The present invention relates to wearable elements for use with implantable distension devices.
Obesity is becoming a growing concern, particularly in the United States, as the number of obese people continues to increase, and more is learned about the negative health effects of obesity. Morbid obesity, in which a person is 100 pounds or more over ideal body weight, in particular poses significant risks for severe health problems. Accordingly, a great deal of attention is being focused on treating obese patients. One proposed method of treating morbid obesity has been to place a distension device, such as a, spring-loaded coil inside the stomach. Examples of satiation and satiety inducing gastric implants, optimal design features, as well as methods for installing and removing them are described in commonly owned and pending U.S. patent application Ser. No. 11/469,564, filed Sep. 1, 2006, and pending U.S. patent application Ser. No. 11/469,562, filed Sep. 1, 2006, which are hereby incorporated herein by reference in their entirety. One effect of the coil is to more rapidly induce feelings of satiation defined herein as achieving a level of fullness during a meal that helps regulate the amount of food consumed. Another effect of the coil is to prolong the effect of satiety which is defined herein as delaying the onset of hunger after a meal which in turn regulates the frequency of eating. By way of a non-limiting list of examples, positive impacts on satiation and satiety may be achieved by an intragastric coil through one or more of the following mechanisms: reduction of stomach capacity, rapid engagement of stretch receptors, alterations in gastric motility, pressure induced alteration in gut hormone levels, and alterations to the flow of food either into or out of the stomach.
With each of the above-described stomach distension devices, safe, effective treatment requires that the device be regularly monitored and adjusted to vary the degree of distension applied to the stomach.
Furthermore, requiring a patient to travel to a physician to have the implant powered and monitored is time consuming for both the patient and the physician. Monitoring the implant during a visit to a physician is also not necessarily the best indication of how the implant is performing when compared with data taken regularly during every day activities. Thus, there is a need for methods and devices that allow a patient to carry monitoring and powering systems. This would greatly improve the ease of use, reliability and efficiency of the implantable distension device for both the patient and the physician. In addition, being able to monitor the conditions of the implant and of physiological conditions on a regular basis by providing devices which are wearable by the patient during daily activities may reduce the risk of missing a problem with an adjustment that could cause damage to the patient's stomach and overall health.
The invention will be more fully understood from the following detailed description taken in conjunction with the accompanying drawings, in which:
Certain exemplary embodiments will now be described to provide an overall understanding of the principles of the structure, function, manufacture, and use of the devices and methods disclosed herein. One or more examples of these embodiments are illustrated in the accompanying drawings. Those of ordinary skill in the art will understand that the devices and methods specifically described herein and illustrated in the accompanying drawings are non-limiting exemplary embodiments and that the scope of the present invention is defined solely by the claims. The features illustrated or described in connection with one exemplary embodiment may be combined with the features of other embodiments. Such modifications and variations are intended to be included within the scope of the present invention.
The present invention provides wearable elements which allow for a more comfortable and efficient way of carrying external devices related to powering and monitoring an implantable distension device. The distension device may also be adjustable. Exemplary non-limiting examples of adjustable implantable distension devices (e.g., satiation and satiety inducing gastric implants), optimal design features, as well as methods for installing and removing them are described in commonly owned and pending U.S. patent application Ser. No. ______, filed on even date herewith and entitled “Devices and Methods for Adjusting a Satiation and Satiety-Inducing Implanted Device” [Atty. Docket No. END6514USNP], which is hereby incorporated herein by reference in its entirety. In one exemplary embodiment, a system for forming a distension in a stomach is provided and includes an implantable distension device adapted to cause a distension in a stomach and an implantable communicating member configured to send and/or receive a wireless signal. The distension device can include, for example, a gastric coil and a housing in communication with the gastric coil. The system can further include a wearable element configured to be worn by a patient and an external device coupled to the wearable element which is configured to send and/or receive a wireless signal to communicate with the implantable communicating member. In an exemplary embodiment, the external device is disposable at a plurality of locations relative to the wearable element.
The external device can have a variety of configurations, and in one embodiment the external device can be an antenna positionable in proximity to the implantable communicating member and configured to receive data from the implantable communicating member. In another embodiment, the external device can be configured to send power to the implantable communicating member. In still another embodiment, the implantable communicating member can be an internal inductive coil and the external device can be an external inductive coil and the coils can be configured to resonate at substantially the same frequency to maximize power coupling. The wearable element can also include an alignment mechanism configured to indicate proper alignment between the external device and the implantable communicating member.
