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484
resultados
Última actualización
30/07/2026 [08:11:00]
Resultados 275 a 300 de 484
Resumen de: KR20260108808A
일 실시예에 따른 출력 장치는 환자의 골절 부위를 촬영하여 생성된 CT 데이터를 수집하는 단계; 상기 수집된 CT 데이터를 이용하여 소정의 조직에 대응하는 3차원 출력을 위한 골절 모델을 생성하는 단계; 상기 생성된 골절 모델을 분할하는 단계; 상기 분할된 골절 모델을 출력하기 위한 설정값을 결정하는 단계; 및 상기 결정된 설정값에 기초하여 상기 분할된 골절 모델의 3차원 출력물을 출력하는 단계를 수행할 수 있다.
Resumen de: WO2026146504A2
A curable formulation usable as a support material formulation in additive manufacturing of a three-dimensional object such as a denture structure, which forms a hardened mixed layer with a modeling material formulation and provides an object that features improved toughness (e.g., fracture toughness), and additive manufacturing methods employing same are provided. The curable formulation comprises at least one non-curable material which comprises at least one polymeric material featuring water solubility (e.g., ECAH) lower than 200 grams/liter, at least one mono-functional (meth)acrylate featuring low Tg and miscibility in the non-curable material, at least one multi-functional (meth) acrylate featuring at least 10 ethoxylated groups and/or Tg lower than 0 °C, and at least one mono-functional (meth)acrylate. Additive manufacturing of a three- dimensional assembly which comprises a hardened object and a hardened sacrificial structure, and systems employing same are also provided.
Resumen de: WO2026147853A1
A biosensor system for telemedicine and remote physiological monitoring is provided. The biosensor system may include a sensor subsystem comprising a piezoelectric film sensor configured to detect and transduce human or animal body acoustics into electrical signals. The biosensor system may include an electronics subsystem removably coupled to the sensor subsystem. The electronics subsystem may include an interface for interacting with the sensor subsystem, pre-processing circuitry for generating a pre-processed signal from a signal received from the sensor subsystem, a processor configured to receive the pre-processed signal, a communications interface operably coupled to the processor and configured to send the preprocessed signal to a receiving device, and a power supply configured to provide power to the biosensor system. The pre-processing circuitry may include a preamp and a filter.
Resumen de: WO2026147825A1
The present invention relates generally to the fields of cancer therapy and patient stratification. More particularly, the specification relates to determining a likelihood of a patient response to cancer treatment.
Resumen de: US20260191440A1
A system for detecting oximetry parameters of a user may include a reusable, wireless, and flexible near-infrared spectroscopy (NIRS) monitoring wearable system. The NIRS system may include a first component having a plurality of light sources configured to emit visible and infrared light at a plurality of wavelengths. The first component may have a first detector configured to detect a first plurality of signals from the plurality of light sources at a first source-detector distance of approximately 6 millimeters (mm) to 10 mm. The NIRS system may include a second component having a plurality of second detectors configured to detect a second plurality of signals from the plurality of light sources at multiple source-detector distances ranging from about 25 mm to about 45 mm. The NIRS system may include a memory, rechargeable battery, and processor configured to execute multi-depth tissue analysis.
Resumen de: US20260195728A1
This application describes systems and methods for locating, securing, accessing and utilizing a discrete enclosure or workspace. The discrete enclosure or workspace may be located in a public, private or semi-private setting and may comprise a combination of working platforms or surfaces, seats, desks and other apparatus, as well as computer hardware and software. Systems may comprise natural language processing, artificial intelligence, machine learning and other adaptive learning capabilities to enhance the use of the discrete workspace. The workspace may be dimensioned to be used for a wide variety of activities by one or more users.
Resumen de: WO2026148163A1
An article organizer for use with plural articles to be loaded and removed includes a housing including a chamber for removably receiving at least one cartridge, each cartridge removably storing at least one article, an organizer communication module, and an organizer communication module. The housing includes an organizer opening through which the at least one cartridge is insertable into and removable from the housing. The organizer communication module can communicate with the at least one cartridge, and send data to and/or receive data from the at least one cartridge. The organizer controller can process data from the organizer communication module and output information based on the data.
