1549results about How to "Reduce exercise" patented technology

In various embodiments of the present invention, a piece of buttress material can be configured to match a curved profile of the anvil and / or staple cartridge of a surgical stapler. In at least one embodiment, the piece of buttress material can include first and second edges extending between first and second ends. In these embodiments, the first edge can be defined by a first radius of curvature and the second edge can be defined by a second radius of curvature wherein the second radius of curvature is larger than the first radius of curvature. In at least one embodiment, the anvil and / or staple cartridge can include a surface configured for receiving a piece of buttress material thereon and a lip which at least partially extends along the periphery thereof wherein the lip can be configured to reduce relative movement between the piece of buttress material and the surface.

A stent valve insertable in a body vessel containing a body fluid. The stent valve includes: a valve for at least partially controlling the flow of the body fluid in the body vessel; and a scaffold, the scaffold including : an anchoring section for anchoring the scaffold to said body vessel and a valve supporting section supporting the valve. The scaffold is substantially radially expandable from a scaffold retracted configuration to a scaffold expanded configuration. The valve supporting section is expandable over a greater range of radial expansion than the anchoring section.

An adaptive alarm system is responsive to a physiological parameter so as to generate an alarm threshold that adapts to baseline drift in the parameter and reduce false alarms without a corresponding increase in missed true alarms. The adaptive alarm system has a parameter derived from a physiological measurement system using a sensor in communication with a living being. A baseline processor calculates a parameter baseline from a parameter trend. Parameter limits specify an allowable range of the parameter. An adaptive threshold processor calculates an adaptive threshold from the parameter baseline and the parameter limits. An alarm generator is responsive to the parameter and the adaptive threshold so as to trigger an alarm indicative of the parameter crossing the adaptive threshold. The adaptive threshold is responsive to the parameter baseline so as to increase in value as the parameter baseline drifts to a higher parameter value and to decrease in value as the parameter baseline drifts to a lower parameter value.

A self-powered medical device, for example a pacemaker uses the variations of blood pressure inside the heart or a major artery to create a mechanical resonance in an electromagnetic or piezoelectric generator. The resonance extends the time power is generated during the cardiac cycle. The pressure variations compress a bellows carrying the resonant generator. The inside of the bellows may be evacuated to a partial or full vacuum, and a spring restores the bellows to the desired equilibrium point, acting against the blood pressure. The current pulses are stored in a capacitor. Eliminating the battery allows dramatic miniaturization of the medical device to the point it can be implanted at the point of desired stimulation via a catheter.

Some embodiments of the present invention provide stimulation systems and components for selective stimulation and / or neuromodulation of one or more nerve root ganglia through implantation of an electrode on, in or around a nerve root ganglia. Some other embodiments of the present invention provide methods for selective neurostimulation of one or more dorsal root ganglia as well as techniques for applying neurostimulation to the spinal cord. Still other embodiments of the present invention provide stimulation systems and components for selective stimulation and / or neuromodulation of one or more nerve root ganglia through implantation of an electrode on, in or around a nerve root ganglia in combination with a pharmacological agent.

The invention is directed to a trocar assembly having a channel defined along an elongate axis, the trocar assembly being adapted to receive a surgical instrument, the trocar assembly comprising a septum seal disposed in the channel including a seal tip having a proximal facing surface, the seal tip including portions defining an orifice; and a septum shield including a tubular member having a proximal end and a distal end, and a plurality of blades or leaflets protruding distally from the distal end of the tubular member, the septum shield being placed inside the septum seal such that the blades engage the proximal facing surface of the seal tip. The trocar assembly may further comprise a zero closure seal such as a double duckbill valve disposed in the channel outside of the septum seal. The septum shield operates to reduce the drag force and to minimize axial movement of the septum shield and the instrument during insertion and removal of the instrument through the septum seal. The septum shield may be formed from a rigid plastic material, and the septum seal may be formed of an elastomeric material. The blades or leaflets may overlap or offset one another. The orifice may be expandable to accommodate the instrument having a diameter of about 5-15 mm. The blades or leaflets have distal tips that glide or roll against the instrument during placement of the instrument. The distal tips may comprise of a combination of material, durometer and shield geometry to control the behavior of the septum shield. The trocar assembly may further comprise a second septum shield disposed outside of the septum seal.

