ASSEMBLY COMPRISING A SUCTION DEVICE SUITABLE FOR BEING PLACED ON A WOUND AND/OR AN INCISION

Abstract

An assembly including a suctioning device suitable for being placed on an incision and/or a wound of a patient to disinfect and/or dry the incision or wound, the device including a drape. The drape includes an outer layer with an upper face and a lower face, the upper face being impermeable, an inner layer, made of non-woven sterile material, including an upper face and a lower face, the lower face to come into contact with the wound and/or the incision. The drape is wound around a limb or around the body of the patient. The assembly also includes a suctioning zone having cavities, a discharge tube connected to the suctioning zone, and a suctioning member is a system for recovering portable or mobile autologous blood.

Claims

1-8. (canceled)

9. An assembly, comprising: a suctioning device suitable for being placed on an incision and/or a wound of a patient to disinfect and/or dry said incision or said wound, said device comprising a drape comprising: an outer layer comprising an upper face and a lower face, an inner layer comprising an upper face and a lower face, wherein the lower face is arranged so as to come into contact with the wound and/or the incision, and a suctioning member, wherein the upper face of the outer layer of the drape is impermeable, the drape is suitable for being wound around a limb or around the body of the patient, the outer layer and the inner layer of the drape are made of one single part such that the winding of said drape around a limb of the body of the patient leads to the simultaneous winding of said outer layer and said inner layer, a suctioning zone having cavities, is arranged between the lower face of the outer layer and the upper face of the inner layer, the periphery of said suctioning zone being sealed, a discharge tube is connected to the suctioning zone, said tube ending by a nozzle suitable for being connected to the suctioning member to create a suctioning depression in the suctioning zone, and the suctioning member is a system for recovering portable or mobile autologous blood.

10. The assembly according to claim 9, wherein the inner layer is formed of a neutral gauze, so as to minimize the interactions with red blood cells.

11. The assembly according to claim 9, wherein the suctioning zone is formed of a multiperforated catheter maze.

12. The assembly according to claim 9, wherein the suctioning zone is formed of multiperforated foam.

13. The assembly according to claim 9, wherein the suctioning zone is formed of a catheter grid network.

14. The assembly according to claim 9, wherein the drape is formed of a separable male portion and a female portion.

15. The assembly according to claim 9, wherein one of a total or partial incision window is installed in the drape, so as to have access to the wound and/or incision.

16. A method for installing an assembly, comprising: a suctioning device suitable for being placed on an incision and/or a wound of a patient to disinfect and/or dry said incision or said wound, said device comprising a drape comprising: an outer layer comprising an upper face and a lower face, an inner layer comprising an upper face and a lower face, wherein the lower face is arranged so as to come into contact with the wound and/or the incision, and a suctioning member, wherein the upper face of the outer layer of the drape is impermeable, the drape is suitable for being wound around a limb or around the body of the patient, the outer layer and the inner layer of the drape are made of one single part such that the winding of said drape around a limb of the body of the patient leads to the simultaneous winding of said outer layer and said inner layer, a suctioning zone having cavities, is arranged between the lower face of the outer layer and the upper face of the inner layer, the periphery of said suctioning zone being sealed, a discharge tube is connected to the suctioning zone, said tube ending by a nozzle suitable for being connected to the suctioning member to create a suctioning depression in the suctioning zone, and the suctioning member is a system for recovering portable or mobile autologous blood, positioning the suctioning protective device by: placing the lower face of the inner layer of the drape, facing the incision and/or facing the wound, winding the drape around the limb or around the body of the patient where the incision and/or the wound is situated, and connecting the suctioning member to the nozzle of the discharge tube.

Description

DESCRIPTION OF THE FIGURES

[0037] Other advantages and features of the invention will best appear upon reading the description of a preferred embodiment below, in reference to the appended drawings, made as indicative and non-limiting examples, and wherein:

[0038] FIG. 1 is a schematic, cross-sectional view of a drape constituting a suctioning device according to the invention,

[0039] FIG. 2 is a schematic, top view of the drape of FIG. 1, this being equipped with an incision window,

[0040] FIG. 3 is a schematic, top view of a drape according to the invention, said drape being constituted of a separable female portion and male portion,

[0041] FIG. 4 is a schematic view of a patient, the suctioning device of FIG. 1 being installed under the limb of said patient,

[0042] FIG. 5 is a schematic view of a patient, the suctioning device of FIG. 1 being wound around the limb of said patient,

[0043] FIG. 6 is a schematic view of a multiperforated catheter used in the suctioning zone of a drape used in the invention,

[0044] FIG. 7 is a schematic view of a suctioning zone example, this being presented in the form of a multiperforated foam,

[0045] FIG. 8 is a schematic view of a catheter of a known type, used in an embodiment of the suctioning zone according to the invention.

