WO2021110598A1 - Appareil pour mesurer des paramètres vitaux, ayant un agencement d'étanchéité avantageux - Google Patents

Appareil pour mesurer des paramètres vitaux, ayant un agencement d'étanchéité avantageux Download PDF

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Publication number
WO2021110598A1
WO2021110598A1 PCT/EP2020/083964 EP2020083964W WO2021110598A1 WO 2021110598 A1 WO2021110598 A1 WO 2021110598A1 EP 2020083964 W EP2020083964 W EP 2020083964W WO 2021110598 A1 WO2021110598 A1 WO 2021110598A1
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WO
WIPO (PCT)
Prior art keywords
housing part
alignment
sealing element
line connection
fixing device
Prior art date
Application number
PCT/EP2020/083964
Other languages
German (de)
English (en)
Inventor
Aaron Weber
André Hein
Achim Biener
Nestor Garcia
Original Assignee
Pulsion Medical Systems Se
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
Application filed by Pulsion Medical Systems Se filed Critical Pulsion Medical Systems Se
Publication of WO2021110598A1 publication Critical patent/WO2021110598A1/fr

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording for evaluating the cardiovascular system, e.g. pulse, heart rate, blood pressure or blood flow
    • A61B5/021Measuring pressure in heart or blood vessels
    • A61B5/022Measuring pressure in heart or blood vessels by applying pressure to close blood vessels, e.g. against the skin; Ophthalmodynamometers
    • A61B5/02233Occluders specially adapted therefor
    • A61B5/02241Occluders specially adapted therefor of small dimensions, e.g. adapted to fingers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording for evaluating the cardiovascular system, e.g. pulse, heart rate, blood pressure or blood flow
    • A61B5/021Measuring pressure in heart or blood vessels
    • A61B5/02141Details of apparatus construction, e.g. pump units or housings therefor, cuff pressurising systems, arrangements of fluid conduits or circuits
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording for evaluating the cardiovascular system, e.g. pulse, heart rate, blood pressure or blood flow
    • A61B5/021Measuring pressure in heart or blood vessels
    • A61B5/022Measuring pressure in heart or blood vessels by applying pressure to close blood vessels, e.g. against the skin; Ophthalmodynamometers
    • A61B5/0225Measuring pressure in heart or blood vessels by applying pressure to close blood vessels, e.g. against the skin; Ophthalmodynamometers the pressure being controlled by electric signals, e.g. derived from Korotkoff sounds
    • A61B5/02255Measuring pressure in heart or blood vessels by applying pressure to close blood vessels, e.g. against the skin; Ophthalmodynamometers the pressure being controlled by electric signals, e.g. derived from Korotkoff sounds the pressure being controlled by plethysmographic signals, e.g. derived from optical sensors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/70Means for positioning the patient in relation to the detecting, measuring or recording means
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B2560/00Constructional details of operational features of apparatus; Accessories for medical measuring apparatus
    • A61B2560/04Constructional details of apparatus
    • A61B2560/0406Constructional details of apparatus specially shaped apparatus housings
    • A61B2560/0425Ergonomically shaped housings

Definitions

  • the present invention relates to a measuring device and a provision device for such a measuring device, in particular for recording vital parameters of living beings.
  • the recording of vital parameters can preferably be carried out non-invasively by the measuring device.
  • the provision device is particularly preferably a device which provides radiation and / or pressure for determining blood pressure, in particular a provision device for providing radiation and / or pressure for continuous determination of the intra-arterial blood pressure on at least one finger of a hand.
  • the measuring device is preferably a blood pressure measuring device, in particular a measuring device for the continuous determination of the intra-arterial blood pressure on at least one finger of a hand.
  • the (in particular arterial) blood pressure of a patient is one of the most important measured variables in medical technology, and the known associated, in particular also non-invasive, measurement technology is extremely diverse. This applies above all to measurement technology for the continuous monitoring of blood pressure over a longer period of time, for example in intensive care medicine but also in emergency medicine and during surgical interventions.
  • the blood pressure measuring device is often attached to the patient's limbs, for example an applanation tonometric sensor in the radial artery on the forearm or a photoplethysmographically based on the so-called “sogn. "Vascular Unloading Technique” according to Pegoz operated finger sensor.
