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WO1991007204A2 - Dispositif pour l'alimentation externe de sondes percutanees - Google Patents

Dispositif pour l'alimentation externe de sondes percutanees Download PDF

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Publication number
WO1991007204A2
WO1991007204A2 PCT/EP1990/001942 EP9001942W WO9107204A2 WO 1991007204 A2 WO1991007204 A2 WO 1991007204A2 EP 9001942 W EP9001942 W EP 9001942W WO 9107204 A2 WO9107204 A2 WO 9107204A2
Authority
WO
WIPO (PCT)
Prior art keywords
passage
ring
adapter
probes
groove
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP1990/001942
Other languages
German (de)
English (en)
Other versions
WO1991007204A3 (fr
Inventor
Ferdinand +Di Frimberger
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of WO1991007204A2 publication Critical patent/WO1991007204A2/fr
Publication of WO1991007204A3 publication Critical patent/WO1991007204A3/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • 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
    • A61M25/00—Catheters; Hollow probes
    • A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
    • A61M25/02—Holding devices, e.g. on the body
    • 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
    • A61M25/00—Catheters; Hollow probes
    • A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
    • A61M25/02—Holding devices, e.g. on the body
    • A61M2025/0246—Holding devices, e.g. on the body fixed on the skin having a cover for covering the holding means
    • 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
    • A61M25/00—Catheters; Hollow probes
    • A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
    • A61M25/02—Holding devices, e.g. on the body
    • A61M2025/0266—Holding devices, e.g. on the body using pads, patches, tapes or the like
    • A61M2025/0273—Holding devices, e.g. on the body using pads, patches, tapes or the like having slits to place the pad around a catheter puncturing site
    • 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
    • A61M25/00—Catheters; Hollow probes
    • A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
    • A61M25/02—Holding devices, e.g. on the body
    • A61M2025/028—Holding devices, e.g. on the body having a mainly rigid support structure

