WO1981002516A1 - Cushion for holding an element of grafted skin - Google Patents
Cushion for holding an element of grafted skin Download PDFInfo
- Publication number
- WO1981002516A1 WO1981002516A1 PCT/DE1980/000025 DE8000025W WO8102516A1 WO 1981002516 A1 WO1981002516 A1 WO 1981002516A1 DE 8000025 W DE8000025 W DE 8000025W WO 8102516 A1 WO8102516 A1 WO 8102516A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- pillow
- recess
- skin
- graft
- cushion
- Prior art date
Links
- 239000007788 liquid Substances 0.000 claims abstract description 8
- 230000036074 healthy skin Effects 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 4
- 239000000853 adhesive Substances 0.000 claims description 3
- 230000001070 adhesive effect Effects 0.000 claims description 3
- 239000012780 transparent material Substances 0.000 claims description 3
- 230000035876 healing Effects 0.000 description 5
- 206010040954 Skin wrinkling Diseases 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 230000028327 secretion Effects 0.000 description 3
- 239000002985 plastic film Substances 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 210000004243 sweat Anatomy 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- 230000002411 adverse Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- 230000037237 body shape Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F5/00—Orthopaedic methods or devices for non-surgical treatment of bones or joints; Nursing devices; Anti-rape devices
- A61F5/01—Orthopaedic devices, e.g. splints, casts or braces
- A61F5/30—Pressure-pads
- A61F5/34—Pressure pads filled with air or liquid
-
- A61F13/05—
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M27/00—Drainage appliance for wounds or the like, i.e. wound drains, implanted drains
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F2013/00089—Wound bandages
- A61F2013/00157—Wound bandages for burns or skin transplants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F2013/00089—Wound bandages
- A61F2013/00165—Wound bandages not touching the wound
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F2013/00089—Wound bandages
- A61F2013/0017—Wound bandages possibility of applying fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F2013/00089—Wound bandages
- A61F2013/0017—Wound bandages possibility of applying fluid
- A61F2013/00174—Wound bandages possibility of applying fluid possibility of applying pressure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F2013/00089—Wound bandages
- A61F2013/00182—Wound bandages with transparent part
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F2013/00361—Plasters
- A61F2013/00795—Plasters special helping devices
- A61F2013/00829—Plasters special helping devices rigid or semi-rigid backing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F2013/00361—Plasters
- A61F2013/00846—Plasters with transparent or translucent part
Definitions
- the invention relates to a cushion for pressing skin grafts.
- a cushion for pressing skin grafts When transplanting skin, especially when the skin; in Whole thickness is transplanted, it is critical that the entire graft is pressed onto the area of the body with even pressure. This constant pressure must be maintained for six to eight days, it can vary somewhat individually.
- it is known to apply a pressure bandage that contains a pillow that is larger than the skin graft and presses it evenly over the entire surface onto the sore body part (Ferris Smith: Plastic and Eeconstructive Surgery, WB Saunders Co. 1950, pages 26 and 27).
- the object of the invention is to develop a pressure bandage for a skin graft which avoids these disadvantages.
- This object is achieved according to the invention in that the pillow has on its side facing the body a recess which is at least almost as large as the graft.
- this pillow When applying the pressure bandage, this pillow is then placed on the graft so that the recess comes to lie over the graft and the edge of the recess is glued to the skin, whereby the sand can also be sewn onto the skin and the prick parts additionally with adhesive o.
- Can be sealed provided that they are in the area of the tape to be sealed.
- the recess has the shape of the skin graft. In embodiments of the invention, the recess may be slightly smaller than the skin graft so that the edge of the recess still lies on the graft, or the recess is somewhat larger than the graft, in which case the edge of the recess lies on the healthy skin.
- the graft can be sewn on the edges of the wound in the usual way, but the seam can also be omitted if, in the first-mentioned embodiment of the invention, the edge of the recess not only on the edge of the skin graft, but also on the healthy skin is stuck on.
- Advantages of the pillow according to the invention are first of all that the skin does not sweat in the area of the recess and the secretion of protein and other secretions either does not occur or does not lead to irritation of the skin.
