A medical station comprises a base and an upper module formed of a structure positioned atop the base. At least one vertical mounting post is attached to at least one of the base and the upper module and a first mounting clamp is slidably mounted to the vertical mounting post. A horizontal rail is attached to the at least one vertical mounting post via the first mounting clamp, wherein a vertical position of the horizontal rail is adjustable via sliding the first mounting clamp along the horizontal rail and wherein a storage bin can be removably attached to the horizontal rail.
A61B 50/10 - Mobilier spécialement adapté aux appareils ou aux instruments chirurgicaux ou de diagnostic
A61B 50/30 - Récipients spécialement adaptés à l'emballage, la protection, la distribution, la collecte ou l'élimination des appareils ou des instruments chirurgicaux ou de diagnostic
2.
SYSTEM AND METHOD FOR DETECTING OVER-INFUSION DUE TO MECHANICAL FAILURE OF AN INFUSION PUMP
An apparatus, method, and system for detecting an over-infusion of a fluid due to a mechanical failure of an infusion pump. A pressure sensor of an infusion pump measures a pressure of a fluid in an infusion line loaded into the pump over at least a portion of a pumping cycle. The pumping cycle includes application of at least one occluder and at least one pumping finger to the infusion line to move the fluid through the infusion line. A control unit associated with the pump determines a metric based on measuring the pressure over the at least the portion of the pumping cycle, determines whether the metric satisfies a fault threshold corresponding to a pump fault and, responsive to the determination, provides an alert indicating the pump fault and terminates or reduces the pumping of the fluid through the infusion line.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
3.
ADHESIVE FOR BONDING DISSIMILAR MATERIALS IN MEDICAL DEVICE
Bonding dissimilar materials of medical device components can be carried out by applying an adhesive on at least one surface of two components which are composed of dissimilar materials and contacting the surfaces and exposing the contacted surfaces to heat and/or irradiate the adhesive to cure the adhesive and bond the surfaces. One medical component, e.g., medical tubing, can be composed of a non-polar, polyvinyl chloride free thermoplastic polymeric material and the other medical component, e.g., a medical connector, can be composed of polyacrylate, polyacrylonitrile, acrylonitrile-butadiene-styrene (ABS), methyl methacrylate-acrylonitrile-butadiene-styrene (mABS), polyester, and/or a polycarbonate material. The adhesive formulation can include: (a) a polyolefin oligomer having reactive acrylate groups and alkenyl groups, (b) an initiator, and optionally (c) a solvent.
The priming attachment for a vacuum syringe can prevent air that is drawn out of the IV set and into the vacuum syringe from being released into the environment or back into the IV set. The priming attachment couples to the vacuum syringe and prevents the syringe plunger from reentering the syringe barrel. One embodiment of the priming attachment includes arms that fit inside the barrel and are pulled distally until they are released from the barrel. Once the arms released, the arms cannot reenter the barrel, which prevents distal movement of the plunger relative to the barrel. Another embodiment of the priming attachment includes a key that couples with a notch in a modified plunger. The modified plunger can rotate between a free position, where it can reciprocate within the barrel, and a locked position, where the notch aligns with the key and prevents translation of the modified plunger.
The priming attachment for a vacuum syringe can prevent air that is drawn out of the IV set and into the vacuum syringe from being released into the environment or back into the IV set. The priming attachment couples to the vacuum syringe and prevents the syringe plunger from reentering the syringe barrel. One embodiment of the priming attachment includes arms that fit inside the barrel and are pulled distally until they are released from the barrel. Once the arms released, the arms cannot reenter the barrel, which prevents distal movement of the plunger relative to the barrel. Another embodiment of the priming attachment includes a key that couples with a notch in a modified plunger. The modified plunger can rotate between a free position, where it can reciprocate within the barrel, and a locked position, where the notch aligns with the key and prevents translation of the modified plunger.
A method of adjusting a position of an infusion container includes determining a current fluid pressure of a first fluid in a fluid path at or upstream of a fluid junction. When the determined current fluid pressure satisfies a predetermined threshold: display an indication of a fault condition associated with the current fluid pressure of the fluid being above the predetermined threshold. A motor operatively coupled to an adjustment device automatically changes a height of the infusion container, relative to a reference point, to an adjusted height that causes a reduction in a flow of the first fluid beyond the fluid junction, which mixes with a flow of a second fluid from the infusion container. The method includes determining an updated fluid pressure of the first fluid in the fluid path after the motor automatically changes the height of the infusion container to the adjusted height.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A flow stop system is disclosed. A flow stop is configured, in a first position, to prevent a flow of a fluid through a tubing, and in a second position, to permit the flow of the fluid through the tubing, and a tubing fitment coupled to the flow stop and configured to receive the tubing and align the tubing with the flow stop. One or more conductive connections electrically are connected to a non-transitory machine readable memory, and the flow stop system is shaped to be loaded and engaged to a receptacle of an infusion device, and shaped to cause, when loaded and engaged, the one or more conductive connections to engage with one or more corresponding conductive connections provided by the infusion device.
A61M 5/172 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte électriques ou électroniques
H01R 13/15 - Broches, lames ou alvéoles ayant un ressort indépendant pour produire ou améliorer la pression de contact
H02J 50/10 - Circuits ou systèmes pour l'alimentation ou la distribution sans fil d'énergie électrique utilisant un couplage inductif
A clamp assembly for adjusting the fluid flow rate in an infusion set includes a housing having two opposing side walls with guide grooves, a guide wall disposed between the side walls, an elastomeric segment disposed between the two opposing side walls, the elastomeric segment being a hollow tube, tubing ports disposed on each end of the elastomeric segment, and a flow regulating member having portions disposed in the guide grooves, the flow regulating member configured to move along a longitudinal axis of the housing over a movement range as the portions slide in the guide grooves, wherein the flow regulating member is configured to remain in a set position during use of the infusion set based on the compression set performance of the elastomeric segment until the flow regulating member is moved by a user. A method of operating a clamp assembly is also provided.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
In order to accurately monitor fluid flow through an infusion line, it can be desirable to position a pressure transducer along the infusion line and a noise-filtering mechanism between the pressure transducer and the fluid. Fluid in the infusion line transmits a pressure wave that is partially transmitted through the noise-filtering mechanism, such that the parts of the pressure wave with high amplitudes are received by the pressure transducer and the rest of the pressure wave (i.e., the noise) is reflected back towards the fluid. The noise-filtering fluid measurement system disclosed herein utilizes a layered structure of gel and air to gradually change the impedance of the materials through which a pressure wave must travel to ensure that only the meaningful parts of the pressure wave reach the pressure transducer while also preventing the entirety of the pressure wave from being reflected back towards the fluid.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
In order to maintain the patency of an intravenous (IV) catheter while limiting the risk of occlusions, it can be desirable to use a keep vein open (KVO) infusion flow control device to continuously deliver fluid to a patient's catheter line in a controlled manner. The KVO infusion flow control device disclosed herein utilizes super absorbent polymers (SAPs) (150), which expand when in contact with water (particularly, distilled water) (162), to gradually deliver a consistent flow of saline to the patient's catheter line. The KVO infusion flow control device includes a spiking system (114) that can be used to spike a distilled water chamber and expose distilled water to a SAP block. When the SAP block expands, the SAP block compresses a flush chamber filled with saline and advances the saline out of the KVO infusion flow control device and into the patient's catheter line.
A61M 5/148 - Perfusion sous pression, p. ex. utilisant des pompes utilisant des réservoirs sous pression, p. ex. au moyen de pistons flexibles
A61M 5/152 - Perfusion sous pression, p. ex. utilisant des pompes utilisant des réservoirs sous pression, p. ex. au moyen de pistons flexibles mis sous pression par contraction de réservoirs élastiques
11.
MODULAR POWER AND CONNECTIVITY SYSTEM FOR INFUSION DEVICES
A modular power and connectivity assembly and system are provided. The modular power and connectivity assembly includes a rectangular housing comprising an open rectangular cavity disposed in a corner portion of the rectangular housing, a cavity coupling member configured to receive a device coupling member of an infusion device comprising one of a sensor and an infusion pump, a power assembly configured to provide power to an infusion device, and a communication assembly configured to provide communication with the infusion device, wherein the modular power and connectivity assembly is configured to be removably coupled to the infusion device. A method of operating a modular power and connectivity system is also provided.
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
G16H 20/17 - 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 administrés par perfusion ou injection
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
In order to accurately monitor fluid flow through an infusion line, it can be desirable to position a pressure transducer along the infusion line and a noise-filtering mechanism between the pressure transducer and the fluid. Fluid in the infusion line transmits a pressure wave that is partially transmitted through the noise-filtering mechanism, such that the parts of the pressure wave with high amplitudes are received by the pressure transducer and the rest of the pressure wave (i.e., the noise) is reflected back towards the fluid. The noise-filtering fluid measurement system disclosed herein utilizes a layered structure of gel and air to gradually change the impedance of the materials through which a pressure wave must travel to ensure that only the meaningful parts of the pressure wave reach the pressure transducer while also preventing the entirety of the pressure wave from being reflected back towards the fluid.
