479 results about "Percutaneous" patented technology

The invention discloses a treatment monitoring method and system for a percutaneous ear vagus nerve stimulation device, and the method comprises the steps: carrying out the multi-source treatment situation monitoring of a target user in a treatment course, obtaining the multi-source treatment situation monitoring data, and constructing a multi-mode treatment situation feature; real-time treatment situation analysis is carried out according to the multi-mode treatment situation features, and real-time treatment situation analysis information is generated; performing dynamic state classification based on the real-time treatment situation analysis information, evaluating the treatment condition of the target user in the current treatment course, and generating a treatment regulation and control scheme to perform treatment management and control on the current treatment course when an abnormal treatment condition exists; and constructing a treatment situation prediction model, obtaining the regulated and controlled multi-mode treatment situation characteristics, generating a floating regulation and control boundary in combination with the treatment situation prediction model, and dynamically correcting the diagnosis and treatment regulation and control scheme by using the floating regulation and control boundary to ensure the curative effect and treatment safety. The treatment effect can be accurately perceived; and the treatment safety is ensured.

A medical system may include a pump disposed along a longitudinal axis of a blood flow assist system and including an impeller disposed in a pump housing; a power lead coupled with the first end portion of the pump; and a tether coupled with a second end portion of the pump opposite the first end portion. During operation of the blood flow assist system with the pump disposed within the blood vessel, the power lead may be configured to extend from within the blood vessel within which the pump is disposed to outside the first vascular access site to couple to the control system, and the tether may be configured to extend from within a blood vessel within which the pump is disposed to an anchoring position disposed away from the second end portion.

The invention relates to the field of medical treatment, and discloses a method for treating chronic insomnia by percutaneous magnetic stimulation of stellate ganglion block, which comprises the following steps: preprocessing: determining the initial position of stellate ganglion, tissue initial parameters and initial stimulation parameters through multi-modal image positioning and initialization to obtain reference data; dynamic sensing: collecting neck tissue displacement data, temperature field data and electromyographic signals in real time, and calculating spatial position variation of stellate ganglions and time-varying parameters of tissue electromagnetic characteristics; and modeling optimization: constructing a time-varying electromagnetic field distribution model based on the reference data, the spatial position variable quantity and the time-varying parameters. The method comprises the following steps: acquiring neck tissue displacement, a temperature field and an electromyographic signal in real time through reference data, capturing a stellate ganglion space position change and tissue electromagnetic property time-varying rule, constructing a time-varying electromagnetic field distribution model, and solving target stimulation parameters adaptive to a real-time tissue state through an optimal control algorithm.

The invention relates to the technical field of intelligent wearing monitoring, in particular to a multifunctional head-mounted device for improving anxiety and depression symptoms in the perioperative period, which comprises a main body base, an electric treatment assembly and a power supply assembly are arranged on the main body base, extending ear hooks are arranged at two ends of the main body base, binding straps are arranged on the extending ear hooks, and a nose pad block is arranged at the bottom of the main body base. The electric treatment assembly is in signal connection with an evaluation and control system, heart rate monitoring assemblies are arranged on the extension ear hooks, and an eye movement monitoring assembly is arranged at the bottom of the main body base; a displacement monitoring assembly is arranged on the main body base, and a respiration monitoring assembly is arranged on the nose pad block. According to the invention, physiological parameter monitoring, anxiety and depression assessment and percutaneous nerve stimulation treatment functions are integrated, and multi-node fixed design and real-time dynamic data processing are combined, so that redundant steps depending on preposed medical assessment in the traditional technology are omitted, doctors can remotely and accurately adjust personalized schemes based on dynamic data, and the accuracy of diagnosis and treatment is improved. The anxiety depression intervention efficiency and reliability in the perioperative period are improved.

A delivery device for percutaneously delivering a stented prosthetic heart includes a sheath, a handle, and adjustment device including a fine adjustment mechanism, and an outer stability shaft. The sheath defines a lumen and is configured to compressively constrain the stented prosthetic heart valve. The handle is coupled to the proximal portion of the sheath and includes an actuator mechanism coupled to a proximal portion of the sheath that is configured to selectively move the sheath relative to the housing to release the stented prosthetic heat valve. The adjustment device is coupled to the handle and includes an adjustment lumen through which the sheath and the handle slidably extend. The outer stability shaft is coupled to the adjustment device. The fine adjustment mechanism is configured to selectively move the handle and the sheath relative to the adjustment device and the outer stability shaft.