- the graft is ventilated through the recess.
- the transplant can be supplied with oxygen or a nutrient solution through the cutout, so that the healing process can thereby possibly be accelerated or the healing process can be corrected.
- the pillow cannot fold in the area of the recess, ie above the graft, so that this disadvantage of the known pillow is avoided.
- the side of the pillow facing away from the body is made of a transparent material, the healing process can be checked through the recess or the degree of blood flow to the skin graft can be observed and, if necessary, by filling the pillow with a Treatment medium can be corrected. Therefore, in one embodiment of the invention, the pillow is made of a transparent material, for example of a suitable plastic film or the like, at least in the region of the side opposite the recess.
- the recess in the pillow can be cut out of the pillow in the form of the skin graft immediately before the pressure bandage is put on.
- the edge of the recess follows the edge of the skin graft exactly, the edge of the recess in the pillow can run partly on the skin graft and partly on the healthy skin.
- the recess can also be significantly larger than the transferred skin piece, without the healing process being adversely affected in the aforementioned cases. Therefore, pillows with different sized, prefabricated recesses can be made and made available to the surgeon. In these cases, the edge of the recess can be provided with an adhesive for attaching the pillow to the skin or the skin graft.
- the cushion has a valve for adjusting the pressure within the cushion.
- a valve which is known per se, for generating, controlling and / or maintaining the pressure in the cushion can be connected to this valve.
- the pillow has on its side facing away from the body a rigid plate which, according to the aforementioned embodiment, can also be transparent.
- This plate can be adapted to the body shape on which the pillow is to be placed.
- This embodiment of the invention has the advantage that the risk of wrinkles forming in the non-recessed area of the side of the cushion lying on the body when the pressure bandage is applied is substantially reduced.
- the pillow according to the invention can be pressed onto the body with an elastic bandage with or without the rigid plate being interposed; an elastic stocking can also be used on the extremities for this purpose.
- only one valve is provided which is suitable for generating, maintaining or controlling the pressure within the cushion and / or for filling a liquid into the interior of the cushion, but two connections are provided so that air and liquid can be exchanged within the pillow without the pressure in the pillow changing significantly.
- a liquid in the pillow can be forced out by introducing air into one port to the other port and vice versa, air in the pillow can be displaced from the pillow through the one port .
- the two connections can also be used to constantly renew the liquid or pressurized air in the cushion or to circulate it through a device which treats this medium, for example removing moisture from the air, so that in no sweat or wound water accumulates on the pillow.
- liquid can also be drawn off through one of the connections.
- a mass can also be embedded in the pillow, which binds moisture and therefore dries the air in the pillow.
- a substance that dries the air can also be separated from the cavity of the cushion by a semi-permeable wall, for example made of a suitable plastic, this wall only permitting the moisture in the direction of the drying substance.
- Fig. 1 shows a view of that side of a
- Embodiment of the pillow according to the invention which is intended to rest on the body part to be treated,
- FIG. 4 shows a third embodiment in a section corresponding to FIG. 2.
- the cushion has two film cuts 1 and 2 made of latex or a suitable elastic plastic, which are connected airtightly at their edges by a seam 3.
- the cushion 2 which is placed on the upper side of the body to be treated when the pressure bandage is put on, has a recess 4 in the film 2.
- a valve 5 is welded into the film 1 near the edge of the cushion.
- the recess 4 is larger than the skin graft, so that the edge 6 in this embodiment of the invention is glued to the body completely outside the seam with which the skin graft is attached to the healthy skin.
- the valve 5 is designed so that it can be connected to known means for generating, maintaining and controlling a certain pressure within the cushion.
- the film 1 is transparent so that the skin graft can be observed through this film and through the recess 4 without the pressure dressing being released.
- the prerequisite for this is that a window is also provided in the part of the dressing arranged above the pillow, which permits this observation or that this part is also transparent.
- the embodiment of the invention shown in Fig. 3 differs from the embodiment shown in Figs. 1 and 2 in that a rigid plate 7 is welded or glued or otherwise fixed in position on the film 1, which has the shape of Has surface of the body part 8 to be treated.
