Resumen de: JP2026115517A
0001 【課題】授乳指導に有効な情報を視覚化する授乳支援システム、授乳指導支援装置、授乳指導支援方法、およびプログラムを提供する。 【解決手段】授乳指導支援装置200は、乳児の舌運動を示す舌運動指標を取得する第1取得部202と、乳児の養育者から取得した情報に基づいた第1授乳指標を取得する第2取得部204と、養育者に対して乳児の養育に関するアドバイスを行う専門家から取得した情報に基づいた第2授乳指標を取得する第3取得部206と、舌運動指標、第1授乳指標、および第2授乳指標を、同時または異なるタイミングで表示させるための表示画面データを生成して出力する出力部208と、を備える。 【選択図】図1
Resumen de: KR20260108675A
본 발명은 운동시 관절의 건의 피로도 정보에 기반하여 운동지속여부를 판단하는 방법 및 시스템으로서, 더욱 상세하게는, 건측정장비 및 제어부를 포함하고, 건측정장비의 초음파트랜스듀서모듈로 착용자의 팔뚝 조직의 구성을 스캔하고, 팔뚝과 팔꿈치 사이에 위치하는 힘줄인 CET의 두께변화를 측정하여 CET의 피로 축적 정도를 확인 후, 그에 따라 운동지속여부를 판단하는 방법 및 시스템에 관한 것이다.
Resumen de: KR102986905B1
0001a 일 실시예에 따른 방법은 사용자의 인지 능력(cognitive capability)을 향상시키기 위한 퀴즈를 디스플레이 또는 지면(ground) 중 적어도 하나에 출력하는 단계, 카메라를 포함하는 적어도 하나의 센서를 통해 획득된 사용자의 위치 정보에 기반하여 퀴즈와 관련된 복수의 선택지에 대한 정보를 포함하는 복수의 아이콘을 디스플레이 또는 지면 중 적어도 하나에 출력하는 단계, 적어도 하나의 센서를 통해 사용자의 발이 복수의 아이콘 중 하나의 아이콘에 접촉되었는지 식별하는 단계 및 사용자의 발이 접촉된 아이콘이 퀴즈의 정답인 경우, 사용자 스코어에 퀴즈에 대응되는 점수를 합산하는 단계를 포함할 수 있다.
Resumen de: US20260192132A1
0000 Systems and methods for generating radiotherapy plans are provided. One or more medical images are received. One or more anatomical objects are segmented from the one or more medical images. Radiotherapy configurations for one or more objectives are determined based on the one or more medical images and the segmentations of the one or more anatomical objectives. A candidate radiotherapy plan is generated based on the radiotherapy configurations. A quality assessment of the candidate radiotherapy plan is performed. The one or more objectives are updated based on results of the quality assessment and the determining, the generating, and the performing are repeated for one or more iterations using the updated one or more objectives as the radiotherapy objectives to generate the candidate radiotherapy plan for a last iteration as a final radiotherapy plan. The final radiotherapy plan is output. Since the pipeline is automatic, the plan generation can be scaled. The data can serve large-scale AI model training.
Resumen de: WO2026145647A1
The present application provides a data scanning method and apparatus, an electronic device, and a storage medium. The method comprises: acquiring first scan data of an oral cavity in a first state, wherein the oral cavity in the first state refers to the oral cavity having at least one abutment implanted therein, and the first scan data comprises initial abutment data and gingival data; acquiring second scan data of the oral cavity in a second state, wherein the oral cavity in the second state refers to the oral cavity having a corresponding scan post mounted on the abutment, and the second scan data comprises scan post data; determining a first transformation relationship between the scan post data in the second scan data and target abutment data; and processing the first scan data and the second scan data on the basis of the initial abutment data, the target abutment data, and the first transformation relationship between the scan post data and the target abutment data, to obtain a target three-dimensional model. The present application can be utilized to solve the problems of a complicated scanning process for implants, high scanning costs, and being prone to causing physical discomfort to users.
Resumen de: DE112023006984T5
Computerimplementiertes Verfahren zur Bereitstellung von Anzeigedaten für ein halbtransparentes Durchsichtanzeigegerät in einer medizinischen Umgebung, wobei das Verfahren die Schritte umfasst: Bereitstellen eines 2D- und/oder 3D-Modells eines ersten Objekts (Schritt S1); Empfangen von ersten Positionsdaten des ersten Objekts (Schritt S2); Empfangen von zweiten Positionsdaten eines zweiten Objekts (Schritt S3); Erfassen eines Freiraums basierend auf den zweiten Positionsdaten (Schritt S4); Bestimmen von Anzeigedaten zur Anzeige auf einem halbtransparenten Durchsichtanzeigegerät basierend auf dem 2D- und/oder 3D-Modell, dem erfassten Freiraum, den ersten Positionsdaten und den zweiten Positionsdaten (Schritt S5); und Bereitstellen der bestimmten Anzeigedaten zur Anzeige auf dem halbtransparenten Durchsichtanzeigegerät (Schritt S6).
