Patent Application
20230338674
The present disclosure relates to an open surgery medical gases delivery system, and more particularly a patient interface for use in an open surgery medical gases delivery system.
Insufflation gases can be used in surgery for a variety of purposes. In open surgery, gas can be insufflated into a body cavity for de-airing, as in cardiac or thoracic surgery, for example. The insufflation gas can be selected from air or carbon dioxide (CO2).
One of the biggest barriers that prevents the successful delivery of gas into a surgical wound or cavity is the integration of the gas delivery system into the surrounding surgical work field. This is primarily due to the large amount of variation that exists in surgical procedures, incision types and locations, patient demographics, surgeon preferences, wound preparation techniques, wound retraction systems and patient draping and warming systems.
In this specification, where reference has been made to external sources of information, including patent specifications and other documents, this is generally for the purpose of providing context for discussing the features of the present disclosure. Unless stated otherwise, reference to such sources of information is not to be construed, in any jurisdiction, as an admission that such sources of information are prior art or form part of the common general knowledge in the art.
Disclosed is a patient interface for protecting a surgical cavity, comprising:
one or more enclosing or outer layers defining at least in part a gas flow path configured or configurable to direct gases to the surgical site, the gas flow path having a first end and an opposed second end,
Disclosed is a device, for delivering gas into a surgical cavity, comprising
Disclosed is a device, for delivering gas into a surgical cavity, comprising
Disclosed is a device, for delivering gas into a surgical cavity, comprising
Disclosed is a device, for delivering gas into a surgical cavity, comprising
Disclosed is a device, for delivering gas into a surgical cavity, comprising
Disclosed is a device for delivering gas into a surgical cavity, the device comprising:
Disclosed is a device for delivering gas into a surgical cavity, the device comprising:
Disclosed is a device, for delivering gas into a surgical cavity, comprising
Disclosed is a device for delivering gas into a surgical cavity, the device comprising:
Disclosed is a device, for delivering gas into a surgical cavity, comprising
Disclosed is an interface, for delivering gas into a surgical cavity, comprising
Disclosed is a device, for delivering gas into a surgical cavity, comprising
Disclosed is a device, for delivering gas into an open surgical cavity, comprising
Disclosed is a device, for delivering gas into a surgical cavity, comprising
Disclosed is a device, for delivering gas into a surgical cavity, comprising
Disclosed is a device for delivering gas into a surgical cavity comprising
Disclosed is a patient interface for protecting a surgical cavity, comprising an inlet and an outlet, one or more enclosing or outer layers at least partly defining a gas flow path between the inlet and the outlet, the gas flow path including a formable section, and at least one deformable element positioned within the formable section, the at least one deformable element configured to form at least one bending direction for the formable section.
Disclosed is a patient interface for protecting a surgical cavity, comprising
Disclosed is a method of treatment of a surgical cavity comprising positioning an interface as described in or adjacent a surgical site.
Disclosed is a method of protecting a patient from a loss of moisture and/or loss of heat during surgery comprising positioning an interface as described on a surface in or adjacent the surgical site.
Disclosed is a method of protecting a patient from an infection of a surgical site comprising positioning an interface as described on a surface adjacent a surgical site such that the gas from the outlet of the interface forms a protective barrier about the surgical site.
Any one or more of the following embodiments or configurations may relate to any of the above disclosures.
In some configurations the enclosing or outer layer is flexible.
In some configurations the enclosing or outer layer is a film or membrane.
In some configurations the enclosing or outer layer is formed of a breathable material that allows the passage of water molecules through the material
In some configurations the enclosing or outer layer is permeable to water vapour.
In some configurations the enclosing or outer layer is formed at least in part of a material having qualities that resist puckering and/or damage from surgical instruments.
In some configurations the enclosing or outer layer is resiliently deformable.
In some configurations the enclosing or outer layer is formed from polyurethane.
In some configurations the interface further comprises a second layer that surrounds at least in part the enclosing or outer layer.
In some configurations the second layer
In some configurations the conditioned flow of gas comprises a diffused flow.
As used herein, the term “diffused” or “diffused flow” and its grammatical equivalents means that the gas flow has reduced velocity compared to the flow of gas in the delivery assembly.
In one configuration a diffused flow has a velocity reduced by about 10, 20, 30, 40, 50, 60, 70 or 80% relative to the velocity of the gas flow in the delivery assembly, and suitable ranges may be selected from between any of these values.
In one configuration a diffused flow has an expanded cross-sectional gas flow relative to the cross-sectional gas flow in the delivery assembly.
In one configuration the diffused flow has a gas flow expanded by at least 50, 60, 70, 80, 90, 100, 110, 120, 130, 140, or 150% relative to the gas flow in the delivery assembly
As used herein, the term diffuser and its grammatical equivalents means that a device or apparatus that delivers a diffused flow of gas.
In some configurations the interface comprises a delivery assembly fluidly connected between a gas source and the interface.
In some configurations the delivery assembly comprises a conditioning source.
In some configurations the conditioning source is a humidifier, a heater, or a humidifier and a heater.
In some configurations the conditioned flow of gas is humidified.
In some configurations the delivery assembly comprises a gas regulator, a flow meter, or a flow meter and a gas meter.
In some configurations the delivery assembly comprises one or more conduits adapted to connect to the gas supply or gas source and to connect to the interface.
In some configurations the interface comprises a filter between the gas source and the interface.
In some configurations the filter is located filter upstream of the conditioning source, downstream of the conditioning source, or forms part of the conditioning source.
In some configurations the device comprises an attachment mechanism for retaining the delivery assembly, the patient interface, or the delivery assembly and patient interface in a position within, or adjacent to the surgical cavity.
In some configurations the device has a gas flow between 0.1 to 20 Umin.
In some configurations the gas flow path exiting outlet is substantially in a single plane.
In some configurations the gases exiting the outlet are substantially laminar and/or non-turbulent.
In some configurations the gas flow path has substantially the same height or cross sectional area.
In some configurations the gases flow path has a constant width.
In some configurations the interface is configured such that the gas flow exiting the outlet has a velocity that is less than the gas flow velocity at the interface inlet.
In some configurations the device is configured to deliver gas via an interface outlet into the open surgical cavity at a supply pressure of less than 30 mmHg.
In some configurations the gas source is selected from bottled gases, a gas cylinder that provides pressurized gas, wall gases source, reticulated gases source, articulated gas source (e.g. pendant supply), ambient air or a flow generator or compressor that generates a gas flow.
In some configurations the gases source provides a continuous or intermittent flow of gases, that can be at a desired flow rate.
In some configurations the gas source can be any gas or gas mixture suitable for a particular surgical application, including therapeutic gases. Preferably the gas is selected from air, carbon dioxide (CO2), nitrogen gas (N2), nitrogen dioxide N2O, Argon (Ar), Helium (He), or a mixture thereof.
In some configurations the density of the gas provided by the gas source is greater than air. Preferably the density of the gas provided by the gas source is greater than air where the outlet of the patient interface is at, adjacent, or above, the surgical cavity.
In some configurations the density of the gas provided by the gas source is the same, or similar, to air. Preferably the density of the gas provided by the gas source is the same, or similar, to air where the outlet of the patient interface is located within the surgical cavity.
In some configurations the velocity of gas flow in the delivery assembly is at least 2-fold higher than the outlet velocity of the patient interface.
In some configurations the device comprises a gas inlet tube that defines the gas inlet into the patient interface.
In some configurations the gas-permeable material is located distally to the outlet of the patient interface.
In some configurations the surface area of the outlet of the patient interface is about 6 to about 20% of the surface area of the gas-permeable material.
In some configurations the gas-permeable material is located at, or defines, the outlet.
In some configurations the delivery assembly fluidly connected between the gas source and the patient interface.
In some configurations the delivery assembly comprises a conditioning source.
In some configurations the conditioning source is a humidifier, a heater, or a humidifier and a heater.
In some configurations the delivery assembly comprises a gas regulator, a flow meter, or a flow meter and a gas meter.
In some configurations the patient interface comprises a support structure.
In some configurations the interface comprises a support structure at the first end, the support structure defining a housing inlet and housing outlet, the housing outlet being in fluid communication with the interface inlet and/or interface outlet.
In some configurations the support structure is a chamber.
In some configurations the chamber comprises a gas-permeable material.
In some configurations the support structure abuts the gas permeable substrate.
In some configurations the support structure encloses a portion of the gas permeable substrate.
In some configurations the height of the support structure is substantially the same height as the gas permeable substrate.
In some configurations the interface further comprises a tube having a first and second end, the first end connectable to the inlet of the support structure housing inlet.
In some configurations the tube first end connects to the housing inlet via a luer connection, a press fit connection, screw threat or friction fit connection.
In some configurations the tube second end has a luer lock connector.
In some configurations the tube is flexible.
In some configurations the gas permeable material is configured to reduce velocity of the gas flow.
In some configurations the gas-permeable material is: located at, or defines, the outlet of the patient interface to define a cavity in the support structure between the gas-permeable material and the inlet to the support structure inlet, or located distally to the outlet of the patient interface to define a cavity in the support structure between the gas-permeable material and the support structure outlet.
In some configurations about 25 to about 75% by volume of the support structure comprises a gas-permeable material.
In some configurations the gas permeable substrate has a front and rear face. An end of each of the front and rear face of the gas permeable substrate can abut the support structure.
In some configurations the support structure is a chamber and the gas permeable substrate fills at least a portion of the chamber. The gas permeable substrate may be contained within the chamber or at least a portion may extend outwardly of the chamber at or adjacent the outlet.
In some configurations the patient interface includes one or more adhesive layers.
In some configurations the interface defines a front surface and a rear surface.
In some configurations the rear surface further comprises an adhesive.
In some configurations the patient interface includes an adhesive layer on at least a portion of the rear surface of the patient interface, the front surface of the patient interface, or both the front and rear surface of the patient interface.
In some configurations the patient interface includes an adhesive layer on at least a portion of the front surface of the patient interface device.
In some configurations the adhesive is an adhesive layer.
In some configurations the adhesive layer comprises a removable backing that once removed exposes the adhesive layer.
In some configurations the interface comprises a removal tab.
In some configurations the removal tab is provided by the enclosing wall or outer membrane, or the second layer.
In some configurations the enclosing or outer layer includes a cut-out on the rear surface adjacent the interface outlet.
In some configurations at least a portion of a side region of the gas permeable material is absent any covering, as might otherwise be provided by the enclosing wall or outer membrane, the second layer, or the adhesive layer.
In some configurations the interface outlet is substantially rectangular in cross section.
In some configurations the edge of interface outlet is rounded.
In some configurations the patient interface includes a layer of material intended to protect the interface.
In some configurations the layer of material intended to protect the interface is provided by a separate protective layer of material.
In some configurations the layer of material intended to protect the interface is provided by a thickening of a layer of the interface.
In some configurations the support structure or chamber is formed of a rigid material such as plastic. The chamber may be at least partly formed of a flexible material such as silicon.
In some configurations the gas permeable substrate is enclosed by the wall or outer membrane.
In some configurations a portion at least of the surface area of the gas permeable substrate is coated or layered in one or more gas-impermeable layers.
In some configurations a gas-impermeable layer is a gas-impermeable film.
In some configurations a portion of the gas permeable substrate not coated or layered in a gas-impermeable layer defines the interface outlet.
In some configurations the gas permeable substrate is, or comprises, an open cell foam.
In some configurations the gas permeable substrate is flat.
In some configurations the gas permeable substrate is rectangular.
In some configurations the length and/or width of the gas permeable substrate is greater than height.
In some configurations the length of the gas permeable substrate is greater than the width.
In some configurations the width of the gas permeable substrate is greater than the length.
In some configurations the patient interface is configured to locate at least partly in the surgical cavity with at least part of the rear face of the patient interface adhered to a surface in or adjacent the surgical cavity, such as a surface of a surgical retractor.
In some configurations the patient interface is configured to locate with the outlet arranged at or adjacent the wound edge of the surgical cavity.
In some configurations at least a portion of the patient interface is flexible and/or deformable to allow the patient interface to be bent and to retain its shape.
In some configurations the patient interface comprises a deformable element to allow the patient interface to be bent and to retain its shape.
In some configurations the deformable element attaches to the support structure.
In some configurations the deformable element is malleable.
In some configurations the deformable element is formed from stainless steel or plastic.
In some configurations the deformable element is resiliently deformable.
In some configurations the deformable element is located within the gas permeable substrate, between an enclosing or outer layer and the gas permeable substrate, within an enclosing or outer layer, or outside of an enclosing or outer layers.
In some configurations the deformable element is shaped to conform substantially to the shape of a perimeter of the gas permeable substrate.
In some configurations the patient interface is bendable to substantially correspond with a configuration of the wound edge, and to retain its shape once bent into that configuration.
In some configurations the gas permeable substrate is removable from the support structure or chamber.
In some configurations the gas permeable substrate reduces the velocity of gases at the outlet relative to the inlet.
In some configurations the velocity of gas flow at the outlet of the patient interface is less than about 2 m/s.
In some configurations the velocity of gas flow at the outlet of the patient interface is less than about 0.8 ms−1.