PREFERRED EMBODIMENTS OF THE INVENTION

[0046] The invention relates to an assembly comprising a device for suctioning a wound and/or an incision intended to disinfect them and/or dry them for autologous blood recovery and possibly to avoid the development of infections. Such a suctioning device comprises a drape 1 constituted of two layers 3, 4 surrounding a suctioning zone 6a, 6b, 6c.

[0047] In FIG. 1, the drape comprises a suctioning zone 6a, 6b, 6c arranged between an outer layer 3 and an inner layer 4.

[0048] The outer layer 3 comprises an upper face 3a and a lower face 3b in contact with the suctioning zone 6a, 6b, 6c (described above in the description). This layer 3 can, for example, be made of a non-woven sterile material of the cellulose cotton type, single-layer or multilayer. Any other material known to a person skilled in the art and suiting the production of the drape 1 can however be used.

[0049] Preferably, and with the aim of effectively isolating the body of the patient P of the outer environment and in particular, introducing a contaminated fluid, the upper face 3a of the outer layer 3 of the drape 1 is preferably impermeabilized. This impermeabilization can be done by means of a plastic film, of a material which is impermeable to liquids, of a hydrophobic material, or also using any other material suiting a person skilled in the art.

[0050] The inner layer 4 comes into contact with the patient P when the suctioning device is installed. It makes it possible to avoid the suctioning zone 6a, 6b, 6c (described above in the description) being in direct contact with the incision and/or the wound, and thus improves the comfort and the safety of the patient P. Preferably, the inner layer 4 is presented in the form of a neutral gauze such that it is the least amount of interactions possible with the red blood cells contained in the blood of the patient P. Thus, the embodiment preferred for the inner layer 4 is a neutral gauze of a known type, like for example, sterile compresses.

[0051] In the same manner as the outer layer 3, the inner layer 4 can be made of a non-woven sterile material of the cellulose cotton type, single-layer or multilayer. Any other material known to a person skilled in the art and suiting the production of a drape 1 can however be used.

[0052] The outer layer 3, as well as the inner layer 4 each have a width of between 20 cm and 40 cm, a total length of between 20 cm and 60 cm, and a thickness varying from 1 mm to 2 mm. However, these dimensions are not limiting and can be adapted by the person skilled in the art, according to the type of surgical intervention carried out.

[0053] In a preferred embodiment, the inner layer 4 and the outer layer 3 are made of one single part surrounding the suctioning zone 6a, 6b, 6c. Such a configuration makes it possible to facilitate the design of the suctioning protective device and thus limit the costs.

[0054] The suctioning zone 6a, 6b, 6c is arranged between the upper face 4a of the inner layer 4 and the lower face 3b of the outer layer 3. It comprises cavities 61a, 61b, 61c, wherein the blood of the patient P will be collected then suctioned, in order to be able to recycle it and thus reuse it.

[0055] The suctioning zone 6a, 6b, 6c is connected to a suctioning member 8 by means of a tube 7. The tube 7 is advantageously perforated on a distal portion, and ends, on the proximal portion thereof, by a nozzle intended to be connected to the suctioning member 8. In practice, a Luerlock® connector is used, which could be connected to a pump or any other type of suctioning member.

[0056] The suctioning member 8 is preferably presented in the form of a system for recovering autologous blood of Cell Saver® type. Such a device makes it possible for the practitioner, after washing and centrifugation, to auto-transfuse the patient P during the intervention. Such a feature being particularly useful during emergency intervention or also to avoid risks of allogenic transfusions. This recovery system 8 is preferably portable, so as to be able to transport it easily over the places of intervention. It can, however, in the case of an intervention occurring in an operating room, being presented in the form of a wall-fixed system. It can create a suctioning depression which could vary between −50 mmHg and −300 mmHg, thus making it possible for the practitioner to adjust the suctioning force according to the degree of hemorrhage.

[0057] The suctioning zone 6a, 6b, 6c is sealed, the periphery 9 thereof being closed such that the suctioned blood in said suctioning zone 6a, 6b, 6c can only escape through the tube 7. The sealing can be achieved through welding, or also by adding a material surrounding the whole periphery 9. The suctioning zone 6a, 6b, 6c has dimensions similar to those of the inner 4 and outer 3 layers. It has a length of between 20 cm and 60 cm, a width varying from 20 cm to 40 cm, and a thickness of between 1 mm and 1 cm.

[0058] In a first embodiment, the suctioning zone 6a is presented in the form of a multiperforated catheter maze 63a. These catheters 63a are known to a person skilled in the art and can be made of materials such as polyamide or also polyurethane. The number of multiperforated catheters 63a can vary according to the necessary suctioning capacity. The suctioning zone 6a can, for example, comprise between 1 and 100 catheters.

