U.S. patent application number 11/230048 was filed with the patent office on 2006-01-19 for catheter and method of fluid removal from a body cavity.
Invention is credited to Allen J. Meglin, Matthew Meglin.
Application Number | 20060015089 11/230048 |
Document ID | / |
Family ID | 28677938 |
Filed Date | 2006-01-19 |
United States Patent
Application |
20060015089 |
Kind Code |
A1 |
Meglin; Allen J. ; et
al. |
January 19, 2006 |
Catheter and method of fluid removal from a body cavity
Abstract
A catheter comprises a catheter body having a wall defining a
lumen therein and having plural holes defined through the wall in a
pattern which prevents loculation, migration and blockage of a
fluid flow through the lumen, the catheter body having a
tissue-puncture resistant shape; and a port having a reservoir
capable of multiple needle accesses. The catheter is useful for
draining fluids from a patient's body cavity, for example the
peritoneal cavity.
Inventors: |
Meglin; Allen J.;
(Wilmington, NC) ; Meglin; Matthew; (Wilmington,
NC) ; Meglin; Allen J.; (Wilmington, NC) |
Correspondence
Address: |
LOWRIE, LANDO & ANASTASI
RIVERFRONT OFFICE
ONE MAIN STREET, ELEVENTH FLOOR
CAMBRIDGE
MA
02142
US
|
Family ID: |
28677938 |
Appl. No.: |
11/230048 |
Filed: |
September 19, 2005 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10172160 |
Jun 14, 2002 |
|
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11230048 |
Sep 19, 2005 |
|
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60370558 |
Apr 4, 2002 |
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Current U.S.
Class: |
604/890.1 ;
604/523 |
Current CPC
Class: |
A61M 27/00 20130101 |
Class at
Publication: |
604/890.1 ;
604/523 |
International
Class: |
A61K 9/22 20060101
A61K009/22 |
Claims
1. A catheter for removing fluid from a body cavity, comprising: a
catheter body extendible substantially within the body cavity
having a wall defining a lumen therein and having at least one hole
defined in the catheter body in a location that is within the body
cavity when implanted, and which in combination with a shape of the
catheter body prevents loculation, migration and blockage of a
fluid flow through the lumen when the fluid flow is induced in a
direction defined as running from a distal end to a proximal end
thereof, the catheter body having a tissue-puncture resistant
shape; and a port having on a first surface a septum capable of
multiple needle accesses, and having on a second surface an outlet
in communication with the catheter body and arranged so the
catheter body extends substantially without bends in a direction
perpendicular to the first surface, into the body cavity.
2. The catheter of claim 1, wherein the plural holes are located in
a protected region of the catheter body.
3. The catheter of claim 2, having a pigtail coil shape.
4. The catheter of claim 3, wherein the plural holes are located in
a protected region defined by an inner curve of the pigtail
coil.
5. The catheter of claim 2, having a helix coil shape.
6. The catheter of claim 5, wherein the plural holes are located in
a protected region defined by an inner curve of the helix coil.
7. The catheter of claim 2, having a T-bar shape.
8. The catheter of claim 7, wherein the plural holes are located in
a protected region defined adjacent an angle between a stem and a
crossbar of the T-bar.
9. The catheter of claim 1, having a tulip shape.
10. The catheter of claim 9, wherein the plural holes are located
on a broad surface of a petal of the tulip.
11. The catheter of claim 10, the tulip collapsible when advanced
by a pusher rod.
12. The catheter of claim 1, further comprising: another port
coupled to the first port and to the body of the catheter for fluid
communication therewith.
13. The catheter of claim 1, further comprising: a cage surrounding
at least part of the catheter body including the plural holes.
14. The catheter of claim 13, wherein the cage is integral with the
catheter body.
15. The catheter of claim 13, wherein the cage is memory metal.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a divisional application claiming the
benefit under 35 U.S.C. .sctn..sctn. 120 and 121 of U.S.
application Ser. No. 10/172,160 filed on Jun. 14, 2002, which
claims domestic priority under 35 U.S.C. .sctn. 119(e) to
provisional Patent Application No. 60/370,558 filed Apr. 4, 2002,
all of which are hereby incorporated by reference.