Definitions

  • the invention relates to a device for the external supply of percutaneous probes.
  • These are probes that are inserted into the human body from the outside, for example into hollow organs or organs with a duct system.
  • they are used to drain bile to the outside if the internal discharge is obstructed, for example, by a tumor.
  • they Placed in the stomach or intestines, they enable percutaneous nutrition for patients whose food intake is impaired for various reasons.
  • a fistula tract forms in the area of the probe passage, the inner surface of which is formed by wound tissue. This wound tissue permanently secretes wound secretion that escapes inwards and outwards along the fistula canal.
  • the percutaneous probes are usually supplied externally by: secured against slipping by a single skin seam and compresses are placed over the probe exit point to soak up the wound secretion and fastened with plaster.
  • the disadvantages of this known external supply are that the plaster has to be torn off and the compress has to be removed each time to inspect the probe exit point, and that a moist chamber is formed between the compress and the skin through wound secretions and body sweat, the microbes optimal
  • the wound care agent e.g. Wundsekret aufaugen.de Gauze
  • the perforation also allows the wound secretion to drain freely into the space enclosed by the retaining ring, in which it can be sucked up by the gauze.
  • medications can also be used as wound care agents, for example.
  • the perforation can comprise a passage for the probes, which preferably has a larger diameter than the probes and thereby also enables the passage of fluid, such as the discharge of wound secretions, and, if the diameter is sufficiently large, also enables inspection of the probe exit point.
  • the perforation can comprise at least one further passage that allows the fluid to pass through.
  • the perforation comprises the pores of a fluid-permeable porous material surrounding the passage.
  • the adhesive plaster is inside the retaining ring is transparent at least in places.
  • the diameter of the passage is substantially equal to the inside diameter of the mounting ring. In this way, wound care and inspection of the probe exit point can be carried out particularly easily.
  • the space enclosed by the mounting ring can preferably be covered by a cover.
  • This cover can be designed as a substantially rigid cover attached to the mounting ring, which serves as an additional retention means and protection for the gauze.
  • the lid can be lockable.
  • a hood is preferably provided as a cover or as an additional cover, the free edge of which can be detachably fastened below a circumferential projection on the mounting ring. This hood can be made watertight and thus allow the patient to shower and bathe.
  • the holder advantageously comprises a holding groove formed in the holding ring for receiving and fixing the probes and fitting pieces for the probes.
  • the adapters can be designed as couplings, such as Luer connections, for connecting the probes to further supply probes and / or as an adapter for fixing probes with smaller diameters than the holding groove.
  • the holding groove can be directed towards the passage or at a location remote from the passage.
  • An essentially straight course of the retaining groove is possible, for example essentially radially or essentially along or parallel to a secant on the retaining ring.
  • the fitting pieces are secured against rotation about their longitudinal axis and against longitudinal displacement by means of a positive reception in the holding groove.
  • Holding groove have a substantially semicircular cross section, two webs projecting on both sides into the holding groove are provided for engagement in slots in the fitting pieces.
  • the holding groove it is also possible for the holding groove to have an angular cross section corresponding to the fitting and, at each end, to have a projection securing the fitting against longitudinal displacement.
  • Adapters in the form of adapters advantageously have a channel which is provided for receiving the respective probe and which comprises a continuous, open groove at the top in the upper adapter surface facing away from the adhesive plaster or a through channel which is enclosed on all sides and runs inside the adapter. It is expedient if the adapter is divided into two adapter halves in the middle or off-center along the channel. Both adapter halves can be connected to one another by a hinge piece for easier handling.
  • a holding groove closure which extends across the holding groove is provided for fixing the probes or the fitting pieces.
  • the retaining groove closure is expedient to design the retaining groove closure as a force-locking closure, preferably as an elastic ring which can be fastened to two projections formed on the side of the retaining groove.
  • the probe is designed with a free end section which is bent essentially at right angles.
  • the end region thereof which projects into the space enclosed by the mounting ring when the adapter is fastened in the holding groove, can be bent downwards and directed towards the passage in the adhesive plaster.
  • Adapters with a groove open at the top are advantageously provided with a through hole instead of the downwardly bent end region, into which the groove opens and which runs essentially perpendicular to the same and is directed towards the passage in the adhesive plaster when the adapter is fastened in the holding groove.
  • the adhesive plaster connected to it via the mounting ring can be pushed onto the transcutaneously placed probe and guided along it until it adheres to the patient's skin. In this way it is ensured that the passage point of the probe through the skin is arranged within the passage in the adhesive plaster, for example in the center of this passage when the through hole is directed coaxially onto the same.
  • the mounting ring can preferably be placed on a mounting ring permanently attached to the adhesive plaster and detachably attached to it.
  • a conventional adhesive plaster such as is used, for example, for stoma care of patients with an artificial intestinal exit.
  • a placement device which can be inserted into the space enclosed by the mounting ring or mounting and mounting ring, which can be detachably attached to the mounting or mounting ring and has a continuous opening which is aligned with the passage in the adhesive plaster and its Diameter is smaller than that of the passage.
  • the adhesive plaster can be transcutaneously applied to the transcutaneously in the same way as with the adapter having the through hole the placed probe is pushed on and guided along it until it adheres to the patient's skin;
