269results about How to "Minimize injury" patented technology

Methods and devices for maintaining a space-occupying device in a fixed relationship relative to a patient's stomach by manipulation of the stomach. In one variation, two or more regions of the stomach wall are brought into appromixation with one another and secured together in a manner that secures a space-occupying device within the stomach of the patient. In another variation, two or more regions of the stomach wall are wrapped around a space-occupying device to maintain the position of the space-occupying device relative to the stomach wall. In another variation, a system having a space-occupying member and a locking member capable holding the space-occupying member against the inner wall of the stomach are provided. In a further variation, a pouch is created within the stomach that receives and retains a space-occupying device.

Devices, systems, and method for treating urinary incontinence generally rely on energy delivered to a patient's own pelvic support tissue to selectively contract or shrink at least a portion of that pelvic support tissue so as to reposition the bladder. The energy will preferably be applied to the endopelvic fascia and / or an arcus tendineus fascia pelvis. The invention provides a variety of devices and methods for applying gentle resistive heating of these and other tissues to cause them to contract without imposing significant injury on the surrounding tissue structures. Alternatively, heat-applying probes are configured to heat tissue structures which comprise or support a patient's urethra. By applying sufficient energy over a predetermined time, the tissue can be raised to a temperature which results in contraction without significant necrosis or other tissue damage. By selectively contracting the support tissues, the bladder neck, sphincter, and other components of the urinary tract responsible for the control of urinary flow can be reconfigured or supported in a manner which reduces urinary leakage.

A flexible spinal fixation device having a flexible metallic connection unit for non-rigid stabilization of the spinal column. In one embodiment, the fixation device includes at least two securing members configured to be inserted into respective adjacent spinal pedicles, each securing member each including a coupling assembly. The fixation device further includes a flexible metal connection unit configured to be received and secured within the coupling assemblies of each securing member so as to flexibly stabilize the affected area of the spine.

A flexible spinal fixation device having a flexible connection unit for non-rigid stabilization of the spinal column. In one embodiment, the fixation device includes at least two securing members configured to be inserted into respective adjacent spinal pedicles, each securing member each including a coupling assembly. The fixation device further includes a flexible connection unit configured to be received and secured within the coupling assemblies of each securing member so as to flexibly stabilize the affected area of the spine.

Methods are provided herein for affecting a region of a subject's body, comprising exposing the region to a cooling element under conditions effective to cool subcutaneous adipose tissue in said region; and increasing the blood flow rate to the cooled tissue by exposing the tissue to an energy source. Methods are also provided for treating subcutaneous adipose tissue in a region of a subject's body, comprising exposing said region to a cooling element under conditions effective to cool said tissue; and exposing the tissue to an energy source to increase the blood flow rate to the cooled tissue, thereby stimulating reperfusion in, and / or causing an ischemia-reperfusion injury to, the cooled tissue.

Methods and devices for maintaining a space-occupying device in a fixed relationship relative to a patient's stomach by manipulation of the stomach. In one variation, two or more regions of the stomach wall are brought into approximation with one another and secured together in a manner that secures a space-occupying device within the stomach of the patient. In another variation, two or more regions of the stomach wall are wrapped around a space-occupying device to maintain the position of the space-occupying device relative to the stomach wall. In another variation, a system having a space-occupying member and a locking member capable holding the space-occupying member against the inner wall of the stomach are provided. In a further variation, a pouch is created within the stomach that receives and retains a space-occupying device.

A method of repairing a defect in an annulus fibrosus of an intervertebral disc, without excising the entire nucleus pulposus of the disc. The method includes inserting an introducer needle through the annulus fibrosus by puncturing the annulus fibrosus with the introducer needle, injecting an in situ curable, bio-compatible polymerizable or polymeric material composition into the disc through the introducer needle directly or indirectly so that the in situ curable composition contacts a defect in the annulus fibrosus; and curing said material in situ.