In some configurations the patient interface has an outlet having an effective outlet area of at least 1 mm2, the outlet venting a conditioned flow of gas at an outlet velocity of less than about 2 ms−1.
In some configurations the gas source provides a gas flow of about 5 to about 20 L/min.
In some configurations the patient interface has an effective outlet area of at least 180 mm2.
In some configurations the pressure of the gas flow at the outlet of the patient interface is less than 30 mmHg.
In some configurations the delivery assembly comprises one or more conduits adapted to connect to the gas supply or gas source and to connect to the patient interface.
In some configurations the device comprises a retractor, to maintain the surgical cavity in an accessible condition, wherein the retractor is
In some configurations the delivery assembly comprises a conditioning source to condition the gases prior to delivery to the surgical cavity. In some configurations, the conditioning source is a humidifier to humidify the gases delivered to the surgical cavity.
In some configurations the delivery assembly comprises a gas control unit, wherein the gas control unit controls the supply of gas.
In some configurations the device comprises a heating source, for heating the gas flow.
In some configurations the device comprises a gas control unit inlet and outlet, a humidifier inlet and outlet, and a patient interface inlet and outlet, the gas control unit in fluid communication with a gas source, the gas control outlet in fluid communication with the humidifier inlet, and the humidifier outlet in fluid communication with the interface inlet.
In some configurations the cross-sectional size of the patient interface expands between the patient interface inlet and patient interface outlet.
In some configurations the patient interface outlet is expanded relative to the patient interface inlet.
In some configurations the cross-sectional size of the total outlet area of the patient interface is 10, 15, 20, 25 or 30 times that of the cross-sectional size of the patient interface inlet.
In some configurations the patient interface comprises a smooth transition between the patient interface inlet and outlet.
In some configurations the flow rate of the gas flow through the delivery assembly is less than 10 L/min.
In some configurations the interface outlet surface area is about 6 to about 20% of the surface area of the gas-permeable material.
In some configurations the device is adapted to deliver gas at a flow rate of up to 20 L/min.
In some configurations the patient interface is adapted to vent gas at a velocity of less than 2 ms−1.
In some configurations the patient interface is adapted to function as a retractor to maintain the surgical cavity in an open condition.
In some configurations the retractor and the patient interface are integrated.
In some configurations the patient interface is an extendable and lockable scaffold and comprises one or more outlets, the scaffold adapted for radial extension and retraction within the surgical cavity.
In some configurations the patient interface comprises an inflatable member, and wherein at least a portion of the inflatable member is located at, or about, the surgical cavity and comprises one or more outlets.
In some configurations the patient interface is an inflatable tube comprising one or more outlets and is adapted for inflation to apply radial force to the walls of the surgical cavity.
In some configurations the outlet(s) are positioned on the internal edge of the inflatable tube.
In some configurations the patient interface forms part of a surgical drape that at least partly surrounds the surgical cavity, the surgical drape having one or more gas pathways and one or more outlets adjacent the surgical cavity.
In some configurations the patient interface is L-shaped.
In some configurations the patient interface is U-shaped.
In some configurations the patient interface outlet on a lower surface of the patient interface, to direct air downwards into the surgical cavity.
In some configurations the patient interface outlet on a vertical surface of the patient interface, to direct air horizontally.
In some configurations the patient interface is a flexible pad comprising a gas outlet zone having one or more gas flow paths for delivering air into the surgical cavity.
In some configurations the flexible pad includes an adhesive zone, preferably in the form of a film having a front gas venting surface and a rear adhesive surface.
In some configurations the pad is formed at least in part by a material that retains its shape when subjected to plastic deformation.
In some configurations the flexible pad includes an adhesive zone.
In some configurations the form of a flexible pad comprising a gas outlet surface an adhesive surface on an opposed side of the pad to the outlet.
In some configurations the pad is formed at least in part by a material that may be manipulated into a desired shape and retain to that desired shape
In some configurations the patient interface comprises one or more elongate portion(s) having a substantially tubular profile.
In some configurations a plurality of secondary elongate portions that stem off from a primary elongate portion.
In some configurations the elongate portion(s) (have one or more articulations. In one embodiment the primary elongate portion(s) has one or more articulations.
In some configurations the elongate portion(s) are made from material that may be manipulated into a desired shape and retain to that desired shape.
In some configurations at least one of the elongate portions are adapted to locate above the surgical cavity and wherein the outlet is directed downwards to the surgical cavity.
In some configurations the patient interface comprises a projection adapted to penetrate the tissue of patient.
In some configurations the projection is a hook.
In some configurations the patient interface includes a zone of greater weight and/or density.
In some configurations the zone of greater weight and/or density is located distal to the patient interface inlet.
In some configurations the patient interface comprises a grip handle and a shaft, the outlet of the patient interface located on the shaft distally from the handle.
In some configurations the patient interface comprises one or more arms that each comprises one or more interface outlets or a plurality of outlets for the patient interface.
In some configurations the patient interface is substantially “Y”-shaped.
In some configurations the patient interface comprises at least two separate arms.
In some configurations the patient interface comprises at least one outlet on the inner surface of each arm of the patient interface.
In some configurations the patient interface comprises one or more adjustable loop(s).
In some configurations the patient interface comprises a slidable collar that forms a loop.
In some configurations the patient interface has one or more gas colliding surfaces to which the gas collides prior to exiting the patient interface at the patient interface outlet.
In some configurations the patient interface comprises two or more interference gas flow paths between the patient interface inlet and patient interface outlet.
In some configurations the patient interface comprises two or more gas outlets, and wherein the outlets are directed substantially at each other.
In some configurations the outlets are positioned on opposed sides of the surgical cavity relative to each other.
In some configurations the patient interface is suspended over the surgical cavity, and wherein either the patient interface or the delivery assembly is positionable above the surgical cavity by an attachment mechanism.
In some configurations a portion of the patient interface, or the delivery assembly, is wound about a reel.
In some configurations the patient interface is held in position by a moveable elongate stand.
In some configurations the patient interface comprises a vent, and wherein the vent is located above the surgical cavity.
In some configurations the vent is located in the ceiling above the surgical cavity.
In some configurations the patient interface integrates to, or connects into, an existing air conditioning or ventilation system.
In some configurations the patient interface comprises a plurality of outlets.
In some configurations the outlets are distributed evenly along a length of the patient interface.
In some configurations the outlets are distributed irregularly along a length of the patient interface.
In some configurations the outlets are holes in the surface of the patient interface, and the holes are of uniform size.
In some configurations the outlets are holes in the surface of the patient interface, and the holes vary in size.
In some configurations the patient interface or the patient interface outlet comprises a porous medium, the porous medium having a plurality of gas flow paths and plurality of outlets.
In some configurations the porous medium is a soft porous medium selected from weaved fabric, felt, porous films, woven mesh, fibrous materials.
In some configurations the porous medium is a hard and/or rigid porous medium selected from sintered metal, sintered polymer, sintered plastic or sintered ceramic.
In some configurations the porous medium is a granular substrate selected from sand, carbon, garnet or anthracite.
In some configurations the patient interface comprises a hinged or articulated portion, wherein the patient interface outlet is located on the hinged or articulated portion.
In some configurations the hinged or articulated portion is connected to a first portion of the patient interface via a pair of pins and corresponding recesses.
In some configurations the hinged or articulated portion is connected to a first portion of the patient interface via a cylinder located at or adjacent the interface between the first portion and the hinged or articulated portion.
In some configurations the cylinder has a plurality of apertures.
In some configurations the retractor is formed of a malleable material and comprises one or more attachment mechanisms for the delivery assembly, patient interface, or delivery assembly and patient interface.
In some configurations the retractor includes a heating source to heat the gas.
In some configurations the retractor comprises one or more gas flow paths between the gas source and the patient interface outlet.
In some configurations the retractor comprises a replaceable component, and wherein the replaceable component comprises the gas flow path.
In some configurations the retractor comprises at least two arms to retract the surgical cavity, and wherein the two arms are located on opposed sides of the surgical cavity.
In some configurations at least a pair of arms of the retractor (each member located on opposed sides of the surgical cavity), comprise a gas flow path and a diffusion outlet.
In some configurations an attachment mechanism that attaches the patient interface and/or delivery assembly to any one or more of a surgical drape, the patient, a retractor, a surgical tool or furniture.
In some configurations the attachment mechanism incorporates a two-part clip or bracket that comprises a base and a bracket interposed over the base, wherein the clip comprises an aperture between the clip and bracket.
In some configurations the clip additionally comprises a slot.
In some configurations the two-part clip retains the retractor, the patient interface, or the retractor and patient interface.
In some configurations the retractor is held within the aperture.
In some configurations the bracket connects to the base with magnetic interactors.
In some configurations fasteners connect the bracket to the base.
In some configurations the base comprises a rotating joint.
In some configurations the clip is in the form of a ring clip element, comprising a ring with a central aperture and a pair of fastening arms.
In some configurations the clamping surface of the ring clip element comprises foam, rubber, silicone or a combination thereof.
In some configurations the ring clip element is fastened or clipped to the patient's skin, a surgical drape, or surgical equipment.
In some configurations the ring clip element is formed integrally with the delivery assembly.
In some configurations the attachment mechanism comprises a suction cup for attachment to a surgical drape, the patient, a surgical tool or furniture.
In some configurations the attachment mechanism comprises an adhesive pad or strip for attachment to a surgical drape, the patient, a surgical tool or furniture.
In some configurations the adhesive pad or strip comprises adhesive on both the top and lower surfaces of the adhesive pad or strip.
In some configurations the adhesive pad or strip is attached to a surface within the surgical site.
In some configurations the attachment mechanism attaches to the delivery assembly, patient interface, or delivery assembly and patient interface to the retractor.
In some configurations the attachment mechanism is a clip, a tie, a band, a releasable mechanical fastener such as a hook and loop structure (e.g. Velcro® strap), an elastic strap, bent wire or knotted string.
In some configurations the tie is a resilient adhesive tie.
In some configurations the attachment mechanism comprises a releasable mechanical fastener (e.g. Velcro® strap), having an adhesive surface for attachment to a surgical drape, the patient, a surgical tool or furniture, and a corresponding Velcro® sleeve about the delivery assembly, the patient interface or the delivery assembly and patient interface.
In some configurations the attachment mechanism is a bracket that covers the delivery assembly, the patient interface, or the delivery assembly and patient interface, the bracket attaching to the patient's skin, the surgical drape or surgical instrument or furniture.
In some configurations the cover is a sleeve.
In some configurations the bracket is secured to the patient's skin with sutures, glue or adhesive.
In some configurations the attachment mechanism comprises a magnetic pad, magnetic strip or pad for positioning on, or about, a surgical drape, the patient, a surgical tool or furniture, and a corresponding mating element about the delivery assembly, the patient interface or both the delivery assembly and the patient interface.
In some configurations the magnetic pad includes an adhesive surface.
In some configurations a surface of the patient interface is substantially planar and comprises glue for attachment to a surface of the surgical cavity, a surgical drape, a surgical tool or furniture.
In some configurations a cover that extends over the delivery assembly, the patient interface, or both the delivery assembly and the patient interface, the cover being attachable to a surgical drape, or patient surface by a suitable fastener.
In some configurations the cover is formed of a rigid material, a resilient material, or a soft and pliable material.
In some configurations the cover is moulded to form about or over the wound edge.
In some configurations the attachment mechanism is a clamp for attachment about the wall of the surgical cavity, the clamp comprising an attachment for the delivery assembly, the patient interface or the delivery assembly and patient interface.
In some configurations the device comprises two complementary pieces that combine, with one piece having an aperture or slot, and the other piece a complementary projection.
In some configurations the clamp is height adjustable.
In some configurations the height adjustable mechanism is a ratchet mechanism.
In some configurations the clamp is a C-clamp or a G-clamp.
In some configurations the attachment mechanism comprises
In some configurations the elongate rail is integrated into a retractor.
In some configurations the rail may comprise two vertically spaced tracks for attachment of the delivery assembly, the patient interface, or both the delivery assembly and the patient interface.
In some configurations the rail comprises an “L”-shape or is in the form of a ring.
In some configurations the attachment mechanism is attached to a surgical drape, and wherein the drape covers at least the edge of the surgical cavity, and optionally at least a portion of the wall of the surgical cavity.
In some configurations the attachment mechanism is attached to a frame that extends the perimeter of the edge of the surgical cavity.
In some configurations the rail is a circular railing system provided in a ring configuration located in the surgical site such that it surrounds the surgical cavity.
In some configurations the attachment mechanism comprises one or more projections for passage through a surgical drape, each projection including a screw thread.
In some configurations the delivery assembly, the patient interface or the delivery assembly and patient interface comprise a plurality of projections less than 5 mm in length, the projections formed from a soft and/or flexible material.
In some configurations one or more zones of the delivery assembly, the patient interface or the delivery assembly and patient interface are covered in the projections, and wherein the projections lead to an at least 5-fold increase in the surface area of the zones.
In some configurations the attachment mechanism is one or more weighted anchors located on the patient interface, or on the delivery assembly adjacent the patient interface, and wherein the patient interface or delivery assembly are adapted to position the one or more weighted anchor in or adjacent the surgical cavity when in use.
In some configurations the attachment mechanism comprises a mechanical claw having two or more fingers, the mechanical claw adapted to include a release mechanism.
