83 results about "Patient acceptance" patented technology

The invention relates to the technical field of rehabilitation treatment of chronic obstructive pulmonary patients, and discloses a therapeutic scheme matching method for rehabilitation treatment of chronic obstructive pulmonary patients, comprising the following steps: step 1, a data acquisition and integration module which is responsible for collecting multi-dimensional data of patients; according to the treatment scheme matching method for the rehabilitation treatment of the chronic obstructive pulmonary disease patient, unnecessary medical resource waste can be avoided, the patient can be timely and properly treated, the overall utilization efficiency of the medical resources is improved, detailed treatment information and self-management suggestions are provided for the patient, and the patient is prevented from suffering from chronic obstructive pulmonary disease. A patient can better know the illness state and the treatment process of the patient, a personalized treatment scheme is easier to accept and execute by the patient, the treatment compliance of the patient can be improved, a large amount of real-world patient data is accumulated by the system, rich materials are provided for medical research, and through deep mining and analysis of the data, the treatment compliance of the patient can be improved. Pathogenesis, treatment effect influence factors and the like can be further explored.

Systems and methods for providing an intelligent network to onboard patients to specialty medications are described herein. A server system for managing communication is configured to receive from a user at a healthcare practice, an electronic request to obtain a medical prior authorization (medPA) for a specialty drug to administer for a patient of the healthcare practice; select, using a rules service, a communication pathway to submit the medPA to a healthcare payer from a plurality of communication pathways; and initiate a connection with the healthcare payer using the selected communication pathway.

The invention discloses a visual pain assessment report system and method, and relates to the technical field of medical treatment, three groups of algorithm units are matched with one another to form a core architecture of the visual pain assessment report system, a basic pain value Pd is calculated by considering pain intensity Pi, pain time Pct and a sensitivity coefficient Sp, and the basic pain value Pd is calculated by taking the pain intensity Pi, the pain time Pct and the sensitivity coefficient Sp into consideration. The comprehensive pain value Ps is calculated by combining the real-time physiological data (such as heart rate and blood pressure) of the patient, more comprehensive and more detailed visual pain assessment is provided, and compared with subjective description singly depending on the patient, the pain assessment mode can reflect the actual pain condition of the patient more accurately, and the pain assessment accuracy is improved. The planned drug application amount Dp is calculated by comprehensively considering the basic drug application amount Db, the body weight We of the patient and the comprehensive pain value Ps through the planned drug application amount algorithm unit, it can be ensured that the patient receives proper drug treatment, the situation that the drug amount is insufficient or excessive is avoided, and therefore the treatment effect on the patient can be improved, and adverse reactions are reduced.

The present invention is in the field of ocular disease therapy. In particular, the invention relates to a composition comprising pimecrolimus for use in the topical treatment of moderate to severe blepharitis, in particular in a patient group comprising subjects with a clinical diagnosis of moderate to severe blepharitis, wherein the subjects to be treated have signs and symptoms of moderate to severe blepharitis characterised by swelling of the eyelid margin, ocular debris and ocular discomfort. In particular, the present invention relates to an ophthalmic composition that shows a high patient acceptance and a clinically meaningful improvement in the signs and symptoms of treated patients.

To provide an information sharing system capable of tracking PICS information over a long period.SOLUTION: A PICS information sharing system according to the present invention includes a management server that manages PICS information, an ICU terminal, a general ward terminal, and an outpatient terminal, wherein the ICU terminal, the general ward terminal, and the outpatient terminal are connected to the management server via a network and view and update PICS information of a patient, the ICU terminal inputs function evaluation information when the patient leaves the ICU, and the management server registers the input function evaluation information as PICS information. A general ward terminal inputs function evaluation information when a patient leaves a general ward, a management server registers the input function evaluation information as PICS information, an outpatient terminal inputs function evaluation information when the patient receives medical care at an outpatient, and the management server registers the input function evaluation information as PICS information.SELECTED DRAWING: Figure 1

The utility model relates to the field of medical equipment, in particular to a monitoring probe fixing device which comprises a fixing band, an installation window is arranged on the fixing band, a fixing seat is arranged on the installation window, a groove matched with a monitoring probe in shape is formed in the fixing seat, a light hole is formed in the bottom wall of the groove, and a light source is arranged in the light hole. And a limiting cover capable of being opened and closed is arranged at the opening part of the groove. According to the monitoring probe fixing device, the fixing belt is arranged, the monitoring probe is detachably connected with the fixing belt, when a patient needs to move, the limiting cover is opened, the monitoring probe is taken out, the fixing belt does not need to be taken down from the arm of the patient, repeated binding and disassembling operation is avoided, use is easier and more convenient, and the cost is reduced. And the patient acceptability is higher.