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
In order to maintain the patency of an intravenous (IV) catheter while limiting the risk of occlusions, it can be desirable to use a keep vein open (KVO) infusion flow control device to continuously deliver fluid to a patient’s catheter line in a controlled manner. The KVO infusion flow control device disclosed herein utilizes super absorbent polymers (SAPs), which expand when in contact with water (particularly, distilled water), to gradually deliver a consistent flow of saline to the patient’s catheter line. The KVO infusion flow control device includes a spiking system that can be used to spike a distilled water chamber and expose distilled water to a SAP block. When the SAP block expands, the SAP block compresses a flush chamber filled with saline and advances the saline out of the KVO infusion flow control device and into the patient’s catheter line.
A system and method is disclosed for converting drug library packages. An existing drug library software package is automatically analyzed to identify one or more first drug parameters within the existing drug library software that are compatible with a target medical device type, and one or more second drug parameters not compatible with the target medical device type and which would cause an error response from a respective device of the target medical device type if loaded by the respective device. Replacement parameters compatible with the target medical device type are determined to replace the one or more second drug parameters, and a new drug library software is generated that includes the one or more first drug parameters and including the determined one or more replacement parameters in place of the one or more second drug parameters.
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
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 coupler including a first connector having a mating portion with a first opening, and a first torsion member disposed within the mating portion with a first channel. The first torsion member being rotatable relative to the mating portion. The coupler including a second connector having a second torsion member with a second channel, and a coupling portion having a second opening and at least partially disposed within the second torsion member. The second torsion member configured to couple to the first torsion member to couple the first connector to the second connector such that rotation of the second torsion member causes rotation of the first torsion member to cause alignment of the first channel, the first opening, the second channel, and the second opening to form a fluid pathway. The first connector is configured to decouple from the second connector in response to a force exceeding a threshold force.
F16L 37/367 - Accouplements du type à action rapide avec moyens pour couper l'écoulement du fluide avec un obturateur dans chaque extrémité de tuyau avec deux vannes à plaque ou tiroirs
A chromic sensor for an intravenous catheter may include a first region disposed to be proximal to an insertion site at which the intravenous catheter is inserted into a patient. The first region includes a chromic material that changes color in response to a stimulus. A second region of the chromic sensor is disposed to be distal to the insertion site, spaced apart from the first region along a portion of the intravenous catheter inserted into the patient. The second region includes the chromic material. The first and second regions are configured to respond identically to identical stimuli.
A61B 5/01 - Mesure de la température de parties du corps
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 5/103 - Dispositifs de mesure pour le contrôle de la forme, du dessin, de la dimension ou du mouvement du corps ou de parties de celui-ci, à des fins de diagnostic
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 5/1477 - 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 procédés chimiques ou électrochimiques, p. ex. par des moyens polarographiques non invasifs
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
C09K 19/00 - Substances formant des cristaux liquides
G01K 11/12 - Mesure de la température basée sur les variations physiques ou chimiques, n'entrant pas dans les groupes , , ou utilisant le changement de couleur, de translucidité ou de réflectance
G01N 21/29 - CouleurPropriétés spectrales, c.-à-d. comparaison de l'effet du matériau sur la lumière pour plusieurs longueurs d'ondes ou plusieurs bandes de longueurs d'ondes différentes en utilisant la détection visuelle
G01N 21/78 - Systèmes dans lesquels le matériau est soumis à une réaction chimique, le progrès ou le résultat de la réaction étant analysé en observant l'effet sur un réactif chimique produisant un changement de couleur
A chromic sensor for an intravenous catheter may include a first region disposed to be proximal to an insertion site at which the intravenous catheter is inserted into a patient. The first region includes a chromic material that changes color in response to a stimulus. A second region of the chromic sensor is disposed to be distal to the insertion site, spaced apart from the first region along a portion of the intravenous catheter inserted into the patient. The second region includes the chromic material. The first and second regions are configured to respond identically to identical stimuli.
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 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 syringe pump may comprise a main housing. The pump may further comprise a drive head coupled to an elongate body extending out of the main housing. The drive head may comprise an actuator coupled to and rotatable with a threaded shaft, a clutch assembly, and a release body. The drive head may further comprise a carriage engaged with the threaded shaft and displaceable over a range in response to rotation of the shaft. The carriage may drive the release body upon displacement of the carriage. The clutch may transition from an engaged state to a disengaged state when the release body is displaced from a first to second position. The pump may further comprise a drive assembly configured to displace the drive head relative to the main housing. The drive assembly may include a leadscrew which is free to rotate when clutch assembly is in the disengaged state.
Devices for capturing air in a fluid pathway are provided. The device includes IV tubing configured to be disposed within an air-in-line sensor and a flow cannula disposed within the IV tubing. The flow cannula includes a center lumen disposed axially along the flow cannula, wherein the flow cannula is configured to direct an incoming fluid flow from a pump segment through the center lumen into an air capture device and to direct processed fluid received back from the air capture device through the flow cannula externally to the center lumen and internally to the IV tubing. Methods for capturing air in a fluid pathway and flow cannulas for use within IV tubing are also provided.
A61M 5/36 - Dispositifs pour faire pénétrer des agents dans le corps par introduction sous-cutanée, intravasculaire ou intramusculaireAccessoires à cet effet, p. ex. dispositifs de remplissage ou de nettoyage, appuis-bras avec des moyens pour éliminer l'air ou pour empêcher l'injection ou l'introduction d'air dans le corps
A61M 5/165 - Accessoires de filtrage, p. ex. filtres pour le sang, pour les liquides de perfusion
A61M 5/162 - Raccords à aiguilles, c.-à-d. raccordements par perforation entre le réservoir et le tube
Drip chambers are disclosed that can resist the formation of bubbles and turbulence in fluid moving through the drip chamber, and can include an inlet opening to an inner chamber formed at least in part by a sidewall having a portion that intersects a path of fluid droplets moving or falling from the inlet orifice into the inner chamber, where the path of fluid droplets causes the droplets to engage against a tangent impact plane at a location of the sidewall that is transverse relative to the path of fluid droplets such that the fluid droplets can slide from the impact plane into a pool of fluid within the inner chamber and exit the inner chamber through an outlet opening.
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
A61M 5/36 - Dispositifs pour faire pénétrer des agents dans le corps par introduction sous-cutanée, intravasculaire ou intramusculaireAccessoires à cet effet, p. ex. dispositifs de remplissage ou de nettoyage, appuis-bras avec des moyens pour éliminer l'air ou pour empêcher l'injection ou l'introduction d'air dans le corps
Devices for capturing air in a fluid pathway are provided. The device includes IV tubing configured to be disposed within an air-in-line sensor and a flow cannula disposed within the IV tubing. The flow cannula includes a center lumen disposed axially along the flow cannula, wherein the flow cannula is configured to direct an incoming fluid flow from a pump segment through the center lumen into an air capture device and to direct processed fluid received back from the air capture device through the flow cannula externally to the center lumen and internally to the IV tubing. Methods for capturing air in a fluid pathway and flow cannulas for use within IV tubing are also provided.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
22.
MODEL-BASED COMPENSATION FOR ENHANCED INFUSION PUMP DELIVERY ACCURACY
An infusion device includes a display and a pump configured for a predetermined volume per mechanical revolution (“VPMR”) under default environmental conditions. The infusion device receives infusion parameters that include (1) a requested flow rate of a fluid to be infused by the infusion device and, and (2) a head height and/or a patient height. The infusion device determines deviated environmental condition values as a function of (1) the received infusion parameters and (2) the default environmental conditions. The infusion device also determines a flow rate accuracy metric as a function of (1) the deviated environmental condition values and (2) an expected performance metric under the default environmental conditions. Responsive to determining the flow rate accuracy metric, the infusion device (a) displays, via the display, an indication of the flow rate accuracy metric; or (b) adjusts an operating speed of the pump based on the flow rate accuracy metric.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
Drip chambers are disclosed that can resist the formation of bubbles and turbulence in fluid moving through the drip chamber, and can include an inlet opening to an inner chamber formed at least in part by a sidewall having a portion that intersects a path of fluid droplets moving or falling from the inlet orifice into the inner chamber, where the path of fluid droplets causes the droplets to engage against a tangent impact plane at a location of the sidewall that is transverse relative to the path of fluid droplets such that the fluid droplets can slide from the impact plane into a pool of fluid within the inner chamber and exit the inner chamber through an outlet opening.
A cap for coupling to a medical adapter may include a housing with a closed top end and an open bottom end with legs that extend from the housing away from the bottom end. Members may extend from an inner surface of the legs to engage and secure the cap to a medical adapter or an insert configured to mate with a medical adapter. A cap may include angular ridges between a cap housing and an insert to permit rotation of the cap in single direction and prevent removal of the cap from a medical adapter. A cap may include hinged legs to permit the cap to be secured to a medical adapter by rotating the legs toward each other until a portion of a collar on each leg may be matingly joined around the medical adapter.
A61J 1/14 - Récipients spécialement adaptés à des fins médicales ou pharmaceutiques DétailsAccessoires à cet effet
A61M 5/32 - AiguillesParties constitutives des aiguilles relatives au raccordement de celles-ci à la seringue ou au manchonAccessoires pour introduire l'aiguille dans le corps ou l'y maintenirDispositifs pour la protection des aiguilles
A61M 5/50 - Dispositifs pour faire pénétrer des agents dans le corps par introduction sous-cutanée, intravasculaire ou intramusculaireAccessoires à cet effet, p. ex. dispositifs de remplissage ou de nettoyage, appuis-bras avec des moyens pour empêcher la réutilisation ou pour indiquer si le dispositif est défectueux, usagé, non stérile ou si l'on a tenté de l'utiliser
A61M 39/20 - Couvercles ou bouchons d'obturation pour connecteurs ou extrémités ouvertes de tubes
A coupler may include a coupler body including a first end, a second end, an outer surface, an inner surface defining a cavity, and a wall defined between the inner and outer surfaces, a plurality of first retaining fingers disposed adjacent to the first end and extending radially inward into the cavity, and a mounting aperture defined between a free end of each first retaining finger and the wall. The cavity may be configured to receive a first connector and a second connector. The plurality of first retaining fingers may be radially biased inward toward the cavity and configured to engage against a collar of the first connector to prevent axial motion of the first connector relative to the coupler. The mounting aperture may be configured to receive a pivot shaft of the collar to pivotally couple the first connector relative to a central axis of the coupler body.
