EP4149348A1 - Dispositif et procédé pour effectuer des mesures alternées de pressions thoraciques et assurer l'étanchéité vis-à-vis de sécrétions oesophagiennes - Google Patents

Dispositif et procédé pour effectuer des mesures alternées de pressions thoraciques et assurer l'étanchéité vis-à-vis de sécrétions oesophagiennes

Info

Publication number
EP4149348A1
EP4149348A1 EP21734487.8A EP21734487A EP4149348A1 EP 4149348 A1 EP4149348 A1 EP 4149348A1 EP 21734487 A EP21734487 A EP 21734487A EP 4149348 A1 EP4149348 A1 EP 4149348A1
Authority
EP
European Patent Office
Prior art keywords
balloon
pressure
sealing
filling
catheter
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP21734487.8A
Other languages
German (de)
English (en)
Inventor
Fred GÖBEL
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Creative Balloons Maschinenbau GmbH and Co KG
Original Assignee
Creative Balloons Maschinenbau GmbH and Co KG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE102020002932.9A external-priority patent/DE102020002932A1/de
Application filed by Creative Balloons Maschinenbau GmbH and Co KG filed Critical Creative Balloons Maschinenbau GmbH and Co KG
Publication of EP4149348A1 publication Critical patent/EP4149348A1/fr
Pending legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6846—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive
    • A61B5/6847—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive mounted on an invasive device
    • A61B5/6852—Catheters
    • A61B5/6853—Catheters with a balloon
    • 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
    • A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/021—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes operated by electrical means
    • A61M16/022—Control means therefor
    • A61M16/024—Control means therefor including calculation means, e.g. using a processor
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6846—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive
    • A61B5/6885—Monitoring or controlling sensor contact pressure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/72—Signal processing specially adapted for physiological signals or for diagnostic purposes
    • A61B5/7235—Details of waveform analysis
    • A61B5/7246—Details of waveform analysis using correlation, e.g. template matching or determination of similarity
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    • A61B5/72—Signal processing specially adapted for physiological signals or for diagnostic purposes
    • A61B5/7271—Specific aspects of physiological measurement analysis
    • A61B5/7282—Event detection, e.g. detecting unique waveforms indicative of a medical condition
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J15/00—Feeding-tubes for therapeutic purposes
    • A61J15/0026—Parts, details or accessories for feeding-tubes
    • A61J15/003—Means for fixing the tube inside the body, e.g. balloons, retaining means
    • A61J15/0046—Expandable retainers inside body lumens of the enteral tract, e.g. fixing by radially contacting a lumen wall
    • A61J15/0049—Inflatable Balloons
    • 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
    • A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/04—Tracheal tubes
    • A61M16/0434—Cuffs
    • A61M16/044—External cuff pressure control or supply, e.g. synchronisation with respiration
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
    • A61B90/39—Markers, e.g. radio-opaque or breast lesions markers
    • A61B2090/3966—Radiopaque markers visible in an X-ray image
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61B2505/00—Evaluating, monitoring or diagnosing in the context of a particular type of medical care
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B2562/00—Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
    • A61B2562/02—Details of sensors specially adapted for in-vivo measurements
    • A61B2562/0247—Pressure sensors
    • A—HUMAN NECESSITIES
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    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/08—Detecting, measuring or recording devices for evaluating the respiratory organs
    • A61B5/0803—Recording apparatus specially adapted therefor
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/24—Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
    • A61B5/25—Bioelectric electrodes therefor
    • A61B5/279—Bioelectric electrodes therefor specially adapted for particular uses
    • A61B5/296—Bioelectric electrodes therefor specially adapted for particular uses for electromyography [EMG]
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    • A61B5/74—Details of notification to user or communication with user or patient ; user input means
    • A61B5/742—Details of notification to user or communication with user or patient ; user input means using visual displays
    • A—HUMAN NECESSITIES
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    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
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    • A61B5/74—Details of notification to user or communication with user or patient ; user input means
    • A61B5/7475—User input or interface means, e.g. keyboard, pointing device, joystick
    • 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
    • A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/0003—Accessories therefor, e.g. sensors, vibrators, negative pressure
    • A61M2016/0027—Accessories therefor, e.g. sensors, vibrators, negative pressure pressure meter
    • 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
    • A61M25/00—Catheters; Hollow probes
    • A61M25/10—Balloon catheters
    • A61M2025/1043—Balloon catheters with special features or adapted for special applications
    • A61M2025/1052—Balloon catheters with special features or adapted for special applications for temporarily occluding a vessel for isolating a sector
    • 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
    • A61M25/00—Catheters; Hollow probes
    • A61M25/10—Balloon catheters
    • A61M2025/1043—Balloon catheters with special features or adapted for special applications
    • A61M2025/1079—Balloon catheters with special features or adapted for special applications having radio-opaque markers in the region of the balloon
    • 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
    • A61M2205/02—General characteristics of the apparatus characterised by a particular materials
    • A61M2205/0272—Electro-active or magneto-active materials
    • A61M2205/0294—Piezoelectric materials
    • 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
    • A61M2205/33—Controlling, regulating or measuring
    • A61M2205/3331—Pressure; Flow
    • A61M2205/3344—Measuring or controlling pressure at the body treatment site
    • 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
    • A61M2210/00—Anatomical parts of the body
    • A61M2210/10—Trunk
    • A61M2210/1042—Alimentary tract
    • A61M2210/105—Oesophagus
    • 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
    • A61M2230/00—Measuring parameters of the user
    • A61M2230/40—Respiratory characteristics
    • 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
    • A61M25/00—Catheters; Hollow probes
    • A61M25/10—Balloon catheters
    • A61M25/1011—Multiple balloon catheters
    • 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
    • A61M25/00—Catheters; Hollow probes
    • A61M25/10—Balloon catheters
    • A61M25/1018—Balloon inflating or inflation-control devices
    • A61M25/10184—Means for controlling or monitoring inflation or deflation
    • A61M25/10185—Valves

Definitions

  • Device and method for alternating measurement of thoracic pressure and for esophageal secretion sealing dynamically adaptive, trans- or intra-esophageal seal comprising a catheter which is provided with at least one measuring and / or sealing balloon component that changes between two filling states, the filling state of the balloon component (i) in the measuring functional mode being a flaccid, has volume-defined, static filling of the balloon, and (ii) in the sealing function mode is preferably set in a pressure-controlled manner by pressure fluctuations caused by mechanical respiration and transmitted from the thorax to the esophageal or tracheal sealing balloon by a corresponding End displacements of the filling medium can be compensated for by a control unit connected to the catheter unit, and thus a sealing target pressure specified by the user is continuously maintained.
  • the ventilator connected to the patient senses pressure fluctuations or volume movements that occur in the hose system connected to the patient. If, when the patient begins to inhale (inspiration), there is a reduction in the pressure prevailing there in the inspiratory leg of the hose system or a measurable gas movement (flow) directed towards the patient, the device supports the breath initiated by the patient up to one
  • the ventilation pressure specified by the therapist and to be achieved at the end of inspiration (end tidal) or a desired end tidal breath volume (tidal volume) has been reached.
  • the aim of assistive ventilation is to preserve the patient's ability to breathe in the chest as much as possible so that, if necessary, the patient can be disconnected from the device quickly and without complications or the ventilation tube removed (extubation). After extubation, the patient should consistently perform sufficient breathing work without exhausting himself mechanically afterwards.
  • measuring catheters positioned in the esophagus (esophagus) of the patient are used, which are equipped with balloon components, which are usually filled with air in situ in a slack and tension-free manner.
  • the so-called esophageal pressure prevailing in the esophagus corresponds to a good approximation to the so-called intrathoracic pressure and is used as the standard for its clinical measurement.
  • An optimal approximation of the pressures is achieved if the balloon component of the measuring catheter is placed approximately in the area of the transition from the middle to the lower third of the esophagus.
  • the intra-thoracic pressure which is usually outside the patient and converted into an electrical signal via a pressure-sensing element, can be plotted as a coordinate over the respiratory gas volume (flow) measured by the ventilator at the same time as the patient moves.
  • the work of breathing performed by the patient is then mapped as an iterative, circular curve. The respective ability of the patient to breathe himself can thus be assessed over time.
  • the present invention provides esophageal pressure measurement catheters with the ability to seal the respective ones around the catheter shaft adjusting, residual, oesophageal lumen, whereby the rising of stomach contents into the throat of the patient (gastro-pharyngeal reflux) can be reduced or largely prevented.
  • the so-called aspiration of gastro-pharyngeal gastric contents is one of the well-known causes of ventilation-associated pneumonia.
  • the secretion that rises into the throat reaches the deep airways from there, which favors the development of inflammatory pulmonary complications.
  • gastro-pharyngeal reflux the patient's upper body is raised at a certain angle if possible, which can be clinically proven to reduce the incidence of ventilation-associated pneumonia.
  • the present invention should also enable a corresponding effect when the patient, medically indicated, has to remain in a flat body position. If the patient's thorax is already in the upper body position, the reflux-preventive effect can be further improved by the option of a continuous balloon tamponade of the esophageal lumen made possible within the scope of the invention. It is therefore desirable to be able to switch back and forth between two filling states of an esophageally placed balloon element in a simple manner.
