47 results about "Surgery.trauma" patented technology

The invention discloses a thoracoscope-assisted intelligent navigation system and method for thoracic surgery, and the method comprises the steps: recording the respiratory capacity of a patient and shooting a focus image in a breathing state, precisely calculating the position change amplitude and range of a focus in a breathing process, and drawing a dynamic graph for visual presentation; selecting an electromagnetic navigation system positioning method and performing preoperative planning according to lesion characteristics and positions, and adopting a transbronchial or transthoracic navigation positioning technology; wherein different anatomical regions of a human body are divided according to the focus position and the anatomical structure, a navigation path algorithm is planned for each anatomical region, parameters of the electromagnetic navigation system are adjusted according to the characteristics of tissues passed by the navigation path, and final positioning is confirmed; the television is combined with the thoracoscope to assist the thoracoscope, so that the focus is accurately marked and cut off; according to the method, the safety and success rate of the operation are improved, operation wounds are reduced, better treatment effect and experience are brought to patients, and the method conforms to the development trend of precision and intelligence of the medical technology.

The fixing device comprises an X-shaped steel plate and a straight steel plate which are located on the two sides of a bone respectively, a plurality of first penetrating holes are formed in the X-shaped steel plate, and a plurality of second penetrating holes are formed in the straight steel plate; a suture line, a loop turning line and a handle connecting line which are used for connecting the X-shaped steel plate and the straight steel plate are arranged in the first penetrating hole and the second penetrating hole in a penetrating mode, and the loop turning line is used for driving the straight steel plate to turn over relative to the X-shaped steel plate. The four corners of the X-shaped steel plate are all provided with stabs, and the stabs protrude out of the surface of the X-shaped steel plate and are used for stabbing into bone cortex. The X-shaped steel plate and the straight steel plate are arranged on the two sides of the fracture position respectively, meanwhile, the X-shaped steel plate is fixed to the fracture position through the spikes, the X-shaped steel plate and the straight steel plate are bound through the suture lines, so that fixation of the fracture position is achieved, and compared with a traditional operation, trauma is smaller, and fixation is firmer.

The invention discloses a single-incision one-step method TICL implantation method based on a 3D navigation system, and relates to the technical field of medical device.The single-incision one-step method TICL implantation method comprises the steps of S1, data collection, S2, three-dimensional modeling, S3, incision path planning, S4, operation implementation, S5, single-incision TICL implantation and S6, postoperative evaluation.Ocular optical data of a patient is collected through ophthalmology imaging equipment, the three-dimensional modeling, the incision path planning, the operation implementation, the single-incision TICL implantation and the post-operation evaluation are carried out, and the three-dimensional modeling, the three-dimensional modeling, the incision path planning, the operation implementation, the An individualized eye structure model is constructed in combination with a three-dimensional modeling technology, accurate fusion of astigmatism axial direction and cornea morphological parameters is realized, an incision path is planned by using a dynamic optimization algorithm and a genetic algorithm, key anatomical structures such as an iris root and a ciliary body are avoided while the incision length is minimized, operation wounds are reduced, and the operation efficiency is improved. The astigmatism correction angle is automatically optimized through a weighted average formula, manual errors are effectively reduced, and it is ensured that operation planning better fits anatomical features of a patient.

The invention discloses hydrogel for preventing postoperative tissue adhesion and a preparation method thereof, and belongs to the field of medical biological materials. The hydrogel is formed by taking a carboxylated chitin / chitosan derivative with the percentage concentration of 0.5-7% or a low-crosslinking-degree supramolecular derivative of a hydroxyalkylated chitin / chitosan derivative and collagen or gelatin as a solute and water, normal saline, a physiological equilibrium solution, a phosphate buffer solution or a Green's solution as a solvent, the crosslinking degree of the low-crosslinking-degree supramolecular crosslinking derivative is 0.1 to 6 mol percent. The molar ratio of the raw materials to the cross-linking agent is controlled, a small amount of cross-linking agent is used for micro-crosslinking, the prepared low-crosslinking-degree supramolecular derivative can form hydrogel in an aqueous solvent, and the hydrogel has adhesiveness and self-repairing performance, can effectively prolong the residence time and physical barrier time of the hydrogel on the surface of an operative wound, and can be used for preparing the hydrogel. Therefore, the effect of preventing postoperative combined adhesion of the hydrogel is improved, and the hydrogel is an ideal hydrogel material for preventing postoperative abdominal cavity and uterine cavity tissue adhesion.

