39 results about "Post surgical" patented technology

A lift, a head support, and methods for use thereof for use with a surgical frame are provided. The lift and the head support can be used with the surgical frame that is capable of reconfiguration before, during, or after surgery. The surgical frame can include a main beam that can be rotated, raised / lowered, and tilted upwardly / downwardly to afford positioning and repositioning of a patient supported thereon, and the lift and the head support can be used in lifting the patient from a table / gurney and positioning the patient with respect to the main beam.

The invention provides a condyle positioning device and a lower jaw fixator with the condyle positioning device.The condyle positioning device comprises a condyle positioning component, a tooth retention guide plate and a dividing structure formed between the condyle positioning component and the tooth retention guide plate. Wherein the tooth retention guide plate and the condyle positioning component are of an integrated structure and can be separated along the segmentation structure, the condyle positioning component is suitable for being fixed to the front edge of the ramus of the mandible of a patient, and the tooth retention guide plate is manufactured based on the tooth form of the mandible part of the patient and fixed to the corresponding dentition. The condyle positioning component is connected with the lower jaw fixator through a mortise and tenon joint structure so as to position the specific position of the condyle of the patient after the lower jaw operation.

A surgical frame incorporating an electromagnetic-radiation imaging device, and a radiation-mitigation system for use with the surgical frame are provided. The surgical frame can be capable of reconfiguration before, during, or after surgery, and can include a main beam that can be rotated, raised / lowered, and tilted upwardly / downwardly to afford positioning and repositioning of a patient supported thereon. The surgical frame can support the electromagnetic-radiation imaging device. One of an emitter and a receiver of the electromagnetic-radiation imaging device can be positioned under the main beam of the surgical frame, and the other of the emitter and the receiver of the electromagnetic-radiation imaging device can be positioned over the main beam of the surgical frame. The radiation-mitigation system can serve to intercept / block and mitigate at least some of the scatter of the electromagnetic radiation from the emitter.

A surgical frame and method for use thereof is provided. The surgical frame is capable of reconfiguration before, during, or after surgery using a moveable main beam supporting a patient thereon. The surgical frame includes a translating lower beam that is moveable between at least a first lateral position and a second lateral position, and a linkage and / or surgical equipment supportively and moveably attached to the translating lower beam or interconnected with the translating lower beam via the linkage. The linkage and / or the surgical equipment are moveable between a first position at or adjacent a first end of the translating lower beam and a second position at or adjacent a second end of the translating lower beam. The translating lower beam is used to join a first support portion and a second support portion of the surgical frame to one another, and movement of the translating lower beam affords access to a patient receiving area. A linear movement mechanism can be used to facilitate movement of the linkage and / or the surgical equipment along the translating lower beam to avoid interference with the main beam or the translating lower beam.

To provide an ophthalmic device for drug delivery.SOLUTION: An ophthalmic implant for drug delivery is provided. The implant includes a primary intracapsular device coupled to a secondary device. When implanted in a patient's eye, the primary intracapsular device is held in place by the patient's capsular bag, and the secondary device is held in place by the primary intracapsular device. The implant may be inserted in the eye by injecting the primary intracapsular device into the eye either before or after attaching the secondary device to the primary intracapsular device, and subsequently positions the joined secondary device and primary intracapsular device with the primary intracapsular device held in place by the patient's capsular bag and with the secondary device held in place by the primary intracapsular device. The secondary device may be designed to hold a tertiary device that can be implanted and attached at the time of surgery or anytime postoperatively.SELECTED DRAWING: Figure 1

A minimally invasive precision cutting guide, targeting guide, implant, and other instruments comprise a system that permits a physician to surgically correct a bunion or similar deformity with a minimum disruption of surrounding soft tissue. The precision cutting guide ensures that the physician cuts bone in the proper location and orientation. Each of the instruments is designed to minimize disruption to surrounding soft tissue. The system also precisely locates an orthopedic implant such that it can fixate two bone fragments after an osteotomy, or two bones after surgery. The precision cutting guide, targeting guide, implant, and other instruments are provided in a sterile kit for the convenience of the surgeon and safety of the patient.