- This plastic sheet can also be transparent to pass through it to be able to observe the skin graft.
- Their stiffness and size are selected so that they distribute the pressure exerted by the pressure dressing evenly over the surface of the cushion and thereby prevent wrinkling in the area of the underside of the cushion occupied by the film 2.
- the valve 5 can be designed such that it is also suitable for introducing a treatment medium, possibly while maintaining the set pressure in the cushion.
- An additional valve on the cushion can also be provided for this purpose.
- FIG. 4 shows an embodiment which has two feed lines 9 and 10 which open into the interior of the cushion. Devices of any type can be connected to this supply line, which exchange, clean or keep the medium in the interior of the cushion without a drop in pressure or keep it at an adjustable pressure.
- very simple shut-off elements 11 for these feed lines are shown in FIG. 4, which are laterally replaced by more suitable devices in the practical implementation of the invention.
- the recess 4 can be so large that its band 6 lies partly on the healthy skin, partly on the transplant, or entirely on the transplant.
- the pillow can be pressed onto the graft with a bandage or an elastic stocking.
- one of the two films 1 or 2, in particular the lower film 2 can be significantly larger than the other film and can be extended beyond the seam 3 and can be used to fasten the cushion.
Description
Kissen zum Andrücken von Hauttransplantaten
Die Erfindung bezieht sich auf ein Kissen zum Andrücken von Hauttransplantaten . Bei der Transplantation von Haut, insbesondere dann, wenn die Haut; in
ihrer ganzen Dicke verpflanzt wird, ist es entscheidend, daß das ganze Transplantat mit einem gleichmäßigen Druck auf die betreffende Körperstelle aufgedrückt wird. Dieser gleichmäßige Druck muß sechs bis acht Tage aufrechterhalten werden, er kann individuell etwas variieren. Es ist bekannt, zu diesem Zweck einen Druckverband anzulegen, der ein Kissen enthält, das größer als das Hautttransplantat ist und dieses auf seiner ganzen Fläche gleichmäßig auf den wunden Körperteil aufdrückt (Ferris Smith: Plastic and Eeconstructive Surgery, W.B. Saunders Co. 1950, Seiten 26 und 27).
Nachteile liegen jedoch darin, daß, da die be kannten Kissen aus Gummi bestehen, sich zwischen dem Kissen und der Oberfläche des ϊranplantates EiweißSekrete ansammeln und daß das Kissen verhindert, daß Luft an die Oberfläche des Transplantates gelangt. Schließlich läßt sich auch bei Anwendung größter Sorgfalt nicht immer vermeiden, daß die auf dem Transplantat aufliegende Fläche des Kissens durch den Druckverband Falten wirft, insbesondere wenn die Haut auf stark gekrümmte Körperpartien verpflanzt werden muß. Diese Falten bilden sich auf dem übertragenen Hautstück ab und sind auch nach dem völligen Abheilen sichtbar.
Der Erfindung liegt die Aufgabe zugrunde, einen Drυckverband für ein Hauttransplantat zυ entwickeln, der diese Nachteile vermeidet. Diese Aufgabe wird gemäß der Erfindung dadurch gelöst, daß das Kissen an seiner dem Körper zugewandten Seite eine Aussparung aufweist, die zumindest nahezu so groß ist wie das Transplantat.
Beim Anlegen des Druckverbandes wird dann dieses Kissen so auf das Transplantat gelegt, daß die Aussparung über das Transplantat zu liegen kommt und der Rand der Aussparung wird auf die Haut aufgeklebt, wobei der Sand zusätzlich auf die Haut aufgenäht sein kann und die Stichsteilen zusätzlich mit Klebstoff o. dgl. abgedichtet sein können, sofern diese im Bereich des abzudichtenden Bandes liegen. Die Aussparung weist die Form des Hauttransplantates auf. Bei Ausführungsformen der Erfindung kann die Aussparung etwas kleiner sein als das Hauttransplantat, so daß der Rand der Aussparung noch auf dem Transplantat aufliegt, oder aber die Aussparung ist etwas größer als das Transplantat, in welchem Falle der Rand der Aussparung auf der gesunden Haut aufliegt. Das Transplantat kann in der üblichen Weise an den Rändern der Wunde angenäht sein, man kann jedoch auch auf die Naht verzichten, wenn bei der zuerst genannten Ausführungsform der Erfindung der Rand der Aussparung nicht nur auf den Rand des Hauttransplantates, sondern auch auf die gesunde Haut aufgeklebt wird.
