WO2021215586A1 - Isolateur en pression négative pouvant être installé sur mesure pour un patient - Google Patents

Isolateur en pression négative pouvant être installé sur mesure pour un patient Download PDF

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Publication number
WO2021215586A1
WO2021215586A1 PCT/KR2020/009799 KR2020009799W WO2021215586A1 WO 2021215586 A1 WO2021215586 A1 WO 2021215586A1 KR 2020009799 W KR2020009799 W KR 2020009799W WO 2021215586 A1 WO2021215586 A1 WO 2021215586A1
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WO
WIPO (PCT)
Prior art keywords
patient
negative pressure
installable
cover
tailored
Prior art date
Application number
PCT/KR2020/009799
Other languages
English (en)
Inventor
Ki Sub Sung
Ju Young Hong
Original Assignee
Industry-Academic Cooperation Foundation, Yonsei University
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 Industry-Academic Cooperation Foundation, Yonsei University filed Critical Industry-Academic Cooperation Foundation, Yonsei University
Publication of WO2021215586A1 publication Critical patent/WO2021215586A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61G—TRANSPORT, PERSONAL CONVEYANCES, OR ACCOMMODATION SPECIALLY ADAPTED FOR PATIENTS OR DISABLED PERSONS; OPERATING TABLES OR CHAIRS; CHAIRS FOR DENTISTRY; FUNERAL DEVICES
    • A61G10/00—Treatment rooms or enclosures for medical purposes
    • A61G10/02—Treatment rooms or enclosures for medical purposes with artificial climate; with means to maintain a desired pressure, e.g. for germ-free rooms
    • A61G10/023—Rooms for the treatment of patients at over- or under-pressure or at a variable pressure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B42/00—Surgical gloves; Finger-stalls specially adapted for surgery; Devices for handling or treatment thereof
    • A61B42/10—Surgical gloves
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B46/00—Surgical drapes
    • A61B46/20—Surgical drapes specially adapted for patients
    • 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
    • A61B90/40—Apparatus fixed or close to patients specially adapted for providing an aseptic surgical environment
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61G—TRANSPORT, PERSONAL CONVEYANCES, OR ACCOMMODATION SPECIALLY ADAPTED FOR PATIENTS OR DISABLED PERSONS; OPERATING TABLES OR CHAIRS; CHAIRS FOR DENTISTRY; FUNERAL DEVICES
    • A61G10/00—Treatment rooms or enclosures for medical purposes
    • A61G10/005—Isolators, i.e. enclosures generally comprising flexible walls for maintaining a germ-free environment
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61G—TRANSPORT, PERSONAL CONVEYANCES, OR ACCOMMODATION SPECIALLY ADAPTED FOR PATIENTS OR DISABLED PERSONS; OPERATING TABLES OR CHAIRS; CHAIRS FOR DENTISTRY; FUNERAL DEVICES
    • A61G13/00—Operating tables; Auxiliary appliances therefor
    • A61G13/10—Parts, details or accessories
    • A61G13/12—Rests specially adapted therefor; Arrangements of patient-supporting surfaces
    • A61G13/1205—Rests specially adapted therefor; Arrangements of patient-supporting surfaces for specific parts of the body
    • A61G13/121—Head or neck
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F24—HEATING; RANGES; VENTILATING
    • F24F—AIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
    • F24F11/00—Control or safety arrangements
    • F24F11/0001—Control or safety arrangements for ventilation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B2017/00831—Material properties
    • A61B2017/00902—Material properties transparent or translucent
    • 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
    • A61B90/40—Apparatus fixed or close to patients specially adapted for providing an aseptic surgical environment
    • A61B2090/401—Apparatus fixed or close to patients specially adapted for providing an aseptic surgical environment using air flow
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F24—HEATING; RANGES; VENTILATING
    • F24F—AIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
    • F24F11/00—Control or safety arrangements
    • F24F11/0001—Control or safety arrangements for ventilation
    • F24F2011/0002—Control or safety arrangements for ventilation for admittance of outside air
    • F24F2011/0005—Control or safety arrangements for ventilation for admittance of outside air to create underpressure in a room, keeping contamination inside
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F24—HEATING; RANGES; VENTILATING
    • F24F—AIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
    • F24F3/00—Air-conditioning systems in which conditioned primary air is supplied from one or more central stations to distributing units in the rooms or spaces where it may receive secondary treatment; Apparatus specially designed for such systems
    • F24F3/12—Air-conditioning systems in which conditioned primary air is supplied from one or more central stations to distributing units in the rooms or spaces where it may receive secondary treatment; Apparatus specially designed for such systems characterised by the treatment of the air otherwise than by heating and cooling
    • F24F3/16—Air-conditioning systems in which conditioned primary air is supplied from one or more central stations to distributing units in the rooms or spaces where it may receive secondary treatment; Apparatus specially designed for such systems characterised by the treatment of the air otherwise than by heating and cooling by purification, e.g. by filtering; by sterilisation; by ozonisation
    • F24F3/163—Clean air work stations, i.e. selected areas within a space which filtered air is passed

Definitions

  • the present invention relates to a patient tailored-installable negative pressure isolator that can be used to prevent diffusion pathogens (virus, etc.) from spreading through droplet or aerosols.