  • Such pressure measuring devices are for example from US 4,406,289, US 4,524,777, US 4,726,382, WO 2010/050798 A1, WO 2000/059369 A1, WO 2011/045138 A1, WO 2011/051819 A1, WO 2011/051822 A1, WO 2012/032413 A1 and WO 2017/143366 A1 known.
  • near-infrared light is radiated into a finger and the pulsatile (pulse-shaped) blood flow (actually the changing blood volume) in the finger is determined using the non-absorbed portion captured by a photodetector.
  • the (near-infrared) light is usually generated with the help of one or more light-emitting diodes (LED) that work with one or more wavelengths and with the help of one or more light-sensitive receiver diodes (photodiodes) detected.
  • LED light-emitting diodes
  • photodiodes light-sensitive receiver diodes
  • a control system now keeps the plethysmographically registered flow (or the detected blood volume) and thus the resulting photoplethysmographic signal (volume signal v (t)) constant by applying counter pressure in a cuff (cuff pressure) pc (t) to the finger.
  • This counter pressure pc (t) is usually regulated by a fast valve or valve system in conjunction with a pump.
  • the related control of the valve or the valve system is carried out by a control unit, which is preferably implemented with a microcomputer.
  • the main input signals are the PPG signal v (t) and the cuff pressure pc (t).
  • the pressure pc (t) necessary to keep the PPG signal v (t) constant now corresponds to the intra-arterial blood pressure pa (t).
  • the cuff pressure pc (t) can be changed at least as quickly as the intra-arterial blood pressure pa (t) changes, so that the real-time condition is fulfilled.
  • the upper limit frequency of pa (t) and thus the highest rate of pressure change is above at least 20 Hz, which is definitely a challenge for a pressure control system. It follows from this that the pressure regulation by means of a valve or valve system is advantageously located in the immediate vicinity of the cuff. If the air lines are too long, there is a risk of losing this cut-off frequency condition due to the low-pass effect of the lines.
  • a mechanical valve is known from US Pat. No. 4,406,289 which regulates the counter pressure in the finger cuff with the desired accuracy when it is supplied with a linearly operating pump.
  • the valve is housed in a housing on the distal forearm and thus supplies the finger cuff with the pressure pc (t) via a short tube.
  • No. 4,524,777 describes a pressure generation system for the Vascular Unloading Technique, a constant cuff pressure Pc also being generated with a linear pump, which is superimposed with pressure fluctuations ⁇ pc (t) from a parallel-connected "Shaker” or a "Driving Actuator".
  • US Pat. No. 4,726,382 discloses a finger cuff for the Vascular Unloading Technique which has hose connections for the supply of the cuff pressure pc (t). The length of the air tubes extends to the pressure generation system, which in turn is attached to the distal forearm.
  • WO 2000/059369 A1 also describes a pressure generation system for the Vascular Unloading Technique.
  • the valve system here consists of a separate inlet and a separate outlet valve. While a relatively linear proportional pump must be used in US Pat. No. 4,406,289 and US Pat. No. 4,524,777, this system allows the use of simple, inexpensive pumps, since disruptive harmonics can be eliminated by the arrangement of the valves. Furthermore, the energy consumption of the simple pump can be significantly reduced by the valve principle.
  • a system for the vascular unloading technique is known from WO 2004/086963 A1, in which the blood pressure can be continuously determined in one finger, while the measurement quality is checked in the adjacent finger ("watch dog" function). After a while, the system automatically changes the "measuring finger” with the "monitoring finger”.
  • WO 2005/037097 A1 describes a control system for the vascular unloading technique with several interlinked control loops.
  • WO 2010/050798 A1 discloses a pressure generation system ("front end") attached to the distal forearm with only one valve, to which a finger cuff for the vascular unloading technique can be attached.
  • WO 2011/051819 A1 discloses an implementation of the Vascular Unloading Technique which has been improved by means of digital electronics to increase stability and for further miniaturization.
  • WO 2011/051822 A1 describes a method for the vascular unloading technique in which the measured signals v (t) and pc (t) are processed to increase long-term stability and to determine further hemodynamic parameters.
  • a method for eliminating effects resulting from vasomotor changes in the finger arteries and a method for determining cardiac output (Cardiac Output CO) are disclosed.
