NEGATIVE PRESSURE AEROSOL CONTAINMENT UNIT
20210369399 · 2021-12-02
Inventors
Cpc classification
A61B90/40
HUMAN NECESSITIES
International classification
Abstract
A device is disclosed for use by clinicians in medical and dental procedures to contain aerosols generated by patients with known or suspected respiratory pathogen (e.g., a virus such as COVID-19). The device of the invention (a negative pressure aerosol containment unit) may be in the form of a box with an opening at the bottom, the box configured to receive an attached HEPA filter and HVAC unit that creates a localized negative pressure area within the box. The device also may be in a non-rectilinear configuration.
Claims
1. A device for use in medical and dental procedures to contain aerosols generated by a patient with a known or suspected contagious respiratory pathogen, wherein the device is transparent, has an opening at the bottom adapted to fit over the patient, and is configured to receive an attached HEPA filter and HVAC unit that creates a localized negative pressure area within the device.
2. The device of claim 1, wherein the device is in the form of a box with an open bottom.
3. The device of claim 2, wherein the box is defined by a front panel, a back panel, two side panels, a top panel and the open bottom.
4. The device of claim 3, wherein the side panels of the box are made of a clear plastic or non-porous material.
5. The device of claim 4, wherein the side panels of the box are made of plexiglass.
6. The device of claim 1, wherein the patient has a known or suspected virus.
7. The device of claim 1, wherein the virus is COVID-19.
8. The device of claim 1, wherein the device is positioned on a mobile base.
9. The device of claim 1, wherein the device is used to contain aerosols generated by a patient during intubation, extubation, bronchoscopy, tracheostomy placement, and upper endoscopy medical procedures.
10. The device of claim 1, wherein the device is used to contain aerosols generated by a patient during a dental procedure.
11. The device of claim 1, wherein the HEPA filter has a viral filtration efficiency of between 85% and 99.999995%
12. The device of claim 1, wherein the HVAC unit pulls air in a range between 250 cubic ft./minute and 600 cubic ft/minute.
13. The device of claim 3, wherein the front panel is adapted for two openings through which a clinician can engage with the patient using his hands.
14. The device of claim 13, wherein the back panel is adapted to fit over the patient's torso or abdomen.
15. The device of claim 14, wherein one side panel is configured to be fitted with the HEPA filter.
16. The device of claim 15, wherein the other side panel has a large opening configured to be covered with a drape which will allow access by an assistant clinician.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0025] The invention is more fully described by reference to the following detailed description and the accompanying drawings wherein:
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DETAILED DESCRIPTION
[0037] According to one aspect of the invention, the device (also known as the negative pressure aerosol containing unit, or NP-ACU) is a clear plastic (e.g., plexiglass) box mounted on a rolling frame that can be raised or lowered in a manner similar to bedside tables used in other parts of a hospital. The device is used in part to serve as a negative-pressure chamber to help reduce aerosol generation during intubation and extubation for patients with known or suspected respiratory pathogens such COVID-19 (COVID+/PUI).
[0038] The device is not limited to only a hospital setting. Indeed, the device may be used in other medical or dental settings, including in a dental office or clinic. Dental professionals such as dentists or dental technicians are particularly vulnerable to exposure to aerosols generated by patients during dental procedures. Such procedures may include but are not limited teeth cleaning, fillings, extractions, and root canals. In certain cases, the patients may have a respiratory infection and the aerosols generated by the patients can spread pathogens to dental professionals and other patients in the dental setting.
[0039] The device is not limited in shape to a rectilinear configuration (e.g., a box, square or rectangular configuration), but rather may be configured in a variety of shapes (e.g., a three dimensional oval shape or a cylindrical shape) and may be adapted to fit over top a patient in a rested position (e.g., as the patient is positioned in a dental chair or an operating room table).
[0040] According to one aspect of the invention, a high-quality HEPA filter with a viral filtration efficiency in the range of 85% to 99.999995% (of particles 0.3 μm in diameter) is attached to a side panel of the box. This filter is connected to a vacuum which pulls over 250 cubic feet per minute of air (7000 liters per minute). In another embodiment, the vacuum pulls air in a range of 250 to 600 cubic ft/minute. The opposite side panel of the box will have a large opening which should be initially closed with a drape. This opening is intended for access if an assistant clinician (e.g., an airway assistant, nurse or dental technician) is required. The front of the NP-ACU has two holes for the primary clinician's (e.g., anesthesiologist's) hands, and the posterior side is open or partially open, allowing space for the patient's torso or abdomen.