BACKGROUND
[0002] The present invention relates to devices that permit
repeated access to the peritoneal or thoracic cavities. More
particularly, the invention relates to a peritoneal and thoracic
cavity port catheter.
[0003] Certain medical conditions (e.g., ovarian cancer) are
treated by infusing a body cavity with a fluid medical preparation
through a catheter with one or more infusion holes at a distal end
thereof and with an access port or other such device at a proximal
end thereof.
[0004] In the case of ovarian cancer, the radioactive isotope
P.sub.32 is administered in a fluid medium infused into the
peritoneal cavity, in which the patient's ovaries are located. When
ovarian cancer metastasizes or spreads from the ovaries, the cancer
cells simply fall off of the ovaries and spread around the
peritoneal cavity, but generally do not enter the blood stream.
Therefore, a therapy, which floods the peritoneal cavity with
P.sub.32, is effective, without unnecessarily exposing the patient
to radioactivity in undesired areas. However, ovarian cancer cells,
having somewhat defective cell membranes, leak fluids, called
ascites, into the peritoneal cavity. Treatment of ovarian cancer
includes removal of this fluid. The procedure for doing so
typically uses the same catheter through which the infusion is
performed, and takes about four hours, requiring hospitalization,
and is performed about once a week.
[0005] Because conventional infusion catheters are optimized for
infusion, they can only be used to remove fluids from the
peritoneal cavity very slowly, resulting in the long, periodic
hospitalization for ovarian cancer patients.
[0006] There are similar needs under some circumstances to have
access to the thoracic cavity or other body cavities, and current
devices for obtaining such are similarly limited.
SUMMARY OF THE INVENTION
[0007] In accordance with aspects of an embodiment of the
invention, there may be provided a catheter, comprising a catheter
body having a wall defining a lumen therein and having plural holes
defined through the wall in a pattern which prevents loculation,
migration and blockage of a fluid flow through the lumen, the
catheter body having a tissue-puncture resistant shape; and a port
having a reservoir capable of multiple needle accesses.
BRIEF DESCRIPTION OF THE DRAWINGS
[0008] In the figures, in which like reference designations
indicate like elements:
[0009] FIG. 1 is a top view of a catheter and port embodying
aspects of the invention;
[0010] FIG. 2 is a cross sectional detail view of the catheter of
FIG. 1, taken along line 1-1;
[0011] FIG. 3 is a perspective view of the catheter of FIG. 1;
[0012] FIG. 4 is a top view of an alternate port configuration
embodying aspects of the invention;
[0013] FIG. 5 is a top view of an alternate catheter configuration
embodying aspects of the invention;
[0014] FIG. 6 is a top view of yet another alternate catheter
configuration embodying aspects of the invention;
[0015] FIG. 7 is a top view of an alternate catheter and port
configuration embodying aspects of the invention;
[0016] FIG. 8 is an end view of the catheter of FIG. 7;
[0017] FIG. 9 is a top view of the catheter of FIGS. 7-8, extended
by a pusher rod shown in phantom;
[0018] FIG. 10 shows a cross section of a patient's peritoneal
cavity, into whose wall another configuration of port and catheter
has been implanted;
[0019] FIG. 11 is a side view of the distal end of the catheter
body of FIG. 10;
[0020] FIG. 12 is an end view of the catheter body of FIG. 10;
[0021] FIG. 13 is a perspective view of the port and catheter
connection of the embodiment of FIG. 10;
[0022] FIG. 14 is a cross-sectional side view of a removable core
access needle used in various embodiments;
[0023] FIG. 15 is a side view of a catheterless plug;
[0024] FIGS. 16, 17 and 18 are side, top and front views,
respectively, of an alternate port design;
[0025] FIG. 19 is a side view of a combined catheter shape;
[0026] FIGS. 20 and 21 are end and side views, respectively, of an
alternate combined catheter shape; and
[0027] FIGS. 22 and 23 are side and top views, respectively, of a
port design having a right-angle outlet.
DETAILED DESCRIPTION OF EMBODIMENTS
[0028] In accordance with some embodiments of the present
invention, a method and apparatus is provided for removal of fluids
from a patient's body, for example draining fluids from a body
cavity between multiple drug infusion operations (e.g., during the
entire duration of treatment).
