65results about How to "Reduce complications" patented technology

The invention relates to the field of medicine, and discloses a thyroid nodule surgical operation planning and navigation system based on artificial intelligence, which comprises a multi-modal medical image acquisition module, an image preprocessing and enhancing module, an intelligent anatomical structure analysis module, an operation planning decision module and an intraoperative real-time navigation module, the multi-modal medical image acquisition module is used for integrating data of various image equipment such as ultrasonic equipment, CT equipment and MRI equipment, and space-time consistency of multi-modal images is ensured. According to the thyroid nodule surgical operation planning and navigation system based on artificial intelligence, the real-time calculation problem is solved, the system delay is reduced, which is crucial to real-time navigation in an operation, the real-time performance and the operation efficiency are improved, the operation time is shortened, and complications are reduced; by integrating the advantages of different images, the system can provide more comprehensive dissection views, help doctors to more accurately position nodules and important structures and avoid injury to nerves and blood vessels, so that the accuracy is improved, and the surgical risk is further reduced.

The invention discloses an acute kidney injury risk early warning system, and relates to the technical field of clinical decision support systems. In order to solve the problems that in the prior art, due to the fact that a large amount of data preprocessing and model training need long-time data processing and model operation, the early warning opportunity is not accurate, the real-time performance is low, personalized early warning prompting cannot be carried out for patient groups, and early warning fatigue and early warning desensitization are likely to be caused. Through data preprocessing, model construction and risk analysis, real-time monitoring and accurate prediction of the AKI risk of a patient are realized, the early recognition rate is improved, the early warning decision unit generates specific early warning information according to risk scores and kidney function change rules and provides targeted treatment suggestions, and meanwhile, through an early warning threshold adjustment and approach matching module, the early warning decision unit can perform early warning on the AKI risk of the patient. The early warning strategy is optimized, the response speed of medical staff and the compliance of patients are improved, and the user interaction unit continuously optimizes the early warning system through a feedback mechanism.

The invention discloses an anesthesia assessment big data intelligent supervision system, which comprises a user interface module and a supervision system module, and is characterized in that the supervision system module comprises a multi-source data acquisition and integration module, a real-time data analysis and assessment module, an intelligent early warning and decision support module and a visual report and long-term tracking module; by integrating advanced information technology and medical knowledge, intelligentization and precision of anesthesia management are realized, all modules of the system cooperate with one another, data acquisition, processing, analysis and application are completed together, comprehensive, accurate and personalized anesthesia risk assessment and scheme suggestions are provided for users, and the user experience is improved. According to the method, doctors can be helped to master the condition of a patient more accurately, a more reasonable treatment scheme is formulated, risks and complications in the anesthesia process are reduced, the treatment effect and satisfaction degree of the patient are improved, configuration of medical resources can be optimized, the efficiency and quality of medical services are improved, and powerful support is provided for sustainable development of medical institutions.

The invention provides an acetabular prosthesis, which comprises an acetabular cup, an acetabular prosthesis body, an acetabular prosthesis body and an acetabular prosthesis body, wherein a mounting groove is formed in the inner side of the acetabular cup; the lining is adjustably arranged in the mounting groove in the direction perpendicular to the inside and outside direction of the acetabular cup, and an adjusting interval is formed between the outer side wall of the lining and the groove wall of the mounting groove; and the filling piece is filled in the adjusting interval and is matched with the adjusting interval in size so as to limit the movement of the lining relative to the acetabular cup. According to the technical scheme, the problems that in the prior art, an acetabular cup is not easy to install in place, and the rotation center of a hip joint is not easy to reset can be solved.

The invention discloses an endoscope weight reduction support which comprises an upper reducing supporting body, a lower reducing supporting body, a connecting pipe and a membrane pipe. The upper reducing support body and the lower reducing support body are connected through a connecting pipe; and the membrane tube is fixed on the lower reducing support body. The degradable stent is prepared from a poly (p-dioxanone) material, and the degradable stent does not need to be taken out and can be automatically degraded and discharged, so that the step of taking out the stent is omitted, the cost and the risk are reduced, and the comfort of a patient is improved. The fixing effect is more stable, stent displacement is avoided, and stimulation of stent barbs to duodenum bulbar mucosa is avoided; the degradable stent is prepared from a poly (p-dioxanone) material, and the degradable stent does not need to be taken out and can be automatically degraded and discharged, so that the step of taking out the stent is omitted, the cost and the risk are reduced, and the comfort of a patient is improved.

