Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
  • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
  • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
  • A61M5/142—Pressure infusion, e.g. using pumps
  • A61M5/14212—Pumping with an aspiration and an expulsion action
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
  • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
  • A61M5/168—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
  • A61M5/16804—Flow controllers
  • A61M5/16827—Flow controllers controlling delivery of multiple fluids, e.g. sequencing, mixing or via separate flow-paths
• • G—PHYSICS
  • G05—CONTROLLING; REGULATING
  • G05D—SYSTEMS FOR CONTROLLING OR REGULATING NON-ELECTRIC VARIABLES
  • G05D7/00—Control of flow
• • G—PHYSICS
  • G06—COMPUTING; CALCULATING OR COUNTING
  • G06F—ELECTRIC DIGITAL DATA PROCESSING
  • G06F13/00—Interconnection of, or transfer of information or other signals between, memories, input/output devices or central processing units
  • G06F13/14—Handling requests for interconnection or transfer
• • G—PHYSICS
  • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
  • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
  • G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
  • G16H20/10—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
  • G16H20/17—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M2205/00—General characteristics of the apparatus
  • A61M2205/60—General characteristics of the apparatus with identification means
  • A61M2205/6018—General characteristics of the apparatus with identification means providing set-up signals for the apparatus configuration
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M2205/00—General characteristics of the apparatus
  • A61M2205/60—General characteristics of the apparatus with identification means
  • A61M2205/6054—Magnetic identification systems

Definitions

• the invention relates to an injector for the intravenous and intra-arterial administration of parenteral solutions from containers containing a plurality of single doses of the parenteral solution.
• Cartridge injectors are known which apply single doses of cartridges and these cartridges are either empty and to be filled by the user from single or multidose containers of parenteral solution (WO2004 / 091688 A2), or the cartridges are already pre-filled with the parenteral solution (US 6,673,033 B1).
• RFID chip Radio Frequency Identification
• the RFID chip has an electronic data storage and thus allows the reading of information using a reader. With the RFID chip information is transferred from the cartridge to an injector. Transferred information is the product name, quantities, batch number, expiration date of the cartridge, pressure limit on removal from the cartridge.
• the problem with known injectors is that when using a container containing a plurality of doses of a parenteral solution, or from large cartridges containing multiple doses, users run the risk of applying too high doses of the solution, as there are no Limitation by the defined max. Filling volume gives as with the single-dose cartridge. Furthermore, there is a risk that after the first removal of the container or the large cartridge is used longer than acceptable for microbiological reasons, because after the maximum acceptable and specified by the manufacturer service life after opening nor solution in the container or the large cartridge is present.
• the injector may be a pump injector or a cartridge injector for large cartridges.
• multicontainer as used herein encompasses all types of containers, bottles or pouches.
• “Gross cartridge” means a cartridge or large bottle that is deflated by piston pressure and contains multiple doses of a liquid to be administered.
• the injector according to the invention is suitable to be connected to one or more multi-dose containers for fluid transfer.
• the pump injector may be connected via known fluid connections (e.g., tubing connections) to one or more multidose containers on the one hand and to a patient on the other hand.
• the cartridge injector With the cartridge injector, the exit of the cartridge is connected to a patient via known fluid connections (e.g., tubing connections).
• the compound On the patient's side, the compound can be e.g. into a venous catheter.
• parenteral solution can be taken from one or more multidose containers or large cartridges and can be injected individually or possibly in parallel.
• the multidose containers or large cartridges contain parenteral solutions which are administered to the patient.
• Each multidose container contains a variety of cans for application to a variety of patients.
• a container data memory With each multi-dose container or with each large cartridge, a container data memory, which can be read out wirelessly or via a cable connection (READ function), firmly connected.
• the container data memory can also be described in the same way (WRITE function).
• the container data store may be a Radio Frequency Identification (RFID) chip.
• RFID Radio Frequency Identification
• Other types of optical and / or electronic data storage, e.g. One-dimensional codes (barcodes), 2D codes (data matrix) or holographic memories are also suitable as container data storage.
• At least information on the identity of the product contained in the multi-dose container or the large-sized cartridge is stored in the container data memory.
• product data or other relevant data stored in other data stores may be associated with the multi-dose container or cartridge with the corresponding container data store.
• container data store e.g., Product-specific information such as lot number, maximum single dose and maximum useful life after opening the container, expiry date or capacity.
• the multidose containers or large cartridges contain parenteral solutions suitable for the examination, preferably saline or contrast media.
• the pump injector has at least one processor, a pump, an injector data memory and a device for data transfer and on.
• the processor is electronically connected to the injector data memory, to a control unit for the pump, and to the data transfer device.
• the device for data transfer is suitable to read the data from the container data memories.
• the cartridge injector includes at least one processor, a piston propulsion motor that drives the fluid out of the cartridge, an injector data memory and a data transfer device, and on.
• the processor is electronically connected to the injector data memory, to a control unit for the motor and to the device for data transfer.
• the device for data transfer is suitable to read the data from the container data memories.
• Information about different products and / or batch numbers can be stored in the injector data memory. This information is at least the maximum single dose and maximum useful life after opening the container. Other information contained in the operator data may include the lot number, maximum single dose and maximum useful life after opening the container, expiry date or quantity.
• the device for data transfer of the injector is suitable to read data wirelessly or via a cable connection from the container data memory and optionally to send data in the same way for storage in the container data memory.
• the data is transferred from the container data memory to the processor of the injector.
• These data already contain information on the maximum single dose and maximum useful life after opening the container, or the processor extracts this information from the injector data memory on the basis of the transmitted product identity information.
• the processor of the injector controls the control unit for the pump or motor so that no more than the maximum single dose at a time, i. is applied without interruption or within a certain period of time and / or that is not applied from a container or the large cartridge beyond the maximum period of use out.
• the processor checks whether the used Mehrdosenb e knowledgeers or the large cartridge has exceeded the expiration date.
• the expiration date is either taken from the injector data store or transmitted from the container data store to the processor.
• the injector may further include a screen which is also connected to the processor. The product information from the injector data memory or the transmitted product information from the container data memory can be displayed on the screen. Warnings on reaching the maximum dose, the maximum period of use or exceeding the expiration date can also be displayed on the screen and / or made audible by an acoustic signal.
• the device for data transfer of the injector is suitable for exchanging data wirelessly (radio, infrared) or via a cable connection (also for example optical fiber) with further data memories.
• further data memories may be e.g. a scanner for diagnostic purposes, a database within a facility for the medical care of patients or other systems for logistics, ordering processes, billing of services provided.
• Information about the injection protocol or product-specific information about the other data stores can be transferred from the injector.
• Information about the injection protocol includes the type of solution applied, the amount of solution applied, time / period of application, dose, flow rate, max. Pressure during solution injection, scan delay.
• Product-specific information includes product name, concentration, filling quantity, batch number, expiry date.
• the injector can also receive information from the other data stores via its device for data transfer.
• the information transferred from the injector can be used for further electronic data processing in the following ways: a) storing the information together with the image data from the examination with a scanner for diagnostic purposes of a patient, for example in a Radiology Information System (RIS) b ) Transmission of the information to a hospital information system (HIS) for filing
• RIS Radiology Information System
• HIS hospital information system
• FIG. 1 shows a pump injector system 10.
• Several multidose containers 12a to 12d are connected to the pump injector 16 via known hose connections 22a to 22d. Via valves 14a to 14d, the hose connections 22a to 22d can be opened or closed between the multidose containers 12a to 12d and the pump injector 16.
• the pump injector 16 On the output side, the pump injector 16 is connected via a further hose connection 20 to a venous catheter 18 on the patient.
• a container data memory 13a to 13d At each multi-dose container 12a to 12d is a container data memory 13a to 13d, which can be read from a data transfer device on the pump injector 16 attached.
• the pump injector 16 includes a processor 30 that is electronically connected to an injector data memory 32, to a control unit 38 for a pump 39, and to a data transfer device 34.
• the data transfer device 34 is adapted to read the data from the bin data stores 13a to 13d.
• the hose connections 22a to 22d are connected to the manifold 37 on the input side.
• the hose connection 20 leads from the outlet side of the distributor 37 via the pump 39 to the patient.
• Fig. 3 shows the data transfer between the pump injector 16, the container data memories 13a to 13d, a diagnostic scanner 40 and the database 42 of a Hospital Information System (HIS) or similar system.
• the data transfer 44a to 44d between the container data memories 13a to 13d and the means for data transfer 34 of the pump injector 16 preferably takes place wirelessly.
• the data transfer 46 between the device for data transfer 34 of the pump injector and the scanner for diagnostic purposes 40 can be wireless or via a cable connection, e.g. Infrared or optical fiber.
• the data transfer 48 between the device for data transfer 34 of the pump injector and the database 42 of a HIS can be wireless or via a cable connection.

