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333
results.
Updated on
15/11/2026 [06:55:00]
Results 275 to 300 of 333
Absstract of: US20260325305A1
0000 Systems and methods for designing patient-specific orthopedic implants. The systems and methods can include automated collection protocols for available third-party data to use to generate surgical plans or patient-specific orthopedic implant designs. The system can identify triggers for collecting third-party data. The system can determine a confidence score for the collected third-party data based on the type of data, the source of the data, and the similarity of the data to patient data. The system can select parameters in the third-party data to integrate into designing a patient-specific implant or patient treatment.
Absstract of: US20260325872A1
0000 Embodiments of the present disclosure provide methods for training an artificial radiotherapy environment model. The method can include: providing an artificial radiotherapy environment model including: a transition function model configured to predict a next state based on a given state and a given radiation dose for a patient, a radiotherapy outcome estimator model configured to predict a treatment outcome for the next state, the radiotherapy outcome estimator model including at least two artificial neural networks and a logistic function, wherein respective outputs of the at least two artificial neural networks are fed into the logistic function, and a reward function configured to assign a reward for the next state based on the treatment outcome for the next state; and training the artificial radiotherapy environment model with a labeled dataset including a plurality of patient records.
Absstract of: US20260325257A1
0000 A method for manufacturing a dental prosthesis part that can be connected to a tooth stump, in particular a fixed dental prosthesis part includes manufacturing an adapter for a machine tool and a blank for the dental prosthesis part.
Absstract of: US20260331289A1
An artificially intelligent system and method for prognostic evaluation of autoimmune disorders. Certain objects and advantages of the present disclosure include methods and systems configured to aggregate and analyze clinical conversational data, patient biometric data, medical records data, blood biomarker test data, and patient biometric data to tune metrics that are increasingly specific to a patient in the creation of a dynamic patient phenotype to enhance clinical understanding of one or more factors that are specific to the patient's health status. One or more Al framework and engine may facilitate effective integration of communication-related insights into diagnostic and prognostic digital health resources. Exemplary systems, methods, and apparatuses according to the principles herein may comprise machine learning and deep learning techniques for the development of one or more quantitative metrics derived from clinical conversational data.
Absstract of: AU2025271814A1
A patient care system for monitoring injections and/or a patient's adherence to a prescribed treatment regimen comprises: an autoinjector for administering a medicament, such as a growth hormone, in particular to a patient, wherein the autoinjector is configured to receive a cartridge, in particular a dual chamber cartridge, with the medicament, wherein a dose of the medicament corresponds to a complete content of the medicament in the cartridge, wherein the cartridge comprises a code which is indicative of the dose, and wherein the autoinjector comprises a code reader for determining the code, wherein the autoinjector is further configured to administer at least approximately the complete content of the medicament in one administration, a computing device, in particular a mobile and/or a handheld computing device, wherein the autoinjector is configured to send the code which is indicative of the dose of the medicament to the computing device via a wireless or wired connection, in particular in response to or prior to the administering of the medicament, wherein the computing device is configured to store the code in conjunction with a time stamp that is either determined by the computing device or sent together with the code by the autoinjector, wherein the time stamp is indicative of the time and/or the date of the administering of the medicament and wherein the computing device is configured to store the code in conjunction with the time stamp on a storage device, which is
Absstract of: AU2025254558A1
Systems and methods include a component of a bone implant that includes a patient specific bone contacting surface and, optionally, at least one protrusion adjacent to or extending from the patient specific bone contacting surface. The at least one protrusion is configured for engaging a bone preparation in the bone. To prepare the bone for receiving the component, one or more cutting tool templates may be used. The one or more cutting tool templates may be fabricated to have a patient specific bone contacting surface that engages the bone that is to receive the implant component. A cutting tool is engaged in one or more of one or more slots defined by the cutting tool template(s) to remove surface portions of the bone to create the bone preparation for engaging the protrusion. The patient specific bone contacting surface of the component engages the bone.
Absstract of: US20260331294A1
0000 A method for treating a patient with respiratory illness is described according to one embodiment. The method includes the steps of receiving a set of screening spirometry test data measured by a spirometer, generating a first patient performance score based on the received set of screening spirometry test data, generating one of a first high alert when the first patient performance score crosses a first threshold and a first low alert when the first patient performance score fails to cross the first threshold, receiving a set of at-home physiological test data, generating a second patient performance score based on the received set of at-home physiological test data, generating one of a second high alert when the second patient performance score crosses a second threshold and a second low alert when the second patient performance score fails to cross the second threshold, receiving a set of at-home patient survey data entered by the patient, generating a third patient performance score based on the received set of at-home patient survey data, and generating one of a third high alert when the third patient performance score crosses a third threshold and a third low alert when the third patient performance score fails to cross the third threshold.
