Monitoring of a food intake restriction device
First Claim
1. A system for obtaining data from an implanted device, the system comprising:
- (a) an implantable restriction forming device, wherein the implantable restriction forming device is operable to form a restriction in a patient, wherein the implantable restriction forming device comprises an implantable injection port, wherein the implantable injection port defines a fluid reservoir in fluid communication with the implantable restriction forming device, wherein the fluid reservoir of the implantable injection port is configured to receive a fluid, wherein the implantable injection port includes a needle penetrable septum configured to receive a needle for adding fluid to or withdrawing fluid from the fluid reservoir via the needle;
(b) an implantable pressure sensor positioned within the implantable injection port of the implantable restriction forming device, wherein the implantable pressure sensor comprises a diaphragm in fluid communication with the fluid reservoir of the implantable injection port and one or more strain gauges connected with the diaphragm, wherein the one or more strain gauges are configured to sense strain in the diaphragm as a function of the pressure of the fluid such that the implantable pressure sensor is operable to sense the pressure of fluid in the fluid reservoir;
(c) one or more implantable communicators in communication with the implantable pressure sensor, wherein the one or more implantable communicators are operable to communicate data from within a patient;
(d) one or more external communicators in communication with the one or more implantable communicators, wherein the one or more external communicators are operable to externally receive data communicated from within a patient by the one or more implantable communicators; and
(e) a storage device in communication with the one or more external communicators, wherein the storage device is operable to store at least a portion of data received by the one or more external communicators.
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Accused Products
Abstract
An implantable restriction device is configured to provide a restriction in a patient as a function of the pressure of fluid. The implantable restriction device includes one or more pressure sensors configured to sense pressure of the fluid within the implantable restriction device. Pressure data obtained by the one or more pressure sensors may be communicated to a device located external to the patient, such as a data logger, using telemetry coils or other communicators. The data logger may store the pressure data, and may communicate the pressure data to a remote location via a network such as the Internet. A docking station may be provided to couple the data logger to a network and/or to recharge a cell in the data logger.
1640 Citations
15 Claims
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1. A system for obtaining data from an implanted device, the system comprising:
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(a) an implantable restriction forming device, wherein the implantable restriction forming device is operable to form a restriction in a patient, wherein the implantable restriction forming device comprises an implantable injection port, wherein the implantable injection port defines a fluid reservoir in fluid communication with the implantable restriction forming device, wherein the fluid reservoir of the implantable injection port is configured to receive a fluid, wherein the implantable injection port includes a needle penetrable septum configured to receive a needle for adding fluid to or withdrawing fluid from the fluid reservoir via the needle; (b) an implantable pressure sensor positioned within the implantable injection port of the implantable restriction forming device, wherein the implantable pressure sensor comprises a diaphragm in fluid communication with the fluid reservoir of the implantable injection port and one or more strain gauges connected with the diaphragm, wherein the one or more strain gauges are configured to sense strain in the diaphragm as a function of the pressure of the fluid such that the implantable pressure sensor is operable to sense the pressure of fluid in the fluid reservoir; (c) one or more implantable communicators in communication with the implantable pressure sensor, wherein the one or more implantable communicators are operable to communicate data from within a patient; (d) one or more external communicators in communication with the one or more implantable communicators, wherein the one or more external communicators are operable to externally receive data communicated from within a patient by the one or more implantable communicators; and (e) a storage device in communication with the one or more external communicators, wherein the storage device is operable to store at least a portion of data received by the one or more external communicators. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10)
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11. A system for obtaining data from an implantable restriction forming device, the system comprising:
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(a) a gastric band having an inflatable member, the inflatable member being configured to receive fluid, the gastric band being configured to form a restriction in a patient based on the pressure of fluid in the inflatable member; (b) an implantable injection port in fluid communication with the inflatable member of the gastric band, wherein the implantable injection port includes a needle penetrable septum configured to receive a needle for adjusting an amount of fluid in the inflatable member via the needle; (c) a pressure sensor, wherein the pressure sensor is configured to sense the pressure of fluid in the inflatable member; (d) a TET communicator, wherein the TET communicator is operable to provide power to a device implanted within a patient; (e) a telemetry communicator, wherein the telemetry communicator is operable to transmit data communicated from the one or more implantable pressure sensors located within the implantable restriction forming device; (f) a storage device in communication with the telemetry communicator, wherein the storage device is operable to store data transmitted from the telemetry communicator; (g) a microprocessor in communication with the TET communicator, the telemetry coil, and the storage device, wherein the microprocessor is configured to regulate transmission of data from the telemetry communicator to the storage device; and (h) a patient orientation sensor configured to detect orientation data associated with a patient, wherein the patient orientation sensor is in communication with the microprocessor, wherein the microprocessor is configured to account for hydrostatic effects on the fluid pressure caused by patient orientation as detected by the patient orientation sensor. - View Dependent Claims (12, 13, 14, 15)
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Specification