography (EMG) and neuromuscular electrical stimulation (NMES) therapy. For example, some known therapeutic devices include one or more surface electrodes that provide electrical stimulation to portions of a patient's leg to improve the patient's gait mechanics. Such “gait training” therapy can be used, for example, to cause dorsiflexion of the ankle in patients who have lost the ability to dorsiflex following neurological injury.
Known electrodes must be accurately and repeatably positioned on the patient's body to ensure that the electrical signals are delivered to and/or received from the appropriate portions of the body. For example, some known gait training therapeutic devices include a first electrode to be positioned on the patient's leg above the deep peroneal nerve and a second electrode to be positioned on the patient's leg above the superficial peroneal nerve. In some instances, failure to accurately position the electrodes can result in an exaggerated inversion or eversion of the foot.
Some known therapeutic devices include electrodes that can be surgically implanted to maintain their position throughout the patient's rehabilitation. When using such devices, however, the patient is potentially subjected to the risks associated with the surgical procedure to implant the electrodes. Moreover, such electrodes cannot be easily removed between rehabilitation procedures.
Some known therapeutic devices include electrodes that are positioned on an orthosis and/or a garment. During therapy, the patient wears the orthosis or garment to ensure that the electrodes are maintained in their desired position. The positioning of electrodes using an orthosis and/or garment, however can result in a bulky device being attached to the area of the patient's body undergoing therapy. The use of an orthosis and/or garment during therapy may apply pressure to the skin and may prevent ventilation of parts of the skin, potentially also causing skin irritation. Moreover, in some circumstances the electrodes may not be accurately positioned (i.e., when the garment stretches, thereby distorting the relative positions of the electrodes).
Some known therapeutic devices include electrodes that are individually attached on the patient's body by skin adhesion. The placement of such electrodes can be guided by landmarks on the skin. Accordingly, the individual placement of electrodes can be inaccurate and/or not repeatable between therapeutic sessions.
Thus, a need exists for improved apparatuses and methods for placing electrodes on the body.
Apparatuses and methods for placing electrodes on the body are described herein. In some embodiments, an apparatus includes a fitting device and an actuator movably coupled to the fitting device. The fitting device is configured to be disposed about a portion of a body. An inner surface of the fitting device has an attachment portion configured to removably couple an electrode to the inner surface of the fitting device. The actuator is configured to decouple the electrode from the attachment portion of the fitting device when the fitting device is disposed about the portion of the body.
In some embodiments, an apparatus includes a fitting device and an actuator movably coupled to the fitting device. The fitting device, which can include a flexible garment portion, is configured to be disposed about a portion of a body. An inner surface of the fitting device has an attachment portion configured to removably couple an electrode to the inner surface of the fitting device. The attachment portion can include, for example, an adhesive, a hook and loop fastener, a snap fastener and/or a magnetic fastener. The actuator is configured to decouple the electrode from the attachment portion of the fitting device when the fitting device is disposed about the portion of the body.
In some embodiments, an apparatus includes a fitting device configured to be disposed about a first portion of a body, such as, for example, the leg. The fitting device has an indexing portion and an electrode attachment portion. The indexing portion is configured to receive a second portion of the body, such as, for example, the kneecap, to position the fitting device about the first portion of the body at a predetermined location. The electrode attachment portion is configured to removably couple an electrode to an inner surface of the fitting device such that the electrode is disposed at a predetermined location relative to the second portion of the body when the fitting device is disposed about the first portion of the body.
In some embodiments, an apparatus includes a fitting device and an actuator coupled to the fitting device. The fitting device is configured to be disposed about a portion of a body. A distal end portion of the actuator includes a connector configured to removably couple an electrode to the distal end portion of the actuator. The actuator is configured to move the electrode into contact with the portion of the body when the fitting device is disposed about the portion of the body.
In some embodiments, an apparatus includes a sleeve, an electrode and a fitting device. The sleeve has an inner surface and an outer surface, and is configured to be disposed about a first portion of a body. The electrode is coupled to the inner surface of the sleeve. The fitting device has an indexing portion and an attachment portion. The indexing portion of the fitting device is configured to be disposed about a second portion of the body. The attachment portion of the fitting device is configured to removably retain the sleeve within an interior portion of the fitting device such that the electrode is disposed at a predetermined location relative to the second portion of the body when the fitting device is disposed about the first portion of the body.