In some configurations the mechanical claw includes a mechanically or pneumatically operated release mechanism.
In some configurations the delivery assembly, patient interface, or delivery assembly and patient interface comprises an inflatable sleeve, the inflatable sleeve adapted for positioning inside the surgical cavity.
In some configurations the patient interface is suspended over the surgical cavity, and wherein the delivery assembly, patient interface, or delivery assembly and patient interface is positionable by at least two wires attached to opposed sides of the surgical cavity.
In some configurations the delivery assembly, patient interface, or delivery assembly and patient interface comprises a flexible region, wherein the flexible region wraps about a retractor, surgical instrument or furniture.
In some configurations the flexible region comprises corrugations.
In some configurations the delivery assembly, patient interface, or delivery assembly and patient interface is adapted for attachment to the limb of a medical practitioner.
In some configurations the patient interface delivers gas into the surgical cavity via insertion of the patient interface through an incision that creates a passage from the surgical site adjacent the surgical cavity to a patient wall of the surgical cavity.
In some configurations the patient interface comprises a plug, and wherein the plug is adapted for placement inside an incision located in the surgical cavity.
In some configurations the patient interface comprises a compressible component at or adjacent the patient interface outlet that presses into the surgical cavity.
In some configurations the compressible component is, or comprises, the patient interface outlet.
In some configurations the interface is located on a surface within the surgical cavity.
In some configurations the interface is located on or adjacent a wall of the surgical cavity.
In some configurations a gas source is activated to provide a gas flow to the gas flow path.
It is intended that reference to a range of numbers disclosed herein (for example, 1 to 10) also incorporates reference to all rational numbers within that range (for example, 1, 1.1, 2, 3, 3.9, 4, 5, 6, 6.5, 7, 8, 9 and 10) and also any range of rational numbers within that range (for example, 2 to 8, 1.5 to 5.5 and 3.1 to 4.7) and, therefore, all sub-ranges of all ranges expressly disclosed herein are hereby expressly disclosed. These are only examples of what is specifically intended and all possible combinations of numerical values between the lowest value and the highest value enumerated are considered to be expressly stated in this application in a similar manner.
It should be understood that alternative embodiments or configurations may comprise any or all combinations of two or more of the parts, elements or features illustrated, described or referred to in this specification.
Some embodiments of this disclosure may also be said broadly to consist or comprised in the parts, elements and features referred to or indicated in the specification of the application, individually or collectively, and any or all combinations of any two or more said parts, elements or features, and where specific integers are mentioned herein which have known equivalents in the art to which this disclosure relates, such known equivalents are deemed to be incorporated herein as if individually set forth.
The term “enclosing or outer layer”, and its grammatical variants, includes within its definition a film, barrier, wall or membrane and thus defines a layer that is configured to define at least a portion of the gas flow path of the interface.
The term “comprising” as used in this specification means ‘including’. When interpreting each statement in this specification that includes the term ‘comprising’, features other than that or those prefaced by the term may also be present. Related terms such as ‘comprise’ and ‘comprises’ are to be interpreted in the same manner.
As used herein the term ‘(s)’ following a noun means the plural and/or singular form of that noun.
As used herein the term ‘and/or’ means ‘and’ or ‘or’, or where the context allows both.
The disclosure discloses the foregoing and envisages constructions of which the following gives examples only.
Specific embodiments and modifications thereof will become apparent to those skilled in the art from the detailed description herein having reference to the Figures that follow, of which:
The present invention relates to open surgery medical gases delivery systems and to patient interfaces used in medical gases delivery systems.
Insufflation gases can be used in a variety of surgical procedures.
Surgical procedures of relevance are those that result in the creation of a surgical cavity. The surgical site is defined as the entirety of the operating space, including in and out of the surgical cavity. The surgical cavity is defined as the internal volume of the wound after incision, and is the volume intended to be filled with the gas. The wound edge is defined as the edges created by the incision which are then retracted back after the initial surgical incision. The upper patient wall is defined as the top layers of skin, fat, tissue that the surgeon cuts through to create an opening to create the surgical cavity.
In open surgical procedures, the patient's tissues are exposed to the atmospheric conditions of the operating theatre. This can result in cellular desiccation, evaporative cooling and airborne particles entering the wound. The delivery of heated and/or humidified gas has the potential to create a protective space while the surgeon is working within the wound that protects the patient's wound from the operating theatre environment. In open surgery, gases can be used in a body cavity, which can mitigate various risks associated with surgery, such as, but not limited to, decreasing the risk of air embolism or, decreasing the risk of infection. In open surgical applications, the insufflation system provides a generally constant flow of insufflation gas as a desired flow rate over an appropriate time period, which can encompass a portion or the entirety of the surgical procedure.
One or more components of the open surgery medical gases delivery systems may be biocompatible and/or sterilisable. The components that are sterilisable may be sterilizable by suitable means, such as sterilisation by heating and/or radiation.
The term “gases” is used herein broadly to refer to any gas and/or combination of gases that may be used in surgical applications, such as, carbon dioxide, helium, air, carbon dioxide combined with nitrous, carbon dioxide combined with oxygen, among others.
Shown in
The gas supply or gas source 2, 3 can be from a range of sources and types. The gas supply or gas source 2, 3 can be any suitable supply source such as bottled gases, cylinder 3 that provides pressurized gas, wall gases source, reticulated gases source, articulated gas source (e.g. pendant supply), ambient air or a flow generator or compressor that generates a gas flow, for example, from ambient air. The gases supply or gases source 2, 3 can provide a continuous or intermittent flow of gases, that can be delivered at a desired flow rate. For example,
The gas supply or gas source 2, 3 can provide one or more insufflation gases. The insufflation gas can be any gas or gas mixture suitable for a particular surgical application, including therapeutic gases, which may be selected from air or carbon dioxide (CO2) or a mixture thereof. Other insufflation gases that may be used, either singly or in combination with other gases, include nitrogen gas (N2), nitrogen dioxide N2O, Argon (Ar) and Helium (He).
In the medical gases delivery system 1 shown in
The gas control unit 8 is in fluid communication with the conditioning source 7, shown in
The gas supply or gas source 2, 3 and control unit 8 can be in fluid communication with the conditioning source 7 via conduits 9, 10. The flow communication can be a serial connection. The connection may include a connector assembly that connects the gases supply or gases source 2, 3 to the gas control unit 8 and conditioning source 7. For example, the connector assembly may be a screw connector, friction connection, male-female lock connector or any other type of connection known in the art.
The conditioning source 7 may be a humidifier. The gases can be humidified as they pass through the humidifier, which can contain a volume of humidification fluid, such as water. The humidified gases can exit out through the humidifier and into the patient interface conduit/insufflation tube 11. The gases can move through the patient interface conduit/insufflation tube 11 into the surgical cavity 6 of the patient via the patient interface 5.
The conditioning source 7 may be a heater. The gases can be heated as they pass through the heater. The heating of the gas flow may reduce or prevent condensation and may assist in keeping the patient at a desired temperature. The gas may be heated using an appropriate means such as heating element. The heating element may comprise a heater plate. The heated gases can exit out through the heater and into the patient interface conduit 11. The gases can move through the patient interface conduit/insufflation tube 11 into the surgical cavity 6 of the patient via the patient interface 5.
The gases can be humidified and heated as they pass through the conditioning source 7. The conditioning source 7 can comprise a humidifier that both humidifies and heats the gas, as shown in
Environments within a surgical cavity 6 can include cells that are susceptible to damage when exposed to relatively dry and cold gases. Therefore, the application of warming, humidification, or warming and humidification of the insufflation gas flow may reduce or prevent cellular desiccation. This may have a positive effect on patient outcomes and can increase quality of care, reduce recovery time and reduce length of patient hospital stay. Warming and/or humidifying insufflation gases may also reduce intra-operative hypothermia, reduce post-operative complications and improve post-operative recovery.
Some embodiments described provide a surgical humidification system that includes a humidifier control system configured to determine a mode of operation, a mode of control, a heater plate set point, or any combination of these. The humidifier control system can base this determination at least in part on feedback from components of the humidification system. The components of the humidification system can provide feedback through sensors or other electrical components, and feedback can include, for example, outlet and/or inlet gas temperature, ambient temperature, heater plate temperature, heater plate power, gas flow rate, user input through user interface elements, duration of operation, and the like. Some embodiments of the humidifier control system can improve efficiency of the humidification system, provide an output gas with relatively consistent humidity and/or temperature, and provide greater control over temperature and/or humidity of the gas compared to control systems that do not incorporate system component feedback. The humidifier control system can provide at least some of these improvements through modules configured to process system component feedback and adjust output settings according to a control loop feedback mechanism.
The pressure of the gas flow is preferably such that it drives the flow of gas at operational parameters (such parameters are described below). The flow rate of the gas may contribute to how effectively the surgical cavity is filled with gas.
One or more medicaments may be entrained into the gas flow. For example, the medicament may be entrained into the gas flow as a mist or aerosol. The medicament can be entrained into the gas flow in the delivery assembly 4. For example, the medicament may be entrained into the gas flow by being injected into a delivery conduit 9, 10, 11.
Referring to
A flow generator 17 delivers a flow of gas at a desired pressure and/or flow to the patient interface 5. Use of a flow generator 17 may require fewer devices to provide a source of gas to the surgical cavity 6. The flow generator 17 may comprise a motor (with a pump or compressor) that can draw in ambient or room air, and optionally a secondary gas source (e.g. oxygen or CO2), which may be provided by the gas supply or gas source 2, 3. The flow generator 17 may alternatively draw gas primarily or solely from the gas supply or gas source 2, 3. If a secondary gas source is supplied to the flow generator 17, ambient or room air and the secondary gas source may be mixed in the flow generator 17 as the gases flow past one or more sensors, including temperature, flow and oxygen sensors. The flow generator 17 operates to deliver gases to the patient interface 5, and optionally via a humidifier.
The flow generator 17, as the gas supply or gas source, may include an integrated humidifier, heater, or humidifier and heater. For example, the flow generator 17 may include a humidifier having a heater plate or other suitable heating element(s) for heating humidification liquid in the humidifier chamber for use during a humidification process. The heater plate can be in thermal communication with the humidifier heating element. The humidifier heating element may therefore transfer heat to the heater plate. The heater plate can thereby transfer heat from the humidifier heating element to the humidifier chamber.
The humidifier of the flow generator 17 may be controlled by at least one controller, which allows for monitoring and control of various flow and/or pressure parameters. At least one controller controls the humidifier, if present, to humidify the gas flow and/or heat the gas flow to a desired temperature. The controller can be programmed with or can determine a suitable target temperature and/or humidity of the gas flow. The controller can be programmed to, or can determine, a suitable target temperature and/or humidity of the gas flow and use one or more of the heating element(s), humidifier heating element and the flow generator to control flow and/or pressure to the target temperature and/or humidity.
The flow generator 17 may include a user interface (comprising, for example, a display and input device(s) such as button(s), a touch screen, or the like). The flow generator controller may be configured or programmed to control the components of the system, such as operating the flow generator 17 to create a flow of gas (gas flow) for delivery to the patient interface 5, operating the humidifier (if present) to humidify and/or heat the generated gas flow, receive one or more input/s from sensors (such as flow, temperature, humidity, and/or pressure) and/or the user interface for reconfiguration and/or user-defined operation of the flow generator, and output information (for example on the display of the device) to the user. The flow generator 17 may include the gas control unit 8 or have gas control unit functionality built into its controller or control system
The delivery assembly 4 can direct gas flow from gas supply or gas source 2, 3 to the patient interface 5 at a desired flow rate, and at a pressure sufficient to deliver the desired flow rate. Broadly speaking, the delivery assembly 4 comprises one or more conduits 9, 10, 11 adapted to connect to the gas supply or gas source 2, 3, and to connect to the patient interface 5. The delivery assembly 4 may also include a conditioning source 7 (such as a humidifier, heater, or humidifier and heater) and/or gas control unit 8 which may comprise a gas regulator and/or flow meter.
The delivery assembly 4 may include a stand-alone humidifier 7. For example, the humidifier 7 may receive gas flow from the gas control unit 8, which receives gas flow from the gas supply or gas source 2, 3.
In one configuration, the gas control unit 8 is a separate unit to the humidifier 7. In an alternate configuration, the gas control unit 8 may be integrated with the humidifier 7, such as is shown in
In relation to the conduit 9, 10, 11, where the medical gases delivery system 1 comprises a gas supply or gas source 2, 3 and patient interface 5, the conduit 9, 10, 11 may be a single conduit between the gas supply or gas source 2, 3 and patient interface 5. In configurations where the gas supply or gas source is a flow generator 17 that optionally comprises a heater and/or humidifier, the conduit may comprise a conduit between the flow generator 17 and patient interface 5 and between flow generator 17 and gas source. In configurations comprising a flow generator 17 that can draw in ambient or room air, the conduit 9, 10, 11 may be a single conduit between the flow generator 17 and patient interface 5.
