890 results about "Soft tissue injury" patented technology

A method, system and apparatus for augmenting the surgical repair of soft tissue injuries, in which a first end of a bridge member attaches to a first portion of healthy tissue, and a second end of the bridge member attaches to a second portion of healthy tissue. The bridge member (or bridge members) used to augment the soft tissue repair may be interconnected or function independently. Flexibility and elasticity of the bridge member are determined by the situation and may be altered to improve healing. The device may be used in arthroscopic procedures, and may be manufactured in a variety of lengths, or may be manufactured one length and be cut to the desired length, or otherwise altered to provide an optimal length of the bridge member.

An implant for repairing soft tissue injuries is provided comprising at least one channel for receiving a soft tissue graft such as a tendon, ligament, or other soft tissue, to be implanted in a patient. The implant assembled with the graft is designed to fit into a bony defect, such as a graft tunnel, formed in bone of a patient. The implant can be biodegradable, and the implant-graft assembly has a pull-out strength sufficient to withstand everyday use during patient recovery.

A cutting tool to be utilized in the resection or removal of bone tissue from patients includes a handle that tensions a wire or cable-like cutting member with a small diameter between at least two features on the handle to present a thin cutting profile. The design of the cutting tool includes features that protect against soft tissue damage and minimize the incision size necessary to utilize the tool. Some embodiments feature details of the cutting tool that interface with a surgical cutting guide system. Other embodiments describe a cutting tool with a selectively changeable length of the cutting profile of the wire cutting member. In one embodiment, the wire cutting member of the cutting tool is energized by mechanical energy in the form of a unidirectional rotation of the cutting member, a mechanical vibration of the cutting member, or an oscillating movement of the wire cutting member.

A method and soft tissue cleat device for improving the repair of soft tissue damage. A disc having projections pierces soft tissue and securely joins with a second disc to coapt the interposed soft tissue. This provides an increased pull-out strength of the suture and resistance to shear stresses, improving the quality of the repair. The present invention may be used with any bone fixation devices to reattach soft tissue to bone, and may also be used to rejoin soft tissues after a tear in the tissue.

PCT No. PCT / GB97 / 00263 Sec. 371 Date Jul. 8, 1998 Sec. 102(e) Date Jul. 8, 1998 PCT Filed Jan. 30, 1997 PCT Pub. No. WO97 / 27770 PCT Pub. Date Aug. 7, 1997A protective material and a method for the protection of the human head or body from soft tissue damage caused by an impacting object comprises at least two layers of viscoelastic polymeric material to be interposed between head or body and impactor, including at least one first layer of material substantially matched in acoustic impedance to the impacting object and at least one second layer of material selected to produce a large mismatch in acoustic impedance between the first layer and the human head or body. A particular aspect applies the invention to head protection, especially in boxing and like sports, in the form of boxing head guards and boxing gloves.

An optical localization fiber 20 is provided suitable for preoperative localization of soft tissue lesions by x-ray mammography, CT, MRI, ultrasonography, or nuclear medicine. A hook 28 is carried by the optical fiber for retaining the fiber in soft tissue. The tip 26 of the optical fiber is visible through the soft tissue when the proximal end of the optical fiber is attached to a light source 170. Other embodiments include clad or coated 42 optical fibers, bundled optical fibers 156, hooks which are metallic 82, braided 66, and multiple 128, and a helix 162.

The invention discloses a preparation method of sericin hydrogel, the method is as follows: first, weighting domestic silkworm fibroin deletion form mutation variety silkworm cocoon for LiBr or LiCl extraction and dialysis and purification to obtain a non-degradable sericin water solution with a mass percentage concentration of 0.1-4%; concentrating the sericin water solution to 1.5-10%, adding a cross-linking agent to the concentrated sericin water solution (wherein 2-500muL of the cross-linking agent is added into each L of the sericin water solution), fully mixing, and placing at 4-45 DEG C for 5 seconds to 36 hours to obtain the sericin hydrogel. The sericin hydrogel has biological activity and multiple functions, can be used as carrying growth factors, drugs and cell carriers treatment, and can be applied in repair of a variety of soft tissue injuries, including but not limited to skin damages, muscle damages, injuries of blood vessel, nerve injuries, myocardial damages, and the like, and treatment of diseases.