In some embodiments, a method includes disposing a fitting device about a portion of a body. The fitting device includes an electrode coupled to an attachment portion of an inner surface of the fitting device. An actuator is moved relative to the fitting device to decouple the electrode from the attachment portion after the disposing. The fitting device is removed from the portion of the body.
As used in this specification, the words “proximal” and “distal” refer to the direction closer to and away from, respectively, an operator (e.g., surgeon, physician, nurse, technician, etc.) who would use a medical device or a therapeutic device during a procedure. For example, the end of a medical device first to contact the patient's body would be the distal end, while the opposite end of the medical device (e.g., the end of the medical device being operated by the operator) would be the proximal end of the medical device.
The inner surface 112 of the fitting device 110 includes an attachment portion 120 having a coupler 122. The coupler 122 removably couples the electrode 150 to the fitting device 110. The coupler 122 can be, for example, a layer of adhesive, a hook and loop fastener, a snap fastener, a magnetic fastener or any other mechanism suitable for removably coupling the electrode 150 to the fitting device 110. In some embodiments, the electrode 150 can be subdivided into multiple segments, with each segment configured to stimulated separately.
The actuator 140 has a proximal end portion 142 and a distal end portion 144 and is movably coupled to the fitting device 110. The proximal end portion 142 of the actuator 140 is disposed outside of the interior region 113 defined by the inner surface 112. Said another way, the proximal end portion 142 of the actuator 140 is accessible to a user when the fitting device 110 is disposed about the portion of the body B. Accordingly, a user can manipulate the proximal end portion 142 of the actuator 140 to move the actuator 140 relative to the fitting device 110 when the fitting device 110 is disposed about the portion of the body B. In this manner, the actuator 140 can be moved as shown by the arrow AA in
When the medical device 100 is in the first configuration, the distal end portion 144 of the actuator 140 is disposed adjacent the inner surface 112 of the fitting device 110. Additionally, when the medical device 100 is in the first configuration, the distal end portion 144 of the actuator 140 is disposed apart from the electrode 150. When the medical device 100 is in the second configuration, the distal end portion 144 of the actuator 140 is disposed within the interior region 113 defined by the inner surface 112 and is in contact with the electrode 150. In this manner, when the actuator 140 moves from its first position (corresponding to the first configuration of the medical device 100) to its second position (corresponding to the second configuration of the medical device 100) as illustrated by the arrow AA in
As described in more detail herein, when the electrode 150 is positioned on the portion of the body B, the fitting device 110 can be removed from the portion of the body B, leaving the electrode 150 in position on the body B. Alternatively, in other embodiments, the fitting device 110 can remain disposed about the portion of the body B when the electrode 150 is positioned on the body B as desired. For example, in some embodiments, the fitting device 110 can also provide structural support for the portion of the body B during therapy.
The fitting device 110 can be constructed from any suitable material or combination of materials. For example, in some embodiments, the fitting device 110 can be a constructed from a plastic, such as Nylon. In other embodiments, the fitting device 110 can be constructed from a composite material, such as fiberglass. In yet other embodiments, the fitting device 110 can be constructed from several different materials, such as, for example, rigid plastic, metallic materials, foam padding, cloth, elastic materials or the like. In some embodiments, for example, the fitting device 110 can be constructed from a rigid material such that at least a portion of the attachment portion 120 is rigid. In this manner, the attachment portion 120 can maintain the electrode 150 in a predetermined location within the fitting device 110. Said another way, in such embodiments, the attachment portion 120 can maintain a location, orientation and/or position of the electrode 150 relative to the portion of the body B when the fitting device 110 is disposed about the portion of the body B. In other embodiments, at least a portion of the fitting device 110 can include a flexible and/or elastic garment such that the fitting device can conform to different portions of the body B and/or different sizes and/or shapes of different patients.