The invention discloses a closed-loop percutaneous spinal cord electrical stimulation analgesia system and method based on physiological feedback, and belongs to the field of noninvasive electrical stimulation analgesia technologies and stimulation control systems thereof. The system comprises an electrode patch, a flexible substrate of which is provided with at least one pair of electrode units in an integrated manner, and the electrode patch is used for being attached to a corresponding spinal cord segment area of the body surface of a subject; the physiological signal acquisition module is used for acquiring a multi-modal physiological signal of a subject in real time; the stimulator is electrically connected with the electrode patch and used for generating and outputting electrical stimulation signals to at least one pair of electrode units of the electrode patch; the control module is connected with the physiological signal acquisition module and the stimulator and is used for evaluating the pain state of the subject based on the physiological signals acquired by the physiological signal acquisition module; and according to the evaluation result, generating a control instruction to perform closed-loop adjustment on the output state of the stimulator. According to the system, objective feedback is introduced, adaptability is improved, noninvasive individualization is achieved, operation is easy and convenient, and closed-loop automatic control over monitoring, analysis and adjustment is achieved.

The invention belongs to the technical field of DSA, and discloses a DSA platform-based multi-state real-time multi-mode image accurate fusion method. After an angiography image is collected on the basis of DSA equipment under the motion condition, accurate DSA blood vessel subtraction image enhanced display is achieved, meanwhile, hepatic artery extraction in a three-dimensional image in preoperative CT is completed, dynamic intelligent fusion of a precise anatomical structure in a preoperative multi-mode CT image and intraoperative local blood vessel development is combined, and the dynamic and intelligent fusion of the dynamic and intelligent fusion of the dynamic and intelligent fusion of the dynamic and intelligent fusion of the dynamic and intelligent fusion of the dynamic and intelligent fusion of the dynamic and intelligent fusion of the dynamic and intelligent fusion is achieved. The intrahepatic lesions and important blood vessels are accurately and visually displayed, operation planning is completed, fusion of three-dimensional information and two-dimensional DSA is utilized, and transvascular and percutaneous interventional operations are accurately guided.

The invention belongs to the field of human body detection devices, and provides a wearable system for evaluating pain, which comprises wearable equipment in communication connection with a cloud system. The wearable device is used for continuously collecting physiological signals when a patient wears the wearable device. The cloud system is provided with a hierarchical evaluation module, a correction module and an intervention control module, the hierarchical evaluation module extracts physiological features in a long-term time window, extracts skin electroreaction mutation, a myoelectricity activity peak value and skin temperature rapid change in a short-term time window, and deduces an acute pain level in combination with instant self-evaluation information of a patient; the correction module is used for correcting the acute score based on the mapping relation between the long-term stability characteristic and the acute pain level and an individualized threshold value; the intervention control module generates individualized electrical stimulation control parameters according to the correction result and issues the individualized electrical stimulation control parameters to the wearable device, and the electrical stimulation execution unit outputs a stimulation signal through the percutaneous electrode to relieve pain of the patient and uploads a feedback signal to the cloud end to form a closed loop.

The embodiment of the invention provides a self-powered microneedle patch for repairing hypertrophic scars as well as a preparation method and application of the self-powered microneedle patch. The self-powered microneedle patch comprises: a friction nano-generator for generating a current; the conductive drug-loaded microneedle patch is connected with the friction nano-generator, and the friction nano-generator is connected with the conductive drug-loaded microneedle patch; the conductive drug-loaded microneedle patch comprises a conductive microneedle patch body and a crosslinked gelatin-crosslinked hyaluronic acid microneedle bearing Sb4. The surface of the conductive micro-needle patch is provided with a metal coating, and the conductive micro-needle patch is used for mediating current generated by the friction nano-generator and applying percutaneous electrical stimulation; the cross-linked gelatin-cross-linked hyaluronic acid microneedle is coated at the tip of the conductive microneedle patch. According to the self-powered microneedle patch provided by the embodiment of the invention, myofibroblasts of hypertrophic scars are transdifferentiated into adipocytes by providing percutaneous electrochemical stimulation, inflammatory factor release is inhibited, and a tissue microenvironment is remodeled, so that the hypertrophic scars are reversed, and skin repair and tissue regeneration are realized.