  • the present invention relates to a patient tailored-installable negative pressure isolator that can be easily installed and reinstalled on the bed of a patient, etc., can provide an individual isolated space for a patient, and can be used in various ways due to a structure that can be flexibly changed in accordance with circumstances.
  • COVID19 that is presently prevalent in the world in 2020 is a respiratory infection having an airborne spread route through droplet and has been known as being highly infectious, including not only an indirect spread route through a surface infected with droplet, but also the possibility of spread through aerosols.
  • a negative pressure room with internal pressure lower than the outside to efficiently isolate a patient infected with such an infection. Since a negative pressure room requires a facility for pressure control, etc., negative pressure rooms are usually prepared in a separate ward and a sufficient number of negative pressure rooms may not be prepared in hospitals. Accordingly, a technology that temporarily constructs a whole negative pressure room outside in an emergency has been used in the related art (e.g., Korean Patent No. 10-1646524).
  • An object of the present invention is to provide a patient tailored-installable negative pressure isolator that can be installed, removed, and reinstalled at the bed of a patient, can provide an isolation space for each individual patient or new patient, and can be used in various ways due to a structure that can be flexibly changed in accordance with circumstances.
  • a patient tailored-installable negative pressure isolator includes: a base configured to be disposed under the back of the head of a patient lying down; a fixed cover connected to the base, configured to cover the face of the patient, having an intake tube connected to a side thereof to suction air, being maintained at negative pressure, and having an opening formed toward the body of the patient; and a variable cover connected to the opening of the fixed cover, configured to stretch and contract along the body of the patient, configured to cover the patient, and having an internal negative pressure space communicating with the fixed cover.
  • the fixed cover may be at least partially made of a light-transmissive material so that the inside thereof can be visually shown, and may have at least one treatment port through which at least one of the body of a medical staff and medical instruments can go in and out.
  • the treatment ports may be disposed side by side to each other in a pair opposite the opening so that a medical staff can insert both arms from the crown of the head of the patient, and a light-transmissive surface that is an inclined surface disposed toward the gaze of a medical staff may be formed on a surface of the fixed cover close to the treatment port.
  • the patient tailored-installable negative pressure isolator may further include sanitary gloves connected inside the treatment ports.
  • the base may be detachably coupled to the fixed cover.
  • the fixed cover may be coupled to the base by sliding from an end of the base with the head of the patient supported by the base.
  • Rail grooves may be formed at any one of the fixed cover and the base, and protrusions coupled to the rail groove to slide may be formed at the other one.
  • the base may be composed of a plurality of separate plates configured to be disposed at different positions under the back of the head and separably coupled to each other.
  • the separate plates may include a first separate plate and a second separate plate that are respectively inserted under the left and right sides of the back of the head with the neck of the patient therebetween.
  • the patient tailored-installable negative pressure isolator may further include a detachable coupling portion disposed between the variable cover and the fixed cover to detachably couple the variable cover and the fixed cover.
  • variable cover may be made of a flexible material to be fixed in close contact with the body of the patient by stretching or contracting along the body of the patient.
  • variable cover may be formed by connecting a plurality of covers that can overlap each other in multiple steps to be able to slide along the body of a patient.
  • the patient tailored-installable negative pressure isolator may further include extensions protruding from the base to stretch and contract along the body at both sides of the patient, in which the extensions and a side of the variable cover may be detachably coupled to each other.
  • variable cover may be fixed to the extensions by magnetic force or a Velcro tape.
  • the base may have a shock-absorbing pad disposed on the surface that is brought in contact with the head of the patient.
  • the present invention it is possible to provide a patient-fit sealed negative pressure isolation space for each bed through only simple installation. Further, a medical staff can conveniently access a patient and perform necessary treatment or operations even without disassembling the isolation space. Accordingly, protectors, etc. for medical staffs are relatively simplified, so it is possible to reduce a burden on medical staffs and induce more precise operations. Further, since the isolation space is formed to fit the body of a patient, the surrounding space can be more widely used. Further, it is possible to expose only necessary parts of a patient and perform appropriate treatments or operations with the other parts isolated at negative pressure by expanding or reducing the isolation space using a deformable structure, if necessary.
  • the present invention can be very simply installed and removed, so it can be very usefully used by being applied to a necessary bed and then reinstalled on another bed after the patient leave the hospital. Further, it is possible to considerably increase the number of substantial negative pressure beds using existing common beds, etc., by using the present invention. Accordingly, it is possible to effectively deal with rapid spread of infected people through the present invention.