The invention relates to the technical field of ablation path planning, in particular to a liver cancer thermal ablation path planning system based on deep reinforcement learning. The system comprises a target and dangerous area mask generation module, a pipeline distance field construction module, a thermal field prediction module, a breathing deformation prediction module, a multi-scale feature fusion module, a behavior preference reward module, a composite reward function module and a decision output module. Clinical pain points such as breathing interference, dangerous area avoidance and individualized adaptation are broken, the precision and safety of the liver cancer thermal ablation operation are improved, normal tissue damage and complications are reduced, intelligent decision support is provided for interventional therapy, and liver cancer minimally invasive therapy is promoted to be upgraded to precision and intelligence.

The invention relates to a finger-pressing type nucleic acid detection micro-fluidic chip, which comprises a bottom layer, a flow channel layer, a finger-pressing layer and a thin film layer, the flow channel layer comprises an LAMP reaction chamber, a CRISPR reaction chamber, a water storage chamber, a Tesla valve, a finger-pressing chamber and a test paper reaction chamber, the LAMP reaction chamber comprises a nucleic acid extraction-free reaction system based on LAMP, the CRISPR reaction chamber comprises a CRISPR-based cas12b reaction system, and the test paper reaction chamber comprises a Tesla valve, a finger-pressing chamber and a test paper reaction system. The water storage chamber is mainly used for diluting a mixed system, and the Tesla valve is used for preventing crosstalk of the two reaction systems; the finger pressing layer comprises an LAMP reaction chamber button and a CRISPR reaction chamber button, when the LAMP reaction chamber button is pressed, liquid in the LAMP reaction chamber is pumped into the CRISPR reaction chamber, when the two buttons are pressed at the same time, a reaction mixing system is pumped into the water storage chamber to be mixed, and then the reaction mixing system is further pumped into the test paper reaction chamber. The chip can be widely applied to the field of rapid diagnosis of nucleic acid molecules, the detection cost is reduced, manual operation is simplified, and the detection efficiency is improved.

Provided is a tunable biopolymer hydrogel produced from two processed natural polysaccharides for use as a hemostat. If desired, the hydrogel formation can be tuned so that the hydrogel forms within seconds when applied to a tissue lesion. The resulting hydrogel can adhere to tissue and, without swelling, produce hemostasis within seconds after application to tissue of interest. The hydrogel also captures, aggregates and concentrates platelets and red blood cells at the site of the tissue lesion thereby initiating a clotting cascade at the site of the lesion. The hemostat can be used to prevent blood loss during surgical procedures, for example, during brain, spine or other surgical procedures where hemostasis is desirable, and is particularly useful during surgical procedures where swelling of the hemostat (e.g., in the brain or spine) would be detrimental to the subject.

The present application relates to a kind of personalized orthodontic bite gum, the bite gum is used to cooperate with the use of invisible aligner, the bite gum is horseshoe structure in horizontal plane view, it is wedge structure of back thin front thick in sagittal plane view;The bite gum includes bite gum pad, buccal side, lingual side, the buccal side and the lingual side extend to dental arch buccal side and lingual side from the bite gum pad;The bite gum is provided with the avoidance of corresponding arrangement with the invisible aligner, the avoidance is used to avoid weak position on the invisible aligner.The bite gum provided by the present application is mainly aimed at the cases of tooth extraction, tooth defect, replacement tooth period, tooth occlusal surface design, etc.Special device case, by setting avoidance, the bite gum can avoid weak position on the invisible aligner, prevent the deformation of aligner due to the use of bite gum, affect the treatment effect, reduce the use requirement to patient, improve the use efficiency of bite gum, save time.

The utility model 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 lower limb artery embolism by opening a Fogarty catheter to take thrombus. 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 utility model has the advantages of high effectiveness, high safety, strong adaptability, good adaptability, simple structure and convenient operation.

The utility model relates to a self-turning body-position-adjustable anti-bedsore massage air cushion, belongs to the technical field of medical instruments, and solves the problem that the posture of an existing inflatable air cushion cannot be adjusted according to the requirements of a patient. The self-turning-over body-position-adjustable anti-bedsore massage air cushion is divided into three layers, the bottommost part is the anti-bedsore air cushion layer, the middle part is the self-turning-over auxiliary air cushion layer, the uppermost part is the massage cushion, and the massage cushion can provide acupoint stimulation. The air inflation pump, the vacuum pump, the controller and the plurality of sets of electromagnetic valves are arranged, so that different air bag modules can be quickly switched to inflate or vacuumize, and the overall posture of the mattress can be adjusted. According to the utility model, the functions of assisting a patient in turning over and adjusting sitting and lying postures are realized.

