Instrument for skin stretching

11172923 · 2021-11-16

Assignee

Inventors

Cpc classification

International classification

Abstract

An instrument for stretching the skin comprising an elongate, dimensionally stable guide with at last two modules that are disposed on said guide and comprise anchoring means for securing to the skin, wherein at least one of said modules can be moved on the guide in the longitudinal direction thereof, and a non-return device allows movement thereof in a movement direction and blocks movement thereof in the opposite, reverse direction, said non-return device being able to be inverted in terms of the movement direction and the reverse direction.

Claims

1. An instrument for stretching the skin, comprising: an elongate, dimensionally stable guide with at least two modules that are disposed on the guide with a skin anchoring hook for securing the modules to the skin, wherein at least one of the modules and the guide can be moved relative to one another in a longitudinal direction, and a non-return device allows movement of the at least one of the modules and the guide in a movement direction and blocks movement of the at least one of the modules and the guide in an opposite, reverse direction, wherein the non-return device is able to be inverted in terms of the movement direction and the reverse direction.

2. The instrument according to claim 1, wherein a third module is disposed on the guide, wherein the third module can be moved relative to the guide and comprises a second non-return device, and wherein the second non-return device is able to be inverted.

3. The instrument according to claim 1, wherein the non-return device comprises: a toothing formed on the guide and extending in the longitudinal direction of the guide; and at least one pawl disposed on each of the at least two modules, wherein the toothing comprising ribs extending transversely to the longitudinal direction, wherein each rib has vertical support surfaces which are disposed vertically to the longitudinal direction at two end faces of the ribs facing in the longitudinal direction, wherein the pawl engages the toothing with an elastically deflectible free tip, wherein the tip comprises: a chamfer, which passes over the ribs during movement in the movement direction, thereby lifts the pawl out of the toothing against an elastic return force thereof, and wherein the tip of the pawl runs against the vertical support surfaces of the ribs during movement in the reverse direction.

4. The instrument according to claim 3, wherein the at least one pawl is disposed at the end of the at least one of the module trailing in the movement direction, and that the at least one of the module can be slid onto the guide in two orientations rotated by 180° to invert the non-return device.

5. The instrument according to claim 1, wherein the non-return device can be rendered inoperable by a release device.

6. The instrument according to claim 5, wherein the release device lifts the pawl out of the toothing against the elastic return force thereof.

7. The instrument according to claim 1, wherein a second guide is disposed on the rigid frame, wherein movement directions of the two guides extend at an angle with respect to one another in a plane of the frame, and wherein a third module disposed on the third guide can be secured to the rigid frame so that the third guide can be moved in its longitudinal direction with respect to the third module and with respect to the frame.

8. The instrument according to claim 7, wherein the frame is a ring-shaped closed frame in one plane enclosing a free inner surface.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) In the following, the present application is explained in more detail with reference to the accompanying drawings and illustrated in an exemplary embodiment. In the drawings:

(2) FIG. 1 shows the guide of an instrument according to the present disclosure,

(3) FIG. 2 shows a module placed on the guide,

(4) FIG. 3 shows the module in an individual illustration,

(5) FIG. 4 shows the anchoring means of the module,

(6) FIG. 5 shows an axial partial section of the instrument with two modules with oppositely directed non-return devices,

(7) FIGS. 6 to 8 show in a schematic top view various uses of the instrument with two modules,

(8) FIGS. 9 and 10 show in a schematic top view various uses of the instrument with three modules, and

(9) FIG. 11 shows in a schematic top view the use of the instrument with a frame.

DETAILED DESCRIPTION

(10) In the depicted exemplary embodiment, the instrument for stretching the skin comprises a guide 10 shown as an individual part in FIG. 1. Guide 10 is designed as an elongate rod, preferably made of plastic. Guide 10 has a non-circular, in particular rectangular cross section. Guide 10 is dimensionally stable, i.e. stable against axial tensile and compressive forces as well as bending forces. In the depicted exemplary embodiment, guide 10 is designed as a straight rod. To adapt to the body surface of the patient, the guide can optionally be designed with a longitudinal bend.