In another embodiment, the system can include a first external device and a second external device that are coupled to one another and are positionable at a plurality of locations on the wearable element at a distance apart from one another. In one exemplary embodiment, the first external device can be configured to receive data from the implantable communicating member and the second external device can also optionally be configured to provide power to the first external device.
The wearable element can also have a variety of configurations, and in one exemplary embodiment the wearable element can be a flexible battery adapted to flex in response to motion of a user wearing the flexible battery. In another exemplary embodiment, the wearable element can be formed from a plurality of elastic straps. In addition, the wearable element can be adjustable to a variety of patient sizes and shapes. In still another embodiment, the wearable element can be a belt, a vest, a sash, or an adhesive patch. In other aspects, the wearable element can include at least one pocket formed therein which is movable relative to the wearable element. In one embodiment, the pocket includes at least one battery disposed therein which is configured to provide power to the external device.
Methods are also provided for communicating with an implantable distension device. In one embodiment, the method can include positioning an external device on a wearable element worn by a patient at one of a plurality of locations to align the external device with an implantable communicating member on an implantable distension device implanted in the patient. The external device can be activated to wirelessly transfer a signal through tissue to the implantable communicating member. For example, the external device can deliver energy to the implantable communicating member and/or receive data from the implantable communicating member. In addition, the external device can be an external inductive coil and the implantable communicating member can be an internal inductive coil and the method can further include using inductive coupling between the external coil and the internal coil to generate power. The two coils can be tuned to resonate at substantially the same frequency to maximize power coupling.
While the external device can be positioned at a variety of locations, in one exemplary embodiment the external device can be positioned on a skin surface in proximity to the implantable communicating member. The external device can be positioned on the wearable element or at a distance apart from the wearable element. For example, the wearable element can include a plurality of flexible straps, and the external device can be removably mated to the flexible straps in proximity to the implantable communicating member. Alternatively, or in addition, the external device can be disposed within a pocket on the wearable element. In another aspect of the invention, the wearable element can be a flexible battery. The external device can be coupled to the flexible battery and can deliver energy to the implantable communicating member generated by the flexible battery.
While the present invention disclosed herein can be used with a variety of distension systems known in the art,
While not shown in
In one exemplary embodiment, a first external device can be configured to transmit power to the implantable communicating member 60 via a passive telemetry system. For example, a burst of radio frequency power can be sent by the first external device to the implantable communicating member which is sufficient to allow the implantable communicating member 60 to send data and measurements back to the first external device. The first external device can optionally be electrically coupled to a second external device which can record and/or display the various measurement readings or other data received by the first external device. The second external device can also send electrical power to the first external device as needed for communicating with the implantable communicating member 60. The first external device and/or the second external device can be programmed so that the first external device communicates with the implantable communicating member 60 at random intervals or at predetermined time periods so that the patient is not required to activate any device in order for the first external device and the implantable communicating member 60 to communicate. Alternatively, communication between the first external device and the implantable communicating member 60, or between the first external device and the second external device, can be manually activated by the patient or other user.
In one exemplary embodiment, the second external device is a rechargeable battery system configured to send power to the first external device as needed. The second external device can also include circuitry configured to control the amount of power sent through the first external device to the implantable communicating member 60. Alternatively, a single external device can perform all, any one, or any combination of the functions noted above. In still another embodiment, the external device can include multiple battery systems in connection with one another to maximize available power as will be described in more detail below. A person skilled in the art will appreciate that any number of external devices can be used to perform any number of functions needed to power, monitor, and otherwise wirelessly communicate with the implantable communicating member 60. In the same way, a single external device can be configured to perform all of the above noted functions as needed.
The external portion can also include a wearable element that is configured to be worn by a patient, and that is coupled to one or more external devices. The wearable element can be particularly effective to allow the external device(s) to be worn by the user, thus allowing for communication between the external device(s) and the implantable communicating member as may be desired.
As used herein, the term “wearable” can refer to any article of manufacture designed to be worn on or borne by the body or any portion of the body of a wearer. When in the form of a garment, the wearable element can be, for example, in the form of a vest, a shirt, a tank top, a bodysuit, a jacket, or any other form which fits over and/or around the upper torso of a wearer. In addition, the wearable element can also include any other article of clothing in the form of gloves, pants, socks, etc. The term “wearable” can encompass not only garments, but also coils, straps, belts, patches, etc. When in the form of a coil, the wearable element can be, for example, in the form of a torso coil, a waist coil, a neck coil, an arm coil, a head coil, etc. The wearable element can also encompass adhesive patches which can be applied as needed on a patient's body.
As this is a component of the system that is in direct and daily contact with the patient, features that make this interaction more appealing to the patient can serve to increase patient compliance with wearing it.