  • volume-controlled filling state on the one hand, where the balloon element is filled with a predetermined volume of a filling medium
  • a pressure-regulated filling state on the other hand, where the filling pressure within the balloon element is kept approximately constant.
  • the balloon is supposed to perform an esophageal sealing function in order to allow gastric secretions to rise freely into the throat suppress or interrupt. This function can be optimally fulfilled if the balloon is regulated to a specified inflation pressure.
  • the balloon placed in the esophagus should assume a defined filling state, which allows the intra-thoracic pressure to be measured, whereby the catheter can be used for intermittent, respiratory mechanical monitoring of the actively breathing or machine-assisted thorax.
  • pressure regulation would be counterproductive, because then only the filling pressure, which is kept constant, would be measured and not the intra-thoracic pressure.
  • the invention uses a switchover of the control and regulation assembly in such a way that the inflation pressure of the balloon is regulated as constant as possible during a sealing state, while in a measurement state the pressure is not constantly regulated, but only a defined filling volume a filling medium is pushed into the balloon and then left to itself, so to speak, so that it is receptive to the thoracic pressure.
  • the invention provides that a switchover between the two functional states can be triggered manually as well as through a programmable time cycle.
  • Such a manual switchover can be carried out on a regulator unit that produces the pressure in the catheter balloon for the intermittently measuring function or maintains it synchronously with the mechanical pressure changes in the chest, in the sense of a continuous secretion seal.
  • the device or the regulating unit enable the change on the one hand manually, preferably at the push of a button. This enables a doctor or other operating personnel to switch to the measuring function mode at any time, for example, and to check the patient's current ability to breathe by himself and, if necessary, to adjust the ventilator manually.
  • the invention also provides for an automatic switchover, the controller unit automatically switching back and forth between the two functional modes on the basis of a programmable time cycle. Due to such a functionality, the device according to the invention is able to check the parameters for machine support in assisted breathing in a self-adaptive way at regular time intervals and, if necessary, to optimize or redefine them. Therefore, the device according to the invention can be used both as a preventive measure for pneumonia and for respiratory planning purposes. It has proven to be beneficial that the catheter is a nasogastric or orogastric into the esophagus or also through the stomach into the duodenum or into the jejunum, an embryo and / or decompression catheter. There is the possibility that the sealing balloon component tampons or seals the entire thoracic esophagus, or only covers the upper or lower half of the thoracic esophagus.
  • the invention recommends that the sealing and / or the measuring balloon is preformed with a diameter or circumference which exceeds the diameter or the circumference of the respective lumen, in particular the esophageal lumen.
  • the resulting advantage is that the lumen in question can be tamponized without tension, but still filling the space and sealing. Since the surface of the measuring balloon does not have to be stretched, the pressure inside the balloon element is equal to the pressure applied to the outside of the balloon envelope, in the present case the thoracic pressure in the area of the relevant, in particular esophageal, lumen.
  • the sealing and optionally also (the) measuring balloon has a balloon end which is extended proximally towards the extracorporeal catheter end, the diameter of which exceeds the outer diameter of the catheter shaft carrying the balloon and forms a gap through which the sealing balloon can be filled and pressurized.
  • the segment of the balloon that forms the balloon and / or the segment of the balloon that forms the gap can have a partially collapsing, web-like internal structure that at least partially keeps the supply line to the balloon open.
  • a permanently open flow connection between the intracorporeal, esophageally placed balloon on the one hand and an extracorporeal pressure regulator on the other hand ensures that dynamic pressure fluctuations can be regulated immediately at any time.
  • the measuring balloon component should be arranged in such a way that, when the catheter is properly positioned, it is in the lower half of the thoracic esophagus, aslo in the area of the diaphragm where the pressure fluctuations are greatest.
  • the sealing balloon and the measuring balloon are designed as structurally separate components that can be filled separately. If the same can be regulated to different pressures or filling volumes, the sealing balloon can be constantly pressure-regulated, while the measuring balloon is constantly filled only to a flaccid shape.
  • the measuring balloon can be arranged concentrically within the sealing balloon.
  • the measuring balloon it is also possible for the measuring balloon to be arranged in series below or distal to the sealing balloon.
  • Radiopaque markings on the tube of the catheter in particular in the region of the proximal and / or distal end of a balloon component, it is possible to make the length and / or position of the relevant balloon component or balloon components visible by means of an X-ray image. This enables the position of an esophageal catheter according to the invention to be corrected or optimized within a patient, if necessary, in order to achieve the highest level of sensitivity to pressure fluctuations or other signals to be recorded.
  • a control and / or regulator unit is or can be connected to the measuring and / or sealing balloon components of the catheter Function mode to control the filling volume of the respective measuring balloon in such a way that it assumes a slack, tension-free shape due to an incomplete, volume-defined filling, while in the sealing function mode the filling state of the respective sealing balloon is regulated under pressure control.
  • a control and / or regulator unit can be designed in such a way that at least three operating modes can be selected, namely a purely measuring function mode, a purely sealing function mode and an automatic operating mode in which the automatic control permanently changes between the measuring mode Function mode and the sealing function mode is triggered, in particular using a programmable time cycle.
  • a purely measuring function mode namely either the measuring function mode with a constant filling volume or the sealing function mode with a constant filling pressure.
  • there is also a third operating mode with switching back and forth between these two functional modes.
  • a selection module is provided with at least one logic output, the output signal of which is high in one functional state and low in the other.
  • the invention benefits from the fact that two possible functional states, namely measuring functional mode on the one hand and sealing functional mode on the other, can be represented by a single digital signal by assigning the logical value high to a first functional state and the logical value to the other functional state low.
  • the selection module can be constructed in the manner of a flip-flop or a bistable multivibrator, with a set input that sets the output signal at the logic output to high with a rising edge or with a high level of the input signal at this input, and with a reset -Input that sets the output signal at the logical output to low in the event of a rising edge or a high level of the input signal at this input.
  • a bistable flip-flop circuit thus forms a kind of “memory”, which remembers the last function mode set and retains it until a new, different - manual or machine - (toggle) command is issued.
  • a manual input means for example a switch or button.
  • the setting input of the selection module can be coupled to a programmable dead time or delay module, which starts the output signal at the logical output on a falling edge or at an inverting output on a rising edge and after a programmed or programmable time interval has elapsed supplies a rising edge to the set input; and / or the reset input is coupled to a programmable dead time or delay module, which starts the output signal at the logic output on a rising edge or the output signal on the inverting output on a rising edge and, after a programmed or programmable time interval has elapsed, a supplies a rising edge to the reset input.
  • one or more input signals of at least one OR gate can be switched or released by one or more logical blocking and / or release signals are unlocked, in particular via an AND gate each.
  • provision can also be made for one or more logical blocking and / or release signals to be derived from a further input option, in particular an input button.
  • the invention is preferably further characterized by a dynamically adaptive, trans- or intra-oesophageal secretion seal, preferably with one, wherein the actual value of the filling pressure in the balloon component or in a supply line thereof is recorded and kept as constant as possible by regulation to a predetermined setpoint , in particular with a regulator unit, which is constructed as an electro-pneumatic or electronic-pneumatic regulator, which in the sealing function mode, in particular in the state of the esophageal or tracheal seal, continuously maintains a target pressure specified by the user within the sealing balloon, with pressure fluctuations in the sealing balloon, in particular pressure fluctuations caused by mechanical respiration, ie pressure fluctuations occurring in the course of the patient's spontaneous breathing, due to corresponding shifts of Fill medium in and out of the balloon can be compensated to maintain the seal.
  • a regulator unit which is constructed as an electro-pneumatic or electronic-pneumatic regulator, which in the sealing function mode, in particular in the state of the esophageal or tracheal seal
  • the regulator unit connected to the alternately measuring and sealing balloon component of the catheter has at least one electronic, pressure-regulating valve which sets the respective filling pressure in the balloon.
  • This valve serves as an actuator on which the controller acts in accordance with a predetermined control algorithm, with the aim of keeping the filling pressure within the balloon component that can be placed in the esophagus as constant as possible.
  • control and / or regulating unit according to the invention should have a valve function leading to the balloon, via which volume can be supplied to the balloon in a defined manner, as well as a parallel valve function leading away from the balloon, via which volume is withdrawn from the balloon can be.
  • a constant filling volume of the balloon component can thus be set.
  • controllable valve components are designed as piezo-electronically operating actuators. Since only very small filling volumes are required in the case of a balloon placed oesophageally, solenoid valves are generally not fine enough, and therefore the invention prefers the use of piezo-electronic actuators.
  • the invention prefers an arrangement in which the pressure-regulating valve has an integrated or connected sensor function that measures the filling pressure in the balloon, in particular a sensor for the filling pressure in the balloon, the valve regulating the pressure in the balloon in such a way that a predetermined filling pressure can also be maintained in a continuous manner if there are pressure fluctuations in the balloon due to respiratory mechanics.
