Wound packing
11357903 · 2022-06-14
Assignee
Inventors
Cpc classification
A61M1/915
HUMAN NECESSITIES
A61F13/0276
HUMAN NECESSITIES
Y10T83/0341
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
A61F15/001
HUMAN NECESSITIES
Y10T83/04
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
Y10T83/0524
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
Y10T29/49826
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
International classification
A61M1/00
HUMAN NECESSITIES
A61F15/00
HUMAN NECESSITIES
Abstract
A wound packing material is provided, suitable for use in negative pressure wound therapy, including a body of a porous material, the body including frangible regions defining a plurality of portions, the frangible regions allowing the portions to be selectively removed from the body. Methods of manufacturing the wound packing material, and methods of its use are also provided.
Claims
1. A wound packing material comprising: a body of porous material, the body comprising a plurality of outer surfaces and a plurality of outer edges, each of the plurality of outer edges disposed at an interface of a pair of adjacent outer surfaces, each of the outer surfaces delimited by a subset of the plurality of outer edges, the body comprising frangible regions defining a plurality of portions, the frangible regions allowing the portions to be selectively removed from the body, wherein the wound packing material comprises a first partial pre-cut that extends in a first direction from a first outer surface of the body to a second outer surface of the body, wherein the wound packing material comprises a second partial pre-cut that extends in the first direction from the first outer surface of the body to the second outer surface of the body, wherein each of the first and second partial pre-cuts is spaced apart from each outer edge of the subset of outer edges that delimits the first outer surface, and wherein the wound packing material comprises a third partial pre-cut that extends in a second direction from a third outer surface of the body to a fourth outer surface of the body, wherein the third partial pre-cut is spaced apart from each outer edge of the subset of outer edges that delimits the third outer surface.
2. The wound packing material of claim 1, wherein the plurality of portions can be removed manually.
3. The wound packing material of claim 1, wherein the wound packing material is formed from a wound packing foam suitable for use in negative pressure wound therapy.
4. The wound packing material of claim 1, wherein the wound packing material does not substantially collapse when a negative pressure is applied to the wound packing material.
5. The wound packing material of claim 4, wherein the negative pressure is in the range of from 80 to 125 mm Hg below ambient atmospheric pressure.
6. The wound packing material of claim 1, wherein the body further comprises an upper surface, a lower surface, and a thickness defined therebetween, the body comprising at least one first partial pre-cut disposed within the thickness, an upper portion of the thickness being disposed between the at least one first partial pre-cut and the upper surface, a lower portion of the thickness being disposed between the at least one first partial pre-cut and the lower surface.
7. The wound packing material of claim 6, wherein the at least one first partial pre-cut is substantially parallel with the upper surface or the lower surface.
8. The wound packing material of claim 7, wherein the body further comprises at least one second partial pre-cut that is substantially perpendicular to the upper surface.
9. The wound packing material of claim 8, wherein the at least one second partial pre-cut is curved.
10. The wound packing material of claim 9, wherein the at least one second partial pre-cut comprises two or more spaced apart curved planar cuts that are substantially parallel with one another.
11. The wound packing material of claim 10, wherein the at least one second partial pre-cut comprises an additional curved planar cut that is non-parallel with the two or more spaced apart curved planar cuts.
12. A wound packing material comprising: a body of porous material, the body comprising a plurality of outer surfaces and a plurality of outer edges, each of the plurality of outer edges disposed at an interface of a pair of adjacent outer surfaces, each of the outer surfaces delimited by a subset of the plurality of outer edges, the body comprising frangible regions defining a plurality of portions, the frangible regions allowing the portions to be selectively removed from the body, wherein the wound packing material comprises a first plurality of partial pre-cuts that extend in a first direction from a first outer surface of the body to a second outer surface of the body, wherein the wound packing material comprises a second plurality of partial pre-cuts that extend in the first direction from the first outer surface of the body to the second outer surface of the body, wherein each of the first plurality of partial precuts and each of second plurality of partial pre-cuts is spaced apart from each outer edge of the subset of outer edges that delimits the first outer surface, and wherein the wound packing material comprises a third plurality of partial pre-cuts that extend in a second direction from a third outer surface of the body to a fourth outer surface of the body, wherein each of the third and fourth outer surfaces is different from the first and second outer surfaces.