  • the placement device like the aforementioned adapter, ensures that the passage point of the probe through the skin is arranged inside the passage, preferably in the center thereof, and is also at a distance from the holding groove or the fitting, which is the one in the holder or mounting ring enclosed space corresponds to the available probe length; this is particularly important in the case of a passage in the adhesive plaster which has a diameter which substantially exceeds the probe diameter.
  • the use of the placement device is not necessary if the diameter of the passage is equal to the probe diameter or if the adapter with a through hole is used.
  • the placement device is preferably designed in the form of a plate. However, it can also have the shape of a mounting ring with a web projecting into the interior of the mounting ring, the through opening being formed in the web. According to a development of the invention, the opening has a smaller diameter than the diameter of the probes and can be expanded elastically.
  • the plate can be designed as a slotted plate with radial slots that run over part of the plate radius and open into the opening. With the help of these radial slots, the opening can easily be elastically widened. especially if the plate is made of elastic material.
  • the plate can be inserted into the 'surrounded by the mounting support mounting space in a simple manner and be removed therefrom, if one of the radial slots is elongated and opens freely at the periphery of the plate.
  • the plate and the mounting ring can be attached to the mounting ring by means of a locking arrangement.
  • the invention is illustrated below. two exemplary embodiments with reference to the drawing described in more detail. Show it
  • 1 is a radial section of the first embodiment of the device according to the invention before attachment to the skin of a patient
  • FIG. 1 is a radial section of that shown in Fig. 1
  • Fig. 3 is a radial section of the device shown in Fig. 2 with an inserted
  • FIG. 6 is the front view of the adapter according to FIG. 6,
  • FIG. 8 shows a radial section of the second exemplary embodiment of the device according to the invention before attachment to the skin of a patient
  • FIG. 9 shows a radial section of the device shown in FIG. 8 after attachment to the skin of the patient
  • Fig. 10 is a plan view of the holding ring with adapter shown in Figs. 8 and 9, and
  • Fig. 11 is a side view of the adapter of FIG. 10 in the opened state.
  • the device according to the invention according to the first exemplary embodiment comprises an essentially square adhesive plaster 1, a fastening ring 2 fastened to it, a holding ring 3, a placing device in the form of a slotted plate h and a cover 5.
  • the adhesive plaster 1 is a conventional adhesive plaster, as is known for the stoma care of patients with an artificial intestinal exit. It has a centrally arranged passage 6 for a probe 7 or 8 placed percutaneously in, for example, the gallbladder of a patient.
  • the first-mentioned probe 7 has a diameter of 8 mm, while the latter-mentioned probe 8 is shown as a representative of probes of smaller diameter.
  • the diameter of the passage 6 is larger than that of the probe 7 or 8, in order to allow the wound secretion secreted by the granulation tissue in the fistula passage in the region of the probe passage point to drain to the outside.
  • the abdominal wall of the patient is identified by reference number 9.
  • the fastening ring 2 is arranged at a distance coaxially to the passage 6 and provided in the region of its free upper edge with an outer circumferential bead 10 and on its inside with a circumferential inner bead 11, which is deeper than the outer bead 10 and forms a circumferential groove 12 at a distance is arranged by the adhesive plaster 1.
  • the fastening ring 2 consists of elastic plastic material.
  • Retaining ring 3 has an inclined section 13, on the upper edge of which is a circumferential, inwardly directed upper flange 14 and on the lower edge of which is a circumferential, also inwardly directed lower
  • Flange 15 connects.
  • the latter flange 15 forms together with the outer bead 10 on the fastening ring 2 has a latching arrangement for the detachable fastening of the mounting ring 3 on the fastening ring 2.
  • the holder ring 3 is with a holder in the form of a radially extending retaining groove 16 with a semicircular
  • Cross section for receiving adapters in the form of a
  • the Luer connector 17 is used here to fix the probe 8 on the mounting ring 3 and as a coupling for connecting this probe to a further feed probe, not shown, e.g. for the purpose of feeding.
  • the adapter 18 is provided for fixing the probe 7 on the mounting ring 3.
  • a web 19 is formed approximately in the longitudinal center thereof, which extends perpendicular to the longitudinal direction of the retaining groove 16 beyond the upper flange 14 and for engagement in corresponding slots 20 of the Luer connector 17 or the adapter 18 is provided. In this way, both adapters 17, 18 are positively fixed in the holding groove 16 and secured against rotation and longitudinal displacement.
  • Each web 19 is angled at its free upper end in the direction away from the holding groove 16 to form a projection 21.
  • a rubber ring 22 can be fastened in the holding groove 16 as a holding groove closure which extends across the holding groove 16 for the purpose of non-positively holding the probes 7, 8 or the Luer connector 17 or adapter 18 in place.
  • the slotted plate 4 is also made of an elastic plastic material and has a central through opening 23 into which four radial slots un open, each offset by 90 °, open radial slots. Three of these radial slots run over part of the slot plate radius and are designated by the reference number 24.
  • the fourth, designated by reference numeral 25 Radial slot is extended to the mouth at the periphery of the slot plate 4. The latter is intended to be accommodated in the space 26 enclosed by the fastening ring 2 and the holding ring 3 and here within the groove 12 in the fastening ring 2. Accordingly, the thickness and the outer diameter of the slotted plate 4 are substantially equal to the width of the groove 12 and the inner diameter of the fastening ring 2 in the region of the groove 12.
  • edge region 27 of the slotted plate 4 together with the groove 12 represents a latching arrangement for the detachable fastening of the slotted plate 4 on the fastening ring 2.
  • the slot plate 4, c When arranged within the groove 12, the slot plate 4, c is aligned with its opening 23 to the passage 6 in the adhesive plaster 1.