  • the respective valves can optionally be preceded by reservoir-like components that hold an overpressure or underpressure in stock, or the valves are connected to one or more external pressure sources.
  • the controller can have an assembly that applies a defined volume of air to the measuring balloon, and optionally removes it again from it.
  • a further, preferred object of a control and regulating assembly according to the invention is to generate a trigger signal for a connected ventilator as early as possible.
  • the said control and regulating assembly should have an adjustable function and / or assembly that recognizes measured pressure fluctuations in the thorax caused by respiratory mechanics, in particular an initial intra-thoracic pressure drop, as an indication of an incipient, active respiratory excursion of the thorax .
  • the advantage is that an oesophageal pressure drop can be measured much earlier and also more reliably than a pressure drop in the ventilation hose system itself.
  • control and regulation assembly If the control and regulation assembly has recognized an initial, intra-thoracic pressure drop as an indication of a beginning, active breathing excursion of the thorax, it can use such an intra-thoracic pressure drop to develop a trigger signal for the triggering of an assisted mechanical breath by a ventilator .
  • a comparator module which compares the pressure signal with an amount of pressure reduction required for triggering a triggering pulse for a ventilator.
  • Such a comparator can have the relevant pressure signal or a time derivative of the same at one of its inputs receive and at another of its inputs a preset or adjustable setpoint.
  • the control of the regulator assembly be programmed with a latency or dead time that allows a certain pressure drop in the sealing balloon before the volume compensation that maintains the setpoint takes place in order to obtain the trigger option for supporting, mechanical breaths .
  • control loop should remain interrupted until a trigger signal for a supporting, mechanical breath stroke has been generated.
  • the adaptive sealing function can then be resumed immediately.
  • the invention allows the visualized, continuous thoracic pressure signal to be displayed on a display device in order to inform a doctor or other operating personnel about the current status of the assisted ventilation.
  • one or more electrodes for receiving or deriving electrical signals from the patient can be arranged on the esophageal catheter.
  • the present invention thus describes a possible combination of an optionally measuring and / or sealing esophageal balloon catheter with electrode-like components for deriving electrical signals from the patient's diaphragm and from the structures innervating the diaphragm.
  • Corresponding methods are known, for example, in the context of so-called Edi catheter technology or NAVA ventilation methods (neurally adjusted ventilatory assist).
  • NAVA ventilation methods neuroally adjusted ventilatory assist
  • muscle action potentials of the diaphragmatic muscle can recognize the initial, early start of an inspiratory effort on the part of the patient and trigger machine support for the breath initiated by the patient at a point in time when the patient is not yet generating a gas flow directed towards the patient in the connected ventilation hose system the patient's lungs have not yet been folded to an extent that triggers such a patient-directed flow.
  • the invention further provides that the electrode (s) is (are) arranged on the surface of the tube or catheter shaft, in particular distal to the balloon element or all balloon elements. While the sealing function of the balloon component preferably takes place in an upper region of the esophagus, the electrode (s) should be located as close as possible to the diaphragm, that is, distal to the balloon element or elements.
  • Electrodes (s) distributed axially on the surface of the catheter shaft and spaced apart from one another offer the advantage that several electrode signals are available which sense a larger area in the vicinity of the diaphragm and can therefore sense potential fluctuations more reliably.
  • a reference electrode preferably supplies a common reference potential, which is preferably arranged proximally or distally of all other electrode (s).
  • the invention further recommends arranging the electrode (s) in a region of the catheter shaft which, when properly placed in the esophagus, penetrates the diaphragm because the strongest potential amplitudes naturally occur there.
  • the electrodes can be connected to an extracorporeal amplification, evaluation and / or monitoring module via a radio link, for example Bluetooth, in order to transmit the possibly digitized electrode signals;
  • a radio link for example Bluetooth
  • a cable offers a less complex option for information transmission, each electrode preferably being contacted individually, in particular via a multi-core cable with at least one core each for the individual connection of each electrode.
  • Each electrode is preferably contacted individually, in particular via a multi-core cable with at least one core each for the individual connection. each electrode, so that all phases can be evaluated individually and separately from one another.
  • the invention experiences a preferred development in that the extracorporeal amplification, evaluation and / or monitoring module has a module or a function for autocorrelation of the electrode signal or the electrode signals in order to recognize cyclically recurring sequences of the electrode signal or the electrode signals, because only on the basis of such Cyclically recurring sequences can be used to make repeatable statements about a current breathing cycle.
  • a pattern sequence is correlated with subsequent pattern sequences, with the degree or coefficient of correlation required for pattern recognition preferably being adjustable via an input element, for example using a rotary knob, preferably on a scale from -1 to +1 .
  • an input element for example using a rotary knob, preferably on a scale from -1 to +1 .
  • a further module or function can determine the correlation of one or more such reference electrode signals with measured, respiratory-mechanical pressure fluctuations in the thorax, in particular with an initial intra-thoracic one Pressure drop as an indicator of a beginning, active respiratory excursion of the thorax, in order to identify cyclically recurring sequences of one or more electrode signals in the stored reference patterns as indicators for the beginning of neuromuscular respiratory activity, or also typical for an beginning, active respiratory excursion of the thorax Relations between two or more electrode phases.
  • the aim is to find a typical pattern course or typical relationships between several pattern courses, from which it can be concluded that neuromuscular respiratory activity is beginning. This process is preferably fully automated and therefore does not require any assistance from the operator.
  • a pattern sequence or phase pattern sequence identified as typical for the beginning of neuromuscular respiratory activity as part of such an autocorrelation can be stored as a reference sequence or as a plurality of time-synchronous, phase-wise pattern sequences and is then available for a correlation in real time with currently measured electrode signals.
  • the degree or coefficient of correlation required for recognizing a match can be set via an input element, for example via a rotary knob, preferably on a scale from -1 to +1.
  • a trigger signal generated by the system according to the invention for an additional, mechanical breath stroke to a ventilator.
  • the least effort is to output the trigger signal as a pulse signal, e.g. as a voltage signal with 0 V corresponding to a low level and 5 V as a high level, or as a current signal with 4 mA as a low level and 20 mA as a high level if the ventilator has a corresponding logical input.
  • the trigger signal can be transmitted as a short command sequence.
  • Such a command sequence can also be transmitted by radio, for example via Bluetooth.
  • the invention provides that a trigger signal generated by the system according to the invention is sent as a pressure signal to a ventilator is transmitted by venting air from a ventilation hose leading from the ventilator to the patient by means of a pressure relief valve controlled by the control and / or regulating unit according to the invention in order to cause a pressure drop in the ventilation hose that can be detected by the ventilator.
  • a pressure drop is simulated for the ventilator in a recognizable manner, as it would be caused by the patient's diaphragmatic contraction of the diaphragm when inhalation began, and for which the ventilator is waiting anyway, but at a much earlier point in time than would be possible if the pressure drop were to occur would have to be effected by the patient himself.
  • this pressure relief valve must be closed as soon as possible after the ventilator has initiated a supporting mechanical breath so that this breath does not escape through the pressure relief valve but rather reaches the patient's lungs.
  • a pressure sensor is arranged on a ventilation hose, which is connected or can be connected to the control and / or regulating unit in order to signal to the control and / or regulating unit whether the ventilator has triggered an assisting, mechanical breath .
  • This sensor can also be used to sense the degree of the pressure drop caused by the pressure relief valve, so that it can be recognized whether the pressure drop that has occurred is sufficient to activate the ventilator.
  • the pressure relief valve can then be closed briefly, and if an immediately subsequent pressure increase indicates that the mechanical ventilation support has actually already been initiated, the pressure relief valve remains closed; otherwise it can be reopened to increase the pressure drop in the breathing circuit.
  • the pressure relief valve and / or the pressure sensor can be arranged on a Y-shaped connecting piece, where the common The ventilation hose from the endotracheal tube splits into an inspiration hose connected to the ventilator and an expiration hose, or else on a tubular connecting piece, which is preferably connected directly to the ventilator.
  • the invention is further characterized by an endotracheal tube, comprising a tube body penetrated by a lumen, the proximal end of which can be connected to a ventilation device via one or more ventilation tubes, and a cuff surrounding the tube body.
  • the cuff can be connected to the control and regulating device via connecting lines, in particular via hose lines via which the cuff communicates with the control and regulating device. This opens up the possibility for the open-loop and closed-loop control device to fill or (partially) deflate the cuff according to a predetermined and implemented algorithm.
  • a module or a function for dynamically adaptive, tracheal sealing of the cuff against the trachea can be provided in the control and regulator unit, the actual value of the filling pressure in the cuff or in a supply line being recorded and controlled by a controller is kept as constant as possible at a predetermined setpoint.
  • pressure fluctuations in the cuff caused by mechanical respiration i.e. pressure fluctuations occurring during the patient's spontaneous breathing, can be compensated for by shifting the filling medium into and out of the cuff in order to maintain the seal dynamically.
  • the invention can be developed further by a signal input on the control and regulation device for receiving data from a Ventilator, in particular the volume flow moved from or to the patient and / or the pleural pressure.