The application relates to a blood biomarker for evaluating and diagnosing Parkinson's disease and an application thereof. The blood biomarker is SERPINA3 and / or alpha-Syn. By using the biomarker as a diagnostic biomarker for Parkinson's disease, early diagnosis of Parkinson's disease can be assisted by detecting the SERPINA3 level and the alpha-Syn level in a blood sample, the trauma is small, the operation is simple, and the method is suitable for most patients and has high patient acceptance; and the SERPINA3 and alpha-Syn levels in the blood sample can be determined by a photochemical luminescence detection method, the detection sensitivity is high, the accuracy is high, and early, efficient and high-precision diagnosis of Parkinson's disease can be realized.

This invention discloses the application of reagents for detecting biomarker levels in the preparation of products for identifying obstructive sleep apnea. It relates to the field of biomarker technology and aims to overcome the shortcomings of existing technologies that rely on complex polysomnography (PSG) procedures, poor patient compliance, and a lack of effective molecular markers. The biomarkers used in this application consist of CD36 glycoprotein, 9-octadecenal, and protocatechuic acid 3-O-sulfate. This invention enables rapid and objective identification of obstructive sleep apnea by detecting the levels of the above biomarkers in plasma. The procedure is simple and well-accepted by patients. The combined use of multiple biomarkers can improve the accuracy and stability of the identification, making it suitable for screening or auxiliary diagnosis in medical institutions at different levels.

Methods, systems, and apparatuses are described for automated external defibrillation for determining shock / no-shock decisions based on ECG readings taken when a patient is undergoing cardiopulmonary resuscitation (CPR). A device may filter an ECG signal of a patient to reduce artifacts from the signal caused by CPR being performed on the patient. The device may use the filtered ECG signal to determine whether to deliver a therapeutic shock to a patient even if the patient is undergoing CPR.

Reminder of the titleDevice for sleeping with a medical device by Continuous Positive Pressure used for the treatment of sleep apnea. Technical field and statement of the problemThe invention relates to a device for sleeping with a CPAP device without risk of air leakage and removal of the mask. Main characteristics of the solutionIt consists of a T-shirt (1) or a nightie having on its front face a funnel-shaped pocket (2), equipped with a zipper (4) through which the air tube (6) is introduced to keep it in line with the patient's mask (7). Thus, during movements during sleep, the patient moves his mask and the air tube simultaneously in the same direction, canceling any friction force. Intended useThe device according to the invention is particularly intended for better patient acceptance of his Continuous Positive Pressure ventilation treatment.Choice of an illustration to accompany the abstractFigures for the abstract: Fig.1, Fig.2.

The invention belongs to the technical field of medical equipment, and particularly discloses a clinical hemodialysis device and a using method thereof.The clinical hemodialysis device comprises a dialysis box, and a dialysis assembly is arranged on one side of the dialysis box; the dialysis assembly comprises a dialyzer, a liquid inlet pipe, a liquid outlet pipe, a dialysate inlet, a dialysate outlet, a dialysis membrane, an inner partition plate and an adjusting structure. By means of the flow guiding structure, flow guiding can be conducted when blood enters the dialysis cavity, the situation that blood easily flows in a deviated mode after entering the dialysis cavity, so that no blood passes through the surface of a dialysis membrane on one side, the blood and dialysis efficiency is affected is prevented, the treatment duration is shortened, complications are reduced, and the treatment effect is improved by heating the blood. Therefore, the blood is kept at the temperature acceptable by the human body, the comfort of a patient during treatment is improved, and the dialysis treatment is safely and efficiently carried out.