The invention relates to an external application pharmaceutical composition for treating osteoproliferation which comprises semen strychni, Sichuan aconite root, Kusnezoff monkshood root, jack-in-the-pulpit tuber, pinellia tuber, white pepper, buthus martensi karsch, Cinnamomum cassia, white mustard seed, datura flower, wood louse, dragon's blood resin, frankincense, myrrh, notoginseng, asaryl, black-tail snake, cassia twig, mulberry twigs, Chinese ephedra, large-leaf gentian root, peach kernels, safflower, ledebouriella root, spatholobus stem, Chinese angelica root, notopterygium root, pubescent angelica root, campeachy wood, earthworm, Clematis chinensis, curcuma longa, achyranthes root, pawpaw, Ligusticum wallichii, speranskia herb, burred tuber, Japanese yam, zedoary, pyrola, garden balsam seed and hairy birthwort.

A re-usable bandaging system for treating acute soft-tissue injuries and the like provides protection, support and restraint, and optional heating or cooling and uses straps enabling the system to be placed at one of many sites. A flexible, resilient insulating material, covered with loop-bearing fabric comprises (A) a main bandage that is a rectangular panel with a pocket and (B) two straps at diagonally opposite corners. Each strap has an area of complementary hooks at the free end, to adhere to the bandage when in use. A supplementary bandage (C) is for optional use as a strap when stabilising the main bandage. The system provides a sealed flexible gel pack for heating or cooling an injured part when placed in the pocket. The pack is internally baffled to evenly apply a compress therapy by restriction motion of the contents.

The invention relates to a balloon catheter in which the balloon is mounted on the end of the catheter in a manner that creates a recess or pocket between the catheter wall and balloon wall. The recess or pocket opens toward the proximal end of the catheter. The rigid end of an introducer element or finger is received in the recess to attach it to the catheter. The distal end of the catheter, with the end of the introducer element in the recess, is inserted and positioned within the bowel by manipulating the introducer element or finger. After the catheter is properly positioned in the bowel, the introducer element or finger is withdrawn, detaching it from the catheter as the end of the introducer element slides out of the recess and then out of the bowel. The balloon is inflated prior to or after the withdrawal of the introducer element to anchor the end of the catheter in position within the bowel. Since the distal end of the catheter is made entirely of soft, compliant material, no soft tissue damage can occur from use of the device, even when the catheter remains in place within the body over an extended time period.

A pressure monitoring method and system for warning a patient or caregiver that soft tissue pressure has exceeded some predetermined level that over time would necessitate moving the patient to minimize or prevent soft tissue damage. The method and system entail the use of a pressure-sensitive pad assembly adapted to be applied to a surface of the patient's body and generate electrical outputs corresponding to soft tissue pressure sensed at the surface. The system monitors the electrical outputs over a preselected time period and generates a cumulative output signal based on the electrical outputs and corresponding to whether or not the soft tissue pressure has exceeded a predetermined pressure level during the preselected time period. The system generates audible and visual warnings if the cumulative output signal exceeds a predetermined cumulative threshold until the soft tissue pressure drops below the predetermined pressure level.

Pressure monitoring methods and systems for warning a patient or caregiver that soft tissue pressure has exceeded some predetermined level that over time would necessitate moving the patient to prevent or at least reduce a risk of soft tissue damage. The methods and systems entail the use of a pressure sensing unit adapted to be applied to or near a surface of the patient's body, and a sensor associated with the sensing unit to generate electrical outputs corresponding to soft tissue pressure sensed at the surface. The electrical outputs are wirelessly monitored over a preselected time period to generate a cumulative output signal based on the electrical outputs and corresponding to whether or not the soft tissue pressure has exceeded a predetermined pressure level during the preselected time period. An alarm is generated if the cumulative output signal exceeds a predetermined cumulative threshold until the soft tissue pressure drops below the predetermined pressure level.

The present invention is a multi-purpose method and device comprising a therapeutic body containing a plurality of pins. The distal ends of the pins on the therapeutic body are placed in contact with the skin. The apparatus may be used to provide treatment to persons and animals suffering from the symptoms of soft tissue injuries in various regions of the body. The device and method is also useful for relaxation and reenergizing of an injured or tired body.

Minimal Invasive Spine Surgery (MISS) as a surgical approach is increasingly utilized because of the advantages it offers over conventional spine surgery. The smaller incision results in decreased tissue damage, less blood loss, decreased hospital stay & faster postoperative recovery. The drawbacks of MISS are the long learning curve of working through a smaller incision, longer length of surgery, & potential higher complication rate due to compromised visual field. These limitations can be overcome by more effectively using imaging and navigational devices. The pedicle device simplifies the hardest part of MISS instrumented fusion of conventional pedicle screw insertion by introducing a percutaneous temporary device to locate and create the channel for later conventional pedicle screw implantation using available imaging techniques. This results in faster conventional pedicle screw insertion with precision, thereby decreasing implantation error and minimizing soft tissue injury and blood loss, as well as neurological, vascular, and dural injuries and complications.