Disclosed herein are devices and methods for protecting reconstructed nipples, typically post-surgery. The nipple protector may include a circular base portion and an annular ridge concentrically disposed to define a central aperture. The nipple protector In may further include an adhesive layer disposed on a bottom surface of the base portion for adhering the nipple protector to an area surrounding the reconstructed nipple. The nipple protector is fashioned to allow for direct access to the new nipple, which facilitates application of antibiotic ointments. The nipple protector softly adheres to the skin to provide flexible, adherent, comfortable, and water tolerant usage.

A computing system for measuring and monitoring patient biomarkers for detecting or predicting a post-surgical colorectal complication may be provided. A post-surgical colorectal complication may be predicted or detected by comparing measured / processed patient biomarker data with a corresponding determined threshold value. The comparison of the measured / processed patient biomarker data and the corresponding threshold may be performed in association with a context. The context may be based on at least one of a colorectal surgery recovery timeline, at least one situational attribute, or at least one environmental attribute. A notification message associated with a predicted or detected post-surgical colorectal complication may be sent (e.g., sent in real time) to a patient device or a healthcare provider's device. The notification message may be supplemented by a severity level message.

A method includes receiving by a controller, a surgeon-specific surgery profile for an implantation of an implant into a joint, implant profiles, a patient-specific post-surgery desired functional profile of the joint after the implantation, and bone registration data for a first bone member and a second bone member of a patient are inputted into a surgical plan model to generate a surgical plan. The surgical plan model is designed to achieve the patient-specific post-surgery desired functional profile based at least in part on a plurality of dependencies between a plurality of surgical parameters, the implant profiles, at least one functional parameter representative of the expected functional performance of the joint, and movement-related data of the joint. The surgical plan is outputted on a graphical user interface (GUI) on a surgery assistant device to facilitate the implantation.

Described herein are hydrogel-coated surgical meshes and their use in hernia repair, reconstructive surgery, and other surgical procedures. In one aspect, the hydrogel-coated meshes comprise at least one antibiotic or antimicrobial agent for the treatment of hernia repair surgery. In one aspect, the hydrogel coated meshes provide localized, sustained antimicrobial activity for the treatment of surgical site infections. In one aspect, the hydrogel coated meshes provide localized, sustained prophylactic antimicrobial activity for the prevention of surgical site infections. In another aspect, the hydrogel coating may optionally include one or more additional therapeutic components, such as anti-inflammatory compounds or growth factors, to facilitate and enhance recovery following hernia repair, reconstructive procedures, or other surgeries.

The application discloses a method and device for generating a postoperative three-dimensional model of a surgical object. The features include: obtaining a first three-dimensional model of the surgical object through a three-dimensional scanning system, and obtaining a second three-dimensional model of the surgical object through medical imaging technology; determining a surgical correction model of the surgical object based on the second three-dimensional model; and performing correction processing on the first three-dimensional model based on the surgical correction model to obtain a postoperative three-dimensional model of the surgical object. The embodiment of the application realizes accurate and efficient simulation of a postoperative three-dimensional body image of the surgical object, and improves the visualization effect of the postoperative effect.

The invention discloses a limb fixing device after flap surgery, which comprises a basic fixing device, a connecting piece, an upper arm bracket and a forearm bracket, and is characterized in that the basic fixing device is used for binding the upper limb of a patient on a bed body and can be detachably connected with the bed body; the connecting piece is detachably arranged on the foundation fixing device; the upper arm bracket is arranged on the connecting piece and is used for supporting and fixing the upper arm of the affected limb; the forearm bracket is arranged on the upper arm bracket and used for supporting and fixing the forearm of the affected limb. The limb fixing device after the skin flap operation can effectively avoid pressure blood supply disorder, provides a stable anchor point to prevent lateral displacement of an affected limb and meanwhile can avoid raising bedding, and therefore heat preservation of a patient after the skin flap operation is guaranteed.

