103 results about "Traumatology" patented technology

The present invention incorporates new materials for bone regeneration, methods for their manufacture, and application in traumatology surgery, maxillo facial surgery, dental surgery, orthognatic surgery, endodontics, ophthalmology, neurosurgery and / or osteoporotic processes, and other indications where bone regeneration is required. In particular, the present invention incorporates synthetic materials with a 20% to a 95%, preferably between 40% and 90% in mass of monetite [Ca1-XMXHPO4, where 0≦x≦0.05, and where M can be a divalent metallic ion], and which in their final composition incorporate between 5% and 80%, preferably between 0% and 60%, in mass of bioactive calcium compounds chosen from calcium phosphates and between 5% and 80% in total mass of bioactive silicon compounds chosen from calcium silicates and / or bioactive silica glasses and gels.

The invention relates to a high-strength absorbable wire composited internal fixation implantable device and a preparation method of the device, in particular to an internal fixation implantable device taking high-strength magnesium alloy wires in high content as a basal body, wherein the high-strength magnesium alloy wires are bonded and cured at a high temperature by low-content binder polylactic acid polymers and are arranged in a directional dispersion way or in a two-dimension weaving structure or three-dimension weaving structure, and the binder polylactic acid polymers account for 5%-49.9% of the total amount and the magnesium alloy wires account for 50.1%-95% of the total amount according to the weight percentage. The high-strength absorbable wire composited internal fixation implantable device is closer to the magnesium alloy on the aspect of strength, can meet the mechanism safety requirements for large-load fracture fixation with higher strength requirement, and has the advantages of both controllable uniform internal absorption, slow and less hydrogen degradation and separation, etc., thereby being particularly applicable to clinics like departments of bone traumatology, department of bone defect repair, plastic and beauty operations and the like with high strength requirement and large size.

The present invention relates to a plaster for relief pain of viscera muscle joint, and a method for preparing the same. To resolve the problems of worse treating effect and side effect using existing medicine, the medicine provided by the invention is prepared from raw materials added plant oil and yellow lead of unsaturated fatty acid by weight rate as follows: 5-15 parts toad, 2-7 parts lbamboo knot cyperus rotundus l, 0.7-2.2 parts jiazhu, 3-10 parts paris, 5-15 parts crab, 2-7 parts seseli mairei wolff, 2-7 parts dragon arum, 2-7 parts herb of alpine yarrow, 2.5-7.5 parts raw radix aconiti kusnezoffii, 3-8 parts curcuma, 2.5-7.5 parts raw monkshood, 3-8 parts zedoary, 4-12 parts zushima, 2-5 parts olibanum, 2-5 parts myrrh, 2-7 parts qianjin vine, 2-7 parts nux vomica, 3-8 parts xugufeng, 4-9 parts angelica, 4-12 parts hawthorn, 2-7 parts raw pinellia ternate, 3-8 parts naoyanghua, 2-5 parts liquorice, 4-12 parts bamboo knot sanchi, 4-12 parts clematis root, 3-7 parts datura stramonium seed, 3-8 parts aconitum pendulum, 0.02-0.08 moschus. The plant oil is 50-150 parts tung oil and 30-90 parts black sesame oil. The weight rate of plant oil and yellow lead is 120-200 / 14-22. The medicine has wide application effect, and is suitable for treating pain of viscera muscle joint, long chronic illness. The medicine also has obvious cure effects without toxic side effect for treating acute or chronic gastritis, enteritis, diarrhea, dysmenorrhea, low back pain, neck and lumbar disc herniation, orthopaedics and traumatology. The medicine has effects of promoting circulation of qi and blood, clearing meridians and collaterals, using poisons as antidotes, dehydration detumescence, resolving the nodule, promoting blood circulation and removing blood stasis, dispelling wind chill and dampness syndromes, and can reach aim at both temporary solution and permanent control.