  • the diameter of the opening 23 corresponds essentially to the diameter of the smaller probe 8 and can be expanded elastically due to the radial slots 24, 25 and the elastic configuration of the slotted plate 4 to accommodate the larger probe 7.
  • the adapter 18 is of substantially cylindrical shape which fits into the holding groove 16 and projects into the space 26 and is provided with two slots 20 which correspond to the slots 20 of the
  • Luer connection 17 corresponds to 25 Luer connection 17 . It consists of two adapter halves 28, 29, has a through channel 30 for receiving the respective probe 8 and is divided along and off-center of this through channel 30.
  • the through channel 30 is in its end region 31, which continues
  • Bracket ring 3 is for receiving a
  • the cover 5 is provided, which is detachably fastened to the holding ring 3 by means of a latching arrangement.
  • This locking arrangement consists of a peripheral groove 35 formed in the edge of the cover 5 and the free end of the upper flange 14 which engages in it
  • the slit plate 4 is inserted into the groove 12 of the fastening ring 2 and held in this between the adhesive plaster 1 and the inner bead 11.
  • the opening 23 in the slotted plate 4 and the passage 6 in the adhesive plaster 1 are arranged coaxially with one another, so that the percutaneously placed probe 7, 8 guided by the opening 23 without play when the adhesive plaster 1 is subsequently pushed on, passes through the passage 6 centrally and in particular in the case of a pre-curved probe 7 with an essentially right-angled curvature 37, the distance from the Luer connection 17 corresponding to the length of the bent probe end section 38 is arranged in the holding groove 16.
  • the design of the slotted plate 4 as an elastic plate enables the opening 23 to be elastically widened when the probe 7, 8 is pushed through, so that the latter is received by the first without play.
  • the adhesive plaster 1 is then pushed further over the probe 7, 8 until it touches the abdominal wall 9 of the patient, in order then to be attached to it.
  • the mounting ring 3 is on the latter snapped, as shown in Figs. 2 and 3.
  • the probe 7, 8 is attached to the mounting ring 3.
  • the free end of the probe 7, 8 is pushed onto the socket 36 of a Luer connector 17, which is then inserted into the holding groove 16.
  • the webs 19 in the retaining groove 16 engage in the slots 20 of the Luer connector 17 and in this way prevent its longitudinal displacement and rotation within the retaining groove 16.
  • the rubber ring 22
  • a probe 8 of smaller diameter can also be pushed through the passage 30 of an adapter 18.
  • Wound care material such as the gauze 34 shown in FIG. 3, is now introduced into the space 26 enclosed by the fastening ring 2 and the holding ring 3 and this space 26 is closed by a cover 5 which is snapped onto the holding ring 3.
  • the device according to the invention according to the second embodiment differs from that according to the first embodiment by using an adapter 39 instead of the placing device 4 and the adapter 18 and g ⁇ by permanent attachment of the correspondingly adapted
  • the adapter 39 corresponds essentially to the adapter 18, but has g5 instead of the through channel 30 in the
  • the adapter 39 has a length such that when it is fastened in the holding groove 6, the through hole 41 coaxially to the passage 6 in
  • Adhesive patch 1 is directed. Another difference is that the adapter 39 is divided centrally along the groove 40 and thus the through hole 41 into the two adapter halves 28, 29 ', and that these adapter halves are connected to one another at their free ends adjacent to the through hole 41 via a hinge piece 42 .
  • the adapter 39 is the same as that
  • the adhesive plaster 1 is then pushed along the probe 8, which is held taut by a slight pull and previously passed through the through-bore 41, up to the abdominal wall 9 of the patient, in order then to be adhered to the latter. Subsequently, the probe 8 is pressed into the groove 40 formed in the adapter 39 and held there in a force-fitting manner due to the corresponding dimensions.
  • the rubber ring 22 is used to secure the adapter 39 and thus the probe 8 in the retaining groove 6.
  • the probe 8 is to be fixed in such a way that an inner retaining disc (not shown) on the side of the abdominal wall is arranged at a short distance from the abdominal wall to avoid pressure neuroses and is at best very loosely adapted to the mucous membrane.
  • an inner retaining disc (not shown) on the side of the abdominal wall is arranged at a short distance from the abdominal wall to avoid pressure neuroses and is at best very loosely adapted to the mucous membrane.
  • Wound care material such as gauze 34 or an elongated strip of a compress, is introduced in a ring shape when the skin channel is wet, into the space 26 enclosed by the holding ring 3, which can then be closed by a cover 5 which is locked onto the holding ring 3.
  • the adapter 39 is first opened via its hinge piece 42 before being inserted into the holding groove 6, whereupon the percutaneously placed probe 8 is inserted into the through bore 41, the adapter 39 closed and inserted into the retaining groove 6. Then, in the manner already described, the adhesive plaster 1 is moved along the probe 8 to the abdominal wall 9 of the patient and adhered to it, the probe 8 is pushed into the groove 40 and the adapter 39 is secured by means of the rubber ring 22.
  • the latter two steps are carried out in the reverse manner, whereupon the adapter 39 is removed from the holding groove 6 and opened via its hinge piece 42. After removing the probe 8 from the through hole 41, the adhesive plaster 1 can be removed from the
  • Abdominal wall 9 can be removed.
  • Adhesive plasters freely accessible probe exit point can be inspected at any time.
  • the cover 5 is removed and the gauze 34 is removed from the space 26 enclosed by the holding ring 2, 3 in order to be reintroduced into the space 26 after the inspection, whereupon the cover 5 is placed on the
  • Bracket ring 3 is snapped on. If the gauze 34 with Wound secretion is soaked, it is replaced by fresh gauze material. The free access of the probe exit point ensures that the wound secretion can run out undisturbed to be sucked up by the gauze 34.
  • control of the probe passage point can be carried out at any time without tearing off the adhesive plaster, simple change of the wound care material, showering when using a suitable cover, etc.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biophysics (AREA)
  • Pulmonology (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Media Introduction/Drainage Providing Device (AREA)