Surgical systems and methods for correcting a bunion percutaneously including aligning guides are provided herein. At least one embodiment includes a handle including a rod with a first end including a first longitudinal axis and a second end including a second longitudinal axis offset from the first longitudinal axis. The handle can couple to a gadget including a leg that couples to the handle, and a translator that extends and retracts the leg. The gadget can also a slide with a guide body to guide a guide wire for accurate placement of a screw. The surgical system can also include a periscope to assist in pre-visualization of the screw placement.

The invention discloses a percutaneous barrier function evaluation method and system based on precise temperature and humidity control. The method comprises the steps that S1, an individualized skin barrier baseline model containing daytime fluctuation characteristics and temperature and humidity sensitivity parameters and a baseline database are constructed; s2, executing an environment adaptability evaluation scheme through dynamic temperature and humidity spectrum scanning; s3, multi-dimensional skin physiological parameters are collected, a static parameter set and a dynamic parameter set are distinguished, and data standardization is achieved through dynamic baseline subtraction and cross-parameter interference compensation by adopting a physiological constraint type data correction algorithm based on a skin physiological relevance matrix; s4, integrating the standardized parameters to calculate a comprehensive barrier function index; and S5, predicting a barrier function trend. The system comprises a precise environment control module, a multi-parameter acquisition module, an intelligent analysis module, a data storage and interaction module and a central processing module, the accuracy and comprehensiveness of percutaneous barrier function evaluation can be improved, and technical support is provided for skin health management, skin disease diagnosis and treatment and the like.

A method may involve creating a first opening in a right pulmonary artery and a second opening in a superior vena cava. A shunt may be percutaneously delivered into the first opening and the second opening. A stent may be percutaneously delivered into the superior vena cava adjacent to the shunt. The stent can comprise a covering to at least partially prevent flow of blood from the shunt through the stent and / or may be at least partially flexible to allow the stent to bend away from walls of the superior vena cava in response to inflow of blood through the shunt. The stent may be sized to seal against the superior vena cava at a first end and a second end of the stent to trap blood between the stent and the walls of the superior vena cava.

An auricular electroencephalogram (EEG) monitoring system may include an EEG recording module having a plurality of EEG sensor electrodes, configured to be coupled to a wearer's ear, and a processing unit configured to analyze EEG data recorded by the EEG recording module to detect presence or cessation of neuropsychiatric disorders of the wearer. An automatic detection-remedy system may include an auricular electroencephalogram (EEG) monitoring system and a transcutaneous auricular vagus nerve stimulation (taVNS) unit having a stimulating electrode in contact with vagus innervated auricular skin of the wearer's ear. When the presence of EEG signals suggestive of the neuropsychiatric disorder is detected by the processing unit, the processing unit is configured to immediately send signals to the taVNS unit to automatically start sending pre-determined electric stimuli to the vagus innervated auricular skin of the wearer's ear.

An implant assembly for a long bone is adapted to support an exo-prosthesis. The assembly includes a stem, a subdermal component and a percutaneous post. The stem has a proximal end that is adapted to be received in a surgically prepared medullary canal of the long bone, and a distal end having a surface that is adapted to promote bone ingrowth. The subdermal component includes a proximal portion that is adapted for attachment to the distal end of the stem, and a fixation surface that is adapted to promote soft tissue fixation. The percutaneous post has a proximal end that is adapted to be attached to the subdermal component.

A percutaneous circulation support device includes a percutaneous blood pump coupled to a distal end region of an elongate shaft at a junction. The percutaneous blood pump is configured to pump blood through a housing of the percutaneous blood pump during use. The joint includes an end cap at the proximal end of the percutaneous blood pump that surrounds and is secured to the distal end region of the elongate shaft at the joint. The joint may include a wrap filler that surrounds and extends proximally from a proximal end region of the end cap, and surrounds an outer surface of the elongate shaft. The proximal end region of the end cap may include an annular sidewall having one or more apertures and / or one or more grooves extending into the annular sidewall, and the cladding filler extending into the apertures and / or the grooves.

The present disclosure is directed to devices, kits, and methods for treating lumbar spinal stenosis by at least partially decompressing a compressed nerve root. The method can include identifying the compressed nerve root and percutaneously accessing a region of a lamina located adjacent to the compressed nerve root. The method can also include forming a channel through the region of the lamina, wherein the channel can be formed medial to a lateral border of the lamina. Further, the method can include expanding the channel in a lateral direction.