The invention relates to a medicinal and edible compound extract for improving myelosuppression of a tumor patient after chemotherapy, and a preparation method and application of the medicinal and edible compound extract. The compound extract is extracted from a composition at least comprising the following raw material medicines in parts by weight: 0.9-10 parts of tricholoma matsutake, 0.9-10 parts of mulberry and 0.5-10 parts of rhizoma polygonati. The raw material medicine composition further comprises the following raw material medicines in parts by weight: 0.7-10 parts of longan, 0.5-10 parts of pericarpium citri reticulatae, 0.5-10 parts of scorched hawthorn fruit, 0.5-10 parts of fructus amomi, 1.1-10 parts of cordyceps sinensis rice flour and 2.5-15 parts of rice peptide. The selected raw material medicines are all medicinal and edible components, do not cause adverse effects on liver and kidney functions and gastrointestinal tracts of eaters, and are high in safety and high in patient acceptance degree. Effect verification results show that the mulberry compound extract has an improvement effect on the side effect of bone marrow suppression of tumor patients, especially in the early stage, no related adverse reaction is found, and a safe and effective treatment choice is provided for bone marrow suppression.

We provide the system. [Solution] A means of analyzing traffic information using a generative model and deriving the optimal transport route, A means of evaluating the patient acceptance situation at medical institutions and selecting appropriate medical facilities, A means of monitoring a patient's vital signs in real time and issuing a warning signal if an abnormality is detected, A means of controlling transportation methods utilizing autonomous driving technology and optimizing transportation efficiency, A system that includes this.

The invention discloses a primer pair, a kit and a method for detecting echinococcosis based on circulating free DNA, and relates to the field of molecular biological detection. According to the method, a sample to be detected is added into an RPA-CRISPR amplification detection system for synchronous isothermal amplification and CRISPR / Cas reaction, the sample to be detected is cfDNA extracted from blood of a patient, and the RPA-CRISPR amplification detection system comprises an RPA primer pair, crRNA, a Cas12a reporter probe, Cas12a protein, a buffer solution and nuclease-free water. Circulating free DNA of a patient is taken as a detection sample, a tissue sample of the patient does not need to be obtained, the patient cannot be wounded, implementation is easy, and the patient acceptability is high; the RPA-CRISPR amplification detection system constructed by the invention can simultaneously perform nucleic acid amplification and detection, so that the detection period is shortened, the cost is reduced, the operation process is simplified, a nucleic acid amplification product does not need to be uncovered and transferred, and the risk that a sample to be detected is polluted can be reduced.

The utility model discloses an anti-radiation examination suit, which comprises an anti-radiation hood, an upper anti-radiation suit, a lower anti-radiation skirt and anti-radiation shoes, the anti-radiation hood, the upper anti-radiation suit, the lower anti-radiation skirt and the anti-radiation shoes form a set of anti-radiation suit, and the front side of the anti-radiation hood is provided with mask holes. A mask hole is formed in the radiation-proof head cover, a radiation-proof mask is fixedly arranged in the mask hole, the radiation-proof head cover is transparent, longitudinal adjusting frame mechanisms are installed on the left side and the right side in the radiation-proof head cover respectively, and transverse adjusting frame mechanisms are installed on the front side and the rear side in the radiation-proof head cover respectively. The radiation-proof suit solves the problems that a patient receives extra radiation due to the fact that tight radiation-proof measures are not taken for different examination parts of the patient, and meanwhile the radiation-proof suit is inconvenient to adjust and difficult to adapt to different patients.

Methods of metering a pressure reflex response and pressure reflex metering devices and systems are provided herein. Such methods and devices position and expand an expandable structure at a target location within a patient vasculature, preferably an aortic arch, to meter a pressure reflex response to one or more lateral dimensions of the expandable structure. The pressure reflex metering device may optionally expand the structure to a variety of expanded configurations while monitoring the patient's blood pressure to determine an optimal dimension of the pressure reflex response. These metering devices and methods help assess the suitability of a patient to receive treatment and help select or customize implants placed in the vasculature for long term treatment of hypertension. The pressure reflex metering device may be further integrated into an implant delivery system such that partial deployment allows for metered response and full deployment allows for long term treatment.