[0041] According to an aspect of the invention for a non-operating room environment, the device includes a clear plastic (e.g., plexiglass) box mounted with handles on three (3) sides which allows the box to be positioned on top of a patient while they are on a bed, stretcher, or gurney. One purpose of the device is to serve as a negative-pressure chamber to help reduce aerosol generation during medical procedures (e.g., intubation and extubation) or dental procedures for patients with known or suspected respiratory pathogens such as COVID-19 (COVID+/PUI).
[0042] According to an aspect of the invention, the device is a clear plastic (e.g., plexiglass) box with different portals created for surgeons, proceduralists, and airway specialists to manage a patient having an aerosol generating procedure. One purpose of the device is to serve as a negative-pressure chamber to help reduce aerosol generation during other types of aerosol generating procedures such as bronchoscopy, upper endoscopy, tracheostomy for patients with known or suspected respiratory pathogens such COVID-19 (COVID+/PUI).
[0043] A video laryngoscope may be placed, for example, on the operator's left side, and the video scope should be brought in underneath the edge of the device (e.g., a box-shaped device) and placed near the patient's head. Likewise, in the case of a box-shaped device, the anesthesia circuit may be brought in from the right side under the edge of the box.
[0044] In an aspect of the invention with a patient who has contracted COVID-19, full COVID personal protective equipment (PPE), including droplet plus airborne precautions (N95 mask & face shield min), should still be utilized by all healthcare staff in the room on any COVID+, PUI, or high aerosolizing procedure. For safety purposes, it is worth noting that the device of the invention may not completely eliminate the risk of aerosol generation.
[0045] In the event of a difficult intubation, the assistant clinician should slit a hole in a drape on the right side of the device and provide any support as needed. The device of the invention has been tested with a Bougie catheter, and it has operated successfully. A Bougie catheter is much easier to use if an assistant is available to help.
[0046] In a cannot-intubate, cannot-oxygenate scenario, the device of the invention may be rapidly raised and backed up away from the patient. This will provide access to the front of the neck if a surgical airway is required.
[0047] If the patient is to be extubated in the operating room, the device of the invention may also be placed over the patient for extubation and/or recovery. This should help reduce aerosol generation if the patient coughs or vomits during the extubation procedure.
[0048] The device of the invention should be kept on during a procedure regardless of whether it is used on the patient or not. The filtration aspect of the HVAC unit will help keep the air in the procedural room cleaner.
[0049] After each procedure, the device of the invention may require a thorough wipe down and decontamination with appropriate wipes. Other means of decontaminating the device also may be used. The HEPA filter in the HVAC unit does not need to be changed or cleaned immediately after each use; it may be used again in other procedures. The exterior of the HVAC unit, however, should be wiped down after each procedure.
[0050] A thin pre-filter may be used on the inside rim of the device where the HVAC duct connects. This pre-filter should be disposed of between uses and a new pre-filter installed.
[0051] Referring more specifically to the drawings,
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[0054] The panels of the invention in this embodiment are made of clear plastic (e.g., plexiglass) to provide a clear view of the patient from the top and all four sides of the device. Other plastics as well as glass may be used in the device. It is important that the materials used in the device are clear and transparent.
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[0056] A medical assistant may be helpful in performing adjunct tasks, such as touching the anesthesia machine, turning on the ventilator, and helping with difficult intubations.
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[0058] The opposite side of the box may have a large opening which should be initially closed with a drape. The opening is intended for access if an airway assistant is required. The front of the aerosol containment unit has two holes for the anesthesiologist's hands. The posterior end is open, allowing space for the patient's torso or abdomen.
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[0061] In another embodiment of the invention, the arm board of an operating room table may be positioned on their rails so that the tops of the arm boards align with the head of the bed. The device of the invention is then placed over the patient to create the negative pressure environment.
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[0064] Advantageously, the front panel 915, as shown in
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[0069] As the present invention may be embodied in several forms without departing from the spirit or essential characteristics thereof, it will be understood that the invention is not limited by the details of the foregoing description, unless otherwise specified, but rather should be construed broadly within its spirit and scope as defined in the appended claims, and therefore all changes and modifications that fall within the metes and bounds of the claims. Accordingly, the invention is defined by the appended claims wherein: