36 results about "Abdominal Surgical Procedure" patented technology

Surgical training models of the abdominopelvic region of male and female human patient's bodies to assist in training an operator in microsurgical techniques are disclosed. The surgical training models may be used in training in implantation of implantable medical devices, e.g., in the performance of surgical procedures using particular sling implantation tools to implant a urethral sling to support the urethra or bladder to treat incontinence.

Methods, systems, devices and assemblies are provided for treating a patient by: making an incision or puncture though the patient's skin over the abdominal cavity; establishing an initial tract through an opening formed by the incision or puncture; advancing an instrument through the tract; contacting a distal end portion of the instrument against an inner surface of the abdominal cavity; driving at least one stitching needle through the inner surface of the abdominal cavity; continuing the driving until the at least one stitching needle exits the inner surface of the abdominal cavity; anchoring a suture carried by each of the at least one stitching needle to a suture anchor at an exit location, respectively; and applying tension to each of the sutures.

Apparatus, tools, device and methods provided for treating a patient, including: making an incision or puncture though the patient's skin; establishing an initial tract through an opening formed by the incision or puncture; inserting a guide member having a flexible distal portion and a distal tip into the initial tract and extending the initial tract to form a delivery tract leading to a target location within the patient's body; wherein said distal tip and at least a portion of a remainder of said guide member are transparent; and delivering an obturator and conduit assembly over said guide member to place a distal end of the conduit of said obturator and conduit assembly in a location at or near the target location, said obturator having been inserted into said conduit prior to delivering said assembly over said guide member such that a distal end of said obturator extends distally out of a distal opening of said conduit; wherein said obturator comprises a central lumen adapted to closely follow said guide member while sliding thereover.

The invention relates to a prosthesis that can be implanted in the centre of wall wound scarring. The inventive prosthesis, which is intended for use in abdominal surgery, is provided with a geometric shape in the form of sheets that converge in dihedral angles. The sheets or planes are made from a synthetic biotolerated material in porous form with large pores. One of said planes is inserted into the centre of the scarring between the two aponeurotic surfaces to be joined. The other plane(s) of the prosthesis, which is perpendicular to the aforementioned plane, is arranged so as to overlap the aponeurotic edges of the edge of the section. The proliferation obtained around the prosthesis, in the scarring centre and close thereto, provides stress resistance greater than that obtained in standard closures, thereby greatly reducing the risk of hernias caused by a badly healed wound.

Methods, systems, devices and assemblies are provided for treating a patient by: making an incision or puncture though the patient's skin over the abdominal cavity; establishing an initial tract through an opening formed by the incision or puncture; advancing an instrument through the tract; contacting a distal end portion of the instrument against an inner surface of the abdominal cavity; driving at least one stitching needle through the inner surface of the abdominal cavity; continuing the driving until the at least one stitching needle exits the inner surface of the abdominal cavity; anchoring a suture carried by each of the at least one stitching needle to a suture anchor at an exit location, respectively; and applying tension to each of the sutures.

A surgical drain device includes a matrix of biodegradable polymer material and a plurality of drain tubes attached to the matrix. The device is implanted within a surgical wound to treat the presence of seromas, for example, and is used to promote drainage, tissue adhesion, and wound closure. The drain tubes converge into a common collection tube that leads wound fluid outside the body under gravity feed or negative pressure applied to the collection tube. The matrix contains an array of apertures that allow tissue contact across the device. A preferred embodiment comprises a tissue anchoring system including anchor elements such as hooks or barbs. The device can be used with a negative pressure system to further improve the drainage band can also be used with a wound dressing. The device and systems containing the device are particularly useful to promote the healing of surgical wounds from abdominal surgery.

A surgical instrument and methods of use. The surgical instrument can include a control portion having a plurality of tubular shaft portions and a plurality of control rods. Each of the plurality of tubular shaft portions can have a diameter of less than or equal to about 2.5 mm. At least one of the plurality of control rods can extend through each of the plurality of shaft portions. The surgical instrument can also include a tool portion having a plurality of tool rods and a plurality of tool cables. Each of the plurality of tool cables can be connected to one of the plurality of control rods. Further, each of the tool rods can be removably connected to one of the plurality of control rods.

