A physiological information display apparatus includes a heart rate acquisition unit configured to acquire a heart rate of a subject, a respiration rate acquisition unit configured to acquire a respiration rate of the subject, a hemodynamics calculation unit configured to calculate a hemodynamic parameter of the subject, and a respiratory variation of the hemodynamic parameter, based on a plurality of the hemodynamic parameters calculated in a predetermined period, and a display controller configured to output the respiratory variation to a display. The hemodynamics calculation unit is configured to calculate a heart rate in one respiration. The display controller is configured to output a setting screen for setting a length of the predetermined period. The hemodynamics calculation unit is configured to acquire setting information, set the length of the predetermined period based on the acquired setting information; and calculate the respiratory variation in the set predetermined period.
A61B 5/0205 - Évaluation simultanée de l'état cardio-vasculaire et de l'état d'autres parties du corps, p. ex. de l'état cardiaque et respiratoire
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/022 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins par application d'une pression pour fermer les vaisseaux sanguins, p. ex. contre la peauOphtalmodynamomètres
A61B 5/024 - Mesure du pouls ou des pulsations cardiaques
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
2.
IMAGE GENERATION DEVICE, IMAGE GENERATION SYSTEM, IMAGE GENERATION METHOD AND RECORDING MEDIUM
An image generation device according to the presently disclosed subject matter inputs parameter values for a patient monitor from a plurality of medical devices that output the parameter values, and generates a display image of management target-categorized display in which a plurality of the parameter values are collectively arranged by management target functions.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p. ex. ventilateursTubes trachéaux
G06T 11/20 - Traçage à partir d'éléments de base, p. ex. de lignes ou de cercles
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
3.
PHYSIOLOGICAL INFORMATION PROCESSING SYSTEM, PROCESSING DEVICE, AND NON-TRANSITORY COMPUTER-READABLE MEDIUM
A light emitting device emits: first light including a first wavelength at which an absorbance of oxygenated hemoglobin is larger than an absorbance of deoxygenated hemoglobin; and second light including a second wavelength at which the absorbance of deoxygenated hemoglobin is larger than the absorbance of oxygenated hemoglobin. A light detecting device outputs first and second signals respectively corresponding to intensities of the first and second light that have passed through a living tissue. A processing device acquires: a first difference value between light attenuations of the first and second light based on the signals while compression of the living tissue is performed; and a second difference value between the light attenuations based on the signals after the compression is cancelled. A processing device acquires an index corresponding to an oxygen saturation of blood contained in the living tissue based on a difference between the first and second difference values.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/1455 - Mesure des caractéristiques du sang in vivo, p. ex. de la concentration des gaz dans le sang ou de la valeur du pH du sang en utilisant des capteurs optiques, p. ex. des oxymètres à photométrie spectrale
A stimulation electrode unit includes a plurality of electrodes adapted to be attached to a living body. A stimulation control device is configured to form an electric circuitry with the stimulation electrode unit, and to control a stimulation current that is caused to flow into the living body through the electrodes. An information element retains identifier information identifying the stimulation electrode element. The stimulation control device is configured to read out the identifier information through the electric circuitry, and to determine, based on the identifier information, whether the electrical circuit is formed by an adequate stimulation electrode unit
An adapter is configured to be coupled with a mask that is adapted to be attached on a face of a subject to supply air or oxygen gas to an airway of the subject. A base defines a ventilation path adapted to be communicated with an exhaust hole formed in the mask. A retainer is configured to removably retain a sensor including a light detecting element configured to output a signal corresponding to concentration of carbon dioxide as detected optically. The ventilation path is located on a path of light that is to be incident on the light detecting element.
A medical device is configured to issue an alert. An annotation assigning device is configured to provide an input user interface arranged to input managing information indicating whether the alert is an actionable alarm or a non-actionable alarm. The annotation assigning device is configured to assign an annotation corresponding to the managing information to the alert.
G16H 40/20 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour la gestion ou l’administration de ressources ou d’établissements de soins de santé, p. ex. pour la gestion du personnel hospitalier ou de salles d’opération
G16H 40/40 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour la gestion d’équipement ou de dispositifs médicaux, p. ex. pour planifier la maintenance ou les mises à jour
7.
INFORMATION PROCESSING DEVICE, INFORMATION PROCESSING METHOD, AND NON-TRANSITORY COMPUTER-READABLE MEDIUM
An information processing device includes at least one processor, and one or more memories configured to store at least one instruction to be executed by the at least one processor. When the at least one instruction is executed by the processor, the information processing device is configured to generate, based on physiological information on a subject, a plurality of pieces of change tendency information indicating a change tendency of the physiological information during one period or a change tendency of the physiological information from one period to an other period, and generate display data in which the plurality of pieces of change tendency information are displayed side by side or the plurality of pieces of change tendency information are displayed so as to be overlapped with each other.
G06T 11/20 - Traçage à partir d'éléments de base, p. ex. de lignes ou de cercles
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
8.
PATIENT MONITOR, PHYSIOLOGICAL INFORMATION MEASUREMENT SYSTEM, PROGRAM TO BE USED IN PATIENT MONITOR, AND NON-TRANSITORY COMPUTER READABLE MEDIUM IN WHICH PROGRAM TO BE USED IN PATIENT MONITOR IS STORED
A patient monitor (10) acquires a vital sign that is based on a physiological signal of a subject, and an ultrasonic image that is based on a reflected wave of an ultrasonic wave which is irradiated onto the subject. A display section (16) displays information of the subject. A control section (14) switches between a first mode in which a screen containing information of the vital sign is displayed on the display section (16), and a second mode in which a screen containing the ultrasonic image is displayed on the display section (16).
G06F 3/0484 - Techniques d’interaction fondées sur les interfaces utilisateur graphiques [GUI] pour la commande de fonctions ou d’opérations spécifiques, p. ex. sélection ou transformation d’un objet, d’une image ou d’un élément de texte affiché, détermination d’une valeur de paramètre ou sélection d’une plage de valeurs
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
At least one light emitter is configured to emit light. At least one light detector is configured to output a signal corresponding to an amount of incident light. A supporting member has an adhesive face adapted to be attached to a body of a subject. A sheet is peelably attached to the adhesive face. The supporting member includes a first supporting portion, a second supporting portion and a third supporting portion. The first supporting portion supports and covers the light emitter. The second supporting portion supports and covers the light detector. The third supporting portion is located between the first supporting portion and the second supporting portion. The sheet is formed with a foldable portion extending across a portion facing the third supporting portion and including a portion whose cross-sectional shape is changed so as to increase foldability of the sheet.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/145 - Mesure des caractéristiques du sang in vivo, p. ex. de la concentration des gaz dans le sang ou de la valeur du pH du sang
A61B 90/00 - Instruments, outillage ou accessoires spécialement adaptés à la chirurgie ou au diagnostic non couverts par l'un des groupes , p. ex. pour le traitement de la luxation ou pour la protection de bords de blessures
At least one light emitter is configured to emit light. At least one light detector is configured to output a signal corresponding to an amount of incident light. A supporting member is adapted to be attached to a body of a subject. The supporting member includes a first supporting portion, a second supporting portion and a third supporting portion. The first supporting portion supports and covers the light emitter. The second supporting portion supports and covers the light detector. The third supporting portion is located between the first supporting portion and the second supporting portion. At least one of the first supporting portion, the second supporting portion and the third supporting portion includes a portion with higher flexibility than an adjacent portion thereof.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/1455 - Mesure des caractéristiques du sang in vivo, p. ex. de la concentration des gaz dans le sang ou de la valeur du pH du sang en utilisant des capteurs optiques, p. ex. des oxymètres à photométrie spectrale
11.