(11) At one side surface of guide 10, in FIG. 1 at the top, a toothing 12 is formed, which essentially extends over the entire length of guide 10. As can be seen in FIG. 5, toothing 12 consists of ribs 14 spaced apart in the longitudinal direction of guide 10, which extend transversely to the longitudinal direction of guide 10 and/or toothing 12. In the longitudinal section of guide 10, ribs 14 have an essentially rectangular cross section so that their flanks on both sides form support surfaces 16 each facing the opposite longitudinal directions of guide 10, which essentially extend vertically to the longitudinal axis of guide 10.

(12) As shown in FIG. 1, a module 18 is disposed at the one end of guide 10, which, in the depicted exemplary embodiment, is firmly attached to guide 10, preferably integrally formed of plastic with guide 10. It is understood that module 18 can also be a separate component, which is supported on guide 10. Module 18 may optionally be displaceable on guide 10 and lockable in its position on the guide. Module 18 comprises a module body 20 and a receptacle 22 at the bottom below guide 10, into which the anchoring means can be inserted in a manner described below.

(13) Further, at least a second module 24 is placed on guide 10, the structure of which becomes apparent from FIGS. 2 to 5. The second module 24 comprises a module body 20, which is designed with a continuous perforation 26 in the longitudinal direction, the internal cross section of which corresponds to the external cross section of guide 10. Using this perforation 26, second module 24 can be slid onto guide 10 and is thus guided in an axially displaceable and non-rotatable manner on guide 10. Anchoring means are provided at the bottom of module body 20, which serve for securing module 24 to the skin surface of the patient. In the depicted exemplary embodiment, the anchoring means are needle-shaped hooks 28, which can be inserted into the skin of the patient. At least two hooks 28 are disposed next to each other in a row extending transversally to the longitudinal direction of guide 10 and are supported on a hook support 30, which can be inserted removably into receptacle 22 integrally formed at the bottom of module body 20, as can be seen in FIGS. 2 and 5, in particular. Module 24 and hook support 30 are preferably manufactured from plastic. Hooks 28 are needles made of metal or plastic.

(14) Instead of hooks 28, other anchoring means can also be provided at the bottom of modules 18 and 24 to secure modules 18 and 24 to the skin surface of the patient. Such anchoring means can also be adhesive means or the like, for example. It is essential that the anchoring means allow the introduction of forces into the skin parallel to the surface of the skin.

(15) A pawl 32 is disposed at the end of module body 20 opposite to receptacle 22, above perforation 26. In the depicted exemplary embodiment, pawl 32 is integrally formed with module body 20 as an elastically flexible tongue 34 made of plastic. Tongue 34 protrudes above toothing 12 and parallel thereto from module body 20. The free end of tongue 34 is designed as a tip 36, which protrudes downward from tongue 34 against guide 10 and engages toothing 12, as can be seen in FIG. 5. Tip 36 engaging toothing 12 is formed with a chamfer 38, which extends downward from the bottom of tongue 34 towards tip 36 away from module body 20, as shown in FIG. 5. The width of tongue 34 with tip 36 essentially corresponds to the width of toothing 12 and tongue 34 and is only slightly narrower than toothing 12.

(16) A release lever 40 is integrally formed at the top of tongue 34 and protrudes vertically upward from tongue 34. An integrally formed stop lever 42 protruding upward from module body 20 is assigned to release lever 40. An axial gap remains between release lever 40 and stop lever 42.

(17) Pawl 32 together with toothing 12 forms a non-return device, the function of which becomes apparent from FIG. 5. If module 24 is slid onto guide 10, pawl 32 engages toothing 12 with tip 36, under the elastic spring effect of tongue 34. Tip 36 is located between two consecutive ribs 14. In left-hand module 24 in FIG. 5, the non-return device is directed such that module 24 can be moved to the right on guide 10 (in FIG. 5). Pawl 32 is thereby drawn to the right by module 24. Chamfer 38 passes over rib 14. Pawl 32 is thereby lifted out of toothing 12 and can slide over toothing 12 so that module 24 can be moved freely. If module 24 is moved in the opposite reverse direction (towards the left for left-hand module 24 in FIG. 5), tip 36 of the pawl hits vertical surface 16 of next rib 14 thus blocking the movement of module 24.