  • FIG. 1 is a perspective view of a patient tailored-installable negative pressure isolator according to an embodiment of the present invention.
  • FIG. 2 is a perspective view showing the patient tailored-installable negative pressure isolator of FIG. 1 in another direction.
  • FIG. 3 is a perspective view showing the patient tailored-installable negative pressure isolator of FIG. 1 with a variable cover stretched.
  • FIG. 4 is a vertical cross-sectional view of the patient tailored-installable negative pressure isolator of FIG. 3.
  • FIG. 5 is an exploded perspective view of the patient tailored-installable negative pressure isolator of FIG. 1.
  • FIG. 6 is a view showing the process of installing the patient tailored-installable negative pressure isolator of FIG. 1.
  • FIG. 7 is a view showing an example of using the patient tailored-installable negative pressure isolator of FIG. 1.
  • FIG. 8 is a perspective view of a patient tailored-installable negative pressure isolator according to another embodiment of the present invention.
  • FIGS. 9 and 10 are views showing an example of using the patient tailored-installable negative pressure isolator of FIG. 8.
  • FIG. 11 a view showing an example of using the patient tailored-installable negative pressure isolator according to another embodiment of the present invention.
  • FIGS. 1 to 11 An embodiment of the present invention will be described first in detail with reference to FIGS.1 to 7 and then other embodiments will be described in detail with reference to FIGS. 8 to 11.
  • FIG. 1 is a perspective view of a patient tailored-installable negative pressure isolator according to an embodiment of the present invention
  • FIG. 2 is a perspective view showing the patient tailored-installable negative pressure isolator of FIG. 1 in another direction
  • FIG. 3 is a perspective view showing the patient tailored-installable negative pressure isolator of FIG. 1 with a variable cover stretched.
  • patient tailored-installable negative pressure isolator 1 includes a fixed cover 100 in a shape of a case that covers the face of a patient and a variable cover 300 connected to the fixed cover 100 to be deformed.
  • the fixed cover 100 and the variable cover 300 are connected such that their insides communicate with each other, so when air is suctioned through an intake tube 170 connected to a side, the pressure of the entire connected inside decreases lower than that of the outside. Accordingly, a negative pressure isolation space isolated from the outside can be formed in the patient tailored-installable negative pressure isolator 1.
  • the fixed cover 100 is configured to accommodate the head of a patient in a fixed form
  • the variable cover 300 is configured to deform and accommodate the lower body of a patient. That is, the variable cover 300, as shown in FIGS. 1 to 3, is deformed and can be stretched and contracted along the body of a patient, whereby it is possible to form a negative pressure isolation space having an appropriate size to fit the body of a patient. If necessary, it is possible to expand or contract the negative pressure isolation space by adjusting the variable cover 300, and accordingly, it is possible to make the body of patient that requires a specific treatment or operation be exposed outside the negative pressure isolation space. Accordingly, it is possible to perform a more appropriate treatment or operation while considerably decreasing the danger of infection of medical staffs.
  • the detailed configuration of the patient tailored-installable negative pressure isolator 1 of the present invention is as follows.
  • the patient tailored-installable negative pressure isolator 1 includes: a base 200 configured to be disposed under the back of the head of a patient lying down, a fixed cover 100 connected to the base 200 to cover the face of a patient, having an intake tube 170 connected to a side thereof such that the inside is maintained at negative pressure, and having an opening 101 (see FIGS. 4 and 5) open toward the body of a patient; and a variable cover 300 connected to the opening 101 of the fixed cover 100, stretching and contracting along the body of a patient to cover the patient, and having a variable internal negative pressure space communicating with the fixed cover.
  • the internal negative pressure space may be the inside of the variable cover of the negative pressure isolation space in the isolator.
  • the base 200 may be detachably coupled to the fixed cover 100 and may be composed of a plurality of separate plates (a first separate plate (see 200a in FIG. 5) and a second separate plate (see 200b in FIG. 5)) that are separably coupled to each other and configured to be disposed at different positions under the back of a head.
  • the fixed cover 100 can be coupled to the base 200 by sliding from an end of the base 200 with the head of a patient supported on the base 200 (see FIG. 6).
  • the configuration, the operation effect, etc. of the patient tailored-installable negative pressure isolator 1 are described in more detail on the basis of the embodiment of the present invention.
  • other several features of the present invention that are not stated herein will be more clearly understood.
  • the patient tailored-installable negative pressure isolator 1 may be composed of three parts.
  • the base 200 and the fixed cover 100 are connected to each other to surround the head of a patient, and the variable cover 300 is configured to cover the lower body of a patient by stretching from the fixed cover 100.
  • the base 200 is disposed under the back of the head of a patient lying down, thereby supporting the head of the patient.