PHYSIOLOGICAL INFORMATION PROCESSING APPARATUS, PHYSIOLOGICAL INFORMATION PROCESSING METHOD, AND NON-TRANSITORY COMPUTER READABLE STORAGE MEDIUM
A physiological information processing apparatus for evaluating a degree of pain of a patient. The physiological information processing apparatus includes a measurement unit configured to measure physiological information on the patient, a memory configured to store reference physiological information, a processor configured to compare the physiological information with the reference physiological information, and calculate a pain score of the patient, based on a comparison result between the physiological information and the reference physiological information. The processor is further configured to calculate, for each of the physiological information and the reference physiological information, at least one common physiological parameter among a heart rate, a QT interval, a pulse wave propagation time, a perfusion index, and an RR interval, and compare the physiological parameter of the physiological information with the physiological parameter of the reference physiological information.
A physiological information acquisition device includes: a reception interface configured to receive waveform data corresponding to a measured waveform of a physiological parameter of a subject from a sensor; a notifier configured to output an alarm indicating that the physiological parameter is not normally acquired; a processor configured to cause the notifier to output the alarm based on the waveform data; and a predictor configured to predict, based on the waveform data, a probability that the physiological parameter is erroneously calculated. The processor is configured to cause the notifier to perform a notification of at least one of a quality of the waveform data, a state of the sensor, and an action shall be taken by a user, based on the probability.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/0245 - Mesure du pouls ou des pulsations cardiaques utilisant des capteurs engendrant des signaux électriques
A61B 5/33 - Modalités électriques se rapportant au cœur, p. ex. électrocardiographie [ECG] spécialement adaptées à l’utilisation conjointe avec d’autres dispositifs
A61B 5/36 - Détection de l’intervalle PQ, de l’intervalle PR ou de l’intervalle QT
A61B 5/364 - Détection d'intervalle ECG anormal, p. ex. des extrasystoles ou des battements cardiaques ectopiques
13.
PHYSIOLOGICAL SIGNAL MEASUREMENT DEVICE, PHYSIOLOGICAL SIGNAL MEASUREMENT SYSTEM, AND NON-TRANSITORY COMPUTER READABLE STORAGE MEDIUM
A physiological signal measurement device includes: an information processor of one or more processors configured to calculate, based on change in a detected light intensity that is detected by a light detector configured to detect light emitted from a light emitter and transmitted through a physiological tissue, a capillary refilling time after a compression period in which the physiological tissue is compressed. The information processor uses the detected light intensity to determine whether the change in the detected light intensity is appropriate for calculating the capillary refilling time.
A defibrillator includes a controller configured to detect a use state of a defibrillator by an operator, and output guidance of a use method of the defibrillator, according to the detected use state. The controller is configured to detect a change in the use state in a period before a timing at which a pair of pads of the defibrillator are attached to a skin of a subject from a timing at which the defibrillator is started up.
A physiological information measurement system includes: an obtaining unit configured to obtain, from a plurality of sensors that are connected to an air bag containing air and measure pressures received by the air bag from a subject, signals related to the measured pressures; and a determination unit configured to determine at least one of deterioration and failure of at least one of the sensors based on the signals related to the pressures obtained from the plurality of sensors.
An automated external defibrillator configured to deliver an electric shock for defibrillation to a heart of a subject. The automated external defibrillator includes: a sound generator configured to output: a timing sound expressing, by sound, a timing until the electric shock is delivered; and a warning sound expressing a state in which an internal capacitor of the automated external defibrillator has been charged with high voltage; and a sound controller configured to control the sound generator. The sound controller changes the warning sound in accordance with presence or absence of output of the timing sound.
An assist tool to be attached to a finger of a subject. The assist tool includes a support body configured to be placed on a first side of the finger in a case where the support body is attached to the finger, a bag body configured to be placed on a second side of the finger, the second side being opposite to the first side with respect to the finger, a fluid passage communicating with inside of the bag body, and a size adjustment plate configured to be placed on one side, to which the finger is to be attached, in the support body. In a case where the size adjustment plate is accommodated in the support body, a finger accommodating space on a finger side of the bag body is thinned.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/024 - Mesure du pouls ou des pulsations cardiaques
A61B 5/1455 - Mesure des caractéristiques du sang in vivo, p. ex. de la concentration des gaz dans le sang ou de la valeur du pH du sang en utilisant des capteurs optiques, p. ex. des oxymètres à photométrie spectrale
An assist tool to be attached to a finger of a subject. The assist tool includes a support body placed on a first side of the finger in a case where the support body is attached to the finger, a bag body configured to be placed on a second side, the second side being opposite to the first side of the finger with respect to the finger, and a fluid passage communicating with inside of the bag body. A physiological information detector for obtaining the physiological information is configured to be placed between the finger and the support body, and between the finger and the bag body. A spacer is provided in the support body such that the finger does not enter a fingertip side of the bag body.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/024 - Mesure du pouls ou des pulsations cardiaques
A61B 5/1455 - Mesure des caractéristiques du sang in vivo, p. ex. de la concentration des gaz dans le sang ou de la valeur du pH du sang en utilisant des capteurs optiques, p. ex. des oxymètres à photométrie spectrale
19.
PHYSIOLOGICAL INFORMATION PROCESSING SYSTEM AND RELAY DEVICE
A physiological information processing system includes a first information processing device configured to process physiological information, a second information processing device, and a relay device configured to control network communication between the first information processing device and the second information processing device. The relay device includes a controller configured to set network information of the first information processing device as network information of the relay device.
A physiological information processing system includes a first information processing device configured to process physiological information, a second information processing device, and a relay device configured to control network communication between the first information processing device and the second information processing device. The relay device includes a controller configured to control the network communication between the first information processing device and the second information processing device, based on at least one of first device information included in a packet transmitted from the first information processing device or second device information set through a device information setting unit.
H04L 67/12 - Protocoles spécialement adaptés aux environnements propriétaires ou de mise en réseau pour un usage spécial, p. ex. les réseaux médicaux, les réseaux de capteurs, les réseaux dans les véhicules ou les réseaux de mesure à distance
H04L 47/12 - Prévention de la congestionRécupération de la congestion
21.
PREDICTION DEVICE, METHOD OF GENERATING PREDICTION MODEL, AND COMPUTING DEVICE
An interface receives time series data including multiple observed values of an observed parameter that are acquired at different time points for obtaining physiological information of a subject. A processor inputs the time series data into a prediction model to perform prediction of one or more unobserved values of the observed parameter. The processor causes an output device to visualize a range within which the one or more unobserved values may fall. The range is changed in accordance with a time interval between the different time points.
An interface receives time series data including multiple observed values of an observed parameter that are acquired at different time points for obtaining physiological information of a subject. A processor inputs the time series data into a prediction model to output, as a prediction result, a range within which values interpolating the multiple observed values may fall. The processor generates at least one first interpolated value by interpolating the multiple observed values with a first method. The processor generates at least one second interpolated value by interpolating the multiple observed values with a second method that is different from the first method. The processor identifies, as the prediction result, a range defined between a maximum value and a minimum value among the first interpolated value and the second interpolated value.
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
G06F 17/17 - Évaluation de fonctions par des procédés d'approximation, p. ex. par interpolation ou extrapolation, par lissage ou par le procédé des moindres carrés
23.
METHOD OF GENERATING TRAINING DATA, METHOD OF GENERATING PREDICTION MODEL, COMPUTING DEVICE, AND NON-TRANSITORY COMPUTER-READABLE MEDIUM
Training data is used in machine learning of a prediction model adapted to predict physiological information. An original data set includes a first observed value of an observed parameter for obtaining the physiological information acquired from a living body at a first time point, and a second observed value of the observed parameter acquired from the living body at a second time point different from the first time point. A first interpolation data set is generated by interpolating, with a first method, at least one value of the observed parameter in a time period between the first time point and the second time point. A second interpolation data set is generated by interpolating, with a second method different from the first method, at least one value of the observed parameter in the time period. The training data is generated so as to include the first and second interpolation data sets.
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
A medical assistance device includes at least one processor and at least one memory that stores at least one instruction executable by the processor, When the at least one instruction is executed by the processor, the medical assistance device is configured to: obtain past surgery information; generate anticipated surgery schedule information and anticipated auxiliary information; and generate display data. The past surgery information includes past required total time information on a previously performed surgery and past auxiliary information. The past auxiliary information includes at least one of medication information, and transition information. The anticipated auxiliary information includes at least one of anticipated medication information and anticipated transition information, based on the past surgery information. The display data includes the anticipated surgery schedule information and the anticipated auxiliary information.