Natural and / or synthetic materials to form a strong barrier between the skeletal system and the great vessels. In the preferred embodiments, a natural or synthetic material is used to prevent scar tissue from forming around the vessels and / or to act as barrier placed between the vessels and the skeletal system, including the spine. Devices according to the invention may also be used over the dura and nerves following laminectomy procedures, between the sternum and the pericardium or heart following cardiac procedures, in intra-abdominal procedures such as intestinal or vascular surgery, over the brain in intra-cranial surgery, over the ovaries or other organs or tissues in the female genitourinary system, over the prostate or other organ or tissues in the male genitourinary system, or in other surgeries on humans or animals.

A biological adhesive formulation comprising dextrin, at least one adhesiveness modifier agent, and at least one antibiotic is suitable for promoting healing of tissue in a patient, for example, to prevent anastomosis of a surgical wound in the digestive system of a patient, and for affixing a prosthesis during a hernia operation.

Methods, systems, devices and assemblies are provided for treating a patient by: making an incision or puncture though the patient's skin over the abdominal cavity; establishing an initial tract through an opening formed by the incision or puncture; advancing an instrument through the tract; contacting a distal end portion of the instrument against an inner surface of the abdominal cavity; driving at least one stitching needle through the inner surface of the abdominal cavity, continuing the driving until the at least one stitching needle exits the inner surface of the abdominal cavity, anchoring a suture carried by each of the at least one stitching needle to a suture anchor at an exit location, respectively; and applying tension to each of the sutures.

A construct for use in an abdominal surgery is described. The construct contains an allograft having at least one layer of human amnion and chorion tissues, and has a size and shape appropriate for covering an incision or a surgical site resulting from the surgery. Methods of preparing the construct and using it in an abdominal surgery are also described. The products and methods improve the performance of the abdominal surgery, e.g., by reducing adhesions, scar formation while also reducing inflammation and risk of post-operative infection.

Apparatus, tools, device and methods provided for treating a patient including: making an incision or puncture though the patient's skin; establishing an initial tract through an opening formed by the incision or puncture; inserting a guide member having a flexible distal portion and a distal tip into the initial tract and extending the initial tract to form a delivery tract leading to a target location within the patient's body; wherein said distal tip and at least a portion of a remainder of said guide member are transparent and delivering an obturator and conduit assembly over said guide member to place a distal end of the conduit of said obturator and conduit assembly in a location at or near the target location, said obturator having been inserted into said conduit prior to delivering said assembly over said guide member such that a distal end of said obturator extends distally out of a distal opening of said conduit wherein said obturator comprises a central lumen adapted to closely follow said guide member while sliding thereover.

A surgical drain device includes an adhesion matrix of biodegradable polymer material and a plurality of drain tubes attached to the matrix. The device is implanted within a surgical wound to treat the presence of seromas, for example, and is used to promote drainage, tissue adhesion, and wound closure. The drain tubes converge into a common collection tube that leads wound fluid outside the body under gravity feed or negative pressure applied to the collection tube. The matrix contains an array of apertures that allow tissue contact across the device. The device also can include a coating of surgical adhesive and a tissue anchoring system of hooks or barbs. The device and systems containing the device are particularly useful to promote the healing of surgical wounds from abdominal surgery.

Methods, systems, devices and assemblies are provided for treating a patient by: making an incision or puncture though the patient's skin over the abdominal cavity; establishing an initial tract through an opening formed by the incision or puncture; advancing an instrument through the tract; contacting a distal end portion of the instrument against an inner surface of the abdominal cavity; driving at least one stitching needle through the inner surface of the abdominal cavity; continuing the driving until the at least one stitching needle exits the inner surface of the abdominal cavity; anchoring a suture carried by each of the at least one stitching needle to a suture anchor at an exit location, respectively; and applying tension to each of the sutures.

Apparatus, tools, device and methods provided for treating a patient including: making an incision or puncture though the patient's skin; establishing an initial tract through an opening formed by the incision or puncture; inserting a guide member having a flexible distal portion and a distal tip into the initial tract and extending the initial tract to form a delivery tract leading to a target location within the patient's body; wherein said distal tip and at least a portion of a remainder of said guide member are transparent and delivering an obturator and conduit assembly over said guide member to place a distal end of the conduit of said obturator and conduit assembly in a location at or near the target location, said obturator having been inserted into said conduit prior to delivering said assembly over said guide member such that a distal end of said obturator extends distally out of a distal opening of said conduit wherein said obturator comprises a central lumen adapted to closely follow said guide member while sliding thereover.