A felt for repairing soft tissue defects comprising a membranous collagen substrate and a bioresorbable fiber felted onto the collagen substrate. Methods of preparing a felt and methods of repairing soft tissue damage with a felt are also provided.

The invention relates to a balloon catheter in which the balloon is mounted on the end of the catheter in a manner that creates a recess or pocket between the catheter wall and balloon wall. The recess or pocket opens toward the proximal end of the catheter. The rigid end of an introducer element or finger is received in the recess to attach it to the catheter. The distal end of the catheter, with the end of the introducer element in the recess, is inserted and positioned within the bowel by manipulating the introducer element or finger. After the catheter is properly positioned in the bowel, the introducer element or finger is withdrawn, detaching it from the catheter as the end of the introducer element slides out of the recess and then out of the bowel. The balloon is inflated prior to or after the withdrawal of the introducer element to anchor the end of the catheter in position within the bowel. Since the distal end of the catheter is made entirely of soft, compliant material, no soft tissue damage can occur from use of the device, even when the catheter remains in place within the body over an extended time period.

A wireless pressure ulcer alert dressing system for warning a patient or caregiver that soft tissue pressure or health condition has exceeded some predetermined level that over time would necessitate moving the patient to prevent or at least reduce a risk of soft tissue damage. The dressing assembly is adapted to be applied to or near a surface of the patient's body and generate electrical outputs corresponding to soft tissue pressure and other health characteristics sensed at the surface. The dressing assembly generates output signals based on the electrical outputs and corresponding to whether or not the soft tissue pressure has exceeded a predetermined pressure level during the preselected time period. The dressing assembly includes a pocket formed therein for removable, secured and protected insertion of a variety of different sensors such as multiple pressure sensors.

A method including topically administering an effective amount of local anesthetic to a patient is disclosed. The method is effective for inducing analgesia for treating non-neuropathic pain. Non-neuropathic pain suitable for treatment according to the invention includes pain associated with sports injuries; sprains; strains; soft-tissue injury; repetitive motion injury; carpal tunnel syndrome; injury to tendons, ligament, and muscles; conditions such as fibromyalgia, bursitis, castrochondritis, myofascial pain, and pain associated with arthritis, inflammation, contusions, post-surgical pain, and nociceptive pain. Preferably, the lidocaine is applied via a transdermal patch applied near the locus of pain.

The invention discloses a method for simultaneously treating multiple kinds of biological tissue. The method includes the steps of pretreating, degreasing, cell extraction, crosslinking and sterilization. The method for simultaneously treating the multiple kinds of biological tissue can simultaneously treat the multiple kinds of biological tissue, the batch-treated biological tissue amount is large, the treatment degree is uniform, the process is simple, industrialization is easy, and efficient production is achieved. According to the method for simultaneously treating the multiple kinds of biological tissue, use of strong acid, strong base and protease is completely avoided, natural three-dimensional collagen support fiber structures of extracellular matrixes of the multiple kinds of biological tissue can be reserved, and cell components, causing immunogenicity, in the tissue are removed. The biological tissue prepared through the method has good bio-compatibility and mechanical performance, compared with natural biological tissue, high degradation resistance is achieved, and the biological tissue can be used for repairing various kinds of soft tissue injuries.

The invention discloses a 3D (three-dimensional) printing preparation method of an orthopaedic external fixing support, which comprises the following steps of: 1, acquiring limb orthopaedic position information of a patient; 2, based on the orthopaedic position information, establishing a primary three-dimensional model of the orthopaedic external fixing support; 3, establishing a physical constitutive model of the orthopaedic external fixing support, and carrying out biomechanical analysis by adopting a finite element method; 4, based on biomechanical analysis, updating primary three-dimensional model data of the orthopaedic external fixing support; 5, based on the updated three-dimensional model data of the orthopaedic external fixing support, designing a final three-dimensional model of the orthopaedic external fixing support, inputting data of the final three-dimensional model into a 3D printing system, and integrally printing and forming to obtain the orthopaedic external fixing support. The 3D printing preparation method disclosed by the invention solves the technical problems of low coincidence degree with a limb orthopaedic position, easiness for causing soft tissue injuries, insufficient antibacterial property, long customizing time and high cost of an external fixing support in the prior art.

A combination bite block, tongue depressor / retractor and airway for establishing and maintaining an open airway while preventing emergence clenching and the resulting dental and soft tissue damage associated with emergence clenching in procedures where anesthesia and / or sedation are used, or when the patient is not in control of their own airway, regardless of the cause. The inventive subject matter includes a tongue depressor / retractor component in both right and left conformations; and a bite block component. The bite block component is a wedge shaped, compressible component that is inserted between the upper and lower molars on either the right or left side of the mouth. The tongue depressor component is comprised by a flat portion of that is inserted into the side of the bite block, and an optional curved portion that retracts the tongue off of the posterior pharynx when in place.