The invention discloses application of lauromacrogol in preparation of a medicine for treating nasal polyp, and belongs to the technical field of medicines. The invention discloses an application of lauromacrogol in preparation of a medicine for treating nasal polyp. When lauromacrogol is used for treating nasal polyp, the nasal polyp can be reduced, and clinical symptoms can be eliminated. According to clinical data statistics, the lauromacrogol is adopted to treat nasal polyp, the cure rate is 89.56%, the improvement rate is 10.44%, and no recurrent symptoms occur. The invention creatively provides a new application of lauromacrogol, and the lauromacrogol is used for preparing the medicine for treating nasal polyp, and is definite in effect, small in adverse reaction and worthy of popularization and application.

This invention discloses a pre-placed adjustable hernia repair patch and its preparation method, relating to the field of medical device technology. The patch body is a polypropylene woven mesh with a weight of less than 50 g / m². The polypropylene woven mesh has a double-layer gradient structure with different densities on both sides. This pre-placed adjustable hernia repair patch uses a double-layer gradient structure of the same woven mesh. The outer layer has large pores (80-300 μm) to facilitate fibroblast ingrowth and tissue fixation, while the inner layer has small pores (15-80 μm) to form a physical barrier, effectively inhibiting visceral adhesions. It addresses both fixation and anti-adhesion needs. Temporary fixation is achieved through sliding PLGA fixation pins, pre-drilled holes, and elastic rings. The fixation pins are available in various lengths, and the elastic rings enable temporary fixation and position adjustment. Blue marking lines facilitate directional identification, and barium sulfate contrast markers aid in intraoperative positioning and postoperative follow-up.

The scoliosis orthosis comprises a supporting structure, the supporting structure comprises a first supporting unit and a second supporting unit which are connected with each other, the first supporting unit comprises a first supporting face, and the second supporting unit comprises a second supporting face; the first supporting face and the second supporting face are connected through a connecting mechanism, the connecting mechanism comprises a first adjusting belt and a first buckle which are connected with each other, adjusting gears are arranged on the second supporting face, and the second supporting face is connected with a supporting bone. A second adjusting belt and a second buckle which are connected with each other are arranged on the second supporting surface; the scoliosis orthosis is made of a three-dimensional model made according to scoliosis data of a patient. Accurate correction is achieved, the cost for replacing the brace for a long time is greatly reduced, the problem that the brace is not matched is greatly solved, and the effect that multiple sets of orthotics are changed into one set of orthotics is achieved.

The invention discloses an intelligent monitoring electronic nipple, and relates to the technical field of nipples. Comprising a base body, a base body, a sucking head and a handle, the base body and the handle are arranged on the two sides of the base body respectively, the sucking head is arranged at the end of the base body, and the base body, the base body, the sucking head and the handle are integrally formed and manufactured; a circuit board is arranged in the seat body, a power supply part is arranged in the middle of the handle, and a connecting column is arranged on one side, provided with the handle, of the seat body and connected with the power supply part; the base body and the connecting column are internally provided with channels used for wiring. Grooves are oppositely formed in the side faces of the base body, matched groove covers are arranged on the side faces of the base body, and a first pressure sensor and a second pressure sensor are arranged in the oppositely-formed grooves respectively. An embedding groove is formed in the end part of the sucking head, and a camera device is arranged in the embedding groove. Multi-mode, high-synchronization and quantitative monitoring of the sucking process of the premature infant is achieved, the sucking pressure, strength and duration of the premature infant are monitored in real time, the sucking capacity is evaluated and improved, and the swallowing delivery action in the oral cavity is dynamically observed.

The invention relates to the technical field of traditional Chinese medicine, and specifically discloses a traditional Chinese medicine composition for treating varicocele, a preparation method and an application thereof; the traditional Chinese medicine composition is prepared from the following raw materials in parts by weight: 10-20 parts of fennel, 5-10 parts of cinnamon bark, 10-15 parts of angelica sinensis, 5-10 parts of wolfberry, 10-15 parts of lindera striata, 3-5 parts of agarwood, 10-15 parts of curcuma zedoaria, 10-15 parts of turmeric, and 20-30 parts of rhodiola rosea. The formula is formulated based on the principles of breaking up blood and promoting qi, eliminating accumulation and relieving pain. In the formula, Rhodiola rosea and fennel are the main medicines, cinnamon, angelica and Linderae strychnos are the auxiliary medicines, and wolfberry, agarwood, Curcuma zedoaria and turmeric are the adjuvants. It combines movement and stillness, attacks and supplements at the same time, and promotes blood circulation and qi circulation at the same time, which embodies the saying that "qi is the commander of blood" and "blood is the mother of qi". It can significantly improve the various symptoms caused by varicocele. At the same time, it can be combined with surgery for the treatment of varicocele, significantly reducing postoperative complications and the risk of recurrence, and is suitable for large-scale promotion and application.