[0029] Embodiments of aspects of the invention may include a
catheter or a catheterless plug having a catheter body and an
access port, and a method of extracting fluid from a body cavity.
As explained more fully below, the catheterless plug has a body
resembling a catheter body, but which can comprise a fully
integrated unit. References below to the catheter body apply to the
body of the catheterless plug, as well, except where differences
are explicitly mentioned.
[0030] The catheter body should preferably have a shape that is
unlikely to undesirably puncture or injure tissue or organs
encountered in or about the body cavity to be drained. The shape of
the catheter body, together with the placement of one or more fluid
extraction holes in a wall of the catheter body should preferably
be such as to avoid the formation of pockets (referred to by those
skilled in this art as loculation) and/or to avoid creating a fluid
flow that would cause migration of the catheter body, or of tissue
or debris, that could block the extraction holes. For example, the
extraction holes can be positioned in a protected region of the
catheter body, as described below.
[0031] The catheter port should preferably be implantable
subcutaneously, and/or capable of sufficient extraction needle
passages to complete a course of treatment without replacement.
[0032] The invention is now illustrated in further detail with
reference to some embodiments thereof. In the following description
the illustrative example of extracting fluid from the peritoneal
cavity is used. However, it should be understood that the invention
may be employed in connection with treatments requiring the
extraction of fluid from the thoracic cavity or another body
cavity.
[0033] One aspect of the invention is illustrated in connection
with a catheter 10 including a catheter body 100 (FIGS. 1-3) having
a lumen (FIG. 2, 200) that may be closed off at the distal end 101,
i.e., having no end hole. This embodiment includes plural holes 102
covering a combined surface area suitable for withdrawing fluid,
substantially without clogging. Thus, when the catheter 10 is used
to extract fluid from the peritoneal cavity, there is no large
suction through a dominant single point which could attract
occluding masses to migrate to the dominant single point or could
attract the catheter itself to migrate into a position where a
dominant single point is occluded. Optionally, in another
embodiment, an end hole can be provided at the distal end 101 of
catheter body 100, together with one or more other holes 102,
provided neither a hole 102 nor the optional end hole contributes
such a surface area, and consequently large fluid flow, as to
induce loculation or migration of the catheter body 100.
[0034] In order to provide more room for holes 102, the catheter
body 100 of this embodiment is quite long. One danger inherent in
implanting a catheter 10 in many body cavities is the risk of
perforating or puncturing an organ, membrane, or other tissue
unintentionally. The risk is especially large when a long catheter
body 100 is implanted into a closed cavity such as the peritoneal
cavity, with the expectation that the catheter will bunch up like
spaghetti.
[0035] In the embodiment of FIGS. 1-3, the catheter body 100 is a
self-coiling type to facilitate insertion of such a relatively long
catheter into the body. This may be achieved by means known to the
skilled practitioner such as molding the catheter body 100 in a
desired coil configuration, molding the catheter body 100 on a
coiled strength member such as a wire, etc. The coil may be flat, a
straight-sided helix, a conical helix, etc.
[0036] The embodiment of FIGS. 1-3 employs a flat coil pigtail
configuration, although other coil configurations, as well as
configurations that avoid perforation or puncture using other
shapes, as explained below, are possible.
[0037] As stated above, the holes 102 should be positioned to avoid
contact with adjacent tissues or occluding masses. The holes 102 of
this embodiment are positioned on the inner curve 107 of the coil
so as to avoid contact between the holes 102 and adjacent tissues.
The outer curve 108 and the sides 109 can be devoid of holes. Thus,
the holes 102 are in a protected region of the catheter body. As
used herein, "inner curve" refers to that part of the surface of a
coil-shaped catheter body 100 facing a central axis of the coil of
the catheter body 100. Also as used herein, "outer curve" is that
part of the surface of the coil-shaped catheter body 100 facing
away from a central axis of the coil of the catheter body 100.
Finally as used herein, "sides" are surfaces of the coil-shaped
catheter body 100 adjacent to both the inner curve 107 and outer
curve 108 and joining them.
[0038] As mentioned, other shapes can also avoid puncturing
adjacent tissues, organs and membranes, while distributing holes
102 to prevent loculation, migration or occlusion. As shown in FIG.