Vorteile des erfindungsgemäßen Kissens liegen zunächst einmal darin, daß im Bereich der Aussparung die Haut nicht schwitzt und die Absonderung von Eiweiß und anderen Sekreten entweder unterbleibt oder nicht zu einer Irritation der Haut führt. Durch die Aussparung hindurch wird das Transplantat belüftet. Außerdem kann durch die Aussparung hindurch das Transplantat mit Sauerstoff oder aber einer Nährlösung versorgt werden, so daß hierdurch die Abheilung möglicherweise beschleunigt werden kann oder in den Abheilungsprozeß korrigierend eingegriffen werden kann. Schließlich kann das Kissen im Bereich der Aussparung, also über dem Transplantat, keine Falten werfen, so daß dieser Nachteil des bekannten Kissens vermieden ist. Wenn die dem Körper abgewandte Seite des Kissens aus einem durchsichtigen Werkstoff besteht, so kann durch die Aussparung hindurch der Heilungsprozeß kontrolliert werden bzw. der Grad der Durchblutung des Hauttransplantates beobachtet werden und, falls erforderlich, in der oben erwähnten Weise durch Füllen des Kissens mit einem Behandlungsmedium korrigiert werden. Daher besteht bei einer Ausführungsform der Erfindung das Kissen zumindest im Bereich der der Aussparung gegenüberliegenden Seite aus einem durchsichtigen Werkstoff, beispielsweise aus einer geeigneten Kunststofffolie o. dgl.
Die Aussparung im Kissen kann unmittelbar vor Anlegen des Druckverbandes in der Form des Hauttransplantates aus dem Kissen ausgeschnitten werden. Für den Heilungsprozeß ist es jedoch nicht erforderlich, daß der Rand der Aussparung genau dem Rand des Hauttransplantates folgt, der Rand der Aussparung im Kissen kann teils auf dem Hauttransplantat und teils auf der gesunden Haut verlaufen. Schließlich kann auch die Aussparung wesentlich größer als das übertragene Hautstück sein, ohne daß in den vorgenannten Fällen der Heilprozeß ungünstig beeinflußt wird. Daher können Kissen mit verschieden großen, vorgefertigten Aussparungen hergestellt und dem Chirurgen zur Verfügung gehalten werden. In diesen Fällen kann der Rand der Aussparung mit einem Klebstoff zur Befestigung des Kissens auf der Haut bzw. dem Hauttransplantat versehen sein.
Bei Ausführungsformen der Erfindung weist das Kissen ein Ventil zum Einstellen des Druckes innerhalb des. Kissens auf und mit diesem Ventil kann, eine an sich bekannte Einrichtung zum Erzeugen, Kontrollieren und/oder Aufrechterhalten des Druckes im Kissen verbunden sein.
Bei einer Ausführungsform der Erfindung weist das Kissen auf seiner dem Körper abgewandten Seite eine steife Platte auf, die entsprechend der vorerwähnten Ausführungsform auch durchsichtig sein kann. Diese Platte
kann der Körperform angepaßt sein, auf die das Kissen aufgelegt werden soll. Diese Ausführungsform der Erfindung hat den Vorteil, daß die Gefahr, daß sich beim Anlegen des Druckverbandes Falten in dem nicht ausgesparten Bereich der auf dem Körper aufliegenden Seite des Kissens bilden, wesentlich verringert ist.
Das erfindungsgemäße Kissen kann mit einer elastischen Binde mit oder ohne Zwischenschaltung der steifen Platte auf den Körper aufgedrückt werden, an den Extremitäten kann zu diesem Zweck auch ein elastischer Strumpf verwendet werden.