  • This information can be combined with the information generated by the control and regulation unit itself and, for example, displayed visually, preferably in the form of an iterating circle diagram or as a breathing work curve with the continuously measured thoracic or pleural pressure signal, plotted against the pressure signal moving from or to the patient Volume flow.
  • a graphic display device for example in the form of an LCD display, is suitable for this.
  • a method for switching a balloon component of a tube or catheter unit between two filling states namely (i) a first filling state of the balloon component in a measuring function mode, the balloon component being in a flaccid state and having a filling that is set statically in a volume-defined manner , and (ii) a second filling state of the balloon component in a sealing functional mode, the filling of the balloon component being dynamically adjusted in a pressure-controlled manner, in that pressure fluctuations transmitted to the balloon component are compensated for by corresponding displacements of a filling medium by a regulator unit connected to the catheter unit, so that a sealing target pressure specified by the user is continuously maintained, is characterized by a third functional mode, in which an automatic control permanently changes between the measuring functional mode and the sealing fun Action mode is triggered, in particular using a programmable time cycle.
  • the measuring function mode When the measuring function mode is selected, on the one hand, after the balloon has been initially emptied, a defined, predetermined volume of a filling medium is injected into the balloon, which converts the balloon into a flaccid, non-expanded state of filling of the balloon envelope.
  • the sealing function mode when the sealing function mode is selected, the regulating module either supplies or withdraws volume from the balloon in order to achieve and continuously maintain a set sealing pressure target value.
  • the derivation of a relatively early trigger signal to initiate a supporting mechanical breath, somewhat delayed, can also be made possible by measuring or sensing a thoracic pressure fluctuation, the pressure progression being made possible by a pressure sensor placed in the patient's esophagus or trachea Balloon or cuff is detected, and converted by the control and regulation unit or by the connected ventilator (ventilator) into an electrical signal, visualized and processed by its control in a regulating manner.
  • the invention particularly points to the combination of a continuous derivation of an electrical signal with the continuous or intermittent derivation of a thoracic mechanical signal. While electrical signals cannot provide any direct information about the extent to which a breathing excursion of the patient's thorax is actually developing, the mechanical success of a breathing effort can be recorded through the course of the thoracic pressure or pleural pressure, displayed in the course, analyzed for the device control and by the user for ongoing ventilation planning can be used.
  • the combination of the two methods described in the context of the invention enables in particular: the verification of a derived electrical signal as actually belonging to a mechanical diaphragmatic action; the determination of the actual point in time of the transition of an electrical signal into a thoracic measurable change in the pieura Pressure and the quantitative correlation of the electrical signal strength with that of the respective onset of mechanical response;
  • 1 shows an overall overview of the device, comprising a catheter unit, supply lines and connecting elements for identifying the catheter unit, as well as various functional components of a regulation and control unit;
  • 2a shows a schematic cross-section through an esophageally positioned balloon catheter in the balloon-carrying section of the catheter shaft, the balloon assuming a slack tamping state according to the invention;
  • 2b shows a balloon body with a balloon end directed proximally (orally) and shaped beyond the shaft dimension, for the coaxial filling or pressurization of the balloon;
  • 2c shows a special shaft profile of the catheter to ensure an uninterrupted, continuously maintained volume flow between the esophageal balloon and an external volume reservoir or an external pressure or volume source;
  • 3a shows a modified embodiment of the catheter unit with two concentrically arranged, esophageal balloons
  • 3b shows a further embodiment of the device with two serially arranged, esophageal balloons
  • FIG. 4 shows a catheter unit, which is supplemented by electrodes integrated in the catheter shaft for the derivation of electrical signals from the diaphragm and / or efferent nerves to the diaphragm;
  • FIG. 5 shows two module units working in conjunction with the catheter unit described in FIG. 4 for the visualization and processing of patient-derived electrical signals as well as for the synchronous monitoring of the corresponding respiratory response of the patient;
  • FIG. 6 shows a switchover logic for the optional switchover to a measuring function mode or a sealing function mode, whereby the automatic system is not switched off, but only interrupted;
  • FIG. 7 shows another embodiment of a switchover logic, it being possible to switch between an automatic function mode and a manual function mode with a selector switch, in the latter again a manual measuring function mode and a manual sealing function mode can then be selected;
  • FIG. 8 shows a further modified embodiment of the invention, it being possible to switch directly between a purely measuring function mode and a purely sealing function mode and an automatic function mode, in the latter being permanently time-controlled toggling between a measuring function mode and a sealing function mode;
  • 9a shows a further modified embodiment of the invention, the trigger signal being transmitted to the ventilation tube with a valve and then being passed on to the ventilation device as a pressure signal via this tube;
  • FIG. 9b shows an embodiment of the invention similar to the system from FIG. 9a, but with a different type of valve
  • FIG. 10a the valve assembly from FIG. 9a in a larger representation
  • FIG. 10b shows the valve assembly from FIG. 9b in a larger representation
  • FIG. 11 shows a time diagram with the pressure profile within the ventilation hose, the filling pressure within one in the esophagus placed balloon element, and the balloon pressure within the cuff of an endotracheal tube, each applied during two respiration cycles in the case of machine-assisted ventilation, the case being shown on the left in FIG 11 on the right of the illustration according to FIG. 11, the mechanical breath stroke is triggered after the pressure curve within the balloon placed oesophageally;
  • FIG. 12 shows a time diagram corresponding to FIG. 11 with the corresponding pressure profiles, the case being shown again in FIG the mechanical breath is triggered according to the potential curves measured by means of the electrodes placed on the esophageal catheter.
  • the drawing shows the invention using an esophageal sealing catheter 1 as an example. This should not, however, obscure the fact that almost all aspects of the present invention can also be applied to an endotracheal tube with a tracheal sealing balloon element in the form of a cuff.
  • the catheter unit 1 describes the individual components of the device in an exemplary connection representing the functional principle of the invention.
  • the catheter unit 1 is equipped in the thoracic segment of the esophagus 3 with a balloon element 1a which is already molded to the required working size during manufacture.
  • the preferred embodiment of the catheter itself corresponds to the typical design of a naso-gastric decompression or feeding tube. It reaches with its distal end 4a into the stomach of the patient, but in alternative versions it can also, for so-called enteral nutrition, go beyond the stomach into the The duodenum and jejunum are sufficient.
  • the inlet and outlet lumen of the catheter shaft 4 merges into a common connector 4b for the supply of nutritional solution and / or for the decompression or discharge of stomach contents.
  • a hose-like connection 1b which merges distally into a supply lumen, via which the balloon element 1a is filled with a preferably gaseous medium or pressurized.
  • the leading lumen can be integrated, for example, extruded into the wall of the catheter shaft 4, or it can also be formed as a film tube-like extension of the proximal balloon end that envelops the shaft tube.
  • the connecting hose terminates at the end with a connector 1c, which - if necessary via a further hose line 1d - allows a connection to a control unit 5 located outside the body, which cannot be confused.
  • the hose feed line 1d from the regulator 5 to the connector 1c should have a circular lumen of at least 5 mm in diameter in order to avoid flow-related pressure losses and dampening effects between the balloon and the regulator.
  • Upstream of the supply line 1d are two flow or pressure regulating valve units D and U, the unit D regulating the inflow to the patient and the unit U regulating the outflow or the delivery of volume to the environment.
  • the valves D and / or U are preferably based on a piezo-electronic construction and function and are therefore particularly low-noise and energy-efficient.
  • Reservoir chambers PD and PU are connected upstream of the two valves D and U and hold either a specific pressure (PD) or a negative pressure (PU) in stock as a predetermined setpoint value.
  • the valves D and U communicate with the respective associated reservoir PD or PU.
  • a pressure or a negative pressure can take place through a respective connection to an external supply unit ZV.
  • the module 5 also has an assembly Z for volume injection into the balloon element 1a of the catheter 1. Via a piston-cylindrical arrangement KZ, for example, a defined amount of air can flow from the cylinder into the balloon element 1a or the lumen 1b, 1 leading to the balloon element 1a d be moved.
  • the volume is preferably injected in a fixed setting by the controlling software of the module, but it can also be variably set by the user.
  • Other mechanisms are possible as non-adjustable variants, such as those ensured by a hose connector that spontaneously and elastically erects and that is built into a rigid cylinder housing the hose element, the cylinder being pressurized during the injection process and thus the contents of the hose connector to the catheter balloon 1a squeezes out, and automatically straightens up again when the cylinder is decompressed.
  • the balloon is emptied by opening the vacuum valve U.
  • the valve U then closes, and a certain amount of a filling medium is passed from the injecting unit Z via a bypass ZB to the inlet of the pressure valve D, which flows off to the balloon 1a when the valve is open.
  • Valve D then closes.
  • the valve D and / or the valve U have a pressure-measuring function which, in the phase of esophageal pressure measurement, continuously detects the pressure in the balloon and the supply line to the balloon and derives it as a signal for monitoring the pressure profile.
  • the measurement of the esophageal pressure is preferably carried out with a gaseous medium, the volume of which in combination with the medium-carrying volumes of the catheter unit 1 is dimensioned such that the balloon element 1a turns into a flaccid Filling passes over in order to avoid stretching of the balloon envelope, which would impair the quality of the measurement, in any case.