Resumen de: WO2026148102A1
A system and method for monitoring a health status of a patient using one or more radar sensors placed in an environment containing the patient. A processor controls the radar sensors to emit radio waves and measures reflection data including reflected radio waves. The processor processes the reflection data to determine motion state data characterizing position and velocity, isolates motion state data associated with human movement patterns to generate tracked motion state data, and aggregates the tracked motion state data to generate aggregate motion data. Machine learning algorithms process the aggregate motion data to determine health status including fall detection, behavior identification, and characterization of Alzheimer's disease, dementia, Parkinson's disease, fall risk, and sundowning. The system tracks aggregate motion data longitudinally over time and generates reports based on health status.
Resumen de: US20260191454A1
Systems and methods to improve resource utilization in ambulatory patient monitoring are disclosed, including detecting a critical event using the physiologic information, transitioning the ambulatory medical device from a long-term ambulatory monitoring mode to a critical response mode, and controlling, in the critical response mode, transmission of an advertising packet and information about the detected critical event to a remote device in a continuous listening mode or transition of a communication circuit of the ambulatory medical device to a listening mode to receive an advertising packet of the remote device in a continuous advertising mode to transmit a connection response and information about the detected critical event to the remote device to improve resource utilization of the ambulatory patient monitoring.
Resumen de: US20260191458A1
0000 Methods and systems are provided for receiving labor-related data for one or more previous contractions of a patient, the labor-related data at least comprising data obtained with one of a tocodynamometer, an IUPC, and an EHG recording system, predicting labor-related data for a next contraction based on the labor-related data for one or more previous contractions, generating one or more visual indicators and one or more audio indicators based on output from a labor prediction model, the output from the labor prediction model being generated by entering the received labor-related data for the one or more previous contractions into the labor prediction model, the predicted labor-related data, and user input into the labor prediction model, and displaying the one or more visual indicators to a display device that is visible to the patient and outputting the one or more audio indicators to the patient.
Resumen de: WO2026146885A1
This wearable device may comprise at least one sensor, a display, a memory for storing instructions, and at least one processor. The instructions, when executed individually or collectively by the at least one processor, may cause the wearable device to: display a first screen of a watch face through the display; obtain input data through the at least one sensor; generate a second screen related to the input data by using the input data on the basis of identifying that the input data corresponds to defined data; add the second screen to a list of screens to be displayed, in response to at least one swipe input received while the first screen is displayed; receive a swipe input while the first screen is displayed; and change a screen displayed through the display from the first screen to the second screen on the basis of the received swipe input after identifying that the input data corresponds to the defined data.
Resumen de: WO2026147609A1
Certain aspects of the present disclosure provide a therapy management system configured to monitor analyte levels of a host during a time period using one or more analyte sensors to obtain analyte data, the analyte levels comprising at least glucose levels and ketone levels, and determine a metabolic fitness of the host based, at least in part, on the analyte data. The therapy management system is further configured to provide therapy management guidance to the host based, at least in part, on the determined metabolic fitness to improve the metabolic fitness of the host. The therapy management guidance includes at least one of a diet or meal recommendation for the host, an exercise recommendation for the host, or a lifestyle recommendation for the host.
Resumen de: US20260191463A1
0000 Methods and systems for receiving, by at least one processor, for each of a plurality of subjects at defined time intervals during a medical procedure, a subject-specific sensory metric output and a subject-specific sensor dataset. The subject-specific sensory metric output is outputted by a first sensory-monitoring device (SMD) of a first SMD type. The subject-specific sensor dataset is outputted by sensors monitoring a body of each subject from the plurality of subjects, and to be utilized by a second SMD of a second SMD type. The at least one processor executes code to correct for data collection deficiencies, to generate a training dataset for training a machine learning model (MLM) based on the subject-specific sensory metric output and a corrected subject-specific sensor dataset, to train the MLM, and to provide the trained MLM to the second SMD to facilitate medical actions during subsequent medical procedures.