Resumen de: DE112024003806T5
Es werden Systeme, Vorrichtungen und Verfahren zur Erstellung und Verwendung eines personalisierten, segment-spezifischen Endoskop-Rückzugsplans zur Steuerung eines endoskopischen Eingriffs offenbart. Ein Endoskopiesystem umfasst ein Endoskop und eine Steuerschaltung. Das Endoskop umfasst ein Bildgebungssystem zur Erfassung von Bildern oder Videodatenströmen einzelner anatomischer Segmente eines Patienten während eines endoskopischen Eingriffs. Die Steuerschaltung kann die Bilder oder Videodatenströme analysieren, um Bild- oder Videomerkmale für einzelne der unterschiedlichen Segmente der Anatomie zu generieren. Basierend auf den Bild- oder Videomerkmalen kann die Steuerschaltung einen Endoskop-Rückzugsplan generieren, der Ziel- oder empfohlene segment-spezifische Endoskop-Rückzugs-Parameterwerte für jedes der Segmente enthält. Der Endoskop-Rückzugsplan kann dem Benutzer oder einem Robotersystem bereitgestellt werden, um den manuellen oder robotergestützten Rückzug des Endoskops zu erleichtern.
Resumen de: WO2026147842A1
This disclosure relates to planning systems and methods associated with erosion along an articular surface of a joint. The planning systems and methods disclosed herein may be utilized for planning orthopaedic procedures to restore functionality to a joint, may include determining an amount of erosion along or otherwise adjacent to an articular surface of a bone. One or more spherical objects may be utilized to determine the erosion.
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: 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: WO2026147905A1
For each of a plurality of time intervals: a power spectrum is generated using a corresponding portion of EEG data; a normalized power spectrum is generated; and a preferred frequency (a frequency with a largest z-score or a highest normalized power in the normalized power spectrum corresponding to the time interval) or dominant frequency for the time interval is determined. A set of time windows is defined, each including multiple time intervals of the plurality of time intervals. For each of a set of time windows, a number of the time intervals is determined for which the preferred or dominant frequency is within a Beta band (12-30 Hz frequencies) or a portion thereof. For a time window, it is determined that an alert condition is satisfied using the number of the plurality of time intervals where the preferred or dominant frequency is within the Beta band or a portion thereof.
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: 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: US20260188512A1
An interface receives physiological information of a patient. A processor acquires contribution information corresponding to contributions of N first parameters (N is an integer of at least 2) with respect to a status of the patient based on the physiological information. The processor causes a visualizing device to visualize the contribution information under a condition that M first parameters (M is an integer of at least 2 and at most N) included in the N first parameters are substituted by L second parameter (L is an integer less than M).
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: US20260191896A1
Some embodiments provide for a method for identifying an intervention for a subject in furtherance of preventing development of cardiovascular disease in the subject, the method comprising: obtaining cardiometabolic health data for the subject; determining, using at least some of the cardiometabolic health data, a first trained machine learning (ML) model and for each of multiple time intervals, one or more measures of risk that the subject develops cardiovascular disease to obtain multiple measures of risk; determining, using the multiple measures of risk that the subject develops cardiovascular disease and at least one second trained ML model, benefit of administering to the subject one or more therapeutic interventions designed to reduce risk of cardiovascular disease by targeting one or more modifiable causes of the cardiovascular disease; and identifying, using the determined benefit of administering the therapeutic intervention(s), at least one therapeutic intervention to recommend being administered to the subject.
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.
Resumen de: US20260196350A1
The disclosed systems and methods provide systems and methods for rhythm recognition and the analysis of ECG signals.
Resumen de: WO2026146019A1
The invention relates to 3D-printed controlled-release solid oral pharmaceutical compositions comprising a hydrophobic matrix comprising cavities filled with air, allowing flotation in the stomach, one or more regions within the matrix comprising a pharmaceutical, one or more regions within the matrix comprising a swellable material, wherein optionally the one or more regions within the matrix comprise a swellable material and a pharmaceutical one or more fracture zones within the matrix with weaker or less dense structure, one or more hydrophilic channels within the matrix fluidly connecting the outside of the composition with a region within the matrix comprising the swellable material or the pharmaceutical.
Resumen de: WO2026147958A1
This document relates to devices, systems, and methods for fabricating a three-dimensional sample of human tissue. For example, this document relates to techniques for depositing cells according to a predefined pattern and treating the deposited cells to simulate a realistic human tissue sample.
Resumen de: WO2026147879A1
The present disclosure provides novel oligomers and polymerizable compositions comprising the same. Further provided herein are methods of producing polymers, polymer coatings, and devices. Also provided herein are methods of using polymer materials and polymer materials fabricated via additive manufacturing processes (e.g., via 3D printing), such as orthodontic appliances.
Resumen de: WO2026145785A1
A delayed-release oral drug dosage form, and a preparation method related to the oral drug dosage form, such as a three-dimensional printing method.
Resumen de: US20260191430A1
In certain implementations a computer-implemented method, computer program product and systems for performing gait analysis using lidar based three dimensional measurements is provided. Embodiments of the present invention can identify at least one object from received video information. Embodiments of the present invention can then estimate points on the object to depict two dimensional and three dimensional poses of the object based on a threshold number of frames depicting the object. Based on the estimated three dimensional poses, embodiments of the present invention can then generate measurements for biomechanical parameters that characterize movement of the object based on the estimated points on the object.
Nº publicación: WO2026146863A1 09/07/2026
Solicitante:
E SOM CO LTD [KR]
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Resumen de: WO2026146863A1
A color recommendation method utilizing artificial intelligence-based pupil response data, according to various embodiments of the present invention, is disclosed. The method comprises the steps of: acquiring pupil response data of a subject; generating response analysis information corresponding to the acquired pupil response data by utilizing a colorimetric analysis model; and generating color recommendation information on the basis of the response analysis information, wherein the colorimetric analysis model is a deep learning model pre-trained to analyze the response for each color on the basis of the pupil response data of the subject, and the pupil response data can be time-series data generated by continuously measuring, along a time axis, changes in each of pupil size, pupil movement distance and pupil response speed of the subject when a plurality of color wavelengths are sequentially provided to the subject.