Patent Application
20220273414
The present invention relates to a conditioning device.
A conditioning device according to the present invention is particularly adapted to condition an exposed stretch of a blood vessel.
A conditioning device according to the present invention is applicable to condition an exposed stretch of saphenous vein for a surgical procedure to collect material for autologous grafts, by way of non-limiting example for coronary bypasses.
The present invention further relates to a method for collecting biological material for autologous grafts.
Surgical procedures for the revascularization of cardiac tissues are generally known which provide exposing a portion of a patient's saphenous vein and severing a stretch for autologous grafts, e.g. coronary or vascular bypasses. The saphenous vein extends in a superficial portion of the leg between the venous arch of the foot and the groin, passing through the area of the medial malleolus, the knee, and the thigh.
Typically, these surgical procedures provide making a longitudinal incision substantially on the entire medial side of the patient's leg to generate an elongated slit through which a predominant portion of saphenous vein is extracted and exposed, after having severed it near the malleolus forming a free end of the saphenous vein. In this manner, a surgical team is in a position to temporarily extract a predominant stretch of saphenous vein through said elongated slit, thus exposing it.
By virtue of the stretch of exposed saphenous vein, the surgical team can collect biological material intended to form the substrate for an autologous graft, e.g. for applications such as coronary and/or vascular bypass.
After collecting the biological material, usually a section of saphenous vein necessary for the operation (several centimeters in length according to surgical needs), the saphenous stumps are sutured to the malleolus and leg or thigh (according to the length of the harvested stretch) and the surgical closure of the wound is performed in layers.
Typically, this consolidated surgical procedure requires the exposure of a predominant saphenous vein stretch for an interval of time during which the exposed saphenous vein stretch may experience undesirable phenomena due to the temporary interruption of physiological equilibrium, which leads to degradation of the features of the graft material, potentially limiting the service life of the graft. For example, exposure of the saphenous vein imposes oxidative stress on the exposed segment of the vein, which causes a dysfunction of the endothelial tissue forming the vein wall, which can degenerate into a remodeling of the vein walls as well as chronic inflammatory phenomena.
In a time span of even a several years, such remodeling of the walls can result in the formation of a new intimate layer (neointima) and the formation of atherosclerotic plaques which reduce the patency of the graft early, causing an early failure, and imposing the implantation of stents in the graft or its replacement by a new surgical operation.
The need is strongly felt to prevent the onset of mechanisms, which lead to the unwanted remodeling of the vessel wall, minimizing the damage due to the harvesting procedure of the vessel.
To limit the damage due to the vessel harvesting procedure, some palliative remedies have been introduced in surgical practice, e.g. such as the application of gauze soaked in saline solution, to keep the exposed stretch of saphenous vein moist, thus avoiding dehydration.
For example, it is also known from document U.S. Pat. No. 9,579,224 a solution adapted to place a stent about a section of saphenous vein in situ to stimulate an inflammatory reaction to collect inflammatory cells in the area adjacent to the stent.
Conversely, in the technical domain of vascular grafting, it is known, for example, from document WO-98-20027 to create a device for administering active ingredients on the outside of a vascular graft, wherein the device substantially consists of an impermeable cap fitted to the portion of the vessel where the graft is made and fixed thereto surround the vascular graft by means of an impermeable closing system which forms a sealing chamber between the outer walls of the vessel branches comprising the graft. A solution containing vascular endothelial growth factor (VEGF) is then injected into such sealed chamber to promote the tissue vascularization in the zone of the graft.
Although for clinical applications other than the collection of autologous grafts, such a device would not solve the problem because it implies a local alteration of the physiological balance, imposing stress on the vessel wall applied by the impermeable closing system, e.g. comprising elastic bands which press on one or more sections of the vessel itself. This stress does not prevent the onset of mechanisms which lead to the unwanted remodeling of the vessel walls and therefore such a solution is unsuitable for the collection of material for autologous grafts on the saphenous vein.