  • the unstretched state of the balloon envelope ensures that any deflection of the pressure in the esophagus can be recorded, or that values can be recorded that cannot be measured in comparison with an expanded balloon envelope.
  • valve D opens and the pressure in the balloon element 1a is regulated to the sealing pressure DP selected by the user, and is kept there continuously in the subsequent phase of the regulated sealing.
  • the regulation takes place in its ideal form through the interaction of active supply and active removal of filling medium in / to the catheter balloon 1a.
  • This regulation can take place by means of a programmable control, logic and / or regulation unit, whereby a higher-level control logic SL can be used to switch between a measuring function mode FM, in which the filling state of the balloon element 1a is controlled to a constant filling volume, and a sealing function mode FS, in which the filling state of the balloon element 1a is regulated to a constant filling pressure, to switch back and forth.
  • a higher-level control logic SL can be used to switch between a measuring function mode FM, in which the filling state of the balloon element 1a is controlled to a constant filling volume, and a sealing function mode FS, in which the filling state of the balloon element 1a is regulated to a constant filling pressure, to switch back and forth.
  • This higher-level controller SL has an input option with at least two options that switch the system either to the functional state FS of the seal (key S, Sealing) or to the functional state FM of the measurement (key M, monitoring).
  • the change between these two functional states can, on the other hand, also be specified automatically or by a control algorithm, for which a key A (automatic) can be provided.
  • the higher-level controller SL can be constructed as shown in FIG. 6, for example.
  • a bistable multivibrator 22 can preferably have, with a non-inverting output Q1, which is indicated by a high level on Input S1 is set and a high level is reset at input R1.
  • the bistable flip-flop 22 is preferably edge-triggered, that is, the respective rising edge of the input signals at the inputs S1, R1 triggers the setting or resetting process, while the further signal curve at the relevant input has no effect until a subsequent rising edge arrives.
  • the output Q1 always has the inverted signal of the output Q1.
  • the filling state of the balloon member 1a is controlled to a constant fill volume; the output is low for as long.
  • the system according to the invention operates in the sealing functional mode FS, the filling state of the balloon element 1a being regulated to a constant filling pressure; output Q1 is low for as long.
  • the output of a first OR gate 23 is connected to the set input S1; this has two inputs, one of which can be connected to a high level via a button M, but otherwise has a low level. If the button M is pressed, this high level arrives at the input of the OR gate 23 and from there is passed on to the set input S1 of the bistable multivibrator 22; the output Q1 is set to high level and the system immediately goes into the measuring function mode FM.
  • a second OR gate 24 is connected to the reset input R1 of the bistable multivibrator 22; this also has two inputs, one of which can be connected to a high level via a button S, but otherwise has a low level. If the button S is pressed, this high level reaches the Input of the OR gate 24 and is forwarded from there to the reset input R1 of the bistable multivibrator 22; the output Q1 is set to low level and instead the inverting output Q1 to high rule; the system immediately goes into the sealing function mode FS.
  • the inverting output Q1 of the bistable multivibrator 22 is fed back to the second input of the OR gate 23 via a first timer or delay module T1.
  • a positive edge at the output Q1 of the bistable flip-flop 22, i.e. a change from a low to a high rule, is delayed by an adjustable time T1 to the OR gate 23 and is there immediately at the set input S1 of the bistable flip-flop 22 and then triggers an automatic change of the output signal Q1 from low to high rule; the system therefore automatically changes to the measuring function mode FM after a time T1 has remained in the sealing functional mode FS.
  • the switching logic SL from FIG. 6 accordingly shows the behavior of a permanent automatic system that cannot be switched off, with the M or S a type of temporary override function is triggered, namely a time-limited change to a manually selectable state which then remains active for a time interval T1 or T2; then the system automatically returns to the automatic state and switches back and forth between the two functional states FM, FS under time control.
  • the superordinate control logic SL 'from Fig. 7 offers the possibility of being able to switch off the automatic system completely.
  • a switch A is provided for this, which has two stable switching states. If switch A is closed, the system is in an automatic state, ie a high level at the input of switch A reaches one input each of an AND gate 25, 26 when switch A is closed both AND gates are transparent, so to speak, and react immediately to a rising edge at their respective other input.
  • the output signal of the timer module T1 is applied to the other input of the AND gate 25, which in turn, as with the control logic SL, switches a rising edge through at the inverting output Q1 with a time delay T1, and at the other input of the AND gate 26 the output signal of the timer module T2 is applied, which in turn, as with the control logic SL, switches through a rising edge at the non-inverting output Q1 with a time delay T2.
  • a permanent time-controlled mode change i.e. an incessant, time-controlled switching back and forth between the two function modes FM, FS.
  • buttons M, S have their inputs at high level and switch this high when the relevant buttons M, S are pressed manually. Level to the respective AND gate 28, 29 through.
  • the relevant AND gate 28, 29 then also generates a high level at its output, which is passed on to the OR gate 23 at the AND gate 28 and to the OR gate 24 at the AND gate 29.
  • each selected function mode FM, FS including the automatic is stable until a new entry is made.
  • a function mode FM, FS it is necessary first to switch off the automatic system and then to select the respective function mode FM, FS in a second action by pressing a key M, S. Directly pressing a key M, S without switching off the automatic, however, has no effect.
  • switch A from FIG. 7 is transferred to a second, bistable flip-flop circuit 30.
  • the inverting output Q2 of the bistable multivibrator 30 is at the same time low, and thus the two AND gates 25, 26 connected to this inverting output Q2 are blocked and thereby prevent an automatic Operation can come about.
  • the output of a further OR gate 31 is connected to the setting input S2 of the bistable multivibrator 30, the two inputs of which are each connected to the output of the switch M and the switch S, respectively.
  • a rising edge always reaches the set input S2 of the bistable flip-flop 30 and brings it to the previously described state with high levels at output Q2, which in turn has the two AND gates 28, 29 can be made transparent.
  • the bistable flip-flop 30 cannot be reset and remains in this state, the manual one Operation can be designated and where one of the two manually selectable function modes FM or FS is executed, whereby it is possible to switch between these two function modes FM, FS at any time by pressing the respective other key S, M.
  • bistable flip-flop 30 If, on the other hand, button A is pressed, the bistable flip-flop 30 is reset, and a high level is then applied to the inverting output Q2, so that the two AND gates 25, 26 connected to it are now transparent and on the information provided by the timer Blocks T1, T2 respond to delayed edges at the outputs Q1, Q1 of the bistable multivibrator 22, so that there is permanent switching back and forth between the two function modes FM, FS, which corresponds to the automatic mode.
  • pressing a key M, S, A leads immediately to the respective operating mode FM or FS or to the automatic operating mode, and the respective operating mode remains active until another key M, S, A is pressed.
  • the measured pressure values can be monitored in various ways.
  • the pressure signal is displayed as a continuous absolute value, for example. It can also be displayed in conjunction with the volume (flow) actively moved by the patient as an iterating circular curve KK in order to make the patient's work of breathing visible over time.
  • the so-called trans-pulmonary pressure can be determined, which results from subtracting the pleural pressure from the so-called alveolar pressure.
  • the unit can also be used in both functional states to trigger machine-assisted breaths.
  • Corresponding deflections of the intra-thoracic or pleural pressure go hand in hand with the start of mechanical breathing of the patient's thorax, even before measurable movements of the patient Breathing gas comes in the patient-connected hose system.
  • the user specifies a specific thoracic or pleural pressure drop to be generated by the patient as the trigger threshold, with the respective pressure difference being able to be set using a rotary or adjusting knob T, for example steplessly or with a grid.
  • FIG. 2a shows schematically a balloon catheter 1 according to the invention in the functional state of the tamponizing, esophageal seal.
  • the lumen of the esophagus OE is shown as a star-shaped, wrinkled, inverted space F.
  • the balloon envelope BH which is already fully formed during manufacture, lies against the folds of the organ mucous membrane without tension, in the manner of a loosely lying jacket.
  • An expansion of the balloon envelope should be avoided in particular in the functional state of a long-term, esophageal sealing balloon tamponade, since the exposed mucous membrane is on the one hand very sensitive to pressure and on the other hand an irritating bolus perception by the patient should be avoided.
  • the invention proposes an approximately cylindrically shaped balloon body which has a diameter of 15 to 35 mm, preferably 25 to 30 mm.
  • the length is 6 to 12 cm, preferably 8 to 10 cm.
  • the balloon 1a should consist of a thin-walled material with low volume expandability. Polyurethanes with a Shore hardness of 90A to 95A or a hardness of 55D are preferably used.
  • the wall thickness of the balloon body 1a is in the range from 5 to 30 ⁇ m, preferably 10 to 15 ⁇ m.
  • the sealing pressures set in the balloon 1a to avoid gastropharyngeal reflux are typically in a range from 5 to 30 mbar, preferably in a range from 15 to 25 mbar.