Absstract of: AU2025237721A1
A medicinal supply management system manages distribution of medicinal supply. The system may implement a pooling algorithm for pooling studies together, across different countries, with different protocol labeling parameters and/or blinding parameters. The system may allocate unique identifiers for the pooled studies. The system may implement digital display labels on the medicinal product for up-to-date presentation of relevant information to healthcare providers administering the medicinal product. The system may further implement controlled packaging for maintaining proper storage of the medicinal product, e.g., during transport to the treatment site. The controlled packaging may further include sensors for monitoring the internal environment of the controlled packaging, to maintain proper storage of the medicinal product.
Absstract of: US20260331235A1
A patient-specific specimen collection automation system according to an embodiment of the present disclosure includes a management server including specimen information required for respective patients, a tray supply device configured to supply, to a tray, blood collection tubes labeled to correspond to the specimen information, and a tray transport device configured to transport the tray. The tray supply device includes a supply device communication unit configured to communicate with the management server, a blood collection tube supply unit configured to supply the blood collection tubes labeled to correspond to the specimen information, and a tray supply unit configured to classify the labeled blood collection tubes for respective patients into the tray, the tray including identification information. The tray transport device includes a transport device communication unit configured to communicate with the management server, a tray holder configured to receive the tray supplied from the tray supply device, a tray identification unit configured to obtain the identification information of the tray, and an output unit configured to indicate trays matched to respective patients.
Absstract of: WO2026221588A2
The invention relates to an automated processing of 3D dental models to create restoration molds in the field of digital dentistry.
Absstract of: US20260327564A1
A method for generating three-dimensional (3D) cartilage organoids through bioprinting, the method comprising: expanding mesenchymal stem cells (MSCs); preparing a composite bioink; and, bioprinting a cell-laden scaffold to generate the 3D cartilage organoids. Also disclosed is a three-dimensional (3D) cartilage organoid for use in disease modeling and screening, the organoid comprising: human multipotent mesenchymal stem cells (MSCs) and a composite bioink.
Absstract of: WO2026222455A1
A system includes a processor and a storage medium having encoded thereon executable instructions that, when executed by the processor, cause the processor to carry out a method. The method includes receiving surface electrocardiogram (ECG) data of a patient, translating the surface ECG data into 3D spatial coordinates on a right ventricle (RV) anatomical model, and predicting an origin of a ventricular arrhythmia (VA), based on the translated ECG data, on the RV anatomical model.
Absstract of: WO2026221909A1
A method for designing a photon beam bolus for use in photon beam radiation therapy includes receiving three-dimensional imaging data of a patient and delineations of anatomic regions including an external patient contour and an internal target volume. A bolus design algorithm is used to generate a bolus geometry that includes an inner surface conforming to the external patient contour, and an outer surface determined based on the internal target volume and megavoltage photon beam dose deposition characteristics to be applied to the internal target volume. A profile of the photon beam bolus defines a spatially-varying thickness between the inner surface and the outer surface.
Absstract of: US20260326376A1
0000 A hybrid printhead apparatus and method for additive manufacturing that integrates Melt Electrowriting, Fused Deposition Modeling, and Electrospinning into a single device is provided. The disclosed embodiments utilize parallel, independently controlled linear guides to deposit delicate, high precision polymer fibers, and subsequently reinforcing them with thicker macroscale fibers. This hybrid method preserves the structural integrity of the delicate underlying meshes despite varying processing temperatures. Furthermore, the disclosed embodiments enable the incorporation of bioactive compounds, such as those derived from Opuntia ficus-indica. By altering the physical pore size of the underlying framework, the disclosed embodiments provide tunable, sustained release kinetics for advanced tissue engineering and chronic wound care.
Absstract of: US20260330798A1
Systems and methods for real time three-dimensional left atrial appendage (LAA) quantification. Deep learning is used to perform LAA segmentation, tracking and live quantification on critical measurement in 4D ultrasound sequences. The collected information may be used for device selection and anomaly detection to assist early-phase disease finding.
Absstract of: US20260325741A1
A system and method for detecting failure of an infusion pump is disclosed. The system includes a communication module that is separate and independent of a pump operating system of the pump. The communication module periodically monitors the pump operating system to determine the operational status of the pump operating system, and establishes a failure of the pump operating system when signals are no longer detected from the pump operating system within a specific predetermined timeout interval. The communication module then communicates with a remote computing device regarding a failure to determine the operational status of the pump operating system. According to various examples, the timeout interval is determined based on predetermined technical factors associated with the infusion pump and/or clinical factors associated with a patient receiving a therapy from the infusion pump, the therapy, or a care area associated with the patient.
