WO2022199745A1 - Medizintechnisches gerät, system medizintechnischer geräte sowie verfahren zur konfiguration eines medizintechnischen geräts - Google Patents
Medizintechnisches gerät, system medizintechnischer geräte sowie verfahren zur konfiguration eines medizintechnischen geräts Download PDFInfo
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- WO2022199745A1 WO2022199745A1 PCT/DE2022/100170 DE2022100170W WO2022199745A1 WO 2022199745 A1 WO2022199745 A1 WO 2022199745A1 DE 2022100170 W DE2022100170 W DE 2022100170W WO 2022199745 A1 WO2022199745 A1 WO 2022199745A1
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- medical device
- medical
- mode
- configuration
- ventilation
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- 238000000034 method Methods 0.000 title claims abstract description 19
- 230000006978 adaptation Effects 0.000 claims description 2
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- 239000001301 oxygen Substances 0.000 description 8
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- 208000001953 Hypotension Diseases 0.000 description 3
- 208000008784 apnea Diseases 0.000 description 3
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- 101100407030 Arabidopsis thaliana PAO2 gene Proteins 0.000 description 2
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- 238000013194 cardioversion Methods 0.000 description 2
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- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 208000010496 Heart Arrest Diseases 0.000 description 1
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Classifications
-
- 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
- G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
- G16H40/60—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices
- G16H40/63—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
-
- 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
- G16H20/30—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to physical therapies or activities, e.g. physiotherapy, acupressure or exercising
-
- 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
- G16H20/40—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to mechanical, radiation or invasive therapies, e.g. surgery, laser therapy, dialysis or acupuncture
Definitions
- Medical device system of medical devices and method for configuring a medical device
- the invention relates to a medical device, for example in the sense of a ventilator or a defibrillator.
- the invention relates to a system of medical devices, wherein at least one of the medical devices is designed as a respirator or as a defibrillator.
- the invention relates to a method for configuring a medical device.
- a medical device be it a ventilator, a defibrillator or a system of medical devices, for example a ventilator and a defibrillator, that has a configuration suitable for all applications.
- a further object of the invention is to create a system of medical devices in which individual modes or processes can be configured by an operator or user of the system of medical devices without new device software having to be developed and installed on at least one medical device of the system .
- a further object of the invention is to specify a method for configuring a medical device that allows the configuration of new modes or sequences of control of a medical device by an operator or user of the medical device without new device software having to be developed and installed. According to the invention, this object is achieved by a method for configuring a medical device having the features of patent claim 8 .
- a medical device has at least one display, one input device, one memory device and one control unit.
- GUI graphical User Interface
- the input device is used to record user inputs, in particular also with regard to the configuration of the control sequence of the medical device, and in embodiments of the invention has one or more buttons, switches or rotary switches, or is additionally or exclusively as a touch input of the display educated.
- the medical device also has a therapy module that is designed for the therapeutic treatment of a patient.
- the medical device has a monitoring module that is used to record and/or monitor at least one vital parameter of a patient and/or at least one device-related measured value.
- the medical device has an acoustic output device, which is designed for the acoustic output of instructions to a human helper and/or for the acoustic output of alarms.
- the medical device has, in addition to the display, at least one optical output device which is designed to output optical signals, in particular to output alarms optically.
- the optical output device is designed as at least one light that lights up in color to output an alarm signal.
- optical alarms can also be output via the display in embodiments of the invention.
- a medical device enables its operator or user to configure their own modes for controlling the medical device.
- An operator of a medical device within the meaning of this document is, for example, an emergency service or a hospital.
- a user of a medical device within the meaning of this document is, for example, a paramedic or a paramedic of a rescue service.
- a mode is a sequence of the control of the medical-technical device, the control of the medical-technical device being defined by the sequential and/or parallel execution of functional elements.
- IPPV intermittent positive pressure ventilation
- the mode has various functional elements, which in the "IPPV” example include "actuation of the blower”, “measurement of pressure”, “evaluation of the measurement data” and “alarm”.
- the functional elements of a mode are usually parameterized, so that the manner in which the respective functional element is actually implemented can be configured via one or more parameters.
- the following parameters are mapped to the corresponding functional items: tidal volume (Vt), ventilation rate (f), positive end-expiratory pressure (PEEP), maximum inspiratory pressure (pMax), and the inspiratory-expiratory ratio (l:E).
