Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H31/00—Artificial respiration or heart stimulation, e.g. heart massage
  • A61H31/02—"Iron-lungs", i.e. involving chest expansion by applying underpressure thereon, whether or not combined with gas breathing means
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H31/00—Artificial respiration or heart stimulation, e.g. heart massage
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H31/00—Artificial respiration or heart stimulation, e.g. heart massage
  • A61H31/004—Heart stimulation
  • A61H31/006—Power driven
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H31/00—Artificial respiration or heart stimulation, e.g. heart massage
  • A61H31/008—Supine patient supports or bases, e.g. improving air-way access to the lungs
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H31/00—Artificial respiration or heart stimulation, e.g. heart massage
  • A61H2031/001—Artificial respiration or heart stimulation, e.g. heart massage fixed on the chest by suction
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H31/00—Artificial respiration or heart stimulation, e.g. heart massage
  • A61H2031/003—Artificial respiration or heart stimulation, e.g. heart massage with alternated thorax decompression due to lateral compression
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H2201/00—Characteristics of apparatus not provided for in the preceding codes
  • A61H2201/12—Driving means
  • A61H2201/1238—Driving means with hydraulic or pneumatic drive
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H2201/00—Characteristics of apparatus not provided for in the preceding codes
  • A61H2201/16—Physical interface with patient
  • A61H2201/1602—Physical interface with patient kind of interface, e.g. head rest, knee support or lumbar support
  • A61H2201/1619—Thorax
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H2201/00—Characteristics of apparatus not provided for in the preceding codes
  • A61H2201/16—Physical interface with patient
  • A61H2201/1602—Physical interface with patient kind of interface, e.g. head rest, knee support or lumbar support
  • A61H2201/165—Wearable interfaces
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H2201/00—Characteristics of apparatus not provided for in the preceding codes
  • A61H2201/16—Physical interface with patient
  • A61H2201/1683—Surface of interface
  • A61H2201/169—Physical characteristics of the surface, e.g. material, relief, texture or indicia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H2205/00—Devices for specific parts of the body
  • A61H2205/08—Trunk
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H2205/00—Devices for specific parts of the body
  • A61H2205/08—Trunk
  • A61H2205/084—Chest