  • the base 200 may be integrated with the fixed cover 100, but may be detachably coupled to the fixed cover 100, as in this embodiment. Since the base 200 of this embodiment can be attached to/detached from the fixed cover 100, it can be more conveniently slid under the back of the head of a patient lying down. Further, the fixed cover 100 and the variable cover 300 can also be more easily installed with the base 100 disposed in this way. A detailed installation process will be described in more detail below.
  • the base 200 may have an area that is enough to support the head of a patient and may be formed entirely in a rectangular panel shape.
  • the base 200 has a shock-absorbing pad 210 on the surface that is brought in contact with the head of a patient, thereby being able to protect the patient's head from a shock.
  • the base 200 is composed of a plurality of separate plates (see 200a and 200b in FIG. 5) that can be detachably coupled to each other and configured to be disposed at different positions under the back of a head, so it is possible to easily install and apply the base for intensive care patients who have difficulty in controlling their heads. Accordingly, the negative pressure isolation space can also be more conveniently formed.
  • the shock-absorbing pad 210 may also be formed in separate form to correspond to the base 200. Since the base 200 can be changed into various shapes as long as it can support the back of the head of a patient, it is not necessarily limited to this embodiment.
  • the fixed cover 100 is connected to the base 200 to cover the face of a patient. That is, the base 200 supports the back of the head of a patient and the fixed cover 100 is stretched away from the base 200 to cover the face of a patient, so the patient's head can be placed in the space defined by the fixed cover 100 and the base 200. As shown in FIGS. 1 to 3, the fixed cover 100 is connected to the base 200 to seal the internal space from the outside and is connected to the variable cover 300 through the opening (see 101 in FIGS. 4 and 5) that is open toward the body of a patient.
  • the fixed cover 100 may be formed in a three-dimensional housing shape such as a hard case, as described above, and the intake tube 170 for suctioning air may be connected to a side of the fixed cover 100.
  • a hole may be formed through a side of the fixed cover 100, and an end of the intake tube 170 may be fixed to the fixed cover 100, as shown in the figures.
  • the other end of the intake tube 170 not shown in the figures may be connected to pressure control equipment including an intake pump (not shown), etc.
  • the fixed cover 100 is at least partially made of a light-transmissive material so that the inside can be visually shown. That is, it is possible to prevent droplet, etc. from spreading outside by disposing the fixed cover 100 between a patient and medical staffs, and medical staffs can perform necessary treatments while checking the condition of a patient through the transparent fixed cover 100.
  • the fixed cover 100 may be made of a light-transmissive plastic having high hardness, and if necessary, the light-transmissive material may be applied to a portion or the entire of the fixed cover 100.
  • the fixed cover 100 further has a treatment port on a side through which at least one of the body of a medical staff and medical instruments can go in and out. For example, the treatment port, as shown in FIGS.
  • first treatment ports 110a and 110b may include a plurality of treatment ports of first treatment ports 110a and 110b and a second treatment port 110c disposed at different positions.
  • a medical staff can more easily access a patient in the negative pressure isolation space by putting both arms inside the first treatment ports 110a and 110b, and the second treatment port 110c can be used to more conveniently put in/out medical instruments, such as an intubation tube, for various treatments. That is, a pair of treatment ports may be formed side by side opposite the opening 101 of the fixed cover 100, like the first treatment ports 110a and 110b, in order that a medical staff can insert both hands toward the crown of the patient's head.
  • the treatment ports are also not necessarily limited thereto and the number of treatment ports may be appropriately changed, if necessary. Further, the use of the treatment ports is not limited and the treatment port may be used for other purposes, which does not depart from the spirit of the present invention.
  • a surface of the fixed cover 100 that is adjacent to the treatment ports may have a light-transmissive surface 130 inclined toward the gaze of a medical staff.
  • the entire light-transmissive surface 130 may be made of the light-transmissive material described above and may be a smooth curved or flat inclined surface that does not excessively refract light such that an internal image is not distorted.
  • the arrangement toward the gaze of a medical staff may mean that when a medical staff looks inside the fixed cover 100, the gaze passes through the light-transmissive surface 130 perpendicularly to the light-transmissive surface 130 or a tangential line of the light-transmissive surface 130.
  • the gaze of the medical staff is formed downward at a predetermined angle to the patient from the medical staff's head positioned higher than the crown of the head (see FIG. 7b), whereby a clearer and wider visual field following the gaze can be provided by the appropriately inclined light-transmissive surface 130. Accordingly, the medical staff can more accurately and smoothly perform an operation. Further, since the outer surface of the fixed cover 100 has the inclined surface, a medical staff can access the patient inside the fixed cover 100 closer. That is, a medical staff can access a patient closer and perform an accurate treatment or operation while checking the patient through the light-transmissive surface 130 that is an inclined surface.
  • the fixed cover 100 may have various structures having various functions as long as it covers the face of a patient. Accordingly, the fixed cover 100 may have an amorphous three-dimensional shape, as shown in FIG. 2.