  • WO 2012/032413 A1 describes novel finger sensors which have a disposable part for single use. The cuff that comes into contact with the finger is housed in the disposable part for reasons of hygiene, whereas the associated pressure generation and pressure control system is housed in a reusable part. Accordingly, a separable pneumatic connection between the disposable part and the reusable part must be provided here.
  • Such accesses can be blocked by the pressure generation and pressure control system and its attachment.
  • the system can slip or tilt during operation. This can have a detrimental effect on the fit of the sensors.
  • the fit of the sensors would also improve if the finger to be measured or the corresponding hand is in a certain rest position.
  • the publication WO 2017/143366 A1 proposes a measuring system for the continuous determination of the intra-arterial blood pressure on at least one finger of a hand, with at least one finger sensor, with a plethysmographic system, with at least one light source, preferably LED, with one or several wavelengths and at least one light sensor and at least one inflatable cuff, as well as with a pressure generation system with at least one
  • the measuring system having a housing with a surface that serves as a support surface for the at least one finger and the adjacent areas of the palm.
  • the hand rests here on a support under which there are essential components that were attached to the forearm in conventional systems.
  • the cuff is accommodated in a disposable part that can be separated from the housing (and thus from the hand rest).
  • a separable pneumatic connection between the disposable part and the reusable part must again be provided.
  • the light-emitting diodes and photodiodes for emitting and detecting the near-infrared measurement radiation are arranged directly on the finger. If the light-emitting diodes and photodiodes are arranged in a reusable part, there is the problem that the exposed light-emitting elements must be subjected to cleaning and disinfection before they can be reused.
  • the need for an easy-to-clean design restricts the degree of freedom in the design. Otherwise, the need to accommodate the light-emitting diodes and photodiodes in the immediate vicinity of the finger is a limitation of the geometric configuration of the device.
  • the light-emitting diodes and photodiodes are arranged in a disposable item, however, there is the problem that electrical connections are provided between the disposable item and the reusable base unit and that the cost of manufacturing the disposable item increases. The heat input from electrical components with skin contact is also perceived as negative.
  • this object is achieved with a device according to claim 1.
  • Provisioning device for providing at least exposure radiation, in particular for determining vital parameters.
  • the provision device preferably has at least: a first housing part and a second housing part, the first housing part and the second housing part being coupled to one another, in particular releasably, in a defined alignment.
  • the provision device preferably has at least or precisely one first radiation source for providing the impinging radiation.
  • the provision device preferably has at least or precisely one first detection device for detecting detection radiation.
  • the first housing part and the second housing part preferably form a receiving space for holding at least the first radiation source and for holding at least the first detection device.
  • a sealing element is preferably arranged circumferentially between the first housing part and the second housing part.
  • the sealing element is preferably on a first Side with the first housing part in contact and wherein the sealing element is preferably in contact on a second side with the second housing part.
  • the provision device can have a line connection for introducing data, electricity and / or substances into the receiving space and / or for discharging data, electricity and / or substances from the receiving space.
  • the distance between the first side of the sealing element and the second side of the sealing element in the direction of extension of the sealing element is greater in a first section than in a second section.
  • the line connection is arranged in the first section between the first side of the sealing element and the second side of the sealing element, the line connection extending into the receiving space.
  • This embodiment is advantageous because the interface between the housing parts and the interface between the line connection and at least one housing part can be sealed by means of a single seal or a single sealing element.
  • an alignment and fixing device for aligning and fixing at least one section of the line connection, the alignment and fixing device being arranged at least partially in the receiving space and the sealing element, the alignment and fixing device in the circumferential direction of the Alignment and fixing device completely encloses.
  • the sealing element preferably encloses the aligning and fixing device in the longitudinal direction of the aligning and fixing device in sections, in particular mostly or up to 50% (of the length).
  • the sealing element is preferably in contact with the first housing part on a first side and the sealing element is preferably in contact with the second housing part on a second side.
  • the provision device preferably has a line connection for introducing data, electricity and / or substances into the receiving space and / or for discharging data, electricity and / or substances from the receiving space.
  • the line connection is arranged between the first side of the sealing element and the second side of the sealing element, the line connection extending into the receiving space and / or preferably an alignment and fixing device for aligning and fixing at least one section of the line connection is provided, with the alignment and fixation device is arranged at least partially in the receiving space and wherein the sealing element completely encloses the alignment and fixation device in the circumferential direction of the alignment and fixation device.