In contrast, it is generally known to reduce the risk of proliferation of viral and bacterial infections in wounds by applying patches made of selectively permeable materials, and in particular materials non-permeable to viruses and bacteria, to form a barrier which limits the risk of contamination.
Patches of this type are made to adhere tightly against the skin around the wound to be treated and typically comprise a layer of hydrogel intended to contact the tissue inside the wound to be treated by promoting the collection of wound exudates to be collected in a container through the body of the hydrogel by providing a fluid suction duct connected at one end to the wound to be treated and leading to the opposite end in the exudate collection container. A negative pressure generator is usually associated with the suction line. Solutions of the type described above are disclosed, for example, in document WO-2004-37334.
However, these solutions are not applicable in the procedure of collecting grafts from an exposed stretch of blood vessel, e.g. such as the saphenous vein, because they require the presence of a suction system for exudates of the wound.
Therefore, the need to provide a solution capable of avoiding or at least minimizing the onset of undesirable phenomena due to the interruption, albeit temporary, of physiological equilibrium which leads to a degradation of the features of the material for grafts, to extend the service life of the graft itself.
At the same time, the need is felt to maintain the conditions of physiological balance in an exposed section of a blood vessel intended for the collection of autologous grafts.
It is an object of the present invention to solve the described drawbacks of the prior art and to provide a solution to the needs mentioned above.
These and other objects are achieved by a device according to claim 1 and by a method according to claim 16.
Some advantageous embodiments are the object of the dependent claims.
According to an aspect of the invention, a conditioning device for conditioning at least one portion of an exposed stretch of a blood vessel for collecting biological material for grafts, comprising an envelope and at least one conveying channel which extends entirely within the envelope; wherein said envelope comprises a first layer comprising a first surface intended to face said exposed stretch, and a second layer comprising a second surface, opposite to said first surface; and wherein said at least one conveying channel comprises at least one first aperture which leads out of the envelope, so that said at least one conveying channel can be supplied with working fluid through said at least one first aperture. Said first layer is permeable to at least one component of the working fluid, so that, when said working fluid is in said at least one conveying channel, said at least one component, permeating said first layer diffuses until it reaches said first surface, to apply a conditioning action on said exposed stretch of the blood vessel.
By virtue of the suggested solutions, improved performance is provided in terms of conditioning an exposed stretch of a blood vessel, e.g. the saphenous vein during the collection of graft material.
The suggested solutions provide improved control over the conditioning of an exposed stretch of a blood vessel, such as the saphenous vein during the collection of graft material.
Further features and advantages of the device and of the method will appear from the following description of its preferred embodiments, by way of non-limiting examples, with reference to the accompanying figures, in which:
According to a general embodiment, it is provided a conditioning device 1.
Said conditioning device 1 is adapted to condition at least a portion of an exposed stretch 2 of a blood vessel 3.
Preferably, said conditioning device 1 is used in the collection of biological material for grafts.
Preferably, the term “exposed stretch” means a stretch of a blood vessel 3, which is temporarily taken outside the body of a patient.
Preferably, the term “exposed stretch” means a stretch of a saphenous vein of a patient who, according to current surgical practice, is temporarily placed in paracorporeal position, with one end of the blood vessel stretch 3 still connected to the inside of the patient's body 37, and preferably the other end 24 severed and incannulated by a cannula 39 by an operator 9, typically a surgeon.
Said conditioning device 1 comprises an envelope 4 or bag 4.
Preferably, said envelope 4 of the conditioning device 1 comprises a casing 5 which at least partly delimits an inner volume 6. In this manner, said inner volume 6 is located inside said envelope 4 of the conditioning device 1. Preferably, said casing 5 encloses said inner volume 6. Preferably, said casing 5 is made of flexible material, e.g. in the form of film.