The invention discloses an anti-adhesion coating for an implantable device and the implantable device, and belongs to the technical field of implantable device coatings. The preparation method of the anti-adhesion coating comprises the following steps: blending carboxymethyl chitosan and hyaluronic acid, adding a cross-linking agent to enable the carboxymethyl chitosan to be subjected to a cross-linking reaction to generate cross-linked carboxymethyl chitosan, and after the cross-linking reaction, obtaining hydrogel in which the hyaluronic acid is distributed in pores of the cross-linked carboxymethyl chitosan; and stirring the hydrogel, shearing and thinning, coating the surface of the implanted device with the hydrogel, and drying to obtain the anti-adhesion coating. According to the implantable device with the anti-adhesion coating attached to the surface, the adhesion effect between the implantable device and biological tissue can be reduced, the biocompatibility and the performance of the device are improved, complications caused by adhesion are reduced, and the service life of the implantable device is prolonged.

The application discloses a glaucoma drainage device and belongs to the technical field of medical devices. The glaucoma drainage device comprises a drainage sheet, the inside of which is a cavity structure, the drainage sheet is divided into a left cavity and a right cavity through a first partition plate, the upper surface of the left cavity is provided with a drainage hole, and the first partition plate is provided with a drainage opening; a drainage assembly is in communication with the inside of the drainage sheet through a connecting hole provided on the drainage sheet; and a fixing mechanism is arranged on the drainage sheet and used for fixing the drainage sheet and the drainage assembly. The glaucoma drainage device can fix the drainage assembly and the drainage sheet of the device through a mechanical fixing structure, avoids the problems of the suture fixation of the drainage device in the prior art, simplifies the operation process, shortens the operation time, reduces the complications caused by the suture foreign matter, and improves the fixing reliability and safety.

The utility model discloses a nose shaping ectogenic silica gel nose tip support structure which comprises an ectogenic extension support, a nose tip section is arranged at the front end of the ectogenic extension support, a forked nose tip support section is arranged on the side wall of the ectogenic extension support, and the forked nose tip support section and the ectogenic extension support are integrally connected. The bifurcate nose tip support section and the ectogenic extension support are arranged in a relatively bent mode, and relates to the technical field of medical instruments. Through an integrated nose tip extension lifting silica gel material, the nose shaping ectogenic silica gel nose tip support is arranged, the concept and method for extending the nose tip through the ectogenic support are well applied, and the nose tip extension effect and stability are enhanced; the nasal tip lengthening and lifting surgical operation can be simplified, complications are reduced, the support is attached to the nose bridge bone, and the nasal tip lengthening and lifting stability is improved.

The invention relates to an anti-fogging self-cleaning laparoscope which is characterized in that a transparent glass sheet is fixedly arranged at the outer end of an objective lens at the far end of the laparoscope, and a closed carbon dioxide gas groove is formed in a gap between the transparent glass sheet and the objective lens; an air inlet pipeline is fixed along the inner wall of an outer tube of the laparoscope, a corresponding air inlet hole is formed in the near end of the air inlet pipeline, and the far end of the air inlet pipeline penetrates through the objective lens and extends into the carbon dioxide gas groove; a gas outlet pipeline is fixed along the inner wall of the outer tube of the laparoscope, the far end of the gas outlet pipeline extends into the carbon dioxide gas groove, and the near end of the gas outlet pipeline exhausts gas through a gas exhaust hole; and the air inlet is externally connected with a carbon dioxide air source. The laparoscope solves the technical problems that an existing laparoscope is prone to causing fogging of an objective lens and infection of tissue fluid in a minimally invasive abdominal surgery, consequently, the surgical field is blurred, and surgical operation needs to be interrupted due to the fact that a real-time processing function does not exist.