The proposed invention relates to the field of physical therapy and can be used for the treatment and prophylaxis of a number of diseases, and also for health-improving purposes, including improving the stamina, for instance, of athletes. The installation for conducting general air cryotherapy comprises a closed-type cryogenic chamber (1) with a door (2) with heat insulation (3) and a heat sensor (8), a refrigeration machine (7) with a condenser and a power and control unit (9), and a coolant supply line (6), wherein the refrigeration machine (7) has two cascades, and an evaporator (4) with a ventilator (5) is installed into the ceiling or wall of the cryogenic chamber (1) and is connected by means of the coolant supply line (6) to the double-cascade refrigeration machine (7), and wherein a heat control valve (12) is installed at the inlet to the evaporator (4), and the cryogenic chamber (1) is equipped with a valve for equalizing pressure with the outside environment (11), and wherein said valve (11) has an electric heater, the door (2) of the cryogenic chamber (1) is made entirely transparent and is equipped, as is the frame thereof, with an electric heater, and a control console with a sensor panel (13) is installed on the external surface of the cryogenic chamber (1). The proposed installation is more reliable than the prototype and the dimensions and cost of the installation are significantly decreased. The proposed installation can be used for the purposes of treatment and prophylaxis in the fields of rheumatoid arthritis, neurology, dermatology, traumatology and orthopedics, states of depression and stress, and in sports medicine.

The present invention relates generally to an antibacterial coating which is composed of silver, to medical tools and to implants comprising such a coating and to a method as well to an apparatus for the production of such a coating. The medical tools or the dental or orthopaedic implant comprises a metal or metal alloy having a treated surface wherein the treated surface is at least partially converted to an oxide film by plasma electrolytic oxidation using a colloid-dispersed system and wherein the converted surface is partially covered by islands formed by colloid-dispersed silver-particles of the colloid-dispersed system. An Ag—TiO2 coating shows excellent properties in terms of antibacterial efficacy (even against multi-resistant strains), adhesion and biocompatibility. The life-time of an implant in a human body is increased. The antibacterial coating can be used in the field of traumatology, orthopaedic, osteosynthesis and / or endoprothesis, especially where high infection risk exists.

The invention discloses an externally applied traditional Chinese medicine composition for curing diseases of orthopedics and traumatology, relates to a method for preparing plaster with the externally applied traditional Chinese medicine composition, and belongs to the technical field of traditional Chinese medicines. The externally applied traditional Chinese medicine composition is composed of 30 types of traditional Chinese medicines such as Chinese angelica, garden balsam stem, clove, native copper and dragon's blood, is prescribed according to the assistant and guide principle and compatibility, is nontoxic, has no side effects, is fast in healing, short in treatment course, and low in price, and has an obvious curative effect for diseases of orthopedics and traumatology such as various bone fracture, bone and muscle contusion, joint injury, acute and chronic soft tissue injury, joint and muscle strain, and neck, shoulder and lumbocrural pain, wherein the efficacy is higher than 95 percent.

The invention relates to an adhesive amniotic membrane, which is a double layer or multi-layer adhesive amniotic membrane bonded with amniotic membrane and fibrin albumen glue. The preparing method comprises: bonding the fresh amniotic membrane of epithelium removed with fresh amniotic membrane without removing epithelium by using fibrin albumen glue; or condensing the amniotic membrane immersing in the glycerol, and then bonding the fresh amniotic membrane of epithelium removed with fresh amniotic membrane without removing epithelium by using fibrin albumen glue; or bonding with the fresh amniotic membrane without removing epithelium by using fibrin albumen glue; finally putting the bonded adhesive amniotic membrane into pure glycerol under 0-6 Deg C for closed and sterile conservation. The product not only maintains the biological property and various biological activity of the amniotic membrane, but also the increases the clinical treating effect distinctively. The preparing process id simple and economical, the conservation time is as long as one year and with a high biological safety, which is facilitate for clinical spead. The product can be widely used in tissue engineering rebuilding and restoring, traumatology department, ulcerative tissue restoring, burn, scald biological dressing, plastics for eye rebuilding operation, and etc.