Bei einer Ausführungsform der Erfindung ist nur ein Ventil vorgesehen, das zum Erzeugen, zum Erhalten oder Kontrollieren des Druckes innerhalb des Kissens und/oder zum Einfüllen einer Flüssigkeit in das Innere des Kissens geeignet ist, sondern es sind zwei Anschlüsse vorgesehen so daß Luft und Flüssigkeit innerhalb des Kissens ausgetauscht werden können, ohne daß sich der Druck im Kissen wesentlich ändert Eine im Kissen befindliche Flüssigkeit kann durch Einleiten von Luft in den einen Anschluß zum anderen Anschluß hinausgedrückt werden und umgekehrt im Kissen befindliche Luft durch den einen Anschluß aus dem Kissen verdrängt werden. Die beiden Anschlüsse können auch dazu verwendet werden, um die im Kissen befindliche, unter Druck stehende Flüssigkeit oder unter Druck stehende Luft ständig zu erneuern oder durch ein Gerät zirkulieren zu lassen, das dieses Medium behandelt, beispielsweise der Luft Feuchtigkeit entzieht, so daß sich in dem Kissen kein Schweiß oder Wundwasser ansammelt. Selbstverständlich kann durch einen der Anschlüsse auch Flüssigkeit abgesaugt werden.
Bei einer anderen Ausführungsform der Erfindung kann in dem Kissen auch eine Masse eingelagert sein, die Feuchtigkeit bindet und daher die im Kissen befindliche Luft trocknet. Eine die Luft, trockende Substanz kann auch durch eine semipermeable Wand, z.B. aus einem geeigneten Kunststoff von dem Hohlraum des Kissens abgetrennt sein, wobei diese Wand die Feuchtigkeit nur in Richtung zu der trocknenden Substanz hindurchläßt.
In der Zeichnung sind Ausführungsformen der Erfindung dargestellt.
Fig. 1 zeigt eine Ansicht auf diejenige Seite einer
Ausführungsform des erfindungsgemäßsen Kissens, die zur Auflage auf der zu behandelnden Körperpartie bestimmt ist,
Fig. 2 zeigt einen Schnitt nach der Linie II-II durch die Ausführungsform nach Fig. 1,
Fig. 3 zeigt eine andere Ausführungsform der Erfindung in Seitenansicht ,
Fig. 4 zeigt eine dritte Ausführungsform in einem der Fig. 2 entsprechenden Schnitt.
Bei der in Fig. 1 und 2 dargestellten Ausführungsform der Erfindung weist das Kissen zwei Folienzuschnitte 1 und 2 aus Latex oder einem geeigneten elastischen Kunststoff auf, die an ihren Rändern durch eine Naht 3 luftdicht miteinander verbunden sind. An derjenigen Seite des
Kissens, die heim Anlegen des Druckverbandes auf die zu behandelnde Körperoherfläche aufgelegt wird, weist die Folie 2 eine Aussparung 4 auf. In der Nähe des Randes des Kissens ist in die Folie 1 ein Ventil 5 eingeschweißt. Die Aussparung 4 ist größer als das Hauttransplantat, so daß der Rand 6 bei dieser Ausführungsform der Erfindung vollständig außerhalb der Naht auf den Körper aufgeklebt wird, mit der das Hauttransplantat an der gesunden Haut befestigt wird. Das Ventil 5 ist so ausgebildet, daß an dieses bekannte Einrichtungen zum Erzeugen, Aufrechterhalten und Kontrollieren eines bestimmten Druckes innerhalb des Kissens angeschlossen werden können. Die Folie 1 ist durchsichtig, so daß durch diese Folie und durch die Aussparung 4 hindurch das Hauttransplantat beobachtet werden kann, ohne daß der Druckverband gelöst wird. Voraussetzung hierzu ist, daß in dem über dem Kissen angeordneten Teil des Verbandes ebenfalls ein Fenster vorgesehen wird, das diese Beobachtung zuläßt oder daß dieser Teil ebenfalls durchsichtig ist.