  • the sealing element preferably encloses the alignment and fixing device in the longitudinal direction of the alignment and fixing device in sections, in particular mostly or up to 50% (of the length) or at least 30% (of the length) or 40% (of the length).
  • the provision device it is also possible for the provision device to have a plurality of radiation sources, in particular at least or precisely one second radiation source. If, for example, several examination areas are provided, a radiation source can be provided for each examination area. If not only one vital parameter, but several vital parameters are recorded, the provision device can have one radiation source per vital parameter and / or per examination area. If, for example, three examination areas are provided and three vital parameters are recorded, up to, exactly or at least nine radiation sources can be provided. However, it is also conceivable that one or more radiation sources for the provision of radiation are arranged in several examination areas. The same applies analogously to the detection device.
  • the receiving space is preferably completely encapsulated, ie the receiving space is preferably liquid-tight.
  • Liquid-tight here preferably means that less than 1g of deionized water (fully decalcified water) from a water bath into which the Provisioning device is completely submerged and which is subjected to 2 bar pressure, penetrates into the receiving space within 1 hour.
  • the distance between the first side of the sealing element and the second side of the sealing element in the direction of extension of the sealing element is greater in a first section than in a second section, the line connection being arranged in the first section.
  • the alignment and fixing device forms a deflection area for deflecting the line connection, the deflection area of the line connection providing a defined curved course.
  • This embodiment is advantageous because the portion of the line connection extending into the receiving space can be very precisely oriented or arranged in the receiving space.
  • This embodiment is advantageous because the receiving space can be made very small. This is advantageous because it allows weight and thus resources to be saved during manufacture.
  • the provision device can be coupled with smaller positioning and loading devices, so that the vital parameters can also be recorded and / or evaluated from small living beings, in particular small people, such as children.
  • Embodiment is advantageous because the alignment area provides protection against undesired Buckling of the line connection is effected in the area of the housing. This is advantageous because it prevents the sealing element from being compressed to such an extent that moisture can penetrate into the receiving space. Furthermore, by connecting the alignment and fixing device by means of the connection point to a housing part and the deflection area, which holds the line connection in a bent or kinked shape, strain relief is realized. Tensile forces introduced into the line connection outside the receiving space are thus decoupled from the end of the line connection arranged in the receiving space, since they are introduced into the housing via the alignment and fixing device.
  • the portion of the alignment region formed outside of the receiving space is preferably largely or completely surrounded by the sealing element on its outside.
  • the deflection area and the connection point lie in a first plane and the alignment area lies in a second plane, the first plane and the second plane being inclined, in particular orthogonally, aligned with one another.
  • This embodiment is advantageous since the aligning and fixing device can thereby be easily connected to the housing. Additionally or alternatively, the deflection area, the connection point and the alignment area can be connected to one another in one piece. This embodiment is advantageous because these three areas and preferably the alignment and fixing device can be provided or produced as a whole as a one-piece component.
  • the alignment and fixing device is preferably produced on the line connection by means of an injection molding process.
  • the aligning and fixing device consists of a first material or a first material combination and the sealing element preferably consists of a second material or a second material combination, the first material or the first material combination having a first hardness and / or first Having strength and wherein the second material or the second material combination has a second hardness and / or second strength, wherein the first hardness is greater than the second hardness and / or wherein the first strength is greater than the second strength and / or wherein the alignment and fixing device has a first rigidity and the sealing element has a second rigidity in an area surrounding the alignment and fixing device, the first rigidity being greater than the first rigidity.
  • This embodiment is advantageous because the kink protection and / or the strain relief is brought about by the internal alignment and fixing device and the sealing against moisture is effected by the sealing element.
  • Having functional fluid supply device It is additionally or alternatively possible for the functional fluid to be provided via the first supply line. Furthermore, it is additionally or alternatively possible that a further line connection, in particular a detachable line connection, is provided or designed to provide power to operate the control device, the first radiation device and / or the first detection device and / or to exchange data. Additionally or alternatively, it is possible that an interface for coupling a further line connection, in particular for providing power to operate the control device and / or the first radiation device and / or the first detection device and / or for the exchange of data, is provided or designed.
  • Functional fluid supply device is preferably designed as a valve device which regulates, in particular enables, limits or prevents the forwarding or the onward flow of the functional fluid preferably provided via a supply line.