The invention discloses a cheekbone and zygomatic arch fracture reduction guide plate, and relates to the technical field of cheekbone and zygomatic arch reduction, the cheekbone and zygomatic arch fracture reduction guide plate comprises a guide plate body and a fixing structure, the guide plate body is provided with an attaching inner surface matched with the anatomical form of an affected side cheekbone and zygomatic arch bone surface in a target reduction form; the fixing structure is arranged on the guide plate body and used for fixing the guide plate body to the healthy bone surface around the zygomatic arch of the diseased side cheekbone, the problems that in the prior art, operation trauma is large, accuracy is low, the reduction effect is not ideal and the like are solved, and the zygomatic arch fracture reduction fixing operation is completed accurately, safely and efficiently.

The invention relates to the field of auxiliary instruments for wrist arthroscopic surgery, and particularly discloses a wrist arthroscopic channel stabilizing device which comprises a groove type sleeve made of a disposable vein infusion tube, the tube wall of the groove type sleeve is cut off in the longitudinal direction to form an open groove, the two ends of the groove type sleeve are cut to be smooth, and the length of the groove type sleeve is suitable for a wrist arthroscopic surgery approach; by establishing the stable channel, the instrument can freely slide along the groove wall of the stable channel, repeated friction and injury of the surgical instrument to subcutaneous tissues around an approach, such as joint capsules, blood vessels, nerves and tendons, are effectively avoided, surgical wounds are remarkably reduced, multiple times of access of the same channel can be ensured, no tissue implication is caused, and the surgical efficiency is improved. By the adoption of the structure, intra-articular operation can be rapidly transferred to be conducted outside the joint, the annular design reduces compression damage to channel tissue, it is guaranteed that the sleeve always exists, and the open type notch design enables an operation instrument to obtain a free operation space.

The invention discloses a facial ligament lifting method, which comprises the following steps of S1, accurately marking a subcutaneous attachment end or a body surface projection area corresponding to a target facial ligament on the surface of facial skin on the basis of facial anatomical positioning and anatomical walking of the target facial ligament, so that the subcutaneous attachment end or the body surface projection area corresponding to the target facial ligament is accurately marked on the basis of facial anatomical positioning; acting force is accurately focused on the target ligament through a special instrument, and surrounding tissue is prevented from being damaged. The whole process is only operated on the skin surface, no incision or implantation is needed, surgical wounds and wire foreign matter risks are thoroughly avoided, the composite force can be effectively conducted to the deep ligament to enable the deep ligament to generate controllable folding deformation, stable fixation is achieved through a subsequent biological healing mechanism, ligament relaxation is fundamentally improved, the effect is more natural and lasting, and the application range is wide. Due to the fact that skin breaking is not needed and energy is controllable, the operation safety is greatly improved, and dynamically-adjusted mechanics and selectable hot-cold collaborative procedures aim at optimizing experience and ensuring the comfort degree of the process.

The invention relates to a diameter-variable blood vessel sheath structure, which solves a series of problems of large operative wound, incapability of intraoperative radiography and the like in the process of treating arterial embolism of lower limbs through open thrombus extraction of a traditional Fogarty catheter. The device comprises an outer sheath, an inner sheath and a sheath core which are sequentially nested from outside to inside, the outer sheath comprises an outer sheath main body and an outer sheath base arranged at the near end of the outer sheath main body; the inner sheath comprises an inner sheath body, an inner sheath base is arranged at the near end of the inner sheath body and connected with a hemostasis valve, the far end of the inner sheath body is connected with a self-expansion covered stent sample structure with two open ends, and the length of the inner sheath is larger than that of the outer sheath. The sheath core comprises a sheath core body, a sheath core base is arranged at the near end of the sheath core body, a conical end with the outer diameter gradually reduced is arranged at the far end of the sheath core body, a middle hole for a guide wire to penetrate through is formed in the sheath core body, and the length of the sheath core is larger than that of the inner sheath. The device has the advantages of high effectiveness, high safety, strong adaptability, good adaptability, simple structure and convenience in operation.