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p. ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p. ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
G16H 20/10 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p. ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des médicaments ou des médications, p. ex. pour s’assurer de l’administration correcte aux patients
G16H 70/40 - TIC spécialement adaptées au maniement ou au traitement de références médicales concernant des médicaments, p. ex. leurs effets secondaires ou leur usage prévu
A medical support device includes at least one processor, and a memory configured to store at least one instruction executable by the processor. When the at least one instruction is executed by the processor, the medical support device generates display data including expected procedure schedule information indicating an expected procedure schedule set for each of a plurality of procedures included in a surgery and progress information indicating progress of each of a plurality of procedures included in a current surgery.
G16H 40/20 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour la gestion ou l’administration de ressources ou d’établissements de soins de santé, p. ex. pour la gestion du personnel hospitalier ou de salles d’opération
G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p. ex. pour des dossiers électroniques de patients
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p. ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p. ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
26.
BLOOD VOLUME MEASUREMENT METHOD, BLOOD VOLUME MEASUREMENT DEVICE, AND PROGRAM
A blood volume measurement method for calculating a cardiac output includes a first measurement step of measuring a first value in a predetermined section of a first physiological information parameter, a second measurement step of measuring a second value in a section longer than the predetermined section of a second physiological information parameter, and the pulse pressure of the subject, a baseline determination step of determining whether or not a difference between the measured first value and the measured second value is equal to or less than a threshold value, a calibration step of, when it is determined in the baseline determination step that the difference between the first value and the second value is equal to or less than the threshold value, calculating a subject-specific coefficient of the subject based on the second value, and a calculation step of calculating the cardiac output based on the first value and the subject-specific coefficient calculated in the calibration step.
A blood volume measurement method for calculating a cardiac output, includes an instantaneous value measurement step of measuring an instantaneous value of a first physiological information parameter, a division moving average value measurement step of measuring a plurality of times a division moving average value in a first predetermined section of a second physiological information parameter, a comprehensive moving average value calculation step of calculating a comprehensive moving average value which is an average value of a plurality of the division moving average values when a number of times the division moving average values are measured in a second predetermined section is a threshold value or more, in the division moving average value measurement step, a calibration step of calculating a subject-specific coefficient of the subject based on the comprehensive moving average value calculated in the comprehensive moving average value calculation step, and a calculation step of calculating the cardiac output based on the instantaneous value and the subject-specific coefficient calculated in the calibration step.
A defibrillator configured to execute a defibrillation process of delivering an electric shock for defibrillation to a heart of a subject. The defibrillator includes: a processor, and a memory that stores a computer-readable instruction that when executed by the processor, causes the defibrillator to perform operations including: receiving a raw data related to at least one of a plurality of components configuring the defibrillator and an accessory of the defibrillator; and transmitting the received raw data and an identification information of the defibrillator to a management server. The raw data is used to determine presence or absence of an abnormality in at least one of the plurality of components and the accessory.
The physiological information measurement system includes: a detector configured to detect a candidate QRS complex from an electrocardiogram of a subject; and an estimator configured to estimate whether the candidate QRS complex is a QRS complex based on the candidate QRS complex and information on a cardiac function of the subject.
An automated external defibrillator is configured to automatically execute a defibrillation process of delivering an electric shock for defibrillation to a heart of a subject. The defibrillator includes: a processor; and a memory that stores a computer-readable instruction that when executed by the processor, causes the defibrillator to perform operations including: receiving a physiological signal of the subject through an electrode pad; determining whether the defibrillation process is necessary based on the physiological signal; and determining whether the electrode pad is attached to the subject and a predetermined operation has been performed on the defibrillator. When the defibrillation process is necessary, the defibrillator cancels the defibrillation process while maintaining an on-state of a power supply thereof, in response to a result of the determination as to whether the electrode pad is attached to the subject and the predetermined operation has been performed on the defibrillator.
[ABSTRACT]
[ABSTRACT]
An automated external defibrillator (1) includes: a display (100) that presents at least one of time information regarding a time length until an electric shock is delivered, an illustration regarding reception of the electric shock, and a warning text regarding the reception of the electric shock, and a display controller (103A) that controls the display (100), wherein the display controller (103A) changes a color presented on the display (100) in accordance with the time length until the electric shock is delivered.
A bone conduction hearing-aid system includes an intracorporeal unit that is embedded under a scalp and that includes an intracorporeal vibration generator configured to generate vibration by receiving a magnetic field frequency, and an extracorporeal unit that is disposed extracorporeally, that is configured to generate the magnetic field frequency and to apply the magnetic field frequency to the intracorporeal unit, and that is configured to generate vibration by an extracorporeal vibration generator. The vibration generated by the intracorporeal unit and the vibration generated by the extracorporeal unit vibrate a skull.
A bone conduction hearing-aid unit embedded under a scalp. The bone conduction hearing-aid unit includes a vibration generator configured to generate vibration, and an anchor. A magnetic field frequency is applied to the vibration generator from the outside of the scalp to generate vibration. The vibration is transmitted to a skull via the anchor.
An input interface receives at least one of first data corresponding to actual measured values of arterial oxygen partial pressure and arterial oxygen saturation of a subject, and second data corresponding to a value of at least one of arterial carbon dioxide partial pressure, pH of arterial blood, body temperature, and concentration of 2, 3-Diphosphoglycerate in blood of the subject. A processor determines a rule for converting the arterial oxygen saturation of the subject into an estimated value of the arterial oxygen partial pressure of the subject based on at least one of the first data and the second data. In response to reception of third data corresponding to transcutaneous arterial oxygen saturation of the subject at the input interface, the processor calculates the estimated value based on the third data and the rule.
A bone conduction hearing-aid unit that is entirely embedded under a scalp. The bone conduction hearing-aid unit includes a vibration generating device configured to generate vibration, and an anchor fixed to a skull and configured to transmit the vibration to the skull. The vibration generating device is detachably fixed to the anchor.
A temperature measuring device (10) is adapted to be disposed on a referential surface (S) covering a heat source (H). A first temperature sensor (11) is configured to detect first temperature at a first position (P1) that is a first distance from the referential surface (S) in a first direction (D1). A second temperature sensor (12) is configured to detect second temperature at a second position (P2) that is a second distance longer than the first distance from the referential surface (S) in the first direction (D1). A temperature specifier is configured to specify temperature of the heat source (H) based on the first temperature and the second temperature. Each of the first temperature sensor (11) and the second temperature sensor (12) includes multiple temperature detecting elements that are arrayed in a second direction (D2) intersecting with the first direction (D1) and are thermally coupled to each other.
G01K 7/42 - Circuits pour la compensation de l’inertie thermiqueCircuits pour prévoir la valeur stationnaire de la température
G01K 3/06 - Thermomètres donnant une indication autre que la valeur instantanée de la température fournissant des valeurs moyennesThermomètres donnant une indication autre que la valeur instantanée de la température fournissant des valeurs intégrées par rapport à l'espace
G01K 13/20 - Thermomètres médicaux par contact pour les humains ou les animaux
A61B 5/01 - Mesure de la température de parties du corps
37.
INFORMATION PROCESSING DEVICE, INFORMATION PROCESSING METHOD, AND NON-TRANSITORY COMPUTER READABLE STORAGE MEDIUM
An information processing device includes an input interface to which physiological information on a subject is input, at least one processor, and a memory configured to store at least one command. In a case where the at least one command is executed by the processor, the information processing device is configured to classifies the physiological information input to the input interface into a first physiological information group and a second physiological information group, and generates display data including the first physiological information group, the second physiological information group, a first line that is a timeline, and a second line that indicates a value related to the physiological information, and the display data is generated in a form in which the first physiological information group and the second physiological information group are displayed in a state where the first lines overlap each other and the second line is common.
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
G06F 3/14 - Sortie numérique vers un dispositif de visualisation
38.