The actuator 140 can be any suitable actuator constructed from any suitable material. For example, in some embodiments, the proximal end portion 142 of the actuator 140 can have a size and/or a shape that can be easily manipulated by a user. Similarly, in some embodiments, the distal end portion 144 of the actuator 140 can have a size and/or a shape that corresponds to a size and/or a shape of the electrode 150. For example, in some embodiments, the distal end portion 144 of the actuator 140 can have a shape that corresponds to a shape of the electrode 150. Accordingly, when the actuator 140 is moved into contact with the electrode 150, the distal end portion 144 of the actuator 140 can transmit a spatially uniform force to the electrode 150. In this manner, the electrode can be evenly and securely positioned on the portion of the body B.
The electrode 150 can be any suitable electrode for transmitting an electrical signal to the body B and/or receiving an electrical signal from the body B. For example, in some embodiments, the electrode 150 can be a surface electrode capable of transmitting an electrical signal having an amplitude of between 0.2 mA and 80 mA at a frequency of between 20 and 60 pulses per second. In other embodiments, the electrode 150 can be a surface electrode capable of receiving an electrical signal of between 20 μA and 10 mA at a frequency of between 10 Hz and 5 KHz. In yet other embodiments, the electrode 150 can be capable of transmitting a polarized electrical signal (i.e., the electrode 150 can have a negative or positive polarity).
Similarly, the electrode 150 can be constructed from any suitable components and can have any suitable features. In some embodiments, for example, the electrode 150 can include a cloth backing (not shown in
Similarly, the electrode 150 can have any suitable size and/or shape. For example, in some embodiments, the electrode 150 can be a surface electrode having a circular shape ranging in size between 0.5 inches and 2 inches. In other embodiments, the electrode 150 can be a surface electrode having a rectangular shape. Such rectangular shaped electrodes can range in size from a 1.5 inch square electrode to a 3 inch by 5 inch rectangular electrode.
In some embodiments the electrode may be divided into plurality of segments, electrically insulated from each other and serving as separate electrodes.
In some embodiments, a fitting device can include an indexing portion to orient and/or position the fitting device about the body at a predetermined location. For example,
The inner surface 212 of the fitting device 210 includes an attachment portion 220 having two couplers 222. The couplers 222 removably couple the electrodes 250A, 250B to the fitting device 210. The couplers 222 can be, for example, a layer of adhesive, a hook and loop fastener, a snap fastener, a magnetic fastener or any other mechanism suitable for removably coupling the electrodes 250A, 250B to the fitting device 210. In some embodiments, for example the couplers 222 can be bands of Velcro® configured to engage a backing 256B (see
The fitting device 210 includes an indexing portion 230 that defines a curved edge 231. As described in more detail herein, the curved edge 231 has a shape that corresponds to a shape of the patient's kneecap K (see, e.g.,
As shown in
The application of the medical device 200 on a patient's leg L is described with reference to
When the fitting device 210 is disposed about the patient's leg L with the patient's kneecap K disposed within the curved edge 231, as shown in
As shown by the arrow BB in
When the actuator 240B is in the second position, the distal end portion 244B of the actuator 240B is disposed within the interior region 213 defined by the inner surface 212 and is in contact with the electrode 250B such that the electrode 250B is spaced apart from the coupler 222. Said another way, when the actuator 240B moves from its first position to its second position as illustrated by the arrow BB in
As described above, the fitting device 210 can be constructed from any suitable material or combination of materials. For example, in some embodiments, at least a portion of the attachment portion 220, at least a portion of the indexing portion 230, and/or at least a portion of the fitting device 210 disposed therebetween can be constructed from a rigid material, a flexible material or a semi-flexible material. Similarly stated, in some embodiments, at least a portion of the attachment portion 220, at least a portion of the indexing portion 230 and/or at least a portion of the fitting device 210 disposed therebetween can be constructed from an inelastic material. In this manner, the geometrical relationship between the attachment portion 220 and the indexing portion 230 can be maintained, such that the fitting device 210 can be used to repeatably and/or accurately position the electrodes 250A, 250B at a predetermined position and/or orientation relative to the kneecap K, as described above. Similarly stated, in this manner, the distance between the attachment portion 220 and the indexing portion 230 can be substantially constant or fixed.
The fitting device 310 has an inner surface 312, an outer surface 314, an attachment portion 320, an indexing portion 330 and two attachment straps 326. The inner surface 312 of the fitting device 310 defines an interior region 313 within which a portion of a patient's body B can be disposed. As described above, in some embodiments, the inner surface 312 of the fitting device 310 can have a shape that corresponds to a shape of the patient's body B (e.g., the patient's hand, leg, foot, arm or the like). In this manner, the fitting device 310 can be disposed about the portion of the body B such that the inner surface 312 is in contact with and/or is adjacent the body B.