An electro diagnostic functional assessment unit (EFA-2) that diagnoses age of and treats soft tissue injuries. The EFA-2 utilizes sensor(s) including EMG, Range of Motion, FCE, pinch and grip, and allows for monitoring of muscles and muscle groups to ascertain compliance, pain and function. The EFA-2 also monitors disc pathology and determines whether a person requires surgery or conservative care and, the age of the disc. Additionally, the EFA-2 monitors EEK activity and NCV, as well as invasive EMG that monitors nerve damage. Previously, with NCV the temperature and the position of electrodes would effect readings and produce false positive or false negative readings. The EFA-2 eliminates these problems by incorporating temperature sensor(s) and electrode placement sensor(s). The EFA-2 also provides direct treatment by means of ultrasound and electrical stimulation. Thus, the EFA-2 allows diagnosis any treatment by means of a single unit.

The invention discloses a method for preparing collagen / bioglass / hyaluronic acid tissue repairing materials, comprising the following steps: combining I-type collagen and bioglass, static layering, filtering, adjusting pH value, adding hyaluronic acid, cross linking, molding, freezing and drying and the like. In the process of preparing the collagen / bioglass / hyaluronic acid tissue repairing materials, the diameter of the collagenous fiber bundle composing the network structure of the tissue repairing materials is increased by adjusting the ratio of the I-type collagen and bioglass and the pH value of the combined solution, and the microstructure of the materials is adjusted, thus achieving the aim of improving mechanical strength thereof. The collagen / bioglass / hyaluronic acid tissue repairing materials prepared by the invention has improvement in mechanical property and degradation performance, can be widely used in medical field, also can be used in tissue engineering scaffolds and bone defects and soft tissue injuries repairing.

The invention relates to a traditional Chinese medicine composition and a preparation thereof, and especially relates to a pharmaceutical composition with effects of dispelling wind, relieving pain, dispelling cold, removing dampness, warming meridians and collaterals, relaxing meridians, and invigorating blood circulation, a hot-compress preparation and a preparation method thereof. The pharmaceutical composition for dispelling wind, relieving pain, dispelling cold, and removing dampness is mainly characterized by comprising the following raw materials by weight: 10-20 parts by weight of notopterygium roots, 10-20 parts by weight of radix angelicae pubescentis, 10-20 parts by weight of rhizoma atractylodis, and 10-20 parts by weight of radices sileris. Through clinical treatment demonstration by a lot of cases, the pharmaceutical composition of the invention has significant effect, is nontoxic, and good in stability; and a new traditional Chinese medicine preparation is provided with treatment, rehabilitation and health care effect on rheumatic joint swelling and pain, limb crymodynia, muscle and bone pain caused by wind-cold invasion, swelling and pain caused by soft tissue damage, ankylosis, and the like.

The invention relates to an external preparation made from Chinese herbal medicines, specifically to a film-spraying agent for treating acute soft tissue injuries. 1000ml of the film-spraying agent in the invention is composed of the following raw materials: a Chinese herbal extract extracted from 20-60g of rheum officinale, 20-60g of Cacumen Platycladi, 10-30g of Cortex Phellodendri amurensis, 10-30g of Herba Lycopi and 10-30g of mint by ethanol, 2-6g of borneol, 0.4-1.2g of menthol, 2-6g of chlorobutanol, 30-60g of polyvinylpyrrolidone, 1-8g of hydroxypropyl methyl cellulose, and the rest ethanol water with a volume concentration of 30-40%. During application, the film-spraying agent of the invention is directly sprayed on the injured part and can form a film in 8 minutes. With good anti-inflammation, pain easing, stasis removing, acute soft tissue injury improving and microcirculation improving, as well as antibacterium effects, the film-spraying agent provided in the invention has an obvious effect in treating acute soft tissue injuries such as sprains, contusions and other local injuries, and redness, swelling, heat, pain, wound surface infection, as well as other aspects.

The invention relates to a medicinal medicament for treating osteoarthrosis which comprises the following constituents: drynaria, frankincense, safflower, achyranthes and cyathula root, Ligusticum wallichii, Clematis chinensis, ledebouriella root, notopterygium root, pubescent angelica root, myrrh, and large-leaf gentian root, the preparing process comprises proportioning, mixing homogenously, charging water by the weight ratio of 1:4, boiling for 1 hour, filtering and extracting.