Resumen de: WO2026148109A1
A device may receive physical activity data for a subject, wherein the physical activity data comprises raw acceleration data. A device may derive a plurality of metrics from the raw acceleration data, wherein the plurality of metrics comprise a plurality of pattern-related metrics. A device may input the plurality of metrics into a deployed machine learning model. A device may be configured to perform receiving, from the deployed machine learning model, a physical activity score. A device may calculate a risk score for at least one disease or condition based on the physical activity score.
Resumen de: WO2026147654A1
A method of delivering a medicament to a subject for the treatment of diabetes includes: receiving glucose data and lactate data for the subject; adjusting medicament therapy to be delivered to the subject based at least in part on the glucose data and the lactate data; and delivering the adjusted medicament therapy to the subject.
Resumen de: WO2026147606A1
A device for measurement of a concentration of glycated serum protein is disclosed, the device comprising: an analyte sensing portion configured to generate a signal associated with a concentration of a glycated serum protein, the analyte sensing portion comprising a flavin adenine dinucleotide (FAD)-dependent enzyme or an adenosine triphosphate (ATP)- dependent enzyme; a working electrode (WE); and a counter electrode (CE) and/or a reference electrode (RE). Methods of monitoring kidney disease in a subject using the device are also disclosed.
Resumen de: WO2026145627A1
Disclosed in embodiments of the present application are an intraoral three-dimensional scanner, an intraoral three-dimensional scanning method and system, and a system design method. The scanner comprises: a dental arch tray, a plurality of three-dimensional scanning heads, and a swing driving device. The plurality of three-dimensional scanning heads are located on the dental arch tray; the swing driving device is connected to the plurality of three-dimensional scanning heads and is configured to drive the plurality of three-dimensional scanning heads to swing; and the plurality of three-dimensional scanning heads are configured to scan, during swinging, a target oral cavity that has bitten the dental arch tray. The technical solution of the embodiments of the present application can reduce scanning time and learning costs.
Resumen de: WO2026148164A1
An inhaler tracking device for use with an inhaler or cannister configured to release a substance upon actuation includes a housing including a chamber for receiving the inhaler or cannister, the housing configured to hold the inhaler or cannister at a predetermined orientation, plural sensors sensing plural conditions or events including those of the inhaler or cannister, at least one indicator providing feedback to a user, and a controller configured to receive data from the plural sensors, analyze dispensing from the inhaler or cannister based on the received data, and output feedback signals to the at least one indicator. The analyzing includes determining duration and/or intensity of shaking of the device prior to dispensing, orientation of the device during dispensing, and number of actuations of the inhaler or cannister.
Resumen de: AU2025279596A1
SYSTEMS AND METHODS FOR GENERATING PATIENT-SPECIFIC IMPLANTS FOR ANATOMICAL STRUCTURES OF PATIENTS Embodiments for generating patient-specific implants for anatomical structures of patients are disclosed. One embodiment includes a method that includes receiving image data of an anatomical structure of a patient, where the image data indicates a fracture site associated with the anatomical structure; receiving manipulation data associated with manipulation of one or more parameters associated with the fracture site in a virtual reality environment; visualizing a three- dimensional (3D) model of the anatomical structure based on the image data, the one or more parameters, and the manipulation data, where the 3D model is visualized in a 3D space; generating a set of instructions for a printer based on the 3D model, and controlling the printer for generating a 3D printed model of the anatomical structure based on the set of instructions. The 3D printed model is configured to receive an implant, such that the implant is contoured to match the fracture site. FOR ANATOMICAL STRUCTURES OF PATIENTS site. ec - e c ec e c
Resumen de: WO2026145594A1
The present application discloses a digital segmentation line design method, a dental appliance forming method, a dental appliance, an apparatus, an electronic device, and a storage medium. The digital segmentation line design method comprises: acquiring a three-dimensional dental model and an attachment added on the three-dimensional dental model; determining a traversable region on the surface of the three-dimensional dental model, wherein the traversable region avoids the attachment; and generating a segmentation line in the traversable region, wherein the segmentation line extends from a first gingival line on a buccal-labial surface of the three-dimensional dental model to a second gingival line on a lingual surface. In the present application, the segmentation line can be generated by designing the traversable region, so that the design of the segmentation line is more reasonable; and the segmentation line extends from the first gingival line to the second gingival line, thereby enabling the present application to be applicable to multiple application scenarios. When a corresponding dental appliance is subsequently generated on the basis of the three-dimensional dental model, the dental appliance comprises an attachment accommodating cavity corresponding to the attachment and segment lines corresponding to the segmentation line, wherein the segment lines avoid the attachment accommodating cavity.