  • the functional fluid is preferably provided via the supply line at a pressure that is higher than the ambient pressure.
  • the supply device preferably forms a coupling point for receiving a further device, in particular a positioning and loading device, or has such a coupling point.
  • exposure radiation is preferably understood to mean radiation which is provided by a radiation source, in particular the first radiation source and / or a further radiation source, and / or which is supplied to a part of the body or emitted in the direction of an exposure point or an examination area becomes.
  • detection radiation is understood to be the portion of the exposure radiation that was scattered or deflected by the body part or passed through the body part and is fed or fed to the detection device or reaches the detection device.
  • the provision device has a positioning and application device for defined arrangement on at least one body part of a living being, in particular for applying radiation and / or pressure to the body part, in particular for determining at least one vital parameter of the living being.
  • the positioning and application device preferably has at least: A guide and support structure for delimiting an examination area and preferably for holding at least one force application device, the body part being positionable in the examination area during the application, in particular the application of radiation and / or pressure.
  • the force application device is preferably connected to the guide-support structure, wherein the body part can be subjected to pressure by means of the force application device.
  • the guide / support structure preferably forms at least one radiation entry area in a section delimiting the examination area, with radiation being able to be introduced into the examination area through the radiation entry area. Additionally or alternatively, the guide support structure forms a radiation exit area in a further section delimiting the examination area, radiation that can be introduced into the examination area via the radiation exit area being diverted from the examination area through the radiation exit area.
  • the provision device can alternatively be referred to as a base part.
  • the positioning and loading device, in particular the guide-support structure, can alternatively be referred to as a cuff part and preferably designed within the scope of the present invention.
  • the above-mentioned object is also achieved by a measuring device according to claim 13.
  • the measuring device is preferably used to determine at least one vital parameter of a living being, in particular to continuously determine the intra-arterial blood pressure on at least one finger of a hand and preferably on two fingers, at least two fingers or exactly two fingers of the hand
  • the sealing element preferably encloses the aligning and fixing device in the longitudinal direction of the aligning and fixing device in sections, in particular mostly or up to 50% (of the length). Additionally or alternatively, the distance between the first side of the sealing element and the second side of the sealing element in the direction of extension of the sealing element is greater in a first section than in a second section.
  • the measuring device preferably has a positioning and loading device for the defined arrangement on at least one body part of a living being, the positioning and loading device having a guide support structure for delimiting one or at least one examination area, in particular two, at least two or exactly two examination areas, wherein the exposure radiation can be introduced into the examination area (s) for exposure to the body part, and portions of the
  • Exposure radiation can be fed as detection radiation to the first detection device.
  • the supply device has a first coupling point and the positioning and loading device has a second coupling point, the first coupling point and the second coupling point particularly preferably being able to be physically coupled and / or decoupled with one another without tools and / or non-destructively.
  • the provision device can be designed to be reusable, ie the components that are expensive or complex to manufacture can be used multiple times.
  • the positioning and loading device can be provided as a single-use part or single-use product or for single use.
  • the overall device can be made available to a large number of people in a cost-effective manner while complying with hygienic requirements.
  • the alignment and fixing device has an alignment area for the defined alignment and stabilization of the line connection, the alignment area being at least predominantly arranged outside the receiving space and the alignment area being at least mostly enclosed by the sealing element in the longitudinal direction of the alignment area and completely in the circumferential direction of the alignment area is.
  • the alignment area preferably forms a tubular portion or area, the tubular portion or area preferably extending at least partially and particularly preferably for the most part or completely in a straight line.
  • the alignment area particularly preferably encloses the line connection at least in sections and preferably completely for the most part.
  • the production method or production method has the step of producing a one-piece sealing element, the sealing element being produced or arranged on the aligning and fixing device.
  • the sealing element preferably encloses the alignment and fixation device in the circumferential direction of the alignment and fixation device at least in sections completely and preferably only in sections.
  • the manufacturing method for manufacturing the measuring device can further include the step of manufacturing or providing a positioning and loading device for defined arrangement on at least one body part of a living being, the positioning and loading device having a guide support structure for delimiting an examination area.
  • the positioning and loading device can preferably be coupled to the delivery device via a coupling device, in particular the delivery device forms a first coupling point and the positioning and loading device preferably forms a second coupling point.