A system and method for predicting an inventory update for the medication dispensing machine is disclosed. A care area is determined based on location of a medication dispensing machine and one or more prescribing patterns for one or more physicians in the determined care area is identified for the care area and for a period of time associated with the care area. An inventory update for the medication dispensing machine is determined based on the care area and the prescribing patterns being provided to a predictive algorithm, and a current inventory of the medication dispensing machine is adjusted based on the inventory update.
G16H 20/13 - 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 delivrés par des distributeurs
G06Q 50/22 - Aide sociale ou assistance sociale, p. ex. activités de développement communautaire ou services de consultation
G07F 17/00 - Appareils déclenchés par pièces de monnaie pour la location d'articlesInstallations ou services déclenchés par pièces de monnaie
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 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 50/20 - 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 diagnostic assisté par ordinateur, p. ex. basé sur des systèmes experts médicaux
27.
VIRTUAL ASSISTANT FOR INTERCONNECTING MEDICAL DEVICES
A method may include receiving a selection of an order associated with a patient. A scannable token, such as a barcode, may be generated for interacting with one or more medical devices involved in a patient encounter to fulfill the order. In some cases, the same scannable token may be further associated with one or more additional patient encounters associated with the same patient or different patients and conducted by a same clinician or different clinicians. The scannable token may be sent to a client device. In response to the scannable token being scanned at the one or more medical devices, at least a portion of information associated with the order may be sent to the one or more medical devices. Related methods and articles of manufacture are also disclosed.
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
G06F 21/34 - Authentification de l’utilisateur impliquant l’utilisation de dispositifs externes supplémentaires, p. ex. clés électroniques ou cartes à puce intelligentes
G16H 10/65 - 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 stockées sur des supports d’enregistrement portables, p. ex. des cartes à puce, des étiquettes d’identification radio-fréquence [RFID] ou des CD
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
A needleless fluid delivery device can be coupled to a valve to deliver fluid to a patient. When the device is withdrawn from the valve, the fluid inside the valve can leak out of the valve. This problem can be addressed with an anti-leak valve. The anti-leak valve can include a housing having a reception lumen and a delivery lumen that is transverse to the reception lumen. A guide bush is positioned in the reception lumen, and a silicon tube bears outwardly against the delivery lumen. When the device is inserted into the reception lumen, the device displaces the guide bush and compresses the silicon tube. This compression fluidly connects a hole in the guide bush to the delivery lumen, which facilitates delivery of the fluid. When the device is removed, the silicon tube seals the delivery lumen and restricts fluid from leaking out of the valve.
F16K 7/06 - Dispositifs d'obturation à diaphragme, p. ex. dont un élément est déformé, sans être déplacé entièrement, pour fermer l'ouverture à diaphragme tubulaire dont l'étranglement est assuré par une force extérieure radiale par tige filetée, came ou autre moyen mécanique
F16L 33/18 - Dispositions d'assemblage des manches avec des organes rigidesRaccords rigides pour manches, p. ex. éléments unitaires s'engageant à la fois dans deux manches caractérisées par l'emploi de moyens d'étanchéité additionnels
29.
SCAN-LESS AUTOMATED PROGRAMMING OF INFUSION DEVICES
A system for automatically programming an infusion device is disclosed. An infusion device can be activated to send a first message indicating that the medical device is ready to receive automated programming. A terminal, separate from the infusion device, may be used by a user to request an automated programming message be sent to an unidentified medical device, and the terminal displays the medical device as being ready to receive automated programming. The user may then confirm, using the terminal, that the automated programming message is for the medical device and the system automatically causes, responsive to receiving the confirmation, the automated programming message to be transmitted to the medical device, the automated programming message causing the medical device to be configured according to predetermined operational parameters.
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
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
A needleless fluid delivery device can be coupled to a valve to deliver fluid to a patient. When the device is withdrawn from the valve, the fluid inside the valve can leak out of the valve. This problem can be addressed with an anti-leak valve. The anti-leak valve can include a housing having a reception lumen and a delivery lumen that is transverse to the reception lumen. A guide bush is positioned in the reception lumen, and a silicon tube bears outwardly against the delivery lumen. When the device is inserted into the reception lumen, the device displaces the guide bush and compresses the silicon tube. This compression fluidly connects a hole in the guide bush to the delivery lumen, which facilitates delivery of the fluid. When the device is removed, the silicon tube seals the delivery lumen and restricts fluid from leaking out of the valve.
An infusion device receives an instruction indicating a total volume to be infused (VTBI) of a fluid for a pumping element to pump through a fluid tube into a patient connector. The infusion device pumps the fluid according to a pumping rate, and causes 2024/102124 an air-in-line sensor to measure an amount of air within the fluid tube according to a sensitivity level. The infusion device determines that a first VTBI threshold has been met, and outputs a notification or reduces the pumping rate. The infusion device determines that second VTBI threshold has been met, and increases the sensitivity level of the air-in-line sensor based on the first and second VTBI thresholds having been met.
A61M 5/36 - Dispositifs pour faire pénétrer des agents dans le corps par introduction sous-cutanée, intravasculaire ou intramusculaireAccessoires à cet effet, p. ex. dispositifs de remplissage ou de nettoyage, appuis-bras avec des moyens pour éliminer l'air ou pour empêcher l'injection ou l'introduction d'air dans le corps
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
Syringes are provided that include a syringe body defining a syringe cavity, a syringe port, and an indicator window, a medication plunger disposed within the syringe cavity and defining a medication chamber in the syringe cavity, a priming indicator comprising a first indicator portion and a second indicator portion, the priming indicator coupled to a plunger shaft of the medication plunger, wherein the priming indicator presents the first indicator portion through the indicator window in an unprimed position and presents the second indicator portion through the indicator window in a primed position, and a saline plunger disposed on the plunger shaft, the saline plunger disposed within the syringe cavity and defining a saline chamber in the syringe cavity. Medication delivery systems and methods to deliver medication via medication delivery systems are also provided.
Devices for creating positive fluid displacement are disclosed. Converting a device or system that typically creates a negative fluid displacement, either by design or through accidental misuse of the equipment, into a device or system that creates a positive fluid displacement can minimize risks associated with negative fluid displacement, including risks of infection. Existing devices for use in patient IV lines, such as needle-free connectors and slide clamp designs, can be modified to create positive fluid displacement.
Data is received that characterizes infusions administered to a patient among each of a plurality of infusion channels. Thereafter, a plurality of infusion events and respective event times are identified based on the received data. A temporal view of the infusion events can then be displayed in a graphical user interface and/or the temporal view of the infusion events can form part of a report. The temporal view segregates each channel into a separate swim lane with each swim lane visualizing infusion events for the corresponding channel at the respective event times. Related apparatus, systems, techniques and articles are also described.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
G16H 20/17 - 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 administrés par perfusion ou injection
G16H 40/60 - 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
Devices for creating positive fluid displacement are disclosed. Converting a device or system that typically creates a negative fluid displacement, either by design or through accidental misuse of the equipment, into a device or system that creates a positive fluid displacement can minimize risks associated with negative fluid displacement, including risks of infection. Existing devices for use in patient IV lines, such as needle-free connectors and slide clamp designs, can be modified to create positive fluid displacement.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
A sensor assembly for determining a receptacle fill level. The sensor assembly includes a bar having an adjustable feature that adjusts in response to a change in a fill level of the receptacle, one or more sensors configured to detect the adjustable feature of the bar, and a controller configured to determine, based at least on the adjustable feature of the bar, the fill level of the receptacle.
G06F 3/0481 - Techniques d’interaction fondées sur les interfaces utilisateur graphiques [GUI] fondées sur des propriétés spécifiques de l’objet d’interaction affiché ou sur un environnement basé sur les métaphores, p. ex. interaction avec des éléments du bureau telles les fenêtres ou les icônes, ou avec l’aide d’un curseur changeant de comportement ou d’aspect
37.
INTRAVENOUS SET INTEGRATION INTO INFUSION INTEROPERABILITY WORKFLOW
Methods are provided that include scanning, by a scanner, a barcode of an intravenous (IV) set, placing the IV set into service and automatically populating, by one or more processors in response to the scanning of the IV set barcode, fields of an electronic medical record system associated with a patient or fields of an infusion pump display. Systems and non-transitory machine-readable storage medium are also provided.