  • Fig. 2b shows a special shape of the combined esophageal sealing and measuring balloon 1a, this on the distal, the stomach facing end 1e is fixed on the shaft tube SS, and is tapered at the proximal end 1f such that there is a gap SR between the surface of the shaft tube SS and the balloon end 1f, via which the balloon is filled from the extracorporeal side or with a filling pressure
  • the gap space SR thus makes it possible for the balloon
  • Fig. 2c shows a special embodiment of the catheter shaft SS in the area above the sealing balloon 1a as a transverse cutting plane [2c] peristaltically occurring contraction, a residual space 7 for the displacement of filling medium, so that an interruption of the communication of the balloon 1a with the extracorporeal, regulating unit 5 can be avoided.
  • the profile 6 is preferably made of an elastic, self-erecting material such as polyurethane. The profile extends from the proximal end of the balloon 1f to the area of the transition from the shaft tube to the supply line 1b. In an alternative embodiment, the profile also extends distally into the area of the sealing balloon body or through to the lower fixing point of the balloon 1a on the catheter shaft SS.
  • Fig. 3a shows an alternative embodiment of the catheter unit 1, wherein the 'catheter having two concentric balloons 8, is equipped 9, and wherein the inner balloon 9 has a measuring function, and the outer balloon 8 the esophagus in organ acceptable, tampon Schlder manner seals.
  • the two balloons are filled and switched on through separate supply lines 10 and 11 connected to a controller 5 modified with corresponding accesses.
  • the supply line filling the measuring balloon is connected directly to the volume injector Z.
  • the measuring balloon 9 preferably has a diameter of 8 to 12 mm; Hardness (according to Shore) of 95A.
  • the sealingly tamponizing balloon 8 corresponds in its dimensions and the materials used to the designs described above for the esophageal seal.
  • 3b shows an alternative, sequential arrangement of two balloon bodies, the measuring balloon 9 preferably being arranged distally in order to be able to be placed preferably in the transition of the lower to the middle third of the esophagus, which is preferred for the detection of the thoracic pressure.
  • the sealing balloon 8 is to be positioned in the area of the upper thoracic half of the esophagus.
  • the procedure for handling the system comprising the catheter unit 1 and the control module 5 according to FIG. 1, possibly with characteristics of the catheter unit 1 according to one or more of FIGS. 2a to 3b, is structured as follows:
  • the catheter unit 1 is typically positioned nasogastrically. Correct positioning of the catheter balloon 1a, which seals and measures the tampon, between the upper and lower sphincter muscle of the esophagus is confirmed by an X-ray of the thorax, the upper and lower ends of the balloon 1a being highlighted by correspondingly contrasted markings 14 on the shaft tube SS of the catheter 1 . After the position of the balloon 1a has been checked and the catheter 1 has been fixed in the area of the nasal opening, it is connected to the regulator unit 5.
  • the first functional step of the regulator unit 5 is the opening of the valve U, as a result of which the balloon body 1a is maximally emptied.
  • a predetermined volume of a filling medium is passed through a volume injection unit Z directly to the opened valve D and displaced over the valve into the catheter balloon.
  • the valve D closes and, by means of a pressure-receiving function, preferably integrated in the valve, now measures the filling pressure prevailing in the balloon 1a, which corresponds to a good approximation to the intra-thoracic pressure, as a continuous value.
  • a first visualization of the intra-thoracic pressure then takes place, either as a continuous pressure curve or as a continuous, iterating circular diagram of a breathing work diagram.
  • the correct positioning of the balloon 1a is confirmed by a typical image of the esophageal pressure curve.
  • the user checks the continuous thoracic pressure signal for typical subsidence that is triggered by the patient's own thoracic breathing. If the image is sufficiently clear, these depressions can be used to trigger a machine-assisted breath. The trigger threshold or pressure difference to be achieved can then be set by the user using a rotary control T.
  • the user can view the thoracic pressure as a continuous curve / signal, iterating pressure / volume curves (breathing work curves) or the calculated, so-called trans- pulmonary pressure can be displayed.
  • the transition from the measuring to the sealing mode takes place by manual switching (button S) by the user.
  • the valve P, the pressure reservoir PD, and the valve U the PU vacuum reservoir switched on.
  • Volume is now either added to or withdrawn from the balloon in order to achieve the respectively set, esophageal sealing pressure setpoint DP or to keep it continuously.
  • the control of the regulator can be programmed with a certain latency, which allows a certain pressure drop in the balloon body before the volume shift directed towards the balloon, which receives the sealing setpoint, begins.
  • FIG. 4 shows a catheter unit 1 according to the invention, which has additional discharge electrodes 12 for electrical action potentials of the diaphragmatic muscle ZF and / or of the neural structures innervating the diaphragm.
  • the electrodes 12 are spaced apart from one another on the surface of the catheter shaft 4, arranged axially distributed, preferably at the distal catheter end 13 distal of the balloon 1a or a balloon assembly 8, 9.
  • the electrodes are arranged below or distal the esophageal balloon component 8 or 9, and capture in the preferred embodiment both the area above and below the diaphragm.
  • the individual electrodes 12 are led out of the catheter shaft in the area of the extra-corporeal end of the catheter via a cable 12a that bundles all phases.
  • the connection to the connected hardware is made by a corresponding multi-pole connector 12b.
  • the electrodes 12 are connected to a reference electrode 12c in each case or in total during the derivation.
  • the distal end 13 of the catheter is optionally designed such that it opens into the patient's stomach, or through the stomach into the Duodenum, or through the duodenum into the jejunum of the patient.
  • FIG. 5 shows an exemplary arrangement of signal receiving, processing and signaling modules 15, 18, which allow the user to use modular options for synchronous derivation of an electrical and a mechanical respiration-associated signal.
  • an amplification and monitoring module 15 and, on the other hand, a respiratory mechanical module 19 are shown and / or U, pressure reservoirs PD and / or PU, an assembly Z for volume injection into the balloon element 1a of the catheter 1, a control logic SL, input elements M and S for manual selection of a measurement function on the one hand or a sealing function on the other hand, and possibly also rotary knobs DP , T for entering an esophageal sealing pressure setpoint or a trigger threshold.
  • the amplification and monitoring module 15 is connected to one or more electrodes 12, 12c via cables 12a, 12d and preferably a detachable plug connection 12b, 12b 'and enables the continuous visualization of the electrical diaphragmatic activity in the form of a continuous signal curve 16
  • Signal analyzing algorithm certain, cyclically recurring segments of the signal can be recognized and identified as an effective beginning of "neuro-muscular" respiratory activity.
  • the point in time of the detection of patient-generated, neuromuscular activity 17 can be sent to the ventilator (ventilator) V of the patient and there trigger an assisting breath that optimally supports the patient's spontaneous breathing attempt early on, at a point in time that is the effective volume flow to the patient triggering Self-breathing precedes it in time, ie already takes place in the state of “isometric” patient breathing, whereby the thoracic lumen has not yet enlarged, or has enlarged only to a small extent, or the elastic restoring force of the lungs has not yet been overcome.
  • This option for particularly early support is essential for many patients.
  • the signal detection or the calculation and triggering of a trigger pulse can for example be done by an autocorrelation algorithm that correlates a sample action with subsequent actions.
  • the degree or coefficient of correlation required for triggering can be set by the user by manual input on an input element, for example a rotary knob 18a, preferably on a scale from -1 to +1.
  • the respiratory mechanical module 19 In parallel with the electric. Signal is from the. Thorax of the patient derived a mechanical signal, with the currently prevailing thoracic pressure recorded via the esophageal balloon 8, 9, 1a, and via one or more hose-like supply lines 1b, 1d and preferably via a detachable plug or screw connection 1c, 1c 'to the respiratory mechanical module 19 is conducted.
  • the thoracic or pleural pressure curve is shown, for example, as a continuous pressure curve. The curve enables the user to follow the patient's thoracic ability to breathe spontaneously over the course of time.
  • Relative deflections of the pressure curve into the negative can be interpreted as the beginning of the mechanical respiratory action by an identifying, correlating algorithm and transmitted to the ventilator V as a trigger pulse will.
  • the signal detection or the calculation and triggering of a trigger pulse can for example be done by an autocorrelation algorithm that correlates a pattern course of the pressure curve with subsequent signal courses of the pressure curve.
  • the degree or coefficient of correlation required for triggering can be set by the user by manual input on an input element, e.g. a rotary knob 18b, preferably on a scale from -1 to +1,
  • pleural pressure In addition to a continuous display of the pleural pressure, it can be plotted against the volume flow moved by the patient, visualized as an iterating circle diagram or as a breathing work curve 20 in the breathing mechanical module 19.
  • the number of iterations of the respiratory work curve 20 to be shown on the display can be entered manually by the user at an input option, for example an input rotary knob 21.
  • the respiratory mechanical module 19 interacts with the ventilator V in both directions, i.e. it takes over current flow values measured by the ventilator V and in turn transmits control or triggering impulses to it.
  • the combination of electrical and mechanical signals described enables, in particular, the correlation of neuromuscular electrical activity with effective, mechanically performed work of breathing, and thus allows the user, on the one hand, to identify an electrical signal with a mechanical response as belonging to one another.
  • the evaluating algorithm of the two signals can correlate the respective signal intensities with one another.