- a user of a medical device according to the invention is thus provided with configurable ventilation modes, sequence control, guideline support, free choice of adjustable parameters and/or possibly setting ranges for parameters based on preprogrammed modes.
- the configurability of a medical device or a system of medical devices according to the invention is thus made possible by providing the options for selecting functional elements, determining the order of the functional elements and/or setting the parameters of the individual functional elements for an individual operating mode.
- individual modes for supraglottically intubated patients or for desaturated COPD patients can be configured freely or on the basis of predefined modes by an operator or a user of a medical device according to the invention.
- a configuration of a mode or the selection of specific parameters or settings on the medical device e.g. after a machine-assisted anamnesis of a patient, is also contemplated.
- the GUI provides a user interface for the graphical or programming language-based configuration of the medical device. For example, configuration by programming in XML is possible.
- the configuration also makes it possible to define decision trees, guidelines or expert systems.
- the adaptation of the control of the medical-technical device in a defined mode thus takes place in embodiments of the invention by the operator or user of the medical-technical device configuring the medical-technical device itself and not by installing adapted firmware.
- the GUI of the medical device has free “slots” for storing and selecting such individual modes.
- the medical device has a tool for graphically programming the modes, so that the configuration of individual modes is also supported by people who do not know a classic programming language.
- a medical device or a system of medical devices can be configured in a tree-like manner. In the sense of this document, this means that one or more subordinate parameters that are wholly or partially configurable are linked to a configurable parameter.
- the parameters assigned to a functional element are automatically configured to default values when the functional element is selected and arranged during the course of a mode.
- the at least one subordinate parameter is assigned to a configurable parameter
- the at least one subordinate parameter is also configured to a standard value when the configurable parameter is configured.
- the value of the at least one sub-parameter can be adjusted if required, provided that it is a configurable sub-parameter.
- dependent parameters are defined whose setting values influence one another, i.e. if a parameter is changed, the at least one dependent parameter that may be present is also automatically changed in accordance with a stored regulation.
- the modes and parameters mentioned below can be selected and/or configured for medical devices according to the invention designed as respirators or defibrillators.
- Possible modes for a ventilator are, for example: IPPV, aPCV (assisted Pressure Control Ventilation) possibly in conjunction with ASB (Assisted Spontaneous Breathing), PRVC (Pressure Regulated Volume Control) possibly in conjunction with ASB, BiLevel, possibly in conjunction with ASB , PCV, SIMV (synchronized intermittent mandatory ventilation) possibly in conjunction with ASB, S-IPPV, CPAP (continuous positive airway pressure) possibly in conjunction with ASB and CCSV (Chest Compression Synchronized Ventilation).
- the aPCV mode is used for pressure-controlled, assisted ventilation with a fixed mandatory ventilation frequency. If there is spontaneous breathing, the patient has the option of increasing the frequency and thus the minute volume. If the patient makes a spontaneous effort to breathe within a certain time window of expiration, the mandatory ventilation stroke is synchronized with the patient's breathing.
- the time window or trigger window can be set as a percentage of the expiration time (T e ) before the next expected mandatory ventilation stroke. If the patient makes a spontaneous effort to breathe outside the set trigger window, no mandatory ventilation stroke is triggered.
- the following ventilation parameters can be configured in this mode: plnsp: inspiratory pressure
- the controlled-assisted ventilation mode PRVC + ASB combines the advantages of pressure-controlled and volume-controlled ventilation.
- the set tidal volume is applied with the lowest possible ventilation pressure. Ventilation begins with three volume-controlled breaths at the set tidal volume.
- the device selects the measured plateau pressure as the starting value for the inspiratory pressure plnsp of the following pressure-controlled ventilation. It measures the administered volumes and adjusts the ventilation pressure. If the lung parameters change during ventilation, the device changes the inspiratory pressure plnsp in steps of a maximum of 3 mbar in order to reach the set tidal volume again and thus automatically compensate for changes in the patient. Measurement of applied volume is improved by compensating for tubing compliance.
- the set maximum pressure limit (pMax) ensures patient safety.
- the following ventilation parameters can be configured in this mode:
- Vt tidal volume (breath volume)
- the BiLevel + ASB mode is used for pressure-controlled ventilation combined with free spontaneous breathing at the pressure levels plnsp and PEEP throughout the respiratory cycle and adjustable pressure support at the PEEP level.
