389 results about "Hernia" patented technology

A method of tracking the location of a hernia defect is disclosed, the method including providing a display device, a camera adapted to transmit an image to the display device, a marking surface disposed on the display device and a marker adapted to alter the marking surface when applied to the marking surface. The method includes receiving an image of a hernia defect from the camera and displaying the received image on the display device and marking the shape and position of the hernia defect on the marking surface by applying the marker to the marking surface. Alternatively the display device may be marked by executing by the processor a computer program to mark the shape and position of the hernia defect on the display device.

Provided herein is a device and system for measuring an object geometry. The device comprises a probe with contacting and tracking ends and a tracking means and actuation control unit positioned on the probe. The system further comprises a measurement and post processing unit in electronic communication with the tracking means and / or the actuation control unit. Also provided is a method for measuring a geometry of an anatomic object, for example, a hernia. One or more locations of interest on the object are touched directly with the contacting probe end and the location or motion data of the probe end and of the tracking means are tracked and transmitted to the measurement and post processing unit as the point(s) of interest are touched. The data is processed into the geometric measurement and a representative image may be displayed.

A surgical prosthesis including a sheet formed of one or more layers of a thin flexible material suitable to promote or prevent biological tissue adherence thereto and a grid formed of intersecting lines provided on at least one main surface of the sheet. The grid helps the surgeon trim the prosthesis to proper size, deploy the prostheses into optimal position and fix the prosthesis with optimal alignment and tension. The prosthesis may be used as a hernia patch.

Methods and devices are provided for effecting movement of one or more components of a multifire device, such as a clip applier, hernia tacker, or skin stapler. In one exemplary embodiment, a surgical fastening instrument is provided having an elongate shaft with an end effector coupled thereto and adapted to apply one or more surgical fasteners to tissue. An electrically expandable and contractible actuator, such as an electroactive polymer actuator, can be used to drive a fastener advancing or forming assembly through the elongate shaft, thereby driving a surgical fastener into tissue. In another embodiment, an electrically expandable and contractible actuator, such as an electroactive polymer actuator, can be used to effect movement of an articulation joint formed between the elongate shaft and the end effector.

Methods and devices are provided for effecting movement of one or more components of a multifire device, such as a clip applier, hernia tacker, or skin stapler. In one exemplary embodiment, a surgical fastening instrument is provided having an elongate shaft with an end effector coupled thereto and adapted to apply one or more surgical fasteners to tissue. An electrically expandable and contractible actuator, such as an electroactive polymer actuator, can be used to drive a fastener advancing or forming assembly through the elongate shaft, thereby driving a surgical fastener into tissue. In another embodiment, an electrically expandable and contractible actuator, such as an electroactive polymer actuator, can be used to effect movement of an articulation joint formed between the elongate shaft and the end effector.

In some embodiments, a method of repairing a hernia may include one or more of the following steps: (a) introducing a patch prosthesis into a patient, (b) positioning the patch prosthesis over the hernia, (c) removing a wire frame from the patch prosthesis and the patient, (d) wrapping the patch prosthesis, (e) allowing the patch prosthesis to unwrap, (f) removing a removable stitch coupling the wire frame and a prosthetic fabric, and (g) securing the prosthetic fabric to the patient.

The present invention relates to new reinforced biodegradable scaffolds for soft tissue regeneration, as well as methods for support and for augmentation and regeneration of living tissue, wherein a reinforced biodegradable scaffold is used for the treatment of indications, where increased strength and stability is required besides the need for regeneration of living tissue within a patient. The present invention further relates to the use of scaffolds together with cells or tissue explants for soft tissue regeneration, such as in the treatment of a medical prolapse, such as rectal or pelvic organ prolapse, or hernia.

A physical model representing an anatomic model of the abdominal wall that provides for the option of: tactile feedback, the option for photo realism, the inclusion of various pathologies (including, but not limited to, abdominal wall defects such as hernia), and the customizability to mount the model to various training boxes or frames. This medical / anatomic simulation model is composed of various material layers including, but not limited to, non-elastomeric and elastomeric materials such as papers, fabrics, metallic sheets, metallic meshes, rubber-like foams, and other materials. This is a physical / mechanical model that simulates skin, tissue, and organs associated with abdominal wall morphology and pathology.

A patch for repairing an intra-abdominal defect is disclosed in one embodiment of the present invention as including a mesh layer providing a grid of material perforated by apertures through the mesh. This mesh is used to reinforce an area around an intra-abdominal defect. A containment layer is secured proximate an edge of the mesh layer. A filler is distributed across the apertures of the mesh to contain a fluid from passing through the mesh. The mesh layer, containment layer, and filler are connected to form a chamber to selectively expand upon receipt of a quantity of fluid between the containment layer and the filler.