5, an alternate embodiment of a catheter 500 has a catheter body
501 with a shape such as a simple helix or corkscrew, that avoids
punctures. Holes 102 are disposed on the inner curve 502 of the
catheter body 501 to avoid contact between the holes 102 and
adjacent tissues. Again, the holes 102 are located in a protected
region of the catheter body. This catheter 500 and the catheter 10
of FIGS. 1-3 can optionally include an end hole (not shown) at the
distal end 503 provided the area of the end hole is properly
balanced against the areas of the holes 102.
[0039] Another catheter body shape possessing desirable
characteristics of avoiding punctures, loculation, migration and
occlusion is shown in FIG. 6. In this example, catheter body 600
has a T-bar shape. The terminuses 601 may be closed or may
optionally include end holes (not shown) at the terminuses 601.
[0040] Yet another suitable catheter body shape is shown in FIGS.
7-9. This catheter body 700 has what is referred to as a "tulip"
shape. The surfaces of the tulip "petals" 701 can be opened into
holes 702. The center 703 of the tulip may be a closed end nipple
704, which captures a pusher rod 705 by which the catheter body 700
is advanced during implantation. When the pusher rod 705 is
extended, the end of the catheter body 700 stretches, collapsing
the tulip petals 701 as shown in FIG. 9. When the pusher rod 705 is
withdrawn, after implantation, the tulip petals 701 expand as shown
in FIGS. 7 and 8. This configuration can be shorter then those of
FIGS. 1-3 and 5-6 because the shape of petals 701 permits holes 702
to have a large surface area compared to holes 102.
[0041] Another suitable arrangement for the catheter body that
prevents blockage, puncture or loculation is shown in FIGS. 10-12.
This embodiment has a short body 1001 terminating in one or more
fluid extraction holes 1002. The fluid extraction holes 1002 are
surrounded by a spherical cage 1003 that prevents organs, e.g. the
bowels 1004, or debris from blocking the extraction holes 1002. The
cage 1003 may have other shapes, but a spherical cage 1003 presents
no sharp edges or steps that are likely to cause problems during
implantation or removal. Because the cage 1003 surrounds the fluid
extraction holes 1002, the extraction holes 1002 are in a protected
region of the catheter body.
[0042] The spherical cage 1003 of this embodiment can be formed of
plastic, metal, or any other suitable material. If formed of
plastic, the cage 1003 can be molded integrally with the body 1001
of the catheter, in the expanded spherical shape shown in FIGS.
10-12. If formed of metal, the cage 1003 can be preformed, also in
the expanded spherical shape shown in FIGS. 10-12. The metal can be
Nitinol or another so-called "memory metal" which can be
alternately stowed or deployed, for example by alternate
application of room ambient temperature and of the patient's own
body heat. A metal spherical cage 1003 would also be formed
integrally with and molded into the plastic of catheter body 1001.
In an alternative method of stowing and deploying the device, as in
the case of the tulip design described above in connection with
FIGS. 7-9, the spherical shape can be collapsed by a pusher rod
engaging an end tab 1005 during insertion and extraction. The
pusher rod is withdrawn completely from the catheter body while the
catheter is in situ in a patient's body.
[0043] The catheter body (FIG. 1, 100; FIG. 5, 501; FIG. 6, 600,
FIG. 7, 700, FIG. 10, 1001) may be constructed of any suitable
materials, using any suitable methods. Holes 102, 702, where
applicable, may be molded into the catheter or formed by any other
suitable technique, e.g., laser drilling, which can produce holes
suitable for rapid fluid extraction. The size, shape and location
of the holes should be selected to be suitable for fluid
extraction, as explained above. However, infusion can also be
performed through the holes. Without limitation, suitable materials
include plastics and elastomers such as silicone, polyurethane and
polyethylene and the like.
[0044] Ports usable in connection with the catheter bodies
described above are now described.
[0045] In the embodiment of FIG. 1, the proximal end 103 of the
catheter body 100 terminates at and is connected for fluid
communication to a subcutaneously implantable port 104. The port
has a membrane (referred to as a septum) 105 for percutaneous
access to the port 104 by a suitably sized extraction needle, e.g.,
a 14-gauge needle. In one embodiment, the septum 105 is durable
enough to permit at least 50 or more non-coring, self-healing
passages by a 14 gauge or larger needle. In other embodiments, the
septum 105 can withstand at least 100 or more, and preferably 200
or more passages.