The invention relates to an AI-assisted lumbar intervertebral disc resection visual navigation device with a postoperative care monitoring function, and belongs to the technical field of medical equipment.The AI-assisted lumbar intervertebral disc resection visual navigation device comprises an AI assisting module, a visual navigation module, a postoperative care monitoring module and a data processing and transmission module, and the AI assisting module is internally provided with an image recognition model and a risk prediction model; the system is used for performing lesion recognition and positioning on image data of a patient before an operation, performing operation risk assessment in combination with multi-source information of the patient, and overlapping and displaying the operation risk in a three-dimensional model to realize real-time navigation in the operation, the AI auxiliary module realizes accurate lesion positioning and risk quantitative assessment, and the visual navigation module provides real-time guidance with the precision smaller than or equal to 0.5 mm. The postoperative nursing monitoring module achieves all-around real-time monitoring of physiological parameters, wound states and rehabilitation training, and the abnormity early warning subunit discovers the risks in time and treats suggestions in a grading mode to improve nursing pertinence.

The invention discloses an arthroscope positioning method and system for knee joint minimally invasive surgery. The anatomical mark points are recognized and tracked in real time through the operation video stream collected by the arthroscope camera in combination with the computer vision algorithm. The pre-planned ideal bone tunnel position and the anatomical marker in the real-time image are accurately registered, so that the system can dynamically generate surgical navigation information and visually display the position of the entrance point of the bone tunnel. According to the scheme, dependence of a traditional navigation system on a special surgical instrument and a complex calibration process is avoided, the visual field of the arthroscope familiar with a surgeon can be fully utilized, and more visual and convenient surgical guidance is provided, so that the surgical precision and efficiency are remarkably improved, and the risk of surgical wounds and complications is reduced.

The invention relates to the technical field of medical instruments, in particular to a 3D (three-dimensional) biological knee joint and a preparation method thereof.The 3D biological knee joint comprises a femoral condyle component, a tibia support component, a meniscus component and a patella component; according to the method, individualized knee joint data of a patient is obtained through CT / MRI scanning, reverse modeling is conducted in combination with Mimics software, a precisely-matched prosthesis three-dimensional model is generated, and the success rate is increased; based on specific anatomical features of a patient, adaptability errors of a traditional standardized prosthesis are avoided, operative wounds are reduced, and the initial stability of the prosthesis and a bone interface is improved. According to the invention, through the combination of technological processes such as individualized modeling, gradient functional coating, multi-process printing and post-treatment, the defects of a traditional knee joint prosthesis are overcome, and the properties such as remarkably improved biocompatibility, excellent antibacterial property, optimized mechanical matching property and accurate individualized adaptation are improved.

The invention relates to the technical field of medical treatment, and discloses a postoperative rectum finger force stimulation method which comprises the following steps: step 1, targeted excitation work of stomach colon reflex: remotely starting colon group movement mainly by simulating physiological feeding stimulation; and 2, after the step 1 is completed, executing broad-spectrum enhancement work of the intestinal tract body peristalsis function through preset physiological response delay time, mainly enhancing and maintaining the intensity and duration of the intestinal tract peristalsis wave excited by the previous steps through composite physical and chemical stimulation. Through four steps, a plurality of links such as stomach colon reflex excitation, whole intestinal tract movement enhancement, rectum end pre-sensitization and key nerve reflex accurate triggering are organically integrated, and a complete manual intervention system is constructed and used for simulating and repairing a normal defecation physiological chain interrupted by an operative wound; and the method has high systematicness, logicality and synergy.

The utility model belongs to the technical field of medical instruments, and discloses a tissue resection device which comprises a pushing catheter, a first snare wire and a second snare wire, the first snare wire and the second snare wire penetrate through the pushing catheter, the two near ends of the first snare wire extend out of the near end of the pushing catheter, and the two near ends of the second snare wire extend out of the near end of the pushing catheter. The first snare wire forms a cutting ring outside the far end of the pushing catheter; the two near ends of the second snare wire extend out of the near end of the pushing catheter, and the second snare wire forms a fixing ring outside the far end of the pushing catheter. According to the tissue resection device, the tissue is tightened through the fixing ring, the effect of pulling the tissue is achieved, the form of the tissue can be stabilized, cutting of the tissue by the cutting ring is facilitated, the tissue cutting speed is effectively increased, operation wounds and operation time are reduced, and operation risks are reduced.

