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Description  |
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BACKGROUND OF THE INVENTION
The invention relates to a device for implanting self-expanding endoprostheses. Endoprostheses of the generic type can be inserted, for example, in veins, bile ducts or urinary tracts to maintain patency. They are also used to prevent recurring
stenoses in the sense of an elastic recoiling or a cicatrized constriction following balloon dilation of arteries.
In most known devices, the axial length of the endoprosthesis is considerably longer when it is folded up than when it is expanded. Therefore, positioning in vessels, etc., is relatively difficult, since the exact length and location of the
endoprosthesis is not apparent until after it unfolds. In most known devices, the endoprostheses can be released by way of a relative motion between the tubular body and the core element.
A common feature of all the devices currently available on the market, however, is the fact that once the endoprosthesis is partially released, it can no longer be folded back up again. This means that once even just a small piece of the
endoprosthesis is released, the device can only be removed from the body by completely releasing the endoprosthesis and leaving it in the body. Moreover, once the endoprosthesis is partially released, it can only be pulled proximally but not pushed,
since the expanded distal end of the endoprosthesis would inevitably injure the vessel in which it was supposed to be introduced if it were pushed. Also, the shape of the endoprosthesis would be affected by this forcing action; it would be compressed
and its supporting elements would buckle.
If it is discovered when the endoprosthesis is released and unfolded that the final location does not correspond to the desired position, the possibility should thus exist of pulling the endoprosthesis back into the device again after it is
partially released so that it can accordingly be repositioned in a folded state.
A device of this type, described as an instrument for inserting a self-expanding implant, is outlined in [design patent] DE-GBM G 90 10 130.8. This device consists basically of an outer casing inside of which is an axial hollow core. The core
has a diameter that increases incrementally at its distal end, whereby the distal end of the core strikes against the distal end of the casing. Around the distal end of the core is a gripping component that firmly holds a self-expanding implant in such
a way that it can be separated. In order to produce a friction-locking connection between the core or the gripping component and the expanding prosthesis, the gripping component is made of a high-friction material. In addition, another type model
provides for coating the gripping component with an agent for gluing the expanding implant in such a way that it can be separated.
A disadvantage of this device is the fact that the outer casing must tightly enclose the expanding implant so that a friction-locking connection is ensured between the gripping component and the self-expanding implant as proposed. As a result of
this, a relative displacement creates a great deal of friction between the core and the outer casing, and naturally between the expanding implant and the inner wall of the outer casing, so that consequently forces exerted to release the expanding implant
and to withdraw it are great. Furthermore, there is a risk that due to the relatively strong forces being exerted, reliability with respect to precise positioning of the implant will be adversely affected accordingly, because in addition to the friction
between the expanding implant and the outer casing, there is also the friction between the core and the outer casing along the entire remaining length of the device. Moreover, it is more expensive to ensure by creation of the corresponding friction
coefficients that the relative movement actually occurs as intended between the expanding implant and the outer casing, although there the normal force on the friction surfaces is higher by the total expansion force of the expanding implant than the
normal force between the core and expanding implant.
With this device it is crucial, in order to achieve a very specific friction between the core and the expanding implant, that a normal force also be required that is just as precise. In this case, the amount of normal force is determined by the
elasticity of the outer casing, the elasticity of the expanding implant, and the elasticity of the core, on the one hand, and by the inner diameter of the outer casing, the thickness of the expanding implant and the outer diameter of the core, on the
other. Moreover, the expansion force of the expanding implant further determines the amount of normal force; it works against the normal force. The required normal force must be met exactly in order to produce a specific friction force; on the other
hand, however, the normal force is very sensitive to the determining factors cited. Mass production of this device therefore presents great problems.