PHYSIOLOGICAL INFORMATION MEASUREMENT DEVICE, PHYSIOLOGICAL INFORMATION MEASUREMENT METHOD, AND NON-TRANSITORY COMPUTER READABLE STORAGE MEDIUM
A physiological information measurement device includes a sensor connected to an airbag containing air, the sensor being configured to measure pressure received by the airbag from a subject, and a processor configured to process a measurement result of the sensor to obtain information on a dynamic pressure and a static pressure of the subject, and a detector configured to detect an abnormality in a path from the airbag to the sensor, based on a change in the dynamic pressure and/or the static pressure.
G01M 3/26 - Examen de l'étanchéité des structures ou ouvrages vis-à-vis d'un fluide par utilisation d'un fluide ou en faisant le vide par mesure du taux de perte ou de gain d'un fluide, p. ex. avec des dispositifs réagissant à la pression, avec des indicateurs de débit
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
39.
INFORMATION PROCESSING APPARATUS AND ULTRASOUND SYSTEM
An information processing apparatus configured to process information acquired from a probe including a base having flexibility to bend along a surface of subject's body and a plurality of ultrasound transducers arranged on the base at predetermined intervals. The information processing apparatus includes a controller configured to acquire transmission information, which relates to ultrasound emitted from the ultrasound transducers of the probe whose base is attached to the subject along the surface of the subject's body, and first reception information, which relates to first reflection received by first ultrasound transducers of the ultrasound transducers after the ultrasound is reflected by a first target, and calculate parameters, which relate to a curve of the base, from the transmission information, the first reception information, and the predetermined intervals between the first ultrasound transducers.
A muscle relaxation monitoring device includes a stimulation output unit configured to stimulate a nerve via a stimulation electrode attached to a living body of a subject, a signal detection unit configured to detect, as an electrical signal, a physiological signal generated from a muscle in response to the stimulation to the nerve by the stimulation output unit, via a lead-out electrode attached to the living body, and a controller configured to cause the stimulation output unit to stimulate the nerve, and determine an abnormal installation cause of the lead-out electrode, based on the electrical signal detected by the signal detection unit.
A physiological information processing method for automatically acquiring information relevant to a fluid flowing through a body of a subject using an ultrasonic sensor. The ultrasonic sensor includes a plurality of ultrasonic elements. The physiological information processing method includes acquiring reflection signals of ultrasonic waves, identifying, among the ultrasonic elements, two or more ultrasonic elements facing a vessel through which the fluid flows, analyzing a reflection signal of an ultrasonic wave associated with a first ultrasonic element of the two or more ultrasonic elements, analyzing a reflection signal of an ultrasonic wave associated with a second ultrasonic element of the two or more ultrasonic elements, identifying an angle of the vessel with respect to the irradiation direction of the ultrasonic wave, analyzing the reflection signal of the ultrasonic wave associated with the first ultrasonic element or the second ultrasonic element, and acquiring information relevant to the fluid.
An alarm control system includes an obtaining unit configured to obtain a message signal related to measurement of physiological information and an output value of the physiological information, a first alarm signal generator configured to generate a first alarm signal based on the message signal related to the measurement, a second alarm signal generator configured to generate a second alarm signal based on at least one of the message signal related to the measurement or a period in which a measurement value is invalid, the period being calculated based on the output value of the physiological information, and an output controller configured to perform control to output the first alarm signal and the second alarm signal.
A physiological information analysis device includes an obtaining unit, a determination unit, and a notification controller. The obtaining unit obtains a plurality of pieces of physiological information related to a subject. The determination unit determines effectiveness of the plurality of pieces of physiological information. The notification controller issues, when effectiveness of corresponding first physiological information and second physiological information among the plurality of pieces of physiological information matches, predetermined notification according to the effectiveness, and issues the predetermined notification according to the effectiveness of any physiological information of the first physiological information and the second physiological information when the effectiveness of the first physiological information and the effectiveness of the second physiological information do not match.
A physiological information measurement device includes: a pressure controller executes a measurement of increasing or decreasing an applied pressure of a cuff with respect to a predetermined site of a subject from an initial value; a pulse detector detects a pulse from a pressure received by the cuff from the predetermined site; a pulse determination unit determines whether the pulse detected by the pulse detector is a correctly detected pulse; a blood pressure calculation possibility determination unit determines whether calculation of a blood pressure of the subject is possible based on the pulse detected by the pulse detector; and a blood pressure calculator calculates the blood pressure of the subject based on a plurality of the pulses determined to be correctly detected by the pulse determination unit.
A61B 5/022 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins par application d'une pression pour fermer les vaisseaux sanguins, p. ex. contre la peauOphtalmodynamomètres
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/021 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins
A61B 5/0225 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins par application d'une pression pour fermer les vaisseaux sanguins, p. ex. contre la peauOphtalmodynamomètres la pression étant commandée par des signaux électriques, p. ex. dérivés des bruits de Korotkoff
46.
PHYSIOLOGICAL INFORMATION MEASUREMENT DEVICE, PHYSIOLOGICAL INFORMATION MEASUREMENT METHOD, AND NON-TRANSITORY COMPUTER-READABLE STORAGE MEDIUM
A physiological information measurement device includes a pressure controller configured to control an applied pressure of a cuff to a predetermined site of a subject, a pulse detector configured to detect pulses from a pressure received by the cuff from the predetermined site, a physiological information detector configured to detect physiological information on the subject, a noise classification unit configured to classify whether detection data detected by the pulse detector is noise based on the physiological information, and a blood pressure calculator configured to calculate a blood pressure of the subject based on a plurality of the pulses that are classified as not noise by the noise classification unit.
A61B 5/0225 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins par application d'une pression pour fermer les vaisseaux sanguins, p. ex. contre la peauOphtalmodynamomètres la pression étant commandée par des signaux électriques, p. ex. dérivés des bruits de Korotkoff
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/021 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins
A61B 5/022 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins par application d'une pression pour fermer les vaisseaux sanguins, p. ex. contre la peauOphtalmodynamomètres
A61B 5/352 - Détection des crêtes de l'onde R, p. ex. pour la synchronisation d'appareils de diagnosticEstimation de l’intervalle entre crêtes R
A sensor system includes a bedding sensor including a detector that detects vital signs information of a subject on bedding and an accommodation portion that accommodates the detector, and an information processing device configured to process the detected vital signs information and capable of being in an attached state in which the information processing device is attached to the bedding sensor and a separated state in which the information processing device is separated from the bedding sensor.
ST. MARIANNA UNIVERSITY SCHOOL OF MEDICINE (Japon)
NIHON KOHDEN COPRPRATION (Canada)
Inventeur(s)
Fujitani, Shigeki
Yoshida, Toru
Fukuhara, Itaru
Oura, Mitsuhiro
Kawamura, Syuhei
Abrégé
The patient information processing method includes a step of obtaining a plurality of pieces of vital data of a patient, a step of obtaining information indicating a content and a time of a treatment performed on the patient, and a step of causing a display to display information indicating at least one of the plurality of pieces of vital data or an index associated with the plurality of pieces of vital data, and to display information indicating the content and the time of the treatment.
G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p. ex. pour des dossiers électroniques de patients
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
49.
PATIENT INFORMATION PROCESSING METHOD, PATIENT INFORMATION PROCESSING DEVICE, AND PATIENT INFORMATION PROCESSING SYSTEM
A patient information processing method is executed by one or more processors, and the method includes obtaining a plurality of pieces of patient information each of which is associated with respective one of a plurality of patients, and determining a display order of the pieces of patient information to be displayed on a patient information list screen based on first information and second information different from the first information. The determining the display order includes determining the display order of the pieces of patient information based on the first information such that the pieces of patient information to be displayed on the patient information list screen are displayed early according to a value of the first information, and determining a display order of patient information of patients having the same value of the first information based on the second information.
G06F 3/0482 - Interaction avec des listes d’éléments sélectionnables, p. ex. des menus
G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p. ex. pour des dossiers électroniques de patients
50.