When the fitting device 310 is disposed about the portion of the body B, the straps 326 can extend around the portion of the body B to secure the fitting device 310 in position. Each strap 326 includes a coupler 327 configured to removably couple the ends of the straps 326 together. The couplers 327 can be, for example, a hook and loop fastener, a snap fastener, an adjustable buckle fastener or the like. The straps 326 can be constructed from any suitable flexible material, such as, for example, an elastic material or an inelastic material.
As shown in
As shown in
The indexing portion 330 of the fitting device 310 defines a curved edge 331 having a shape and/or size that corresponds to a shape of a portion of the patient's body B. For example, in some embodiments, the curved edge 331 can have a shape and/or size corresponding to a kneecap, an ankle, a wrist, an elbow, a thumb or any other suitable portion of the body for indexing the position of the fitting device 310. Accordingly, the indexing portion 330 can receive a portion of the patient's body to position the fitting device 310 about the patient's body B at a predetermined location, orientation and/or position. In this manner, when the fitting device 310 is disposed about the body B with a portion of the patient's body B disposed within the curved edge 331, the electrodes 350A, 350B are positioned at a predetermined location, orientation and/or position on the patient's body B.
As shown in
The distal end portion 344A of the actuator 340A includes a coupler 348A configured to removably couple the electrode 350A to the actuator 340A. The coupler 322 can be, for example, a layer of adhesive, a hook and loop fastener, a snap fastener, a magnetic fastener or any other mechanism suitable for removably coupling the electrode 350A to the actuator 340A. In some embodiments, for example the coupler 322 can be a band of Velcro® configured to engage a cloth backing (not shown in
In use, the fitting device 310 is disposed about a portion of the body B such that a portion of the body B is received within the indexing portion 330 of the fitting device 310, as described above. When the fitting device 310 is positioned as desired about the patient's body B, the actuator 340A is moved from a first position (see, e.g.,
After the electrodes 350A, 350B are positioned on the patient's leg L, the actuator 340A is moved from the second position back to the first position, as shown by the arrow DD in
As shown in
Although the actuators are shown and described above as being actuated by manipulating a proximal end portion of the actuator, in some embodiments, an actuator can be actuated by manipulating any suitable portion of the actuator. For example,
The attachment portion 420 of the fitting device 410 includes a recess 424, defined by the inner surface 412 of the fitting device 410 and a lumen 416 defined by the fitting device 410 in communication with the recess 424. A coupler 422 is disposed on the inner surface 412 of the fitting device 410 within the recess 424 to removably couple an electrode 450 within the recess 424. As described above, the coupler 422 can be, for example, a layer of adhesive, a hook and loop fastener, a snap fastener, a magnetic fastener or any other mechanism suitable for removably retaining the electrodes 450 within the recess 424.
In some embodiments, the size and shape of the recess 424 corresponds to the size and shape of the electrode 450. This arrangement allows the electrode 450 to be “loaded” into the fitting device 410 in a predetermined orientation and/or position. Similarly, in some embodiments, the recess 424 can be uniquely associated with a particular type of electrode 450.