Such conditioning device 1 comprises at least one conveying channel 7, or perfusion duct 7, extending entirely within said inner volume 6 of the envelope 4.
Said envelope 4 comprises a first layer 15 comprising a first layer surface 15′ or first surface 15′ or first face 15′ intended to face said exposed stretch 2.
According to an embodiment, said first layer 15 and said first surface 15′ are part of said casing 5, so that said casing 5 of the envelope 4 comprises said first layer 15.
Said envelope 4 further comprises a second layer 16 comprising a second layer 16′ or second surface 16′ or second face 16′, opposite to said first surface 15′.
According to an embodiment, said second layer 16 and said second surface 16′ are part of said casing 5, so that said casing 5 of the envelope 4 also comprises said second surface 16′, opposite to said first surface 15′ of the first layer 15 with respect to said inner volume 6.
Said at least one conveying channel 7 comprises at least one first aperture 11 which leads out of the envelope 4, in other words, which leads out from the casing 5, so that said at least one conveying channel 7 can be supplied with working fluid 14 through said at least one first aperture 11. In this manner, said at least one first aperture 11 leads out from the inner volume 6.
According to an embodiment, the conveying channel 7 comprises a single aperture 11 and acts as a working fluid collection vessel 14.
Advantageously, said first layer 15 is permeable to at least one component 14′ of the working fluid 14.
In this manner, said working fluid 14, when there is in said at least one conveying channel 7, permeates with said at least one component 14′ said first layer 15′ of the envelope 4, so that said at least one component 14′ reaches said first surface 15′ of the envelope 4, to apply a conditioning action on said exposed stretch 2 of the blood vessel 3.
In other words, when under operating conditions, said at least one component 14′ of said working fluid 14, when said working fluid 14 is in said at least one conveying channel 7, spreads to said first surface 15′ of the first layer 15 of the envelope 4, to apply a conditioning action on said exposed section 2 of the blood vessel 3.
In this manner, it is possible, if necessary, to wet said first surface 15′ by means of said first component 14′.
Preferably, said first layer 15 forms a barrier for at least one additional component of said working fluid 14, except for said at least one component 14′. Advantageously, said first layer 15 is selectively permeable to at least one component 14′ of the working fluid 14.
Preferably, the term “conditioning action” means a homeostatic regulating action applied to the exposed stretch 2.
Preferably, the term “conditioning action” means indicating an action to regulate environmental parameters, such as temperature and/or humidity and/or chemical composition.
By virtue of the prevision of said conveying channel 7, it is possible to achieve a convective conveying of said working fluid 14 inside the conveying channel 7.
By virtue of said first layer 15 permeable to said at least one component 14′ of the working fluid 14, it is possible to make a diffusive, or mainly diffusive, or a slow convective conveying of said at least one component 14′ of the working fluid 14 from the conveying channel 7 to the first surface 15′.
Preferably, said second layer 16 is impermeable to said working fluid 14. According to a preferred embodiment, said second layer 16 forms at least one portion of an impermeable wall 23″ of the conveying channel 7 which is impermeable to said working fluid 14.
By virtue of the provision of said second impermeable layer 16, a barrier can be formed which prevents the transfer of the working fluid 14 and/or of each of its various components 14′ to the outside of the envelope 4, i.e. of the casing 5. For example, the evaporation of the working fluid 14 is prevented. In this manner, a predetermined moisture level is maintained near the exposed stretch 2 of the blood vessel 3.
By providing such a second layer 16, it is possible to improve the efficiency of said conditioning action.
According to an embodiment, said conveying channel 7 is delimited at least partially by said first layer 15 permeable to said at least one component 14′ of the working fluid 14. In this manner, at least a portion of wall 23 of the conveying channel 7 is made from said first layer 15. According to an embodiment, said inner volume 6 of the envelope 4 forms at least one portion of the wall 23′ of the conveying channel 7.
According to an embodiment, said inner volume 6 of the envelope 4 is in contact with said first layer 15.