The additional proposal in the aforementioned design patent with respect to coating the gripping component with an agent for gluing the expanding implant in such a way that it can be separated brings with it the risk that the expanding implant,
especially when stored for longer periods, will no longer expand on its own after the outer casing is pulled back, since its opening force is too weak, or that the adhesive coat will undergo chemical changes with time and consequently that the desired
friction-locking connection will no longer be guaranteed. Applying the adhesive coat also presents problems; every effort must be made to prevent the adhesive coat from getting between elements of the expanding implant, which must move toward one
another when the implant expands. Separable adhesive agents derive their properties from the fact that they always retain certain rheological properties; they do not harden. Consequently, the danger exists that adhesive agents that are properly applied
originally will begin to run during the time the device is stored and that the expanding implant will become stuck together.
Another type model of the design patent provides for supplying the gripping component with a roughened surface. However, with a roughened surface, there is the danger that the expanding implant will become deformed and, as a result, that its
shape will be affected, particularly when it expands.
It should be noted in general that a sure method of operation cannot be achieved in every case by means of type models such as those proposed in the aforementioned design patent, since with the manufacturing of expanding implants and, in
particular, with the type of compression, high tolerances with respect to accuracy to gauge and expansion force must be reckoned with.
SUMMARY OF THE INVENTION
It is therefore the purpose of the invention to provide a simple device for implanting endoprostheses and folding them back up again in which, compared to devices that do not permit the endoprosthesis to be folded back up again, the operating
force is not increased and the free and undeformed unfolding of the endoprosthesis is not affected, which can be manufactured easily and inexpensively, which guarantees sure operation even after long storage periods, and in which even certain unavoidable
manufacturing tolerances of the endoprosthesis do not have any adverse affect on its sure operation, particularly in releasing the endoprosthesis and folding it back up again.
Another purpose of the invention consists of providing a process for impressing a stamping on this device and for doing so easily.
Designing the endoprosthesis in such a way that the core element exhibits on a portion of its surface an impressed relief that corresponds to the structure of the inner surface of the endoprosthesis guarantees, on the one hand, that the forces
exerted to move the core element in relation to the outer body can be kept to a minimum and, on the other hand, that a sure radial separation of the self-expanding endoprosthesis from the core element is still ensured even after a long storage period.
Thus sure and reliable operation is achieved by means of such a design. This type of endoprosthesis can also be manufactured easily and inexpensively.
A preferred type model of the invention provides for the relief impressed on the core element to be individually adapted to the structure of the inner surface of the endoprosthesis. Such a design ensures that an optimal form-locking connection
is achieved between the core element and the endoprosthesis and therefore guarantees the greatest possible operational reliability. In this case, the individual form-locking meshing sites are individually matched to one another with respect to their
position, arrangement, and design.
A preferred process provides for using the individual endoprosthesis that is to be inserted in the device to form the relief. An advantage of this process is that great tolerances with respect to accuracy to gauge of the endoprosthesis do not
themselves adversely affect the operational reliability of the device.
BRIEF DESCRIPTION OF THE DRAWINGS
Two examples of the invention's design are explained in greater detail in the following using the drawings. The drawings show:
FIG. 1. A device in a partial cutaway view with a separate representation of a folded endoprosthesis;
FIG. 2. The device in partial cutaway view with an enclosed endoprosthesis;
FIG. 3. An enlarged cross section through a first type model of the device along line A--A in FIG. 2;
FIG. 3a An enlarged cross section through a second type model of the device along line A--A in FIG. 2; and
FIG. 4 The device in a partial cutaway view with a partially unfolded endoprosthesis.
DETAILED DESCRIPTION OF THE INVENTION
The device represented in FIG. 1 for implanting endoprosthesis 1 has basically a tubular, flexible outer body 2 and an elongated, flexible core element 3.
