GB2162752A

GB2162752A - A device for lengthy fixation of a tube introduced into the patient's body

Info

Publication number: GB2162752A
Application number: GB08420428A
Authority: GB
Inventors: Nikolai Mikhailovich Shiskov; Vladimir Evgenievic Zelenetsky; Nadezhda Alexeevna Demina; Ivan Mikhailovich Bondarev; Alexandr Nikolaevich Cherny; Alisa Arnoldovna Ertli; Semen Ivanovich Marina; Anatoly Grigorievich Avxentiev; Stanislav Nikolaev Lepetchenko; Ivan Petrovich Serzhantu
Original assignee: BELGOROD DNESTROVSKY Z MED IZD; MED POLIMEROV VNII; MO NII TUBERKULEZA
Current assignee: BELGOROD DNESTROVSKY Z MED IZD; MED POLIMEROV VNII; MO NII TUBERKULEZA
Priority date: 1984-08-10
Filing date: 1984-08-10
Publication date: 1986-02-12
Also published as: GB2162752B; GB8420428D0

Abstract

A device for fixation of a tube (1) in the patient's body (3) comprises a housing (4) provided with a flexible annular base, a means (5) for securing the tube (I) in the housing (4), comprising a bushing (10) which is stationary mounted coaxially with respect to the base of the housing (4) by ribs (II) extruding therebetween, the ribs being spaced from the patient's body (3); and a cover (13). <IMAGE>

Description

SPECIFICATION A device for lengthy fixation of a tube introduced into the patient's body The present invention relates to medical instruments, and more specifically to devices for lengthy fixation of a tube introduced into the patient's body.

The present invention can find application in the course of an extended treatment carried out by way of administering medicinal preparations to a patient through a tube introduced into his body for a period of not less than two months. The invention may be successfully used when treating, for instance, cavernous forms of tuberculosis.

Known in the art is a device for fixing a tube such as a drain tube, introduced into the patient's body, comprising a housing whose extending portion is made as a cap accommodating a pneumatic annular chamber which contacts and rests upon the patient's body in the intermediate area between the support surface and the tube. The cap and the annular chamber are provided with an opening into which the drain tube is introduced and is clamped therein while some medium, for instance, air under an excessive pressure is filling up the annular chamber. The support portion of the housing is essentially an annular cavity which is depressurized (is under vacuum) to provide for drawing-in of a portion of the skin integument over a circumference.The cap is secured to the patient's body by means of a sticky surface provided on the support portion of the housing, as well as by means of elastic belts.

However, this device has a number of disadvantages. The support portions of the housing, employed in the device, may cause trauma of the skin integument due to its pressing- in or drawing-in by the support surface, which also results in skin irritation and formation of bedsores particularly during an extended application of the device.

Excretions in the form of sweat drops accumulating on the surface of contact of the support portion of the pneumatic annular chamber made of resin and the patient's body may also cause irritation of the skin integument.

Presence of the pneumatic annular chamber does not allow for a sanitary and hygienic treatment of the skin integument portion at the point of the drain tube introduction without removing the device, which is necessary when the tube is kept in the patient's body for a length time period.

The-pneumatic rubber chambers employed in the device complicate the design and the process of manufacture of the product.

Also known in the art is a device for fixing a tube, for example, a drain tube, a catheter, a trocar, etc. in the patient's body, comprising a housing secured to the patient's body and provided with a flexible annular base made as an elastic disk having a central opening.

The housing has an extending portion shaped as a tube which has a branch for inflation. The rubber parts of the housing are interconnected by a permanent joint.

Hermetically mounted inside the tube which is the extending portion of the housing is a resilient bushing the thickness of whose wall is much smaller than that of the wall of the outer tube. The central portion of the bushing is mounted freely, i.e. with some gap in the tube, thereby providing for an annular cavity communicated with the inflating branch. In the course of inflation the central portion of the bushing forms two projections that are disposed opposite each other, clamp and fix the surgical instrument placed into the central opening of the disk. The device is secured to the patient's body with the aid of an adhesive substance.

The known device has the following disadvantages: -during the use of the device there is possible an accidental displacement of the tube while the patient is asleep or as a result of his movement, which may cause paid caused by traumatizing of walls of the cavity by the displaced tube; -strong irritation and damage of the skin integument, which, in its turn, causes strong pain, may take place during an extended contact (for 2-3 months) between the support portion of the housing and the skin integument; -the design of the support portion of the housing does not allow for a sanitary and hygienic treatment of the skin integument at the point of introduction of the tube without removing the device, which is necessary when the tube is kept in the patient's body for a length time period.

Besides, connection of the structure separate parts made of rubber into an integral part is a labour-consuming process.

According to the present invention there is provided a device for securing a tube introduced into a patient's body, comprising a housing to be secured to the patient's body and including a flexible annular base and means for holding the tube, said means including a bushing supported coaxially with respect to the base by ribs extending therebetween, said ribs being arranged to be spaced from the patient's body to enable sanitary and hygienic treatment of the skin integument portion around the tube, and a cover for enclosing a cavity with the base and the patient's body.

