123 results about "Joint capsule" patented technology

A permanent non-resorbable implant allows surgical replacement of cartilage in articulating joints, using a hydrogel material (such as a synthetic polyacrylonitrile polymer) reinforced by a flexible fibrous matrix. Articulating hydrogel surface(s) are chemically treated to provide a negative electrical charge that emulates the negative charge of natural cartilage, and also can be treated with halogenating, cross-linking, or other chemical agents for greater strength. For meniscal-type implants, the reinforcing matrix can extend out from the peripheral rim of the hydrogel, to allow secure anchoring to soft tissue such as a joint capsule. For bone-anchored implants, a porous anchoring layer enables tissue ingrowth, and a non-planer perforated layer can provide a supportive interface between the hard anchoring material and the softer hydrogel material.

The methods shown provide for the minimization of extravasation during arthroscopic surgery. Use of an anti-extravasation sheath having at least one drainage aperture allows a surgeon to drain excess fluids from the tissue surrounding the surgical field during an arthroscopic surgical procedures when the drainage aperture is disposed within the tissue surrounding an arthroscopic surgical field outside of the joint capsule. The method of performing arthroscopic surgery may further include providing fluid inflow and outflow to the joint capsule through inflow / outflow holes in the anti-extravasation sheath.

A single unit surgical fastener and system and method for repairing torn meniscus tissue in an arthroscopic, all-inside procedure. The desired length of the single unit surgical fastener is first determined by measuring the distance from the interior of the meniscus across the tear and across the joint capsule, and then a single unit surgical fastener of desired length is then inserted across the tear in one or more places through a curved, slotted cannula.

A spine prosthesis is provided and in particular, related to the facet joint of a spine. A spinal implant comprises a facet prosthesis including an insert to be positioned within a joint capsule between facets of a zygapophyseal joint. The insert may comprise a member having two opposing facet interfacing portions. A facet prosthesis exerts a distraction force between facets of a facet joint and may comprise a curable material to be injected into the facet joint. A facet prosthesis may also comprise a pair of magnets, each magnet coupled to a facet and oriented with like poles facing each other to provide a distracting force away from each other. A spine implant may also include an insert to be positioned within the joint capsule, a securing member comprising an elongate portion extending through part of a facet, and an anchor to anchor the securing member to the facet.

Devices, systems and methods are disclosed for repairing soft tissue. The surgical system allows for the creation of tissue repair by grasping, aligning and sewing or fixing tissue. For example, this system may be used for clipping together excessive capsular tissue and reducing the overall capsular volume. The deployment device includes a central grasping mechanism and an outer clip delivery system. The clip embodiments may be single or multi-component (penetration and locking base components) that penetrate tissue layers and deploy or lock to clip the tissue together. An example of the system is used to reduce the joint capsule tissue laxity and reduces the potential for subluxation or dislocation of the joint by either restricting inferior laxity (anterior or posterior) and resolving or eliminating pathologic anterior or posterior translation.

The invention discloses methods and devices for repairing, replacing and / or augmenting natural facet joint surfaces and / or facet capsules. A facet joint restoration device of the invention for use in a restoring a facet joint surface comprises: a cephalad facet joint element comprising a flexible member adapted to engage a first vertebrae and an artificial cephalad joint; and a caudad facet joint element comprising a connector adapted for fixation to a second vertebrae and an artificial caudad joint adapted to engage the cephalad facet joint. In another embodiment, the invention discloses a facet joint replacement device for use in replacing all or a portion of a natural facet joint between a first vertebrae and a second vertebrae comprising: a first cephalad facet joint element having a fixation member adapted to engage a lamina or spinous process of the first vertebrae and a first caudad facet joint element, the first caudad facet joint element comprising a first caudad connector adapted to fixate to the second vertebral body and an artificial caudad facet surface adapted to engage with the cephalad facet joint element.

A method for repairing a facet joint of a human vertebra having a joint capsule surrounding the facet joint. In the method, a synthetic elastic material is introduced into the facet joint. The synthetic elastic material can be a solid, swellable polymer that expands when hydrated upon being placed in the facet joint. The invention includes the implant and the method of making the implant.