Abstract

Pour assurer un positionnement simple et fiable de la sonde ainsi qu'une alimentation simple et fiable en fluide pour faire la toilette de la plaie, un pansement adhésif (1) qui est connu en soi possède une perforation (6) permettant l'insertion des sondes (7, 8) et le passage de fluide, par exemple pour l'évacuation des sécrétions de la plaie, une bague de support (3) entourant la perforation (6) comporte un dispositif de support (16) pour les sondes (7, 8) et un espace (26) entouré par la bague de support (3) et destiné à recevoir un fluide pour la toilette de la plaie (34).
PCT/EP1990/001942 1989-11-14 1990-11-14 Dispositif pour l'alimentation externe de sondes percutanees Ceased WO1991007204A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEP3937849.7 1989-11-14
DE19893937849 DE3937849A1 (de) 1989-11-14 1989-11-14 Vorrichtung zur aussenversorung von perkutanen sonden

Publications (2)

Publication Number Publication Date
WO1991007204A2 true WO1991007204A2 (fr) 1991-05-30
WO1991007204A3 WO1991007204A3 (fr) 1991-12-12

Family

ID=6393497

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1990/001942 Ceased WO1991007204A2 (fr) 1989-11-14 1990-11-14 Dispositif pour l'alimentation externe de sondes percutanees

Country Status (2)