PATIENT INFORMATION PROCESSING METHOD, PATIENT INFORMATION PROCESSING DEVICE, AND PATIENT INFORMATION PROCESSING SYSTEM
A patient information processing method is executed by one or more processors, and the method includes obtaining a plurality of pieces of vital data of a patient, calculating a vital score indicating a condition of the patient using at least the plurality of pieces of vital data, and generating summary information related to the vital score and/or the plurality of pieces of vital data during a specific period.
G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p. ex. pour des dossiers électroniques de patients
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
51.
SPHYGMOMANOMETER, CONTROL DEVICE, AND NON-TRANSITORY COMPUTER-READABLE MEDIUM
A control device is configured to: cause an inflating/deflating device to initiate a first air feeding to a cuff with a prescribed flow rate; calculate an estimated value of a capacity volume of the cuff based on a time length for which the internal pressure inflates from a first value to a second value; cause the inflating/deflating device to perform at least air exhausting before an inflation of the internal pressure reaches a steady state to deflate the internal pressure; determine, based on the estimated value, an air feeding flow rate for obtaining a prescribed inflating speed; cause the inflating/deflating device to initiate a second air feeding to the cuff with the air feeding flow rate before the internal pressure reaches zero; and measure blood pressure of the subject while the second air feeding is performed.
A61B 5/0225 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins par application d'une pression pour fermer les vaisseaux sanguins, p. ex. contre la peauOphtalmodynamomètres la pression étant commandée par des signaux électriques, p. ex. dérivés des bruits de Korotkoff
A61B 5/022 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins par application d'une pression pour fermer les vaisseaux sanguins, p. ex. contre la peauOphtalmodynamomètres
52.
PHYSIOLOGICAL INFORMATION PROCESSING APPARATUS, PHYSIOLOGICAL INFORMATION PROCESSING METHOD, AND PHYSIOLOGICAL INFORMATION PROCESSING PROGRAM
A physiological information processing apparatus includes an ECG data detector configured to detect ECG data of a subject, a pulse wave data detector configured to detect pulse wave data of the subject, and a pulse wave transit time measurement unit configured to measure pulse wave transit time of the subject, based on the ECG data and the pulse wave data, The pulse wave transit time measurement unit includes a candidate value measurement unit configured to set one of rising timings of pulse waves as reference time, and configured to measure, as candidate values of the pulse wave transit time, time from the heartbeats to the reference time for a plurality of heartbeats before the reference time, and a specifying unit configured to specify, as the pulse wave transit time of the subject, the candidate value satisfying a prescribed condition, among the candidate values.
An information processing apparatus (2) includes an acquisition unit (2012) configured to acquire sensor information from each of a plurality of sensors including an ultrasonic sensor (3, 3A, 3B) coming into contact with or in proximity to a subject, and a derivation unit (2015) configured to derive a predetermined parameter indicating a body state of the subject based on the acquired sensor information.
A reception interface is configured to receive physiological information of a subject. A communication interface is configured to allow communication with a terminal device provided with a display. A processor is configured to create data for visualize information including at least the physiological information. The processor is configured to selectively execute either one of: a first communication protocol configured to transmit the data from the communication interface as a reply to a request transmitted from the terminal device; and a second communication protocol configured to transmit the data from the communication interface at a prescribed timing while maintaining connection established by a request transmitted from the terminal device. Information corresponding to the data transmitted by the second communication protocol has a higher priority for requiring an immediate display on the display than the information corresponding to the data transmitted by the first communication protocol.
To provide an immunoassay method capable of detecting a non-specific reaction. An immunoassay method for detecting an object to be measured in a sample, including: reacting a sample with fluorescent particles on which a specific binding substance for the object to be measured is immobilized and latex particles on which a specific binding substance for the object to be measured is immobilized to obtain a reactant; and detecting the object to be measured by obtaining size information and fluorescence information of the reactant using flow cytometry.
G01N 33/53 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet
G01N 33/536 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet avec formation d'un complexe immunologique en phase liquide
56.
VITAL SIGNS INFORMATION PROCESSING APPARATUS, VITAL SIGNS INFORMATION PROCESSING METHOD, AND NON-TRANSITORY COMPUTER READABLE STORAGE MEDIUM
A vital signs information processing apparatus includes an obtaining unit configured to obtain vascular dynamic information indicating a circulation state of blood of a subject; and a processor configured to perform a normalization processing on the vascular dynamic information to obtain an index value of pain evaluation of the subject. The processor is configured to calculate a reference value, based on the vascular dynamic information obtained in a reference period before a start of a treatment event related to a treatment for the subject, calculate a target value, based on the vascular dynamic information obtained after the start of the treatment event, and calculate a ratio of the target value to the reference value as the index value, as the normalization processing.
A61B 5/352 - Détection des crêtes de l'onde R, p. ex. pour la synchronisation d'appareils de diagnosticEstimation de l’intervalle entre crêtes R
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
57.
DISPLAY CONTROL DEVICE, NON-TRANSITORY COMPUTER-READABLE STORAGE MEDIUM, AND MONITOR DEVICE
An input interface receives a trigger signal. A processor displays a first screen or a second screen on a display device based on the trigger signal. The first screen provides first medical information for each of a plurality of subjects. The second screen provides, for at least one of the plurality of subjects, second medical information that is not included in the first medical information.
G06F 3/04845 - Techniques d’interaction fondées sur les interfaces utilisateur graphiques [GUI] pour la commande de fonctions ou d’opérations spécifiques, p. ex. sélection ou transformation d’un objet, d’une image ou d’un élément de texte affiché, détermination d’une valeur de paramètre ou sélection d’une plage de valeurs pour la transformation d’images, p. ex. glissement, rotation, agrandissement ou changement de couleur
G06Q 10/0631 - Planification, affectation, distribution ou ordonnancement de ressources d’entreprises ou d’organisations
58.
DISPLAY DATA GENERATION DEVICE, DISPLAY DATA GENERATION METHOD, AND NON-TRANSITORY COMPUTER-READABLE STORAGE MEDIUM
A display data generation device includes an input interface configured to receive vital signs information of a subject, one or more processors, and one or more memories configured to store at least one instruction executable by the processor. When the at least one command is executed by the processor, the display data generation device generates display data, the display data including the vital signs information and background information that indicates a background corresponding to a condition of the subject determined based on the vital signs information and a determination method for determining the condition of the subject, the background information overlapping with the vital signs information.
A display data generation apparatus includes an input interface configured to receive vital signs information on a subject, one or more processors, and one or more memories configured to store at least one instruction to be executed by the processor. In a case where the at least one instruction is executed by the processor, the display data generation apparatus generates display data. The display data includes, among the vital signs information received by the input interface a first vital signs information that is used in a determination method for determining a condition of the subject, the first vital signs information being displayed in a first area, and a second vital signs information that is not used in the determination method, the second vital signs information being displayed in a second area different from the first area.
An airway adapter includes a measurement flow path through which at least one of expired air or inhaled air of a subject passes through. A water absorption member is provided in a lower portion of the measurement flow path in a state where the airway adapter is placed. The water absorption member is exposed to an outside, and is configured to discharge water to the outside.
The cannula includes an attachment portion configured to be attached in nasal cavities of a subject, and a junction portion configured to be connected to the attachment portion. A first connection portion is provided with a single medical gas flow path for supplying, to the subject, a medical gas from the medical gas supply device. The first connection portion being provided to the junction portion on a side of a medical gas supply device. A second connection portion is provided with a single measurement pipe for measuring a respiratory condition of the subject. The second connection portion being provided to the junction portion on a side of a respiration measurement module.
An information processing device for processing ultrasonic wave information obtained from an ultrasonic wave sensor including a plurality of ultrasonic wave elements. The information processing device includes an obtainer configured to obtain the ultrasonic wave information from the ultrasonic wave sensor provided on a body surface of a subject, a recognizer configured to recognize a first blood vessel of the subject and a second blood vessel, based on the ultrasonic wave information, the second blood vessel being different from the first blood vessel, and a controller configured to cause a display to display comparison information in which first blood vessel information relating to the first blood vessel and second blood vessel information relating to the second blood vessel are compared with each other.