  • An electrical signal can also be differentiated into a leading, motor-efferent neural signal and the subsequent muscle action potential.
  • the user can also verify whether a neuronally efferent electrical signal changes into a muscle action potential, or determine the intensity of the potential.
  • the user can use the appropriate How to determine whether and with what intensity a muscle action potential changes into a mechanical contraction of the diaphragmatic muscle.
  • the shaft tube SS is provided with radiopaque markings 14 which make the upper and lower ends of the esophageally positioned balloon 1a or the balloon arrangement 1a, 8, 9 visible in the X-ray image.
  • the sealing effect of the balloon 1a, 8 should be established in the entire area between the upper and lower esophageal sphincter.
  • the positioning of the preferably ring-shaped markings 14 on the shaft tube SS should then approximately correspond to the respective sphincters.
  • the invention also describes a method for reflux-minimizing and pneumonia-preventive mechanical ventilation of patients, the user being able to switch from an esophageal dynamic sealing mode to an esophageal static measuring mode during the ventilation process.
  • the invention also describes a method for alternating, esophageal measuring and esophageal sealing application of a catheter unit 1, with the acquisition of neuromuscular, electrical signals of the patient's diaphragm being made possible via a trans-diaphragm or near-diaphragm electrode arrangement 12.
  • the catheter unit 1 accordingly has a structural combination of an esophageal positioned, measuring and / or sealing catheter balloon 1a and electrical discharge electrodes 12.
  • the procedure for handling the system comprising the catheter unit 1 and modules 15, 18 according to FIG. 4 is as follows:
  • the catheter unit 1 is typically positioned nasogastrically.
  • the correct positioning of the tampon-sealing and measuring catheter balloon 1a between the upper and lower sphincter muscle of the The esophagus is confirmed by an X-ray of the thorax, the upper and lower ends of the balloon 1 a being highlighted by appropriately contrasted markings 14 on the shaft tube SS of the catheter 1.
  • the probe-like catheter 1 has the functions of a naso-gastric feeding catheter; it enables both gastric decompression and gastric feeding of the patient.
  • the discharge electrodes 12 positioned distal to the balloon component 1a are preferably positioned in such a way that they come to lie on both sides of the diaphragm, that is to say trans-diaphragmatically.
  • the lead electrodes 12 are connected to the reinforcement and monitoring module 15, for example via the cable feed line 12a, 12b, 12b 'and 12d, and the balloon 1a, 8, 9 is connected via the hose supply lines 1b, 1c, 1c 'and 1d are connected to the respiratory mechanical module 19.
  • a total potential of several individual electrodes 12 or a signal from one or more individual electrodes 12 can then be shown as a continuous signal curve 16.
  • the derivation takes place relative to the signal of a reference electrode 12c also arranged on the catheter shaft SS.
  • a module-integrated control algorithm determines an identification spike 17 within the signal 16 which is as early as possible and with whose specific morphology the potentials that follow cyclically are correlated.
  • the precision of the correlation can be set by the user by entering a correlation coefficient required for the detection of the signal spike.
  • the module sends a triggering pulse to the ventilator V connected to the patient, whereby the device is informed of the onset of electrical diaphragmatic activity.
  • the trigger pulse can be used by the ventilator V to trigger a breath that supports the patient's breathing effort.
  • the respiratory mechanical module 19 visualizes the course of the thoracic or pleural pressure in a display, either as a continuous curve or as an iterating circular curve (loop).
  • a continuous loop is created in that the ventilator V continuously determines the flow of breathing gas to and from the patient and sends it as a corresponding electronic signal, for example as a voltage curve, to the respiratory mechanical module 19, which it applies to the continuously determined thoracic pressure .
  • the combination of the two modules 15, 19 enables the beginning of a muscular action (diaphragmatic action potential) with the beginning of an associated, mechanically effective contraction of the diaphragm and an associated deflection or lowering of the diaphragm in a manner that is optimal for the ventilation planning of the user to connect thoracic pressure in a correlating manner.
  • a supportive volume support that supports the patient's breath or inspiratory effort can already be initiated when the patient has not yet developed any or only slight mechanical respiratory effort.
  • the patient can contribute a greater or lesser amount of his / her own contribution to achieving a certain tidal volume.
  • the specification thus enables optimized, respiratory “training of the breathing apparatus” without the patient having to tire himself respiratory and having to abandon the patient's supported self-breathing.
  • the breathing mechanical module 19 already integrates or has the functionalities and elements of the regulator module 5, parallel or alternatively to a connection of the catheter balloon 1a to a breathing mechanical module 19, the hose-like supply line 1b to the catheter balloon 1a can also be connected to a module representing the thoracic pressure curve 5, which, in addition to the option of intermittent measurement of the thoracic pressure, also offers the option of continuous, sealing tampon-acting pressure regulation in the catheter balloon 1a, the sealing balloon pressure regulating the thoracic pressure fluctuations caused by the patient's own breathing in a dynamic manner compensated.
  • continuous triggering of a ventilator that supports the patient's breathing can be carried out by an action potential of the diaphragm.
  • the point in time at which the device is triggered can in turn be specified with a certain time offset from the onset of an electrical diaphragmatic signal, which can be set by the user.
  • FIG. 9 a a further example is used to show how the trigger signal generated by the control and regulator unit 5 can be transmitted to a ventilator V.
  • an adapter 33 is connected to the control and regulator unit 5 via a cable 32a, which in turn is connected to a ventilation hose 34a of the ventilation device V, for example - as shown in FIG. 9a - with a Y-shaped connector 35 which on the one hand connected or connectable to the proximal end of the breathing tube 34a leading to the patient and on the other hand it can be connected to two separate tubes 34b for inspiration and expiration.
  • the adapter 33 is arranged directly on a tubular connecting piece 36, which in turn can be connected directly to the ventilator V.
  • the main component of the adapter 33 is a pressure relief valve 37, which is opened and closed by a magnet 38, which in turn is activated by the control and regulator unit 5 via the cable 32a.
  • this trigger signal As soon as a trigger signal has been generated by this control and regulator unit 5, that is to say an assisting, mechanical breath stroke is requested by the ventilator control and regulator unit 5, this trigger signal must be communicated to the ventilator V.
  • the trigger signal - if necessary in a sufficiently amplified form - is switched to the magnet 38 via the cable 32a and causes the magnet to open the pressure relief valve 37.
  • air can escape from the ventilation tubes 34a, 34b communicating with one another and / or from the Y-shaped distributor piece 35 or from the tubular connecting piece 36.
  • the resulting pressure drop in the ventilation hose 34b leading to the ventilation device V is sensed by the ventilation device V and interpreted as an attempt by the patient to close his chest lift in order to suck air into his lungs by means of negative pressure, and then the ventilator V triggers the desired, assisting mechanical breath.
  • the pressure relief valve 37 should only remain open until the desired, assisting mechanical breath stroke has been triggered. The pressure relief valve 37 should then be closed as quickly as possible so that the overpressure generated by the ventilator V does not escape, but rather reaches the patient's lungs.
  • a pressure sensor 39 is arranged in the area of the pressure relief valve 37, which is connected to the control and regulator unit 5 via a cable 32b and allows the pressure sensor 39, which increases as a result of the now active ventilator V, in the To recognize ventilation hose 34b and to close the pressure relief valve 37 immediately.
  • the catheter unit 1 from FIG. 1, which has no electrodes, and the catheter unit 1 according to FIG , 12c are arranged. Then these electrodes 12, 12c are connected via a cable connection 12a, 12b, 12d to the control and regulation unit 5, which then preferably also has the functionality of the monitoring module 15 and the respiratory mechanical module 19 or can be connected to modules of this functionality.
  • the trigger signal can then be derived not only from the esophageal pressure within the balloon element 1a, but also from the signals from the electrodes 12, 12c, which pick up the activity potential of the diaphragm directly from the patient.
  • the ventilation or endotracheal tube 40 is also shown in FIG. 9a. This comprises the actual tube 41 as well as a cuff 42a that encloses it.
  • the ventilation hose 34a can be connected to the proximal or extracorporeal end 43 of the ventilation tube 40.
  • the cuff 42a of the ventilation tube 40 is also subject to a similar sealing problem as the balloon element 1a of the esophageal catheter 1. This sealing problem is based on the fact that the intra-thoracic pressure is subject to regular fluctuations during a patient's breathing cycle, particularly when the pressure is temporarily reduced can lead to the fact that the cuff 42a as well as the balloon element 1a is no longer completely tight.
  • the invention provides - as for the esophageally placed balloon element 1a - also for the cuff 42a of the ventilation tube 40, an adaptive pressure control so that the cuff 42a is permanently tight during the entire breathing cycle without the consequent prolonged stay in it Patients with atrraumatic impairment results.
  • the pressure within the cuff 42a is measured - either directly in the cuff 42a itself or in a supply line 42b, 42c, 42d of the same - and this measured pressure is then preset by the control and regulation unit 5, if possible Setpoint regulated.
  • This can be the same control algorithm as the balloon element 1a placed in the esophagus, with the only difference that the cuff 42a does not require a switch to a measuring function mode.