  • the first treatment ports 110a and 110b may be positioned under the light-transmissive surface 130 and may partially protrude. Handles 140 may be formed at the top of the fixed cover 100 for easy dealing and a detachable filter 120 may be coupled to a side of the fixed cover 100.
  • a detachable coupling portion 150 that detachably connects the variable cover 300 and the fixed cover 100 may be formed between the variable cover 300 and the fixed cover 100 to be described below for easy coupling and separating.
  • FIG. 4 is a vertical cross-sectional view of the patient tailored-installable negative pressure isolator of FIG. 3, and FIG. 5 is an exploded perspective view of the patient tailored-installable negative pressure isolator of FIG. 1.
  • the variable cover 300 is connected to the opening 101 of the fixed cover 100 and covers a patient by stretching and contracting along the body of the patient. Accordingly, as shown in FIG. 4, the internal negative pressure space communicating with the fixed cover 100 is also variable. That is, the fixed cover 100 and the variable cover 300 are connected to each other, whereby a negative pressure isolation space isolated from the outside can be formed therein and can be varied by stretching/contracting the variable cover 300. Variation is usually implemented as the negative pressure space inside the variable cover 300 is deformed by stretching/contracting the variable cover 300.
  • the variable cover 300 is made of a flexible material and is fixed in close contact with the body of the patient while stretching or contracting along the body of the patient.
  • the variable cover 300 may be made of a flexible plastic material and may be made of a light-transmissive material.
  • the variable cover 300 may include a material such as vinyl.
  • a frame may be formed at a side of the variable cover 300 using a plastic material or other materials that have high hardness, and the variable cover 300 may be appropriately formed to stretch and contract into predetermined shapes.
  • the variable cover 300 for example, may be formed in a shape of bellows to easily stretch and contract.
  • a contact portion 310 that comes in close contact with the body of a patient may be formed at the end of the variable cover 300.
  • the contact portion 310 has elasticity, thereby being able to come in close contact with the body of a patient or plastically deform to follow curves of the body.
  • the detachable coupling portion 150 described above is formed between the variable cover 300 and the fixed cover 100, the covers can be easily coupled and separated.
  • the detachable coupling portion 150 may be a structure having a zipper, but may include other various detachable structures.
  • the detachable coupling portion 150 may have a structure that can implement sealing through thorough coupling, and the coupling structure may have same or different one or two or more combined coupling types.
  • the detachable coupling portion 150 may be formed in various ways that can easily detachably couple the variable cover 300 and the fixed cover 10 and can effectively form a sealing structure.
  • the detachable coupling portion 150 for example, may be formed at the opening 101 of the fixed over 100 and the end of the variable cover 300 being in contact with the opening 101 to correspond to each other.
  • the variable cover 300 is connected to the fixed cover 100, but is also connected to the base 200, whereby structural stability can be increased.
  • extensions 220 protruding from the base 200 may be formed to stretch/contract along the body of a patient at both sides of the patient, and sides of the extensions 220 and the variable cover 300 may be detachably coupled to each other.
  • fixing portions 230 corresponding to each other may be formed on the extensions 220 and the side of the variable cover 300 that is in contact with the extensions 200.
  • the fixing portion 230 for example, may be coupled to each other by magnetic force or may be formed using Velcro tapes. That is, the variable covers 300 may be fixed to the extensions 220 by magnetic force or Velcro tapes.
  • variable cover 300 it is possible to connect the variable cover 300 to the base 200 using a relatively simple detachable structure in order to easily finish a sealing structure.
  • the extensions 220 as shown in the figure, are slidably coupled to the base 200, and if necessary, may be folded into multiple steps. When the extensions 220 are coupled to the variable cover 300, they can support the variable cover 300 while stretching/contracting with the variable cover 300.
  • the base 200 is composed of the first separate plate 200a and the second separate plate 200b, as in this embodiment, the extensions 220 may protrude outward from the separate plates in a pair.
  • the base 200 may be made of a plurality of separate plates that can be separately coupled to each other and are configured to be disposed at different positions under the back of a head.
  • the base 200 may include the first separate plate 200a and the second separate plate 200b that are respectively positioned under the left and right sides of the back of the head of a patient with the patient's neck therebetween.
  • the first separate plate 200a and the second separate plate 200b may be symmetrically formed, and each may have a shock-absorbing pad 210.
  • the shock-absorbing pads 210 are in close contact with each other, thereby supporting the back of a head as a single pad.
  • the first separate plate 200a and the second separate plate 200b can also be detachably coupled to each other, and for example, they may be coupled by a coupling structure composed of a hook 201 and a holder 202.
  • the holder 202 may be a kind of protrusion and the hook 201 may be locked to the holder 202 while elastically swinging.
  • This structure may be symmetrically disposed at one or more positions facing each other on the first separate plate 200a and the second separate plate 200b so that the separate plates can be easily detachably coupled.
  • this is only an example and does not limit the present invention, and the separate plates can be detachably coupled to each other in various ways using various other coupling structures.