- This mode is used with patients who are not breathing spontaneously or with patients who are breathing spontaneously.
- the patient can trigger a mandatory, pressure-controlled ventilation stroke during a defined trigger window.
- the trigger window is 20% of the expiration time T e before the mandatory ventilation stroke to be expected.
- the rest of the time the patient can breathe spontaneously or with the help of pressure support.
- Tidal volume and minute volume result from the set plnsp, the lung compliance and the set inspiratory time T i .
- the following ventilation parameters can be configured in this mode: plnsp: Inspiratory pressure Freq.: Ventilation rate PEEP: Positive end-expiratory pressure pMax: Maximum inspiratory pressure
- the PCV mode is used for mandatory, pressure-controlled ventilation with fixed pressure levels. This mode is used in patients without spontaneous breathing. However, a spontaneously breathing patient can breathe freely during expiration. the The set maximum pressure limit (Pmax) ensures the safety of the patient.
- the following ventilation parameters can be configured in this mode: plnsp: inspiration pressure Freq.: ventilation frequency PEEP: positive end-expiratory pressure pMax: maximum inspiration pressure l:E: inspiration-expiration ratio
- SIMV is a form of ventilation in which a fixed minimum frequency is specified, but at the same time the ventilation frequency can be increased by self-breathing.
- the mechanical ventilation strokes are synchronized with the spontaneous breathing.
- the following ventilation parameters can be configured in this mode:
- Vt tidal volume
- the SIMV + ASB mode is used for volume-controlled ventilation with a fixed mandatory minute volume (MV).
- MV mandatory minute volume
- the patient can breathe spontaneously between the mandatory ventilation strokes and thus increase the minute volume. If there is spontaneous breathing, the mandatory ventilation stroke is synchronized with the patient's breathing. The mandatory minute volume and the mandatory respiratory rate remain unchanged.
- the set maximum pressure limit (pMax) ensures patient safety.
- the ventilation mode SIMV + ASB is also used as the mode for apnea ventilation.
- the patient can trigger a mandatory, pressure-controlled ventilation stroke during a defined trigger window.
- the trigger window is available in the last 20% of the expiratory time Te. The rest of the time, the patient can breathe spontaneously or with the help of pressure support.
- the following ventilation parameters can be configured in this mode:
- Vt tidal volume
- PEEP Positive end-expiratory pressure
- pMax Maximum inspiratory pressure
- ⁇ pASB pressure support (relative to the set PEEP)
- the S-IPPV mode is a volume-controlled ventilation mode with a variable mandatory minute volume (MV).
- MV variable mandatory minute volume
- a trigger is active during the entire expiration phase, which enables the patient to initiate another ventilation stroke. The patient thus has the opportunity to increase the respiratory rate and thus the minute volume MV and to adapt it to his needs. As a rule, this mode is used in patients with insufficient spontaneous breathing. Ventilation in S-IPPV mode corresponds to ventilation in IPPV mode, with the difference that synchronization with the patient's inspiratory efforts is possible. The patient can spontaneously trigger mandatory ventilation strokes due to the lower respiratory rate setting. A trigger window that extends over the entire expiration time is available for synchronization.
- the following ventilation parameters can be configured in this mode:
- Vt tidal volume
- InTr Inspiratory trigger pMax: Maximum inspiratory pressure
- CPAP ventilation is a form of ventilation that combines the patient's spontaneous breathing with a permanent positive pressure (PEEP) that is maintained during inspiration and expiration.
- PEEP permanent positive pressure
- CCSV mode In CCSV mode, a ventilation stroke is triggered synchronously with each chest compression. This means that no volume of gas can escape from the lungs and the increased pressure in the lungs ensures greater compression of the heart during cardiac massage. A frequency tacho helps the user to maintain the optimal compression frequency.
- An advantage of CCSV is that the ventilation mode can be used with mechanical chest compression devices.
- the monitoring of at least one vital parameter of a patient can be both an independent process, for example, through the functional elements "reading a Sensors”, “processing of the measured values” and “output of the measured values” can be defined in sequential order, or be part of a sequence in a specific mode, for example in the course of ventilation and/or defibrillation.
- the monitoring can be parameterized, for example, by the vital parameter(s) to be recorded, the sampling frequency and the form of the output (eg display of a measured value or output of a diagram with a progression over time).