A display controller acquires a first inferential result corresponding to a clinical decision with regard to a prescribed item made for a subject. The first inferential result is obtained by inputting subject information related to the subject to a first inferential model. The display controller acquires a second inferential result corresponding to a clinical decision with regard to the prescribed item made for the subject. The second inferential result is obtained by inputting the subject information to a second inferential model. The display controller causes a display device (20) to display the first inferential result on the display device together with a first identifier (211) identifying the first inferential model, and causes the display device (20) to display the second inferential result together with a second identifier (212) identifying the second inferential model.
G16H 50/70 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour extraire des données médicales, p. ex. pour analyser les cas antérieurs d’autres patients
64.
CONTROL METHOD, CONTROL PROGRAM, AND ALARM DISTRIBUTION SYSTEM
A control method for an alarm distribution system including a plurality of medical devices. The control method including a step (a) of outputting an explanation or a question related to a patient management method, in accordance with a workflow corresponding to a state of a patient or a placed situation of the patient, and of receiving a response or an answer to the explanation or the question, a step (b) of performing setting to the plurality of medical devices, in accordance with the response or the answer, the setting being related to alarms associated or linked with each other, and a step (c) of controlling the alarms of the plurality of medical devices in coordination with each other, in accordance with the setting, the plurality of medical devices being simultaneously used for the same patient or the same patient group.
G16H 40/00 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux
65.
VITAL SIGN OBTAINING DEVICE, NON-TRANSITORY COMPUTER READABLE STORAGE MEDIUM, AND VITAL SIGN OBTAINING SYSTEM
A vital sign obtaining device includes an interface configured to receive, from a first sensor, a first detection signal corresponding to a vital sign of a subject, the first sensor configured to obtain the vital sign, an inference model configured to output a probability that the first detection signal is classified into each of a plurality of classes, and a processor configured to output data corresponding to a vital sign associated with the first detection signal, the probability that the first detection signal is classified into one of the plurality of classes being equal to or greater than a threshold.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
The presently disclosed subject matter provides a circulating blood volume determination apparatus includes a detection unit configured to detect a pulse wave from a sensor attached to a predetermined portion of a living body, an analysis unit configured to analyze a state of a venous component in the detected pulse wave, and a determination unit configured to perform a determination as to a circulating blood volume based on the analysis result of the analysis unit.
A61B 5/02 - Détection, mesure ou enregistrement en vue de l'évaluation du système cardio-vasculaire, p. ex. mesure du pouls, du rythme cardiaque, de la pression sanguine ou du débit sanguin
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/021 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins
A61B 5/022 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins par application d'une pression pour fermer les vaisseaux sanguins, p. ex. contre la peauOphtalmodynamomètres
67.
PROCESSING DEVICE, NON-TRANSITORY COMPUTER READABLE STORAGE MEDIUM, METHOD FOR GENERATING TRAINING DATA, AND METHOD FOR GENERATING PREDICTION MODEL
A processing device includes an interface configured to receive electrocardiographic waveform data corresponding to an electrocardiographic waveform of a subject, and a processor configured to divide the electrocardiographic waveform into a plurality of partial electrocardiographic waveforms, based on the electrocardiographic waveform data, calculate a probability that a waveform portion in which a heart disease is suspected is included in each of the plurality of partial electrocardiographic waveforms, and cause a display to display an index together with information, the index corresponding to the probability, the information corresponding to the partial electrocardiographic waveform from which the probability is calculated.
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
68.
PHYSIOLOGICAL INFORMATION PROCESSING APPARATUS AND PHYSIOLOGICAL INFORMATION PROCESSING METHOD
A physiological information processing apparatus includes one or more processors, and one or more memories configured to store a computer readable instruction, when the computer readable instruction is executed by the processor, the physiological information processing apparatus is configured to: cause a plurality of physiological sensors to intermittently operate such that an operation time and a standby time are alternately repeated; obtain a plurality of pieces of physiological information on a patient from the plurality of physiological sensors during the operation time; and change an operation mode of the plurality of physiological sensors that intermittently operate in accordance with a condition related to at least a part of the plurality of pieces of physiological information or a condition related to at least a part of the plurality of physiological sensors.
A defibrillator electrode pad includes a metal foil configured to diffuse electricity transmitted from a defibrillator via a cable, a conductive adhesive layer configured to be attached to a living body, the conductive adhesive layer being provided on a part of a first surface of the metal foil, a base member provided on a second surface of the metal foil, and an insulating part covering a portion, of the first surface, at which the conductive adhesive layer is not provided, the insulating part fixing, to the metal foil, a cable terminal provided at an end portion of the cable.
A gas inhalation mask (1) includes a mask body (11) formed of paper, nonwoven fabric, or fabric, and a tube attachment member (12). The tube attachment member is attached to an attachment opening (111) provided in the mask body. In a case where the mask body is attached to a subject, an axis of a tube does not directly face toward a face of the subject. The tube is connected to a tube connecting portion (122a) of the tube attachment member.
An airway adapter includes an airway adapter body including a first tube connection portion, a second tube connection portion, and a detection portion provided between the first tube connection portion and the second tube connection portion, and a support base configured to support the airway adapter body. The support base is configured to support the first tube connection portion at a position higher than a position of the second tube connection portion.
A monitoring method includes a calculation step and an output step. The calculation step includes calculating an alarm generation time, in which at least one of a vital alarm notifying an abnormality of physiological information and a technical alarm is generated, or a ratio of the alarm generation time. The output step includes outputting the calculated alarm generation time or the calculated ratio.
A physiological information processing method executed by a computer. The physiological information processing method includes obtaining a plurality of electroencephalogram signals indicating an electroencephalogram of a subject, using a plurality of electrodes attached to a head of the subject, each of the plurality of electroencephalogram signals being associated with a respective one of the plurality of electrodes, obtaining, from each of the plurality of electroencephalogram signals, a plurality of artifact component signals indicating different types of artifacts, calculating effective values of the plurality of artifact component signals of each of the electroencephalogram signals, determining whether the effective value of each of the artifact component signals of the electroencephalogram signal satisfies a predetermined condition, and visually presenting information related to the artifact associated with the artifact component signal of which the effective value satisfies the predetermined condition.
RESPIRATION INFORMATION OBTAINING APPARATUS, RESPIRATION INFORMATION OBTAINING SYSTEM, PROCESSING APPARATUS, AND RESPIRATION INFORMATION OBTAINING METHOD
A respiration information obtaining apparatus includes: a light emitter configured to emit a first light including a first wavelength and a second light including a second wavelength different from the first wavelength; a light detector that outputs a first signal and a second signal respectively corresponding to an intensity of the first light and an intensity of the second light after an interaction with a tissue of a subject, and a processor that calculates an index value based on a ratio between the first signal and the second signal, and obtains respiration information of the subject based on a change over time in the index value.
A physiological information processing apparatus includes a calculator configured to calculate a moving average value of a pulse wave transit time of a subject, and a hemodynamic parameter of the subject, using the calculated moving average value. The calculator is configured to switch a calculation target between a first hemodynamic parameter and a second hemodynamic parameter. The first hemodynamic parameter is calculated using the moving average value of a first pulse wave transit time. The second hemodynamic parameter is calculated using the moving average value of a second pulse wave transit time that is shorter than the moving average time of the first pulse wave transit time.
A61B 5/02 - Détection, mesure ou enregistrement en vue de l'évaluation du système cardio-vasculaire, p. ex. mesure du pouls, du rythme cardiaque, de la pression sanguine ou du débit sanguin
A61B 5/021 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
76.
NEURAL MONITORING SYSTEM, PROCESSING APPARATUS, AND NON-TRANSITORY COMPUTER-READABLE STORAGE MEDIUM
A neural monitoring system includes a stimulation device configured to generate a stimulation signal corresponding to stimulation applied to a subject, and a processing apparatus configured to: acquire a waveform corresponding to a change over time in an evoked potential of the subject based on the stimulation, and cause a display device to display an index indicating any one of a plurality of colors, based on an amplitude value of the waveform and an amplitude change rate. the amplitude value is acquired based on a predetermined rule. The amplitude change rate is a ratio of the amplitude value to an amplitude value of a reference waveform.