  • the fixed cover 100 and the base 200 may be combined to be able to slide with respect to each other. That is, as described above, it is possible to support the head of a patient with the separable base 200 and then couple the fixed cover 100 by sliding it from an end of the base 200.
  • rail grooves 160 may be formed at any one of the fixed cover 100 and the base 200, and protrusions 240 slidably coupled to the rail grooves 160 may be formed at the other one so that they are slidably combined.
  • rail grooves 160 parallel with each other may be formed on the lower end of the fixed cover 100 at both sides of the opening 101, and rail-shaped protrusions 240 may be formed at corresponding positions on the base 200 in parallel with the rail grooves 160.
  • the protrusions 240 can be inserted in the rail grooves 160 and slid or discharged. A very effective sliding coupling structure can be achieved by the structure.
  • the protrusions 240 and the rail grooves 160 may be switched, and the numbers of the protrusions 240 and the rail grooves 160 may be increased for stability. It is possible to form a slidable structure by appropriately arranging the protrusions 240 and the rail grooves 160.
  • the treatment ports of the fixed cover 100 each may have a multi-sealable structure. As shown in FIGS. 4 and 5, the treatments ports can be protected by overlapping an outermost valve 111, an intermediate shield diaphragm 112, and an inner shield plate 113.
  • the valve 111 for example, can be opened/closed in an iris type and may have the shape of a common iris valve. It is possible to open/close the valve 111 by operating a lever 111a at a side.
  • the shield diaphragm 112 may be a flexible film with a hole at the center, and as shown in FIG. 4, decreases in thickness toward the end, so when an arm of a medical staff, etc.
  • the shield diaphragm 112 can form a sealed structure by coming in close contact with the arm, etc.
  • the shield plate 113 may be formed in a circular flexible plate corresponding to the treatment port and circumferentially symmetrically cut. Accordingly, when an arm of a medical staff, etc. are inserted, the shield plate is developed outward from the center, thereby being able to open the treatment port. This multiple structure makes it possible to effectively surround and seal a body or a medical instrument inserted into the fixed cover 100 from the outside.
  • the valve 111 is not limited to the structure of an iris valve, and if there are other effective opening/closing structures, they may be used.
  • the shield diaphragm 112 and the shield plate 113 are made of an elastic material, so when a deformation factor is removed, they can be restored into the initial shapes and can immediately seal the treatment port.
  • the multi-sealable structure is applied to each of the treatment ports (including the first treatment ports 110a and 110b, and the second treatment port 110c), whereby it is possible to effectively prevent spread of sources of infection.
  • sanitary gloves 180 may be provided and used inside the treatment ports of the fixed cover 100.
  • sanitary gloves 180 may be connected inside the first treatment ports 110a and 110b through which a medical staff can insert both arms.
  • the sanitary gloves 180 may be detachably provided using various detachable structures, and if necessary, they may be coupled and used, as shown in FIG. 5. Accordingly, it is possible to increase the sealing effect, reduce the number of protectors for medical staffs, and decrease a burden. However, if necessary, it is possible to separate the sanitary gloves 180 anytime and come back into the state shown in FIGS. 1 to 4, and accordingly, a medical staff can have a larger access space and more efficiently perform treatments or operations.
  • the sanitary gloves 180 may be a stretchable rubber material.
  • FIG. 6 is a view showing the process of installing the patient tailored-installable negative pressure isolator of FIG. 1,and FIG. 7 is a view showing an example of using the patient tailored-installable negative pressure isolator of FIG. 1.
  • the patient tailored-installable negative pressure isolator 1 can be very conveniently installed and used on a bed, etc. as follows.
  • a patient A may be already lay down on a bed, but, as shown in (a) and (b) of FIG. 6, the first separate plate 200a and the second separate plate 200b may be inserted under both sides of the back of the heads to support the head of the patient A. That is, as described above, the first separate plate 200a and the second separate plate 200b are respectively separately inserted under the left and right sides of the back of the head with the neck of the patient A therebetween and then coupled at the middle portions, whereby it is possible to very conveniently and effectively put the base 200 under the back of the head of the patient A lying down.
  • the fixed cover 100 with the patient A stably lying down, as shown in (c) of FIG. 6, using the sliding structure described above. That is, it is possible to very conveniently couple the fixed cover 100 and the base 200 by sliding the fixed cover 100 in parallel with the protrusions 240 of the base 200.
  • the variable cover 300 may be coupled in advance to the fixed cover 100 or may be coupled after the fixed cover 100 is coupled to the base 200. In this manner, it is possible to install an independent negative pressure chamber by connecting the base 200, the fixed cover 100, and the variable cover 300 to fit the patient A, and then adjusting the variable cover 200. It is possible to finish fixing the variable cover 300 by aligning and coupling the extensions 220 and the fixing portions 230. When the isolator needs to be removed, it is possible to very conveniently remove the isolator in the reverse order of the installation.