  • the positioning and loading device and the supply device can preferably be connected to one another, in particular releasably, by coupling the first coupling point to the second coupling point.
  • the first housing part can be designed as a positioning and loading device.
  • the line connection is preferably held by means of a holding device during the creation of the alignment and fixing device.
  • the first orientation is preferred to the second orientation at an angle of more than 3 °, in particular at an angle between 5 ° and 85 °, in particular at an angle between 15 ° and 60 °, in particular at an angle between 25 ° and 60 ° , in particular at an angle between 30 ° and 60 °, in particular at an angle between 35 ° and 50 °.
  • the manufacturing method or Manufacturing method includes the step of producing a one-piece sealing element, the sealing element being produced or arranged on the alignment and fixing device and preferably completely enclosing it at least in its circumferential direction.
  • FIG. 1a shows a first schematic view of a measuring device according to the invention
  • 2a is a perspective view of an exemplary alignment
  • Fig. 2b is a sectional view of the alignment and shown in Fig. 2a
  • Fixation device, 2c shows a plan view of an arrangement according to which the alignment and fixing device is arranged around a line connection and according to which the alignment and fixing device is partially enclosed by a sealing element,
  • Fig. 3a is a schematic representation of a line connection, wherein the
  • Line connection has a defined shape in sections
  • FIG. 3b shows the line connection from FIG. 3a with the alignment and fixing device according to FIG. 2a arranged thereon
  • FIG. 3c shows the arrangement from FIG. 3b with it arranged or generated
  • FIG. 4a shows the arrangement from FIG. 3c with a first housing part arranged underneath and two fastening elements
  • FIG. 4b shows the components shown in FIG. 4a, the sealing element being arranged on the housing part
  • FIG. 4c shows the components shown in FIG. 4b, the fastening elements holding the alignment and fixing device and the housing part against one another, in particular pressing them against one another,
  • FIG. 5a schematically shows an exemplary sectional illustration through a first and second housing part, through the alignment and fixing device and through the sealing element
  • FIG. 5b exemplarily shows a perspective view of a connection of the arrangement shown in FIG. 3c to a housing part
  • FIG. 6a shows a sectional illustration of the arrangement shown in FIG. 5b
  • the detection device (s) 8 (see FIG. 1b) and the radiation source (s) 6 (see FIG. 1b) are preferably arranged analogously, in particular on a carrier structure 66 (see FIG. 1b) in the provision device 1.
  • the reference numeral 18 denotes a line connection which extends partially outside the provision device 1 and which extends at least partially into the interior of the provision device 1.
  • the line connection 18 is in the transition area between the area outside the provision device 1 and the The area within the provision device 1 is provided with a sealing element 12 or surrounded by it, in particular completely in the circumferential direction.
  • FIG. 2b shows schematically a first orientation 88 or first direction 88 along which the alignment area 31 extends and a second orientation 90 or second direction 90 in which the deflection area 26 deflects the tubular or tube-like course of the alignment and fixing device 24.
  • the reference symbols “U” and “UA” identify the circumferential direction of the alignment and fixing device 24 and the circumferential direction of the alignment region 30.
  • FIG. 2 c shows that the sealing element 12 can for the most part enclose the alignment region 30 of the alignment and fixing device 24.
  • the deflection area 26 and / or the connection point (s) 28, 29 are preferably not enclosed by the sealing element 12, but rather are particularly preferably designed without a sealing element.
  • the reference number 68 denotes a jacket of the line connection 18 and the reference number 36 denotes a line, in particular a supply line.
  • the jacket 68 covers the supply line preferably only in sections in the longitudinal direction of the line connection 18; additionally or alternatively, the jacket 68 preferably covers the majority of the supply line 36 in the longitudinal direction of the line connection 18.
  • a plurality of supply lines can particularly preferably be provided in the line connection 18; all supply lines 36 are preferably overlaid by the jacket 68 at least in sections and preferably only in sections.
  • FIG 4a shows three assemblies: the first housing part 2, the line sealing and alignment / fixing device and two fastening elements 72, 74, in particular screws or pins. It can be seen that the first housing part 2 is brought into contact with the first side 14 of the sealing element 12.
  • FIG. 4 b shows a state in which the sealing element 12 is brought into contact with the first housing part 2.