A physiological information display apparatus includes a heart rate acquisition unit configured to acquire a heart rate of a subject, a respiration rate acquisition unit configured to acquire a respiration rate of the subject, a hemodynamics calculation unit configured to calculate a hemodynamic parameter of the subject, and a respiratory variation of the hemodynamic parameter, based on a plurality of the hemodynamic parameters calculated in a predetermined period, and a display controller configured to output the respiratory variation to a display. The hemodynamics calculation unit is configured to calculate a heart rate in one respiration. The display controller is configured to output a setting screen for setting a length of the predetermined period. The hemodynamics calculation unit is configured to acquire setting information, set the length of the predetermined period based on the acquired setting information; and calculate the respiratory variation in the set predetermined period.
A61B 5/024 - Mesure du pouls ou des pulsations cardiaques
A61B 5/0285 - Mesure de la vitesse de propagation de l'onde pulsatile
A61B 5/029 - Mesure du débit de sang à la sortie du cœur, p. ex. volume éjecté par minute
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/02 - Détection, mesure ou enregistrement en vue de l'évaluation du système cardio-vasculaire, p. ex. mesure du pouls, du rythme cardiaque, de la pression sanguine ou du débit sanguin
78.
PHYSIOLOGICAL INFORMATION DISPLAY APPARATUS AND PHYSIOLOGICAL INFORMATION DISPLAY METHOD
A physiological information display apparatus includes a reception unit configured to receive a start signal and an end signal, the start signal indicating a start timing of a treatment for a subject, the end signal indicating an end timing of the treatment, a calculation unit configured to calculate a moving average value of a pulse wave transit time of the subject, a hemodynamic parameter of the subject, using the calculated moving average value, and a change rate of the hemodynamic parameter in a period from the start timing to the end timing, based on the start signal and the end signal received by the reception unit, and a display controller configured to output, to a display, the change rate calculated by the calculation unit.
A61B 5/02 - Détection, mesure ou enregistrement en vue de l'évaluation du système cardio-vasculaire, p. ex. mesure du pouls, du rythme cardiaque, de la pression sanguine ou du débit sanguin
A61B 5/0205 - Évaluation simultanée de l'état cardio-vasculaire et de l'état d'autres parties du corps, p. ex. de l'état cardiaque et respiratoire
A61B 5/021 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins
A61B 5/024 - Mesure du pouls ou des pulsations cardiaques
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
A61B 5/339 - Affichages spécialement adaptés à cet effet
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/0215 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins par des moyens introduits dans le corps
A61B 5/352 - Détection des crêtes de l'onde R, p. ex. pour la synchronisation d'appareils de diagnosticEstimation de l’intervalle entre crêtes R
A medical instrument is adapted to be attached to a subject. A nasal adapter includes cannulas adapted to be disposed so as to face nostrils of the subject when the medical instrument is attached to the subject. A bite block includes a hollow member-adapted to be disposed in an oral cavity of the subject when the medical instrument is attached to the subject. A flexible joint connects the nasal adapter and the bite block.
A61B 1/00 - Instruments pour procéder à l'examen médical de l'intérieur des cavités ou des conduits du corps par inspection visuelle ou photographique, p. ex. endoscopesDispositions pour l'éclairage dans ces instruments
A61M 16/06 - Masques respiratoires ou pour l'anesthésie
NATIONAL UNIVERSITY CORPORATION TOKAI NATIONAL HIGHER EDUCATION AND RESEARCH SYSTEM (Japon)
UNIVERSITY PUBLIC CORPORATION OSAKA (Japon)
Inventeur(s)
Nagata, Shinya
Suzuki, Akane
Shioyama, Takahiro
Sugimoto, Tadanori
Shinozaki, Yukino
Satsu, Masakazu
Ohtsuki, Chikara
Nakamura, Jin
Akiyoshi, Hideo
Nishida, Hidetaka
Mie, Keiichiro
Abrégé
Provided is a porous body for capturing cancer cells, including a biocompatible inorganic material, the porous body for capturing cancer cells having biocompatibility and also having stability in a living body. The porous body for capturing cancer cells can be used for application related to cancer such as a treatment, a treatment assistance, a test, or a diagnosis.
A61L 31/12 - Matériaux composites, c.-à-d. en couches ou contenant un matériau dispersé dans une matrice constituée d'un matériau analogue ou différent
A61L 31/14 - Matériaux caractérisés par leur fonction ou leurs propriétés physiques
81.
STIMULATING SYSTEM, STIMULATION ELECTRODE UNIT, RELAY CABLE, AND STIMULATION CONTROL DEVICE
A stimulation electrode unit (11) includes a plurality of electrodes (111) adapted to be attached to a living body. A stimulation control device (12) is configured to form an electric circuitry (14) with the stimulation electrode unit (11), and to control a stimulation current that is caused to flow into the living body through the electrodes (111). An information element (15) retains identifier information identifying the stimulation electrode element (11). The stimulation control device (12) is configured to read out the identifier information through the electric circuitry (14), and to determine, based on the identifier information, whether the electrical circuit (14) is formed by an adequate stimulation electrode unit.
A physiological information processing device includes one or more processors, and one or more memories for storing computer-readable commands. When the computer-readable commands are executed by the processors, the physiological information processing device executes processing of acquiring attribute information associated with an attribution of an infant, acquiring state information related to a state of the infant before a start of a pain event that causes pain in the infant, acquiring physiological information data of the infant, acquiring facial expression information associated with infant's facial expression after the start of the pain event, calculating a pain assessment index for assessing the pain of the infant in the pain event based on the attribute information, the state information, the physiological information data, and the facial expression information, and outputting the calculated pain assessment index.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/0205 - Évaluation simultanée de l'état cardio-vasculaire et de l'état d'autres parties du corps, p. ex. de l'état cardiaque et respiratoire
A61B 5/145 - Mesure des caractéristiques du sang in vivo, p. ex. de la concentration des gaz dans le sang ou de la valeur du pH du sang
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
83.
PHYSIOLOGICAL INFORMATION PROCESSING APPARATUS, PHYSIOLOGICAL INFORMATION PROCESSING METHOD, PROGRAM AND STORAGE MEDIUM
A physiological information processing apparatus comprising: a processor; and a memory that stores a computer-readable instruction that when executed by the processor, causes the physiological information processing apparatus to perform operations comprising: displaying on a display unit, first attachment position information representing a position where a first physiological information sensor is attached; acquiring first physiological information data of a subject from the first physiological information sensor; and displaying, on the display unit, information relevant to the first physiological information data. The physiological information processing apparatus displays the first attachment position information on the display unit before displaying the information relevant to the first physiological information data on the display unit.
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p. ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p. ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p. ex. ventilateursTubes trachéaux
G16H 40/67 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement à distance
An automated external defibrillator includes: an operation accepter that accepts an operation input from a user; and a self-test executor that executes a self-test for checking a state of the automated external defibrillator when a first condition or a second condition has been satisfied. The first condition is that a setting time instant set in advance comes. The second condition is that the operation accepter accepts a predetermined operation input.
A gas measurement adapter includes a flow tube portion configured to allow gas to pass through the flow tube portion and a window portion configured to allow measurement light for measuring a component of the gas passing through the flow tube portion to pass through the window portion. The adapter is prepared by using an adapter forming material containing a cycloolefin-based resin as a main component.
An automated external defibrillator includes: a high voltage generator configured to charge or discharge electric energy for giving a subject an electric shock for defibrillation; an outer housing configured to house the high voltage generator and defining an exterior of the automated external defibrillator; and a potting material containing an insulating material. The high voltage generator includes: a high voltage circuit board; and a high voltage electronic component disposed on the high voltage circuit board. The potting material covers the high voltage circuit board and a terminal of the high voltage electronic component, and is in contact with the high voltage circuit board and the outer housing to fix the high voltage circuit board to the outer housing.