Absstract of: US20260325214A1
A system and method for transseptal puncture site selection are disclosed. The system includes a processor and a memory communicatively connected to the processor, the memory containing instructions configuring the processor to receive a 3D organ model pertaining to an organ of a subject, receive a treatment plan pertaining to the subject, wherein the treatment plan includes at least an area of interest, and a procedure type, generate treatment guidance as a function of the treatment plan, and generate an overlay for the 3D organ model as a function of a puncture site and an optimized access route.
Absstract of: WO2026220200A1
This invention relates to a routine management system. In particular, the present invention relates to a routine management system for supporting daily scheduling and self-regulation in children with ADHD. A routine management system according to the invention is provided which comprises a physical routine planner including generally, a plurality of variable activity elements that represent discrete tasks forming part of a varying routine, a user‑wearable reminder device configured to deliver sensory‑regulating feedback to prompt a user regarding the status of tasks, while also logging compliance data, and a mobile application, in electronic communication with both the physical planner and the user-wearable reminder device, which enables the authoring, synchronization, and dynamic updating of the routine based on pre‑determined cycles to facilitate unified tangible task interaction, multisensory prompting, adaptive feedback, and multi‑party communication into a cohesive framework for enhancing self‑regulation and adherence to a routine by a user.
Absstract of: US20260331285A1
0000 Embodiments described relate to techniques for identifying and characterizing biological structures using machine learning techniques. These techniques may be employed to enable a device to identify the particular type of tissue and/or cells (e.g., platelets, smooth muscle cells, or endothelial cells) in, for example, a biological structure, which may be a tissue or a lesion of a duct (e.g., vasculature) in an animal (e.g., a human or non-human animal), among other structures. The machine learning techniques may use raw impedance spectroscopy measurement data in addition to values derived from that raw data. In addition, the machine learning techniques may be used to select frequencies at which to measure impedance and select features to extract from the measured impedance at the selected frequencies to arrive at a small set of frequencies that allow for reliable differentiation.
Absstract of: WO2026222296A1
A system for assessing breastfeeding performance may include a detection unit that may include at least one motion detection sensor, wherein the motion detection sensor may be configured to acquire motion data from a subject. The system may include a processing unit storing instructions that, when executed by the processing unit, may cause the system to acquire, from the detection unit, the motion data. The instructions may further cause the system to determine a facial deformation metric from the motion data, and to determine, based on the deformation metric and based on one or more control datum, an intraoral pressure metric. The instructions may further cause the system to convert the intraoral pressure metric into a pressure quality result. In the event the pressure quality result corresponds to a deficit associated with a breastfeeding abnormality, the instructions may cause the system to generate a deficit-responsive protocol.
Absstract of: US20260325751A1
0000 A medical timer device has processors and memory including instructions that, when executed by the processors, cause timer logic to set a timer for a delivery of a medication by intravenous infusion, to obtain an infusion variable, to calculate a time period for an operational parameter of the infusion based on the infusion variable and to generate an indicator about the operational parameter. An infusion pump and a method of using a medical timer device are also provided.
Absstract of: WO2026222080A1
Systems, devices, and methods for pain management and wellness are disclosed. Some methods described herein include correlating various user and sensor data to improve treatment outcomes. Devices for user treatment are also disclosed.
Absstract of: WO2026222275A1
The disclosure relates to a melanin-detecting pulse oximetry system and a method of calibrating a pulse oximetry measurement. A pulse oximeter sensor obtains an oxygen saturation measurement from a patient, and a reflectance sensor positioned on a finger of the patient by a finger clamp obtains skin reflectance data at wavelengths of about 415 nm, about 515 nm, and about 630 nm. A processor receives the oxygen saturation measurement and the skin reflectance data and generates a calibrated oxygen saturation value based on the oxygen saturation measurement and the skin reflectance data. The reflectance sensor may comprise a spectrometer, and a computing device may apply a regression model and output the calibrated oxygen saturation value through a graphical user interface.
Absstract of: WO2026220883A1
A medical image processing device according to an embodiment comprises: an observation image generation unit that generates a medical observation image from a medical captured image; a depth estimation processing unit that generates depth information related to a depth in the medical captured image so that the depth resolution of a site of interest in the medical captured image is higher than that of a region other than the site of interest; and a display image generation unit that generates a display image including the medical observation image and the depth information.
Nº publicación: US20260325040A1 22/10/2026
Applicant:
STRYKER CORP [US]
Stryker Corporation
Absstract of: US20260325040A1
0000 An example method includes continuously recording high-fidelity data at a medical device in a circular buffer. The high-fidelity data can include physiological parameter data, user operational data, and medical device data. The method also includes detecting a trigger event. In response to detecting the trigger event, the medical device can store, in a memory associated with the medical device, a portion of the high-fidelity data corresponding to a period of time after the trigger event. The method further includes transmitting the portion of the high-fidelity data to an external device.
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