A device embodying the invention allows trauma to the walls of the cavity into which the tube is introduced to be avoided. At the same time it permits convenient sanitary and hygienic treatment of the skin integument at the point of introduction of the tube without having to remove the whole device. The device may be suitable for treatment of out-patients, and is not complicated to manufacture.

It is expedient to provide the device with tabs to facilitate removal of the cover, one tab being disposed on the cover and another tab being disposed on the flexible annular base such that, with the cavity closed by the cover, the tabs are displaced in the circumferential direction with respect to each other by a distance providing for a convenient removal of the cover.

It is also expedient to make the cover with a spherical portion having at least one ventilation port made therein.

To secure the whole device to the patient's body, the flexible annular base may have projections with openings made in each of them. Alternatively a securing mernber may be used, the member being an elastic ring mounted on the flexible annular base co-axially between the latter and the cover, and having at least two radial tabs extending outwardly beyond the ring and the flexible annular base.

It is expedient for the free ends of the tabs of the base and cover, and/or the securing member, to be rounded.

It is also expedient to mount inside the bushing an insert of elastic material for holding the tube introduced into the patient's body.

Use of the device of the present invention makes it possible to eliminate pain during an extended treatment of the patient.

Other features and advantages of the present invention will be more readily understood from the following description of its exemplary embodiments and the accompanying drawings, in which: Figure 1 is a sectional view of a device for lengthy fixation of a tube introduced into the patient's body, according to the invention; Figure 2 shows the same device with the removed cover, a view taken along arrow A; Figure 3 shows the same device closed with the cover, a view taken along arrow A; Figure 4 shows the same device with the removed cover and a member used for securing it to the patient's body, according to the invention; Figure 5 shows the same device closed with the cover, a section taken along line V-V in Figure 4.

A device for lengthy fixation of a tube I (Figure I) introduced into a cavity 2 of a patient's body 3, comprises a housing 4 secured to the patient's body 3, and a means 5 for securing the tube I in the housing 4 (Figures 1, 2), with all the parts and units of the device made of a polymeric material.

The housing 4 has a flexible annular base 6 (Figure 2) provided with projections 7 which are made therein and of which each has an opening 8 for securing the whole device to the patient's body 3 by way, for instance,#of placing a silk ligation onto the skin.

The surface of the base 6 is also provided with projections 9 made therein (Figures 1, 2).

In accordance with the invention, the means 5 for securing the tube I in the housing 4 comprises a bushing 10 (Figure I) stationary mounted coaxially with respect to the base 6, and ribs II (Figure 2) which connect the bushing 10 with the base 6 and which mount the bushing 10. Ribs II may be of any number, and the invention embodiment under description shows three ribs II which are arranged in one and the same plane at an angle of 1200 with respect to one another. The ribs II are somewhat lifted over the base 6, and, consequently, over the surface of the body 3, thereby simultaneously lifting the bushing 10 too.

The ratio between the height of each rib II and its length is selected to be within the range of 1:47, which makes the ribs resilient, particularly in the case when they are made of a polymeric material.

The ribs II are raised above the base 6 in such a manner that a cavity 12 is formed between the latter and the patient's body 3 around the tube 1. The cavity 12 is closed with a cover 13 (Figures I and 3) having a spherical portion which is provided with severaiven#ilation ports 14 (Figure 3) made therein. The cover 13 has an end face having openings 15 made therein, the number of the openings 15 corresponding to the number of the projections 9 (Figures 1, 2), and the latter entering the openings 15 when the cavity 12 is closed with the cover 13 in the manner shown in Figure I.

The device is also provided with a means for removing the cover T3, which is made as tabs 16 and 17 (Figures 2, 3).

The tab 16 is disposed on the flexible base 6, and the tab 17 is disposed on the cover 13, whereby, with the cavity 12 closed with the cover 13, the tabs 16 and 17 will necessarily be displaced with respect to each other in such a manner that there will be some distance "1" between their axes, said distance making it possible for the servicing personnel, by having conveniently gripped# the tab 17 disposed on the cover 13 and by holding the other tab 16 (by pressing it against the patient's body), to remove the cover 13 without damaging the fixation of the introduced tube or causing unpleasant feelings on the part of the patient. To decrease traumatizing, the free ends of the tabs 16 and 17 are made rounded.

To make it easier to secure the whole device to the patient's body, it is possible to do this without any operation, for which purpose theAdevice is provided with a member for securing it to the patient's body. The member is made as an elastic plate ring 18 (Figure 4) which is mounted on the base 6 coaxially thereto so that the ring 18 is positioned between the base 6 and the cover 13 (Figure 5).

The ring 18 has at least two radial tabs 19 (Figure 4) made therein and extending outside the ring 18, the free ends of the tabs 19 being rounded.