The present disclosure relates to predicting a survival rate of a patient with cancer following a treatment. In some embodiments, one or more processors: apply a large language model to a clinical report to extract a plurality of clinical features; acquire a pre-treatment image and a post-treatment image of the patient with cancer; apply a segmentation algorithm on an annotated volume of interest (VOI) of the pre-treatment image to obtain a first segmented VOI; apply the segmentation algorithm on the annotated VOI of the post-treatment image to obtain a second segmented VOI; determine a plurality of radiomics features and a plurality of deep learning features from the first segmented VOI and the second segmented VOI; and apply a machine learning model to the plurality of clinical features, the plurality of radiomics features, and the plurality of deep learning features to predict the survival rate of the patient with cancer.

The invention relates to a feedback control and audio and video combined tinnitus adjuvant therapy method, which comprises the following steps of: firstly, constructing a tinnitus therapy process set by combining audio and video related functions of multimedia, and constructing a basic tinnitus therapy scheme according to the tinnitus therapy process set; when a basic tinnitus treatment scheme is carried out for a user, the treatment cycle of the tinnitus treatment scheme can be adjusted according to the treatment feedback effect, and recommendation can be carried out according to the completed tinnitus treatment process and the tinnitus treatment process of a non-running tinnitus treatment scheme with concentrated tinnitus treatment processes. And a personalized tinnitus treatment process scheme is formulated for the user. According to the tinnitus treatment system and method, clear and easy-to-understand audios and videos can be combined during tinnitus treatment, so that patients can accept the tinnitus treatment system and method easily, remote treatment compliance is improved, curative effect tracking and intervention adjustment are achieved in cooperation with scoring and feedback mechanisms, the tinnitus treatment process can be pushed to the user, and then a personalized tinnitus treatment scheme is customized for the user.

The invention provides a foldable scoliosis correcting device which comprises a main framework, a lifting mechanism, an adjusting chassis, a rotating mechanism, an inclining mechanism and a seat cushion part, the adjusting chassis is connected with the main framework through the lifting mechanism, the rotating mechanism and the inclining mechanism are arranged on the adjusting chassis, the seat cushion part comprises a stool part, the rotating mechanism comprises a rotatable disc, and the rotatable disc is arranged on the stool part. The tilting mechanism comprises a base part fixedly connected with the rotatable disc, a first tilting part arranged on the base part in a spherical contact manner and a second tilting part arranged on the first tilting part in a spherical contact manner, and the second tilting part is fixedly connected with the stool part; according to the foldable scoliosis correction device, the correction angle can be adjusted in real time in a multi-dimensional mode, the individualized requirement for scoliosis treatment is met, the patient acceptability is high, and the treatment effect is good.

The invention relates to the technical field of gynecological disease adjuvant therapy instruments, in particular to a vagina drug delivery device which comprises a tube body, a drug storage bag, a threaded push rod, an injection tube, a rotating assembly, a protective cap and a liquid storage bag, a fixing ring is installed at one end of the tube body, and internal threads are arranged on the inner wall of the fixing ring; according to the vagina drug delivery device, through the scale strip on the outer wall of the first threaded sleeve, a user can intuitively set the needed drug delivery dosage, rotate the rotating cylinder anticlockwise to enable the first threaded sleeve to stretch out, observe the scale strip to be adjusted to the preset position, and the user can conveniently and rapidly deliver the drug delivery dosage. The liquid storage bag is filled with the medical lubricant, the medical lubricant is adhered to the outer wall of the injection tube through the sponge ring, friction and discomfort during insertion are reduced, and the acceptability and compliance of a patient are improved, especially under the condition that multiple times of administration are needed, through the design, the dosage of the liquid storage bag is ensured to be accurate, and the liquid storage bag is filled with the medical lubricant and is adhered to the outer wall of the injection tube through the sponge ring.