A shoulder model and methods of shoulder arthroscopy using the shoulder model. The shoulder model includes an acromioclavicular (AC) joint assembly, a joint capsule assembly, a scapula mount, a shoulder musculature, a skin, and a base. The AC joint assembly is mounted on the scapula mount and the joint assembly is attached to the AC joint assembly and fastened using a screw / nut to form the shoulder assembly. The shoulder assembly is placed in the shoulder musculature and the skin is rolled over the shoulder musculature and zipped in place. The bones of the shoulder assembly are made of foam-cortical shell, the shoulder musculature is made of foam, the soft tissue components are made of thermoplastic elastomers, and the skin is made of vinyl. A method of practicing shoulder arthroscopy using the shoulder model includes mounting the shoulder model in a beach chair position, making anatomical references, establishing a posterior viewing portal, inserting cannulas into the glenohumeral joint or the subacromial space, creating a labral disruption or a rotator cuff tear, and repairing the rotator cuff tear or labral disruption.

Instrumentation and a method for resurfacing a joint capsule having cartilage and meniscal surfaces such as a knee joint includes resecting a central portion of the joint cartilage on one joint member such as the tibia while leaving a meniscal rim attached to the peripheral joint capsule. A cavity is then formed in the bone underlying the central portion of the joint surface such as the lateral tibial surface. A resurfacing implant is then coupled, by cementing for example, to the cavity. A soft prosthetic meniscal implant is then coupled to the remaining meniscal ring such as by suturing.

A spine prosthesis is provided and in particular, related to the facet joint of a spine. A spinal implant comprises a facet prosthesis including an insert to be positioned within a joint capsule between facets of a zygapophyseal joint. The insert may comprise a member having two opposing facet interfacing portions. A facet prosthesis exerts a distraction force between facets of a facet joint and may comprise a curable material to be injected into the facet joint. A facet prosthesis may also comprise a pair of magnets, each magnet coupled to a facet and oriented with like poles facing each other to provide a distracting force away from each other. A spine implant may also include an insert to be positioned within the joint capsule, a securing member comprising an elongate portion extending through part of a facet, and an anchor to anchor the securing member to the facet.

An implantable medical device for treating the back of a patient. Stimulation energy is delivered to muscles or joint capsules or ligaments or nerve fibers to improve the heath of the back.

An implantable medical device for treating the back of a patient. Stimulation energy is delivered to muscles or joint capsules or ligaments or nerve fibers to improve the heath of the back.

Various methods for treating a joint are disclosed herein. According to one method, a joint is surgically treated by performing a surgical repair treatment on tissue within the joint capsule; implanting a load reducing device at the joint and entirely outside of the joint capsule to reduce load transmitted by the treated tissue to allow for the tissue within the joint capsule to heal; and partially unloading the joint during healing of the surgical repair site.

The invention discloses methods, devices, systems and kits for repairing, replacing and / or augmenting natural facet joint surfaces and / or facet capsules. An implantable facet joint device of one embodiment comprises a cephalad facet joint element and a caudal facet joint element. The cephalad facet joint element includes a member adapted to engage a first vertebra, and an artificial cephalad bearing member. The caudal facet joint element includes a connector adapted for fixation to a second vertebra at a fixation point and an artificial caudal bearing member adapted to engage the cephalad bearing member. The artificial caudal bearing member is adapted for a location lateral to the fixation point. In another embodiment, an implantable facet joint device comprises a cephalad crossbar adapted to extend mediolaterally relative to a spine of a patient, the crossbar having opposite first and second ends, a connector element adapted to connect the crossbar to a first vertebra, a first artificial cephalad bearing member adapted for connection to the first end of the crossbar and adapted to engage a first caudal facet joint element connected to a second vertebra, and a second artificial cephalad bearing member adapted for connection to the second end of the crossbar and adapted to engage a second caudal facet joint element connected to the second vertebra. In yet another embodiment, an implantable facet joint device comprises a caudal cross-member adapted to extend mediolaterally relative to a spine of a patient and adapted to connect to a first vertebra, a first artificial caudal bearing member adapted for connection to the caudal cross-member, and adapted to engage a first cephalad facet joint element connected to a second vertebra, and a second artificial caudal bearing member adapted for connection to the caudal cross-member at a predetermined spacing from the first bearing member, the second bearing member being adapted to engage a second caudal facet joint element connected to the second vertebra.