Tubular outer body 2 is represented in lengthwise section from break line x to its distal end. At its proximal end, tubular body 2 is provided with a handle 5. Elongated core element 3 is placed in tubular body 2, where core element 3 is
designed to be longer than tubular body 2 and also has a handle 6. Toward its distal end, core element 3 exhibits a region B, which serves to receive endoprosthesis 1. This region B exhibits at its proximal end a shoulder 8 made from X-ray opaque
material. Distally contiguous to this is a section 9, the diameter of which is reduced. Following section 9 is an area 10 in which a relief in the form of a stamping 11 is impressed and which exhibits a somewhat larger diameter than section 9 preceding
it. The form of relief or stamping 11 corresponds to the structure of the inner surface of folded endoprosthesis 1. Contiguous to area 10 lies a section 13 that exhibits approximately the same diameter as section 9. Following this is a ring 14, which
is also made of X-ray opaque material and which is designed to be somewhat larger in diameter than section 13. Finally, at its distal end, core element 3 has a blunt, cone-shaped tip 15.
Extending the entire length of core element 3 is a lumen 16 in which a guide wire 17 can be inserted. For the sake of better clarity, endoprosthesis 1 is depicted outside of the device and folded up in this representation. In this way, the
correlation between the form of stamping 11 and that of folded endoprosthesis 1 can be seen. It can also be clearly seen from this representation that the length of area 10, which is provided with stamping 11, is shorter than the length of the
endoprosthesis; it preferably totals approximately 10-50% of the length of the endoprosthesis. As a result of this length of stamping 11, the flexibility of the device in region B of endoprosthesis 1 is affected as little as possible by the piled up
material and the form locking in the stamping area. On the other hand, however, a reliable form-locking connection between enclosed endoprosthesis 1 and core element 2 is guaranteed.
FIG. 2 shows the device in a ready-to-use condition. Here endoprosthesis 1 is enclosed folded up between core element 3 and tubular outer body 2. At the same time, the inner surface of endoprosthesis 1 meshes with core element 3 along stamping
11 impressed in area 10. Stamping 11 corresponds to the structure of the inner surface of endoprosthesis 1, so that a large number of form-locking meshing sites are formed between area 10 of core element 3 and endoprosthesis 1. Since the individual
threads of a layer of endoprosthesis 1 diverge when the latter is folded up, differences in the location of the threads with respect to stamping 11 could result in the region of the proximal and distal ends of endoprosthesis 1. For this reason, it is
advantageous to provide sections 9 and 13, which have a smaller diameter than area 10, between the latter, which is provided with stamping 11, and the ends of endoprosthesis 1.
A first type model of the device can be seen in FIG. 3 in an enlarged cross section along line A--A of FIG. 2. Endoprosthesis 1 is enclosed between tubular outer body 2 and core element 3. The distance between the outer diameter of core element
3 and the inner diameter of tubular outer body 2 is chosen in such a way that the inner layer of endoprosthesis 1 is pressed into the recesses resulting from stamping 11. The depth of stamping 11 corresponds to approximately 50% of the thickness of the
inner layer of the semifinished material used in endoprosthesis 1. In this case, a thin wire is used as the semifinished material for manufacturing endoprosthesis 1. However, the same ratio applies if endoprosthesis 1 is punched out, for example, from
thin sheet metal or is made of strip metal. The above-mentioned depth of stamping 11 ensures a good form-locking connection between core element 3 and endoprosthesis 1 by means of a large number of form-locking meshing sites 20 and guarantees, in
addition, sure radial separation and unfolding of released endoprosthesis 1, because the form-locking connection does not affect the relative motion of the layers of semifinished material in relation to one another.
A second type model of the device is illustrated in FIG. 3a in an enlarged cross section along line A--A in FIG. 2. In this example, core element 3 has a coating or sheath 3a. The advantage of such a coating or sheath 3a is that it can exhibit
properties other than those of core element 3. The change in diameter required in this area can be easily obtained as well by means of this sheath or coating 3a. Thus, for example, the thermoplasticity of core element 3 can be lower than that of
coating or sheath 3a. Consequently, the depth of stamping 11 can be easily influenced by the thickness of coating or sheath 3a. Sheath 3a can be manufactured very easily, for example, by shrinking a contracting tube onto core element 3.