[0046] The port 104 is constructed of any suitable materials, using
any suitable methods. In one embodiment, the side walls and back
wall of the port 104 may be formed of titanium, but other metals or
plastics such as acetal homopolymers that are bioinert can be used,
for example. The top surface is the septum 105, which may be formed
of silicone or other elastomer or plastic. In embodiments capable
of withstanding 200 passages by a 14-gauge needle, the septum 105
of silicone has a surface area of about 1-6 cm.sup.2 and be about
2-4 mm thick. Typically, but without limitation thereto, the septum
105 may have dimensions of about 1-2 cm by 1-3 cm.
[0047] The walls and septum 105 of the port 104 define a reservoir
within that has a low, wide profile to minimize the volume of fluid
held in the reservoir, and to maximize the comfort to the patient
in whom the port 104 is implanted. The port may, without limitation
thereto, have overall dimensions of 2 cm by 4 cm by 1 cm. Such a
port 104 can be implanted in a large pocket formed on the patient's
abdominal wall or in another location that avoids interference with
patient mobility. The catheter body 100 and port 104 may include
any suitable connector feature for connecting one to the other. For
example, a conventional hub connection (not shown) can be used.
[0048] FIG. 4 shows an alternate embodiment of the invention
directed to a multi-septum configuration. This multi-septum
configuration is useable in combination with any of the catheter
body configurations disclosed herein, and any other catheter body
configurations. In the embodiment of FIG. 4, the port 401 at the
proximal end 103 of the catheter 100 has two chambers 402, each
have a septum 403, allowing two needles to be placed for more rapid
drainage. The chambers 402 may be interconnected 404, and may be
connected to a single catheter 100 through a single hub 405.
[0049] In the alternative embodiment shown in FIG. 13, the port
1301 has a ribbed outlet 1302 to which the catheter body 1303 is
attached. A ribbed outlet 1302 such as shown can be used instead of
a conventional hub, such as mentioned above. In this embodiment,
the port outlet 1302 is disposed opposite the septum 1304, an
arrangement also thought to be advantageous in some cases.
[0050] Use of a ribbed outlet 1302 simplifies the construction and
assembly of the catheter and port. The proximal end 1305 of the
catheter body 1303 is simply slipped over the ribbed outlet 1302,
and is held in place by friction between the catheter body 1303 and
the ribbed outlet 1302.
[0051] Placing the ribbed outlet 1302 opposite the septum 1304 is
advantageous at least in that the impedance of the structure to
fluid flow is reduced relative to placing the outlet to the side of
the port, as in the embodiments of FIG. 1-7. Moreover, implantation
can be simplified using this arrangement because the entire
assembly is inserted straight into the cavity to be drained, rather
than at an angle or along a convoluted path. Yet another advantage
of this arrangement is that the catheter is less likely to kink
than in a configuration where the catheter body has to transition
from a position parallel to the abdominal wall to one perpendicular
to the abdominal wall.
[0052] In another alternative embodiment, shown in FIGS. 22 and 23,
exhibiting advantages similar to those of the embodiment of FIG.
13, a right-angle outlet 2201 is employed. Port 2200 is
substantially similar in construction and arrangement to port 104
of FIG. 1. However, outlet 2201 makes a right-angle bend towards
the direction of implantation of a catheter body (not shown), so
that kinks or bends are not introduced into the catheter body.
Outlet 2201 may terminate in a conventional hub (not shown) or
ribbed section (not shown) to grip the catheter body.
[0053] The port may also include other useful features. For
example, the port may include suture loops 1306 by which the port
can be secured to tissue in the patient's body. The port may have
funnel shape to further reduce the impedance of the assembly to
fluid flow during extraction.
[0054] As identified above, the port (FIG. 1, 104) can be accessed
through the system 105 by a conventional access needle, for example
a 14-gauge needle. Alternatively, a removable core access needle
1400, such as shown in FIG. 14, can be used. Such a needle may
include a large bore, e.g., 14 gauge, hollow point 1401. The point
1401 may be made of metal, perforated on the sides thereof 1402,
and have a beveled entry edge 1403 to prevent occlusion while in
use. The point 1401 is affixed to a right-angle end 1404 of a
suitable type of tubing 1405 that resists collapse under suction.