Die in Fig. 3 dargestellte Ausführungsform der Erfindung unterscheidet sich von der in den Fig. 1 und 2 dargestellten Ausführungsform dadurch, daß auf die Folie 1 eine steife Platte 7 aufgeschweißt oder aufgeklebt oder auf andere Weise in ihrer Lage fixiert ist, die die Form der Oberfläche der zu behandelnden Körperpartie 8 aufweist. Diese Kunststoffplatte kann ebenfalls durchsichtig sein, um durch sie hindurch
das Hauttransplantat beobachten zu können. Ihre Steifigkeit und ihre Größe ist so gewählt, daß sie den von dem Druckverband ausgeübten Druck gleichmäßig über die Oberfläche des Kissens verteilt und dadurch eine Faltenbildung in dem von der Folie 2 eingenommenen Bereich der Unterseite des Kissens verhindert.
Das Ventil 5 kann so ausgebildet sein, daß es auch zum Einführen eines Behandlungsmediums, gegebenenfalls unter Aufrechterhaltung des eingestellten Druckes im Kissen, geeignet ist. Auch kann für diesen Zweck ein zusätzliches Ventil am Kissen vorgesehen sein.
Fig. 4 zeigt eine Ausführungsform, die zwei Zuleitungen 9 und 10 aufweist, die in das. Innere des Kissens münden. An diese Zuleitung können Geräte beliebiger Art angeschlossen werden, die das in dem Innern des Kissens befindliche Medium ohne Druckabfall austauschen, reinigen oder auf einem einstellbaren Druck halten. Zur Demonstration sind in Fig. 4 sehr einfache Absperrorgane 11 für diese Zuleitungen eingezeichnet, die bei der praktischen Ausführung der Erfindung seitlich durch geeignetere Geräte ersetzt sind.
Die Aussparung 4 kann abweichend von dem in Verbindung mit Fig. 1 beschriebenen Ausführungsbeispiel so groß sein, daß ihr Band 6 teils auf der gesunden Haut, teils auf dem Transplantat, oder aber ganz auf dem Transplantat aufliegt.
Das Kissen kann mit einer Binde oder einem elastischen Strumpf auf das Transplantat aufgedrückt sein. Auch kann eine der beiden Folien 1 oder 2, insbesondere die untere Folie 2, wesentlich größer als die andere Folie und über die Naht 3 hinaus verlängert sein und zum Befestigen des Kissens dienen.
Claims
1. Kissen zum Andrücken von Hauttransplantaten, dadurch gekennzeichnet, daß das Kissen an seiner dem Körper zugewandten Seite eine Aussparung (4) aufweist, die zumindest nahezu so groß ist wie das Transplantat.
2. Kissen nach Anspruch 1, dadurch gekennzeichnet, daß die Gestalt der Aussparung (4) so gewählt ist, daß ihr Hand (6) auf den Rand des Transplantates zu liegen kommt.
3. Kissen nach Anspruch 1, dadurch gekennzeichnet, daß die Aussparung (4) größer als das Transplantat gewählt ist und ihre Form so gewählt ist, daß der Rand (6) der Aussparung (4) zumindest teilweise auf der gesunden Haut aufliegt.
4. Kissen nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet, daß das Kissen zumindest auf der der Aussparung (4) gegenüberliegenden Seite aus einem durchsichtigen Werkstoff besteht.
5. Kissen nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet, daß das Kissen ein Ventil (5) aufweist, das zum Anschluß einer Einrichtung zum Erzeugen, Aufrechterhalten und/oder Kontrollieren des Druckes innerhalb des Kissens geeignet ist.
6. Kissen nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet, daß das Kissen ein Ventil aufweist, das zum Einführen eines Behandlungsmediums in den Raum innerhalb des Kissens geeignet ist.
7. Kissen nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet, daß der Rand (6) der Aussparung (4) mit einem Klebstoff zum Befestigen des Kissens auf der Haut versehen ist.
8. Kissen nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet, daß das Kissen auf der dem Körper abgewandten Seite eine steife Platte (7) aufweist.