The actuator 440 has a first end portion 442, a central portion 446, and a second end portion 444. The first end portion 442 and the second end portion 444 are coupled to the outer surface 414 of the fitting device 410. The actuator is movably coupled to the fitting device 410 between a first configuration (
When the actuator 440 is in the second configuration, the central portion 446 of the actuator is in contact with the electrode 450. In this manner, when the actuator 440 moves from its first configuration to its second configuration, as illustrated by the arrow EE in
In some embodiments, the actuator 440 can be constructed from a resilient material, such as, for example, a thin metallic strip, a polymer or the like. In this manner, when the actuator 440 is in its second configuration and when the user releases the actuator 440, the central portion 446 of the actuator will return to the first configuration as shown in
As shown in
Two electrodes 550A, 550B of the type shown and described above are fixedly coupled to the inner surface 562 of the sleeve 560. In some embodiments, the electrodes 550A, 550B can be positioned on the inner surface 562 of the sleeve 560 such that when the sleeve 560 is disposed about the patient's leg L, the electrode 550A is disposed adjacent the superficial peroneal nerve and the electrode 550B is disposed adjacent the deep peroneal nerve. In other embodiments, the electrodes 550A, 550B can be positioned on the inner surface 562 of the sleeve 560 such that when the sleeve 560 is disposed about the patient's leg L, the electrodes 550A, 550B can be positioned and/or oriented adjacent any anatomical feature of the patient's body (e.g., nerves, muscles, or the like). In some embodiments, the inner surface 562 of the sleeve 560 can include a recess or multiple recesses (not shown in
An electronic stimulator 556 is coupled to the outer surface 564 of the sleeve 560 and is electronically coupled to the electrodes 550A, 550B. The electronic stimulator 556 can provide electrical signals to the electrodes 550A, 550B as a part of a therapeutic program. For example, in some embodiments, the electronic stimulator 556 can provide electrical signals to the electrodes 550A, 550B to cause dorsiflexion of the ankle in patients who have lost the ability to dorsiflex following neurological injury. The stimulator 556 can be any stimulator suitable for providing electrical signals to the electrodes 550A, 550B. For example, in some embodiments, the electronic stimulator 556 can be capable of providing a signal of between 0.2 volts and 1.0 volts at a frequency of between 25 pulses per second and 35 pulses per second.
As shown in
The couplers 527 and 567 can be any suitable mechanism for removably coupling the sleeve 560 to the fitting device 510. For example, in some embodiments, the couplers 527 and 567 can be hook and loop fasteners. In other embodiments, the couplers 527 and 567 can be snap fasteners. In yet other embodiments, the couplers 527 and 567 can be zippers. Although shown as including two sets of mating couplers 527 and 567, in some embodiments, the fitting device 510 and the sleeve 560 can include a single coupler.
In some embodiments, the inner surface 512 of the fitting device 510 can have a shape that corresponds to a shape of the patient's leg L. In this manner, the fitting device 510 can be disposed about the leg L such that the inner surface 512 is in contact with and/or is adjacent the leg L.
The indexing portion 530 of the fitting device 510 defines a curved edge 531 having a shape that corresponds to a shape of the patient's kneecap K. Accordingly, the indexing portion 530 can receive a portion of the patient's kneecap K to position the fitting device 510 about the patient's leg L at a predetermined location, orientation and/or position. In this manner, when the fitting device 510 is disposed about the patient's leg L with the patient's kneecap K disposed within the curved edge 531, the sleeve 560, and therefore the electrodes 550A, 550B are positioned at a predetermined location, orientation and/or position on the patient's leg L.
The stimulator housing portion 525 defines a recess 524 within which the electronic stimulator 556 can be disposed when the sleeve 560 is coupled to the fitting device 510, as shown in
In use, the sleeve 560 is coupled to the fitting device 510 and the fitting device 510 is disposed about the patient's leg L. When the fitting device 210 is disposed about the patient's leg L such that the patient's kneecap K is within the curved edge 531, the sleeve 560 is positioned such that the first electrode 550A is positioned above or adjacent the superficial peroneal nerve SP of the leg L and the second electrode 250B is positioned above or adjacent the deep peroneal nerve DP of the leg L. In this manner, the fitting device 510 can be used to position the sleeve 560 at a predetermined location, orientation and/or position on the patient's leg L. Similarly stated, the indexing portion 530 of the fitting device 510 is positioned and/or oriented relative to the couplers 527 of the fitting device 510 such that when the fitting device 510 and the sleeve 560 are disposed about the patient's leg L with the patient's kneecap K disposed within the curved edge 531, the sleeve 560 is disposed adjacent the leg L at a predetermined position and/or orientation relative to the kneecap K.
After the fitting device 510 is positioned as desired about the patient's leg L, the sleeve 560 is coupled about the patient's leg L. The sleeve 560 can be removably coupled to the leg L by couplers (not shown in
Upon completion of the therapy, the fitting device 510 can be used to remove the sleeve 560 from patient's leg, by following the above operations described above in the reverse order. In this manner, the sleeve 560 can be stored within the fitting device 510 when not being used for therapy.