According to an embodiment, said first layer 15′ allows said component 14′ to permeate by capillarity towards said first surface 15′.
According to an embodiment, said first layer 15′ allows said component 14′ to permeate by diffusion towards said first surface 15′.
For example, said at least one component 14′ of said working fluid 14 comprises at least one of either: water in liquid form, water vapor, dissolved oxygen, gaseous oxygen, bound oxygen, gaseous carbon dioxide, dissolved carbon dioxide, bound carbon dioxide, dissolved solutes, ionic solutes, bound solutes, non-soluble substances, gaseous substances, drug molecules bound to a dissolved carrier, drug molecules in suspended form, drug molecules in colloidal form, drug molecules in gaseous form, nano-particles, vesicles, combination of the above.
For example, said working fluid 14 is a mixture and/or solution and/or suspension.
For example, said working fluid 14 comprises, in addition to said component 14′, at least one of either: water, saline solution, preferably in liquid form.
For example, said working fluid 14 is in gaseous or aeriform form and comprises water vapor and/or a gas mixture.
The construction of interconnected pores in the body of the inner volume 6 and/or the first layer 15 may be envisaged; such interconnected pores are preferably not to be considered as parts of the said conveying channel 7.
By virtue of the provision of such a conditioning device 1, it is possible to transfer at least one component 14′ of the working fluid 14 to the first surface 15′ controlling the chemical-physical conditions thereof. In this manner, a portion with controlled chemical-physical conditions faces an exposed stretch 2 of the blood vessel 3 placed near or in contact with said first surface 15′.
For example, said first layer 15 may allow the transfer of the aqueous component of working fluid 14 to the first surface 15′, thus wetting it. In this manner, it overlooks an exposed stretch 2 of blood vessel 3 placed near or in contact with said first surface 15′ a damp or moistened face of conditioning device 1. Therefore, the risk of dehydration of the exposed stretch 2 of the blood vessel 3, e.g. a saphenous vein, is avoided or at least minimized.
Such working fluid 14 acts as a carrier element for conveying of conditioning factors in exposed stretch 2 of the vessel 3, e.g. the saphenous vein, such as humidity and/or temperature.
Such a working fluid 14 may also act as a carrier element for the conveying of soluble and/or suspended chemical and/or biochemical components, for the conditioning of exposed section 2 of vessel 3, e.g. the saphenous vein.
Preferably, when under exercise conditions, the first surface 15′ and preferably the first layer 15 is in chemical balance with the exposed stretch 2 of the blood vessel 3. For example, the oxygen saturation value is substantially the same in the first surface 15′ and in the wall 40 of the exposed section 2 of the blood vessel 3.
According to a preferred embodiment, said at least one conveying channel 7 further comprises at least a second aperture 13 which leads out from said casing 5 of the envelope 4. In this manner, said at least one first aperture 11 and said at least one second aperture 13 leads out from the casing 5. Preferably, said at least one first aperture 11 acts as an inlet aperture and said at least one second aperture 13 act as an outlet aperture for the working fluid 14, so that a flow of working fluid 14 passes through said first aperture 11, said conveying channel 7, and said second aperture 13.
By virtue of the provision of said inlet aperture 11 and of said outlet aperture 13, a convective flow of working fluid 14 through said inlet aperture 11 flows inside said envelope 4, flows into said conveying channel 7 and flows out from said outlet aperture 13 out from the envelope 4, in other words out from the inner volume 6 and/or out from the casing 5.
The walls 23′ which delimit said at least one conveying channel 7 may be made from said same inner volume 6 and may comprise porosity, being wettable, e.g. they can be adapted to absorb of at least one component of the working fluid 14 and/or a fraction of the working fluid flow.