The utility model belongs to the field of medical instruments, and provides a bed body extending mechanism which comprises a bed frame. The extending mechanism is slidably arranged in the bed frame and used for extending the using length of the bed frame; the limiting mechanism is arranged at the bottom of the bed frame and used for limiting and fixing the extension mechanism; the sliding mechanism is fixedly arranged on the inner wall of the bed frame and assists the extension mechanism in sliding use; the supporting mechanism is arranged outside the bed frame; due to the fact that the bed leg transverse supports are connected to one side of the bed frame in the sliding mode through the two extending inner frames, after the feet and legs of a patient are subjected to an operation, when the using length of the bed frame needs to be prolonged, the two extending inner frames can be pulled out of the interior of the bed frame and are limited and fixed through matching of the pin shafts and the front holes, and therefore the using length of the whole bed frame is increased; a patient can adjust and use conveniently.

1. The name of the product under this design: Bra (post-operative breast support and breast binding). 2. Purpose of this design product: bra for use after surgery. 3. The design key points of this appearance design product are: the main view. 4. The picture or photo that best illustrates the key points of the design: main view. 5. The top view of this design product is a part that is difficult to see or cannot be seen when in use, so the top view is omitted; the bottom view of this design product is a part that is difficult to see or cannot be seen when in use, so the bottom view is omitted. 6. The model in the design image is a background and does not belong to the design content for which protection is requested.

The present invention relates to a magnetised physiological water solution containing 0.9% by weight of sodium chloride for use in the healing treatment of skin or tissue injuries or wounds, in particular post-surgical surgical wounds or injuries. The present invention also relates to a process for preparing the above magnetised physiological water solution and to the magnetised physiological water solution obtained by means of said process.

A method for preparing a bionic injectable polypeptide hydrogel is provided. The hydrogel is formed using a brain extracellular matrix laminin-derived peptide DDIKVAV modified with 9-fluorenylmethoxycarbonyl (Fmoc) (Fmoc-DDIKVAV) and an immunostimulatory peptide FTKPRF modified with Fmoc (Fmoc-FTKPRF) as hydrogel monomers. These monomers further utilize non-covalent bond forces such as hydrogen bonds, hydrophobic interactions, and x-x stacking to co-assemble into a hydrogel within a short time at 37° C. The bionic hybrid polypeptide hydrogel is injectable and can serve as a drug reservoir implanted into cavities formed after tumor surgery. The drugs loaded in the hydrogel are slowly released at a stable and controlled rate and appropriate concentration within the post-surgical cavity, thereby effectively killing residual tumor cells while avoiding the toxic side effects of systemic drug administration.

The present invention relates to a screw device for spinal surgery, which can easily prevent a screw from loosening, detaching, or coming out from a vertebra after the screw is press-fit and fixed into a vertebra for surgery, and a method for injecting bone cement using same. That is, the objective of the present invention is to provide a screw device for spinal surgery, which, during spinal surgery for fixing a screw into a vertebra, injects bone cement into the interior of the vertebra through an injection channel formed in the screw, thereby allowing the screw and the bone cement to bond together within the vertebra and thus effectively preventing the screw from loosening or coming out from the vertebra, and a method for injecting bone cement using same.

Systems, methods, and instrumentalities for managing surgical consequences in a simulated surgical task may be provided. A simulation environment to simulate a surgical task defined by a set of environmental parameters may be received. Surgical interaction data may be received. In examples, the surgical interaction data may comprise an indication of a triggering event and / or an indication of consequence environmental parameters. The surgical interaction data may be associated with a surgical task. The consequence environmental parameters may be associated with the triggering event. User interaction data may be received. The user interaction data may be based on a user action within the simulation environment and may be associated with a surgical task. On a condition that the received user interaction data matches the triggering event, the simulation environment may be modified, for example, based on the consequence environmental parameters.