The invention discloses a self-suction type throat atomization administration device, and belongs to the technical field of medical instruments. Comprising a shell and an atomizer installed on the shell. The rotary drum is rotationally mounted in the shell, and a premixing cavity is formed in the rotary drum; the one-way air inlet valve is installed on the shell, and the one-way air inlet valve and the atomizer are both communicated to the left end of the premixing cavity; the valve seat is installed in the shell and abuts against the right end of the rotary drum, and an inner cavity of the shell on the right side of the valve seat is a mixing cavity. The one-way ventilation assembly is installed on the valve seat and used for communicating the premixing cavity with the mixing cavity in a one-way mode. The suction nozzle is arranged at the right end of the shell and is communicated with the mixing cavity; wherein the shell is further provided with an air distribution hole communicated with the mixing cavity, and an adjusting cylinder is installed outside the air distribution hole. The device is small in overall size and convenient to carry and operate, a patient can accept and insist in use more easily, and the treatment effect is improved; the atomized liquid medicine is uniformly mixed, and the gas distribution amount is adjustable; the one-way ventilation assembly can be automatically opened and closed, and liquid medicine waste is reduced.

The application discloses an oral orthodontic anchorage nail implantation operation patient's physical and mental state monitoring system and method, relates to the oral orthodontic treatment technical field, and comprises a patient physiological signal information acquisition unit, which is used for collecting patient physiological signal information and transmitting the patient physiological signal information to a processing and analysis unit for processing and analysis; the processing and analysis unit is used for processing and analyzing the collected patient physiological signal information, determining the patient's physical and mental state according to the patient physiological signal information, and triggering an early warning mode; and a mobile terminal platform is used for displaying the early warning mode output by the processing and analysis unit to doctors and patients and recommending a treatment mode according to the early warning mode. The application can record, analyze and feedback the patient's physical physiological information and changes before, during and after operation in a whole cycle, help doctors and nursing staff understand the real-time health condition change trend of the patient, provide guidance and support for clinical operation, help the patient better accept and adapt to the anchorage nail treatment, and improve the patient's acceptance and satisfaction.

The invention relates to a method in which xylitol is heated until liquified, to be added to hydroxyapatite and zinc citrate, the mixture subsequently being subjected to a process of controlled crystallisation. This produces crystals for dental care with active agents that maximise the bioactive effect of same in the mouth, the crystals also providing slow and controlled release of the active agents, thereby increasing effectiveness in comparison with conventional forms of application. In summary, the invention represents a significant advance in dental care technology. It not only improves the therapeutic efficacy of the hydroxyapatite and zinc citrate through innovative release technology, but also increases patient acceptance and environmental sustainability.

This disclosure provides a method for identifying patients requiring treatment for pressure ulcers and treating such patients with clinical interventions selected based on subcutaneous water content. This disclosure also provides a method for stratifying patient groups based on the risk of pressure ulcers and a method for reducing the incidence of pressure ulcers in care facilities. [Solution] A method is provided and includes for identifying and providing an appropriate level of pressure ulcer care to a patient based on multiple subcutaneous moisture (SEM) measurements. In one aspect, the patient receives progressively more effective intervention for pressure ulcers based on changes in SEM measurements. In another aspect, the patient receives low-intensity intervention for pressure ulcers based on changes in SEM measurements.

The application belongs to the technical field of medical equipment, and discloses a waist and abdomen plasma therapeutic instrument, which comprises a supporting frame, a therapeutic head, a plasma generator and a tail gas collecting device, the therapeutic head is arranged on the supporting frame, the therapeutic head is provided with a hollow groove and a matching opening communicated with the hollow groove, the waist or abdomen of a patient can be matched with the matching opening to form a closed treatment cavity with the hollow groove, the plasma generator is installed on the therapeutic head and communicated with the hollow groove, plasma gas and waste gas generated by discharge of medium gas in the plasma generator can be sprayed into the hollow groove, the tail gas collecting device is communicated with the hollow groove, and the tail gas collecting device can collect gas in the hollow groove. The waist and abdomen plasma therapeutic instrument can ensure that waste gas cannot spread to the environment outside the treatment cavity when a patient receives treatment, so that the safety of the patient is ensured.

The invention discloses a composite material for detecting HCG (human chorionic gonadotropin) protein in sweat, a preparation method of the composite material and application of the composite material in AD diagnosis, and belongs to the technical field of biosensing. The composite material comprises a composite substrate material composed of carbon nanotubes and 1T-phase molybdenum disulfide, and polypeptide molecules which are fixed on the substrate through a cross-linking agent and can be specifically combined with HCG protein. The preparation method comprises the following steps: synthesizing a CNTs / 1T-MoS composite substrate by adopting a one-pot solvothermal reaction, carrying out carboxylation modification on the CNTs / 1T-MoS composite substrate, and then coupling with polypeptide molecules. The material is also fixed on the surface of a working electrode to prepare a sensor, and the sensor can be integrated on a micro-fluidic chip to form a wearable detection patch. The composite material and the sensor have ultrahigh sensitivity (the detection limit reaches 0.45 pg / mL) and specificity on AD sweat marker HCG protein, non-invasive and convenient early diagnosis of AD is realized, and the acceptance of patients is remarkably improved.