  • the first and second connection points 28, 29 are aligned, in particular aligned, with respect to a first receiving part 73, in particular a blind hole, and a second receiving part 75, in particular a blind hole.
  • the sealing element 12 is preferably designed in such a way that it can only be connected in exactly one alignment with the first housing part 2, in particular with a connecting device 80 (cf. FIG. 7) that is negative to the first side 14.
  • the receiving part 73 or the receiving parts 73, 75 it is also possible for the receiving part 73 or the receiving parts 73, 75 to be arranged or formed in the second housing part 4.
  • the sealing element 12 preferably forms a circumferential depression or groove or recess on the first side 14
  • FIG. 4c shows an exemplary illustration according to which a state can be recognized in which the fastening elements 72, 74 fix the alignment and fixing device 24 on the first housing part 2.
  • FIG. 5a shows an exemplary sectional illustration. It can be seen from this sectional illustration that the sealing element 12 is in flat contact with the alignment and fixing device 24 via a first contact surface 76 and is in flat contact with the line connection 18 via a second coupling surface 78. In addition, it should be added that the sealing element 12 is in contact with the first and second housing parts 2, 4 via the connection points 81 and 83.
  • the sealing element 12 thus has at least two and preferably at least three and particularly preferably four or at least four or exactly four contact surfaces 81, 83, 76, 78 with other components 2, 4, 24, 18.
  • Fig. 7 shows an example of a cross-sectional shape of the sealing element 12 in a defined section, such as in section 22 (see Fig. 3c).
  • the features shown in FIG. 7 have already been mentioned and described in the description part of FIG. 4b.
  • FIG. 8c shows that the supply device 1, in addition or as an alternative to the line connection 18, has an interface 38 or several interfaces for coupling a line connection, in particular for transmitting or exchanging power and Data, may have.
  • the interface 38 can be at a distance from the sealing element 12 or have no direct contact therewith.
  • Fig. 8c shows that the line connection 18 is aligned inclined with respect to a longitudinal direction of the supply device 1, in particular at an angle between 5 ° and 85 °, in particular an angle between 15 ° and 75 ° or an angle between 35 ° and 55 ° or a Angle between 40 ° and 50 °.
  • the line connection preferably enters the provision device 1 in an area which forms an interface between the longitudinal extension and the width extension. This embodiment is advantageous because the line connection 18 is spaced apart from one another The wrist or forearm of a user is arranged and, as a result, the wrist or the forearm does not press together with the line connection during a vital parameter measurement.
  • the line connection 18 is preferably arranged between the first side 14 of the sealing element 12 and the second side 16 of the sealing element 12, the line connection 18 being in the Receiving space 10 extends into it. Additionally or alternatively, an alignment and fixing device 24 can be provided for aligning and fixing at least one section of the line connection 18, the alignment and fixing device 24 being at least partially arranged in the receiving space 10 and the sealing element 12 in the alignment and fixing device 24 in Circumferential direction U of the aligning and fixing device 24 completely encloses. Additionally or alternatively, the distance between the first side 14 of the sealing element 12 and the second side 16 of the sealing element 12 in the direction V of the sealing element 12 is greater in a first section 20 than in a second section 22.
  • first fastening element functional fluid supply device 73 first receiving part control device 74 further or second fastening element supply line or first
  • Supply line 75 second receiving part interface for coupling a 76 contact surface between further or second sealing element and line connection alignment and fixing device measuring device 78 contact surface between

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Cardiology (AREA)
  • Vascular Medicine (AREA)
  • Biomedical Technology (AREA)
  • Molecular Biology (AREA)
  • Veterinary Medicine (AREA)
  • Biophysics (AREA)
  • Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Medical Informatics (AREA)
  • Physics & Mathematics (AREA)
  • Surgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Physiology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Dentistry (AREA)
  • Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)

Abstract

La présente invention concerne un dispositif de distribution (1) pour délivrer au moins un rayonnement d'exposition, en particulier pour déterminer des paramètres vitaux, le dispositif de distribution (1) ayant au moins : une première partie de boîtier (2) et une seconde partie de boîtier (4), la première partie de boîtier (2) et la seconde partie de boîtier (4) étant accouplées, en particulier de manière détachable, dans un alignement défini l'une avec l'autre ; une première source de rayonnement (6) pour délivrer le rayonnement d'exposition ; un premier dispositif de détection (8) pour détecter un rayonnement de détection, la première partie de boîtier (2) et la seconde partie de boîtier (4) formant un espace de réception (10) pour stocker au moins la première source de rayonnement (6) et stocker au moins le premier dispositif de détection (8), un élément d'étanchéité (12) s'étendant autour de la première partie de boîtier (2) et de la seconde partie de boîtier (4), l'élément d'étanchéité (12) étant en contact avec la première partie de boîtier (2) sur un premier côté (14), et l'élément d'étanchéité (12) étant en contact avec la seconde partie de boîtier (4) sur un second côté (16) ; et un raccordement de conduite (18) pour introduire des données, de l'électricité et/ou des substances dans l'espace de réception (10). Selon l'invention, la distance entre le premier côté (14) de l'élément d'étanchéité (12) et le second côté (16) de l'élément d'étanchéité (12) est plus grande dans une première section (20) que dans une seconde section (22) dans la direction de déplacement (V) de l'élément d'étanchéité (12).