The invention relates to a new drug combination for treating diseases of traumatology, a preparation method and application of the drug combination, a medicinal preparation containing the drug combination and quality control method thereof. The drug combination provided by the invention can quickly and durably relieve pains, obviously and rapidly alleviate edema, facilitate callus growth and accelerate fracture healing; compared with the drug combination prepared by the prior art, the new drug combination has better curative effect and high safety.

The invention relates to the technical field of medical instruments, in particular to an auxiliary device for orthopedics and traumatology department rehabilitation. The device comprises a supportingplate, a supporting box body is slidably connected to the supporting plate, a seat plate is arranged on the supporting box body, and a massage mechanism matched with the seat plate is arranged in theseat plate; a pedal mechanism is slidably connected to the supporting plate, a pair of supporting arms are fixedly connected to the supporting plate, and movable arms are rotatably connected to the supporting arms; through pipes are arranged in the supporting arms and the movable arms; a pull rope is arranged in the through pipe, one end of the pull rope is fixedly connected with a pull ring, andthe other end of the pull rope is connected with a reciprocating adjusting mechanism; moving wheels and a brake are arranged below the supporting plate. The problems that the patient cannot effectively exercise the coordination of the limbs of the orthopedic patient and the orthopedic patient needs a period of time to do body coordination exercise after leaving the hospital are effectively solved;and meanwhile, the four limbs of the patient are exercised, so that the problems of muscle atrophy and the like of other parts due to the fact that the patient only exercises the upper limbs or the lower limbs and ignores exercise of other parts during illness are solved.

The invention discloses a high-efficiency magnetic medicament waist belt for treating acute and chronic soft tissue injury, hyperosteogeny and neck shoulder pain or lumbocrural pain of orthopedics and traumatology and a preparation method thereof. The waist belt comprises three parts, namely a waist belt main body, a magnetic sheet and a medicament patch, wherein the medicament patch comprises the following raw material medicaments: orientvine, kadsura pepper stem, Chinese starjasmine stem, suberect spatholobus stem, Japanese honeysuckle stem, common monkshood mother root, kusnezoff monkshood root, nux vomica, dahurian angelica root, drynaria rhizome, safflower, trogopterus dung, ground beeltle, himalayan teasel root, cassia bark and the like. The high-efficiency magnetic medicament waist belt of the invention is worn on the waist of a patient to treat various acute and chronic lumbocrural pain with good treatment effect based on the treatment principle of the magnetic medicament. The magnetic medicament waist belt has the function of treating both symptoms and root causes of the lumbocrural pain caused by various symptoms. The magnetic medicament waist belt has the advantages of simple and convenient method, short treatment period, no surgery, no pain, low medical expense and safe and reliable treatment when used for treating the diseases such as acute and chronic soft tissue injury, hyperosteogeny, neck shoulder pain or lumbocrural pain of orthopedics and traumatology and the like.

The invention relates to the technical field of medical apparatus and instruments, and discloses an external fixing frame for postoperative nursing of the bone traumatology department, the external fixing frame comprises a nursing bed, a side plate is fixedly mounted at the edge of the nursing bed, a U-shaped frame is slidably arranged on the outer wall of the side plate, and a driving device is arranged on the U-shaped frame and is used for driving the U-shaped frame to slide back and forth on the side plate. The legs of a patient are placed in the lower clamping sleeve, when the upper clamping sleeve gradually gets close to the lower clamping sleeve, magnetism of a magnetic block is utilized to push a piston, the piston moves along an arc-shaped cavity, the piston moves along the arc-shaped cavity so that air in the arc-shaped cavity can be inflated into an air bag through a communication opening, the air bag is inflated and swelled to be attached to the legs of the patient, and fixing is firmer and more comfortable; certain buffering and damping functions are also achieved, and the legs of the patient are prevented from being secondarily hurt. The external fixing frame is novel in design and simple in structure, and has the advantages that stretching traction and knee bending exercise can be achieved at the same time, legs are firmly and comfortably fixed, and limbs can be conveniently kept warm.