Orthopedic implants having a bone interface member and a water swellable IPN or semi-IPN with a stiffness, hydration, and / or compositional gradient from one side to the other and physically attached to the bone interface member. The invention also includes an orthopedic implant system including an implant that may conform to a bone surface and a joint capsule. The invention also includes orthopedic implants with water swellable IPN or semi-IPNs including a hydrophobic thermoset or thermoplastic polymer first network and an ionic polymer second network, joint capsules, labral components, and bone interface members. The invention also includes a method of inserting an orthopedic implant having a metal portion and a flexible polymer portion into a joint, including inserting the implant in a joint in a first shape and changing the implant from a first shape to a second shape to conform to a shape of a bone.

A shoulder model and methods of shoulder arthroscopy using the shoulder model. The shoulder model includes an acromioclavicular (AC) joint assembly, a joint capsule assembly, a scapula mount, a shoulder musculature, a skin, and a base. The AC joint assembly is mounted on the scapula mount and the joint assembly is attached to the AC joint assembly and fastened using a screw / nut to form the shoulder assembly. The shoulder assembly is placed in the shoulder musculature and the skin is rolled over the shoulder musculature and zipped in place. The bones of the shoulder assembly are made of foam-cortical shell, the shoulder musculature is made of foam, the soft tissue components are made of thermoplastic elastomers, and the skin is made of vinyl. A method of practicing shoulder arthroscopy using the shoulder model includes mounting the shoulder model in a beach chair position, making anatomical references, establishing a posterior viewing portal, inserting cannulas into the glenohumeral joint or the subacromial space, creating a labral disruption or a rotator cuff tear, and repairing the rotator cuff tear or labral disruption.

An automated method for detecting a disease state is presented. The method includes identifying a bone surface in one or more image data sets, wherein the one or more data sets correspond to a region of interest in an object of interest. Furthermore, the method includes segmenting a joint capsule region corresponding to the one or more image data sets based on a corresponding identified bone surface. In addition, the method includes analyzing the segmented joint capsule region to identify the disease state. Systems and non-transitory computer readable medium configured to perform the automated method for detecting a disease state are also presented.

Devices, systems and methods are disclosed for repairing soft tissue. The surgical system allows for the creation of tissue repair by grasping, aligning and sewing or fixing tissue. For example, this system may be used for clipping together excessive capsular tissue and reducing the overall capsular volume. The deployment device includes a central grasping mechanism and an outer clip delivery system. The clip embodiments may be single or multi-component (penetration and locking base components) that penetrate tissue layers and deploy or lock to clip the tissue together. An example of the system is used to reduce the joint capsule tissue laxity and reduces the potential for subluxation or dislocation of the joint by either restricting inferior laxity (anterior or posterior) and resolving or eliminating pathologic anterior or posterior translation.

A surgical procedure for replacing a destructed hip joint with an artificial joint is disclosed. The present invention provides a two-incision minimally invasive surgery for total hip arthroplasty. This method comprises positioning of the patient on a lateral decubitus position and a series of surgical techniques including a first skin incision over the anterior side of the trochanteric area of the femur (ranging from 3 cm to 10 cm), intermuscular dissection between the Gluteus muscle (Gluteus minimus and medius) and Tensor fascia lata muscle, incision of the anterior joint capsule, osteotomy of the femoral neck, removal of the femoral head and neck, acetabular reaming and socket insertion, secondary skin incision over the Gluteus maximus muscle (ranging from 1 cm to 6 cm), dissection through the muscle fiber of the Gluteus maximus, intermuscular dissection between the Gluteus medius and Piriformis, partial incision of the joint capsule, femoral reaming, femoral stem insertion, femoral head insertion, joint capsule closure and skin closure.