  • the curve a represents the pressure curve over time within the ventilation hose 34a, 34b during machine-assisted ventilation, as measured by the ventilation device V during the inhalation phase 44 and the exhalation phase 45 of a breathing cycle 46, 47 * , 47 ", but
  • the pressure along the ordinate in mbar is plotted as the abscissa over the time axis t.
  • All breathing cycles 46, 47 ', 47 “have in common that at the end of a complete, preceding exhalation phase 45, the pressure within the ventilation tube 34a, 34b has dropped to an approximately constant value 48, which is the positive, end-expiratory pressure (positive end- expiratory pressure, PEEP) and is around +5 mbar.
  • PEEP positive end- expiratory pressure
  • a corresponding stimulus reaches the ZF diaphragm via the phrenic nerve, whereupon this begins - at least in patients with at least a rudimentary ability to breathe contract. After a certain time it becomes somewhat conical, with a simultaneous enlargement of the pleural cavity. As soon as the pleural cavity has increased noticeably, the pressure within the ventilation hose system 34a, 34b drops somewhat according to curve a. This pressure drop 49 is referred to as the initial respiratory pressure drop (IRPD).
  • IRPD initial respiratory pressure drop
  • the pressure curve b is measured in the cuff 42 of the endotracheal tube 40 in synchronism with the pressure curve a within the ventilation hose system 34a, 34b according to curve a. At the end of an exhalation phase 45, this has reached approximately a constant pressure value 52 of approximately 25 mbar. As soon as the diaphragm ZF begins to contract, the beginning of patient breathing (onset of patient breathing, OPB) can be recognized from a slight pressure drop 53 within the cuff 42. The pressure drop 53 is only about 2 to 3 mbar below the initial, constant pressure value 52 of about 25 mbar. In the case of machine-assisted breathing, this pressure drop 53 remains approximately constant until the ventilator V becomes active and presses air into the lungs.
  • the cuff pressure b also rises to approximately the peak or PEAK value 50 and then follows the pressure curve a within the ventilation tube system 34a, 34b up to the increased inhalation pressure plateau 51, PLATEAU, which is already close to the initial pressure value 52 of curve b lies at about 25 mbar, towards which curve c finally approaches again in the exhalation phase 45.
  • the pressure curve c can be measured in synchronism with the pressure curves a and b in the balloon element 1a of the catheter unit 1 placed in the esophageal. At the end of an exhalation phase 45, this has reached approximately a constant pressure value 54 of approximately 15 mbar.
  • the beginning of the patient's breathing OPB can again be recognized from a pressure drop 55 within the esophageal balloon element 1a.
  • the pressure drop 55 in curve c is significantly more pronounced than in curve b and lies typically at about 6 to 7 mbar below the initial, constant pressure value 54 of about 15 mbar.
  • this pressure drop 55 remains approximately constant or continues to drop slightly until the ventilator V becomes active and presses air into the lungs.
  • the pressure c in the esophageally placed balloon element 1a also rises to approximately the peak or PEAK value 50 of curve a - i.e.
  • this pressure drop 55 within the esophageally placed balloon element 1a at the beginning of the patient's breathing OPB is significantly more pronounced than the approximately simultaneous pressure drop 53 within the cuff 42a on the endotracheal tube 40, this pressure drop 55 can be made easier and faster by the control and / or regulating unit 5 according to the invention can be recognized as the pressure drop 53 in the cuff 42a, and can be used to generate a trigger signal for the ventilator V.
  • a ventilation cycle 46 is shown with a conventional triggering on the pressure drop 49, IRPD in the ventilation hose system 34a, 34b.
  • This pressure drop 49, IRPD is recognized by the ventilator V at time 56 and the mechanical, assisting breath stroke 44 is then initiated or triggered.
  • a pressure drop 49 in the pressure curve a in the ventilation hose system 34a, 34b is not waited for, but rather the triggering takes place on the basis of the pressure drop 55 in the oesophageally placed balloon element 1a according to curve c.
  • This is clearly pronounced and can therefore be used reliably as a basis for the generation of a trigger pulse.
  • this trigger time 56 ' is much closer to the start 57 of the contraction of the diaphragm ZF than the trigger time 56 determined by the ventilator V in a conventional manner.
  • the time interval 58' between the start 57, BMO of the muscular activity of the diaphragm ZF and the assisting activation of the ventilator V is therefore significantly shorter than the corresponding time interval 58 for conventional triggering of the ventilator.
  • triggering based on output signals from electrodes 12, 12c on the shaft 4a of the esophageally placed catheter 1 is shown as a further case.
  • the electrodes 12 can come into direct contact with the diaphragm ZF in order to measure its electrical muscle activity as part of an electromyography (EMG), especially if the electrode phalanx 12 is positioned on the catheter shaft 4a about half distal and the other half proximal of the diaphragm ZF.
  • EMG electromyography
  • the trigger time 56 ′′ can therefore be determined before an oesophageal pressure drop 55 even occurs This can be seen in FIG. 12 from the fact that before the rising edge of all curves ac at the beginning of the inhalation phase 44, no pressure drop 49, 53, 55 is recognizable.
  • the two times 56 ", 57 "together, the response time interval 58" is equal to zero.
  • controller unit 24 OR gates

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Abstract

La présente invention concerne un dispositif et un procédé permettant d'effectuer des mesures alternées de la pression thoracique et/ou pleurale et d'assurer l'étanchéité gastropharyngienne ou trachéale, le composant ballonnet d'un tube ou d'un cathéter placé dans la trachée ou l'œsophage se modifiant entre deux états de remplissage et/ou de fonctionnement, le niveau de remplissage du composant ballonnet adoptant une valeur faible, en mode de mesure, de volume constant et de volume défini, pendant la mesure, et le niveau de remplissage du ballonnet conservant une pression d'étanchéité constante prédéfinie par l'utilisateur, en mode de fonctionnement à effet étanchéifiant au niveau de l'œsophage ou de la trachée. Le dispositif de régulation relié à l'ensemble tube ou cathéter garantit en mode d'étanchéité de la trachée ou de l'œsophage un déplacement rapide de milieu de remplissage dans ou hors du tube ou du ballonnet, la pression cible à effet étanchéifiant de la trachée ou de l'œsophage étant maintenue en continu, dans la mesure où les variations de pressions liées au mécanisme de la respiration intervenant dans le ballonnet sont compensées par un déplacement continu à effet compensatoire de volumes de remplissage. L'utilisateur peut permuter entre les deux états de fonctionnement par une fonction manuelle de commutation ou par un cycle temporel pouvant être programmé. Outre la possibilité de permettre un monitorage intermittent du mécanisme de la respiration et une tamponnade par ballonnet à effet étanchéifiant continu dans la trachée ou l'œsophage, le ballonnet placé dans la trachée ou l'œsophage permet dans les deux états de fonctionnement la dérivation thoracique d'un signal de mécanisme de la respiration à effet déclencheur, lequel peut déclencher dans un respirateur connecté au dispositif le mouvement de respiration assistée du patient. L'invention concerne en outre des options structurales et fonctionnelles pour la dérivation simultanée d'un signal électrique neuronal et/ou musculaire du diaphragme du patient et d'un signal du mécanisme de la respiration sur la base de variations de pressions thoraciques et/ou pleurales, dérivées par voie trachéale ou œsophagienne.
EP21734487.8A 2020-05-15 2021-05-17 Dispositif et procédé pour effectuer des mesures alternées de pressions thoraciques et assurer l'étanchéité vis-à-vis de sécrétions oesophagiennes Pending EP4149348A1 (fr)

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DE102020002932.9A DE102020002932A1 (de) 2019-05-15 2020-05-15 Vorrichtung und Verfahren zur wechselweisen Messung thorakaler Drucke und ösophagealen Dichtung gegen aufsteigendes Magensekret
DE102021000221 2021-01-19
DE102021000220 2021-01-19
PCT/IB2021/054222 WO2021229552A1 (fr) 2020-05-15 2021-05-17 Dispositif et procédé pour effectuer des mesures alternées de pressions thoraciques et assurer l'étanchéité vis-à-vis de sécrétions œsophagiennes

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Publication number Priority date Publication date Assignee Title
US4622979A (en) * 1984-03-02 1986-11-18 Cardiac Monitoring, Inc. User-worn apparatus for monitoring and recording electrocardiographic data and method of operation
US7967780B2 (en) * 2007-08-29 2011-06-28 Kimberly-Clark Worldwide, Inc. Gastro-esophageal reflux control system and pump
US20090120439A1 (en) * 2007-11-08 2009-05-14 Fred Goebel Method of triggering a ventilator
GB2496074B (en) * 2010-07-13 2016-07-20 Sandhill Scient Inc Apparatus and method for detecting and measuring condition of esophageal mucosa and indications of gastroesophageal reflux disease
DE102020002932A1 (de) * 2019-05-15 2020-11-19 Creative Balloons Gmbh Vorrichtung und Verfahren zur wechselweisen Messung thorakaler Drucke und ösophagealen Dichtung gegen aufsteigendes Magensekret

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