- a patient In the inhalation mode, a patient is supplied with a constant volume flow of oxygen via a loose breathing mask or breathing cannula, but breathes spontaneously himself.
- Another mode that can be configured in embodiments of the invention is pre-oxygenation, in which a prophylactic enrichment of oxygen in the lungs of a patient is carried out before an induced respiratory arrest (apnea), for example as part of an anesthetic.
- the oxygen source of a medical device designed as a ventilator is controlled in such a way that the oxygen content of the breathing air supplied to a patient is made with pure or almost pure oxygen.
- the patient breathes freely and the ventilator or the ventilator's blower is only activated to compensate for the hose system.
- a timer preferably counts up the time of the intervention and this value is displayed to the user of a corresponding device.
- alarms can be configured in embodiments of a medical device according to the invention, which can be triggered, for example, by exceeding or falling below specified and possibly configurable threshold values.
- Such alarms are linked to one or more of the following parameters, for example: F high, F low (measurement of the patient's respiratory rate), PAW high, PAW low (PAW: Pressure Airways, airway pressure measured at the distal end or patient valve), CO2 high , Low CO2, High Vt, Low Vt, Hands Off (time of cessation of chest compressions), High CPR Rate, Low CPR Rate, Apnea (Not breathing), Patient Leak, High O2 Concentration, Low O2 Concentration, Medical Device Battery low, remaining time O2 short (ventilator's oxygen source), low inlet pressure, oxygen overdose, medical device temperature (device hot, device cold), medical device input voltage low, medical device input voltage high.
- the parameters can be set by free configuration by the user or within predetermined value ranges.
- the operator of a medical device can specify in an extended configuration mode protected by a password, for example, which parameters are fixed and which parameters may be configurable for a user and, if necessary, whether the configuration is free for a user or not can take place within predetermined value ranges.
- Adjustable parameters of the various functional elements of the modes are, for example, the inspiratory pressure (plnsp), the positive end-expiratory pressure (PEEP), the respiratory rate or ventilation rate, the tidal volume (Vt), Delta-P-ASB, the end-inspiratory pause, the ramp of the Inspiration, the expiration ramp, the waveform (decelerating flow yes/no), the inspiration trigger, the expiration trigger, the trigger levels, the l/E ratio and the maximum pressure (P Max).
- plnsp the positive end-expiratory pressure
- Vt tidal volume
- Delta-P-ASB Delta-P-ASB
- P Max maximum pressure
- the inhalation or exhalation effort of a patient is triggered (e.g. based on a volume flow or pressure measurement and exceeding or falling below a corresponding threshold value).
- a ventilator or, in particular, the blower of a ventilator can be controlled on the basis of such triggers to support the breathing of a patient.
- the medical device is designed as a defibrillator
- the following modes can be selected and/or configured in embodiments of the invention: monitoring, pacemaker (pacing), cardioversion (establishing the normal sinusoidal heart rhythm) and defibrillation (triggered manually).
- the charge (corresponding to the energy of the shock), rate and synchronization source of a cardioversion.
- an operator can specify whether these can be set by a user (yes, no). It is also possible for a user to specify an actual value and the maximum and/or minimum of the setting range for a parameter. Further functional elements with possibly assigned parameters (indented) are in embodiments of the invention:
- bradycardia slow heartbeat
- the view is configurable in embodiments of the invention in the sense that an operator and/or a user can select an individual representation on the display of the medical device for a mode.
- the operator can thus arrange setting fields, measured value fields, curves and trends on the display as desired, provide a user with various preconfigurations to choose from and/or block the user from changing the layout.
- a system of medical devices according to the invention has at least two of the following medical devices: ventilator, defibrillator, monitor, medical pad.
- at least one respirator or a defibrillator as a therapeutic medical device is always part of the system of medical devices according to the invention.
- a medical pad within the meaning of this document is used to issue instructions or, in general, guidelines to be used for a therapeutic procedure to a user of a system of medical technology devices, in particular to a human helper. Furthermore or alternatively, the medical pad can be designed to control a ventilator and/or a defibrillator.
- a monitor as an independent medical device within the meaning of this document is a medical device for monitoring at least one vital parameter of a patient.
- the monitor can also be part of the ventilator and/or the defibrillator and, if necessary, can be designed to monitor at least one device-related measured value.