(18) According to the present disclosure, the movement direction and the reverse direction of the non-return device can be inverted. To do so, module 24 is slid rotated by 180° onto guide 10, as illustrated in FIG. 5 for module 24 on the right-hand side. In this arrangement, module 24 in FIG. 5 can be moved to the left, wherein pawl 32 passes over toothing 12, while a movement in the reverse direction, i. e. to the right, is blocked. In FIG. 5, the respective movement direction of module 24 relative to guide 10 for both positions is represented by an arrow.

(19) It is understood that in the corresponding operating mode, the non-return device also allows guide 10 to be displaced relative to fixed module 24 in a movement direction and to be blocked in the opposite direction. If, for example, in FIG. 5, left-hand module 24 is fixed, guide 10 can be moved to the left in this left-hand module 24, wherein guide 10 takes the right-hand module 24 along.

(20) If release lever 40 is pushed manually against stop lever 42, release lever 40 pivots tongue 34 upward against the elastic return force thereof and lifts tip 36 out of toothing 12. The non-return device is thereby released and module 24 can be displaced freely on the guide in both directions. This is in particular required to be able to slide module 24 onto guide 10 against the reverse direction of the on-return device, to release the tensile force applied to the skin.

(21) It will be readily appreciated that instead of first module 18 firmly connected to guide 10, a module designed according to second module 24 can also assume the functionality of first module 18. It will further be readily appreciated that in addition to second module 24, a correspondingly designed third module 44 can also be slid onto guide 10, with the movement direction and the reverse direction of second module 24 and third module 44 being able to be inverted independently from one another in any way.

(22) When using hooks 28, it is important to insert these into the skin in the tensile direction, to prevent them from slipping out of the skin under the tensile effect.

(23) In the following, the use of the inventive instrument is explained for various treatment methods.

(24) FIG. 6 shows the use of the instrument for the known method of skin stretching for the purpose of wound closure. This method is preferably used for traumatic skin defects. A first module 18 and a second module 24 are anchored in skin 46 at the two edges of a wound 48 by means of the anchoring means. The two modules 18 and 24 are moved towards one another, as indicated by the arrows, to stretch the skin outside the modules and to draw the edges of wound 48 towards one another, until they can be sutured. The stretching of the skin outside the modules anchored to the wound edges results in a mechanical enlargement of the skin and in a reduction of the tissue edema, which allows the wound edges to be brought together until they can be connected to one another by skin suture.

(25) FIG. 7 shows how the two modules 18 and 24 can be moved away from each other by the inventive inversion of the movement direction of module 24, as also indicated by arrows. The undamaged skin 46 between the anchoring points of modules 18 and 24 can thus be temporarily drawn apart. This causes a stretching of the dermal and subdermal cells, which results in a biochemical stimulation of the tissue proliferations and matrix synthesis in addition to the mechanically induced surface enlargement. If high compressive forces are introduced in the skin, a temporary ischemia can be induced, which results in a beneficial hyperfusion upon relaxation of the skin. A controlled damage to the dermal fiber system caused by very high compressive forces activates healing forces, which lead to reconstruction of the fiber system and regeneration of body tissue (remodelling).

(26) FIG. 8 shows how the skin stretching explained in FIG. 7 can be used for the treatment of a chronic wound 48. Two instruments are anchored to skin 46 at the two sides of a chronic wound, and skin 46 is stretched in these two areas adjacent to the wound by drawing the modules apart. In doing so, a skin injury in the areas adjacent to wound 48 is achieved, which can then be used for closing the wound.

(27) FIGS. 9 and 10 show the use of the instrument with three modules 18, 24 and 44.

(28) In the method shown in FIG. 9, first module 18 and second module 24 are anchored to the skin in the two opposite edges of wound 48. Modules 18 and 24 are moved towards one another to bring the wound edges together. Skin 46 outside modules 18 and 24 is thereby stretched. A third module 44 is placed on guide 10 outside second module 24, with the movement direction and the reverse direction being disposed opposite to second module 24. The skin outside second module 24 can thus be additionally stretched by means of third module 44. This triggers the release of biochemical growth factors in an additional skin area, which initiate and optimize regenerative processes by stimulating tissue regeneration and wound healing (see FIG. 7).