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
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
G06K 7/14 - Méthodes ou dispositions pour la lecture de supports d'enregistrement par radiation électromagnétique, p. ex. lecture optiqueMéthodes ou dispositions pour la lecture de supports d'enregistrement par radiation corpusculaire utilisant la lumière sans sélection des longueurs d'onde, p. ex. lecture de la lumière blanche réfléchie
A method includes receiving, by a master infusion device from a server, at least one fluid delivery protocol. The fluid delivery protocol includes one or more parameters for delivering a fluid to a user. The method also includes configuring, by the master infusion device, a first slave infusion pump with a first fluid delivery protocol of the at least one fluid delivery protocol. The method further includes configuring, by the master infusion device, a second slave infusion pump with a second fluid delivery protocol of the at least one fluid delivery protocol. The method also includes delivering, by the first slave infusion pump and based on the first fluid delivery protocol, the fluid to the user. Related methods and articles of manufacture, including apparatuses and computer program products, are also disclosed.
G16H 20/17 - 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 administrés par perfusion ou injection
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A secure receptacle includes within it a vertically-aligned carousel having a plurality of securable containers horizontally disposed around the carousel. Each container includes a securable lid preventing access to the contents of the container, and the vertically-aligned carousel is configured to lock in a secured position. A sensor within the secure receptacle determines a position of the carousel, and a motorized controller rotates the carousel to a requested position. On determining a requested container, the carousel is rotated so that the requested container is moved from a current position to the opening of the secure receptacle, and the securable lid of the requested container is actuated to provide access to its contents.
Certain aspects of the disclosure provide techniques for personalized chronotherapy. An example method includes obtaining sensor data associated with one or more sensors; determining a circadian rhythm based on the sensor data; determining a control schedule, for a device configured to deliver a therapeutic, based on the circadian rhythm and pharmacological data associated with the therapeutic; and controlling the device in accordance with the control schedule.
G16H 20/17 - 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 administrés par perfusion ou injection
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61M 5/172 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte électriques ou électroniques
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
A pumping segment recovery device coupled to a pumping mechanism is disclosed. The pumping segment recovery device includes a first arm segment, a second arm segment, a tube receiving space between the first arm and the second arm, and a connecting segment coupling the first arm segment with the second arm segment. The connecting segment is arranged below the tube receiving space. The first arm segment includes a first flared end to contact a pumping element before the pumping element contacts a fluid tube received in the tube receiving space, and the second arm segment includes a second flared end to contact the pumping element before the pumping element contacts the fluid tube received in the tube receiving space.
A method and system identifies interactions of a user with one or more medical devices, determines, for each of a plurality of clinicians, a performance score based on interactions data from one or more treatment devices pertaining to the clinician interacting with the one or more treatment devices to treat one or more patients in a healthcare facility, and receives identifying information for a clinician of the plurality of clinicians using a treatment device. When the performance score does not satisfy a threshold performance score, a restriction is set to display, on a display device, an alert pertaining to a follow-up activity to the clinician when the clinician interacts with the treatment device. The restriction is removed when the performance score satisfies the threshold performance score.
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
G06F 3/14 - Sortie numérique vers un dispositif de visualisation
G06Q 10/0631 - Planification, affectation, distribution ou ordonnancement de ressources d’entreprises ou d’organisations
G06Q 10/0639 - Analyse des performances des employésAnalyse des performances des opérations d’une entreprise ou d’une organisation
G06Q 30/018 - Certification d’entreprises ou de produits
G09B 19/00 - Enseignement non couvert par d'autres groupes principaux de la présente sous-classe
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 20/17 - 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 administrés par perfusion ou injection
G16H 40/60 - 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
G16H 50/20 - 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 diagnostic assisté par ordinateur, p. ex. basé sur des systèmes experts médicaux
G16H 70/20 - TIC spécialement adaptées au maniement ou au traitement de références médicales concernant des pratiques ou des directives
A method includes providing, on a computing device, when a user of the device is authorized, a user interface including respective representations of first medication administration functions and second medication administration functions associated with storage of the one or more medications and, in response to determining that the computing device is within the first predetermined area, enabling the computing device to perform the one or more first medication administration functions associated with the first predetermined area to cause, responsive to a selection of a displayed representation of the one or more first medication administration functions, a respective electronic medication storage cabinet associated with the selected displayed representation to perform an operation regarding a physical storage of a medication associated with a patient of the one or more patients, and preventing the computing device from performing the one or more second medication administration functions not associated with the first predetermined area.
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
A47F 3/02 - Vitrines ou meubles d'exposition avec systèmes de distribution
A47F 3/04 - Vitrines ou meubles d'exposition à air conditionné ou réfrigéré
A61J 7/00 - Dispositifs pour administrer les médicaments par voie buccale, p. ex. cuillèresDispositifs pour compter les pilulesDispositions pour l'indication ou le rappel du moment où l'on doit prendre des médicaments
B65D 83/04 - Réceptacles ou paquets comportant des moyens particuliers pour distribuer leur contenu pour distribuer de petits objets en forme d'anneau, de disque, de sphère ou similaire, p. ex. des comprimés ou des pilules
G06F 3/04842 - Sélection des objets affichés ou des éléments de texte affichés
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 20/13 - 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 delivrés par des distributeurs
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
H04W 4/029 - Services de gestion ou de suivi basés sur la localisation
44.
INTRAVENOUS SET INTEGRATION INTO INFUSION INTEROPERABILITY WORKFLOW
Methods are provided that include scanning, by a scanner, a barcode of an intravenous (IV) set, placing the IV set into service and automatically populating, by one or more processors in response to the scanning of the IV set barcode, fields of an electronic medical record system associated with a patient or fields of an infusion pump display. Systems and non-transitory machine-readable storage medium are also provided.
G16H 20/17 - 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 administrés par perfusion ou injection
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 40/63 - 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
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
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
45.
PATIENT CARE DEVICE CONFIGURED FOR AUTOMATIC ADJUSTMENT BASED ON IMAGE DATA
The present disclosure regards an infusion system that includes an infusion device, an imaging device, and a processor. The processor is configured to pump a fluid, and the imaging device is configured to convert a received image signal into image data. The processor is configured to receive an identifier for the fluid and determine that the fluid is associated with an imaging-based infusion protocol based on the fluid identifier. The processor is also configured to detect whether the imaging device is connected to the imaging probe and, responsive to detecting that it is connected, operate the infusion device at a first operating speed. Additionally, the processor is configured to receive the image data from the imaging device and determine a second operating speed based on the image data. Further, the processor is configured to operate the infusion device at the second operating speed.
G16H 20/17 - 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 administrés par perfusion ou injection
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
An infusion module operates an infusion pump to provide a patient therapy according to clinical information received from a first control module to which the infusion module is physically coupled. The infusion module is decoupled from the first control module and, while the infusion module is physically decoupled from the first control module, continues to provide the patient therapy according to the clinical information received from the first control module. When and based on the infusion module becoming physically coupled to a second control module, the infusion module provides the clinical information to the second control module and operates, while the infusion module is coupled to the second control module, the infusion pump to continue providing the patient therapy according to the clinical information.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/172 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte électriques ou électroniques
A61M 5/36 - Dispositifs pour faire pénétrer des agents dans le corps par introduction sous-cutanée, intravasculaire ou intramusculaireAccessoires à cet effet, p. ex. dispositifs de remplissage ou de nettoyage, appuis-bras avec des moyens pour éliminer l'air ou pour empêcher l'injection ou l'introduction d'air dans le corps
G16H 20/17 - 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 administrés par perfusion ou injection
47.
Patient care device configured for automatic adjustment based on image data
The present disclosure regards an infusion system that includes an infusion device, an imaging device, and a processor. The processor is configured to pump a fluid, and the imaging device is configured to convert a received image signal into image data. The processor is configured to receive an identifier for the fluid and determine that the fluid is associated with an imaging-based infusion protocol based on the fluid identifier. The processor is also configured to detect whether the imaging device is connected to the imaging probe and, responsive to detecting that it is connected, operate the infusion device at a first operating speed. Additionally, the processor is configured to receive the image data from the imaging device and determine a second operating speed based on the image data. Further, the processor is configured to operate the infusion device at the second operating speed.
A61M 5/00 - Dispositifs pour faire pénétrer des agents dans le corps par introduction sous-cutanée, intravasculaire ou intramusculaireAccessoires à cet effet, p. ex. dispositifs de remplissage ou de nettoyage, appuis-bras
A61M 5/172 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte électriques ou électroniques
Monitoring systems are disclosed that can include a fluid pathway formed in a housing to receive and direct a fluid through the housing, a sensor coupled to the fluid pathway to detect data for a fluid in the fluid pathway, a communication unit for conveying data sensed by the sensor, and a power source, where the systems of the present disclosure can be used for intravenous monitoring when coupled to a catheter or intravenous set, or can include a catheter needle extending from the housing, and in which the systems of the systems of the present disclosure can detect characteristics such as placement of a catheter, fluid pathway occlusion or patency, and catheter extravasation or infiltration.
Certain aspects of the disclosure provide techniques for personalized chronotherapy. An example method includes obtaining sensor data associated with one or more sensors; determining a circadian rhythm based on the sensor data; determining a control schedule, for a device configured to deliver a therapeutic, based on the circadian rhythm and pharmacological data associated with the therapeutic; and controlling the device in accordance with the control schedule.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
G16H 20/17 - 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 administrés par perfusion ou injection
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
Monitoring systems (100, 200, 300) are disclosed that can include a fluid pathway formed in a housing (120, 220, 320) to receive and direct a fluid through the housing, a sensor (130) coupled to the fluid pathway to detect data for a fluid in the fluid pathway, a communication unit (140) for conveying data sensed by the sensor, and a power source (152), where the systems of the present disclosure can be used for intravenous monitoring when coupled to a catheter (12) or intravenous set, or can include a catheter needle (380) extending from the housing (320), and in which the systems of the systems of the present disclosure can detect characteristics such as placement of a catheter, fluid pathway occlusion or patency, and catheter extravasation or infiltration.