Mounted inside the bushing 10 (Figures 1, 5) is another bushing 20 which is made of an elastic material and holds the tube I after it has been introduced into the cavity 2 of the patient's body 3, the tube I being rigidly secured in the bushing 20.

In order to place and fix the tube I in the patient's body 3, it is necessary to perform the following.

The bushing 20 and the tissue of the patient's body are punched at a required spot with a stiletto (not shown in the drawing) having the tube I tightly adhering thereto. The device is moved' along the tube I until the base 6 contacts the skin of the patient, whereupon the base 6 is secured to the patient's body by way, for example, of placing through the openings 8 in the projections 7 a silk ligation onto the skin. With the base 6 secured, the stiletto is removed and the tube I remains in the body 3 of the patient.

To prevent the tube I from accidental displaced ment when the patient is asleep or during his movement, the cover 13 is positioned on the base 6 in such a manner that the projections 9 of the base 6 are closely aligned with the respective openings 15 in the cover 13. Thereby, the cavity 12 confined by the patient's body 3 portion and the base around the tube I will be closed. However, owing to the ventilation ports 14 the cavity 12 is communicated with atmosphere, which makes it possible to eliminate almost completely any maceration of the skin integument on this portion of the body.

Elimination of possible displacements of the tube is achieved due to the resilience of the ribs II and the resilience of the device as a whole, as it is made of polymeric materials.

To eliminate the possibility of appearance of pneumothorax and to determine the position of the tube I, the latter has a mandrin 21 (Figure I) made of a roentgen-contrast material, introduced therein.

The device may also be secured to the patient's body by means of the ring 18 mounted on the base 6. The tabs 19 of the ring 18 are secured to the patient's body by means of an adhesive band 22 (Figure 4), whereby, after some time, the ring 18 may be turned through some angle with respect to the base 6, and the tabs 19 may be moved to another portion of the body 3.

To remove the cover 13, it is sufficient to press the tab 16 against the body 3 and pull the tab 17 which is either secured to or made integral with the cover 13, whereupon the projections 8 will leave one after the other the openings 15, and the cover 13 will be removed to make an access to the tube I. During all this the patient feels no pain, and it is possible to treat easily and quickly the portion of the skin integument around the tube I.

Thus, the device under description makes it possible to eliminate the possibility of accidental displacements of the tube introduced into the patient's body for a lengthy time period, thereby doing away with pain caused by traumatizing walls of the cavity by the displaced tube.

The device provides for a convenient access to the tube, prevents maceration of the skin integument in the zone of the device fixation and allows for a sanitary and hygienic treatment of the wound formed during ari extended stay of the tube in the cavity.

The device is simple to manufacture, for example, by the method of injection moulding.

Claims

1. A device for securing a tube introduced into a patient's body, comprising a housing to be secured to the patient's body and including a flexible annular base and means for holding the tube, said means including a bushing supported coaxially with respect to the base by ribs extending therebetween, said ribs being arranged to be spaced from the patient's body to enable sanitary and hygienic treatment of the skin integument portion around the tube, and a cover for enclosing a cavity with the base and the patient's body.

2. A device according to claim 1, wherein tabs are provided to facilitate removal of the cover, a first tab being disposed on the cover and a second tab being disposed on the base such that said tabs are displaced circumferentially with respect to each other when the cover is attached to close the cavity.

3. A device according to claim 2, wherein the free ends of the tabs are rounded.

4. A device according to claim 1, 2 or 3, wherein the cover comprises a substantially hemispherical portion having at least one ventilation port therein.

5. A device according to any one of claims 1-4, wherein the flexible annular base is provided with openings for securing the housing to the patient's body.

6. A device according to any one of claims 1-4, wherein a securing member is provided for securing the housing to the patient's body, the member comprising a ring mounted coaxially on the annular base and having at least two radially outwardly extending tabs projecting beyond the outer periphery of the base.

7. A device according to claim 6, wherein the free ends of the tabs are rounded.

8. A device according to any one of claims 1-7, wherein an insert of elastic material is located in the bushing for holding the tube therein.

9. A device for securing a tube introduced into a patient's body, substantially as herein described with reference to the accompanying drawings.

Amendments to the claims have been filed, and have the following effect: (a) Claims 1 and 7 above have been deleted or textually amended.

(b) New or textually amended claims have been filed as follows: (c) Claims 8 and 9 above have been re-numbered as 7 and 8 and their appendancies corrected.

1. A device for securing a tube introduced into a patient's body, comprising a housing to be secured to the patient's body and including a flexible annular base and means for holding the tube, said means including a bushing supported coaxially with respect to the base by ribs extending therebetween, said ribs being arranged to be spaced from the patient's body to enable sanitary and hygienic treatment of the skin integument portion around the tube, and a cover for enclosing a cavity with the base and the patient's body, the cover preventing accidental displacement of the tube to eliminate pain.