In an embodiment shown for example in
According to an embodiment, said casing 5 is interrupted only at said at least one inlet aperture 11 and said at least one outlet aperture 13. In this manner, the casing 5 encloses and confines the inner volume 6 even if inner volume 6 is permeated by said working fluid 14 or component 14′ thereof.
According to an embodiment, said at least one conveying duct 7 is associated with at least one inlet duct 10 associated with said at least one first aperture 11 and at least one outlet duct 12 associated with said at least one outlet aperture 13, said at least one outlet duct 10 and said at least one outlet duct 12 extend outside said inner volume 6 of the envelope 4, preferably through said casing 5. Preferably, so-called ducts 10 and 12 are formed by flexible sleeves.
According to an embodiment, said conveying channel 7 is made by digging into the second layer 16. For example, the second layer 16 is made of polymeric material, e.g. polyurethane and/or polyester.
According to an embodiment, said conveying channel 7 is made by removing material from said second layer 16, on the side of the second layer 16 opposite to said second surface 16′. For example, said connecting channel 7 is made by laser etching.
According to an embodiment, said conveying channel 7 is made by molding or casting. For example, the geometry of said conveying channel 7 is made in negative on a mold.
According to an embodiment, said conveying channel 7 comprises at least one duct in which the working fluid 14 flows substantially in laminar flow.
According to an embodiment, said conveying channel is made by hot embossing.
Preferably, the first layer 15 and the second layer 16 are glued and/or welded together either directly or indirectly by overlapping at least one more layer, e.g. a third layer consisting of said inner volume 6.
According to a preferred embodiment, said conditioning device 1 further comprises at least one locking device 8 or closing device 8, adapted to lock said envelope 4 at least temporarily in a predefined geometric configuration.
Preferably, said predefined geometric configuration is a closed geometric configuration which forms a device lumen 17 adapted to receive said at least one exposed stretch 2 of the blood vessel 3. In this manner, it is possible to arrange said first surface 15′ of said first layer 15 of the conditioning device 1 about the outer wall 40 of the exposed stretch 2 of the blood vessel 3.
Preferably, said device lumen 17 forms a longitudinal cavity through which it passes. Said device lumen 17 may have a tapered shape or in any case be suitably shaped to adapt to accommodate the volumetric conformation of an exposed section 2 of a natural vessel.
According to an embodiment, said device lumen 17 forms a longitudinal cavity adapted to be placed on or wrapped about the exposed stretch 2 of the blood vessel 3. In this manner, said envelope 4 substantially forms a sleeve to embrace said exposed stretch 2.
According to a variant, device lumen 17 is not a passing lumen, i.e. it is a vessel comprising a bottom portion opposite the access aperture of the lumen 17, forming a cap for said exposed stretch 2.
Preferably, in said envelope 4 a longitudinal direction X-X, substantially parallel or coincident with the longitudinal development axis of said exposed stretch 2 of blood vessel 3 is defined when said conditioning device 1 is in working condition, a transverse direction T-T, orthogonal to, and incident to longitudinal direction X-X, and a thickness direction, orthogonal to both longitudinal direction X-X and transverse direction T-T, and defining an envelope thickness 33. Preferably, said casing 5 defines said envelope thickness 33. Preferably, said envelope thickness 33 is much smaller than the extensions of said envelope 4 in longitudinal direction X-X and transverse direction T-T, so that said envelope 4 essentially forms a sheet.
According to an embodiment, said at least one locking device 8 is placed on a transverse margin 22, 22′ of said envelope 4. Preferably, the term “transverse margin” indicates a portion of said envelope 4 placed near or at the transverse edge of said envelope 4, wherein the longitudinal dimension of the envelope 4 is significantly larger, and preferably much larger, than the transverse extension of said envelope 4. Not necessarily said transverse margin 22, 22′ is placed at edge 35 of envelope 4, although in accordance with a preferred embodiment it is.
By virtue of said locking device 8, it is possible to keep said envelope 4 of conditioning device 1 around the exposed stretch 2 in wound configuration, like a sleeve.