Such features include matching the patient's skin color, providing chest support for women, designed to avoid bunching together, making it small, light weight, portable, and body contouring, including additional pockets for holding miscellaneous items such as iPods, making it of materials that don't interfere with airport security such as any non-metallic materials, etc
In use, the wearable element can generally be wearable over some portion of a patient's body. The wearable element can be configured to be fitted tightly to the portion of the patient's body so as to fit under a patient's clothing. It can also be configured to fit loosely over a patient's body or over a patient's clothing. Adjustability elements can be included on the wearable element so that the wearable element can be adapted to fit patients of various sizes and shapes. The wearable element can be made of various materials, but a light and resilient material is preferred to optimize comfort and ease of use for the patient. In an exemplary embodiment, the wearable element is made from materials commonly used in fabric and textile applications. For example, the wearable element can be made from elastomeric yarns (such as spandex) and/or comfort yarns (such as nylon, polyester, or cotton). Any combination of materials can be formed as necessary to maximize comfort and ease of use for the patient, as well as to provide ease of cleaning. The wearable element may be comprised of a plurality of fabrics such that portions are elastic and other portions are soft or non distensible. Some portions may be more or less rigid or moldable about the patient's anatomy whereas other portions may be moldable. The wearable element can also be adapted to be worn for extended lengths of time by the patient or it can be adapted to be worn only at specific times as needed for powering, monitoring, and/or otherwise communicating with the implantable communicating member.
In one exemplary embodiment shown in
As also shown in
In another exemplary embodiment shown in
In use, for example, one pocket attached to a wearable element can be placed in proximity to an implantable communicating member and can hold an external device, such as an antenna, for communicating with the implantable communicating member. Simultaneously, another pocket can be disposed towards the bottom of the wearable element and can hold another external device, such as a rechargeable battery system or reader device, that is connected to the antenna.
As another example, two pockets can be disposed next to each other on a wearable element in proximity to the implantable communicating member, each holding an external device. A first external device can be an antenna for obtaining data or measurements from the implantable communicating member and a second external device can be an inductive coil for providing power to the implantable communicating member. Alternatively or in addition, one pocket can hold an alignment mechanism for monitoring proper alignment of the first and/or second external devices with the implantable communicating member.
In a final example most clearly illustrated in
The vest 300 can generally be wearable over a patient's torso and can be configured to be fitted tightly to the torso so as to fit under a patient's clothing or to fit loosely over a patient's body or over a patient's clothing. The external inductive coil 306 can be formed from wound metal wire, for example copper wire, and can conform to various sizes and shapes as needed for powering the internal inductive coil 310, as is well known in the art. The external inductive coil 306 can be adapted to be positioned adjacent to a tissue surface and in proximity to the internal inductive coil 310. For example, the external inductive coil 306 can be formed in a front panel 330a or a rear panel 330b of the vest 300. The external inductive coil 306 can be formed integrally with the vest 300 or can be disposed on an exterior or interior surface of the vest 300 and can be attached to or disposed within the vest 300 in any way known in the art which is effective to allow proper alignment of the external inductive coil 306 with the internal inductive coil 310. Thus, the external inductive coil 306 can optionally be removably attached to the vest 300 so that the external coil 306 can be moved and aligned as needed. Alternatively, the external inductive coil 306 can be integrally formed in an interior portion of the vest 300 with a predetermined alignment based on where the internal inductive coil 310 will be positioned. The internal coil 310 can also be formed of metal wire, for example copper magnet wire, and can be of a size and shape to achieve the desired power and/or signal coupling from the corresponding external inductive coil 306 or inductive coils 306a-306d.
In an exemplary embodiment, the external inductive coil 306 can be in electrical communication with the external reader 370. The external reader 370 can provide power to the external inductive coil 306 taken from any power source 340 known in the art, for example a battery or wall electrical outlet. The external reader 370 can be configured so that a user can control the amount of power coupled through the external inductive coil 306 to the internal inductive coil 310, as well as other aspects of using the external inductive coil 306. The external reader 370 can be configured in various ways. For example, it can be positioned on the vest 300, in a hand-held device, or at a position remote from the vest 300, as shown in
In another embodiment shown in
In another embodiment,
In the embodiment illustrated in
In an exemplary embodiment, in use, each of the wearable elements of
In another embodiment, the wearable element can be in the form of an adhesive patch that can be applied to the patient directly, or to one of the other embodiments of wearable elements described herein. The adhesive patch can be formed from a flexible battery, and it can be attached directly to a wearable element or disposed within a pocket that is attached to a wearable element, as described above in reference to
As further shown in
In use, in each of the various embodiments disclosed herein, the external device can be positioned on a wearable element worn by a patient at one of a plurality of locations to align the external device with an implantable communicating member on an implantable distension device implanted in a patient. Once positioned as desired, the external device can be activated to transfer a signal through tissue to the implantable communicating member.