A surgical procedure for replacing a destructed hip joint with an artificial joint is disclosed. The present invention provides a two-incision minimally invasive surgery for total hip arthroplasty. This method comprises positioning of the patient on a lateral decubitus position and a series of surgical techniques including a first skin incision over the anterior side of the trochanteric area of the femur (ranging from 3 cm to 10 cm), intermuscular dissection between the Gluteus muscle (Gluteus minimus and medius) and Tensor fascia lata muscle, incision of the anterior joint capsule, osteotomy of the femoral neck, removal of the femoral head and neck, acetabular reaming and socket insertion, secondary skin incision over the Gluteus maximus muscle (ranging from 1 cm to 6 cm), dissection through the muscle fiber of the Gluteus maximus, intermuscular dissection between the Gluteus medius and Piriformis, partial incision of the joint capsule, femoral reaming, femoral stem insertion, femoral head insertion, joint capsule closure and skin closure.

A surgical instrument particularly suited to endoscopic use articulates an end effector by including a fluid transfer articulation mechanism that is proximally controlled. A fluid control, which is attached to a proximal portion, transfers fluid through the elongate shaft through a first fluid passage to a first fluid actuator that responds by articulating an articulation joint. Two opposing fluid actuators may respond to differential fluid transfer to effect articulation. Thereby, design flexibility is achieved by avoiding the design constraints of transferring a mechanical motion through the tight confines of the elongate shaft sufficient to effect articulation.

An automated method for detecting a disease state is presented. The method includes identifying a bone surface in one or more image data sets, wherein the one or more data sets correspond to a region of interest in an object of interest. Furthermore, the method includes segmenting a joint capsule region corresponding to the one or more image data sets based on a corresponding identified bone surface. In addition, the method includes analyzing the segmented joint capsule region to identify the disease state. Systems and non-transitory computer readable medium configured to perform the automated method for detecting a disease state are also presented.

Various methods for treating a joint are disclosed herein. According to one method, a joint is surgically treated by performing a surgical repair treatment on tissue within the joint capsule; implanting a load reducing device at the joint and entirely outside of the joint capsule to reduce load transmitted by the treated tissue to allow for the tissue within the joint capsule to heal; and partially unloading the joint during healing of the surgical repair site.

Configurations are described for conducting minimally invasive medical diagnoses and interventions utilizing elongate instruments and assemblies comprising one or more imaging devices, and one or more remote retraction and distraction devices. Retraction and distraction devices, such as balloons, mechanical retraction members, and / or trocar screw geometries may be utilized to access, investigate, and intervene at the joint capsule, or inside of the joint capsule. Imaging devices, such as optical image capture devices, ultrasound transducers, and optical coherence tomography fibers, may be utilized to assist with navigation of the pertinent tools during diagnostic and interventional steps.

A corrective element for the articulation between the femur and the pelvis, comprising a contoured body that can be inserted, without dislocation of the head of the femur, in the iliac acetabular region after incision of the articular capsule; the contoured body has a smooth outer surface that is substantially adapted to the iliac acetabular region and an inner surface that forms a seat for accommodating the femur head.

The present invention comprises methods and systems / devices for non-invasively measuring baseline collagen and collagen changes during treatment of tissue, e.g., denaturation by the application of RF energy, through linear dichroism, circular dichroism, or birefringence. The invention optionally uses polarization sensitive optical measurements to discriminate between denaturation of unidirectionally oriented strands of collagen, such as a ligament or tendon, and denaturation of planar collagen surfaces, such as the dermal layer of the skin or collagen in joint capsules.

Medical implants and methods useful in treating postoperative pain are described. The implants comprise one or more electrospun drug-loaded fibers, which fibers comprise a drug useful in the treatment of pain. The implants are implanted at sites of interest including joint capsules, bones, and subcutaneous spaces, and are secured with tissue flaps or fasteners.

Disclosed are novel methods of maintaining articular cartilage health in an atraumatic, non-diseased joint of a mammal, either human or non-human. The methods involve injecting into the joint capsule of the mammal an amount of a lubricin polypeptide to prevent shear-induced chondrocyte apoptosis and to maintain a lubricin-expressing phenotype of chondrocytes.