The joint provision of said second impermeable layer 16 and said locking device 8 allows, by wrapping said envelope 4 of the conditioning device 1 about the exposed stretch 2 of blood vessel 3, to form a containment barrier which helps to maintain the desired chemical-physical conditions in the device lumen 17, and therefore in the exposed stretch 2 of blood vessel 3 received in the device lumen 17 and facing said first surface 15′, allowing an improved control over the conditioning action applied by the conditioning device 1 on the exposed stretch 2 of blood vessel 3.
When in closed and wound configuration, the second layer 16 forms an impermeable barrier to working fluid 14 for conditioning the exposed section 2.
According to a preferred embodiment, the inner volume 6 of said envelope 4 of the conditioning device 1, as well as said envelope 4, is flexible at least in a transverse direction, transverse to the longitudinal direction, so that it can be wound, in other words wrapped, about the exposed stretch 2 to embrace the exposed stretch 2 of blood vessel 3, e.g. the saphenous vein. The provision of the locking device 8 allows the envelope 4 to be locked in wrapped configuration about the exposed stretch 2 of blood vessel 3.
Preferably, said envelope 4 comprises a locking device 8 on each transverse margin 22, 22′, so that the envelope 4 can be wrapped to embrace said exposed stretch 2 of blood vessel 3 and locked in this geometric configuration, at least when under operating conditions, e.g. during collecting operation of the grafts.
According to an embodiment, said at least one locking device 8 forms a releasable coupling. In this manner, the envelope 4 can be reopened if necessary, e.g. when the graft collection operation has ceased.
According to an embodiment, said locking device 8 is adapted to form a slot-hook type coupling. Preferably, said at least one locking device 8 comprises Velcro.
According to an embodiment, said locking device comprises a snap coupling system.
According to an embodiment, called at least one locking device 8 is adapted to form an adhesive bond and is preferably made at least partially of adhesive material. Not necessarily said at least one locking device 8 comprises glue, although according to an embodiment which comprises it. According to an embodiment, said locking device 8 is adapted to form an adhesive bond by adjusting the surface features, such as the choice of the material of clamping device 8, the surface affinity of a material to the same material or a different material.
According to an embodiment, said at least one locking device 8 is adapted to form a magnetic coupling. Preferably, said at least one locking device 8 comprises a permanent magnet. According to an embodiment, said at least one locking device 8 comprises at least one electromagnetic which can be activated as required.
When in operating conditions in which the envelope 4 assumes a closed geometric configuration and wrapped around the exposed stretch 2 of the blood vessel 3, the device lumen 17 is oriented substantially in the X-X longitudinal direction.
By virtue of the locking device 8, the envelope 4 can switch from an open configuration, as diagrammatically shown in
The provision of such a locking device 8 allows a quick locking of the envelope 4 in closed and wound configuration around the exposed stretch 2 of the blood vessel 3 while providing a firm locking of the envelope 4 in closed and wound configuration.
According to an embodiment, said conveying channel 7 defines at least one coil-like perfusion path 28, 28′ to maximize the exchange area of the internal volume 6 of the envelope 4 with the conveying channel 7. According to an embodiment, said conveying channel 7 defines at least two opposed coil-like paths 28, 28′ which extend along the extension in longitudinal direction X-X of the envelope 4 and are joined together by a union duct 29, preferably placed on a longitudinal side 30 or 30′ of the body of the envelope 4.
According to an embodiment, said conveying channel 7 defines stagnation zones, e.g. having increased cross-section, to favor the diffusion of said at least one component 14′ towards said first surface 15′ of the device 1 and thus towards said exposed stretch 2 of blood vessel 3. According to an embodiment, said conveying channel 7 defines shuffling zones, e.g. forming an increased tortuosity, to obtain a mixing effect of said working fluid 14.
According to an embodiment, said conveying duct 7 substantially extends along the entire longitudinal extension of the envelope 4.