Methods and devices for partitioning or plicating a region of a hollow body organ are described herein. These methods and devices relate generally to medical apparatus and methods and more particularly to devices and methods for affecting a change in the function of a hollow body organ, particularly a stomach, intestine or gastrointestinal tract. These changes can include reducing the volume capacity of the hollow body organ, disrupting or altering the normal function of the organ, functionally excluding certain sections of the organ either by affixing adjacent tissue or excising certain regions, or affecting or correcting the response of the organ to naturally occurring stimuli, such as ingestion.

An apparatus for sensing at least one physiological parameter of a patient and transmitting data related to the sensed physiological parameter to an external device. The apparatus comprises a detecting portion comprising at least one sensor interconnected with a connector, an acquisition portion comprising a connector interface configured to receive the connector, electronics for controlling the at least one sensor via the connector interface, receiving data related to the at least one physiological parameter from the at least one sensor via the connector interface and processing the received data, and a wireless interface for transmitting the processed data to the external device, and a power source for supplying energy to the acquisition module.

A capsule type medical device is of a type of a capsule type medical device that is introduced inside the living body to gather in-vivo information, and comprises a capsule shaped casing; an in-vivo information acquisition device for acquiring the in-vivo information; a communication device for sending the in-vivo information acquired by the in-vivo information acquisition device to outside of the living body by wireless; at least one pair of first electrodes provided in a vicinity of one end along an axis of the casing for giving electric stimulation to body tissue in the living body; a first current control device for sending current to the first electrodes; and an interelectrode distance variation device for changing a distance between the electrodes.

A rotating irradiation apparatus includes a rotating gantry 3 including a front ring 19 and a rear ring 20 and is provided with a beam delivery device 11 and an irradiation device 4. The beam delivery device 11 delivers an ion beam used for particle radiotherapy. Radial support devices 61A and 61B support the front ring 19 and radial support devices 61A and 61B support the rear ring 20. Each radial support device includes a linear guide 41, an upper support structure disposed above the linear guide 41, and a lower support structure disposed below the linear guide 41. The upper support structure is movably mounted on the lower support structure and is movable in the direction of the rotational axis of the rotating gantry 3.

Systems and related methods control movement of an end effector. A method of controlling movement of an end effector includes receiving, by a controller, a command to close or open an end effector that includes a first jaw member, a second jaw member, a wrist, and an instrument shaft. In response to the command, the controller controls movement of the end effector to simultaneously move the first jaw member relative to the second jaw member and actuate the wrist to orient the end effector so that at least one of a position and an orientation of a reference aspect of the end effector is substantially maintained in space.

Methods and apparatus are provided for repairing or replacing a defective cardiac valve including an anchor having a double helix configured to engage the cardiac valve leaflets of a diseased or defective cardiac valve, and a replacement valve body disposed in an expandable stent configured to be disposed within the anchor so that the anchor limits expansion of the expandable stent. The expandable stent of the replacement valve body may be self-expanding or mechanically expanded, e.g., using a balloon catheter or catheter-based mandrel and the valve body may be formed of animal tissue or a synthetic fabric.

Some embodiments of the present invention provide neurostimulation systems and components for selective stimulation and / or neuromodulation of one or more dorsal root ganglia through implantation of an electrode on, in or around a dorsal root ganglia. Some other embodiments of the present invention provide neurostimulation systems adapted for selective neurostimulation of one or more nerve root ganglia as well as techniques for applying neurostimulation to the spinal cord. Still other embodiments of the present invention provide stimulation systems and components for selective stimulation and / or neuromodulation of one or more dorsal root ganglia through implantation of an electrode on, in or around a dorsal root ganglia in combination with a pharmacological agent.