In order to control access through such a needle, and to prevent
coring of the septum (FIG. 1, 105) during insertion, the removable
core access needle 1400 has a removable stylete 1406 that resides
within the hollow of the point 1401 when not accessing the port,
and that is withdrawn when accessing the port. Stylete 1406 removal
is facilitated by providing a diaphragm or septum 1407, through
which the stylete 1406 passes and may be inserted or withdrawn.
[0055] It has been found that no cuff, as is often conventionally
provided, is necessary. However, if desired, a bacteriostatic cuff
106 may provided near the proximal end 103 of the catheter body
100, so as to prevent inward migration of an infection. The cuff
106 promotes fibrous tissue ingrowth. Bacteriostatic cuffs of
polyester impregnated with bacteriostatic compounds are
suitable.
[0056] Leaking around the catheter can be prevented by use of a
tissue collagen injection at one or more sites around the implanted
system. Tissue collagen acts as a kind of biocompatible glue
between the catheter body 100 and port 104, and the surrounding
tissues.
[0057] In yet another embodiment, a fully integrated, catheterless
fluid extraction plug 1500 is shown in FIG. 15. This embodiment
combines several features described above in connection with other
embodiments, as now described.
[0058] The exemplary catheterless drainage plug 1500 has an
expanded port section 1501 and an elongated body section 1502. Any
suitable port section shape can be used in combination with any
suitable body section shape, including those shown in the other
exemplary embodiments.
[0059] The catheterless plug embodiment is advantageous because of
its simplicity. Without joints and rough edges that may be found in
other designs, there are fewer locations to harbor potentially
infectious matter or irritate the implantation site in the patient.
The device is also less expensive and easier to manufacture than
designs using multiple components and joints.
[0060] The devices described herein are all implanted using
suitable techniques, including techniques known in the art. One
such technique is now described.
[0061] First an incision is made in the patient's skin above the
location where the device is to be implanted. The incision exposes
a small area of the underlying cavity wall. A hollow needle is
inserted through the cavity wall until a "fluid flash" is seen,
that is an outflow of fluid from within the body cavity. The fluid
flash indicates that the needle has been inserted into the desired
location. Next, a guide wire is inserted through the needle to
provide a defined path for the remainder of the devices employed.
The needle is then withdrawn over the guide wire. A sheath and
dilator are next inserted, over the guide wire. The dilator
enlarges the hole through the cavity wall sufficiently to allow a
catheter to be inserted. After the dilator has enlarged the hole,
it is removed. The catheter is then slid over the wire and sheath
and through the enlarged hole. Finally the sheath, and optionally
the wire, is withdrawn, leaving the catheter in place.
[0062] Various modifications to the port could now be evident to
the skilled artisan. For example, the bottom of the port could be
curved to follow the curve of the patient's abdomen, for patient
comfort. Alternatively, the port could be "almond-"shaped to leave
room for two extraction needles. Preferably, the port shape
accommodates a septum large enough to permit rotation of the
skin/septum puncture site, so as to avoid skin breakdown as a
result of repeated needle punctures. See, for example, FIGS. 16-18.
The almond shape would allow room for deep needles, for example
needles including side holes. Hollow needles with side holes would
permit higher extraction flow rates than hollow needles having only
an end hole. The eyelets 1306 may be filled with a membrane or not,
as desired.
[0063] According to yet other variations, the shapes and features
described above, and others, can be combined, as for example as
shown in FIGS. 19-21. FIG. 19 shows a helix 1901 combined with a
pigtail 1902. FIGS. 20 and 21 show a helix 2001 combined with a
straight section 2002. In each case, the geometry is such that it
allows straightening followed by self-coiling or bunching, for
implantation.
[0064] The present invention has now been described in connection
with a number of specific embodiments thereof. However, numerous
modifications, which are contemplated as falling within the scope
of the present invention, should now be apparent to those skilled
in the art. Therefore, it is intended that the scope of the present
invention be limited only by the scope of the claims appended
hereto.
* * * * *