According to an embodiment, said conveying channel 7 defines at least one bifurcation. For example, at least one bifurcation is located just downstream of inlet duct 10.
According to an embodiment, said inlet aperture 11 and said outlet aperture 13 of the conveying channel 7 are placed on the same longitudinal side 30 or 30′ of the envelope 4, and preferably are both placed on the longitudinal side 30 of the envelope 4 adapted to face the free end 24 of the exposed stretch 2 of the blood vessel 3, e.g. the saphenous vein 3, when in operating conditions.
According to a preferred embodiment, said first layer 15 comprises hydrogel so that a hydrogel body is interposed between said conveying channel 7 and the first surface 15′ to allow at least one component 14′ to be transferred from said conveying channel 7, through said hydrogel, to said first surface 15′ facing the exposed section 2 of the blood vessel 3, e.g. the saphenous vein.
According to an embodiment, the inner volume 6 inside the envelope 4 comprises hydrogel, preferably between and in contact both with said conveying channel 7 and with said first layer 15.
According to an embodiment, said hydrogel is hydrogel that can be photopolymerized, e.g. cross-linked by exposure to ultraviolet radiation.
The first permeable surface 15′ can be corrugated to bias the conditioning action either near or in contact with the exposed stretch 2 of the blood vessel 3.
The first layer 15, as well as the inner volume 6, can be made using a variety of materials and methods.
According to an embodiment, said first layer 15 is made of composite material. For example, said composite material of the first layer 15 comprises an essentially porous matrix impregnated with a material permeable to said at least one component 14′. According to an embodiment, said composite material of the first layer 15 comprises a non-woven fabric impregnated with hydrogel.
According to an embodiment, said first layer 15 comprises a semi-permeable membrane. For example, said first layer 15 comprises a selectively permeable membrane.
According to an embodiment, said first layer 15 and/or said inner volume 6 is made of gas-permeable polymeric material, e.g. comprises a layer of silicone material.
According to an embodiment, said first layer 15 and/or said inner volume 6 comprises silicone gel.
According to an embodiment, said first layer 15 and/or said inner volume 6 comprises silk. The term “silk” also means a silk derivative, such as silk fibroin.
According to an embodiment, said first layer 15 and/or said inner volume 6 comprises at least one layer made by electro-spinning. For example, an electro-threaded scaffold can be placed in said inner volume 6.
According to an embodiment, said first layer 15 and/or said inner volume 6 comprises an organized nano-mesh.
According to an embodiment, said first layer 15 and/or said inner volume 6 comprises a non-woven fabric.
According to an embodiment, said conditioning device 1 comprises at least one fluid supply device 18 connected to at least one of said apertures 11, 13 to supply said conveying channel 7 with the working fluid 14. Preferably, said feeding device 18 comprises at least one pump 25 adapted to generate a pressure difference to handle said working fluid 14. According to an embodiment, said supply device 18 comprises at least one reserve tank 27, adapted to contain a predefined volume of working fluid 14.
According to an embodiment, said at least one fluid supply device 18 comprises at least one working fluid conditioning system 21, adapted to regulate the temperature and/or the composition of the working fluid 14, e.g. before it flows in said at least one conveying channel 7.
According to an embodiment, said working fluid conditioning system 21 comprises at least one heat exchanger 31, adapted to regulate the temperature of the working fluid 14. According to an embodiment, said working fluid conditioning system 21 comprises at least one mass exchanger 32, e.g. a gas exchanger. According to an embodiment, said conditioning system of the working fluid 21 comprises at least one delivery and/or collection device 34, e.g. comprising syringe or an auxiliary pumping system, adapted to deliver and/or withdraw a predefined volume of fluid into and/or from the inlet duct 10 of the conditioning device 1. Preferably, said dispensing and/or withdrawal device 34 is adapted to dispense a predetermined volume of active substance into the conveying channel 7, and thus in the inner volume 6 of the envelope 4, and consequently through the first layer 15 onto the exposed stretch 2 of the blood vessel 3.