The invention discloses a gas chromatography finger printing quality control method for volatile ingredient in bone-knitting pharmaceutical preparation added with internal standard in the department of traumatology, which comprises the following steps: (1) preparing internal standard liquor: methyl salicylate is accurately weighed, and absolute ethyl alcohol or ethyl adetate is used for dissolving the methyl salicylate; (2) preparing test sample liquor: internal standard solution is added into the bone-knitting pharmaceutical preparation in the department of traumatology and after the ultra audible sound extraction, the test sample solution can be obtained; (3) analyzing and detecting the programmed temperature gas chromatography of sample solution of the bone-knitting pharmaceutical preparation in the department of traumatology; (4) building up the standard finger printing and analyzing the finger printing of the volatile ingredient of the bone-knitting pharmaceutical preparation in the department of traumatology. The invention has the advantages that the method is simple and stable, the precision is high, the reproduction quality is good, the method is reliable, scientific and effective evaluation can be done to the bone-knitting pharmaceutical preparation in the department of traumatology, and the method can be used for the quality control in practical production, which has beneficial effect on the whole control of producing quality of bone-knitting pharmaceutical preparation in the department of traumatology.

The invention relates to a traditional Chinese medicine for treating ankylosing spondylitis, belonging to the technical field of treatment of orthopedics and traumatology. The traditional Chinese medicine is characterized by comprising the following traditional Chinese medicine materials in parts by weight: 25-30 parts of rhizoma cibotii, 25-30 parts of cervus nippon temminck, 50-60 parts of epimedium herb, 15-20 parts of lingxian, 15-20 parts of twotooth achyranthes root, 15-20 parts of myrrh, 15-20 parts of eupolyphaga and 20-25 parts of rhynohophylla. According to the invention, based on the pathological principle of ankylosing spondylitis and the reasons causing the ankylosing spondylitis, a pure traditional Chinese medicine formula is adopted, and effective components are extracted and then prepared into internal oral liquid, or powder, or tablets or capsules. After being taken orally or externally used, the traditional Chinese medicine can effectively treat the ankylosing spondylitis and achieve ideal effect.

The present invention relates generally to an antibacterial coating which is composed of silver, to medical tools and to implants comprising such a coating and to a method as well to an apparatus for the production of such a coating. The medical tools or the dental or orthopaedic implant comprises a metal or metal alloy having a treated surface wherein the treated surface is at least partially converted to an oxide film by plasma electrolytic oxidation using a colloid-dispersed system and wherein the converted surface is partially covered by islands formed by colloid-dispersed silver-particles of the colloid-dispersed system. An Ag—TiO2 coating shows excellent properties in terms of antibacterial efficacy (even against multi-resistant strains), adhesion and biocompatibility. The life-time of an implant in a human body is increased. The antibacterial coating can be used in the field of traumatology, orthopaedic, osteosynthesis and / or endoprothesis, especially where high infection risk exists.

The invention relates to a patella fracture fixing device based on traumatology and orthopedics of traditional Chinese medicine and is applicable to undisplaced patella fracture. Patients suffering from fissural fractures or stellate fractures with small displacement can be purely utilize the patella fracture fixing device to fix the knee joints in an extending position, and patients transverse fractures with displacement within 1 cm can be treated through massage and then fix the knee joints in the extending position. The patella fracture fixing device has the advantages of being simple and flexible in application, low in production cost and capable of well meeting the individual demands of patients, embodies the characteristics of traumatology and orthopedics of traditional Chinese medicine and has wide application values.

The invention belongs to the technical field of application of traditional Chinese medicine, and in particular relates to an external application plaster combination for treatment of fracture injuries and a preparation method thereof. The external application plaster combination is characterized by comprising two parts of, namely traumatology extinction paste, and traumatology bone-setting paste. During the treatment of a fracture injury, different pastes are used at different stages, wherein the traumatology extinction paste is externally applied at the injury position in the early fracture reduction, and before and after a surgery; while the traumatology bone-setting paste is applied in the middle and late period to reduce local swelling and pain of the injury, and effectively promote the healing of the fracture, allowing a patient to perform effective functional training relatively early for prevention and treatment of joint stiffness. Clinical applications have proves that the external application plaster combination which is prepared from pure Chinese medicinal herbs, has advantages of being fast in relieving swelling and pain, short in the recovery period, definite in curative effects, and non-side effects.