The utility model discloses a guide baffle for patella outer side supporting belt joint capsule external debonding operation, which relates to the technical field of medical instruments and comprises a guide plate, edges on two sides of the guide plate are gradually recessed towards the middle to form an arc-shaped sliding groove, and the arc-shaped sliding groove of the guide plate is gradually lowered and narrowed from one end to the other end. The width of the arc-shaped sliding groove of the guide plate is gradually narrowed from the high end to the low end, and the low end of the arc-shaped sliding groove of the guide plate penetrates through the gap between the joint capsule and the outer side supporting belt. The whole guide plate penetrates through the gap between the joint capsule and the outer side supporting belt, and a protection channel is established between the joint capsule and the outer side supporting belt, so that it is ensured that a release path is accurately found in a subcutaneous tunnel, deviation is avoided, the success rate and speed of an operation are improved, meanwhile, the integrity of the joint capsule is comprehensively protected, and the working efficiency is improved. And by adopting the guide plate, the subcutaneous tunnel separation area in the operation can be reduced, and large damage to subcutaneous blood vessels is avoided.

The invention discloses a skin mucosal disinfectant and a preparation method thereof, belonging to the technical field of disinfection, wherein the disinfectant comprises, by weight percentage, 0.15%-0.20% of povidone iodine, 0.05%-0.10% of cyclodextrin-iodine complex, 0.18%-0.22% of composite quaternary ammonium salt, 1%-2% of stabilizer, and the balance is purified water. The skin mucosal disinfectant provided by the invention can effectively kill Staphylococcus aureus, Escherichia coli, Candida albicans, Pseudomonas aeruginosa, poliovirus, rabies virus CVS-11 strain, etc. in a short time, and meets strict disinfection requirements, and has the advantages of broad-spectrum and efficient sterilization, no skin irritation, good storage stability, easy cleaning without yellowing, and no unpleasant odor.

The orthopedics external fixing frame support capable of being accurately pressurized or expanded comprises an upper fixing assembly, a lower fixing assembly, an adjusting base, an adjusting screw rod and an external supporting rod, wherein the adjusting screw rod and the external supporting rod are parallel to each other; the adjusting base is arranged at the bottom ends of the outer supporting rod and the adjusting screw rod in a sleeving mode and can limit the position relation between the outer supporting rod and the adjusting screw rod at the bottom ends of the outer supporting rod and the adjusting screw rod, the lower fixing assembly is arranged in the middle of the outer supporting rod and the adjusting screw rod, and the position of the lower fixing assembly can be adjusted along the outer supporting rod and the adjusting screw rod. The upper fixing assembly is arranged at the tops of the outer supporting rod and the adjusting screw rod; the upper fixing assembly comprises an upper three-dimensional moving mechanism, an upper platform module, an upper adjusting bolt and two upper outer fixing frame clamps. The lower fixing assembly comprises a lower three-dimensional moving mechanism, a lower platform module, a lower adjusting bolt and two lower outer fixing frame clamps. The external fixing device can be well matched with an external fixing frame, accurate pressurization, distraction or stretching of fractures and joints of a patient can be achieved, a doctor can operate the external fixing device easily and conveniently, and blood vessels and nerves can be avoided so as to reduce complications.

The present application belongs to the technical field of medical devices, and particularly relates to a micro catheter with variable rigidity. The micro catheter with variable rigidity comprises a catheter, a handle and a balloon. The catheter has a device conveying cavity and a liquid filling cavity, the liquid filling cavity is arranged outside the device conveying cavity, and the balloon is arranged in the liquid filling cavity. The device conveying cavity is used for conveying devices, and the liquid filling cavity is used for conveying fluid to the balloon. The handle is arranged at the proximal end of the catheter, and the handle has a first luer joint and a second luer joint. The first luer joint is in communication with the liquid filling cavity, and the second luer joint is in communication with the device conveying cavity. The micro catheter with variable rigidity can adjust the rigidity according to requirements, and can balance the good bending performance and support performance.

The pulmonary artery micro catheter comprises a catheter body, a guide wire channel penetrating through the catheter body and a balloon channel arranged in the catheter body, the wedge-shaped balloon is arranged at the far end of the catheter body, the far end of the wedge-shaped balloon is closed, and the other end of the wedge-shaped balloon is communicated with the balloon channel.