Resumen de: WO2026145316A1
An interaction method, device and medium are disclosed. The method includes: obtaining first teeth digital model groups respectively corresponding to M orthodontic treatment stages of a patient and a quantity of actual worn steps corresponding to each of the orthodontic treatment stages, where a first teeth digital model group of a first orthodontic treatment stage includes a first teeth model and first designed teeth models respectively corresponding to N orthodontic treatment steps; and in response to an operation of presenting a multi-stage orthodontic treatment plan of the patient, displaying a first orthodontic treatment interface, where the first orthodontic treatment interface includes second teeth digital model groups respectively corresponding to K orthodontic treatment stages sequentially arranged according to a first timeline, a second teeth digital model group of the first orthodontic treatment stage includes the first teeth model and first designed teeth models respectively corresponding to L orthodontic treatment steps.
Resumen de: WO2026148219A1
An inhaler apparatus (800) includes a receiver port (228) of a dispenser (102) that receives a canister (108) with an inhalant. The apparatus (800) includes a wireless data module (204) that reads encrypted data from and writes encrypted data to a memory chip (230) affixed to the canister (108) and a canister code module (802) that, if data read from the memory chip (230) does not including a cannister code, writes a cannister code of the dispenser (102) to the memory chip (230). The apparatus (800) includes a dispenser module 804 that enables dispensing the inhalant from the canister (108) in response to determining that the memory chip (230) includes the cannister code and that locks the dispenser 102 from dispensing the inhalant in response to determining that the canister (108) does not have a cannister code or determining that the canister (108) includes a different cannister code.
Resumen de: US20260193617A1
0000 Disclosed herein are organoid compositions that are manipulated to form shaped or elongated morphologies that more closely resemble native organ structures. These shaped organoids are advantageous for purposes such as studying organellar organization and for transplants compared to unformed organoids. Also disclosed herein are methods of producing said shaped or elongated organoid compositions.
Resumen de: US20260191471A1
0000 A system and method to confirm the insertion of an analyte-selective sensor comprising an array of microneedles possessing vertical extent between 200 and 2000 μm into viable tissue is disclosed herein. Mechanical insertion of an analyte-selective sensor is firstly attempted by means of an application of external force. Either during or following this routine, an electrical stimulus is applied between at least two distinct electrodes located within the said analyte-selective sensor; a resultant response is measured. This response is compared with a reference value to determine if insertion was successful. If insertion was successful, no further effort is required and the sensor can operate as intended. However, if insertion was not successful, the user can be instructed to continue to apply additional force to said sensor to achieve successful insertion or otherwise re-apply the said sensor altogether.
Nº publicación: US20260192047A1 09/07/2026
Solicitante:
CAREFUSION 303 INC [US]
CAREFUSION 303, INC.
Resumen de: US20260192047A1
0000 An infusion device includes a display and a pump configured for a predetermined volume per mechanical revolution (“VPMR”) under default environmental conditions. The infusion device receives infusion parameters that include (1) a requested flow rate of a fluid to be infused by the infusion device and, and (2) a head height and/or a patient height. The infusion device determines deviated environmental condition values as a function of (1) the received infusion parameters and (2) the default environmental conditions. The infusion device also determines a flow rate accuracy metric as a function of (1) the deviated environmental condition values and (2) an expected performance metric under the default environmental conditions. Responsive to determining the flow rate accuracy metric, the infusion device (a) displays, via the display, an indication of the flow rate accuracy metric; or (b) adjusts an operating speed of the pump based on the flow rate accuracy metric.
BOPI
Sede Electrónica