According to an embodiment, said working fluid conditioning system 21 comprising said heat exchanger 31 and/or said mass exchanger 32 is situated outside the envelope 4, in other words outside the casing 5.
According to an embodiment, said at least one fluid supply device 18 comprises at least one control device 26, e.g. comprises a programmable logic controller PLC, to transmit control signals for automating said fluid supply device 18, e.g. to said pump 25 and/or said working fluid conditioning system 21.
According to an embodiment, a sensing device, e.g. including sensors such as flow meters and/or level sensors and/or temperature sensors and/or humidity sensors and/or concentration sensors of the chemical species of interest, shall be associated with such a control device 26. According to an embodiment, valves 38, e.g. check valves, are provided in said fluid supply device 18 to determine the working fluid path 14.
According to an embodiment, a collection tank 20 is provided to collect the working fluid 14 which flows out of said outlet aperture 13 of the conveying channel 7.
According to a preferred embodiment, said at least one fluid supply device 18 is connected to both said at least one apertures 11,13 of the conveying channel 7, to form a recirculation path 19 for the working fluid 14. A filtering device can be placed in the recirculation path 19.
According to an embodiment, said fluid supply device 18 is integrated inside the body of a handpiece which can be associated with said envelope 4 of the conditioning device 1.
A method of collecting autologous biological material for grafts, e.g. for coronary bypasses, will be described below.
The method of collecting autologous biological material for grafts comprises the step of exposing a stretch 2 of blood vessel 3, e.g. a stretch of saphenous vein.
The method of collecting autologous biological material for grafts also comprises the step of providing a conditioning device 1 according to any of the embodiments described above.
The method of collecting autologous biological material for grafts further comprises the step of making the first surface 15′ of the conditioning device 1 face the exposed stretch 2.
The method of collecting autologous biological material for grafts further comprises the step of feeding working fluid 14 into the conveying channel 7 of the conditioning device 1.
The method of collecting autologous biological material for grafts further comprises the step of permeating said first layer 15 with at least one component 14′ of the working fluid 14 so that at least one component 14′ diffuses to said first surface 15′ of the first layer 15.
By virtue of such a method, a conditioning action is applied on said exposed stretch 2 of the blood vessel 3 through said first surface 15′ of the first layer 15.
According to a possible mode of operation, the method of collecting autologous biological material for grafts further comprises the step of temporarily wrapping said conditioning device 1 about the exposed stretch 2 of the blood vessel 3. In this manner, a device lumen 17 is formed which acts as a conditioning chamber for the exposed stretch 2 of the saphenous vein 3.
According to a possible mode of operation, the method of collecting autologous biological material for grafts further comprises the step of adjusting the humility in the device lumen 17.
According to a possible mode of operation, the method of collecting autologous biological material for grafts comprises the step of adjusting the acid-base balance, as well as the concentration of oxygen and/or carbon dioxide and/or other substances, in device lumen 17.
According to a possible mode of operation, the method of collecting autologous biological material for grafts comprises the step of administering a pharmacological agent, by means of the delivery of the conditioning device 1 to the exposed stretch 2 of the saphenous vein in said conveying channel 7.
According to a possible mode of operation, the method of collecting autologous biological material for grafts further comprises the step of proceeding with the collection of biological material for autologous grafts from said exposed stretch 2.
By virtue of the features described above, provided either separately or in combination, where applicable, it is possible to respond to the needs mentioned above, and to obtain the listed advantages, in particular:
The person skilled in the art may make many changes and adaptations to the embodiments described above or may replace elements with others, which are functionally equivalent, to satisfy contingent needs without however departing from the scope of the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 102019000012537 | Jul 2019 | IT | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2020/056750 | 7/17/2020 | WO |