9. Kissen nach Anspruch 8, dadurch gekennzeichnet, daß die Platte (7) der Form der Körperpartie (8) angepaßt ist, zu deren Bedeckung das Kissen bestimmt ist.
10. Kissen nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet, daß in das Kissen eine die Feuchtigkeit bindende Substanz eingelagert ist.
11. Kissen nach Anspruch 10, dadurch, gekennzeichnet, daß die die Feuchtigkeit bindende Substanz durch eine semipermeable Wand von dem Hohlraum des Kissens getrennt ist, der mit dem Transplantat in Verbindung steht.
12. Kissen nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet, daß das Kissen zwei Anschlußstutzen aufweist.
13. Kissen nach Anspruch 12, dadurch gekennzeichnet, daß die Anschlußstutzen ein Absperrorgan (11) aufweisen.
14. Druckverband mit einem Kissen nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet, daß die Ränder der Aussparung flüssigkeits- und/oder luftdicht mit der Körperhaut und/oder dem Transplantat verbunden sind.
15. Druckverband nach Anspruch 14, dadurch gekennzeichnet, daß die Ränder der Aussparung (4) auf der benachbarten Haut aufgeklebt sind.
16. Druckverband nach Anspruch 14 oder 15, dadurch gekennzeichnet, daß die Ränder der Aussparung (4) auf der benachbarten Haut aufgenäht sind.
17. Druckverband nach Anspruch 16, dadurch gekennzeichnet, daß die Stichstellen der Naht abgedichtet sind.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT80101233T ATE14835T1 (de) | 1980-03-11 | 1980-03-11 | Hauttransplantations-druckverband. |
PCT/DE1980/000025 WO1981002516A1 (en) | 1980-03-11 | 1980-03-11 | Cushion for holding an element of grafted skin |
US06/321,169 US4480638A (en) | 1980-03-11 | 1980-03-11 | Cushion for holding an element of grafted skin |
EP80101233A EP0035583B1 (de) | 1980-03-11 | 1980-03-11 | Hauttransplantations-Druckverband |
AU67314/81A AU6731481A (en) | 1980-03-11 | 1980-03-14 | Skin transplant bolster pressure dressing |
AU67313/81A AU6731381A (en) | 1980-03-11 | 1980-03-14 | Pressure bolster for skin grafts |
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
WODE80/00025 | 1980-03-11 | ||
PCT/DE1980/000025 WO1981002516A1 (en) | 1980-03-11 | 1980-03-11 | Cushion for holding an element of grafted skin |
US06/321,169 US4480638A (en) | 1980-03-11 | 1980-03-11 | Cushion for holding an element of grafted skin |
EP80101233A EP0035583B1 (de) | 1980-03-11 | 1980-03-11 | Hauttransplantations-Druckverband |
AUPE275780 | 1980-03-14 | ||
AU67314/81A AU6731481A (en) | 1980-03-11 | 1980-03-14 | Skin transplant bolster pressure dressing |
AU67313/81A AU6731381A (en) | 1980-03-11 | 1980-03-14 | Pressure bolster for skin grafts |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1981002516A1 true WO1981002516A1 (en) | 1981-09-17 |
Family
ID=27542814
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/DE1980/000025 WO1981002516A1 (en) | 1980-03-11 | 1980-03-11 | Cushion for holding an element of grafted skin |
Country Status (5)
Country | Link |
---|---|
US (1) | US4480638A (de) |
EP (1) | EP0035583B1 (de) |
AT (1) | ATE14835T1 (de) |
AU (1) | AU6731481A (de) |
WO (1) | WO1981002516A1 (de) |
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- 1980-03-11 WO PCT/DE1980/000025 patent/WO1981002516A1/de unknown
- 1980-03-11 AT AT80101233T patent/ATE14835T1/de not_active IP Right Cessation
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Also Published As
Publication number | Publication date |
---|---|
EP0035583B1 (de) | 1985-08-14 |
US4480638A (en) | 1984-11-06 |
AU6731481A (en) | 1981-09-17 |
ATE14835T1 (de) | 1985-08-15 |
EP0035583A1 (de) | 1981-09-16 |
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