A61M 25/06 - Aiguilles avec un guide pour piquer le corps ou analogues
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61M 1/36 - Autre traitement du sang dans une dérivation du système circulatoire naturel, p. ex. adaptation de la température, irradiation
A61M 1/00 - Dispositifs de succion ou de pompage à usage médicalDispositifs pour retirer, traiter ou transporter les liquides du corpsSystèmes de drainage
A61B 17/00 - Instruments, dispositifs ou procédés chirurgicaux
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61B 5/15 - Dispositifs de prélèvement d'échantillons de sang
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
A male luer connector is provided that includes a luer slip comprising a first material, the luer slip sized and shaped to mate with a female connector, a collar disposed on an outer surface of the luer slip, the collar comprising a second material, a plurality of first grip features disposed on an outer surface of the collar and a notch sized and shaped to receive a protrusion disposed on an outer surface of the luer slip and a grip coupled to the luer slip. Infusion sets and infusion set luer connector assemblies are also provided.
A pump system is disclosed that comprises a control unit and one or more modular infusion devices removably docked to the primary control unit. Each modular infusion device comprises a pumping mechanism and a processor configured to control the pumping mechanism and communicate with the control unit. The modular infusion device is configured to operate and pump a fluid while it is undocked from the control unit. The modular infusion device may wirelessly receive programming from a mobile device and may report operational status to the mobile device and/or a server remote from the modular infusion device.
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A method includes receiving, by an infusion pump administration (IPA) device from a first data tag coupled to a fluid storage, a fluid delivery protocol. The fluid delivery protocol includes a fluid parameter associated with the delivery, from a fluid pump, of a fluid from the fluid storage to a patient. The method also includes receiving, by the IPA device from a second data tag coupled to a patient ID, a patient parameter associated with the patient. The method also includes comparing, by the IPA device, the fluid parameter to the patient parameter. The method further includes configuring, by the IPA device, the fluid pump with the fluid parameter and the patient parameter. Related methods and articles of manufacture, including apparatuses and computer program products, are also disclosed.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
G16H 20/17 - 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 administrés par perfusion ou injection
The present disclosure regards a cabinet for cleaning medical devices. The cabinet includes a housing, a mechanical retainer, a robotic cleaning head, and a processor. The housing includes an enclosure for receiving one or more medical devices and a door configured to secure the enclosure. The mechanical retainer is positioned on a surface of the enclosure and configured to immovably couple the medical device to the surface while the medical device is received within the enclosure. The robotic cleaning head is movably coupled to another surface of the enclosure and configured to move therein and apply a cleaning agent to the medical device. The processor is configured to cause the cleaning head to move within the enclosure and apply the cleaning agent to clean the one or more medical devices after determining that the one or more medical devices are received within the enclosure and the door is securing it.
A61B 90/70 - Dispositifs de nettoyage spécialement adaptés aux instruments chirurgicaux
A61L 2/10 - Procédés ou appareils de désinfection ou de stérilisation de matériaux ou d'objets autres que les denrées alimentaires ou les lentilles de contactAccessoires à cet effet utilisant des phénomènes physiques des radiations des ultraviolets
A61L 2/24 - Appareils utilisant des opérations programmées ou automatiques
Methods and systems for infusing a user. An infusion pump includes a housing with an elastic component configured to expand and store potential energy. The infusion pump includes a first tube fluidically coupled to an outlet of the housing. The first tube is configured to conduct the fluid from the housing at a first flow rate. The infusion pump includes an air filter fluidically coupled to a distal end of the first tube via an air filter inlet. The infusion pump includes a second tube fluidically coupled to the air filter via an air filter outlet. The second tube is configured to adjust the first flow rate of the fluid conducted from the housing to a second flow rate. The infusion pump further includes one or more components for distributing the fluid to a user, the one or more components fluidically coupled to an outlet of the second tube.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/165 - Accessoires de filtrage, p. ex. filtres pour le sang, pour les liquides de perfusion
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
An apparatus for preserving an elasticity of a pumping segment of an infusion set into an infusion pump. The apparatus includes a rigid tubing support surface and one or more rotating members each comprising a keyway configured to receive one or more respective support keys fixedly attached to the pumping segment such that a rotation of a compressible tubing of the pumping segment is prevented from rotating with respect to the respective support keys. The rotating members at least partially rotate the pumping segment about a central axis of the pumping segment by causing the one or more respective support keys to at least partially rotate, while constraining the pumping segment in a predetermined linear position between the rigid tubing support surface and a pumping mechanism of the infusion pump and while the pumping mechanism applies a periodic compression force to the pumping segment.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/152 - Perfusion sous pression, p. ex. utilisant des pompes utilisant des réservoirs sous pression, p. ex. au moyen de pistons flexibles mis sous pression par contraction de réservoirs élastiques
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
The present disclosure regards a cabinet for cleaning medical devices. The cabinet includes a housing, a mechanical retainer, a robotic cleaning head, and a processor. The housing includes an enclosure for receiving one or more medical devices and a door configured to secure the enclosure. The mechanical retainer is positioned on a surface of the enclosure and configured to immovably couple the medical device to the surface while the medical device is received within the enclosure. The robotic cleaning head is movably coupled to another surface of the enclosure and configured to move therein and apply a cleaning agent to the medical device. The processor is configured to cause the cleaning head to move within the enclosure and apply the cleaning agent to clean the one or more medical devices after determining that the one or more medical devices are received within the enclosure and the door is securing it.
A61L 2/18 - Procédés ou appareils de désinfection ou de stérilisation de matériaux ou d'objets autres que les denrées alimentaires ou les lentilles de contactAccessoires à cet effet utilisant des substances chimiques des substances liquides
A61L 2/10 - Procédés ou appareils de désinfection ou de stérilisation de matériaux ou d'objets autres que les denrées alimentaires ou les lentilles de contactAccessoires à cet effet utilisant des phénomènes physiques des radiations des ultraviolets
A61L 2/24 - Appareils utilisant des opérations programmées ou automatiques
58.
DEVICES, SYSTEMS, AND METHODS FOR VALIDATING AUTOMATED PROGRAMMING REQUESTS
An infusion device includes a fluid pump and a processor. The processor is configured to receive an automated programming request (APR) from a device manager, where the APR includes an indicated order type. The processor is also configured to determine an implied order type for the APR based in part on whether the fluid pump is active. Additionally, the processor is configured to determine whether the indicated order type is compatible with the implied order type. If the indicated order type is compatible with the implied order type, the processor sends an acknowledgment message to the device manager and programs the fluid pump according to the operating parameters. However, if the indicated order type is incompatible with the implied order type, the processor sends a non-acknowledgment message and an error message to the device manager and rejects the command to automatically program the fluid pump according to the operating parameters.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/172 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte électriques ou électroniques
G16H 20/17 - 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 administrés par perfusion ou injection
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
Features relating to a wasting station that provides for secure collection, anonymous auditing, and safe disposal of medication are provided. The wasting station securely receives and stores wasted medication for later analysis. The wasting system may provide for waste containers that may include electronic tags, biomarkers, and/or reagents that may be used to analyze waste items. The wasting system may include support for witnessing the wasting process, either locally or remotely.
G06Q 50/26 - Services gouvernementaux ou services publics
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
An apparatus for preserving an elasticity of a pumping segment of an infusion set into an infusion pump. The apparatus includes a rigid tubing support surface and one or more rotating members each comprising a keyway configured to receive one or more respective support keys fixedly attached to the pumping segment such that a rotation of a compressible tubing of the pumping segment is prevented from rotating with respect to the respective support keys. The rotating members at least partially rotate the pumping segment about a central axis of the pumping segment by causing the one or more respective support keys to at least partially rotate, while constraining the pumping segment in a predetermined linear position between the rigid tubing support surface and a pumping mechanism of the infusion pump and while the pumping mechanism applies a periodic compression force to the pumping segment.
A syringe may be pre-filled with fluid and connected to a rapid infusion attachment to deliver a rapid bolus of fluid to a patient. The rapid infusion attachment may comprise a spring that, when compressed, provides a spring force to the plunger of the syringe. The device comprising the syringe and the rapid infusion attachment may be shipped and stored such that the syringe is pre-filled and the spring is pre-loaded, or compressed. The device may also be shipped and stored with the spring uncompressed, and a clinician or other user may compress the spring prior to attaching the device to an IV set or other fluid pathway. The device may further comprise a mechanism that allow the clinician to control the fluid flow. The device may also further comprise a locking mechanism that can be released when the fluid in the syringe is to be injected.
A61M 5/145 - Perfusion sous pression, p. ex. utilisant des pompes utilisant des réservoirs sous pression, p. ex. au moyen de pistons
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A syringe may be pre-filled with fluid and connected to a rapid infusion attachment to deliver a rapid bolus of fluid to a patient. The rapid infusion attachment may comprise a spring that, when compressed, provides a spring force to the plunger of the syringe. The device comprising the syringe and the rapid infusion attachment may be shipped and stored such that the syringe is pre-filled and the spring is pre-loaded, or compressed. The device may also be shipped and stored with the spring uncompressed, and a clinician or other user may compress the spring prior to attaching the device to an IV set or other fluid pathway. The device may further comprise a mechanism that allow the clinician to control the fluid flow. The device may also further comprise a locking mechanism that can be released when the fluid in the syringe is to be injected.