  • the patient tailored-installable negative pressure isolator 1 can be used in various ways, as shown in FIG. 7.
  • a negative pressure isolation space fitting the patient A is formed by connecting the base 200, the fixed cover 100, and the variable cover 300 through the process described above, adjusting the variable cover 300 to come in close contact with the body of the patient, and then connecting the intake tube 170 and suctioning air.
  • the negative pressure isolation space which is the area surrounded by the fixed cover 100 and the variable cover 300, is formed outside the body of the patient A and does not necessarily surround the entire body of the patient A. That is, as shown in (a) of FIG.
  • variable cover 300 when the variable cover 300 is contracted and fixed in the state, the negative pressure isolation space formed inside the fixed cover 100 and the variable cover 300 can be contracted in the minimum size and the other parts of the body of the patient A such as the stomach can be further exposed outside the isolation space. Accordingly, a medical staff can apply necessary treatments to the patient A more safely outside the negative pressure isolation space in the negative pressure isolator.
  • the variable cover 300 can be completely brought in close contact with the body of the patient A by adjusting the contact portion 310 at the end, as described above, can also be connected to the base 200 through the fixing portion 230 other than the fixed cover 100, so it can be structurally stable. Further, a medical staff can increase the negative pressure isolation space and perform necessary treatments by stretching the variable cover 300, as shown in (b) of FIG. 7.
  • the extensions 220 are pulled out to fit the variable cover 300, whereby it is possible to maintain the structural stability. Further, if necessary, it may be possible to make the isolation space tighter by fastening an attachment band 320 on the body of the patient A and the connecting then end of the variable cover 300 to the attachment band 320.
  • the attachment band 320 may be an elastic band with a Velcro tape on the outer side and a Velcro tape may be attached to the contact portion 310 at the end of the variable cover 300 to attach them.
  • variable cover 300 it is possible to reinforce the negative pressure isolation space by making at least a portion of the variable cover 300 in a double or multiple structure, and for example, it is possible to effectively seal the negative pressure isolation space by forming an additional extension structure, which covers the contact portion, outside the contact portion 310 that comes in close contact with the body of the patient A, etc.
  • the additional extension structure forms an additional space between the internal negative pressure isolation space and the outside, thereby being able to implement a kind of exclusive chamber.
  • the negative pressure isolation space By varying the negative pressure isolation space, as described above, it is possible to safely and smoothly perform even treatments or operations that were difficult to apply to an infected patient or a suspected patient. Even though the negative pressure isolation space is contracted, the surrounding including the face of the patient A is still surrounded and sealed by the fixed cover 100 and the variable cover 300 and maintained at pressure lower than the outside, so the damage of contamination from the outside due to droplet or aerosols is considerably reduced and a medical staff can perform necessary treatments more safely and accurately. For example, as shown in (a) of FIG. 7, it is also possible to apply CPR to an urgent patient A suspected to be infected with his/her body exposed or induce parturition of an infected pregnant woman while protecting the unborn child.
  • a medical staff B can conveniently perform an operation by inserting both arms through the first treatment ports 110a and 110b and accessing the crown of the head of the patient A, and can perform an operation closer to the patient A while more clearly looking at the patient A through the light-transmissive surface 130 that is an inclined surface disposed toward the gaze of the medical staff (see the arrows of dotted lines). Even in this process, the medical staff can be safely protected from droplet or aerosols from the patient A by the fixed cover 100. It is possible to increase the number of substantial negative pressure beds by installing the patient tailored-installable negative pressure isolator 1 of the present invention for each bed, and it is possible to disassemble and apply the isolators to other beds. Further, it is possible to maintain the negative pressure isolation space even if moving the bed equipped with the negative pressure isolator, so it is possible to smoothly perform various examinations even in a ward not completely equipped with isolation facilities.
  • FIG. 8 is a perspective view of a patient tailored-installable negative pressure isolator according to another embodiment of the present invention
  • FIGS. 9 and 10 are views showing an example of using the patient tailored-installable negative pressure isolator of FIG. 8.
  • a patient tailored-installable negative pressure isolator 1-1 include different types of variable covers 300-1a and 300-1b, and one of the variable covers can be selectively coupled to the fixed cover 100.
  • Detachable coupling portions 150 described above may be formed at the variable covers 300-1a and 300-1b and the fixed cover 100, and accordingly, the different types of variable covers 300-1a and 300-1b can be exchanged and used.
  • the variable covers 300-1a and 300-1b may include a variable cover 300-1a having a relatively small area and a variable cover 300-1b having a relatively large area, and may include other shapes of variable covers not shown.
  • any one variable cover 300-1a may be formed in a relatively simple shape that can freely bend, or fold or unfold, and the other variable cover 300-1b may be stretched and contracted like a corrugated tube or a bellows by extending to have a long length outward from the fixed cover 100.