The invention discloses a multi-parameter monitoring pressure-adjustable recoverable hydrocephalus shunting device and a treatment method, and belongs to the technical field of medical instruments. The device comprises a shunt pipe assembly and a recovery device. The shunt tube assembly forms a cerebrospinal fluid shunt passage from a ventricle to veins, a front-end brain pressure monitoring module, an automatic pressure regulation flow rate valve, a central processing and transmission module and a multi-parameter function monitoring module are integrated, and automatic regulation and control of intracranial pressure and real-time monitoring of multiple parameters of thrombus, blood pressure and blood oxygen are achieved. The flow velocity of cerebrospinal fluid is autonomously adjusted through the automatic pressure adjusting flow velocity valve according to dynamic changes of intracranial pressure, traditional manual adjustment is replaced, and adjustment and control accuracy and timeliness are improved; meanwhile, the shunt tube is safely and conveniently replaced through a magnetic recovery structure, and operation wounds and infection risks are reduced. The system is suitable for precise treatment and postoperative comprehensive monitoring of adult hydrocephalus.

Methods and devices for the nasal administration of compositions comprising glutathione trisulfide (GSSSG), pantethine trisulfide (PTN-SSS), or lipoic acid trisulfide (LA-SSS) in neuroprotection, e.g., in neurodegenerative diseases and to reduce the risk of ischemic injury. The methods can be used, e.g., to reduce risk of injury to brain, spinal cord, and peripheral nerves from ischemia or low blood flow states possibly caused by surgery, trauma, and other conditions that decrease / impair blood flow and or oxygen delivery to the nervous system.

The utility model relates to the technical field of hand and foot surgery, and discloses a hand and foot surgery minimally invasive operating table which comprises a fixing plate, a base is fixedly connected to the middle of the upper surface of the fixing plate, a fixing column is fixedly connected to the middle of the upper surface of the base, and an operating table body is fixedly connected to the top of the fixing column. According to the minimally invasive surgery operating table, a doctor can observe a surgical site more clearly through the arrangement of the camera device, so that the accuracy and safety of a surgery are improved, due to the design of the minimally invasive surgery operating table, a surgical incision is smaller, surgical wounds are reduced, and a patient can recover more quickly; the operating table is provided with various auxiliary devices such as a drainage groove and a bandage, the limbs of a patient can be better fixed, dirty liquid generated in the operation process can be better collected, the surface of the operating table is kept relatively dry, the liquid is prevented from affecting the operation, and meanwhile cleaning work after the operation is facilitated.

The invention relates to the technical field of medical instruments, and discloses an aortic arch intracavity cerebral blood perfusion and radiography dual-purpose sheath which comprises a sheath tube, the sheath tube is a hollow tube, the sheath tube has flexibility and fracture resistance, the two ends of the sheath tube are divided into a near end and a far end, a side hole is formed in the middle end of the sheath tube, the near end of the sheath tube is fixedly connected with a sheath connector, and the sheath connector is fixedly connected with the sheath tube. A connecting tube is led out of the side face of the sheath joint, a rubber sheet is arranged at the joint of the sheath joint, a crack is formed in the middle of the rubber sheet, the guide wire / sheath core penetrates through the crack, the position of a puncture femoral artery is guided through B ultrasound, the guide wire / sheath core and the sheath tube are matched to the right common carotid artery, then the sheath tube is placed through the guide wire / sheath core, and the far end of the sheath tube is located in the right common carotid artery. After the long guide wire / sheath core is pulled out and the short guide wire / sheath core is placed, blood flow is transferred to the carotid artery through the side hole in the middle section of the sheath tube, so that blood is supplied to the inside of the brain, the effect of relieving cerebral ischemia caused by covering the carotid artery after the stent body is released is achieved, and the surgical wound surface is small.