A61M 5/145 - Perfusion sous pression, p. ex. utilisant des pompes utilisant des réservoirs sous pression, p. ex. au moyen de pistons
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
An infusion pump determines a distance between a first element and a second element of an air-in-line sensor using a position sensor coupled to a housing and configured to detect a position of the second element. The first element is coupled to the housing behind a tubing receiving area, and the second element is configured to be positioned over the tubing receiving area and biased by a constant force toward the first element. The infusion pump sets a baseline tubing thickness of fluid tubing installed in the tubing receiving area according to the distance between the first element and the second element, configures an alarm threshold of the air-in-line sensor according to the baseline tubing thickness, and performs an infusion while operating the air-in-line sensor according to the alarm threshold.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A locking slide clamp includes a uniform body. The uniform body includes an aperture configured to allow a tubing to pass through the body. The aperture is configured to allow unrestricted flow of a fluid within the tubing when the tubing is at a first position of the aperture and restrict the flow of the fluid within the tubing when the tubing is at a second position of the aperture. The uniform body includes an engageable coupling mechanism, which may include a clasp, disposed at a first portion of the flexible uniform body. The coupling mechanism is configured to, when engaged, cover at least a portion of the release point of the aperture such that the tubing is locked in place within the pinch point of the aperture.
A61M 39/28 - Moyens de serrage pour l'écrasement des tubes flexibles, p. ex. brides de serrage à rouleaux
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A vision-enabled fluid flow rate detection system is disclosed. The system includes an image sensing device that images an infusion container supplying a fluid to an infusion pump and a pattern of markings associated with a surface of the container, and identifies a visual difference in the pattern from a default state of the pattern to determine a volume of fluid infused from the infusion container, and used to calculate a volume of fluid in the container and a flow rate of the fluid. When the amount of fluid, as determined by the vision system, differs from the amount reported by the pump, the pump's motor may be adjusted to correct the expected volume or flow rate, as needed. When a severe infusion inaccuracy is detected, an alarm or other indication may be provided, or the infusion terminated.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
66.
NEEDLELESS CONNECTOR DISINFECTION DEVICES AND METHODS
Needleless connector disinfecting devices are provided that include a body having a top surface and a bottom surface, a cavity in the body, the cavity configured to receive a needleless connector, a cartridge housing pivotably disposed on the top surface of the body, an activation arm disposed on the cartridge housing, a swab cartridge disposed in the cartridge housing and a disposal chamber disposed in the body, the disposal chamber configured to receive used cleaning swabs. Methods of using needleless connector disinfecting devices are also provided.
A61L 2/18 - Procédés ou appareils de désinfection ou de stérilisation de matériaux ou d'objets autres que les denrées alimentaires ou les lentilles de contactAccessoires à cet effet utilisant des substances chimiques des substances liquides
A61L 2/24 - Appareils utilisant des opérations programmées ou automatiques
A61L 2/28 - Dispositifs pour tester l'efficacité ou l'intégralité de la stérilisation, p. ex. indicateurs qui changent de couleur
A connector assembly can serve to couple first and second connectors using a clamp component. The first connector can have a central bore, an outer surface, and a slot extending radially inwardly from the outer surface to the bore. The slot can be configured to receive at least a portion of the clip component therein for restricting longitudinal movement of the clip relative to the first component. The second component can have a mating groove configured to engage with the engagement member of the clip component when the second component is positioned in the central bore of the first component for securing the second component in an engaged configuration relative to the first component. The second component can be removable from the central bore upon exertion of a separating force that dislodges the engagement member from the mating groove of the second component.
Needleless connectors are described that can include a housing and a flexible valve element, the flexible valve element positioned within a cavity of the needleless connector to selectively permit flow between proximal and distal fluid ports of the housing, and the flexible valve element including a valve head, a valve stem, and a valve diaphragm, the flexible valve element further including features to resist obstruction of fluid flow between the valve head and the valve diaphragm, including a fluid flow pathway along any of a shoulder of the valve head and the valve diaphragm, where the fluid flow pathway can be formed by any of a channel and a rib. The flexible valve element can further include a diaphragm formed as a bellows to resist or reduce strain on the flexible valve element when the needleless connector is activated.
A medication compounding system is described that is capable of receiving one or more medications and diluents and that includes an array of moveable transfer cartridges to access a medication container and to transfer medication. The transferred medication may be joined with a diluent to form a compounded medication. The resulting compounded medication may then be directed to a filling port where a compounded medication container may be coupled. A second medication container may align with a second transfer cartridge to transfer a second medication. Because the device may comprise one or more medications and diluents, a series of compounded medications may be created using an individual transfer cartridge for each medication.
A61J 3/00 - Dispositifs ou procédés spécialement conçus pour donner à des produits pharmaceutiques une forme physique déterminée ou une forme propre à leur administration
A61J 1/20 - Dispositions pour le transfert des liquides, p. ex. du flacon à la seringue
A61J 7/00 - Dispositifs pour administrer les médicaments par voie buccale, p. ex. cuillèresDispositifs pour compter les pilulesDispositions pour l'indication ou le rappel du moment où l'on doit prendre des médicaments
A connector assembly can serve to couple first and second connectors using a clamp component. The first connector can have a central bore, an outer surface, and a slot extending radially inwardly from the outer surface to the bore. The slot can be configured to receive at least a portion of the clip component therein for restricting longitudinal movement of the clip relative to the first component. The second component can have a mating groove configured to engage with the engagement member of the clip component when the second component is positioned in the central bore of the first component for securing the second component in an engaged configuration relative to the first component. The second component can be removable from the central bore upon exertion of a separating force that dislodges the engagement member from the mating groove of the second component.
A system for programming infusion devices for target controlled infusion is disclosed. The system includes a docking station and one or more processors configured to determine a first infusion device docked with a docking station and accept user input of one or more of patient-specific parameters, drug-related parameters, and a desired target concentration of a therapeutic agent in a workflow on the first infusion device for programming a target controlled infusion (TCI) therapy. After receiving a particular set of parameters, the set of parameters can be copied to the second infusion device to pre-complete and bypass a number of workflow steps of a second workflow of another infusion device. When the second workflow is accessed, the number of workflow steps of the second graphical interface workflow are pre-completed and bypassed.
G16H 20/17 - 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 administrés par perfusion ou injection
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
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
Needleless connectors are described that can include a housing and a flexible valve element, the flexible valve element positioned within a cavity of the needleless connector to selectively permit flow between proximal and distal fluid ports of the housing, and the flexible valve element including a valve head, a valve stem, and a valve diaphragm, the flexible valve element further including features to resist obstruction of fluid flow between the valve head and the valve diaphragm, including a fluid flow pathway along any of a shoulder of the valve head and the valve diaphragm, where the fluid flow pathway can be formed by any of a channel and a rib. The flexible valve element can further include a diaphragm formed as a bellows to resist or reduce strain on the flexible valve element when the needleless connector is activated.
A system for programming infusion devices for target controlled infusion is disclosed. The system includes a docking station and one or more processors configured to determine a first infusion device docked with a docking station and accept user input of one or more of patient-specific parameters, drug-related parameters, and a desired target concentration of a therapeutic agent in a workflow on the first infusion device for programming a target controlled infusion (TCI) therapy. After receiving a particular set of parameters, the set of parameters can be copied to the second infusion device to pre-complete and bypass a number of workflow steps of a second workflow of another infusion device. When the second workflow is accessed, the number of workflow steps of the second graphical interface workflow are pre-completed and bypassed.
A61M 5/172 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte électriques ou électroniques
G16H 20/17 - 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 administrés par perfusion ou injection
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
A method may include receiving, from a volume meter at a pump configured to deliver medication to a patient, data indicative of a volume of a medication present in a syringe inserted in the pump. A first counter may be updated, based on the data, in response to the medication being delivered to the patient as a first dose type. A second counter may be updated, based on the data, in response to the medication being delivered to the patient as a second dose type. The volume of the medication delivered to the patient may be determined based on the first counter and/or the second counter. An electronic alert may be sent to a mobile device in response to one or more anomalies being present in the volume of the medication delivered to the patient. Related methods and articles of manufacture, including apparatuses and computer program products, are also disclosed.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/315 - PistonsTiges de pistonGuidage, blocage, ou limitation des mouvements de la tigeAccessoires disposés sur la tige pour faciliter le dosage
H04W 4/14 - Services d'envoi de messages courts, p. ex. SMS ou données peu structurées de services supplémentaires [USSD]
H04W 4/20 - Signalisation de servicesSignalisation de données auxiliaires, c.-à-d. transmission de données par un canal non destiné au trafic
A connector assembly may include a cover defining a cavity, a luer portion extending through an open end of the cover, a proximal connector disposed at least partially in the cavity of the cover, a pusher mounted on the proximal connector, a distal connector at least partially disposed in the cover, and a stopwatch mounted on the cover and including at least one contact. The pusher may include a body portion and first and second pusher legs extending from the body portion. When the distal connector is coupled to a mating connector, the stopwatch may abut the first pusher leg such that the at least one contact is recessed within the stopwatch. When a force applied to the proximal connector exceeds a predetermined threshold the stopwatch may be separated from the first pusher leg and the at least one contact may extend proximally to activate a timer of the stopwatch.