Definitions

• the invention relates to a device for the selective regionalization of pulmonary aeration, for selectively surrounding the posterior part of the thoracic cage of a patient, to create a depression therein by means of a negative pressure generator.
• the invention finds applications in the medical field, and in particular in the field of ventilatory assistance for patients with respiratory pathology associated with inhomogeneous pulmonary lesions.
• the invention is particularly suitable for the treatment or prevention of acute or chronic respiratory failure.
• Acute or chronic respiratory failure is a condition affecting several million people around the world. In some cases, the inability of the respiratory system to ensure sufficient oxygenation of the body must be compensated for by ventilatory support.
• ventilatory support by positive intrathoracic pressure is delivered via an invasive (intubation probe or tracheostomy cannula) or non-invasive (nasal mask, face mask, or helmet) interface, connected to a positive pressure generator.
• ventilatory assistance by extrathoracic negative pressure is delivered globally via a shell or breastplate (placed on the anterior part of the trunk), a cage or a waterproof garment (notably containing the entire trunk), connected to a negative pressure generator.
• pulmonary lesions have a clear posterolateral predominance.
• the overall delivery of ventilation then exposes the risk of non-recruitment of injured areas and overdistension of healthy areas, likely to cause or aggravate the injuries induced by ventilatory assistance ("ventilator-induced lung injury", or VILI). .
• VILI ventilatory assistance
• the present invention makes it possible to redistribute in a more homogeneous manner the ventilation delivered by ventilatory assistance and / or naturally by the respiratory muscles, so as to preferentially apply the injured areas, rather than the healthy areas of one or more lungs, in a patient. with respiratory failure most often requiring ventilatory assistance, if their respiratory muscles are unable to ensure sufficient ventilation of the lungs.
• the object of the invention is to at least partially solve the problem associated with overventilation of healthy areas to the detriment of injured areas in one or both lungs of a patient in need of artificial respiratory assistance.
• the invention proposes a device allowing the selective regionalization of the distribution of pulmonary aeration, so as to preferentially recruit the damaged areas of a lung during ventilatory assistance or during spontaneous ventilation.
• the damaged areas of a lung are most often located in the posterolateral part.
• the invention proposes to create locally a depression capable of promoting the opening and aeration of the damaged posterolateral areas of the lung to make them available to the ventilation delivered by ventilatory assistance (in positive pressure) and / or naturally by the respiratory muscles.
• the device according to the invention selectively surrounds the dorsal part of the patient's thoracic cage, in a hermetic manner.
• the space between the patient's body and the device is advantageously filled with a material capable of conforming to the contours of the patient's body and which allows a distance between the negative pressure orifice and the skin of the dorsal wall to be kept as a spacer. (in order to avoid a contact point between the skin of the dorsal wall and the shell at the level of the negative pressure orifice which would generate a depression that is too focal and too strong at this point of contact). A depression is created in this space and in the posterolateral part of the patient's lungs.
• the device according to the invention is non-invasive and can be used in a hospital or non-hospital environment.
• the device is molded to the dimensions of the patient, in order to ensure optimum sealing.
• the device according to the invention can be used alone or in combination with a conventional, invasive or non-invasive ventilatory assistance system.
• the subject of the invention is therefore a device for selective regionalization of pulmonary aeration, intended to apply a depression on a posterolateral part of the thoracic wall of a patient, said device comprising a rigid or semi-rigid shell, intended in selectively surrounding a posterior part of the chest wall of the patient, and a layer of alveolar material covering an internal wall of the rigid shell, intended to be in contact with the chest wall of the patient, said shell comprising at least one through orifice, intended to be connected to a negative pressure generator.
• the invention relates to a device for selective regionalization of pulmonary ventilation, intended to apply a depression on a posterolateral part of the thoracic wall of a patient, said device comprising a rigid or semi-rigid shell. , intended to surround a posterior part of the thoracic wall of the patient, and a layer of alveolar material covering an internal wall of the rigid shell, intended to be in contact with the thoracic wall of the patient, said shell comprising at least one through orifice, intended to be connected to a negative pressure generator.
• the subject of the invention is also a system for applying a localized transpulmonary pressure, said system comprising at least one device for selective regionalization of pulmonary aeration according to the invention, at least one negative pressure generator connected to the device by the through orifice on the shell, so as to impart negative pressure from the generator to the shell and create a depression between the posterior thoracic wall of a patient to which the device is applied and said shell.
• the subject of the invention is also a ventilatory assistance kit comprising a system for applying localized transpulmonary pressure according to the invention and an invasive or non-invasive artificial ventilation system (operating in positive pressure).
• the negative pressure generator is able to deliver constant or variable negative pressures.
• an invasive or non-invasive artificial ventilation system is coupled with the negative pressure generator (s)