Country Link
DE (1) DE3937849A1 (fr)
WO (1) WO1991007204A2 (fr)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2288538A (en) * 1994-04-19 1995-10-25 Alan David Mogg Catheter retainer
WO1995033508A1 (fr) * 1994-06-02 1995-12-14 Nikomed Aps Dispositif pour la fixation d'un drain et systeme de drain
WO1997021459A1 (fr) * 1995-12-13 1997-06-19 Nikomed Aps Dispositif pour fixer un drain
US5690616A (en) * 1996-01-16 1997-11-25 Mogg; Alan David Catheter clamp
FR2787336A1 (fr) * 1998-12-22 2000-06-23 Francis Navarro Dispositif de maintien d'au moins un drain ou analogue
US6273873B1 (en) 1996-10-04 2001-08-14 Maersk Medical A/S Fixation device for fixating a catheter relative to a skin surface part of a person
WO2006085085A1 (fr) 2005-02-11 2006-08-17 Unomedical Limited Dispositif de fixation d'un tube par rapport a la peau d'un patient et assemblage du tube et du dispositif

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5807341A (en) * 1996-12-11 1998-09-15 Team Medical Llc Medical catheter dressing device
DE10310631A1 (de) * 2003-03-10 2004-09-23 Nagy, Gabor M. Medizinisches Wundpflaster

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Publication number Priority date Publication date Assignee Title
US3699956A (en) * 1970-10-01 1972-10-24 Tecna Corp Percutaneous lead device
US3765420A (en) * 1971-12-16 1973-10-16 Kendall & Co Eccentric locking device for surgical drainage members
US4397641A (en) * 1981-04-03 1983-08-09 Jacobs Daimon C Catheter support device
JPS5897364A (ja) * 1981-11-27 1983-06-09 バクスター、インターナショナル、インコーポレイテッド 皮膚部位の無菌隔離
US4516968A (en) * 1982-09-28 1985-05-14 Marshall Charles A Catheter shield and method of use
US4533349A (en) * 1982-11-08 1985-08-06 Medical Engineering Corporation Skin mounted drainage catheter retention disc
US4659329A (en) * 1984-07-27 1987-04-21 The Kendall Company Liquid drainage system
GB2162752B (en) * 1984-08-10 1988-03-30 Med Polimerov Vnii A device for lengthy fixation of a tube introduced into the patient's body
US4717385A (en) * 1985-04-12 1988-01-05 The Beth Israel Hospital Association Surgical tube anchoring device and method for using same
US4699616A (en) * 1986-06-13 1987-10-13 Hollister Incorporated Catheter retention device and method
EP0266091A3 (fr) * 1986-10-20 1988-07-13 City Of Hope National Medical Center Dispositif de fixation d'un cathéter transdermique à longueur réglable pour drainage

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2288538A (en) * 1994-04-19 1995-10-25 Alan David Mogg Catheter retainer
WO1995033508A1 (fr) * 1994-06-02 1995-12-14 Nikomed Aps Dispositif pour la fixation d'un drain et systeme de drain
US5685859A (en) * 1994-06-02 1997-11-11 Nikomed Aps Device for fixating a drainage tube and a drainage tube assembly
EP1029555A3 (fr) * 1994-06-02 2000-09-06 Maersk Medical A/S Dispositif de fixation d'un drain
EP1719537A3 (fr) * 1994-06-02 2006-11-29 Unomedical A/S Dispositif de fixation d'un drain
WO1997021459A1 (fr) * 1995-12-13 1997-06-19 Nikomed Aps Dispositif pour fixer un drain
US5690616A (en) * 1996-01-16 1997-11-25 Mogg; Alan David Catheter clamp
US6273873B1 (en) 1996-10-04 2001-08-14 Maersk Medical A/S Fixation device for fixating a catheter relative to a skin surface part of a person
FR2787336A1 (fr) * 1998-12-22 2000-06-23 Francis Navarro Dispositif de maintien d'au moins un drain ou analogue
WO2000037136A1 (fr) * 1998-12-22 2000-06-29 Francis Navarro Dispositif de maintien d'au moins un drain
US6682506B1 (en) 1998-12-22 2004-01-27 Francis Navarro Device for maintaining at least a tube
WO2006085085A1 (fr) 2005-02-11 2006-08-17 Unomedical Limited Dispositif de fixation d'un tube par rapport a la peau d'un patient et assemblage du tube et du dispositif

Also Published As

Publication number Publication date
WO1991007204A3 (fr) 1991-12-12
DE3937849A1 (de) 1991-05-16

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