The traumatological Chinese medicine composition for promoting blood circulation is prepared with rhubarb, raw aconite root, safflower, dragon's blood, Sichuan achyranthes root and other 15 kinds of Chinese medicinal materials, and through crushing, soaking, percolation, mixing, filtering, packing and other steps. It has the functions of promoting blood circulation to disperse blood clots, eliminating swelling and pain, activating vital energy, etc., and is used in treating acute closed soft tissue damage caused local swelling, pain, cyanosis, clot spot, etc in fast and long time acting and short treating period.

The present invention relates to a Chinese medicine for curing traumatic injuries, its preparation process and dosage form. Said Chinese medicine has the functions of quickly subduing swelling and stopping pain, promoting growth of callus and union.

The invention discloses a traditional Chinese medicine for treating chronic infectious arthritis, belonging to the technical field of treatment of orthopedics and traumatology. The traditional Chinese medicine is characterized by being prepared from the Chinese medical herbs in parts by weight: 15-20 parts of Chinese angelica, 15-20 parts of rhizoma rehmannia, 10-15 parts of cocklebur fruit, 20-25 parts of garter snake, 10-15 parts of eupolyphaga, 3-5 parts of scorpio, 10-15 parts of roasted squamamanitis into puffy with sand, 30-35 parts of rhizoma dioscoreae nipponicae, 20-25 parts of epimedium, 25-30 parts of caulis spatholobi, 15-20 parts of cortex erythrinae, 5-8 parts of dung beetle, 2-4 parts of centipede and 15-20 parts of medicinal cyathula root. According to the pathological mechanism principle of the chronic infectious arthritis and the reason causing the chronic infectious arthritis, a pure Chinese medicine formula is adopted, an oral liquid, or powder, or a tablet, or a capsule is prepared through extracting effective components; and an externally applied agent plaster can also be prepared. After the traditional Chinese medicine is orally taken, the chronic infectious arthritis can be effectively treated, and an ideal effect is achieved.

The invention relates to a medicine for treating ankylosing spondylitis, belonging to the technical field of orthopedics and traumatology treatment. The medicine is characterized by being prepared from the following active components in parts by weight: 2-4 parts of rhizoma cibotii, 1-3 parts of rhizoma curculiginis, 2-8 parts of dried body of ground beetle, 1-9 parts of rhynohophylla, 5-9 parts of astragalus membranaceus, 2-7 parts of cornu cervi degelatinatum, 2-6 parts of rhodiola rosea, 3-5 parts of asarum, 1-8 parts of myrrh, 3-7 parts of the root of bidentate achyranthes, 2-6 parts of radix clematidis, 1-8 parts of radix angelicae, 1-9 parts of pyrola, 2-8 parts of black semen sesame, 1-7 parts of poria cocos, 1-8 parts of divaricate saposhnikovia root, 2-8 parts of notopterygium root, 3-7 parts of ligusticum wallichii, 1-8 parts of the root of red-rooted salvia and 2-6 parts of lycopodium clavatum. According to the pathology principle of the ankylosing spondylitis and the reason for the ankylosing spondyliti, the medicine employs a pure traditional Chinese medicine formula, effective components are extracted to prepare the medicine into oral liquids, powder, tablets or capsules; when the medicine is orally taken and externally used, the ankylosing spondyliti can be effectively treated, and ideal effect is achieved.

The veterinary orthopedic kit relates to veterinary science and more specifically to orthopedics and traumatology, and can be used in veterinary clinics in the treatment and restoration of function to damaged limbs of dogs, cats and other animals. The technical problem to be solved consists in the timely and quality provision of emergency care to injured animals, an increase in the effectiveness of treatment and the prevention of serious complications. This problem is solved in that orthopedic external fixation systems are provided in a universal and multifunctional set. The veterinary orthopedic kit consists of a rectangular container in the form of a box having a lid and being divided by partitions into a plurality of sections. The sections accommodate a set of components and instruments for the purposes of external fixation: polyfunctional monoblocks, plates, rods and pins, bars, fasteners and instruments.