• the invasive or non-invasive artificial ventilation system is capable of delivering constant or variable positive pressures.
• [Lig 1] schematically represents a cross section of the thoracic cage of a patient with inhomogeneous lesions, with condensation of the posterolateral part of the right and left lungs.
• FIG. 2 schematically shows side view (A) and top view (B) a device for selective regionalization of pulmonary ventilation according to an example of the invention.
• [Lig 3] shows a cross section of a device for selective regionalization of pulmonary aeration according to an example of the invention, in position around the dorsal part of the thoracic cage of a patient, a selective increase in pressure transpulmonary in the posterolateral zones which have been represented by arrows (the pulmonary aeration resulting from artificial or spontaneous ventilation is thus better distributed in the posterolateral zones of the two lungs).
• FIG 4 shows an example of a seal that can be used with the device for selective regionalization of pulmonary ventilation according to the invention.
• the present invention provides a device intended to selectively surround the posterior (dorsal) part of the thoracic cage of a patient and capable of applying a depression to all or part of the posterior part of said thoracic cage.
• the term "patient” denotes a mammal, and preferably a human, including an adult, a child or an infant.
• the term “patient” can also refer to a non-human animal, in particular a non-human primate.
• the device according to the invention comprises a shell made of rigid or semi-rigid material, forming the structure which will receive the patient's body.
• the shell is for example plastic such as polypropylene, polyethylene, polyamide, composite material such as glass, carbon, aramid, or resin fibers. It can be modeled for example by thermoforming or three-dimensional printing.
• the shell preferably has an elliptical shape having a concave curvature to match a contour of the posterior part of the patient's chest wall.
• the dimensions of the shell are such that the shell covers the posterior and lateral part of the thorax, from the lower costal rim at the bottom to the inter-scapular region at the top at the height of the axillary hollows, and transversely of a line middle axillary to the other.
• the shell is obtained by molding, taking into account the dimensions of the patient.
• the shell is obtained by means of a 3D printing scan.
• the general shape of the shell is such that it hermetically conforms to a contour of the dorsal part of the thoracic wall of the patient, when the patient is lying on said shell.
• the shape of the shell is such that it makes it possible to receive the dorsal part of the thorax of a patient, from the lower costal edge at the bottom to the inter-scapular region at the height of the axillary hollows at the top and one middle axillary line to another on the sides.
• the shell thus delimits a volume intended to receive a dorsal and lateral part of the thoracic cage of a patient.
• a layer of alveolar (or porous) material lines the internal wall of the shell, directed towards the patient's body.
• the dorsolateral part of the patient's body is therefore in contact with the layer of alveolar material.
• the layer of cellular material has a structure allowing, when a depression is created in the shell, to distribute the depression evenly over the entire contact surface of the dorsal part of the patient's chest wall.
• the layer of cellular material is made of polymer, preferably chosen from polyurethane, polyethylene, polyether.
• the layer of alveolar or cellular material is, for example, a homogenization foam, preferably with open porosity, thus allowing the pores of the foam to be connected to each other and to distribute the negative pressure homogeneously.
• the foam used has low density and low rigidity, in particular in order to conform to the contours of the dorsal part of the patient.
• the foam can in particular be a polymeric foam, in particular made of polypropylene or polystyrene.
• the seal between the hermetic shell and the patient's body is obtained by means of sealing means, extending over a peripheral part of the shell, intended to be placed in sealed abutment against the thoracic wall. of the patient.
• the sealing means include a seal.
• the connection between the seal and the shell can also be reinforced with an adhesive.
• the seal comprises two sealing lips, intended to come into contact with the patient's skin, on either side of the peripheral part of the shell.
• the shell may have one or more reinforcing grooves, extending over the inner and outer wall of the shell.
• the cross section of each groove forms a concavity at the level of the internal wall and a convexity at the level of the external wall.
• at least one reinforcing groove opens into an orifice passing through the shell.
• the groove or grooves can also be used to suck and evacuate any serosities.
• the device comprises a central support means, extending longitudinally on the internal wall of the shell, and intended to come into contact with the body of the patient facing the spine.
• the support means is made of a sufficiently dense and / or resistant material so as not to collapse under the weight of the patient and to support the patient's spine.
• the central support means is made of waterproof material, capable of hermetically separating the parts of the shell arranged on either side of said central support means when the shell is held around the part. posterior rib cage of the patient.
• the central support means makes it possible to divide the internal volume of the shell into two parts, in which it is possible to independently create the vacuum.
• the support means is made of a viscoelastic material, in particular a viscoelastic gel.