PCT/EP2020/083964 2019-12-01 2020-11-30 Appareil pour mesurer des paramètres vitaux, ayant un agencement d'étanchéité avantageux WO2021110598A1 (fr)

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DE102019008320.2 2019-12-01
DE102019008320.2A DE102019008320B4 (de) 2019-12-01 2019-12-01 Vorrichtung zum messen von vitalparametern mit vorteilhafter dichtungsanordnung

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US4406289A (en) 1980-09-12 1983-09-27 Nederlandse Centrale Organisatie Voor Toegepast-Natuurwetenschappelijk Device for the indirect, non-invasive and continuous measurement of blood pressure
US4524777A (en) 1983-02-25 1985-06-25 Ueda Electronic Works Limited Automatic, continuous and indirect blood pressure measurement apparatus
US4726382A (en) 1986-09-17 1988-02-23 The Boc Group, Inc. Inflatable finger cuff
WO2000059369A2 (fr) 1999-03-30 2000-10-12 Cnsystems Medizintechnik Gmbh Tensiometre non invasif a mesure continue
WO2004086963A2 (fr) 2003-04-01 2004-10-14 Cnsystems Medizintechnik Gmbh Dispositif et procede pour mesure non invasive continue de la tension arterielle
US20050148885A1 (en) * 2003-08-22 2005-07-07 Eppcor, Inc. Non-invasive blood pressure monitoring device and methods
WO2005037097A1 (fr) 2003-10-21 2005-04-28 Cnsystems Medizintechnik Gmbh Dispositif et procede pour reguler la pression dans un manchon gonflable d'un tensiometre
WO2010050798A1 (fr) 2008-10-29 2010-05-06 Bmeye B.V. Dispositif de mesure de pression sanguine, extrémité antérieure, corps gonflable et produit informatique
WO2011045138A1 (fr) 2009-10-15 2011-04-21 Finapres Medical Systems B.V. Dispositif de commande de la pression dans un capteur de pression gonflable
WO2011051822A1 (fr) 2009-10-29 2011-05-05 Cnsystems Medizintechnik Ag Appareil et procédés pour améliorer et analyser des signaux à partir d'un dispositif non invasif de mesure en continu de la pression sanguine
WO2011051819A1 (fr) 2009-10-29 2011-05-05 Cnsystems Medizintechnik Ag Procédé de régulation numérique pour mesure de tension artérielle
WO2012032413A2 (fr) 2010-09-07 2012-03-15 Cnsystems Medizintechnik Ag Capteur jetable et amovible pour la mesure continue non invasive de la pression artérielle
EP2858469A2 (fr) * 2013-10-03 2015-04-08 Valeo Powertrain Energy Conversion AS Dispositif d'enceinte électronique
WO2017143366A1 (fr) 2016-02-22 2017-08-31 Cnsystems Medizintechnik Ag Procédé et système de mesure pour la détermination continue de la pression sanguine intra-artérielle
US20180019637A1 (en) * 2016-07-18 2018-01-18 Sunonwealth Electric Machine Industry Co., Ltd. Motor with an Improved Damp Proof or Dustproof Effect
US20190254188A1 (en) * 2018-02-14 2019-08-15 Mtd Products Inc Sealing system for electronics enclosure

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DE102019008320B4 (de) 2021-07-15

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