The operation of the device is explained by means of FIG. 4. Using the device, endoprosthesis 1 is inserted folded (FIG. 2) in a body canal 22, which is only indicated schematically, in the known manner and is advanced until the distal end
region B of the device is positioned so that enclosed endoprosthesis 1 is at the desired location in body canal 22. At the same time, the advance of folded endoprosthesis 1 in body canal 22 is monitored by means of known processes such as fluoroscopy.
The location of endoprosthesis 1 is readily visible due to X-ray opaque rings 8 and 14, which are fitted on core element 3 in the area of the two ends of enclosed endoprosthesis 1.
Once endoprosthesis 1 is in the intended final position, core element 3 is locked into position and endoprosthesis 1 is slowly released by pulling back tubular outer body 2. The two handles 5 and 6 are used for this purpose. Since
endoprosthesis 1 is self-expanding, the released portion begins to unfold and rest against the inner wall of body canal 22. In unfolding, the length of endoprosthesis 1 is shortened accordingly. Since there is a direct connection between the shortening
of endoprosthesis 1 and the inner diameter of body canal and the diameter of endoprosthesis 1 in its inserted, unfolded state but the final amount of expansion is not known exactly, the final position of unfolded endoprosthesis 1 cannot be determined
with certainty beforehand. Thus the position of endoprosthesis 1 must also be monitored during the unfolding. If monitoring shows that it is positioned correctly, endoprosthesis 1 can be completely released by pulling back tubular body 2 to the area of
shoulder 8 of core element 3. If, however, it is discovered during the unfolding that endoprosthesis 1 is not in the correct position, it can be folded back up again in tubular body 2 by moving tubular body 2 forward. This makes it possible for
endoprosthesis 1 to then be repositioned accordingly and released again in the new position in the manner described above.
By means of a form-locking connection between endoprosthesis 1 and core element 3, which is achieved via stamping 11, which corresponds to the structure of the inner surface of endoprosthesis 1, and via endoprosthesis 1, which meshes with
stamping 11, it can be ensured, on the one hand, that the forces exerted to move core element 3 with respect to outer body 2 can be kept to a minimum and, on the other hand, that sure radial separation of self-expanding endoprosthesis 1 from core element
3 is still guaranteed even after a long period of storage. In short, sure and reliable operation is achieved by way of a device with this design. It can also be manufactured easily and inexpensively.
The process for producing a stamping for this type of device can go as follows: An endoprosthesis 1 is pushed unfolded onto region B of core element 3. Then endoprosthesis 1 is folded up in the area of section 9 of core element 3 in which there
is no stamping. Next, tubular outer body 2 is pushed forward up to the proximal end of area 10 of core element 3. Endoprosthesis 1 is secured in position in this way. Endoprosthesis 1 is subsequently folded up in the area where it is exposed by a
pressing die, which is in itself known, and pressed by the pressing die on area 10 of core element 3. The pressing die is now warmed with hot air so that endoprosthesis 1, which has been pressed together, is heated and in this way pressed into the
thermoplastic material of core element 3 or into its coating or sheath 3a. After removing the pressing die, tubular outer body 2 is pushed forward until its distal end lies against the back side of tip 15 of core element 3 and endoprosthesis 1 is thus
completely enclosed. A corresponding process is utilized if a hardened plastic is used instead of the thermoplastic material. While this process is being carried out, it is absolutely imperative that shoulder 8 does not rest against the proximal end of
endoprosthesis 1. It automatically rests against the proximal end of endoprosthesis 1 once endoprosthesis 1 comes unmeshed from core element 3 upon release. Shoulder 8 serves then as an abutment for endoprosthesis 1 when the remaining portion of the
endoprosthesis still enclosed in tubular body 2 is released.
Obviously, processes are also conceivable in which the same endoprosthesis is always used to form the stamping. Furthermore, it is also possible to impress the stamping by means of a positive cast of an endoprosthesis formed on the pressing die.
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