The invention is applied to the technical field of medical treatment, and discloses a thoracic surgery postoperative complication intelligent prediction system, which comprises a data acquisition and transmission module, a feature extraction and model training module, a real-time monitoring and prediction module and a decision support module. According to the intelligent prediction system for the postoperative complications of the thoracic surgery department, the flexible silica gel intelligent pectoral girdle integrating the pulse oximeter, the respiratory rate sensor and the micro-pressure sensor is adopted, and continuous and real-time collection of physiological data such as the heart rate, the blood oxygen saturation degree, the respiratory rate and the thoracic tiny pressure change is achieved; the problem of prediction lag caused by traditional intermittent manual monitoring is solved, the endurance of equipment reaches 72 hours or above, the integrity and comfort of data acquisition are ensured by combining a low-power reminding function, the monitoring effect is prevented from being influenced by equipment defects, key information such as operation types, duration and bleeding amount is automatically obtained through a hospital information system (HIS), and the operation efficiency is improved. The postoperative physiological status and the operative wound influence of the patient are comprehensively reflected.

The utility model belongs to the technical field of orthopedic instruments, particularly relates to a hollow traction needle giving consideration to reduction and fixation, and solves the problems of complex operation, insufficient reduction precision and unstable fixation in the traditional fracture reduction and fixation process. A hollow traction needle with resetting and fixing functions comprises a fixing guider, a positioning needle, a guide needle and a hollow screw, and the fixing guider is provided with a main body and a handle arranged on the main body; a first through hole and a second through hole are formed in the length direction of the main body in a penetrating manner; the handle is held by an operator; the positioning needle is configured to be implanted into the bone through the second through hole so as to fix the angle and the position of the fixed guider; the guide pin is configured to be implanted into the bone through the first through hole; the hollow screw is provided with a center channel, can be arranged on the guide pin in a sleeving mode and is configured to be implanted into the bone through the first through hole under the guidance of the guide pin. The traction and internal fixation device has traction and internal fixation functions, can provide a stable fixation effect during fracture reduction, reduces operative wounds, and reduces postoperative complications.

The present invention discloses a biological acetabular partial reconstruction prosthesis for treating hip dysplasia, which comprises a specific base and an articular surface coating. The upper end of the specific base is pointed and small, while the lower end is thick and large. It includes an acetabular contact surface, a soft tissue contact surface and a femoral head joint engagement surface. The acetabular contact surface and the soft tissue contact surface enclose the side surface of the specific base, and the femoral head joint engagement surface constitutes the bottom surface of the specific base. The specific base is a three-dimensional porous network structure. The biological acetabular partial reconstruction prosthesis for treating hip dysplasia disclosed by the present invention enables patients to improve the biomechanical environment of the hip joint, delay the progression of hip arthritis, and avoid the disadvantages of large surgical trauma and poor morphological combination of the existing periacetabular osteotomy. At the same time, it can be applied to the early treatment of sequelae of hip dysplasia, delay or avoid joint replacement, and has a significant effect on the treatment of patients with mild hip dysplasia.

The utility model provides an integrated internal iliac sitting steel plate of resetting and fixing relates to rehabilitation tool technical field, including bevel angle plate body, connecting plate body and arc-shaped plate body, connecting plate body is connected with one end of bevel angle plate body, arc-shaped plate body is connected with one end of connecting plate body, the inner side of arc-shaped plate body is provided with the inner extension bulge, the inner side of arc-shaped plate body is provided with the inner extension bulge, the inner side of arc-shaped plate body is provided with the outer extension bulge. An inner groove is formed in the inner side of the inner extending bulge; a plurality of groups of fixing holes are formed in the oblique angle plate body, the connecting plate body and the arc-shaped plate body; the anterior approach surgery fixing plate is composed of the oblique angle plate body, the connecting plate body and the arc-shaped plate body, the oblique angle plate body is matched and fixed with an iliac wing, the arc-shaped plate body is matched and fixed with an arcuate line, and the inward extending protrusion is matched with the inner groove to be matched and fixed with an ischial large incisura, so that the anterior approach surgery is matched, the treatment effect can be improved, and surgical wounds are reduced; the rehabilitation curve is shortened, and considerable social and economic benefits are achieved.