A minimally invasive orthopedic bone attachment system comprising a pedicle screw and guide support sleeve for insertion of the screw. The pedicle screw is a self-boring, self-tapping integral screw having a distal sharply pointed end for guiding the insertion of the screw as well as forming a borehole for the self-tapping threads of the screw. The proximal end of the screw provides a cylindrical extension which can include a recess for receiving a rotational drive tool or wrench. The length of the threads and the type of threads provided in the screw are designed for the type of orthopedic surgery that is intended. A relatively thin hollow support sleeve including an internal threaded section in the distal end is provided to match the threads and the length of the threaded portion of the pedicle screw. The proximal end of the sleeve includes a central passageway having an internal diameter that can receive the extension portion of the screw and also guide and receive a drive device for the screw. A retainer clip associated with circumferential slots spacedly indexed along the longitudinal surface of the drive device can be used to limit the depth of the screw upon insertion as well as to lock the drive device as an assembly with the screw and sleeve to form the attachment system. A small diameter passageway can be provided along the longitudinal axis of the assembly extending from the proximal end of the drive device through the screw to exit through the pointed distal end of the screw. A thin rigid rod having a point at the distal end is slidably positioned within the narrow passageway. The proximal end of the road includes a cap. A flange surface on the under portion of the cap limits the travel of the rod through the assembly. The length of the rod is determined so that it equals the length of the assembly plus an additional dimension corresponding to the anticipated installed depth of the screw. Prior to insertion of the screw, the rod is driven into the bone through the assembly. The location of the rod is ascertained by an image guidance system to determine the correct final projected location of the screw upon installation.

Disclosed are a means and method for rapidly and accurately positioning a toroidal balloon with its distal surface placed tightly against the endocardial surface of the left atrium at a location that is close to the ostium of a pulmonary vein. On the exterior surface of the toroidal balloon can be an electrically conducting wire that is capable of causing rf energy to be placed into the tissue of the left atrium so as to ablate that tissue to alter the conduction of aberrant electrical signals of the heart that are associated with atrial fibrillation. The toroidal balloon is wrapped circumferentially around a tapered balloon that is placed into the pulmonary vein. This system can be applied successively to at least one or as many as all four of the pulmonary veins that enter the left atrium to treat the patient's atrial fibrillation.

A balloon catheter having a multi-layered balloon which has a first layer and at least a second layer, and which has noncompliant limited radial expansion beyond the nominal diameter of the balloon. By selecting the polymeric materials forming the balloon layers, and arranging and radially expanding the multiple layers of the balloon in accordance with the invention, a balloon is provided having an improved low compliance, preferably in combination with high flexibility and softness.

Methods are provided herein for affecting a region of a subject's body, comprising exposing the region to a cooling element under conditions effective to cool subcutaneous adipose tissue in said region; and increasing the blood flow rate to the cooled tissue by exposing the tissue to an energy source. Methods are also provided for treating subcutaneous adipose tissue in a region of a subject's body, comprising exposing said region to a cooling element under conditions effective to cool said tissue; and exposing the tissue to an energy source to increase the blood flow rate to the cooled tissue, thereby stimulating reperfusion in, and / or causing an ischemia-reperfusion injury to, the cooled tissue.

A sphincter treatment apparatus includes an elongated member having at least one lumen including an inflation lumen and a basket assembly with first and second arms. The basket assembly is coupled to the elongated member and has deployed and non-deployed configurations. An inflatable member is coupled to the elongated member and positioned in an interior of the basket assembly. The inflatable member has deployed and non-deployed states and is coupled to the inflation lumen. In the deployed state, the inflatable member expands the basket assembly to its deployed configuration. A first energy delivery device is positionable in the first arm and advanceable from the first arm to a selected treatment site. A second energy delivery device is positionable in the second arm and advanceable from the second arm to a selected treatment site.

An adjustable spinal stabilization system having a flexible connection unit for non-rigid stabilization of the spinal column. In one embodiment, the spinal stabilization system includes a flexible connection unit having a tether running through a hollow portion of the flexible connection unit, wherein the tether limits bending of the flexible connection unit. In a further embodiment the tether is pre-tensioned. In a further embodiment, the tension upon or compression of the tether is adjustable.

An article of cleated footwear comprises an upper for holding a foot of a wearer to a sole having an outsole plate. The outsole plate includes a predetermined first metatarsal region that generally overlies the respective skeletal structure of a human foot. Several ground engaging members extend downwardly from the outsole plate to provide traction on a ground surface. The outsole plate includes a downwardly extending metatarsal head cradle located on a lateral side and a medial side of the first metatarsal region to reduce stud pressure and provide traction control. The outsole plate may include a distal phalanx region and a predetermined proximal phalanx region. A first ground engaging member is located in the distal phalanx region and a second ground engaging member is located in the proximal phalanx region for toe off movements.

A wireless system that detects the presence of a child in a safety seat located in the passenger cabin of a vehicle includes a controller responsive to signals generated by sensors monitoring predefined functions of the vehicle, RFID tag device attached to the safety seat and RFID tag reader mounted in the cabin. The system generates control signals which activate an alarm, open the doors of the vehicle and roll down windows if the child is left in the safety seat of an unattended vehicle.