An information processing device includes an acquisition unit configured to acquire subject information including at least one of information about a patient and information bout a medical practitioner, measurement information about a physiological parameter of the patient, and prediction information about the physiological parameter of the patient predicted by the medical practitioner, an analyzing unit configured to analyze a relationship between the subject information and a degree of divergence between the prediction information and the measurement information, and an output that configured to output analysis information representing the relationship between the subject information and the degree of divergence.
An automated external defibrillator includes: a detector that detects an abnormality of the automated external defibrillator; and a notifier that notifies a user of the detection of the abnormality. The notifier has a display unit that includes a light source, and a sounder that generates an alert sound. The display unit executes a first mode and a second mode lower in power consumption alternately. The sounder executes a third mode and a fourth mode lower in power consumption alternately. At least a half part of each of periods in which the first mode is executed overlaps timewise with a corresponding one of periods in which the fourth mode is executed. At least a half part of each of periods in which the third mode is executed overlaps timewise with a corresponding one of periods in which the second mode is executed.
A sensor attachment system includes: a sensor configured to detect a state of respiratory gas of a subject; and a compatible airway adaptor compatible with the sensor. The sensor includes a respiratory gas detector configured to detect the state of the respiratory gas of the subject, and a sensor-side engagement portion engageable with the compatible airway adaptor. The compatible airway adaptor includes a tube portion having a respiratory gas ventilation passage through which the respiratory gas passes, and an adapter-side engagement portion engageable with the sensor-side engagement portion. The sensor is attachable to the compatible airway adaptor in a state in which the compatible airway adaptor and the sensor do not interfere with each other, and the sensor is not attachable to an incompatible airway adaptor that is not compatible with the sensor in a state in which the incompatible airway adaptor and the sensor interfere with each other.
A signal processing device is mounted on a physiological information processing device switchable between a first state in which the physiological information processing device is operable by a first function and a second state in which the physiological information processing device is operable by a second function higher than the first function. The signal processing device processes a signal corresponding to physiological information output from a sensor included in a probe connected to the physiological information processing device based on a state designation information for designating whether the physiological information processing device operates in the first state or in the second state. The signal processing device, when the probe holding type specific information is connected to the physiological information processing device, receive the type specific information, and when a switching device holding switching information is connected to the physiological information processing device, receive the switching information.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
91.
NON-TRANSITORY COMPUTER-READABLE MEDIUM, PORTABLE INFORMATION TERMINAL, SYSTEM, AND METHOD FOR NOTIFICATION ABOUT ACTIVATION OF AUTOMATED EXTERNAL DEFIBRILLATOR
A non-transitory computer-readable medium has recorded thereon a program that makes circuitry of a portable information terminal execute: a detection step of detecting presence/absence of an automated external defibrillator in an activated state based on presence/absence of a wireless signal sent from the automated external defibrillator, the wireless signal becoming detectable in response to activation of the automated external defibrillator having a wireless communication module; and a first transmission step of transmitting notification information for notification about the activation of the automated external defibrillator to a management computer in response to the automated external defibrillator in the activated state being detected in the detection step.
A first input interface receives measured values of non-invasive blood pressure of a subject intermittently at a first frequency. A second input interface receives measured values of pulse wave transit time of the subject at a second frequency higher than the first frequency. A processor executes regression analysis processing based on the measured values received until when a measured value acquired by Nth (N is an integer that is no less than 2) measurement of the non-invasive blood pressure is received to acquire a regression equation in which the measured value is set as an explanatory variable. An information presenting device visibly presents estimated values of the non-invasive blood pressure calculated with the regression equation and the measured values, until a measured value acquired by (N+1)th measurement of the non-invasive blood pressure is received.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/0205 - Évaluation simultanée de l'état cardio-vasculaire et de l'état d'autres parties du corps, p. ex. de l'état cardiaque et respiratoire
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
A defibrillator includes: processing circuitry; and a memory storing a program. When executed on the processing circuitry, the program causes the processing circuitry to: calculate battery usage of a battery configured to supply power to the defibrillator; record, on a battery memory, information related to the battery usage; and record, on the battery memory, battery information indicating battery failure in response to voltage of the power supplied from the battery being below a threshold.
A physiological information processing method executed by a computer. The physiological information processing method includes acquiring, from a plurality of electrodes attached to a body surface of a subject, a plurality of electrocardiogram signals indicating an electrocardiogram waveform of the subject, separating, through independent component analysis, each of the plurality of electrocardiogram signals into one or more first waveform components indicating the electrocardiogram waveform and one or more second waveform components indicating a waveform other than the electrocardiogram waveform, acquiring an activity evaluation index indicating a respiratory muscle activity amount of the subject based on an electrocardiogram signal that is obtained from a predetermined electrode among the plurality of electrodes attached to the body surface of the subject and from which the one or more first waveform components have been removed, and outputting information on the activity evaluation index.
A defibrillator configured to execute a defibrillation process of delivering an electric shock for defibrillation to a heart of a subject. The defibrillator includes: a processor; and a memory that stores a computer-readable instruction that when executed by the processor, causes the defibrillator to perform operations including: receiving a raw data related to at least one of a plurality of components configuring the defibrillator and an accessory of the defibrillator; and transmitting the received raw data and an identification information of the defibrillator to a management server. The raw data is used to determine presence or absence of an abnormality in at least one of the plurality of components and the accessory.
An automated external defibrillator includes: a self-test executor that executes a self-test for checking a state of the automated external defibrillator; and a display unit that indicates the state of the automated external defibrillator. The display unit makes: a first display when the automated external defibrillator is in a normal state; a second display when the automated external defibrillator is in an abnormal state, and the first display and the second display simultaneously or in a predetermined pattern when the automated external defibrillator is self-testing.
An automated external defibrillator (AED) includes: a battery configured to supply electric power to the AED; an indicator configured to visually provide predetermined information related to the AED and a remaining level of the battery; and an indicator controller configured to change a visual aspect of the indicator according to the remaining level.
An automated external defibrillator is configured to automatically execute a defibrillation process of delivering an electric shock for defibrillation to a heart of a subject. The defibrillator includes: a processor; and a memory that stores a computer-readable instruction that when executed by the processor, causes the defibrillator to perform operations including: receiving a physiological signal of the subject through an electrode pad; determining whether the defibrillation process is necessary based on the physiological signal; and determining whether the electrode pad is attached to the subject and a predetermined operation has been performed on the defibrillator. When the defibrillation process is necessary, the defibrillator cancels the defibrillation process while maintaining an on-state of a power supply thereof, in response to a result of the determination as to whether the electrode pad is attached to the subject and the predetermined operation has been performed on the defibrillator.
A medical photometer includes a signal producing section that produces a first control signal to emit a first light having a first wavelength, a second control signal to emit a second light having a second wavelength, a third control signal to emit a third light having a third wavelength, and a fourth control signal to emit a fourth light having a fourth wavelength, a signal acquiring section that acquires a first to fourth intensity signals, a processor, and a memory that stores instructions. In the medical photometer, the first wavelength and the second wavelength are selected as two wavelengths at each of which an extinction coefficient of blood is a first value. The third wavelength and the fourth wavelength are selected as two wavelengths at each of which the extinction coefficient of the blood is a second value which is different from the first value.
A61B 5/1455 - Mesure des caractéristiques du sang in vivo, p. ex. de la concentration des gaz dans le sang ou de la valeur du pH du sang en utilisant des capteurs optiques, p. ex. des oxymètres à photométrie spectrale
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p. ex. ventilateursTubes trachéaux
An automated external defibrillator (1) includes: a sound generator (101) that outputs a timing sound expressing, by sound, a timing until the electric shock is delivered, and a warning sound expressing a state in which an internal capacitor in the automated external defibrillator has been charged with high voltage; and a sound controller (103B) that controls the sound generator, wherein the sound controller (103B) changes the warning sound in accordance with presence or absence of output of the timing sound.