The invention provides a biodegradable medical abdominal surgical suture material. The biodegradable medical abdominal surgical suture material, a composite biodegradable material, consists of a cylindrical core layer, a middle layer wrapping the core layer and a cover layer wrapping the middle layer, wherein the core layer is selected from polyglycolic acid, polylactic acid, polycrylactone or a copolymer thereof, the middle layer is selected from carboxymethyl chitosan, chitosan fibers or collagenous fibers, and the cover layer is selected from polyglycolic acid, polylactic acid, polycrylactone or a copolymer thereof. The biodegradable medical abdominal surgical suture material has the advantages of no toxicity, no irritation, biocompatibility and capability of avoiding causing inflammatory reaction since a degradation product of a surgical suture is finally decomposed into carbon dioxide and water which are free of toxicity.

Methods, systems, devices and assemblies are provided for treating a patient by: making an incision or puncture though the patient's skin over the abdominal cavity; establishing an initial tract through an opening formed by the incision or puncture; advancing an instrument through the tract; contacting a distal end portion of the instrument against an inner surface of the abdominal cavity; driving at least one stitching needle through the inner surface of the abdominal cavity; continuing the driving until the at least one stitching needle exits the inner surface of the abdominal cavity; anchoring a suture carried by each of the at least one stitching needle to a suture anchor at an exit location, respectively; and applying tension to each of the sutures.

The present invention discloses an abdominal surgery auxiliary device. The abdominal surgery auxiliary device comprises fixing platforms, sliding plate platforms, knife edge fixing platforms, minimally invasive surgery and fixing platforms, the fixing platform comprises a fixing clamp, the fixing clamp clamps a side surface of a surgery bed tightly, when performing a large abdominal surgery, the sliding plate platforms are moved to a specified height by sliding blocks, the knife edge fixing platforms are rotated to a designated position by lower sliding blocks, the knife edge fixing platformsare control to fix fixing pieces to a knife edge of a patient's abdomen, when minimally invasive surgery is conducted, upper sliding blocks drive the minimally invasive surgery and fixing platforms torotate to a designated position, steering machines drive surgical parts to rotate downward, each part of the minimally invasive surgery and fixing platforms is coordinated to perform minimally invasive surgery and open the knife edge, and the abdominal surgery auxiliary device is convenient for doctors to perform the surgery in the minimally invasive knife edge, improves accuracy of the surgery,increases a success rate of the abdominal surgery, avoids problems caused by improper manual operations, and reduces work intensity of the doctors.

Disclosed is a hemostatic agent applicator capable of effectively placing a fluid hemostatic agent on an incision surface. The present invention is a hemostatic agent applicator for use in disposing a fluid hemostatic agent, including a tool body in which a hollow part surrounded by a wall part is formed and which includes an open end part on a downstream side of the wall part, and an inlet provided to a portion of the wall part of the tool body to communicate with the hollow part. This hemostatic agent applicator is useful in medical settings relating to surgical procedures, particularly for surface bleeding of a liver and internal organ surgery such as a spleen and fibroid enucleation. An applicator further reduced in size can be applied not only in abdominal surgery, but in endoscopic surgery as well.

The invention discloses an adjustable sliding type abdominal operation incision retractor which comprises an annular base frame, wherein the annular base frame comprises an annular fixing frame and a supporting assembly arranged at the bottom end of the annular fixing frame; and a traction assembly which comprises a plurality of groups of sliding assemblies and traction assemblies, the sliding assembly comprises a sliding seat and a winding mechanism embedded in the sliding seat, the sliding seat is arranged in a sliding rail on the fixing frame in a sliding mode, the winding mechanism is used for winding a traction arm, the head end of the traction arm is connected with a clamping assembly, and the clamping assembly is clamped on the traction assembly. According to the adjustable sliding type abdominal operation incision retractor, the annular base frame and the matched traction assembly used in cooperation with the annular base frame are arranged, so that the position direction and the traction force of the traction hook are effectively adjusted, and the operation view field is fully exposed.

Systems and methods of reducing pain after surgery in the thoracic or abdominal region and managing chronic nerve pain in the thoracic or abdominal region are provided. Such methods involve an electrode assembly that has a proximal portion and a distal portion with the distal portion including a plurality of electrodes. At least one electrode of the plurality of electrodes is placed over each of a plurality of intercostal nerve bundles in the patient's body. The proximal portion of the electrode assembly is connected to a pulse generator. An electromagnetic field is applied to the plurality of intercostal nerve bundles. The plurality of electrodes is removed from the patient's body after an intercostal nerve block sufficient to alleviate the patient's pain has been achieved.