A flow generator 17 delivers a flow of gas at a desired pressure and/or flow to the patient interface 5. Use of a flow generator 17 may require fewer devices to provide a source of gas to the surgical cavity 6. The flow generator 17 may comprise a motor (with a pump or compressor) that can draw in ambient or room air, and optionally a secondary gas source (e.g. oxygen or CO2), which may be provided by the gas supply or gas source 2, 3. The flow generator 17 may alternatively draw gas primarily or solely from the gas supply or gas source 2, 3. If a secondary gas source is supplied to the flow generator 17, ambient or room air and the secondary gas source may be mixed in the flow generator 17 as the gases flow past one or more sensors, including temperature, flow and oxygen sensors. The flow generator 17 operates to deliver gases to the patient interface 5, and optionally via a humidifier.
Where the medical gases delivery system 1 comprises a conditioning source 7 or gas control unit 8, the conduit 9, 10, 11 may comprise a conduit 9 between the gas supply or gases source 2, 3 and the conditioning source 7 or gas control unit 8 (i.e. a gas supply conduit 9). The medical gases delivery system 1 may have a further conduit 11 (patient interface conduit/insufflation tube) between the conditioning source 7 or gas control unit 8 and the patient interface 5 (i.e. a patient interface conduit 11/insufflation tube).
Where the medical gases delivery system 1 comprises a conditioning source 7 and gas control unit 8, the conduit 9, 10, 11 may comprise:
A delivery assembly 4 having the gas control unit 8 upstream from the humidifier 7 is preferred so that the humidifier chamber is subjected to lower pressure. It is typically preferable to locate the control unit 8 upstream from the conditioning source 7 (humidifier) so the humidifier chamber of the conditioning source 7 is subjected to lower pressure.
In some embodiments the conditioning source 7 may be upstream of the gas control unit 8.
The delivery assembly 4 is configured to provide a pneumatic connection between the gas source 2, 3 and the patient interface 5. The required pressure must be sufficient to overcome the inherent resistance to flow in the delivery assembly 4 and the patient interface 5.
The delivery assembly 4 may include a heated conduit to reduce internal condensation, such as by a heating element that extends through at least part of the delivery assembly conduit 9, 10, 11. The conduit 9, 10, 11, or one or more sections of the conduit (such as the patient interface conduit/insufflation tube 11) may be heated.
For example, in the presence of a conditioning source 7 including a humidifier, the conduit between the conditioning source 7 and the patient interface 5 (i.e. the patient interface conduit 11) may solely be heated. However, each of the conduits 9, 10, 11 may be heated as required.
The heated conduit may comprise a tube having one or more conductive elements embedded, encapsulated or otherwise located in the tube. The one or more conductive elements can be heating filaments (or more specifically, resistance heating filaments). The patient interface 5 may removably or permanently attach to the delivery assembly 4.
The gas control unit 8 may include one or more sensors such as a pressure sensor or flow sensor. The gas control unit 8 may control the pressure and/or flow of the gas being delivered to the patient interface 5. The gas control unit 8 may include a pressure regulator that reduces the input pressure of the gas flow. The gas control unit 8 may mix one or more gas sources and/or gas flow rates. The gas control unit 8 may be located between the gases supply or gases source and the patient interface 5.
The conduit 9 extending between the gas supply or gas source 2, 3 and the gas control unit 8 may be a high-pressure conduit. The high-pressure conduit may have an operating pressure rating of about 200 bar. The operating pressure of the high pressure conduit may depend on one or more of the type and source of gas and the procedure that the gas is being used for. For example, CO2 bottles are typically 50 bar and wall supply CO2 is typically less than 10 bar.
In some configurations, the conduit 9, 10, 11 comprises an electrical connector. The electrical connector may be coupled to one or more sensors and/or power connectors. In some configurations, the electrical connector projects from a portion of the delivery assembly 4.
In some configurations, the electrical connector of the conduit 9, 10, 11 is coupled to one or more sensors. In one embodiment the sensor may be one or more of a temperature, flow or humidity sensor. The sensor(s) may be configured to measure temperature, flow and/or humidity of gas flowing through the delivery assembly 4 at the location of the sensor(s).
As discussed above, the medical gases delivery system 1 comprises a delivery assembly 4 for receiving gases from the gas supply or gas source 2, 3 and directing the gases to the patient interface 5.
The patient interface 5 is attachable to the outlet end of the delivery assembly 4, that being the end of the delivery assembly 4 proximal to the patient interface 5. For example, the patient interface 5 can be connected to the patient interface conduit/insufflation tube 11. The patient interface 5 may be attached with any suitable connection means, such as, for example a luer, screw thread or friction fit connection.
Where the delivery assembly 4 comprises a conditioning source 7 (such as a humidifier and/or heater) and/or gas control unit 8 the patient interface 5 is connected to patient interface conduit/insufflation tube 11 that delivers gas flow to the patient interface 5.
As shown in, for example,
The use of an interface inlet tube 13 may provide for the delivery assembly 4 to be spaced from the surgical cavity 6 as the connection point between the interface inlet tube 13 and the delivery assembly 4 may be spaced from the surgical cavity 6. Such a design may assist in keeping the connection point and/or patient interface conduit/insufflation tube 11 out of, or away from the surgical cavity 6, thereby avoiding the connection point or patient interface conduit 11 taking up space within or impeding access to the surgical cavity 6.
The interface inlet tube 13 may be formed from a soft and/or flexible material such that the interface inlet tube 13 can be manipulated to form any shape but does not have to maintain that shape. Alternatively, the interface inlet tube 13 may be formed of a deformable material that is resilient, such that the material retains its shape when a force is applied.
In some embodiments the patient interface 5 and the interface inlet tube 13 may be integrally formed with the patient interface conduit 11/insufflation tube. In some embodiments, the patient interface 5 may be integrally formed with the patient interface conduit 11/insufflation tube.
The patient interface 5 reduces the velocity of the gas at the patient interface outlet 14 such that it fills the surgical cavity 6. Reduction of velocity of gas at the outlet 14 may influence the nature of the gas flow as it exits the outlet. For example, turbulence may be reduced and/or the gas may exit the outlet 14 as a substantially laminar flow. Depending on the configuration of the patient interface 5, including the configuration of the outlet 14, gas may exit the outlet 14 as a unidirectional, bidirectional or omnidirectional gas flow. The patient interface 5 preferably provides a substantially uniform and even fill of the surgical cavity 6, with gradual flowing/flooding of gas over the upper edge of the surgical cavity 6 as shown in
A substantial portion of the gas may exhibit laminar flow as it fills the surgical cavity 6. As used herein the term “laminar flow” means that there is not substantial disruption between layers of gas flow. As can be seen in
Without wishing to be bound by theory, if the velocity of the gas at the patient interface outlet 14 is too high, jetting may occur and the gas may not form a partial protective environment in the surgical cavity 6. For example, as shown in
Jetting may lead to turbulent mixing which may result in a poorly filled surgical cavity 6 as shown in
The density of the gas provided by the gas source or gas supply 2, 3 may be greater than air. A gas with a density higher than air may assist distributing, settling and/or maintaining the gas in the surgical cavity 6, particularly where the patient interface 5 has an outlet 14 that is at, adjacent, or above, the surgical cavity 6.
In some embodiments the gas may have a density the same, or similar, to air. A gas having a density the same, or similar, to air may be used in conjunction with an interface located in the surgical cavity 6, such that the interface outlet 14 is located within the surgical cavity 6.
The flow rate of the gas in the delivery assembly 4 and/or conduit 8 may be less than 20 L/min, or less than less than 15 L/min, or less than 10 L/min, or less than 9 L/min, or less than 8 L/min, or less than 7 L/min, or less than 6 L/min, or less than 5 L/min, or less than 4 L/min, or less than 3 L/min, or less than 2 L/min, or less than 1 L/min L/min, or less than 0.5 L/min.
The velocity of the gas flow at the patient interface outlet 14 may be less than 2.0 ms−1, or less than 1.5 ms−1, or less than 1.0 ms−1, or less than 0.9 ms−1, or less than 0.8 ms−1, or less than 0.7 ms−1, or less than 0.6 ms−1r, or less than 0.5 ms−1, or less than 0.4 ms−1. The gas flow velocity at the outlet 14 is important to avoid jetting and mixing. The patient interface outlet 14 gas flow is reduced by the passage of the gas flow through or across the patient interface 5. The velocity of gas flow at the patient interface outlet 14 is thus less than the velocity of gas flow entering the inlet tube 13 and/or patient interface inlet. The design of the patient interface 5 is such that it distributes the flow over a large surface area, reducing the velocity of the flow. Preferably the surface area is at least 1110 mm2. A range of designs can be used to achieve this, which are described below.
The volumetric flow rates through the medical gases delivery system 1 may be about 0.1, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20 L/min, and useful ranges may be selected between any of these values (for example 0.1 to about 20, about 0.1 to about 150.1 to about 12, about 0.1 to about 10, about 0.1 to about 5, about 1 to about 20, about 1 to about 16, about 1 to about 13, about 1 to about 10, about 1 to about 8, about 2 to about 20, about 2 to about 15, about 2 to about 10, about 3 to about 20, about 3 to about 17, about 3 to about 12, about 3 to about 10, about 4 to about 20, about 4 to about 13, about 4 to about 10, about 5 to about 20, about 5 to about 16, about 5 to about 12, about 5 to about 10, about 6 to about 20, about 6 to about 15, about 6 to about 13, about 6 to about 10, about 7 to about 20, about 7 to about 16, about 7 to about 10, about 8 to about 20, about 8 to about 14, about 8 to about 10, about 9 to about 20, about 9 to about 15, about 10 to about 20, about 10 to about 15 or about 15 to about 20 L/min).
The velocity of the gas flow into the surgical cavity 6 is about 0.05, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9 or 2.0 m/s, and useful ranges may be selected between any of these values (for example 0.05 to about 2.0, about 0.05 to about 1.5, about 0.05 to about 1.0, about 0.1 to about 2.0, about 0.1 to about 1.6, about 0.1 to about 1.0, about 0.1 to about 0.8, about 0.2 to about 2.0, about 0.2 to about 1.4, about 0.2 to about 1.0, about 0.2 to about 0.8, about 0.3 to about 2.0, about 0.3 to about 1.6, about 0.3 to about 1.0, about 0.3 to about 0.8, about 0.4 to about 2.0, about 0.4 to about 1.6, about 0.4 to about 1.0, about 0.4 to about 0.8, about 0.5 to about 2.0, about 0.5 to about 1.6, about 0.5 to about 1.0, about 0.6 to about 2.0, about 0.6 to about 1.6, about 0.6 to about 1.0, about 0.7 to about 2.0, about 0.7 to about 1.6, about 0.8 to about 2.0, about 0.8 to about 1.6, about 0.8 to about 1.0, about 0.9 to about 2.0, about 0.9 to about 1.6, about 1.0 to about 2.0, about 1.0 to about 1.6, about 1.1 to about 2.0, about 1.1 to about 1.6, about 1.2 to about 2.0 or about 1.2 to about 1.6 m/s).
In one embodiment the patient interface 5 slows the gas flow entering the surgical cavity 6 by converting a portion of the flow's kinetic energy into potential energy of pressure.
In one embodiment the patient interface 5 is placed inside the surgical cavity 6 as shown in
In an alternative embodiment, the patient interface 5 may be placed adjacent to the surgical cavity 6 as shown in
In embodiments where the patient interface 5 is configured to be placed adjacent to the surgical cavity 6, the interface 5 may be configured to direct a flow of gas across the surgical cavity 6. In other words, gas flow may be directed outwardly of the outlet 14 from one side of the surgical cavity 6 to an opposite side thereof. The gas flow may prevent entry of ambient air into the gas flow and/or into the surgical cavity 6. In such embodiments, the patient interface 5 may be placed on a surface adjacent to where a surgical incision is to be made. The interface 5 may be placed on a surface of the patient skin, on film/drape, placed over the patient skin or similar. The interface 5 may be placed such that the interface 5 is close enough to the surface to achieve attachment of a boundary layer of flow of gas toward the surgical site/surgical cavity 6. The flow of gas may be substantially non-turbulent or laminar as it exits the outlet 14 of the interface 5. The flow of gas may be substantially unidirectional, i.e. flows outwardly from the outlet 14 in substantially one direction only.
A substantially non-turbulent or laminar and/or unidirectional flow can be formed by features of the patient interface 5, as will be described below. In such embodiments, the interface 5 may be placed close enough to the surface to achieve attachment of a boundary layer of unidirectional and/or non-turbulent or laminar flow of gas toward the surgical site/surgical cavity 6 along substantially the width of the interface 5 or the outlet 14. In such an embodiment, airborne particles may be prevented from entering the gas flowing out of the outlet 14 and over the surgical cavity 6. Air and airborne particles may be prevented from being entrained into the gas flow or beneath the gas flow and into the surgical cavity 6. The flow of gas may provide a protective layer or seal over the surgical cavity 6. The protective layer may be formed with or without filling of the surgical cavity 6 with the gas.
The position of the patient interface 5 may govern how the surgical cavity 6 is filled. The surgical cavity 6 may be filled from the top of the surgical cavity 6 (top-down filling) as shown in
Gas pumping or organ pumping can occur where the outlet of the patient interface 5 becomes located in gaps between the internal anatomy and body tissues. This may create an inflatable pocket to push body tissue apart and open the pocket to release the now pressurised gas. As the pressure drops, the pocket may contract back to its original shape, causing the body tissue to move back and recreate the sealed pocket. Movement of body tissue may hinder or at least inconvenience surgeons' ability to carry out surgical procedures.