This invention discloses a left atrial appendage closure device, belonging to the field of medical devices. The left atrial appendage closure device of this invention includes a delivery catheter, a support tube, a support plate, a telescopic support rod, a closure clamp assembly, and a control cable. The closure clamp is inserted into the opening of the left atrial appendage via the delivery catheter and is opened at the opening of the left atrial appendage through the cooperation of the telescopic support rod and the control cable. A puncture hook inside the closure clamp pierces the tissue wall of the left atrial appendage opening to achieve closure. Finally, the closure clamp closes the left atrial appendage opening using a straight "I" closure mechanism. Compared with existing left atrial appendage occluders, the puncture hook on the outer periphery of the closure clamp can radially pierce the tissue, and the closure clamp drives the closure of the left atrial appendage opening, making the connection between the closure clamp and the left atrial appendage more secure and less prone to detachment. It also eliminates the problem of decreased reliability of the left atrial appendage seal due to loosening or movement, ensuring the long-term effectiveness of left atrial appendage closure and reducing complications caused by detachment and unreliable sealing.

The utility model discloses a connecting assembly which comprises a first connecting piece, a second connecting piece and a third connecting piece. The end of the first connecting piece is provided with a first locking part and a first positioning groove. The end part of the second connecting piece is provided with a second locking part and a second positioning groove, the first locking part is clamped and matched with the second positioning groove, and the second locking part is clamped and matched with the first positioning groove; the sleeve is used for radially restraining the first locking part and the second locking part; the first connecting piece provides a first moving space, and the second connecting piece provides a second moving space; and when the sleeve retracts to be separated from the connecting area of the first connecting piece and the second connecting piece and the first connecting piece moves relative to the second connecting piece, the first locking part moves into the second moving space, and the second locking part moves into the first moving space, so that the first locking part is separated from the second locking part. According to the utility model, the first moving space and the second moving space are provided, so that the first locking part and the second locking part can move relative to each other after the sleeve is withdrawn, and then the connection is quickly separated.

A disposable visual thoracocentesis drainage device comprises a drainage component, a puncture needle head, a micro camera, an LED light source and a display device. According to the disposable visual thoracocentesis drainage device, the miniature camera, the light source and the puncture needle head are integrated, the puncture process can be monitored in real time, and important structures such as lung tissue and blood vessels are prevented from being damaged. The device is designed to be disposable, sterile operation is ensured, and cross infection is avoided. The device is particularly aimed at a complex environment in the thoracic cavity, the accuracy of puncture positioning is improved through visual guidance, and the safety of an operation is guaranteed. Integration of the miniature high-definition camera and the flexible drainage tube is achieved through the modern microelectronic technology, the puncture needle head is specially designed, and the risk of tissue damage in an operation is reduced in cooperation with a visual system. Through clinical verification, the device can remarkably improve the safety and success rate of the thoracocentesis operation, and is particularly suitable for complex thoracocentesis operation.

The utility model discloses a kind of non-invasive cosmetic injection equipment of multi-channel automatic distribution, including base, it is characterized by: the upper surface of the base is fixedly connected with support block, the upper surface of the support block is fixedly connected with first fixed frame, the fixed connection of the support block has button block, the upper surface of the button block is fixedly connected with threaded rod, the upper surface of the threaded rod is fixedly connected with first gasket.Various injection areas can be adapted, improve the comfort of patient, reduce complication, can ensure that drug is evenly distributed, improve treatment effect, save time, while reducing operation failure and adjustment time in treatment process, the latter can optimize the distribution of drug, so that certain medicament is injected into dermis superficial layer or and injected into muscle layer, ensure the best level distribution of drug, to realize more uniform effect, and improve the individualization and flexibility of treatment, both have stronger practicality.

The utility model discloses and medical equipment technical field discloses a kind of improved broken end anastomosis catheter for prostate cancer radical operation, including catheter body and anti-sewing pipe, catheter body is split into two sections, anti-sewing pipe is arranged between two sections catheter body, the outer diameter of anti-sewing pipe is same with the outer diameter of catheter body, the both ends of anti-sewing pipe are respectively fixedly connected with two sections catheter body, the inside of anti-sewing pipe is filled with rigid structure layer, and channel, which is communicated with catheter body, is equipped on rigid structure layer.The utility model is filled with rigid structure layer anti-sewing pipe by additionally being provided with inside in traditional catheter body, when the broken end anastomosis of minimally invasive surgery is carried out, this improved broken end anastomosis catheter not only can play certain guiding role in urethra and bladder anastomosis during operation, and the rigid structure layer filled inside anti-sewing pipe can prevent sewing needle to be pierced, ensure that needle is sewn to enter and go out without being sewn to catheter rubber part.