The application discloses a percutaneous lung puncture path planning method and device based on lung segment level blood vessel structure constraint, and the method comprises the following steps: performing isotropic resampling, lung lobe segmentation and bronchial tree extraction on CT image data to generate a three-dimensional lung dissection model; inputting the three-dimensional lung dissection model into a lung segment semantic segmentation module to output a lung segment boundary; reconstructing the topological connection relationship between lung segment level blood supply arteries and drainage veins from the lung segment boundary to obtain a structured lung segment level blood vessel atlas; constructing a dynamic puncture risk field voxel map according to the structured lung segment level blood vessel atlas; sampling a plurality of candidate needle entry points in a surface feasible needle entry region to generate an initial path set in the three-dimensional lung dissection model; and weighting the path length, cumulative risk value, puncture angle penalty and high-density lung tissue volume according to a multi-objective optimization function to output a final puncture path. The application significantly improves the safety boundary and clinical applicability of percutaneous lung puncture.

To provide suitable devices, systems, and methods for percutaneous pneumatic cardiac support. [Solution] The cardiac support system includes a pneumatic effector implanted beneath the pericardium and across the myocardial surface covering the patient's left ventricle. A port receives an implanted, percutaneously introduced cannula. The port is connected to supply the drive gas received from the cannula to the pneumatic effector. An external drive unit includes a pump assembly and a control circuit that operates the pump to activate the pneumatic effector in response to the patient's sensed cardiac rhythm. A connecting tube has a pump end connected to the pump and a percutaneous port connection end attached to the implantable port.

Provided is the use of a traditional Chinese medicine composition in preparation of a drug for preventing major adverse cardiac and cerebrovascular events after percutaneous coronary intervention and ameliorating myocardial injury and vascular endothelial dysfunction after percutaneous coronary intervention. The traditional Chinese medicine composition is composed of total salvianolic acid and total hawthorn triterpene acid.

In some embodiments, a bone implant for percutaneous use is provided. The bone implant comprises a head, a body adjacent to the head and a tip opposite the head. At least the head, body or tip is configured to contact bone. An expandable member contacts at least one of the head, tip or body and is movable from an unexpanded configuration to an expanded configuration when deployed at a bone implant site. In some embodiments, a system for percutaneous bone harvesting is provided.

A percutaneous circulatory support system may include a blood pump. The blood pump may include an impeller assembly with an impeller housing having a first central axis. The blood pump may include a motor housing having a second central axis. A magnetic assembly may magnetically couple the impeller assembly with the motor assembly. A flexible connector may couple the impeller housing with the motor housing. The magnetic assembly may bias the impeller housing and the motor housing to a first configuration with the first central axis aligned with the second central axis.

The present disclosure generally relates to systems and methods of use for draining cerebrospinal fluid (CSF) from a brain or a spinal canal in a subject, for example, to treat hydrocephalus or other conditions. In some embodiments, the disclosure relates to a device comprising a flow controller positioned within a conduit that allows CSF to flow through the conduit from a first end to a second end. This may allow the CSF to drain, for example, from an intradural space (such as a thecal sac) into, for example, a paraspinal space, paraspinal vein or other venous space, or peritoneal cavity. A variety of methods may be used to hold or anchor the device in place, for example, an expansion apparatus. In some embodiments, the device can be implanted percutaneously at a location along or within a subject's spinal column, thus reducing the need for surgery, general anesthesia, and hospitalizations.

This device for detecting oxygen saturation of percutaneous muscle comprises a light source for causing light to enter the body, and a first light detector and a second light detector for detecting reflected light reflected in the body. The second light detector is positionally shifted, in the circumferential direction about the light source, from a first imaginary line linking the light source and the first light detector.

The invention provides a navigation method and system for percutaneous transhepatic duct puncture, and the method specifically comprises the steps: S1, reading a liver enhanced CT image, and determining a target bile duct to be punctured; s2, integrating the electromagnetic tracking navigation system and the ultrasonic system to form an ultrasonic-electromagnetic fusion workstation; s3, electromagnetic sensors are installed in the ultrasonic probe and the puncture needle respectively; s4, starting a magnetic field generator to obtain object space vector information; s5, acquiring an ultrasonic medical image, and generating a positioning image according to the object space vector information; s6, setting the positioning image and the ultrasonic medical image according to the same space size proportion; s7, obtaining a superimposed image, and outputting the superimposed image on a display monitor in real time; s8, simulating puncture, offsetting magnetic field interference through parameter adjustment, and adjusting puncture precision; s9, puncturing along the puncturing path; and the like. The percutaneous transhepatic duct puncture navigation system can quickly and accurately complete percutaneous transhepatic duct puncture navigation, is flexible and free of radiation, is short in learning curve, and can be popularized in a homogenized manner.