Alternatively, the surgical cavity 6 may be filled from the bottom (bottom-up filling) as shown in
In top-down filling, gas is delivered above, at the top of, or adjacent an upper edge of the surgical cavity 6. The gas then floods down into the surgical cavity 6 to fill. In bottom-up filling, gas is delivered towards the bottom of the surgical cavity 6 and the gas fills the surgical cavity 6.
It may be advantageous to use a patient interface 5 with an outlet surface area of at least 180, 185, 190, 195, 200, 205, 210, 215, 220, 225, 230, 235, 240, 240 or 250 mm2, and suitable ranges may be selected from between any of these values, (for example, about 180 to about 250, about 180 to about 230, about 180 to about 200, about 185 to about 250, about 185 to about 235, about 185 to about 215, about 190 to about 250, about 190 to about 240, about 190 to about 200, about 195 to about 250, about 195 to about 225, about 195 to about 215, about 200 to about 250, about 200 to about 235, about 200 to about 210, about 205 to about 250 or about 205 to about 240, about 210 to about 250 mm2). The surface area of the outlet may be calculated based on the physical surface area of the patient interface outlet 14 as shown in
In one embodiment the gas pressure at the patient interface outlet 14 is less than 30 mmHg. The gas pressure at the interface outlet may be less than 28 mmHg. The gas pressure at the interface outlet may be less than 26 mmHg. The gas pressure at the patient interface outlet 14 may be less than 24 mmHg. The gas pressure at the patient interface outlet 14 may be less than 22 mmHg. The gas pressure at the patient interface outlet 14 may be less than 20 mmHg. The gas pressure at the patient interface outlet 14 may be less than 18 mmHg. The pressure at the patient interface outlet 14 may be measured by a sensor, such as a pressure sensor. The pressure sensor may generate a signal that is sent to a controller for closed loop control. The controller may increase or decrease the flow of gas to maintain the desired outlet pressure. Alternatively, the controller may increase or decrease the pressure of gas to maintain the desired outlet flow.
The flow rate of the gas through the medical gases delivery system 1 may define at least in part how effectively the surgical wound is filled. The pressure has to be sufficient to deliver the desired flow rate. The flow rate may define at least in part how fast the surgical cavity 6 is filled. Flow rate can be adjusted to allow gas to exit from the interface 5 at a selected velocity and/or as a substantially laminar or non-turbulent flow.
In some embodiments the patient interface 5 comprises a support structure 19 having a connector inlet 47 and a connector outlet 52. The connector inlet 47 of the support structure 19 provides an attachment or coupling means to the interface inlet tube 13. In some embodiments the inlet 47 may include a barbed portion for attachment to the interface inlet tube 13. In alternate embodiments the interface inlet tube 13 may be formed integrally with the support structure 19.
In some embodiments, the support structure 19 can provide an attachment, coupling means and/or housing for a gas-permeable substrate 12. In some embodiments, the support structure 19 may comprise, or define, a chamber 55. In some embodiments, the support structure 19 may comprise a passage between the connector inlet 47 and the connector outlet 52 to allow passage of the flow of gas to the gas-permeable substrate 12. In some embodiments the support structure 19 may be in the form of, or define, a frame for the gas-permeable substrate 12. The support structure 19 may abut, adjoin, comprise or at least partially house the gas-permeable substrate 12, which provides a conditioned flow of gas. Without wishing to be bound by theory the gas-permeable substrate 12 provides a diffuse flow of gas from the interface outlet 14. The gas-permeable substrate 12 may fill a portion of the support structure 19 of the patient interface 5. The support structure 19 may comprise a chamber 55 between the gas-permeable substrate and the connector inlet 47. Alternatively, the entirety of the support structure may be filled with the gas permeable substrate 12.
The gas-permeable substrate 12 allows for gas to pass through the substrate 12 and transforms the inlet gas flow to a diffuse flow into the surgical cavity 6. The gas-permeable substrate 12 may be selected from any material and/or structure that is porous, for example, sintered plastics, open cell foam and other porous permeable substrates 18, for instance paper, felt, sintered metal and/or filter material.
If present, the gas-permeable substrate 12 may:
The cavity within the support structure 19 located upstream of the gas-permeable substrate 12 may allow for the gas flow to distribute about the surface of the gas-permeable substrate 12 providing a larger surface area of gas-permeable material through which the gas flow passes.
Shown in
Gas flow entering the chamber 55 may be via the interface inlet tube 13 or the patient interface conduit 11. The gas flow is conditioned when passing through the gas-permeable substrate 12. For example, the gas flow is conditioned to be a diffuse and/or substantially non-turbulent flow (i.e. a substantially laminar flow) to thereby provide a diffuse and/or non-turbulent gas flow into the surgical cavity 6. The gas flow directed outwardly from the interface outlet 14 may be unidirectional, bidirectional or omnidirectional.
In relation to the patient interface 5 of
Each of the patient interfaces 5 shown in
As shown in
The patient interface devices 5 of
As seen in
In one embodiment the support structure is elongate having a body defining a gas inlet end and a distal end. The support structure 19 may comprise plurality of apertures along its length that define the patient interface outlet 14. The apertures may increase in size towards the distal end of the support structure body. The support structure 19 may be configured as a cylinder or a tube of varying cross section along its length.
Referring to
The patient interface 5 may include an adhesive layer 42 on the rear surface or patient-facing surface of the patient interface 5. An example is shown in
The support structure 19 may be formed of a rigid material such as plastic, a flexible material such as silicon, or a combination of rigid and flexible materials.
At least a portion of the outer surface area of the gas permeable substrate 12 may be coated, covered or enclosed in an enclosing or outer layer. The enclosing or outer later may be formed from one or more layers. The term “outer layer” does not limit the layer to be the outermost layer of the interface device, merely that the outer layer is external to the gas flow path. The enclosing or outer layer may be at least partly flexible. Flexibility may be imparted by physical properties of the material of the wall and/or from design features of the interface 5, as will be described later in this specification. The enclosing or outer layer may be substantially gas-impermeable, such that gas flow is directed through the interface 5 from inlet, through the gas permeable substrate 12 and exiting via outlet 14. The enclosing or outer layer may include a substantially gas-impermeable layer 41, such as is shown in
The enclosing or outer layer or part thereof may comprise a breathable material. A breathable material in the context of this specification is a material that allows the passage of water molecules through a wall of the material, without allowing the bulk passage of liquid water or bulk flow of gases all the way through the enclosing or outer layer is described as a ‘breathable’ material. Passage of water molecules through such an enclosing wall or outer membrane, such as a monolithic wall, may be via the solution-diffusion mechanism. It may be appreciated by one of skill in the art that the water molecules in the wall are molecularly dispersed in the media and are therefore without a state (solid, liquid or gas), sometimes referred to in the art as vapour. The rate of transfer is often referred to as a water vapour transmission rate or the like.
A ‘breathable’ material may be breathable due to its composition, physical structure or a combination thereof. Examples of breathable materials include block copolymers, hydrophilic polyester block copolymers, thermoplastic elastomers, styrene block polymers, copolyester elastomers, thermoplastic polyolefin elastomers, thermoplastic polyurethane elastomers, non-porous monolithic polymers, polyurethanes, hydrophilic thermoplastics, hydrophilic polyesters, perfluorinated polymers, polyamides, and woven treated fabrics exhibiting breathable characteristics.
The enclosing or outer layer defining at least part of the gas flow path through the interface 5 may be made of the breathable material. A variety of designs of the patient interface 5 utilising the breathable material are possible. For example, the entire enclosing or outer layer of the interface 5 may be formed of a breathable material; a portion of the enclosing or outer layer of the interface 5 may be formed of a breathable material; a portion of the enclosing or outer layer over a top of the interface 5 may be formed of a breathable material. A region or regions e.g. portions of the entire enclosing or outer layer of the gas flow path, of the interface 5 may be formed of the breathable material. The breathable material may be placed over the gas permeable substrate 12 and/or may be bonded or otherwise attached to the gas permeable substrate 12. The interface 5 may comprise one or more layers of breathable material. The breathable material can provide a water vapour flow path from the interface 5 to ambient air.
Breathable regions of the interface 5 may allow diffusion of water vapour from the interface 5 to eliminate or mitigate build up of condensation within the interface 5. The breathable regions may reduce the risk of condensation accumulation and possible saturation of the gas permeable substrate 12.
The enclosing or outer layer defining at least part of the gas flow path through the interface 5 may comprise a material that has one or more of the following qualities: is robust to sharp objects; prevents adhesive layers or the like from puckering, or otherwise deforming, when it is applied to such adhesive layers; prevents or minimizes puckering of the enclosing outer layer, particularly when the interface 5 is deformed or bent; is impermeable to gas flow. The material may be a thermoplastic polymer, polyethylene terephthalate (PET), polyester film, biaxially-oriented polyethylene terephthalate (BoPET), or the like.
At least part of the enclosing or outer layer covering or defining at least part of the gas flow path of the interface 5 comprising the aforementioned material may have one or more creases, channels, grooves or slits 51 over at least part of a surface thereof to facilitate or impart flexibility of that layer and hence to the patient interface 5. These slits/grooves can be in any suitable arrangement configuration or pattern to impart flexibility, examples of which are shown in
Referring to
A series of slits/grooves 51 may extend in from opposite sides. A first group of slits/grooves 51 can be oriented in a non-parallel angle with respect to a second group of slits/grooves 51. The slits/grooves 51 of each set may extend past a centreline or centre portion of the interface such that there is no linear path between inlet end and outlet end that is uncut by a slit/groove 51. The first and second groups of slits/grooves 51 may form a substantially herringbone pattern, an example of which is shown in
As shown in
The slits/grooves 51 may be arranged in columns of slits/grooves 51 that extend to opposing sides in alternation. Each of the columns of slits/grooves can comprise slits/grooves 51 with semicircular or crescent shapes that face the opposite direction to and are at least partially offset toward semicircular or crescent shapes of slits/grooves in an adjacent column, such as shown in
The slits/grooves 51 may include a series of parallel ridges and grooves, e.g. corrugations, such as shown in
A gas-impermeable layer 41 may also at least partly coat or cover the support structure 19. The gas-impermeable layer 41 may prevent the flow of gasses such as air, carbon dioxide (CO2), nitrogen gas (N2), nitrogen dioxide N2O, Argon (Ar), Helium (He) through the film. For example, the gas-impermeable layer 41 may block at least 95.0, 96.0, 97.0, 98.0, 99.0 or 99.9% of gas flow through the film. The gas-impermeable layer 41 may have a thickness that allow bending and/or deformation of the patient interface 5 when coated or layered by the gas-impermeable layer 41.
In each embodiment, a portion of the outer surface area of the gas permeable substrate 12 remains uncovered by gas-impermeable layer 41, thereby defining the interface outlet 14. The interface outlet 14 may be axially aligned with the interface inlet tube 13. Alternatively, the interface outlet 14 may be aligned perpendicularly or at an angle to the interface inlet tube 13. A portion of the surface area of the front face and/or side wall of the gas permeable substrate 12 may remain uncovered by the gas-impermeable layer 41. In one embodiment the gas permeable substrate 12 may be cylindrical having the gas-impermeable layer 41 coating or covering its surface wherein the interface outlet 14 is defined by one or more slits in the gas-impermeable layer 41. Such an embodiment may resemble the patient interface as shown in
In some embodiments, one or more portions of the front face of the gas permeable substrate 12 is absent a covering of gas-impermeable layer 41. The patient interface 5 may in use, be located in or adjacent to the surgical cavity 6 with the rear face of the patient interface 5 adhered to a suitable surface, typically a surface of a medical instrument, such as a surgical retractor. The diffused gas flow fills the surgical cavity 6 as it flows out of the portion(s) of gas permeable substrate 12 of the front face not coated or layered in gas-impermeable layer 41.
A bottom side wall of the gas permeable substrate 12 may be absent the gas-impermeable layer 41 such that the interface outlet 14 is located opposite the support structure 19 and distal to the interface inlet tube 13. Examples of such an embodiment are shown in
Alternatively, the patient interface 5 may be located in use at or adjacent the wound edge of the surgical cavity 6. Gas may fill the surgical cavity 6 as it flows out of the interface outlet 14, which may be located at a bottom side wall of the patient interface 5, such as the example shown in
As discussed, the patient interface 5 may comprise an adhesive layer 42 on one side of the patient interface 5 as shown in
The gas permeable substrate 12 and hence the patient interface 5 formed by the gas permeable substrate 12 may be flexible and/or deformable. In order to allow the patient interface 5 to be bent and to retain its shape, the patient interface 5 may comprise one or more deformable elements 40. The deformable element 40 may be in a variety of forms. For example, the deformable element 40 may be in the form of a wire within the patient interface 5. The wire may form a loop as shown in
The deformable element 40 may be located within the gas permeable substrate 12, between the gas-impermeable layer 41/support structure 19 and the gas permeable substrate 12, within or on the outside of the gas-impermeable layer 41/support structure 19. In some embodiments the deformable element 40 may be coextruded with the gas-impermeable layer 41 and/or the support structure 19. The deformable element 40 allows the patient interface 5 to be bent to match or conform to geometry of the wound edge or surface onto which the interface is placed and to retain its shape. This allows the patient interface 5 to be located at the wound edge so that an upper portion of the patient interface 5 is located on the patient's skin or surgical drape.