- a system of medical devices according to the invention comprises at least one medical device according to the invention according to this document.
- the medical devices of a system of medical devices according to the invention are connected to one another for the exchange of data and/or control signals.
- a system of medical devices according to the invention can be configured by making entries on at least one medical device of the system for implementing processes. With the help of these processes, guidelines for the treatment of patients can also be implemented by a system of medical devices according to the invention, which require the use of several various medical devices, such as a ventilator and a defibrillator to implement life-saving measures.
- one of the medical-technical devices of the medical-technical system is designed as a master, which sends the control signals required to implement a selected sequence to the at least one other medical-technical device of the system.
- a medical technology system has a ventilator and a defibrillator.
- a method for configuring a medical device comprises at least the following method steps: - starting a configuration module on a medical device - selecting an existing operating mode of the medical device or a new operating mode to be created - detecting inputs from a user to select the operating mode of the medical device functional elements to be used, for configuring the order of the functional elements used and/or the parameters of individual functional elements of the operating mode using the medical device - saving the configuration of an existing operating mode or a new operating mode determined by the user input
- the configuration of a medical device or a system of medical devices serves to implement a specified sequence of functional elements.
- Such functional elements are, for example, the control of a ventilator and/or a defibrillator or the technical modules for implementing the intended function of the respective medical device.
- By specifically controlling the ventilator and/or the defibrillator special modes for treating a patient can be implemented.
- the individual functional elements can be parameterized by one or more, possibly dependent, parameters according to the above description of a medical device according to the invention.
- the parameterization is carried out, for example, by specifying the fan speed, so that the pressure and/or the volume flow of ventilation as well as the frequency and duration of ventilation can be specified.
- control of the ventilator are, for example, the state of the valve (open/closed), the volume flow source (blower and/or external source) and the pressure and/or flow sensors for the patient gas
- the parameterization takes place, for example, by specifying the number and/or the strength of the shocks (charge) and/or, if necessary, the duration and/or the frequency of the shocks.
- the parameterization takes place, for example, by specifying the position, the frequency, the depth, the direction and/or the relief of the cardiac massage by issuing instructions to a human helper and by a mechanical cardiac massage a corresponding control of a device for carrying out a cardiac massage.
- the configuration mode is implemented as software that is installed and executable on the medical device.
- the configuration mode uses the display of the medical device to output information relating to the configuration or configurations to a user.
- entering a password allows access to an extended configuration mode, which allows specifications about the scope of the normal configuration mode.
- both the normal configuration mode and the extended configuration mode are protected by passwords that are different from one another, so that access to the configuration and the scope of the configuration of the medical device can be reserved for appropriately trained persons.
- the configuration module can be executed independently of the medical device to be configured, for example locally on a PC or on the Internet, and the configuration generated can be stored.
- the configuration created is tested in embodiments of the invention using a device simulation.
- the generated and tested configuration is either manually loaded onto at least one medical device or, using an update server, onto a plurality of devices, for example onto all corresponding devices of an operator who generated the configuration.
- FIG. 1 A schematic representation of the block diagram of a medical device according to the invention
- Figures 2a-2c Schematic representations of a system of medical devices according to the invention.
- FIG. 3 A flow chart of a method according to the invention for configuring a medical device.
- FIG. 1 shows a schematic representation of the block diagram of a medical device (1) according to the invention.
- the medical device (1) has a control unit (2) with which the control sequence of the medical device (1) can be implemented for the various operating modes. Furthermore, the medical device (1) has a display (3), an input device (4), a storage device (5), a monitor (6), a therapy module (7) and an acoustic output device (8).
- the therapy module (7) includes the facilities required for the therapeutic treatment of a patient (20), depending on the configuration of the medical device (1).
- the therapy module (7) of a medical device (1) designed as a ventilator comprises, for example, a blower with the corresponding power electronics, an oxygen source, a tube system, a ventilation mask and a volume flow sensor and/or a pressure sensor and possibly a gas sensor (e.g. CO2 or O2).
- the therapy module (7) of a medical device (1) designed as a defibrillator comprises a charge store, power electronics and electrodes which are designed to deliver shocks to a patient (20).
- an operator or a user of a medical device (1) can adapt existing modes or create new modes by making entries via the input device (4).