A sphincter treatment apparatus includes an energy delivery device introduction member including a proximal end with a first radius of curvature and a distal end with a second radius of curvature. The introduction member is configured to be introduced into the sphincter in a non-deployed state and to be expanded to a deployed state to at least partially expand the sphincter or an adjoining structure. An energy delivery device is coupled to the introduction member. A retainer member is coupled to the energy delivery device introduction member and configured to controllably position the introduction member in an orifice of the sphincter.

A method, computer program product and apparatus for minimizing occupant injury by optimizing occupant restraint properties and / or actions in real time, during pre-crash and crash phases. The restraint system uses three catalogs and a database linking these catalogs. The catalogs include a catalog of possible occupant states, a catalog of possible collision scenarios, and a catalog of potential restraint control laws. The database is an assessment of injury outcome for each possible combination of occupant state, collision scenario, and restraint control law. In addition to the catalogs, the method requires four computational components: an occupant identifier, a collision identifier, a restraint law optimizer, and a restraint controller.

Devices, systems, and method for treating urinary incontinence generally rely on energy delivered to a patient's own pelvic support tissue to selectively contract or shrink at least a portion of that pelvic support tissue so as to reposition the bladder. The energy will preferably be applied to the endopelvic fascia and / or an arcus tendineus fascia pelvis. The invention provides a variety of devices and methods for applying gentle resistive heating of these and other tissues to cause them to contract without imposing significant injury on the surrounding tissue structures. Alternatively, heat-applying probes are configured to heat tissue structures which comprise or support a patient's urethra. By applying sufficient energy over a predetermined time, the tissue can be raised to a temperature which results in contraction without significant necrosis or other tissue damage. By selectively contracting the support tissues, the bladder neck, sphincter, and other components of the urinary tract responsible for the control of urinary flow can be reconfigured or supported in a manner which reduces urinary leakage.

An article of footwear includes an upper for holding a foot of a wearer and a sole having an outsole plate. Several ground engaging members extends downwardly from the outsole plate to provide traction. The outsole plate includes a flex control member composed of a superelastic shape memory material or a nickel-titanium alloy. The flex control member can be coupled to an inside surface, or bottom surface of the outsole plate. The outsole plate may include a rearfoot region, a midfoot region, and a first metatarsal head region, in which the regions generally correspond to the skeletal structure of a human foot. The flex control member extends from a medial side of the rearfoot region through the midfoot region and into the first metatarsal head region of the outsole plate. The ground engaging members may be positioned to extend from the location of the flex control member.

Devices and methods are disclosed for providing a sensing element to scan tissue and detect the presence of structures within the tissue to avoid the structures when performing a procedure on the tissue. A catheter includes a blood vessel sensing assembly and a working lumen adapted to receive a medical appliance or instrument for performing various medical procedures.

An improved cold / compress therapy for the treatment of muscle, tissue, tendon, or cartilage injury or damage. The ICE Power Pack consists of a plurality of hollow vessels filled with water or aqueous solutions or colloids that can be solidified in a conventional domestic or commercial freezer. The encapsulated water or aqueous solutions or colloids rely on the high latent heat of fusion as they undergo a phase change providing an extended therapeutic period in a medically safe temperature zone. The vessels are sandwiched between flexible insulating and non-insulating layers that serve as compresses.

If an impact occurs with an impact energy which exceeds an elastic limit of a bumper while a shock-absorbing member is in a projected position, a bumper stay is forced to move rearward along a first actuating chamber to cause the shock-absorbing member to pivot to a received position. The impact energy is primarily absorbed by an elastic force of a first spring which biases the shock-absorbing member toward the projected position. When the impact energy is not thoroughly absorbed by the first spring, the shock-absorbing member fully pivots into its received position by the bumper stay which is continuously moved rearward. At this time, a second spring which biases the shock-absorbing member forward and is prevented from being stretched forward by the shock-absorbing member, is contacted with the bumper stay via a support plate. Accordingly, the second spring secondarily absorbs the impact energy while being more compressed by the bumper stay which continuously moves rearward after causing the shock-absorbing member to fully pivot to its received position.

A sphincter treatment apparatus includes an energy delivery device introduction member including a proximal end with a first radius of curvature and a distal end with a second radius of curvature. The introduction member is configured to be introduced into the sphincter in a non-deployed state and to be expanded to a deployed state to at least partially expand the sphincter or an adjoining structure. An energy delivery device is coupled to the introduction member. A retainer member is coupled to the energy delivery device introduction member and configured to controllably position the introduction member in an orifice of the sphincter.

Disclosed are device for promoting the clotting of blood comprising a clay material and a release agent. In some embodiments, the clay material is disposed within a substrate and the release agent is disposed within a mesh. The release agent can be configured to make direct contact with a bleeding wound when the device is in particle form and the clay material can promote hemostasis.