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• Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Biomedical Technology (AREA)
• Life Sciences & Earth Sciences (AREA)
• Veterinary Medicine (AREA)
• Animal Behavior & Ethology (AREA)
• Hematology (AREA)
• Heart & Thoracic Surgery (AREA)
• Vascular Medicine (AREA)
• Anesthesiology (AREA)
• Physics & Mathematics (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Primary Health Care (AREA)
• Epidemiology (AREA)
• Medical Informatics (AREA)
• Medicinal Chemistry (AREA)
• Chemical & Material Sciences (AREA)
• General Physics & Mathematics (AREA)
• Theoretical Computer Science (AREA)
• General Engineering & Computer Science (AREA)
• Automation & Control Theory (AREA)
• Infusion, Injection, And Reservoir Apparatuses (AREA)
• External Artificial Organs (AREA)

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Applications Claiming Priority (3)

Publications (1)

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Family Applications (1)

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• 2010
  • 2010-11-24 RU RU2012126603/08A patent/RU2584451C2/ru active
  • 2010-11-24 EP EP10784766A patent/EP2504784A2/de not_active Ceased
  • 2010-11-24 JP JP2012540413A patent/JP6037559B2/ja active Active
  • 2010-11-24 MX MX2012005880A patent/MX2012005880A/es active IP Right Grant
  • 2010-11-24 AU AU2010323215A patent/AU2010323215B2/en not_active Ceased
  • 2010-11-24 US US13/512,548 patent/US9162026B2/en active Active
  • 2010-11-24 BR BR112012012466-8A patent/BR112012012466B1/pt not_active IP Right Cessation
  • 2010-11-24 CN CN201080053708.3A patent/CN102822830B/zh not_active Expired - Fee Related
  • 2010-11-24 CA CA2781816A patent/CA2781816C/en active Active
  • 2010-11-24 KR KR1020127016590A patent/KR101798671B1/ko active IP Right Grant
  • 2010-11-24 WO PCT/EP2010/068100 patent/WO2011064243A2/de active Application Filing
• 2012
  • 2012-05-15 IL IL219800A patent/IL219800A/he active IP Right Grant
  • 2012-05-24 ZA ZA2012/03807A patent/ZA201203807B/en unknown
• 2015
  • 2015-09-30 JP JP2015193504A patent/JP2016027884A/ja active Pending

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