The invention is suitable for the technical field of medical atomizers, and discloses a multidirectional efficient atomization constant-temperature atomizer. The technical problems that in the prior art, the difference between the temperature of liquid medicine and the temperature in the body is large, and the liquid medicine cannot be completely sucked are solved, the breathing device comprises a compressor, a guide pipe, a breathing assembly and an atomizing assembly, the breathing assembly is connected with the atomizing assembly and the guide pipe, the guide pipe is connected with the compressor, and the atomizing assembly is connected with the compressor. Through the arrangement of the double-layer pipeline, on one hand, the sealing performance of the breathing assembly can be guaranteed, external liquid medicine and other dirt can be prevented from entering the breathing assembly and being inhaled into the human body, on the other hand, exhaled gas has certain heat and can be used for heating gas in the pipeline, the temperature of the gas is increased, and therefore atomized liquid medicine can be heated; the body temperature difference between the liquid medicine and the body temperature of a patient is small, the liquid medicine can be accepted by the patient more easily, and the patient does not feel uncomfortable when inhaling the liquid medicine too cold.

The invention relates to a method and apparatus for controlling the inner temperature of a patient, comprising the steps of creating a fluid circuit that comprises a patient and a heat exchanger, the power supply thereto being controlled by a controller; subjecting at least a portion of the fluid in said circuit to the heat exchanger; directing the subjected fluid to and into the patient to control the temperature of the patient; estimating the organ temperature of the patient by a model that has been obtained on a mammal other than the patient; and controlling the power supply to the heat exchanger such that the estimated organ temperature does not exceed a threshold organ temperature, potentially taking into account estimated future organ temperatures. The invention further relates to a method and apparatus for controlling the inner temperature of a patient when subject to whole body hyperthermia, and to a method for obtaining the model.

The application discloses a traditional Chinese medicine sachet for treating insomnia and a preparation method and application thereof. The traditional Chinese medicine sachet comprises a sachet bag and a sachet core, and the sachet core is composed of eleven natural herbal medicinal materials, i.e., wild chrysanthemum, rhizoma acori graminei, rhizoma et radix valerianae, radix morindae officinalis, rose flower, jasmine flower, lavender, amomum villosum, semen cassiae, sandalwood and silkworm sand. The raw materials of the traditional Chinese medicine sachet are homologous to food or traditional anshen medicinal materials, have no dependence and no toxic side effects after long-term use, have a clean and comfortable smell, and have high patient acceptance. The preparation process is simple, raw materials are easy to obtain, and the traditional Chinese medicine sachet is suitable for large-scale production. The traditional Chinese medicine sachet can significantly shorten the sleep time, reduce the number of night awakenings, prolong the sleep time, effectively relieve anxiety, palpitation, bitter taste and other accompanying symptoms, and can be widely applied to home, office, travel and other scenes.

The invention provides a novel model for diagnosis and prognosis of sepsis cardiomyopathy and a construction method thereof. The element TMAD in the new model has the advantages that the element TMAD does not depend on the high cardiac hypersonic image quality and is easy and convenient to operate, no radiation or side effect exists, and the ventricular function can be accurately and rapidly evaluated; compared with LVEF sensitivity, the method has the advantages that left ventricular systolic function changes can be reflected earlier, measurement repeatability is quite good, and the method is particularly suitable for patients with poor cardiac ultrasound image quality; as a relatively new ventricular strain measurement technology, the ventricular strain can be obtained through further analysis by system software, the operation and software image analysis steps are simple, the ventricular strain can be skillfully applied through certain clinical training, the environment is not polluted, the health of an operator is not influenced, and the patient acceptability is relatively high; the method has high feasibility in diagnosis of sepsis cardiomyopathy.