- a mode generated in this way can be stored on the memory device (5) so that it can be called up by the control unit (2) for executing the corresponding mode.
- the control unit (2) can be used to control the therapy module (7), the display (3), the acoustic output device (8) and the monitor (6) and, if necessary, the memory device (5) to implement the selected mode.
- the monitor (6) has the devices required to record at least one vital parameter of a patient (20) and/or to record at least one device-related measured value.
- the monitor (6) and/or the therapy module (7) is/are arranged separately from the configurable medical device (1), so that a system of medical devices (10) according to the invention is formed.
- FIGS. 2a, 2b and 2c show different embodiments of such a system of medical devices (10) according to the invention.
- the system of medical devices (10) has a medical pad and a ventilator.
- the system of medical devices (10) has a medical pad and a defibrillator.
- the system of medical devices (10) has a medical pad, a ventilator and a defibrillator. This third embodiment is shown in FIG. 2a.
- the system of medical devices (10) has a ventilator and a defibrillator. This embodiment is shown in Figures 2b and 2c.
- a stand-alone monitor (6) can be used instead of the defibrillator or in addition.
- only the monitoring function of a defibrillator can be used.
- the embodiments of a system according to the invention shown in FIGS. 2b and 2c differ in the way in which the devices are linked. While communication between the devices takes place in the embodiment according to FIG. 2b, for example in order to exchange configuration data or to carry out synchronization, the devices in the embodiment shown in FIG. 2c operate independently of one another.
- FIG. 3 shows a flowchart of an embodiment of a method according to the invention for configuring a medical device.
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP22708304.5A EP4315351A1 (de) | 2021-03-26 | 2022-03-01 | Medizintechnisches gerät, system medizintechnischer geräte sowie verfahren zur konfiguration eines medizintechnischen geräts |
DE112022001759.7T DE112022001759A5 (de) | 2021-03-26 | 2022-03-01 | Medizintechnisches gerät, system medizintechnischer geräte sowie verfahren zur konfiguration eines medizintechnischen geräts |
CN202280018299.6A CN116917997A (zh) | 2021-03-26 | 2022-03-01 | 医疗技术设备、医疗技术设备系统以及用于配置医疗技术设备的方法 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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DE102021107674.9 | 2021-03-26 | ||
DE102021107674.9A DE102021107674A1 (de) | 2021-03-26 | 2021-03-26 | Medizintechnisches Gerät, System aus medizintechnischen Geräten sowie Verfahren zur Konfiguration eines medizintechnischen Geräts |
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DE102017202821A1 (de) * | 2017-02-22 | 2018-08-23 | Siemens Healthcare Gmbh | Verfahren zum Einstellen eines Betriebsparameters eines medizinischen Geräts und medizinisches Gerät |
DE102019129606A1 (de) * | 2018-11-07 | 2020-05-07 | Löwenstein Medical Technology S.A. | Beatmungsgerät und Verfahren zur Beatmung mit Sauerstoff |
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DE10057585A1 (de) | 2000-11-21 | 2002-05-29 | Erbe Elektromedizin | Vorrichtung und Verfahren zur automatischen Konfiguration von Hochfrequenz-Systemelementen |
DE112014004813T5 (de) | 2013-10-21 | 2016-07-07 | Fisher & Paykel Healthcare Limited | Atmungsunterstützungsgeräte-Benutzer-Schnittstelle |
DE102016015685A1 (de) | 2016-12-22 | 2018-06-28 | Drägerwerk AG & Co. KGaA | Vorrichtung zum Kontrollieren eines Betriebszustandes mindestens eines Medizingerätes in einem medizinischen Datennetzwerk sowie Medizingerät für ein medizinisches Datennetzwerk |
US11633159B2 (en) | 2019-05-06 | 2023-04-25 | Medtronic, Inc. | Personalization of artificial intelligence models for analysis of cardiac rhythms |
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DE102017202821A1 (de) * | 2017-02-22 | 2018-08-23 | Siemens Healthcare Gmbh | Verfahren zum Einstellen eines Betriebsparameters eines medizinischen Geräts und medizinisches Gerät |
DE102019129606A1 (de) * | 2018-11-07 | 2020-05-07 | Löwenstein Medical Technology S.A. | Beatmungsgerät und Verfahren zur Beatmung mit Sauerstoff |
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DE112022001759A5 (de) | 2024-03-28 |
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