The present invention provides articles of footwear adapted for use in extreme and hazardous environments by members of the military, law enforcement personnel and others who require durable and functional footwear. The footwear include protective coverings that may be proof, puncture proof, fire retardant or water repelling. Drainage holes can be positioned in the toe region and along the outsole to enable a wearer to quickly drain water from the article of footwear. Single use or replaceable drainage plugs may cover the holes to prevent entry of water into the boot or other article of footwear. Removable and / or replaceable footbeds may be employed, and such footbeds may provide adjustable sizing of the article of footwear using interchangeable cartridges. A support saddle may be employed with the footbed to enhance foot support under heavy loads. These and other features herein are suited for use in a wide variety of footwear.

An ergometry belt particularly for use in ergometry (ECG stress test) is disclosed. The ergometry belt—according to the present invention—made of a flexible and stretchable material, a plurality of electrodes disposed on the ergometry belt so that stretching of the belt will locate the electrodes in predetermined locations, a plurality of conductors adapted to be connected to a respective electrode, and a cable connected at one end thereof to each conductor and at another end thereof adapted to be connected to an ECG measuring device.

The stent of the present invention combines a helical strut band interconnected by coil elements. This structure provides a combination of attributes that are desirable in a stent, such as, for example, substantial flexibility, stability in supporting a vessel lumen, cell size and radial strength. The structure of the stent of the present invention provides a predetermined geometric relationship between the helical strut band and interconnected coil.

An electronically-controlled roll-up window shade that can easily be installed by a homeowner or general handyman is disclosed. The motorized shade includes an internal power source, a motor, and a communication system to allow for remote control of the motorized shade. One or more motorized shades can be controlled singly or as a group. In one embodiment, the motorized shades are used in connection with a zoned or non-zoned HVAC system to reduce energy usage. In one embodiment, the motorized shade is configured to have a size and form-factor that conforms to a standard manually-controlled motorized shade. In one embodiment, a group controller is configured to provide thermostat information to the motorized shade. In one embodiment, the group controller communicates with a central monitoring system that coordinates operation of one or more motorized shades. In one embodiment, the internal power source of the motorized shade is recharged by a solar cell.

A stabilizer for an optical device that forms part of an electronic device may include a platform that has an optical device mounted thereon. A gimbal mount may retain the platform so that the platform is pivotal about a first axis and the gimbal mount being further pivotal about a second axis so that the optical device is pivotal about both the first and second axes. A first actuator may be controlled to manage movement of the optical device about the first axis and a second actuator may be controlled to manage movement of the optical device about the second axis.

Catheters having selectively insertable or selectively activatable and releasable stiffening mechanisms are provided. In general, the catheter is inserted, navigated and withdrawn from a subject in a relaxed, flexible condition and stiffening mechanisms are deployed to prevent the catheter from shifting during placement or operation of an accessory device or tool through the catheter. Stiffening members(s) may be inserted into and removed from one or more longitudinal channel(s) provided in proximity to the catheter wall and generally coaxial with the primary catheter lumen to change the stiffness properties of the catheter. The properties, configuration and size of the stiffening members and channels may be varied to vary the stiffness properties of the catheter and stiffening members may be constructed from materials having shape change properties or materials that change conformation or stiffness with application of heat, current or electrical field. Stiffening mechanisms may also employ energy absorbing and viscoelastic polymer materials having variable stiffness properties depending on ambient conditions.

A catheter with valve for implantation in a vascular structure of a living being. The catheter is in the general shape of a "T" with the top of the "T" implanted within the lumen of a vascular structure, and the leg of the "T" extending out of the vascular structure through an incision in the vascular structure. The lumen of the implanted portion of the catheter completely occupies the lumen of the vascular structure, causing all blood flow through the vascular structure to be directed through the implanted portion of the catheter. A valve is placed in the wall of the implanted portion of the catheter which opens into the lumen of the leg of the "T" of the catheter upon application of sufficient differential pressure between the lumens of the two portions of the catheter. The leg of the "T" is connected to the side wall of the implant portion of the catheter at an angle, such that the axis of the lumen of the leg of the "T" intersects the axis of the lumen of the implanted portion of the catheter at approximately a 45 degree angle.