The present invention relates to a material, structure, and method for surgical use in traumatology. More particularly, the present invention relates to a composite material, a temporary biocompatible support structure, and related methods of use of the same in aiding osteosynthesis during healing of a bone fracture. The material keeps its strength in a solid phase in vivo and, to aid removal upon healing, can be transformed into a substantially fluid phase, including, for example, a pulverized state, by the application of energy at a chosen time.

The invention discloses a Chinese traditional medicine injection for traumatology and dermatological department and process for preparation, whose essential component is asiatic centella glycosides, its preparing process comprises dissolving asiatic centella glycosides in water, adjusting the pH to 2-3 with hydrochloric acid, extracting with trichloromethane, adjusting pH to 6-7 with 10% sodium hydroxide solution, extracting with water saturation n butanol, decompression concentrating the n-butanol layer, and drying, dissolving with ethanol, filtering, reclaiming ethanol from filtrate, dissolving the refuse with water for injection, obtaining asiaticoside solution, charging suitable adjuvant, treating with activated charcoal, filtering, thus obtaining liquid injection or fluid infusion or powder injection or freeze-dried powder injection.

The invention discloses a quality inspection method for analgesic liquid for the Miao ethnomedicine department of traumatology. The analgesic liquid for the Miao ethnomedicine department of traumatology is prepared from, by weight, 9 parts of Chinese birch velama, 6 parts of garden balsam stems, 6 parts of herba lycopodii, 6 parts of radix scutellariae, 6 parts of rhizoma coptidis, 6 parts of unprepared fructus gardeniae, 6 parts of cortex phellodendri, 6 parts of calcined gypsum, 6 parts of radix arnebiae seu lithospermi, 6 parts of radix trichosanthis, 3 parts of vinegar frankincense, 3 parts of vinegar myrrh, 3 parts of rhizoma curcumae longae, 3 parts of vinegar rhizoma corydalis, 3 parts of radix angelicae sinensis, 3 parts of safflowers, 3 parts of herba lycopi, 3 parts of ligusticum wallichii, 3 parts of scaled drynaria rhizome, 3 parts of radix et rhizome rhei, 3 parts of radix dipsaci, 2 parts of borneol and 2 parts of menthol. The quality inspection method comprises the step of character inspection, wherein the analgesic liquid is tan liquid and is pungent in smell and bitter in taste; the step of identification, wherein thin-layer chromatography of safflowers, thin-layer chromatography of the radix scutellariae and thin-layer chromatography of radix et rhizoma rhei are identified; the step of content assaying, wherein C21H18O11 content is assayed. By means of the method, the quality standard of the analgesic liquid for the Miao ethnomedicine department of traumatology can be formulated, and then the quality of the analgesic liquid for the Miao ethnomedicine department of traumatology can be inspected.

The invention discloses an osteosynthesis medicine for department of traumatology. The osteosynthesis medicine consists of active ingredients and accessories. The osteosynthesis medicine is characterized in that the active ingredients include the following materials in parts by weight: 40-60 parts of pseudo-ginseng, 80-120 parts of natural (forged) copper, 40-60 parts of safflower, 80-120 parts of ground beetle, 15-25 parts of nux vomica powder, 80-120 parts of frankincense (roasted), 80-120 parts of myrrh (roasted), 80-120 parts of chicken bone (roasted), 80-120 parts of muskmelon seed and 5-12 parts of borneol. The osteosynthesis medicine, through intercoordination of a plurality of Chinese herbal medicines, has functions of activating blood circulation and removing stasis, relieving swelling and pain, relaxing tendons and strengthening bone, and is obvious in effect on rapidly stopping bleeding and relieving pain, and promoting rapid growth, resetting and healing of sclerotin and osseocolla. The osteosynthesis medicine is mainly applicable to traumatic injury, lumbus pain and chest pain, injury in sinews or bones, blood stasis and swelling, injure and swelling, and other symptoms.