The sleeve 560 can be constructed from any material or combination of materials suitable for being disposed about the patient's body and for containing the electronic stimulator 556 and/or electrodes 550A, 550B. For example, in some embodiments, the sleeve 560 can be a flexible garment constructed from a polymer and/or natural materials. In some embodiments, the sleeve 560 can include an inelastic portion and an elastic portion. For example, in some embodiments, the portions of the sleeve 560 that include the couplers 567 and the electrodes 550A, 550B can be constructed from an inelastic material and the end portions 566, 568 of the sleeve 560 can be constructed from an elastic material. In this manner, when the sleeve 560 is coupled to the fitting device 510, the position of the electrodes 550A, 550B relative to the indexing portion 530 of the fitting device 510 can be maintained in a predetermined location and/or orientation. Said another way, by constructing a portion of the sleeve 560 from an inelastic material, the sleeve 560 will not stretch when in use, thereby causing the electrodes 550A, 550B to move out of their desired position. Conversely, end portions 566, 568 can be constructed from an elastic material such that the sleeve 560 can be securely coupled about the patient's leg L.
The fitting device 510 can be constructed from any suitable material. For example, in some embodiments, the fitting device 510 can be a constructed from a plastic, such as Nylon. In other embodiments, the fitting device 510 can be constructed from a composite material, such as fiberglass. In yet other embodiments, the fitting device 510 can be constructed from several different materials, such as, for example, rigid plastic, metallic materials, foam padding, cloth, elastic materials or the like.
Although the medical device 500 is shown and described above as including one fitting device 510 and one sleeve 560, in other embodiments, the medical device 500 can include multiple fitting devices 510 and/or sleeves 560. For example, in some embodiments a kit can include a fitting device that includes an indexing portion, similar to those shown and described above, that is custom-fit for a particular patient. The kit can also include multiple sleeves, each having a different configuration of electrodes. For example, one sleeve of the kit can include a single electrode for use in a first therapeutic regiment. A second sleeve of the kit can include multiple electrodes for use in a second therapeutic regiment. In some embodiments, a second sleeve can include electrodes of a different type, electrodes in different location and/or electrodes in a different orientation. In some embodiments, for example, the electronic stimulator 556 can be removably coupled to the sleeve 560 such that it can be used on multiple different sleeve configurations.
Similarly, in some embodiments, a kit can include multiple different fitting devices 510 of the types shown and described above. For example, in some embodiments, a kit can include different fitting devices corresponding to different patient sizes and/or anatomical relationships. In this manner, a practitioner can select a fitting device to best fit the features of a particular patient.
After the fitting device is disposed about the portion of the body, an actuator is moved relative to the fitting device to decouple the electrode from the attachment portion of the fitting device, 674. The actuator can be any actuator of the types shown and describe above. For example, in some embodiments, the actuator can be a linear actuator configured to slide within a portion of the fitting device. In other embodiments, the actuator can be configured to rotate relative to the fitting device.
The fitting device is then removed from the body, 676. In this manner, the electrode can be disposed on the patient's body in a desired position and/or orientation without requiring a garment and/or support device to maintain the position and/or orientation of the electrode.
In some embodiments, the moving can include moving the actuator such that the electrode is removably coupled to the portion of the body. In such embodiments, the electrode can include a layer of conductive hydrogel to couple the electrode to the patient's body.
In some embodiments, the moving can include moving the actuator such that a distal end portion of the actuator contacts the electrode to decouple the electrode from the attachment portion of the fitting device. In some embodiments, for example, the moving can include moving the actuator from a first position to a second position. When the actuator is in the first position a proximal end portion of the actuator is spaced apart from an outer surface of the fitting device. When the actuator is in the second position a distal end portion of the actuator contacts the electrode to decouple the electrode from the attachment portion.
In some embodiments, the moving can include moving the actuator such that a distal end portion of the actuator applies a spatially uniform force to an inner surface of the electrode to decouple the electrode from the attachment portion and/or removably coupled to the portion of the body. In some such embodiments, for example, a distal end portion of the actuator can have a shape and/or size corresponding to a shape and/or size of the electrode.
In some embodiments, the disposing can include receiving a second portion of the body within an indexing portion of the fitting device such that the fitting device is positioned about the first portion of the body at a predetermined location relative to the second portion of the body. For example in some embodiments, the disposing can include receiving a kneecap within an indexing portion of the fitting device such that the fitting device can be positioned at a predetermined location on the patient's leg.