A device (surgical aid) for assisting wound closure in a surgical procedure setting. A flat plastic sheath (retainer) is inserted into the wound to retain the viscera organs and protect them from cuts or punctures while closing the wound after abdominal surgery or any large body cavity surgery. Just before completion of the wound closure, the device is pulled out of the body via a pull cord and then the wound closure is finished.

A biodegradable matrix for preventing post-surgical adhesions, in particular after soft tissue repair in abdominal surgery within the body of a mammal is disclosed. The matrix includes a top layer made of a first biocompatible polymer material and a bottom layer made of a second biocompatible polymer material. The first polymer material comprises poly(lactic acid) as a main component and the second polymer material comprises as a main component at least one polymer selected from the group consisting of poly(glycolic acid), poly(lactic acid), poly(glycolic acid-lactic acid) and mixtures thereof, wherein the poly(lactic acid)content of the first polymer material is higher than in the second polymer material, and wherein both layers are formed as porous scaffolds with the top layer being hydrophilic, having a water contact angle of less than 75°, and the bottom layer being hydrophobic, having a water contact angle of more than 90°.

A surgical instrument and methods of use. The surgical instrument can include a control portion having a plurality of tubular shaft portions and a plurality of control rods. Each of the plurality of tubular shaft portions can have a diameter of less than or equal to about 2.5 mm. At least one of the plurality of control rods can extend through each of the plurality of shaft portions. The surgical instrument can also include a tool portion having a plurality of tool rods and a plurality of tool cables. Each of the plurality of tool cables can be connected to one of the plurality of control rods. Further, each of the tool rods can be removably connected to one of the plurality of control rods.

A device and method for umbilicus protection during abdominal surgery; and, especially plastic reconstructive and aesthetic surgery requiring umbilicoplasty and / or umbilicus transposition is provided. The device embodies an umbilicus shield, which envelops the umbilical pedicle during abdominal surgery. The device can include a tubular element, having a distal end and a proximal end, containing near its proximal end, means for releasabley retaining suture material from tacking stitches taken in the umbilicus to provide means for drawing the umbilical pedicle into the tubular element. The suture material is advantageously drawn through the tubular element by means of a suture shuttle which contains, proximate its distal end, means for releasabley retaining the suture material. The device facilitates umbilicoplasty and umbilicus transposition during abdominal surgery; prevents nicks or cuts during circum umbilicus dissection; prevents nicks, cuts, or amputation of the umbilicus during defattening; and, reduces the possibility of umbilical pedicle strangulation during rectus abdominis musculoaponeurotic plication. The method prevents such strangulation and assures proper positioning of the orifice and umbilicus during umbilicus transpositions.

The invention provides an abdominal operation wound drainage device which comprises a split drainage tube and a negative pressure ball, the split drainage tube is composed of a hose and a drainage apparatus, the drainage apparatus is inserted into one end of the hose, and the other end of the hose is connected with the negative pressure ball; the drainage device comprises an upper arc-shaped pressing piece, a lower arc-shaped pressing piece and an X-shaped supporting piece connected between the two arc-shaped pressing pieces, and two bottom feet on the upper side and the lower side of the X-shaped supporting piece are fixedly connected with the upper arc-shaped pressing piece and the lower arc-shaped pressing piece respectively. A row of drainage holes are distributed in the upper arc-shaped pressing piece in the length direction, and long-strip-shaped drainage grooves distributed in the length direction are formed in the lower arc-shaped pressing piece. The included angle alpha 1 of the two sides of the X-shaped supporting piece ranges from 50 degrees to 70 degrees, the two sides of the upper arc-shaped pressing piece are flush with bottom feet of the X-shaped supporting piece, and distances are reserved between the left side and the right side of the lower arc-shaped pressing piece and the bottom feet of the X-shaped supporting piece. The abdominal operation wound drainage tube can well conduct drainage on an abdominal operation wound, and compared with a traditional cross-shaped drainage tube, the abdominal operation wound drainage tube is beneficial to wound healing.

A method for inhibiting formation of adhesions following abdominal surgery which involves application of an anti-static fatty acid ethoxylated amide (Cocamide DEA) in a matrix that is placed in the peritoneal cavity at the conclusion of an abdominal surgery and which releases this anti-adhesive chemical over a predetermined time in a range up to seven days. Tests conducted on laboratory rats established that the method reduced the incidence of adhesions from 100 percent (100%) in a test model to near zero in the majority of treated animals. In an alternative embodiment, andrographalide was delivered via a pump with similar results. In still another embodiment, an effective amount of 50% phosphatidylchorene and propylene glycol was delivered, via a pump, into the abdominal cavity, again with similar results.