Fluid connector systems that can include first and second valve assemblies that are couplable together to form a fluid pathway through the fluid connector system when the first and second valve assemblies are coupled together, and can resist fluid flow through each of the first and second valve assemblies when the first and second valve assemblies are separated from each other, where the first and second valve assemblies can include a compressible element or post positioned within a channel and configured resist fluid flow through the respective first or second valve assembly in a first position and to reduce the resistance to fluid flow through the first or second valve assembly in a second position, and the first and second valve assemblies including a sleeve and one or more arm configured to engage each other to form a snap fitting feature that can resist separation therebetween.
A flow restriction device may include a housing with first and second end portions forming respective first and second openings, and a cavity configured to receive an insert body defining a fluid passage that extends from a first opening of the housing at the first end portion to a second opening of the housing at the second end portion, where the fluid passage extends in more than one direction along a path between the first and second end portions of the housing to induce a resistance to a fluid flow moving through the device, thereby reducing a flow rate and pressure of the fluid, and where the fluid is blood, reduce the hemolysis index of the blood.
A medical system includes a medical device and a display for displaying a plurality of visual elements. The plurality of visual elements are associated with functions of the medical device. The medical system also includes a plurality of visual profiles for facilitating in controlling visual appearance of the plurality of visual elements displayed on the display, and a visual profile selector for selecting at least one of the plurality of visual profiles based on a state of the medical device.
G16H 20/17 - 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 administrés par perfusion ou injection
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
G06F 3/04847 - Techniques d’interaction pour la commande des valeurs des paramètres, p. ex. interaction avec des règles ou des cadrans
G09G 5/00 - Dispositions ou circuits de commande de l'affichage communs à l'affichage utilisant des tubes à rayons cathodiques et à l'affichage utilisant d'autres moyens de visualisation
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
A vision-enabled fluid flow rate detection system is disclosed. The system includes an image sensing device that images an infusion container supplying a fluid to an infusion pump and a pattern of markings associated with a surface of the container, and identifies a visual difference in the pattern from a default state of the pattern to determine a volume of fluid infused from the infusion container, and used to calculate a volume of fluid in the container and a flow rate of the fluid. When the amount of fluid, as determined by the vision system, differs from the amount reported by the pump, the pump's motor may be adjusted to correct the expected volume or flow rate, as needed. When a severe infusion inaccuracy is detected, an alarm or other indication may be provided, or the infusion terminated.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/172 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte électriques ou électroniques
A system and method for facilitating safe use of a medical device is provided. In one aspect, a method includes receiving an indication that a user has entered a set of parameters into a medical device to provide a medical treatment to a patient, receiving a history of previous medical treatment provided to the patient using the medical device, generating one or more alternative parameters for providing the medical treatment to the patient based on the set of parameters and the received history of previous medical treatment, causing, based on the generating of the one or more alternative parameters, a locking of the medical device to restrict operation of the medical device until an override of the lock is received, providing a notification for display to the user regarding the alternative parameters.
G06Q 10/0631 - Planification, affectation, distribution ou ordonnancement de ressources d’entreprises ou d’organisations
G06Q 10/06 - Ressources, gestion de tâches, des ressources humaines ou de projetsPlanification d’entreprise ou d’organisationModélisation d’entreprise ou d’organisation
G06Q 50/22 - Aide sociale ou assistance sociale, p. ex. activités de développement communautaire ou services de consultation
G16H 20/13 - 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 delivrés par des distributeurs
G16H 20/17 - 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 administrés par perfusion ou injection
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
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 vision-enabled fluid flow rate detection system is disclosed. The system includes an image sensing device that images an infusion container supplying a fluid to an infusion pump and a pattern of markings associated with a surface of the container, and identifies a visual difference in the pattern from a default state of the pattern to determine a volume of fluid infused from the infusion container, and used to calculate a volume of fluid in the container and a flow rate of the fluid. When the amount of fluid, as determined by the vision system, differs from the amount reported by the pump, the pump's motor may be adjusted to correct the expected volume or flow rate, as needed. When a severe infusion inaccuracy is detected, an alarm or other indication may be provided, or the infusion terminated.
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
G01F 22/00 - Procédés ou appareils pour la mesure du volume des fluides ou des matériaux solides fluents, non prévus ailleurs
82.
FLUID CONNECTOR ASSEMBLY WITH NEUTRAL FLUID DISPLACEMENT THAT LIMITS CONNECTOR DAMAGE
Fluid connectors assemblies that provide neutral fluid displacement without overlapping connectors are disclosed. A fluid connector assembly may include a housing and a pair of connectors (e.g., luers) coupled with the housing. A compressible member (e.g., bellow) is located within the housing. The first connector and the second connector each include a post with an opening. The compressible member can seal off the opening of the first connector from fluid entry. However, when the post of the second connector is inserted into the housing, the post of the second connector displaces the compressible member, causing the compressible member to uncover the opening, and further causes the compressible member to open in another location and receive fluid. Further, the compressible member seals each of the first connector and the second connector and forms a fluid path through the posts and the compressible member, with the seals regulating fluid flow.
A coupler having a first connector including a first end having an inlet and a second end opposite the first end having an opening. The first connector including at least one engaging member disposed between the first end and the second end. The coupler having a second connector including a body extending from an outlet portion. The body configured to be at least partially inserted into the opening to couple the second connector to the first connector. The outlet portion including at least one arm having a securing member configured to engage with the engaging member to secure the first connector to the second connector. When the second connector is coupled to the first connector, the outlet portion is exposed. The first connector is configured to decouple from the second connector in response to a pullout force exceeding a predetermined threshold force.
A system and method for enforcing a cleaning of a medical device are disclosed. A first medical device is determined to be exposed to a contaminant based on a use of the first medical device by a user or in a care area during a time period associated with the user or the care area being exposed to the contaminant, and at least one second medical device is identified that was physically associated with the first medical device after the first medical device was exposed to the contaminant and before the first medical device was cleaned. A message pertaining to the first medical device or the at least one second medical device being exposed to the contaminant is then caused to be displayed on a display associated with the first medical device or on a display associated with the at least one second medical device.
A61B 90/70 - Dispositifs de nettoyage spécialement adaptés aux instruments chirurgicaux
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
G05B 19/406 - Commande numérique [CN], c.-à-d. machines fonctionnant automatiquement, en particulier machines-outils, p. ex. dans un milieu de fabrication industriel, afin d'effectuer un positionnement, un mouvement ou des actions coordonnées au moyen de données d'un programme sous forme numérique caractérisée par le contrôle ou la sécurité
G05B 19/4155 - Commande numérique [CN], c.-à-d. machines fonctionnant automatiquement, en particulier machines-outils, p. ex. dans un milieu de fabrication industriel, afin d'effectuer un positionnement, un mouvement ou des actions coordonnées au moyen de données d'un programme sous forme numérique caractérisée par le déroulement du programme, c.-à-d. le déroulement d'un programme de pièce ou le déroulement d'une fonction machine, p. ex. choix d'un programme
G06F 3/041 - Numériseurs, p. ex. pour des écrans ou des pavés tactiles, caractérisés par les moyens de transduction
An infusion pump for detection of a fluid condition in a flexible tubing is provided. The infusion pump includes a memory storing instructions, and a processor configured to execute the instructions to determine a time-decaying parameter associated with a tubing force obtained by a sensor over time, the tubing force characterizing a force-time curve, and determine a fluid pressure value for a fluid in the tube based at least in part on the time-decaying parameter. A machine implemented method for detecting a fluid condition in a flexible tube is also provided.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
G01L 7/04 - Mesure de la pression permanente ou quasi permanente d’un fluide ou d’un matériau solide fluent par des éléments mécaniques ou hydrauliques sensibles à la pression sous forme de jauges, élastiquement déformables sous forme de tubes élastiques, déformables, p. ex. manomètres de Bourdon
G06N 5/04 - Modèles d’inférence ou de raisonnement
G16H 20/17 - 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 administrés par perfusion ou injection
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
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
G16H 50/50 - 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 la simulation ou la modélisation des troubles médicaux
86.
DISPOSABLE PISTON-DRIVEN CASSETTE FOR INFUSION SYSTEMS
A pump cassette is configured to be seated in, and connect to, a cassette recess of an infusion pump system. A cassette drive interface of the cassette is configured to interface with a corresponding pump drive interface provided by the infusion pump system when the cassette is seated in and connected to the cassette recess. The cassette includes multiple pistons that are operatively connected to the cassette drive interface and configured to, when the housing is seated in the cassette recess of the infusion pump system and the pump drive interface is actuated by the infusion pump system, operate in concert with each other to continuously move a fluid received from the inlet port to the outlet port.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
Seals for medical fluid connectors are disclosed. A seal as molded may have an elliptical cross-sectional shape, an aperture on the top face of the seal, a well inside the seal, and a divet on the bottom face of the seal. The seal as molded becomes assembled when it is constrained by a housing. When constrained by the housing, the seal has a circular cross-sectional shape, and the aperture becomes an elongate insertion area. The elongate insertion area is closed such that fluid cannot permeate the seal as assembled. However, the seal as assembled is penetrable by a center post through the elongate insertion area, and the center post creates a fluid path through the seal when the center post penetrates the seal.