A hernia patch supporting tissue in-growth conforms to a tissue wall upon surgical installation and fixation within a patient. The hernia patch can include a base and positioning straps. The base is formed of two layers that are affixed to each other around the perimeter of the patch, for example by stitching. A stabilizing washer is provided between the two layers, and the stitch is provided peripherally around the stabilizing washer, keeping the washer free-floating between the layers. The base, positioning straps, and stabilizing washer are formed of a structure that does not separate the layers of the implant or form a space in the form of a pocket, and promotes more uniform and confluent tissue incorporation or in-growth after implantation. The hernia patch may further include a hydrolysable bioabsorbable cross-linked coating of a fatty acid based material, such as an omega-3 fatty acid based material.

A prosthesis for repairing a hernia includes an adhesion-resistant biodegradable region and an opposing tissue-ingrowth biodegradable region. When the prosthesis is implanted into the patient, the adhesion-resistant biodegradable region covers a fascial defect of the hernia, and the tissue-ingrowth biodegradable region is located above the adhesion-resistant biodegradable region while being exposed substantially only to the host's subcutaneous tissue layer. This orientation allows the tissue-ingrowth biodegradable region to become firmly incorporated with the host's body tissue. The adhesion-resistant biodegradable region faces the internal organs and decreases the incidence of adhesions and / or bowel obstruction.

Surgical implants which include a biocompatible substrate and at least one grip member capable of transitioning between a first non-gripping configuration and a second gripping configuration.

The invention provides a method for preparing an SIS tissue restoring material. The method comprises the following steps: carrying out sterilizing treatment, degreasing treatment, cell free treatment and absterging treatment according to an arbitrary sequence at the lower layer of small intestinal mucosa; and finally preparing the material through freezing and drying. The SIS tissue restoring material can be used as an independent and common support vector for a growth factor, a cell, a drug and the like, and becomes a tissue engineering material through in-vitro culture. The material is a natural and nontoxic biological material without antigenicity and immunity. The SIS tissue restoring material can be used for restoring hernia, defect of skin, urinary system tissue defect, mucosa defect and other periphery and internal parenchyma defects.

A prosthetic repair patch has a sheet and a plurality of retaining structures connected thereto. The sheet, with first and second sheet surfaces, completely under covers a hernia in tissue of a patient with the first sheet surface adjacently abutting a first surface of the tissue that faces away from a person installing the patch. The retaining structures are connected to the sheet in a spaced apart configuration and are configured for retaining a suture passed therethrough, each suture being initially passed from the second tissue surface through the first tissue surface, through at least one retaining structure, and back through the first tissue surface and out of the second tissue surface. Suture ends of each suture may then be drawn away from the second tissue surface to draw the first sheet surface into local and adjacent abutment with the first tissue surface and attached to one another.

The invention relates to an intraluminar method of treating a reflux disease in a patient by implanting a device comprising an movement restriction device that, when implanted in a patient, fills a volume in the patient's abdomen that is close to and at least partially above the patient's cardia when the patient is in a standing position. The invention further relates to a method of restoring the location of the cardia in a patient suffering from a reflux disease and to an instrument suitable to use with intraluminar method and / or restoration method. Also disclosed are instruments treating a patient suffering hiatal hernia and providing a movement restriction device to be invaginated in the stomach fundus wall.

The invention discloses a cosmetic composition which is prepared from lychee seed as raw material, and can be used for treating diseases including diabetes, hernia, orchialgia and lactiferous gland hyperplasia.

The present invention relates to devices and methods for the repair of hernia. One method for repairing a hernia the steps of making an incision through a skin layer of a patient near the hernia, creating an entrance into the preperitoneal space above the peritoneum at a location above the hernia, identifying and freeing a hernia sac, creating a pocket in the preperitoneal space, directing a surgical patch down through the incision and into the preperitoneal space, and expanding the surgical patch in the preperitoneal space. The method further includes the steps of inserting a distal end of a surgical fastening device through the incision and into the surgical patch, actuating the surgical fastening device to drive a fastener through the surgical patch and into the tissue of the patient, moving the distal end of the surgical fastening device to another location, actuating the surgical fastening device to drive a second fastener through the surgical patch and into the tissue of the patient, and closing the incision with stitches. One surgical apparatus for repairing a hernia includes a surgical stapling instrument for applying at least one surgical staple to fasten a surgical hernia patch to internal body tissue. The surgical instrument includes a handle assembly have a longitudinal axis. A staple cartridge housing is mounted to the handle assembly and is adapted to receive the at least one staple. The staple cartridge housing is dimensioned for insertion through an incision and has a staple actuator mechanism for applying the at least one staple into tissue. An actuation mechanism is operatively coupled to the staple actuator mechanism to operate the staple actuation mechanism.

A prosthesis for repairing a hernia includes an adhesion-resistant biodegradable region and an opposing tissue-ingrowth biodegradable region. When the prosthesis is implanted into the patient, the adhesion-resistant biodegradable region covers a fascial defect of the hernia, and the tissue-ingrowth biodegradable region is located above the adhesion-resistant biodegradable region while being exposed substantially only to the host's subcutaneous tissue layer. This orientation allows the tissue-ingrowth biodegradable region to become firmly incorporated with the host's body tissue. The adhesion-resistant biodegradable region faces the internal organs and decreases the incidence of adhesions and / or bowel obstruction.