While various embodiments of the invention have been described above, it should be understood that they have been presented by way of example only, and not limitation. Where methods described above indicate certain events occurring in certain order, the ordering of certain events may be modified. Additionally, certain of the events may be performed concurrently in a parallel process when possible, as well as performed sequentially as described above. Thus, the breadth and scope of the invention should not be limited by any of the above-described embodiments. While the invention has been particularly shown and described with reference to specific embodiments thereof, it will be understood that various changes in form and details may be made.
For example, although the actuators are shown and described above as being manually and/or mechanically actuatable, in some embodiments, an actuator can be automatically actuated. In some embodiments, for example, an actuator can be an electronic actuator that is automatically actuated to position an electrode on the body when a portion of the body is received within an indexing portion of a fitting device. For example, in some such embodiments, the indexing portion of the fitting device can include a sensor configured to output a signal when the portion of the body is satisfactorily received within the indexing portion. In this manner, the fitting device can be configured to prevent premature and/or erroneous placement of electrodes.
Similarly, in some embodiments, an actuator can be a pneumatic actuator, an electronic actuator and/or a hydraulic actuator. In some embodiments, for example, a medical device can include multiple electrodes and a fitting device can include multiple actuators configured to actuate simultaneously after the fitting device is disposed about the body.
In some embodiments, an actuator can be biased in a certain position. For example, in some embodiments, a fitting device can include a spring or other suitable biasing member such that the actuator is maintained in its first (or “loaded”) position. In other embodiments, a fitting device can include a spring or other suitable biasing member such that the actuator is maintained in its second (or “actuated”) position.
Although the fitting devices 200, 300 and 500 are shown and described above as including an indexing portion, in some embodiments a fitting device can include multiple indexing portions. For example, in some embodiments, a fitting device can include a first indexing portion configured to receive a first portion of a patient's body and second indexing portion configured to receive a second portion of a patient's body, different than the first portion. For example, in some embodiments, a fitting device can include a first indexing portion configured to receive a kneecap and a second fitting portion configured to receive an ankle. In other embodiments, a fitting device can include a first indexing portion configured to receive an elbow and a second fitting portion configured to receive a thumb.
Similarly, although the fitting devices 200, 300 and 500 are shown and described above as being disposed on a patient's leg and having an indexing portion configured to receive a portion of a kneecap, in other embodiments, a fitting device can be configured to be disposed about any portion of a patient's body, such as, for example, the arm, hand, foot, torso, head or the like. Similarly, in some embodiments, the indexing portion can be configured to index the location and/or orientation of the fitting device with respect to any suitable anatomical feature of the body. For example, in some embodiments, an indexing portion can be configured to index the location and/or orientation of the fitting device with respect to a thumb, finger, nose, ankle, wrist, elbow, hand, foot or the like.
Although the fitting devices 200, 300 and 500 are shown and described above as including an indexing portion configured to receive a portion of the body, in some embodiments a fitting device can include any suitable indexing portion. For example, in some embodiment, an indexing portion can include a protrusion configured to be disposed within and/or between a portion or portions of the body. For example, in some embodiments, an indexing portion can include a protrusion configured to be received between the patient's fingers.
Although the fitting devices are shown and described above as being configured to place one or more electrodes on a patient's body, in some embodiments a fitting device can be configured to remove electrodes from the patient's body. For example, in some embodiments a fitting device can include a first actuator for placing an electrode on the patient's body prior to a therapeutic session and a second actuator for removing the electrode from the patient's body after the therapeutic session.
Although the medical devices are shown and described above as including one or more electrodes, in some embodiments, a medical device can include a simulated fitting device that is devoid of actual electrodes. In some embodiments, a simulated fitting device can correspond to an actual fitting device, of the types shown and described above, and can be used, for example, to train a user in the placement of electrodes on and/or the removal of electrodes from a patient's body.
This application claims priority to U.S. Provisional Application Ser. No. 60/813,257, entitled “Apparatus and Method for Positioning Electrodes on the Body,” filed Jun. 12, 2006, which is incorporated herein by reference in its entirety.
Number | Date | Country | |
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60813257 | Jun 2006 | US |