The utility model discloses a thyroid post-operation neck dressing which comprises a dressing body, the surface of the dressing body is of an organ pleat structure, a plurality of grooves are formed in the edge of the dressing body, an observation mechanism and a penetrating mechanism are arranged on the surface of the dressing body, and the dressing body is of an arc-shaped structure. According to the utility model, the serrated grooves are particularly formed in the grooves, the organ folds and the edge adhesive part of the dressing main body, so that the adhesion surface of the adhesive and the skin is effectively reduced, the dressing tightening tension possibly caused by a linear edge is further reduced, and a patient can feel more comfortable in the use process; meanwhile, neck movement is easier, discomfort caused by too large tension of the dressing is reduced, meanwhile, the dressing body is provided with the organ pleats, the elasticity of the dressing is increased, and the movement range of the neck of a patient is further improved.

A garment for post-surgical recovery includes a torso covering body formed from a first fabric layer and a second fabric layer bonded together by a thermoplastic polyurethane layer. The thermoplastic polyurethane bonding extends between the fabric layers along contours of the torso covering body to provide a stable layered construction without rigid inserts. The garment may include shoulder straps extending upwardly from the torso covering body and an opening region disposed along either a front or rear central portion. In some embodiments a vertical seam defines a front opening region, and in other embodiments a fastening mechanism defines a rear opening region. The fastening mechanism may include a securing element positioned to maintain closure of the garment. The bonded multilayer construction may be configured to provide extended wear and structural stability for recovery following surgical procedures involving the torso.

SOLUTION: A system for positioning a patient before, during, or after a medical procedure can include an arm assembly and a surgical drape for use with the arm assembly. The surgical drape may be configured to be placed around a surgical site where a surgical procedure is to be performed. The surgical drape includes a transparent viewing window, a plurality of handle covers, and an expandable opening in a top surface of the surgical drape. In addition, the surgical drape may also include an adhesive member on the bottom surface of the drape that may be independently removed to secure the drape around the surgical site.SELECTED DRAWING: Figure 3

The present invention provides a breathing training tool for post-operative lung cancer surgery, comprising a housing and a cover fixed to one side thereof. A rotatable transmission disc is disposed within the housing, and a drive assembly for controlling the rotation of the transmission disc is disposed within the housing. Sliding connection blocks are disposed on both sides of the transmission disc, and sliding sliders are disposed at both ends of the inner side of the housing. Each set of connection blocks is connected to one set of sliders via a rocker mechanism and controls the reciprocating sliding of the sliders at one end of the housing. An elastic band connected by a connecting shaft is disposed at one end of each set of sliders, and one side of the two sets of elastic bands can be connected via Velcro. The tool can control the retraction and extension of the elastic bands, and the patient can adjust the respiratory rate according to the retraction and extension frequency of the elastic bands to improve the efficiency of respiratory function rehabilitation. The retraction and extension amplitude of the elastic bands can also be adjusted according to the patient's chest expansion amplitude, and the respiratory rate and respiratory amplitude can be adjusted according to the indication of an indicator light to adapt to different patients.

The present invention discloses a post-cranial surgery drilling repair device, which relates to the field of skull repair. The device comprises a fixing member and a first sliding sleeve, wherein the first sliding sleeve is symmetrically fixed to the fixing member, the first sliding sleeve is slidably connected to a sliding connector, a protective cover is fixed between the sliding connectors, the protective cover is fixed to a connecting rod, the connecting rod is fixed to a first sliding rod, and a first spring is wound between the connecting rod and the first sliding sleeve. The present invention uses the first sliding rod and the first spring to buffer the impact force exerted on the protective cover, thereby providing space for the protective cover to move and preventing the protective cover from directly squeezing the repair site. The second spring and the guide rod buffer the fixing member, thereby preventing the protective plate from moving up and down with the fixing member and rubbing against the repair site, thereby achieving the purpose of reducing the friction exerted on the repair site.

Methods of maintaining general oral care as well as reducing inflammation, pain, and bruising after oral surgery with a homeopathic recovery kit are disclosed.