The invention provides a quality control method of a traumatology department yellow-water preparation. The method comprises the following steps of (1) weighing phellodendrine chloride, jatrorrhizine hydrochloride, epiberberine chloride, coptisine chloride, palmatine chloride, berberine hydrochloride, geniposide and chlorogenic acid; adding absolute methanol or methanol water solution for preparinga reference product solution; (2) taking contents of the traumatology department yellow-water preparation to be tested; adding absolute methanol or methanol water solution for dissolution; performingfiltering; taking subsequent filtering liquid to be as a solution to be tested; (3) respectively taking the reference product solution and 1 to 5 muL of the solution to be tested; injecting the materials into a liquid chromatography-mass spectrometry instrument for detection; obtaining the contents of phellodendrine, jateorhizine, epiberberine, coptisine, palmatine, berberine, geniposide and chlorogenic acid through calculating a quantitative chromatogram map. The method has the advantages that the original deficient quantitative evaluation index can be completed by once quantitative determination. The quantitative chromatogram map of the method can show good wave peak separation; the identification by the method is fast and accurate.

The invention relates to medicine, and more particularly to physiotherapy, neurology, traumatology, orthopaedics, rehabilitation and sports medicine, and can be used for relaxing spasmed muscles when treating patients with different conditions of the musculoskeletal and nervous systems, and also for prophylaxis in the social sphere. For this purpose, relaxed antagonist muscles are subjected to a stimulating electric impulse effect at an impulse frequency of from 15 to 35 Hz, with an impulse signal duration of from 5 to 60 μs and a working signal level of from 5 to 75% of the strength of a signal at which the patient feels a vibration. Spasmed agonist muscles are subjected to a relaxing thermal effect at a temperature of from 42 to 60° C. In addition, the segments of the spinal cord responsible for innervating the agonist-antagonist muscle pairs undergoing treatment are subjected to a thermal effect at a temperature of from 42 to 60° C. The agonist-antagonist muscle pairs and the segments of the spinal cord responsible for innervating the agonist-antagonist muscle pairs can be acted on simultaneously and alternately. The stimulating electric impulse effect and the relaxing effect can be carried out on individual regions of the body or on all regions simultaneously. The method provides effective physiological relaxation of spasmed muscles by means of a synergistic effect resulting from a combination of effects which engage the central nervous system that regulates and alters the physiological state of the tissues of agonist-antagonist muscle pairs.

The invention discloses a traditional Chinese medicine for treating a cervical disc protrusion disease, belonging to the technical field of treatment of orthopedics and traumatology. The traditional Chinese medicine is characterized by being prepared from the Chinese medical herbs in parts by weight: 25-30 parts of suberect spatholobus stem, 25-30 parts of rhizoma cibotii, 25-30 parts of white paeony root, 10-15 parts of cassia twig, 10-15 parts of epimedium, 15-20 parts of radix clematidis, 12-20 parts of the root of kudzu vine, 25-35 parts of rhizoma wenyujin concise, 15-20 parts of lumbricus, 10-15 parts of gastrodia tuer, 20-25 parts of gamdir vine, 10-15 parts of vegetable sponge and 2 centipedes. According to the pathological mechanism principle of the cervical disc protrusion disease and the reason causing the cervical disc protrusion disease, a pure Chinese medicine formula is adopted, an oral liquid, or powder, or a tablet, or a capsule is prepared through extracting effective components; and an externally applied agent plaster can also be prepared. Through orally taking and externally applying the traditional Chinese medicine, the cervical disc protrusion disease can be effectively treated, and an ideal effect is achieved.

The present invention relates to a material, structure, and method for surgical use in traumatology. More particularly, the present invention relates to a composite material, a temporary biocompatible support structure, and related methods of use of the same in aiding osteosynthesis during healing of a bone fracture. The material keeps its strength in a solid phase in vivo and, to aid removal upon healing, can be transformed into a substantially fluid phase, including, for example, a pulverized state, by the application of energy at a chosen time.