• the device for selective regionalization of the distribution of pulmonary aeration comprises a rigid or semi-rigid hermetic shell, intended to selectively surround a posterior part of the chest wall of the patient, a seal sealing extending over a peripheral part of said shell and intended to be placed in sealed abutment against the chest wall of the patient, a central support means extending transversely on the internal wall of the shell and dividing the shell in two parts, each of the two parts of the shell being lined with a layer of cellular material, the wall of the shell being crossed at each of these parts by an orifice intended to be connected to a negative pressure generator, so that it is possible to create a depression in one and / or the other part of the shell when it is applied to the posterior part of the patient's rib cage.
• the invention also relates to a system for applying a localized transpulmonary pressure, said system comprising at least one device for selective regionalization of the distribution of pulmonary aeration as described above and at least one connected negative pressure generator. to the device through the through orifice on the shell, so as to impart negative pressure from the generator to the shell and create a depression between the posterior thoracic wall of a patient on which the device is applied and said shell.
• the device for selective regionalization of the distribution of pulmonary aeration as described above in combination with an invasive or non-invasive artificial ventilation system (which operates in positive pressure) .
• the device aims to better distribute the pulmonary aeration resulting from the ventilation delivered by ventilatory assistance with an invasive or non-invasive artificial ventilation system in positive pressure, and / or naturally by the respiratory muscles, to preferentially distribute the aeration. in the posterolateral areas of the lungs, by selectively promoting the opening of the alveoli of these usually damaged areas, the latter otherwise remaining (in the state of the known art) occluded to the ventilation generated by an artificial ventilation system and / or naturally by the respiratory muscles.
• Figure 1 shows a cross section of a thoracic cage of a human patient, lying on his back (supine), vertebrae 6 facing down in the figure.
• the posterior parts 3 of the lungs are condensed and poorly ventilated (horizontal hatching), being able to undergo opening / closing cycles causing additional lung damage, while the relatively healthy anterior 4 parts (vertical hatching) are overdistended by ventilatory assistance overall.
• the device 10 overcomes this problem by promoting in a targeted manner the re-aeration of the posterior part of one or both lungs 1, 2 ( Figure 3). More precisely, the dorsal part of the thoracic cage of the patient is housed in the hermetic shell 11, and rests on a homogenization foam 12 lining an internal wall 13 of said shell 11.
• a vacuum pump (not shown) is connected to the shell 11 hermetic by at least one through orifice 14 formed in the shell 11 ( Figures 2 A & 2B) to create a depression capable of lowering the pleural pressure around the posterior part 3 of the lung and thus increasing the transpulmonary pressure in a localized manner , favoring its re-ventilation.
• a pressure sensor can be connected to the vacuum pump to monitor the pressure inside the hull.
• the injured area of the lung can be defined beforehand on the basis of a clinical examination or additional imaging examinations.
• FIGS. 2A and 2B schematically show an embodiment of a device for selective regionalization of pulmonary aeration 10 towards the postero-lateral zones according to the invention.
• the shell has a general shape and a curvature, and is made of a rigid or semi-rigid material, allowing to follow the contours of the dorsal part of the thoracic cage of the patient.
• the shell 11 extends longitudinally from the lower edge of the ribs to the axillary hollow, and transversely to the mid-axillary line.
• Two through orifices 14 are made on the wall of the hermetic shell 11, on either side of a central longitudinal axis (extending substantially along the spine of the patient housed in the shell) dividing said shell 11 into two side parts 15, 16 substantially equal.
• a central support means 17 extends longitudinally along the inner wall 13 of the shell 11, so as to physically separate the two side parts 15, 16.
• the homogenization foam 12 lines each of the side parts 15, 16 from a peripheral contour 18 to the central support means 17.
• the foam 12 can extend over the entire internal wall 13 of the shell 12, and the means central support 17 covers said foam 12 or is covered by said foam 12.
• the presence of the central support means 17 allows to potentially divide into two parts the internal volume of the shell 1 1.
• each part of the shell 11 is provided with a through orifice 14 capable of being connected to a negative pressure generator, it is possible to generate depressions individually in each part or in combination and thus promote the aeration of one or more two lungs.
• the seal 20 comprises two contact lips 21. , 22 of deformable material making it possible to guarantee the sealing of the connection between the shell 11 and the dorsal part of the thoracic wall, during the depression.
• the shell 11 is further provided with reinforcing grooves 2, extending longitudinally or transversely on said shell 11.
• longitudinal grooves extend between the two through holes 14.

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• Health & Medical Sciences (AREA)
• Pulmonology (AREA)
• Cardiology (AREA)
• Heart & Thoracic Surgery (AREA)
• Rehabilitation Therapy (AREA)
• Epidemiology (AREA)
• Pain & Pain Management (AREA)
• Physical Education & Sports Medicine (AREA)
• Emergency Medicine (AREA)
• Life Sciences & Earth Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Percussion Or Vibration Massage (AREA)
• Prostheses (AREA)
• Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)

Applications Claiming Priority (2)

Publications (3)

Family

ID=67441315

Family Applications (1)

Country Status (4)

Family Cites Families (7)

• 2019
  • 2019-03-04 FR FR1902190A patent/FR3093433B1/fr active Active
• 2020
  • 2020-03-03 EP EP20725812.0A patent/EP3934602B1/de active Active
  • 2020-03-03 US US17/435,443 patent/US20220054354A1/en active Pending
  • 2020-03-03 WO PCT/FR2020/050421 patent/WO2020178521A1/fr unknown

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