(29) In FIG. 10, first module 18 and second module 24 are also anchored in the two opposite wound edges, to draw these wound edges together. Third module 44 is placed on guide 10 outside second module 24. The movement direction and the reverse direction of third module 44 are directed in the same direction as for second module 24. Third module 44 can thus additionally stretch skin 46 at the side of third module 44 facing away from wound 48 so that the additionally stimulated skin is pushed towards second module 24 and thus towards wound 48 by third module 44.

(30) The present disclosure makes it possible to perform both a wound contraction for closure of a wound and a skin distraction for stimulation of the cell proliferation and matrix synthesis by using the same instrument. In particular, it is also possible to combine these two functions by means of the instrument.

(31) Another use of the instrument according to the present disclosure is shown in FIG. 11.

(32) In this embodiment, a rigid frame 50 is used, which is preferably ring-shaped and can have the shape of a rectangle, a polygon or also a circular ring, as can be seen in the drawing. Planar frame 50 comprises a free internal space, in which wound 48 to be treated is located during use. One or several modules 24 can be disposed on frame 50. Preferably, modules 24 are secured to the frame in variable positions. For this purpose, frame 50 may, for example, comprise holes 52 offset from one another by circumferential angles, into which modules 24 are inserted using pins integrally formed at the bottom thereof. In this way modules 24 can be positioned on frame 50 in an invertible arrangement. Guides 10 inserted into modules 24 are thus able to be moved in modules 24 secured to frame 50 relative to modules 24 and frame 50. Depending on the arrangement of modules 24 in frame 50, the non-return device can thus act such that guides 10 can be moved inwards in the movement direction to the internal space of frame 50, while the movement thereof to the outside is blocked. When the non-return device is inverted, a movement of guide 10 to the outside relative to frame 50 is enabled, while the movement to the internal space of frame 50 is blocked.

(33) One or several other modules 24 can be disposed on guides 10. These modules can be designed as modules 18 firmly disposed on the guide or as modules 24 that can be displaced on the guide 10 in one direction by means of a non-return device, as described above.

(34) Due to the different positions of modules 24 on frame 50, the movement directions of guides 10 in these respective modules 24 extend at different angles with respect to one another in the plane of frame 50. As can be seen in FIG. 11, the movement directions can extend at angles of, e.g., 30°, 60°, 90°, 180° etc. Depending on the orientation of the non-return device of respective module 24 secured to frame 50, another module 24 supported on guide 10 within frame 50 can be pushed inward to the internal space of frame 50 and/or a module 24 supported on respective guide 10 outside frame 50 can be radially moved outside away from frame 50. This is indicated in FIG. 11 by respective arrows. If modules 24 disposed within frame 50 are anchored to the skin and moved to the internal space of frame 50 by means of guides 10, the edges of a wound 48 enclosed by frame 50 can be pushed towards one another by these modules 24, to stretch the skin at the edge of wound 48 and to close this wound 48, as, for example, explained in FIGS. 6 and 8. If a second module 24 is disposed on guide 10 outside frame 50 and the non-return device of module 24 secured to frame 50 is positioned such that guide 10 can be moved radially outward, additional stretching of the skin outside frame 50 is possible, to achieve an additional skin gain, as, for example, explained with reference to FIG. 7.

(35) With all these uses, the advantage is obtained that frame 50 and in particular guides 10 with modules 24 are located outside the skin area to be treated and wound 48 and do not impede or restrict the free access to the skin area to be treated and to wound 48. This advantage is preserved, even if several instruments are disposed on frame 50, as, for example, shown in FIG. 11, and skin stretching along the entire circumference of wound 48 with different tensile directions is thus possible.

LIST OF REFERENCE NUMERALS

(36) 10 Guide 12 Toothing 14 Ribs 16 Support surface 18 First module 20 Module body 22 Receptacle 24 Second module 26 Perforation 28 Hook 30 Hook support 32 Pawl 34 Tongue 36 Tip 38 Chamfer 40 Release lever 42 Stop lever 44 Third module 46 Skin 48 Wound 50 Frame 52 Holes