13. The wound packing material of claim 12, wherein the plurality of portions can be removed manually.
14. The wound packing material of claim 12, wherein the wound packing material is formed from a wound packing foam suitable for use in negative pressure wound therapy.
15. The wound packing material of claim 12, wherein the wound packing material does not substantially collapse when a negative pressure is applied to the wound packing material.
16. The wound packing material of claim 15, wherein the negative pressure is in the range of from 80 to 125 mm Hg below ambient atmospheric pressure.
17. The wound packing material of claim 12, wherein the body further comprises an upper surface, a lower surface, and a thickness defined therebetween, the body comprising at least one first partial pre-cut disposed within the thickness, an upper portion of the thickness being disposed between the at least one first partial pre-cut and the upper surface, a lower portion of the thickness being disposed between the at least one first partial pre-cut and the lower surface.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) Embodiments of the present invention will now be described, by way of example only, with reference to the accompanying drawings, in which:
(2)
(3)
(4)
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(8)
DETAILED DESCRIPTION OF SOME EXEMPLIFYING EMBODIMENTS
(9) As shown in
(10) As shown in
(11) The three sets of partial pre-cuts 14, 16, 18 are intermittent, the gaps in the pre-cuts defining frangible regions 20 on each internal face of each portion 12 (in other words they are perforated for easy removal of the portions). The frangible regions 20 connect adjacent portions 12 together thereby to ensure the portions 12 remain connected together when the body 10 is stored, compressed or extended, i.e. when being used as a wound packing in NPWT.
(12) The frangible regions 20 extend between face sides of each portion 12 and are elongate. The thickness of each frangible region 20 is suitable to provide adequate strength to ensure adjacent portions 12 remain connected when the body 10 is being compressed or extended during normal use, whilst allowing one or more portions 12 to be easily pulled from the body 10 by compromising the integrity of the frangible regions 20 attaching the portion 12 to the body. For typical NPWT foams, a frangible region of approximately 2 mm of thickness provides a good compromise of strength versus tearability.
(13) One or more portions 12 can be selectively removed by hand from the body 10 to shape the body 10 for a particular wound packing application. Advantageously, cutting tools such as knives, scalpels and scissors are not required to shape the body 10 of porous material.
(14) As shown in
(15) The frangible regions 20 ensure the body 10 retains its structural integrity for storage and handling purposes whilst allowing one or more portions 12 to be selectively removed therefrom.
(16) Of course, the dimensions of the body 10 and the portions 12 may be different to those described above for a particular application and the number and orientation of partial pre-cuts lines 14, 16, 18 may be varied and may be planar or curved to define regular or irregular portions 12 accordingly.
(17) To form a wound packing material similar to the above the following general process may be used. The present process describes a process for converting a single cuboid block of foam into 6 cuboidal wound packing material bodies. The block is initially approximately 200 mm by 100 mm by 180 mm and is cut into 6 blocks of 200 mm by 100 mm by 30 mm. It will be apparent that variations of this method could be used to manufacture wound packing materials of a great variety of different shapes and sizes, and having varying portion size and shapes. A body of porous material is provided which has the dimensions set out above. A first set of parallel planar partial pre-cuts is made in the body using an array of blades 30. The pre-cuts are made perpendicular to, and into, a first face of the body The array (
(18) This process forms 6 cuboids of foam measuring 200 mm×100 mm×30 mm, which are each formed of cuboids measuring approximately 20 mm×20 mm×10 mm, each of the cuboid portions being interconnected with adjacent portions by frangible regions of approximately 2 mm thickness.
(19) It should be noted that where a generally cubic body of foam is being prepared the order of the cuts is not particularly significant as the cube is equally structurally stable in all 3 dimensions. However, when preparing a body with a relatively thin minor dimension, as set out in the method above, it is important that the first cut made is the one perpendicular to the plane of the thin dimension (i.e. the smallest face of the cuboid), or that the shape of the block is supported as the cut is made. If the order is reversed, or the block shape is not supported, there is generally an unacceptable amount of crushing and/or corrugation of the body resulting in a significant distortion to the desired cut geometry.
(20) The result of this process is a wound packing material which can be custom shaped by manually removing cuboid portions by tearing the frangible regions interconnecting the portions making up the body. This allows a medical practitioner to shape the body of wound packing material to fit the wound to be packed or dressed. Once the wound packing material has been shaped appropriately, the wound can be dressed for NPWT.