A hernia prosthesis includes a first portion defining a bag joined to a second portion (B) constituting a one-piece body. A top plate of the first portion comprises a plurality of radial tabs around a central opening. The second portion comprises three distinct successive zones including a first median zone in the form of a very long sheath for introducing and securing an inserter-unfolder device. The median portion is prolonged downwards by a plurality of bands uniformly radially disposed and having bottom ends divided into two each respectively to form two tongues in a Y fastening configuration. Each tongue is fastened by its terminal end to one of the tabs. The body, in a top portion, beyond the sheath, comprises two very high tongues which have, in their top portion, a longitudinal slit in their width for attaching the inserter-unfolder device.

An Invertebral Disc Model Prosthesis, of the type denominated of double articulation, to substitute the function and the movement of intervertebral discs, for universal application due to its principal characteristic of being able to be used as a constrained, semi-constrained or non-constrained prosthesis, specially indicated for treatment of pathological degenerative of the intervertebral discs, discal hernias, by anterior approach, transition syndromes of supra-adjacent disc, chronic lumbagos resistant to conserver treatment, chronic adjacent vertebral instability, made from materials of proved biocompatibility, endowed with a low profile that makes it optimum for its implant in the human being and which consists of three pieces, two plates, upper and lower, and am intermediate piece , which serves for the substitution of the discs of the lumbar and cervical column, capable of being placed by the anterior or lateral approach.

A system for repairing a vertebral disc defect, such as hernia or bulge, a full or partial tear in the annulus, or a weakened annulus wall as a result of an excision procedure. The system introduces a treatment device arranged to repair the defect, and may prevent the leakage of fluid from the nucleus. The components of the device may be resorbable materials, and may induce the ingrowth of cellular material into the components. The system may feature a locating device to ensure proper placement of the treatment device.

An implantable prosthesis and a system and method for repairing, or resisting the formation of, a hernia at an opening or stoma through an anatomical structure such as the abdominal wall. The implantable prosthesis includes a body portion and an opening therethrough, that is adapted to receive an element, such as a section of bowel, that is being externalized through the anatomical structure. The system includes the implantable prosthesis and a cannula having an outer dimension sized to fit within the opening in said implantable prosthesis, and an inner dimension sized to pass through the element. The implantable prosthesis may include a reinforcement member, and it may also include flaps that extend into the opening of the implantable prosthesis. The method includes inserting the cannula into and beyond the opening or stoma, and locating the opening of the prosthesis about the end of the cannula. A portion of the element to be externalized, such as a section of bowel in an enterostomy, is drawn through the end of the cannula such that the bowel section does not contact the implantable prosthesis. The cannula is then removed.

A system for repairing a vertebral disc defect, such as hernia or bulge, a full or partial tear in the annulus, or a weakened annulus wall as a result of an excision procedure. The system introduces a treatment device arranged to repair the defect, and may prevent the leakage of fluid from the nucleus. The components of the device may be resorbable materials, and may induce the ingrowth of cellular material into the components. The system may feature a locating device to ensure proper placement of the treatment device.

A prosthetic repair patch has a sheet and a plurality of sutures integrated therewith and laid securely there across. The sheet, with first and second sheet surfaces, completely under covers a hernia in the abdominal tissue of a patient with the first sheet surface adjacently abutting a first surface of the tissue that faces away from a person installing the patch. The sutures are preconnected, prior to packaging and sterilization of the patch, to the sheet in a spaced apart configuration from one another and each has a longitudinal end thereof that extends from the first sheet surface. Each suture end is adapted to extend through the tissue for locally abutting the first sheet surface to the first tissue surface and to extend from an opposite second surface of the tissue for attachment with another suture end thereat for local fastening of the sheet to the tissue. The present invention also discloses a method of under covering a hernia with the repair patch.

A mesh-device for surgical repair of a hernia which includes a local anesthetic. The local anesthetic may be either embedded within the mesh, or provided in reservoirs, but is generally evenly distributed across the mesh-device. The local anesthetic is released over a predetermined duration at a predetermined rate.

The invention relates to a polypropylene / polyvinylidene fluoride composite hernia patch and a preparation method thereof. The composite hernia patch has a bilayer structure, wherein the bottom layer is a plasma modified polypropylene braid and the surface layer is a polyvinylidene fluoride electrospinning film. The preparation method comprises the following steps: (1) dissolving polyvinylidene fluoride in the mixed solution of dimethylformamide and acetone to prepare polyvinylidene fluoride solution; (2) performing plasma modification to the polypropylene fiber braid; (3) adopting the electrospinning method to spray the polyvinylidene fluoride solution on the modified polypropylene fiber braid; and (4) shaping the composite fabric and drying. The hernia patch of the invention has stable structure and good mechanical properties and biocompatibility; by utilizing the good anti-adhesion property of polyvinylidene fluoride, the problem that the polypropylene hernia patch prepared from a single material is easy to be adhered with intestinal tissues can be overcome; and the preparation method is simple and is suitable for industrial production.