The invention relates to the technical field of orthopedic treatment, and provides a non-invasive orthopedic spinal disease treatment method which comprises the following steps: acquiring orthopedic disease image data of a patient through nuclear magnetic resonance examination; combining a hospital examination report, a nuclear magnetic resonance film and on-site physical examination of a patient, comprehensively analyzing and accurately positioning a pain position; according to the positioned pain position, a skin needle is used for carrying out slight acupuncture treatment on the corresponding skin epidermis; carrying out disinfection treatment on all the acupuncture parts; applying a specially-made detoxifying and repairing plaster to the acupuncture part, and fixing with a medical proof fabric; high risks such as surgical wounds, infection, bleeding and nerve injury operation sequelae caused by traditional operations are avoided, the treatment safety is greatly improved, through the combination of accurate diagnosis of the nuclear magnetic resonance imaging technology and the skin needle therapy and the continuous effect of the specially-made toxin expelling and repairing plaster, the focus can be accurately positioned, and the treatment effect is improved. Local blood circulation is promoted, inflammation is eliminated, pain is relieved, and tissue repair is promoted.

The implant prosthesis comprises a humerus component and a connecting component, one side of the humerus component is provided with an attaching part, the attaching part is attached to a lesion area of a humerus head, and the surface of the side, close to the humerus head, of the humerus component is provided with a first biocompatible coating; one end of the connecting component is connected with the humerus component, the other end of the connecting component is installed on the humerus head, and a second biocompatibility coating is arranged on the surface, making contact with the humerus head, of the connecting component. According to the invention, boning replacement can be carried out on a small lesion area of the shoulder joint, an effective solution is provided for a patient who needs prosthesis replacement in a small lesion area on the surface of the shoulder joint humerus head, the bone mass of the patient can be reserved to the greatest extent, the damage amount to healthy sclerotin is reduced, the operative wound to the patient is reduced, and the rehabilitation of the patient is promoted.

This invention discloses a foreign body removal device, belonging to the field of medical auxiliary device technology. The device includes a malleable support, a connecting rod, and a flexible wrapping band. One end of the connecting rod is connected to the malleable support, and the other end has a handle ring. The malleable support is made of medical-grade stainless steel or titanium alloy closed elastic metal ring, which can be bent and shaped while maintaining its form. Its surface is smooth and polished, the ends are rounded, and it is coated with a hydrophilic coating. The flexible wrapping band is made of medical-grade sterile degreased cotton cloth or non-woven fabric, fixed to the outer periphery of the support and featuring anti-slip texture. In use, the support adapts to the physiological curvature of the rectum to bypass the foreign body, guiding the flexible wrapping band to completely wrap the foreign body. It can then be safely expelled by pulling with the handle. This invention has advantages such as strong adaptability, stable clamping, minimal mucosal damage, and simple operation. It is suitable for minimally invasive removal of various rectal foreign bodies such as plastic, glass, silicone, and fruit pits, reducing surgical trauma and the risk of complications.

The present invention discloses a device for spinal cord stimulation, which includes a programmer, a wireless power supply device, an electrode module, and a wireless power receiving device. The electrode module includes a left electrode, a right electrode, a left guiding tube, a right guiding tube, and a water sac. A hollow blind hole is provided at the head end of the left electrode. The left guiding tube is slidably sleeved outside the head end of the left electrode, and the length of the left guiding tube is slightly longer than the hollow blind hole at the head end of the left electrode. The right guiding tube is hollow, and the right electrode is slidably placed inside the right guiding tube. There is a hollow pipeline inside the right electrode, and the water sac is slidably placed inside the right electrode. The electrode module is detachably electrically connected to the wireless power receiving device and is placed inside the patient's body. The programmer and the wireless power supply device are electrically connected through a USB interface and are placed outside the patient's body. The present invention proposes a brand-new SCS scheme, which reduces the doctor's surgical volume, reduces the surgical trauma for the patient, reduces the patient's economic expenditure, reduces potential safety hazards, and does not affect magnetic resonance imaging.