The patient interface 5 can bend to so that the gas flow path defined by the walls is configured to provide a desired direction of gas flow. In other words, the patient interface 5 and its gas flow path can be configured to position the interface outlet 14 to provide a desired direction of gas flow. A desired direction of gas flow may be into the surgical cavity 6. For example, if the interface 5 is located on the wall of the surgical cavity and the interface outlet 14 is located on the lower surface of the interface 5, then the interface 5 can be bent to direct the gas flow horizontally from the interface outlet 14 if that is desired. If the patient interface 5 is positioned on the surface of the skin adjacent the surgical cavity 6, the patient interface 5 may be bent to position the gas flow path and/or outlet 14 such that gas is directed into the surgical cavity 6.
The adhesive layer 42 on the rear face of the patient interface 5 may be limited to the portion of the patient interface 5 that sits on patient's skin, surgical drape, or other suitable surface adjacent the surgical site/surgical cavity 6 (i.e. not against the patient wall of the surgical cavity).
The gas permeable substrate 12 may be removable from the support structure 19. That is, it may be desirable for the support structure 19 to be reusable and for the gas permeable substrate 12 portion of the patient interface 5 to be disposable. In such an embodiment the gas-impermeable layer 41 may not extend to cover the support structure 19 nor would the gas permeable substrate 12 be adhered with adhesive to the support structure 19. Instead, the gas permeable substrate 12 may be fixed to the support structure 19 by friction fitting a portion of the gas permeable substrate 12 within a portion of the support structure 19, through the use of removable tabs that may overlap the gas permeable substrate 12 and the support structure 19, or by any other suitable method of attachment.
Referring now to
The connector 43 may have a first surface 53 adjacent the interface inlet 47 and a second opposite surface 54 adjacent the gas permeable substrate 12. The connector 43 may comprise one or more passages through the connector from the interface inlet 47 or interface inlet tube 13 to the connector outlet(s) 52. The interface inlet 47 or interface inlet tube 13 may be on the first surface 53 of the connector 52. The connector outlet(s) 52 may be on the second surface 54 of the connector 43. The first surface 53 may be opposite the second surface 54. The gas flow from the connector outlet(s) 52 provide a flow of gas to the gas-permeable substrate 12.
The gas-permeable substrate 12 can abut to a side of the connector 43. In one embodiment the gas-permeable substrate 12 can abut or attach to a side of the connector 43. In the embodiment shown, the gas-permeable substrate 12 abuts or attaches to the second surface of the connector 43 opposite the inlet, so as to substantially cover the second end of the one or more apertures 44. As described above, the gas-permeable substrate 12 may be selected from any material and/or structure that is porous, for example, sintered plastics, open cell foams and other porous permeable substrates 18, for instance paper, felt, sintered metal and/or filter material.
At least a portion of the outer surface area of the gas permeable substrate 12 may be coated or layered in a gas-impermeable layer 41. The gas-impermeable layer 41 may also coat or cover at least a portion of the connector 43. In some embodiments the gas-impermeable layer 41 may also coat or cover a deformable element 40. The gas-impermeable layer 41 may help the gas permeable substrate 12 to remain abutted to the connector 43, without necessarily requiring any direct adhesion to be applied between the gas permeable substrate 12 and the connector 43.
In some embodiments, the gas-impermeable layer 41 may include one or more tabs 45 that extend over or about the connector 43. For example, as shown in
The gas-impermeable layer 41 may define the interface outlet 14. That is, the interface outlet 14 is defined by the portions of the gas permeable substrate 12 not coated or covered by the gas-impermeable layer 41. The interface outlet 14 may locate at the opposite end of the patient interface 5 to the end of gas permeable substrate 12 that abuts the connector 43. The interface outlet 14 provides a flow of gas. The gas flow out of the outlet may be substantially unidirectional, bi-directional or omnidirectional.
In some embodiments the interface outlet may extend to the corners and/or sides of the gas permeable substrate 12. In some embodiments the gas flow out of the outlet may be omnidirectional. In some embodiments the gas flow out of the outlet may be omnidirectional in a single plane. The gas flow out of the outlet may be omni-directional in two or more planes. An omnidirectional flow may be achieved by having exposed gas permeable substrate 12 on two or more surfaces, where those surfaces are in a different plane relative to each other. For example, on a patient facing surface of the patient interface 5 and a side wall surface of the patient interface 5. The gas flow out of the outlet may be omni-directional in a single plane.
As shown in
As shown in
The gas permeable substrate 12 may be flexible and/or deformable. The patient interface 5 may, as mentioned above, comprise one or more deformable elements 40 to allow the interface 5 to be bent as required and to retain its shape once bent. The, or each, deformable element 40 can be located in or adjacent the gas-permeable substrate 12.
In the embodiment shown in
The deformable element 40 may be attached to the connector 43. The deformable element 40 may be fixed or otherwise attached to the second surface of the connector 43. An end or ends of the deformable element 40 may be fixed substantially at or adjacent one side of the second surface of the connector 43. As shown in
The deformable element 40 allows the patient interface 5 to be bent as required. For example, the patient interface 5 can be bent or deformed to match or conform to geometry of the surface, such as wound edge or retractor and to retain its shape. This allows the patient interface 5 to be positioned at or adjacent the wound edge or on the surface as required. The patient interface 5 can bend to allow the outlet 14 to be directed generally downwards towards the surgical cavity 6. This can assist the process of filling the surgical cavity 6 with the gas flow directed outwardly from the interface outlet 14.
At least one adhesive layer 42 may be applied to one or more of the faces of the gas-permeable substrate 12. The at least one adhesive layer 42 may be double-sided. In some embodiments the gas-impermeable layer 41 may partially cover the gas permeable substrate 12. Subsequent layers, such as an adhesive layer 42 may thereby attach to the gas permeable layer 41 and the gas permeable substrate 12.
As shown in
As stated, the at least one adhesive layer 42 may be applied to the face of the gas-permeable substrate 12 that already has the gas-impermeable layer 41 applied. In such an instance, the at least one adhesive layer 42 may be formed to be of a shape, and a size, so that when applied to the face of the gas-permeable substrate 12 it does not extend beyond the area that is covered by the gas-impermeable layer 41.
The patient interface 5 may include a layer, such as a protective backing 48 shown in
With reference to
The at least one adhesive layer 42 may have an external film 50 applied to it. The external film 51 may be composed of a material that has at least the following properties: is robust to sharp objects; prevents adhesive layers or the like from puckering, or otherwise deforming, when it is applied to such adhesive layers; is impermeable to gas flow.
In some embodiments, any of the layers about the gas permeable substrate 12 may include one or more creases, channels, grooves or slits 51 over at least part of a surface thereof to facilitate or impart flexibility of that layer and hence to the patient interface 5. These slits/grooves 51 can be in any suitable arrangement configuration or pattern to impart flexibility.
The patient interface 5 may be positioned in the surgical cavity 6 against the patient wall or a medical instrument such as surgical retractor. The diffused gas flow thus fills the surgical cavity 6 as it flows out of the gas permeable substrate 12 of the patient interface 5. The adhesive layer 42 may be used to attach the patient interface 5 to the patient, retractor, surgical drape, surgical instrument or surgical equipment.
Gas may fill the surgical cavity 6 as it flows out of the interface outlet 14. The patient interface 5 may be adhered to the patient's skin or surgical drape adjacent the wound edge with the interface outlet 14 approximately aligned to the wound edge. The patient interface 5 may be positioned adjacent the wound edge so that the interface outlet 14 is directed at an angle relative to horizontal or to the surface at the wound edge. For example, the interface outlet 14 may be directed at an angle 5, 10, 15, 20, 25 or 30 degrees from horizontal.
The gas-permeable substrate 12 may sit at the outlet of the delivery assembly 4, for example within the outlet 14 of the patient interface 5. The gas-permeable substrate 12 may comprise pores that create a labyrinth of gas flow pathways which spread flow out and engage a larger outlet area consequently slowing the exiting gas's velocity. The pores of the gas-permeable substrate 12 may generate a network of passages for the gas to distribute across.
The porosity of the gas-permeable substrate 12 may be altered to influence the resistance to flow. For a given flow rate, increasing the resistance to flow increases the required driving pressure of the gas supply. For a given flow rate, as the resistance to flow is decreased, this decreases the required driving pressure of the gas supply. The alteration of the resistance to flow may also alter the degree of gas distribution throughout the porous medium and consequently change the reduction in gas velocity.
The porous medium may be selected from soft, resilient and/or flexible materials. Preferably the porous medium is selected from woven fabric, felt, porous films, woven mesh or fibrous materials, such as wool or soft filters. In one embodiment the porous medium is selected from hard or rigid materials. In some embodiments, the porous medium is selected from sintered metal, sintered polymer/plastic or sintered ceramic. In one embodiment the porous medium is selected from granular substrates. Preferably porous medium is selected from one or more of sand, carbon, garnet, anthracite or other suitable particulate material
The patient interface 5 may have a cross sectional area that expands along its length as shown in
The inlet has a smaller cross-sectional area relative to the outlet 14. The chamber 55 widens laterally outwardly from a narrow neck portion adjacent the inlet to a wide portion. The chamber 55 has a bottom or patient-facing surface or wall and an opposing upper wall. The bottom and/or upper surface may each be substantially planar. One or both bottom and upper surface may be generally inwardly or outwardly curving. The inwardly or outwardly curving of the upper and/or bottom surfaces may be generally localised at the wide portion of the chamber 55. In the embodiment shown, the upper surface is generally convex and the patient facing is generally concave. A generally concave lower surface can be configured to match the general shape of the surface to which the patient interface 5 is intended to be applied or placed.
The chamber 55 may have one or more internal structures located or configured to guide gas flow as it enters the chamber 55. The one or more internal structures may comprise flow guide elements, such as baffles. The internal structures are located in the chamber 55 and configured to distribute/direct gas flow from the inlet substantially across the cross-sectional area of the outlet 14.
Gas flow can be additionally conditioned by gas-permeable substrate 12 located in the chamber 55. In the embodiment shown, the gas-permeable substrate 12 is located at or adjacent the outlet 14. The gas-permeable substrate 12 may span the entirety of the outlet 14 and extend a distance inwardly from the outlet. In the embodiment shown, the gas-permeable substrate 12 substantially fills the widest portion of the chamber/patient interface. Alternatively, the gas-permeable substrate may fill a larger volume of the chamber. As per other described embodiments, the gas permeable substrate 12 conditions the gas flow and in the context of this embodiment, conditions the gas flow such that gas exiting the outlet 14 is directed outwardly substantially in one direction or plane and/or as a laminar or non-turbulent flow. The one or more internal structures distribute or direct gas flow from the inlet substantially across the surface of the gas-permeable substrate 12 located at or adjacent the outlet 14. Gas entering the chamber through the inlet can be directed towards the gas-permeable substrate 12 directly from the inlet 13 as well as laterally/outwardly as directed by the internal structures.
The patient interface 5 may additionally comprise a deformable or shape conforming element or component. The deformable element may be substantially as described with reference to the embodiment of
In one embodiment different gas pathway geometries are tuned for specific flowrate ranges. Furthermore, the rate of expansion along the length of the gas pathway of the cross-sectional area may be more gradual for higher flows (e.g. 20 L/m) compared to lower flows (e.g. 5 L/min).
In one embodiment the interface produces a gas flow that comprises incident flow. For example, the gas flow exiting into the surgical cavity 6 is a result of colliding flow leading to a gas flow into the surgical cavity 6 that is dispersed and spread. In one embodiment the gas flow is directed to a surface as shown in
The gas flow into the surgical cavity 6 may result from two or more gas flows colliding as shown in
In one embodiment the collided gas flow may result from the use of internal baffles within the patient interface 5 as shown in
The two or more outlets of the patient interface 5 may be located outside of the surgical cavity 6 on opposed surfaces. As shown in
In the above example, the effective outlet area of the patient interface 5 is notionally the area of turbulence where the two or more jets of gas flow meet.
Due to the collided nature of the gas flow at the interface, the gas flow has an outlet surface area increased compared to the flow of gas exiting the interface prior to the collision. That is, the vector or direction of flow is much more diverse and includes a radial flow component from the point of collision. Additionally, the velocity of the gas flow is reduced at the interface outlet.
As shown in
In some embodiments the substantially L-shaped or U-shaped interfaces are made from soft or compliant materials. In an alternate embodiment the substantially L-shaped or U-shaped interfaces are made from resilient or rigid materials.
In one embodiment as shown in
In one embodiment the patient interface 5 is substantially L-shaped. An example is shown in
In one embodiment the patient interface 5 is substantially L-shaped. An example is shown in
With reference to
Referring now to
As shown in
The hinged or articulated portion 18 of the patient interface 5 can be oriented as desired, at the start of and during surgery to direct gas flow into the surgical cavity 6.