  • the fixed cover 100 and the base 200 may be integrated and not in the detachable type. This is another example of connecting the fixed cover 100 and the base 200, and even in this case, it is possible to perform the installation process described above by appropriately assist a patient.
  • the patient tailored-installable negative pressure isolator 101 can be deformed in different structures and can be used for predetermined purposes. It is possible to expose part of the body of a patient A, as shown in FIG. 9, by coupling the variable cover 300-1b that is formed in a relatively simple shape that can freely bend, or fold or unfold. Further, it is also possible to form a negative pressure isolation space that accommodate the entire body of the patient A, as shown in FIG. 10, by coupling the variable cover 300-1b having a large volume. In the case shown in FIG.
  • variable cover 300-1a it is possible to freely deform the variable cover 300-1a and form various sealing structures corresponding to it to be more suitable for the posture or body shape of the patient A using the contact portion 310 at the end of the variable cover 300-1a.
  • the isolator functions substantially as an individual negative pressure isolator, so the entire body of a patient A can be completely accommodated in the negative pressure isolation space, whereby it is possible to more effectively deal with spread of sources of infection.
  • it is possible to freely deform the variable cover 300-1b since it is possible to freely deform the variable cover 300-1b, if necessary, it is possible to appropriately adjust and use the negative pressure isolation space.
  • FIG. 11 a view showing an example of using the patient tailored-installable negative pressure isolator according to another embodiment of the present invention.
  • variable cover 300-2 may be made of a relatively hard material. That is, in the present invention, the variable cover 300-2 may be implemented in various structures that can be deformed while forming form a negative pressure space therein, and if necessary, the variable cover 300-2 may be made of a less flexible material.
  • the variable cover 300-2 may be formed by connecting a plurality of covers 330 that can overlap each other in multiple steps such that they can slide along the body of a patient A.
  • the covers 330 can come in contact with each other on the inner sides and outer sides thereof, and for example, each can be formed in a tube shape surrounding the body of a patient A.
  • the tubes may be appropriately deformed as long as they can overlap and slide, including a cuboid and cylindrical shape. It is possible to form another shape of variable cover 300-2 using the structure in which the covers 330 are coupled to overlap each other slidably in one direction, as shown in the figure. In this case, it is possible to change the length of the entire variable cover 300-2 by adjusting the protruding lengths of the covers 330 by sliding. Though not shown in the figure, even in this case, a contact portion that comes in close contact with the body of a patient A may be made of a flexible material at the end of the variable cover 300-2, thereby being able to increase the sealing effect. It is possible to implement the prevent invention in various ways, as described above, and use it for curing an infected patient of a suspected patient.
  • the present invention can be easily installed and reinstalled on the bed of each patient, can provide an independent isolation space to each patient, and can be used in various purposes due to the structure that is flexibly deformed, depending on situations, so the industrial applicability is high.

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Abstract

L'invention concerne un isolateur en pression négative pouvant être installé sur mesure pour un patient qui peut être facilement installé sur un lit, etc., peut fournir un espace d'isolement indépendant pour chaque patient, et présente une structure qui peut être déformée de manière flexible, en fonction des situations. L'isolateur en pression négative pouvant être installé sur mesure pour un patient comprend : une base conçue pour être disposée sous l'arrière de la tête d'un patient allongé ; un couvercle fixe relié à la base, conçu pour recouvrir le visage du patient, comprenant un tube d'admission relié à un côté de ce dernier pour aspirer de l'air, maintenu à une pression négative, et comportant une ouverture formée vers le corps du patient ; et un couvercle variable relié à l'ouverture du couvercle fixe, conçu pour s'étirer et se contracter le long du corps du patient, conçu pour recouvrir le patient, et comportant un espace interne de pression négative communiquant avec le couvercle fixe.
PCT/KR2020/009799 2020-04-24 2020-07-24 Isolateur en pression négative pouvant être installé sur mesure pour un patient WO2021215586A1 (fr)

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Cited By (1)

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US6461290B1 (en) * 1998-12-21 2002-10-08 Iit Research Institute Collapsible isolation apparatus
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CN200991385Y (zh) * 2007-01-24 2007-12-19 信山科艺有限公司 防止病菌传播的装置
JP3159341U (ja) * 2010-01-21 2010-05-20 株式会社アイソテック 患者用簡易隔離フード
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JPH07241340A (ja) * 1994-03-07 1995-09-19 Isao Yamada 喘息発作予防装置
US6461290B1 (en) * 1998-12-21 2002-10-08 Iit Research Institute Collapsible isolation apparatus
CN2638703Y (zh) * 2003-07-24 2004-09-08 李素芝 传染病员隔离床
CN200991385Y (zh) * 2007-01-24 2007-12-19 信山科艺有限公司 防止病菌传播的装置
JP3159341U (ja) * 2010-01-21 2010-05-20 株式会社アイソテック 患者用簡易隔離フード
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