The utility model relates to a pair of bipolar electric coagulation forceps for hemostasis of surgical wounds, which aims to solve the technical problem that the conventional bipolar electric coagulation forceps can be used for hemostasis of the surgical wounds only by being continuously pressed by a worker, and comprises two groups of forceps bodies which are symmetrically arranged, the forceps bodies are rotationally connected with the rotating grooves formed in the outer sides of the connecting blocks through the connecting rods, the first adjusting rod is in sliding connection with the limiting grooves in the second adjusting rod, and when the handles are stopped being pressed, the handles of the two forceps bodies can be pushed to move reversely and be opened through the elastic force of the springs in the limiting grooves; the forceps heads at one ends of the forceps bodies move relatively and automatically clamp small blood vessels or small wounds, so that the problem that the forceps heads of the existing bipolar electric coagulation forceps can clamp the small blood vessels or the small wounds for surgical wound hemostasis only by continuously pressing the forceps bodies by working personnel is solved, and the labor intensity of medical personnel is reduced.

The invention discloses a magnetic sleeve for replacing a tong head in an abdominal cavity and a using method, the magnetic sleeve comprises a sleeve body, two ends of the sleeve body are respectively provided with a cavity, a tong head can be arranged in each cavity, and the sleeve body is integrally formed by a magnetic material. Two forceps heads can be carried at a time to enter the abdominal cavity, replacement of the forceps heads can be completed under the condition that an instrument does not leave the abdominal cavity, the situation that the forceps heads of one type are adopted for operation all the time is avoided, the risk that the surgical field is interrupted due to replacement of the forceps heads is also avoided, and the surgical efficiency is improved; the position of the magnetic sleeve in the abdominal cavity is moved in a magnet mode, the acting force of a magnetic field does not bring extra operation wounds to a patient, special operation equipment does not need to be added, and the forceps head can be replaced in a noninvasive mode.

The invention provides a construction method and application of a spontaneous thin uterus mouse model. The mouse model constructed by the invention can spontaneously and stably show thin endometrial pathological characteristics highly consistent with clinical characteristics, is clear in pathogenesis, highly simulates clinical characteristics, does not need any external injury operation, and completely eliminates interference of unstable factors such as operative wounds, inflammatory reactions, non-specific adhesion and the like. The invention provides an efficient and reliable in-vivo screening and verification platform for developing a novel treatment strategy aiming at the thin endometrium, and has important clinical application potential and scientific value.

A device, system and method for neural stimulation, and a storage medium. The device comprises: a stimulation control module, which is disposed outside of a biological body, and is used for generating a stimulation instruction; a remote control module, which is disposed outside of the biological body, is in communication connection with the stimulation control module, and is used for generating a module activation instruction for activating the stimulation control module; and an electrode module, which is used for being implanted into the biological body, and is in communication connection with the stimulation control module, so as to execute the stimulation instruction sent by the stimulation control module. By means of the solution, intervention can be performed in a timely manner when a patient foresees risks, so as to reduce potential risks; and the volume of an implanted part can also be reduced, thereby reducing surgical trauma and also breaking through power consumption limits, and thus neural stimulation therapy with a better effect is implemented by using an algorithm with a higher precision.

The utility model discloses a muscle tendon extracting device capable of reducing operative wounds, which comprises a grab handle, one side of the grab handle is fixedly connected with an extracting rod, one side of the extracting rod is fixedly connected with a sleeve, the outer wall of the grab handle is provided with grooves, the front view of the grooves is arc-shaped, the grooves are distributed on the outer wall of the grab handle at equal intervals, and the sleeve is fixedly connected with the grab handle. The sleeving rod is made of a 630 stainless steel material, the hardness of the sleeving rod is larger than or equal to 42 HRC, the surface roughness Ra of the sleeving rod is smaller than or equal to 1.6 micrometers, the surface roughness Ra of the sleeving rod is smaller than or equal to 1.6 micrometers, a sharp opening is formed in the top end of the sleeve, and the sleeve is made of the 630 stainless steel material. According to the tendon extracting device capable of reducing the operative trauma, through the arrangement of the grab handle, the extracting rod and the sleeve, the condition of reducing the operative trauma during the operation is realized, so that the safety of the operation is improved, and the problems that the trauma is aggravated and the operative risk is increased due to the infection condition in the operation process are avoided.