Wearable electrocardiogram (ECG) systems configured to record ECG from ears (auricular ECG systems), fingers (ear-finger or finger-finger ECG systems) or toes, comprising a processing unit configured to analyze the ECG data to detect serious cardiac arrhythmias or impending serious cardiac arrhythmia. Automatic anti-arrhythmia systems comprise one of the ECG systems and a transcutaneous auricular vagus nerve stimulation (taVNS) unit. When serious cardiac arrythmias are detected, the anti-arrhythmia systems may automatically send pre-determined electric stimuli to a vagus nerve to alleviate or stop the cardiac arrhythmias. The ECG electrodes and the stimulating electrode of the taVNS unit are located on a surface of a housing structure made of flexible elastic and adaptable material such that these electrodes will be naturally and snugly contacting the wearer's skin. These wearable ECG and anti-arrhythmia systems are suitable for easy self-installation, self-removal and daily ambulatory use.

This invention relates to a novel P-approach endoscopic lumbar fusion surgery method, belonging to the field of lumbar fusion surgery technology. This method addresses the high risk of nerve injury and insufficient operational precision in existing endoscopic fusion techniques by proposing an improved solution. It utilizes Kirschner wires for positioning at the inferior articular process to establish a precise entry point avoiding the nerve root pathway; a visually guided circular saw is used throughout the endoscopic procedure to construct a safe triangular working channel directly reaching the spinal canal; under full endoscopic monitoring, a unilateral approach is used for bilateral spinal canal decompression, thoroughly removing diseased tissue and scraping the endplates until punctate bleeding occurs; a bone graft cannula with a curved tip is used to precisely implant the fusion device into the anterior region of the intervertebral space, restoring intervertebral height through a self-locking structure; finally, a universal pedicle screw is percutaneously implanted for fixation. This method reduces the risk of nerve injury, improves surgical safety and efficiency, and is suitable for patients with lumbar spondylolisthesis complicated by spinal stenosis.

This invention belongs to the field of biomedical materials technology, and particularly relates to an analgesic microneedle patch, its preparation method, and its application. The analgesic microneedle patch of this invention uses extracted mesenchymal stem cell exosomes and ginger exosomes as analgesic active substances, and by combining them with microneedle patch technology, it provides a new technical approach for surface anesthesia. The analgesic microneedle patch of this invention combines microneedle technology and photopolymerization 3D printing technology to develop a customizable hydrogel microneedle patch, achieving minimally invasive and precise percutaneous delivery of local anesthetics, providing a new technical approach for surface anesthesia.

1. Name of the product in this design: Transcutaneous acupoint electrical stimulator (ear acupoint). 2. Purpose of this design: To stimulate acupoints on the ear through the skin to prevent and treat diseases. 3. The key design feature of this product is its shape. 4. The image or photograph that best illustrates the design's key points: 3D view 1.

The invention discloses a percutaneous penetration enhancing system as well as a preparation method and application thereof. The percutaneous penetration enhancing system comprises a liquid-liquid condensation phase and an active substance. The anionic surfactant and the cationic surfactant in a certain concentration range are mixed to construct a liquid-liquid condensed phase, and the formed liquid-liquid condensed phase structure can efficiently entrap active substances and has good self-stability. The research field of the percutaneous penetration enhancing system is enriched, and the application of the percutaneous penetration enhancing system in the preparation field of cosmetics, drugs and the like is expanded.

The present invention is related to an extracardiac temporary pacemaker designed for cardiac pacing, particularly for high-grade atrioventricular block and prolonged sinus pauses. The device integrates a pacemaker unit with battery within a transcutaneous patch, featuring thin, needle-like electrodes that penetrate the intercostal muscles to reach the epicardial surface of the heart. The design allows for rapid, significantly reducing the risk of complications associated with traditional intravascular pacemakers and providing a quick, safe, and more efficient solution for temporary cardiac pacing.