In one exemplary embodiment, the wearable element can be placed on or around the patient depending on the form of the wearable element. Once placed on or around the patient, adjustability elements can be adjusted to fit the wearable element to the patient, whether under the patient's clothing or over the patient's clothing. Once a proper and comfortable fit is attained, external devices can be attached to the wearable element as necessary and as will be described in detail below.
In the embodiment shown in
Once the external devices 212 are in the proper location with the proper alignment, if necessary they can be activated by a physician, a user, or by self-actuation to perform any number of actions. For example, where the external device is an antenna, activation of the antenna can be effective to send power or energy to an implantable communicating member to enable the implantable communicating member to send back data to the antenna regarding the data and other measurements taken concerning the implantable distension device. Alternatively, where the external device is an inductive coil, activation of the coil can be effective to communicate with an implantable communicating member, for example an inductive coil, to thereby transfer power to the implantable distension system through inductive coupling.
In the embodiment shown in
In the embodiment shown in
In the embodiment shown in
In the embodiment shown in
Any patent, publication, application or other disclosure material, in whole or in part, that is said to be incorporated by reference herein is incorporated herein only to the extent that the incorporated materials does not conflict with existing definitions, statements, or other disclosure material set forth in this disclosure. As such, and to the extent necessary, the disclosure as explicitly set forth herein supersedes any conflicting material incorporated herein by reference. Any material, or portion thereof, that is said to be incorporated by reference herein, but which conflicts with existing definitions, statements, or other disclosure material set forth herein will only be incorporated to the extent that no conflict arises between that incorporated material and the existing disclosure material.
One skilled in the art will appreciate further features and advantages of the invention based on the above-described embodiments. Accordingly, the invention is not to be limited by what has been particularly shown and described, except as indicated by the appended claims. All publications and references cited herein are expressly incorporated herein by reference in their entirety.
This case is related to the following commonly assigned and concurrently filed U.S. Applications, all of which are hereby incorporated herein by reference: U.S. Ser. No. ______ (Attorney Docket Number END6514USNP) titled DEVICES and METHODS FOR ADJUSTING A SATIATION AND SATIETY-INDUCING IMPLANTED DEVICE; U.S. Ser. No. ______ (Attorney Docket Number END6515USNP) titled Sensor Trigger; U.S. Ser. No. ______ (Attorney Docket Number END6516USNP) titled AUTOMATICALLY ADJUSTING INTRA-GASTRIC SATIATION AND SATIETY CREATION DEVICE; U.S. Ser. No. ______ (Attorney Docket Number END6517USNP) titled OPTIMIZING THE OPERATION OF AN INTRA-GASTRIC SATIETY CREATION DEVICE; U.S. Ser. No. ______ (Attorney Docket Number END6518USNP) titled POWERING IMPLANTABLE DISTENSION SYSTEMS USING INTERNAL ENERGY HARVESTING MEANS; U.S. Ser. No. ______ (Attorney Docket Number END6519USNP) titled WEARABLE ELEMENTS FOR INTRA-GASTRIC SATIETY CREATION SYSTEMS; U.S. Ser. No. ______ (Attorney Docket Number END6520USNP) titled INTRA-GASTRIC SATIETY CREATION DEVICE WITH DATA HANDLING DEVICES AND METHODS; U.S. Ser. No. ______ (Attorney Docket Number END6521USNP) titled GUI FOR AN IMPLANTABLE DISTENSION DEVICE AND A DATA LOGGER; U.S. Ser. No. ______ (Attorney Docket Number END6522USNP) titled METHODS AND DEVICES FOR FIXING ANTENNA ORIENTATION IN AN INTRA-GASTRIC SATIETY CREATION SYSTEM; U.S. Ser. No. ______ (Attorney Docket Number END6523USNP) titled METHODS AND DEVICES FOR PREDICTING INTRA-GASTRIC SATIETY CREATION DEVICE SYSTEM PERFORMANCE; U.S. Ser. No. ______ (Attorney Docket Number END6524USNP) titled CONSTANT FORCE MECHANISMS for Regulating Distension Devices; U.S. Ser. No. ______ (Attorney Docket Number END6525USNP) titled A METHOD OF REMOTELY ADJUSTING A SATIATION AND SATIETY-INDUCING IMPLANTED DEVICE.