In one embodiment the patient interface 5 comprises a flexible pad 23 comprising a gas outlet zone having one or more gas flow paths for delivering gas into the surgical cavity 6. The patient interface 5 comprises an interface tube 13 for connecting to the delivery assembly 4. The patient interface 5 may sit on, adjacent or about the surgical cavity 6. For example, in one embodiment as shown in
In one embodiment the patient interface 5 comprises an adhesive surface for attachment to the surgical area. The adhesive surface may be used for other forms of the patient interface 5 described herein, and may be used for other components of the example medical gases delivery system 1, such as the delivery assembly 4, or the interface inlet tube 13. For example, the patient interface 5 may attach to a surgical gown and/or drape, the patient's skin or surgical equipment. The adhesive may be under a peel off layer. That is, a layer is peeled off a bottom surface of the flexible pad to expose the adhesive surface. The adhesive zone may be located on any part of the flexible pad. For example, it may be located on a portion thereof of the patient interface 5 that sits outside of the surgical cavity 6, or attaches to the gown, patient's skin or retractor. The adhesive zone may be located on the reverse side of the outlet portion of the patient interface 5. The adhesive zone may be located in both the areas: the portion of the patient interface 5 that sits outside of the surgical cavity 6 and the reverse side of the outlet portion of the patient interface 5.
The patient interface 5 may comprise an interface inlet tube 13 providing a gas flow inlet that is distributed the length of the patient interface 5. The interface inlet tube 13 may have a plurality of apertures, slits or other similar openings substantially along its length. This may assist in providing an even outlet flow of gas from the patient interface 5 along its length. The delivery assembly 4 may attach directly to the patient interface 5 and may attach at one end as shown in
The patient interface 5 may have a slim profile (i.e. thin), to assist in keeping the patient interface 5 as unobtrusive as possible.
The patient interface 5 may also connect to a surgical retraction system or surgical retractor 20. A surgical retractor system or surgical retractor 20 is a surgical instrument used to separate the edges of a surgical incision or wound and/or to hold back underlying organs and tissues so that body parts under the incision may be accessed. This is described below. The flexible pad may wrap around, envelop or adhere to the retractor 20. This allows the flexible pad to be retained in place.
In one embodiment the flexible pad 23 may comprise a gas outlet surface and may have an adhesive surface on an opposed side of the pad to the outlet. An example of this is shown in
The flexible pad 23 may be made from a flexible film having a porous membrane. In one embodiment the flexible pad 23 may be formed of a material which may retain to a manipulated shape.
The flexible pad 23 may comprise an interface inlet tube 13 that delivers the gas flow to the flexible pad 23. The interface inlet tube 13 may be integral with the flexible pad 23 or may attach to the flexible pad 23. In one embodiment the interface inlet tube 13 is formed unitarily with the flexible pad 23 and connects to the delivery assembly 4 at a point spaced from the flexible pad. The interface inlet tube 13 may form an inlet to the flexible pad 23 at one end of the pad, or a side wall of the pad.
As shown in
The flexible pad 23 may connect to a retraction system, such as but not limited to one or more ring retractors. The flexible pad 23 may adhere to a portion of the retractor. This allows the flexible pad 23 to be retained in place.
In one embodiment the patient interface 5 comprises one or more elongate body(s) 29 having a substantially tubular profile. An example of this can be seen in
The elongate bodies 29 may be formed of a material that retains to a desired shape. For example, the elongate bodies 29 may comprise soft material comprising a wire along its length. The wire may have a low elastic deformation limit and high fatigue life. A non-limiting example may be armature wire. As the elongate bodies 29 are manipulated into a desired shape, the wire retains the elongate body in that shape.
The elongate bodies 29 may be formed of a material that is resilient (i.e. moves back into shape after bending). The material may be selected from a soft plastic or silicon, or a spring steel.
The elongate body 29 may include one or more secondary elongate bodies 29b that stem off from a primary elongate body 29a. An example of this can be seen in
The interface outlet 14 or outlets are located on at least a portion of the primary elongate body 29a and/or secondary elongate bodies 29. As shown in
One or more of the elongate bodies 29 may sit within the surgical cavity 6. The elongate bodies 29 may be flexible, which facilitates their locating into the surgical cavity 6 as the elongate bodies 29 can be manipulated into convenient positions, particularly around any internal geometry.
In one embodiment the walls of the elongate bodies 29 are formed from a porous medium. In such a design the elongate bodies 29 comprise a tube for transporting the gas flow, the walls of the tube being formed of a porous medium configured to condition the gas flow.
In one embodiment an elongate body 29, or one or more of the elongate bodies 29, may form a loop as shown in
In one embodiment the patient interface 5 is connected to a tube that has one or more articulations. For example,
The articulated tube may form part of the patient interface 5 and may be formed unitarily with the patient interface 5. In this embodiment the articulated tube has an inlet that connects to the delivery assembly 4. The connection may be attached with a screw thread or friction fit connection. The connection point between the articulated tube and the delivery assembly 4 may be spaced from the surgical cavity 6. Such a design may assist in keeping bodily fluids off the delivery assembly 4, which may be a reusable item and so protection from bodily fluids may be useful to ensure it can be reused.
In an alternative embodiment the articulated tube may form part of the delivery assembly 4. The outlet of the articulated tube will then interface with the patient interface 5 that attaches to the end of the articulated tube.
In one embodiment the articulated tube is formed from a soft and/or flexible material such that the articulated tube can be manipulated to form any shape but does not maintain that shape.
The patient interface 5 may be, or comprise, a flexible pad 37. An example is shown in
The interface outlet 14 for the patient interface 5 is located on the flexible pad 37. In some embodiments the flexible pad 37 may be formed from a porous medium. The flexible pad 37 may include an interface inlet tube 13 formed unitarily with the flexible pad 37. In this embodiment the interface inlet tube 13 has an inlet that connects to the delivery assembly 4.
In an alternative embodiment the interface inlet tube 13 may form part of the delivery assembly 4. The outlet of the articulated tube will then interface with the flexible pad 37 that attaches to the end of the articulated tube. The articulated tube may connect to a face of the flexible pad 37, or an end of the pad.
When in use the flexible pad 37 may be cut down to a convenient size and then used in the surgical cavity 6. For example, the flexible pad 37 may be cut to a size to fit the physical dimensions of the cavity or to fit around obstructions in the surgical cavity 6 (e.g. surgical instruments, organs, physiological projections). This allows a single flexible pad 37 to be utilised in a variety of different surgical cavities having different sizes, or being of different types of cavities.
In one embodiment the patient interface 5 comprises a body having an interface outlet 14 at one end and an interface inlet tube 13 for connection to the delivery assembly 4 at the other end.
An example of the interface is shown in
In an alternative embodiment the projection 15 may be located distal from the interface outlet 14 of the patient interface 5, such that retention of the patient interface 5 is carried out by penetration of the projection at the upper patient wall of the surgical cavity 6.
In one embodiment the interface outlet 14 of the patient interface 5 comprises a zone of greater weight and/or density 24. This zone may be provided by employing a material with greater density than the material used to form the body of the patient interface 5. For example, the zone may be formed by a metal or a solid plastic. In one embodiment the zone of greater weight and/or density 24 is provided for by an attachment. The attachment can attach to the body of the patient interface 5 at any point along its length. The attachment may be a sleeve that forms about the body of the patient interface 5 or it may lock into the body of the patient interface 5.
The zone of greater weight 24 may combine with the projection 15 to provide a patient interface 5 that may be held against the upper patient wall of the surgical cavity 6. In one embodiment the combination of the projection 15 and the weighted end of the patient interface 5 provides for a substantially self-locking mechanism once the projection 15 penetrates the tissue layer at the wound edge or the upper patient wall of the surgical cavity 6, particularly when the projection 15 is provided in a hook-like configuration, as shown in
In one embodiment the patient interface 5 is adapted to be connectable to a surgical instrument. The surgical equipment may be an existing instrument, or specifically provided for the patient interface 5. An example is shown in
In some embodiments the patient interface 5 integrates with an existing surgical instrument, such as, for example, a handheld retractor, electro-cautery tool, clamp, or vessel sealing device. In some embodiments, the patient interface 5 may be removably attached to the side of the surgical instrument.
The shaft 16 may be formed of a rigid material such as a plastic or metal. The shaft 16 may have a degree of flexibility. For example, the shaft 16 may be formed of a flexible material (or include one or more zones of flexible material). The flexible material may be formed of a material that retains to a desired shape.
In one embodiment the patient interface 5 comprises one or more arms that each comprises one or more interface outlets 14 or a plurality of outlets for the patient interface 5. An example of this patient interface 5 is shown in
The patient interface 5 may have arms in a bifurcated configuration to resemble a “Y”-shape as shown in
The arms of the patient interface 5 may be formed from a rigid material. In an alternate embodiment the arms are formed from a flexible material. The flexible material may retain a shape or configuration when subjected to plastic deformation
The interface outlet 14 of the patient interface 5 may be located in one or more zones located in the arms of the patient interface 5 that, when in use, will surround the surgical cavity 6. For example, where the arms of the patient interface 5 have a tubular configuration, the outlet may be located on the face or side of the arm that faces the surgical cavity 6, when in use. This means that the interface outlets are generally located in or on the inner portion of the patient interface 5. The interface outlet 14 of the patient interface 5 may comprise one or more apertures, slits or bands of porous material. For example, as shown in
As per previous embodiments, the patient interface 5 may comprise an interface inlet tube 13 for gas flow received from the delivery assembly 4. The patient interface 5 may include an interface inlet tube 13 that extends from one or more of the arms of the patient interface 5 that is adapted for connection to the delivery assembly 4.
In one embodiment the patient interface 5 comprises at least one elongate interface inlet tube 13, adapted to locate above the surgical cavity 6, and wherein the interface outlet 14 of the patient interface 5 is directed downwards toward the surgical cavity 6. An example of this is shown in
The interface inlet tube 13 in the form of a flexible neck may be adapted to locate above the surgical cavity 6 by being bent to form a raised orientation, or may be articulated to form a raised orientation. The interface inlet tube 13 may maintain its shape by being formed of a deformable material that is resilient, such that the material retains its shape when subjected to plastic deformation, or through use of a suitable mechanism such as a series of ball/socket connections, corrugations or pliable material selection.
The interface inlet tube 13 may form part of the patient interface 5 with the interface outlet 14 of the patient interface 5 located at the end of the interface inlet tube 13. The interface inlet tube 13 of the patient interface 5 connects to the delivery assembly 4.
The interface inlet tube 13 allows the user to decide on placement throughout the surgery and maintains the patient interface 5 away from the surgical working space. This patient interface 5 design delivers gases downwardly into the working space of the surgical cavity 6 from a position external to the working space of the surgical cavity 6, including when the patient is positioned at an angle relative to horizontal on the operating table. The gas flow may have a density greater than air to provide effective filling of the surgical cavity 6.
In one embodiment gas flow having a density greater than air is used where the interface outlet 14 is positioned above the surgical cavity 6.
The patient interface 5 may be located above the surgical cavity 6 by being suspended above the surgical cavity 6. For example,
The cables may be attached to the surgical cavity 6 with a clip at or adjacent the wound edge. The cables may be attached to the wound edge using adhesives, glues, or staples. The cables may be tensioned to fix the height of the patient interface 5 above the surgical cavity 6. The length of each cable may be adjustable so that they can be manipulated to alter the position of the patient interface 5 over the surgical cavity 6.
In one embodiment the patient interface 5 is suspended above the surgical cavity 6. For example,
In one embodiment the patient interface 5 may be integrated into, or form part of, a vent that is positioned above the surgical site. For example, shown in
In one embodiment the patient interface 5 forms part of a surgical drape. As shown in
The surgical drape may be marked with an intended line of incision 41. In use, the surgical drape can be placed on the patient such that the intended line of incision 41 is located on top of the intended surgical site. The surgeon can make an incision through the layers of the drape to enter the surgical site and to create the surgical cavity 6. The making of the incision through the gas permeable substrate layer 12 effectively creates outlet(s) 14, located adjacent the wound edge, as shown in
The interface inlet tube 13 extends into the surgical drape and provides gas flow to the interface outlet 14 of the patient interface 5. The interface inlet tube 13 may be interposed between the upper and bottom layers and/or into the gas permeable substrate layer. The interface inlet tube 13 extends out of the surgical drape to connect to the delivery assembly 4.
Incorporating the patient interface 5 into the surgical drape provides for a system that is self-positioning and provides little or no inconvenience to the surgical team. The drape may also include its own heating system to warm gas circulating in and/or flowing through the gas permeable substrate layer. The heating system may therefore effectively warm gas throughout the gas permeable substrate layer, providing heating to a large surface area of the drape and hence to the region of the patient located beneath the drape. The heating system may also contribute to conditioning of the gas. Some embodiments may include gas permeable substrate layer throughout a majority or substantially the entirety of the drape. In such embodiments, heating of the gas introduced into the gas permeable substrate layer can effectively provide patient warming once the drape is placed over the patient body.
In some embodiments the surgical drape may be attached to the patient or other suitable equipment, such as surgical retractor. The drape may stick directly onto the patient and may be designed to be cut through when making the initial surgical incision. This advantageously allows the drape to be used with or sized for a range of wound sizes and shapes.