[0059] FIG. 6 illustrates such a catheter 63a. In this embodiment, the ducts of each of the catheters 63a constitute the cavities 61a wherein the blood of the patient P will be suctioned. The suctioning depression created by the system 8 will suction the blood through perforations 62a so as to recover it in the ducts 61a and then transfer it to said recovery system 8.

[0060] A second embodiment represented in FIG. 7, has a suctioning zone 6b being presented in the form of a multiperforated foam. This foam comprises cavities 61b, preferable arranged uniformly in the whole of the foam 6b. In the same manner as in the preceding embodiment, the suctioning depression created by the system 8 will suction the blood into the cavities 61b through the foam 62b to then send it to said blood recovery system 8.

[0061] In an alternative embodiment, the suctioning zone 6c can be composed of a catheter grid network 63c (represented in FIG. 8). The grids can be interconnected with one another or be separated. In the last case, each of the grids will be connected independently to the recovery system 8. Similarly to that described in the first embodiment, the ducts of the catheters 63c constitute the cavities 61c wherein the suctioned blood is housed. When the suctioning depression is applied using the system 8, the blood of the patient P is suctioned then retransferred to said system so as to be treated and then re-transfused.

[0062] FIG. 2 illustrates a preferred embodiment of the invention, wherein the suctioning device comprises an incision window 2. This can be partial or total and makes it possible for the practitioner to carry out an intervention. This embodiment is particularly useful when the device is used during a surgical intervention and that it is placed at the level of an incision.

[0063] In FIG. 2, the drape 1 is made of one single part. It can however be formed of a separable male portion 1a and a female portion 1b (FIG. 3), the incision window 2 being arranged at the level of the junction between said male portion 1a and said female portion 1b. The use of a drape 1 made of two separable portions 1a, 1b simplifies the design thereof and the implementation thereof by the practitioner. In addition, such a drape 1 makes it possible to make the size of the incision window 2 vary and thus make it possible for the practitioner to adjust it according to the operation to be carried out. To adapt the size of the incision window 2 to the size of the incision or of the wound, the male portion 1a and the female portion 1b of the drape 1 are maintained in position by an adjustable attachment device making it possible to adjust the position of said male portion 1a with respect to said female portion 1b and to make the size of said incision window 2 vary.

[0064] By referring to FIG. 3, the adjustable attachment device is preferably formed of adhesive attachment pads 1c arranged on the male portion 1a and capable of adhering onto the female portion 1b. The adhesive zones can possibly be protected by a removable protective paper that the operator will remove just before the implementation. Any other equivalent adjustable attachment device can be used by a person skilled in the art, like for example, loop straps and hook straps of the VELCRO® type, or also male elements being inserted into female elements.

[0065] FIGS. 4 and 5 represent examples of installing the suctioning device. The limb of the patient P can be placed on the drape 1 (FIG. 4). This configuration is particularly practical when a practitioner operates in an emergency and/or when the blood loss flow is increased.

[0066] In another embodiment represented in FIG. 5, the drape 1 is wound around the limb or the body of the patient where the wound and/or the incision is situated, thus making it possible to maximize the recovery of the blood during an intervention. In this embodiment, the drape 1 preferably has an attachment device 5 making it possible to maintain it in position after having positioned it. This device can, for example, be presented in the form of Velcro® straps, or also a device of the pressure-button type.

[0067] The winding of the drape 1 leads to the simultaneous winding of the outer layer 3 thereof and of the inner layer 4 thereof. The suctioning device can therefore be implemented easily and quickly, in extreme emergency situations, in one single step, contrary to the device described in patent document US2005/0028828 (HEATON), of which the implementation requires several steps.

[0068] The arrangement of the different elements and/or means and/or steps of the invention, in the embodiments described above, must not be understood as requiring such an arrangement in all the implementations. In any case, it will be understood that various modifications can be applied to these elements and/or means and/or steps, without moving away from the sense and the scope of the invention. In particular: [0069] the drape 1 can be positioned differently than the placements described above. It can, for example, be placed at the level of one of the arms, of the torso, etc., [0070] the suctioning zone 6a, 6b, 6c can be different from that described. It can, for example, be presented in the form of a combination of embodiments detailed above. [0071] the suctioning zone 6a, 6b, 6c can be equipped of several tubes 7, making it possible to connect it simultaneously to several suctioning members 8, [0072] the shape of the drape 1 can be different from that described above. It can vary according to the position of the incision and/or the wound. It can, for example, be presented in the shape of a circle, of an ellipsis, or also any other shape suiting a person skilled in the art.