A lift, a head support, and methods for use thereof for use with a surgical frame are provided. The lift and the head support can be used with the surgical frame that is capable of reconfiguration before, during, or after surgery. The surgical frame can include a main beam that can be rotated, raised / lowered, and tilted upwardly / downwardly to afford positioning and repositioning of a patient supported thereon, and the lift and the head support can be used in lifting the patient from a table / gurney and positioning the patient with respect to the main beam.

The utility model relates to the technical field of medical auxiliary instruments, in particular to a gastrointestinal postoperative position adjusting nursing device which comprises a bed frame, the bed frame is composed of supporting legs and a bed board, guide grooves are symmetrically formed in the two sides in the bed board of the bed frame, motors are installed on the two sides of the bottom of the bed board, and first screw rods are rotationally connected to the two sides of the middle of the bottom of the bed board. Output shafts of the motors are connected with the corresponding first screw rods; guide rods are symmetrically arranged on two sides of the bottom of the bed plate. The first screw rod is driven by the double motors, so that the lifting rod jacks the folding base plate, accurate body position adjustment is achieved, the waist and the back are evenly supported, and diaphragm pressure is reduced; the air spraying pipe blows clean air flow to the bed surface after being filtered by the filter cover, so that a dynamic air layer is formed to reduce skin friction and moisture and prevent pressure sores and aspiration; the foldable sponge mattress is attached to a curve in a self-adaptive mode, the shearing force is reduced, the body position mode is switched in cooperation with the controller, adjustment is rapidly completed, and the postoperative nursing quality is remarkably optimized.

The invention discloses an abdominal tightening belt for recovery after surgical operation, which belongs to the field of medical instruments and equipment, and comprises two bridles used for being wound on the abdomen of a user, and the two bridles are connected through a zipper; the main belt body comprises a supporting part and wing plates, the supporting part is used for supporting the waist, and the left side and the right side of the supporting part are each provided with one wing plate; each wing plate is provided with one storage pipe, the storage pipes are arranged in the length direction of the wing plates, through holes are formed in the side walls of the storage pipes, reels are rotationally arranged in the storage pipes, and the ends, away from the zipper, of the bridles pass through the through holes and then are wound on the reels; and the adjusting mechanism is arranged at the end part of the storage pipe and is used for adjusting the rotation of the reel. The problem that in the prior art, operation is inconvenient when an existing binding belt is adopted for binding the abdomen during rehabilitation after a surgical operation and the existing binding belt and a drainage tube are used at the same time is solved.

The Modular Pathways for Gait Therapy, I of the present disclosure, is a system comprising multiple interlocking platform segments. Each platform segment features its own distinctly textured surface, equipped with a hook on top and an interlocking dovetailed eyelet on the bottom. Thus, each platform segment can be easily and securely connected to another. One can rearrange any pathway, of varying lengths, as needed for the post-injury or post-surgery physiotherapy client. Additionally, the relatively compact & lightweight platform segments can be hung on the wall or elsewhere when not in use, ensuring convenient storage & quick setup. The system is designed to enhance diverse sensory feedback during gait therapy, aiding in finer tuning of the client's proprioception, gross & fine locomotor skills, & gait stability during the rehabilitation process.

The present invention relates to a medical device for preserving a prosthetic breast implant in the event of post-surgical infection. The device is configured to ensure effective and homogeneous irrigation of the mammary pocket while simultaneously maintaining the original reconstruction volume and preventing tissue collapse. Said device comprises structural elements adapted to support the breast chamber atraumatically and distribution means allowing a 360-degree washing action. The invention thereby enables the salvage of the prosthetic implant without requiring removal, thus overcoming the limitations of conventional irrigation techniques.

The present disclosure provides machine learning based systems, methods, and non-transitory media for diagnosing and treating patients that have undergone cardiac surgery. Included herein are pre-trained system, methods, and non-transitory media for diagnosing and treating post-surgical cardiac patients based on post-surgical clinical information to address and / or prevent postoperative hyperglycemia or acute kidney injury (AKI) that may arise in the days immediately after surgery. Also included are system, methods, and non-transitory media for diagnosing and treating post-surgical cardiac patients for other ailments that may arise during the period following such surgery.