A clamp assembly for adjusting the fluid flow rate in an infusion set is provided. The clamp assembly includes a housing having two opposing side walls spaced apart from each other and having opposing guide grooves, a guide wall disposed between the side walls, an elastomeric segment disposed between the two opposing side walls and the guide wall, the elastomeric segment having a lower compression set performance that the compression set performance of first and second IV tubes of the infusion set, and first and second tubing ports. A flow-regulating member is seated in the guide grooves and is configured to remain in a set position during use of the infusion set based on the compression set performance of the elastomeric segment until the roller wheel is moved by a user. A method of operating a clamp assembly is also provided.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 39/28 - Moyens de serrage pour l'écrasement des tubes flexibles, p. ex. brides de serrage à rouleaux
89.
FUNCTIONALIZED POLYOLEFIN SOLVENT BLENDS FOR DISSIMILAR MATERIALS BONDING
An adhesive formulation may include a functionalized polyolefin having a polyolefin backbone with a molecular weight in a range from 60,000 Da to 90,000 Da, and a solvent or a solvent mixture present in a range from 52 wt% to 82 wt%. The polyolefin backbone is functionalized by addition of a polar side chain to the polyolefin backbone.
C09J 5/00 - Procédés de collage en généralProcédés de collage non prévus ailleurs, p. ex. relatifs aux amorces
C09J 11/06 - Additifs non macromoléculaires organiques
C09J 151/00 - Adhésifs à base de polymères greffés dans lesquels le composant greffé est obtenu par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneAdhésifs à base de dérivés de tels polymères
C09J 123/28 - Adhésifs à base d'homopolymères ou de copolymères d'hydrocarbures aliphatiques non saturés ne possédant qu'une seule liaison double carbone-carboneAdhésifs à base de dérivés de tels polymères modifiés par post-traitement chimique par réaction avec des halogènes ou des composés contenant des halogènes
Flow path control devices and a method for delivering a medical fluid by flow path control device are disclosed. A flow path control device includes an inner housing and an outer housing. The inner housing includes a knob that rotates the inner housing relative to the outer housing. Rotating the knob activates different flow paths by aligning the flow paths with flow channels on the outer housing. Flow indicators on the inner housing are visible through windows in the outer housing and show a user of the flow path control device which flow channels are open. Additionally, at least one of the flow channels is an access port for a needleless fluid connector. When the flow channels are open, medical fluid can be transported through the flow channels.
Seals for medical fluid connectors are disclosed. A seal as molded may have an elliptical cross-sectional shape, an aperture on the top face of the seal, a well inside the seal, and a divet on the bottom face of the seal. The seal as molded becomes assembled when it is constrained by a housing. When constrained by the housing, the seal has a circular cross-sectional shape, and the aperture becomes an elongate insertion area. The elongate insertion area is closed such that fluid cannot permeate the seal as assembled. However, the seal as assembled is penetrable by a center post through the elongate insertion area, and the center post creates a fluid path through the seal when the center post penetrates the seal.
A clamp assembly for adjusting the fluid flow rate in an infusion set is provided. The clamp assembly includes a housing having two opposing side walls spaced apart from each other and having opposing guide grooves, a guide wall disposed between the side walls, an elastomeric segment disposed between the two opposing side walls and the guide wall, the elastomeric segment having a lower compression set performance that the compression set performance of first and second IV tubes of the infusion set, and first and second tubing ports. A flow-regulating member is seated in the guide grooves and is configured to remain in a set position during use of the infusion set based on the compression set performance of the elastomeric segment until the roller wheel is moved by a user. A method of operating a clamp assembly is also provided.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A method for medical device resource management includes monitoring a plurality of medical devices for adjustments to the medical devices during a period of time; identifying, based on the monitoring, the adjustments to the plurality of medical devices during the period of time; building a therapy profile associated with a patient and the medical devices based on the identified adjustments; identifying an adverse event pertaining the patient or a respective medical device of the plurality of medical devices; and after identifying the adverse event: generating, based on the therapy profile, a plurality of consecutive control signals to correct the adverse event, each being associated with a different one of the medical devices or a different user.
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
G16H 20/00 - 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
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
Flow path control devices and a method for delivering a medical fluid by flow path control device are disclosed. A flow path control device includes an inner housing and an outer housing. The inner housing includes a knob that rotates the inner housing relative to the outer housing. Rotating the knob activates different flow paths by aligning the flow paths with flow channels on the outer housing. Flow indicators on the inner housing are visible through windows in the outer housing and show a user of the flow path control device which flow channels are open. Additionally, at least one of the flow channels is an access port for a needleless fluid connector. When the flow channels are open, medical fluid can be transported through the flow channels.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
95.
DISPOSABLE PISTON-DRIVEN CASSETTE FOR INFUSION SYSTEMS
A pump cassette is configured to be seated in, and connect to, a cassette recess of an infusion pump system. A cassette drive interface of the cassette is configured to interface with a corresponding pump drive interface provided by the infusion pump system when the cassette is seated in and connected to the cassette recess. The cassette includes multiple pistons that are operatively connected to the cassette drive interface and configured to, when the housing is seated in the cassette recess of the infusion pump system and the pump drive interface is actuated by the infusion pump system, operate in concert with each other to continuously move a fluid received from the inlet port to the outlet port.
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/145 - Perfusion sous pression, p. ex. utilisant des pompes utilisant des réservoirs sous pression, p. ex. au moyen de pistons
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/172 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte électriques ou électroniques
96.
FUNCTIONALIZED POLYOLEFIN SOLVENT BLENDS FOR DISSIMILAR MATERIALS BONDING
An adhesive formulation may include a functionalized polyolefin having a polyolefin backbone with a molecular weight in a range from 60,000 Da to 90,000 Da, and a solvent or a solvent mixture present in a range from 52 wt % to 82 wt %. The polyolefin backbone is functionalized by addition of a polar side chain to the polyolefin backbone.
C09J 151/06 - Adhésifs à base de polymères greffés dans lesquels le composant greffé est obtenu par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneAdhésifs à base de dérivés de tels polymères greffés sur des homopolymères ou des copolymères d'hydrocarbures aliphatiques ne contenant qu'une seule liaison carbone-carbone
A method may include receiving a first transaction record indicating a first interaction with a first raw quantity of a first medication and a second transaction record indicating a second interaction with a second raw quantity of a second medication. The first transaction record and the second transaction record may be normalized by generating, based on an equivalent unit, a first normalized quantity of the first medication and a second normalized quantity of the second medication. A machine learning model may be applied to the normalized first transaction record and second transaction record to detect, based on the first transaction record and the second transaction record, an anomalous behavior. An investigative workflow may be triggered in response to the machine learning model detecting the anomalous behavior. Related systems and articles of manufacture, including computer program products, are also provided.
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
G06N 20/20 - Techniques d’ensemble en apprentissage automatique
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 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
The disclosed systems and methods provide hands-free inventory tracking of medical items. A method includes providing an augmented reality device attachable to a face of a user. The method also includes determining, using one or more sensors of the augmented reality device, a user action to be carried out with respect to a medical item. The system automatically determines, based on the information collected by the augmented reality device, an identification of a medical item and that a user currently associated with the augmented reality performed an action pertaining to the medical item at a storage location associated with the medical item. An inventory of medical items is then updated with the medical item based on the determined identification of the medical item, the storage location, and the user performing the action at the storage location.
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
G06F 3/01 - Dispositions d'entrée ou dispositions d'entrée et de sortie combinées pour l'interaction entre l'utilisateur et le calculateur
G06T 19/00 - Transformation de modèles ou d'images tridimensionnels [3D] pour infographie
G06V 10/70 - Dispositions pour la reconnaissance ou la compréhension d’images ou de vidéos utilisant la reconnaissance de formes ou l’apprentissage automatique
G06V 20/20 - ScènesÉléments spécifiques à la scène dans les scènes de réalité augmentée
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
99.
READY-TO-USE, TERMINALLY STERILE PACKAGING FOR SURGICAL ANTISEPTIC AND METHOD OF USE
A ready-to-use, gamma-ray sterilized, surgical antiseptic composition comprising an initial non-toxic concentration of povidone-iodine above a minimum effective concentration of available iodine, iodide in sufficient quantity to provide donor iodine upon gamma irradiation to stabilize said povidone-iodine and maintain said minimum effective concentration of available iodine, and a buffered saline solution.
A61K 31/4025 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à cinq chaînons avec un azote comme seul hétéro-atome d'un cycle, p. ex. sulpiride, succinimide, tolmétine, buflomédil non condensés et contenant d'autres hétérocycles, p. ex. cromakalim
A61K 47/22 - Composés hétérocycliques, p. ex. acide ascorbique, tocophérol ou pyrrolidones
A61L 2/00 - Procédés ou appareils de désinfection ou de stérilisation de matériaux ou d'objets autres que les denrées alimentaires ou les lentilles de contactAccessoires à cet effet
A61M 35/00 - Dispositifs pour appliquer des agents, p. ex. des remèdes, sur le corps humain
An integrated capacitive flowmeter for an infusion pump is disclosed. A conductive plate is attached to a hammer element that moves according to a cam motion in a pumping mechanism of the pump to periodically compress an flexible infusion line loaded in the pumping mechanism. A processor measures a first capacitance between the conductive plate coupled to the hammer element and a conductor opposite the flexible infusion line when the flexible infusion line is loaded between the conductive plate and the conductor in the pumping mechanism. A volume of the fluid within the flexible infusion line during the filling phase is then determined based on the measured capacitance, and a flow rate determined based on the determined volume and a cycle speed of the pump. The speed of the pump can then be adjusted based on a difference between the determined flow rate and a programmed flow rate.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