The medical gases delivery system 1 may also include a surgical retractor or surgical retraction system.
In some embodiments the patient interface 5 is connected to the surgical retractor 20 by an attachment mechanism (such as an attachment mechanism as described below) or integrally formed with the surgical retractor 20 (e.g. see
In some embodiments the surgical retractor 20 includes a heating system which can be incorporated into the surgical retractor or provided upstream of the surgical retractor. The heating system allows the gas flow to be conditioned to a certain temperature, reducing or preventing condensation, and can be configured to heat the patient and/or maintain a desired patient body temperature.
Various forms of retractors 20 are described herein and may be used in combination with any one or more of the diffusors and attachment mechanisms described.
In one embodiment the patient interface 5 is removably connected to the retractor 20 by a suitable connection or fastening means. This may assist in allowing the retractor 20 to be reusable and resterilizable, providing for the patient interface 5 to be replaced as needed. Alternately, the portion of the retractor 20 comprising the gas path may attach to the retractor 20, the portion of the retractor 20 providing the gas path being replaceable. Advantageously, the patient interface 5 can be used on different types of retractors.
Any of the embodiments of the patient interface 5 described above can be utilized with or attached to the retractor. A benefit of this system is that the patient interface 5 can be attached at a range of positions on the retractor 20 to provide for positioning of the patient interface 5 outside of the surgical cavity 6, within the surgical cavity 6, or spanning the surgical cavity 6 as required.
As shown in
The expandable framework or linkage system may position in the surgical cavity 6, such as at the wound edge, or wholly within the surgical cavity 6 to retain the walls of the surgical cavity.
As shown in
In one embodiment the inflatable retractor is formed as an elongate tube having a connection mechanism at the distal end of the tube so that it can be formed into a donut shape.
The body of the inflatable retractor may have one or more interface outlets 14 for the patient interface 5 spaced along the surface of the inflatable retractor. The interface outlets 14 may be in the form of holes or slits as shown in
Without some method of securing the medical gases delivery system 1 to the environment around the surgical cavity 6, any one or more of the components of the medical gases delivery system 1 (e.g. the patient interface 5 or delivery assembly 4) may become prone to movement. This can cause frustrations to the surgeon as components impinge on their working space. Movement of components of the system can also cause gas flow to be directed into tissues or body fluids that cause unwanted noise or splatter and move into gas pockets which can inflate and cause organ movement (see paragraph [0297] above). Effective retention of the patient interface 5 or delivery assembly 4 greatly reduces the likelihood of these problems occurring and improves the usability of the system.
The patient interfaces 5 described can be positioned relative to the surgical cavity 6 by an attachment mechanism 30. The attachment mechanism 30 attaches to any one or more of the delivery assembly 5 or interface inlet tube 13, and to a position on the surgical site. The attachment mechanism can attach to the patient interface 5 (for example, to the interface inlet tube 13 or the body of the patient interface 5) or the delivery assembly 4 to hold the patient interface 5 in a desired position. The attachment mechanism 30 may attach the patient interface 5 or the delivery assembly 4 (or both) to the patient, retractor, surgical drape, surgical instrument or surgical equipment. For example, the described attachment mechanisms 30 may be separate to or unitary with a retractor or surgical equipment.
Various attachment mechanisms 30 for the patient interface 5 systems described above are now described. Any one of the attachment mechanisms 30 described below can be used with any of the above described patient interface 5 embodiments.
In one embodiment the attachment mechanism 30 may be provided as a malleable structure, such as a malleable hook. The attachment mechanism 30 may advantageously be part of or comprise a retractor or retractor system. One example is shown in
As shown in
In one embodiment the bracket 32 of the clip connects to the base 31 by magnetic interactors, although other methods could be used such as the use of adhesive or friction fit.
The clip may include a rotating joint, wherein the clip is attached, (e.g. with adhesive), to the surgical drape, patient, retractor, or surgical instrument, the rotating joint allowing the two-part clip to adjust its position to facilitate positioning and/or movement of the patient interface 5 in the surgical cavity.
In one embodiment the patient interface 5 or delivery assembly 4 (or both) are held by an attachment mechanism 30 in the form of a ring clip element. As shown in
The ring clip element may have a clamping surface formed of a soft material, such as foam, rubber or silicone. The use of soft materials may provide for better grip, or improved safety as the soft material may reduce the likelihood of applying excessive force,
The fastening arms 35 of the ring clip element may be biased to a clamped or closed position. For example, the ring clip element may be spring loaded or be mechanically biased to the clamped position.
The attachment mechanism 30 may alternatively comprise a suction cup to attach to the surgical site, for example to the patient, or to the surgical drape. The suction cup may comprise a holder or ring to attach the patient interface 5, delivery assembly 4 or both.
Referring to
In one embodiment the attachment mechanism 30 for the patient interface 5 or the delivery assembly 4 (or both) may be a clip fastener as shown in
The clamping surface of the clip may use foam, rubber or silicone. The clip may be biased to a closed position, for example with a spring or mechanical closure.
The clip may be a separate component to the patient interface 5 and/or delivery assembly 4. The clip may first be attached to a first component such as a retractor, delivery assembly 4, or interface inlet tube 13. The clip is then attached to another of the components.
In one embodiment the attachment mechanism 30 is a clip, a tie, a band, a releasable mechanical fastener such as a hook and loop structure (e.g. Velcro® strap), an elastic strap, bent wire or knotted string. As shown in
In one embodiment the patient interface 5 or the delivery assembly 4 (or both) could include a unitary bracket that allows a strap, tie, wire or string to pass through in a desired orientation. For example, the delivery assembly and/or patient interface 5 may include a projection with a slot or aperture provided therein to allow insertion of the strap, tie, wire or string. The aperture or slot may be formed by an arm that loops from a surface of the delivery assembly or patient interface 5 to form the aperture or slot. The arm may attach to the delivery assembly or patient interface 5 at one end only to allow the strap, tie, wire or string to be slipped into the aperture or slot.
In one embodiment the attachment mechanism 30 is a resilient adhesive tie that retains the patient interface 5 or the delivery assembly 4 (or both) to a retractor 20, a surgical instrument or surgical furniture as shown in
As shown in
The attachment strip may extend adjacent the surgical cavity 5. The attachment strip may comprise a single strip or a plurality of smaller strips. The attachment strip may allow for detachment of the complementary mating structures allowing re-positioning of the attachment strip.
As shown in
The magnetic pad may be placed below the patient's body. A patient interface 5 comprising a ferrous material or other magnetic metal when placed in the surgical cavity 6 may then be located into position by the magnetic forces from the magnetic pad.
The delivery assembly 4 and/or patient interface 5 may comprise the magnetic material, with the mating element positioning on, or about, a surgical drape, the patient, a surgical tool or furniture.
As shown in
As shown the retention mechanism 30 may be an adhesive pad or strip that sits within the surgical cavity 6. The patient interface 6 may then attach to the adhesive pad or strip.
As shown in
As shown in
As shown in
The clamp may comprise two complementary pieces that combine, with one piece having an aperture or slot, and the other piece a complementary projection. As shown in
In one embodiment the clamp comprises one or more magnetic parts. That is, the elements of the clamp may stick together by a magnetic force. For example, a first part having one polarity and a second part having a different polarity, or a first part being a magnet and a second part formed of a ferrous material. The two parts may be placed either side of a structure to be clamped, the magnetic interaction drawing the two parts together to clamp over the desired structure. The clamp may be a spring-loaded clamp. That is, the spring biases the clamp to a closed position such that opening the clamp against the bias, to span the wound wall thickness, fixes the clamp in place. The spring-loaded clamp may rotate about an axis or move two or more rails.
The clamp may include a release mechanism such as a button to displace and release the projection within a slot.
As shown in
The rail may integrate with a mechanical retraction system. For example, the retraction system may be adapted for attachment of the rail, and wherein the rail can span across a portion at least of the wall of the surgical space.
As shown in
The circular railing system enables the patient interface 5 to track around the ‘circumference’ of the surgical cavity 6 and be repositioned during surgery as required. In one embodiment the circular railing system may be integrated with a retractor 20.
In one embodiment the retention mechanism 30 is attached to a surgical drape, wherein the drape covers at least the wound edge of the surgical cavity 6, and optionally at least a portion of the patient wall of the surgical cavity 6. For example, shown in
The drape may include a rail system (as discussed above) that may comprise horizontal or vertically spaced rails. For example, if horizontally spaced rails, the rail system may travel along the wound edge of the surgical site, either outside of the surgical cavity 6, or along the patient wall of the surgical cavity 6. The rails may be sewn into the surgical drape or attached for example with adhesive.
In one embodiment the retention mechanism 30 comprises a frame that extends the perimeter of the edge of the surgical cavity 6. The frame may be rigid and attach to a retention mechanism 30 or sit over the surgical cavity 6. In an alternative embodiment, the retention mechanism 30 may comprise a frame that extends at least a portion of the perimeter of the surgical cavity 6. The rigid frame may be incorporated into a surgical drape or may be separate to the drape.
The retention mechanism 30 may be a liner for the surgical cavity 6. For example, the liner may be present as a flexible lattice (such as a net or cross-hatched rope) that extends about the edge of the surgical cavity 6, such as the patient wall of the surgical cavity 6, or the upper patient wall of the surgical cavity 6. In some embodiments the liner may traverse inside and outside of the surgical cavity 6 with an attachment for the delivery assembly 4 and/or patient interface 5.
In one embodiment the retention mechanism 30 comprises one or more projections for passage through a surgical drape. For example, the projections may pass through holes already present in the surgical drape, or pierce through the drape when in use allowing the user to place the retention mechanism where they desire.
As shown in
The retention mechanism 30 may comprise plurality of projections, such as at least 2 to 10 projections. When in use the hooks project into the surgical drape at any orientation, the sleeve then holding the delivery assembly 4 and/or patient interface 5 in place relative to the surgical drape.
In one embodiment the attachment mechanism 30 comprises a plurality of projections. As shown in
As shown in
In one embodiment the attachment mechanism 30 comprises a mechanical claw having two or more fingers, the mechanical claw adapted to include a release mechanism.
As shown in
In one embodiment the attachment mechanism 30 comprises an inflatable sleeve 27, the inflatable sleeve 27 adapted for positioning inside the surgical cavity 6. The inflatable sleeve may be located between organs 28, or between an organ 28 and the wall of the surgical cavity 6. As shown in
As shown in
In one embodiment the attachment mechanism 30 comprises a flexible region, wherein the flexible region wraps about a retractor, surgical instrument or furniture. As shown in
As shown in
As shown in
As shown, the gas flow (depicted by “A”) disperses into the surgical cavity 6 from the patient interface 5 located at the patient wall, or adjacent the patient wall.
The patient interface 5 may include an attachment mechanism 30 in the form of a plug, and wherein the plug is adapted for placement inside the incision located in the surgical cavity. An incision made in the side wall of the surgical cavity enables the plug to be inserted and the tube of the patient interface 5 threaded through the plug so that the interface outlet 14 of the patient interface 5 is positioned within the surgical cavity 6.
As shown in
As described above, the attachment mechanism 30 may at least in part comprise an adhesive layer, component or region, such as adhesive layer 42 on the rear surface or patient facing surface of the patient interface 5. Such an adhesive layer or component is useful for attaching the patient interface 5 to a variety of surfaces including surface adjacent the surgical cavity 6 or a surface of a surgical retractor. It will be appreciated that there are many types of surgical retractors available for use in a surgical procedure. Some surgical retractors may have minimal or limited surface area onto which an adhesive surface can be reliably attached to. For example, Balfour retractors may have blades formed from a rod of material, wherein the rod is the only surface of the blade onto which anything could be attached. This may not provide sufficient surface area for satisfactory attachment by adhesive.
To address this potential problem, the attachment mechanism 30 may comprise a fixation structure 49. The fixation structure 49 is adapted to cooperate with the patient interface 5 to secure the patient interface 5 in place as required for a surgical procedure. An example embodiment of a fixation structure 49 is shown in
The first and second portions may be pivotably attached to each other at respective first ends thereof. The first and second portions can in use, be pivoted or folded such that the first and second portions are placed over each side of the retractor blade 20. The first and/or second portion may have an extension or tab extending outwardly from an edge. In the embodiment shown in
The first and second portions can be attached at respective first and second ends, forming a sleeve or pocket which can be placed over the retractor blade 20. The fixation structure 49 can be held in place on the retractor blade 20 by adhesive or other fixation element on surfaces of the first and/or second portions as described above. The surgical cavity facing side of the first portion may provide a surface area onto which the patient interface 5 can be attached.
Reference to any prior art in this specification is not, and should not be taken as, an acknowledgement or any form of suggestion that the prior art forms part of the common general knowledge in the field of endeavour in any country in the world.
Where reference is used herein to directional terms such as ‘up’, ‘down’, ‘forward’, ‘rearward’, ‘horizontal’, ‘vertical’ et cetera, those terms refer to when the apparatus is in a typical in-use position and/or with reference to particular orientations shown in the Figures, and are used to show and/or describe relative directions or orientations.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2021/055346 | 6/17/2021 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 63040376 | Jun 2020 | US | |
| 63061694 | Aug 2020 | US |
