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| United States Patent | 5092850 |
| Link to this page | http://www.wikipatents.com/5092850.html |
| Inventor(s) | Buma; Shelley J. (218 Hill St., Whitinsville, MA 01588) |
| Abstract | A catheter with an adjustable, external locking bolster. The catheter is
for insertion into a body and includes a distal tip which is positioned
inside the body, and a tubular member which is in communication with the
distal tip. A portion of the tubular member exists outside the body and is
provided on its outer surface with engagement elements. An external
coupling has matching engagement elements for selective, adjustable
securement to the tubular member. A compression element is provided which
locks the external coupling to the tubular element and prevents slippage.
The adjustable engagement allows a low profile, close to the skin
appearance, while the compression element securely locks the external
coupling to the tubular member. |
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Title Information  |
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| Publication Date |
March 3, 1992 |
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| Filing Date |
November 29, 1990 |
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Title Information  |
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References  |
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| *references marked with an asterisk below are user-added references |
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| Market Size |
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| Reasonable Royalty |
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Public's "Guesstimation" of Royalty Value
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| Market Size | N/A | [No votes] | | x | Market Share | N/A | [No votes] | | x | Reasonable Royalty | N/A | [No votes] |
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Market Review  |
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Technical Review  |
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Claims  |
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What is claimed:
1. An indwelling medical device wherein said device consists of:
a flexible distal tip with an opening therein,
a flexible tubular member with a lumen connected to the opening on the
distal tip to form a fluid passageway between the tip and the tubular
member to outside the body, said
distal tip adapted to be located within the body and the tubular member
proximal to the distal tip such that after placement a portion of the
tubular member exists outside the body, said
flexible tubular member having multiple engagement elements located on its
outside surface, said
engagement elements on the outside surface of the tubular member clearly
visible outside the body after placement, and
a separate external coupling incorporating at least one matching engagement
element capable of selective engagement with at least one of said elements
on the outside surface of the tubular member wherein said engagement takes
place outside the body, the
separate coupling further capable of being selectively positioned on the
tubular member such that the coupling can rest close to the skin surface,
a compression element capable of locking the coupling to the tubular member
after selective positioning of the coupling on the tubular member, said
compression element preventing engaged elements on both the coupling and
the tubular member from disengagement such that the coupling and the
tubular member become fixed together so that the external coupling
prevents inward migration of the tubular member within the body.
2. An indwelling medical device of claim 1 wherein an anti-reflux valve is
included in the distal tip.
3. An indwelling medical device of claim 1 wherein the tip is of the
deformable mushroom or pezzer type.
4. An indwelling medical device of claim 1 wherein said tip is hollow and
deformable.
5. An indwelling medical device of claim 1 wherein the anti-reflux valve is
housed inside the lumen of the catheter.
6. An indwelling medical device of claim 1 wherein a closure plug is
provided.
7. An indwelling medical device of claim 6 wherein the closure plug is
attached to the external coupling.
8. An indwelling medical catheter for draining or infusion of fluids
consisting of:
a distal tip for positioning inside the body,
an opening in said distal tip,
an inner fluid passageway in said catheter connected to said distal tip,
said
passageway extending substantially the full length of the catheter from
said distal tip to outside the body,
an outer on said passageway wherein said outer wall extends outside the
body and said outer wall incorporates a series of engagement elements
wherein said elements also extend outside the body,
an external bolster with at least one matching engagement element, said
bolster capable of selective engagement with any of the engagement elements
located on the outer wall of the passageway,
a said bolster further capable of being adjustably positioned on said outer
wall such that the external bolster rests close to the skin surface
outside the body,
a compression element capable of locking the bolster in place on the outer
wall of the passageway, said
compression element once in place in the locking mode preventing engaged
elements between the bolster and outer wall from being disengaged to
prevent slippage of the bolster on the outer wall of the passageway.
9. An indwelling medical catheter of claim 8 where said distal tip is a
flexible element larger in diameter than the tubular member.
10. An indwelling medical catheter of claim 8 wherein said distal tip is a
hollow member which is deformable.
11. An indwelling medical catheter of claim 8 wherein said distal tip
opening is surrounded by a hollow member with at least one drainage hole.
12. The indwelling medical catheter of claim 8 wherein an anti-reflux valve
is provided to prevent reflux of fluid from exiting the passageway to the
outside of the body.
13. The indwelling medical catheter of claim 8 wherein an anti-reflux valve
is housed within the distal tip.
14. The indwelling medical catheter of claim 8 including a closure plug to
stop fluid from exiting the passageway.
15. The indwelling medical catheter of claim 8 wherein the distal tip is
flexible and hollow and capable of being deformed and inserted inside the
body using a rigid obturator.
16. An indwelling medical device wherein said device consists of:
a flexible distal tip with an opening therein,
a flexible hollow catheter proximal to said distal tip with an internal
passageway connected to the opening on said distal tip,
said passageway in direct fluid communication with the opening in said
distal tip, said
catheter further having a series of engagement elements progressively
located on an outside wall of the catheter,
at least a portion of the catheter including engagement elements extending
outside the body after placement of the distal tip inside the body,
a separate external coupling with an opening therein, said opening
including matching engagement elements,
said opening and said matching engagement elements cooperating with the
engagement elements on the outside wall of the catheter to form an
interlocking connecting between the coupling and the catheter,
said coupling capable of engagement with any of the elements on the outside
wall of the catheter such that the coupling can be positioned and engaged
so that the coupling can rest close to the skin surface,
a compression element in conjunction with the coupling such that the
coupling can be locked in position with the catheter after compression of
the element such that the coupling and catheter cannot be disengaged
without relieving the compression element.
17. The indwelling medical device of claim 16 wherein the compression
element is a pull tie.
18. The indwelling medical device of claim 16 wherein the engagement
elements on the catheter wall are a series of saw teeth.
19. The indwelling medical device of claim 16 wherein an anti-reflux valve
is included in the distal tip.
20. The indwelling medical device of claim 16 where said distal tip is
hollow and deformable.
21. The indwelling medical device of claim 16 where said distal tip
consists of at least one outwardly extending flange.
22. The indwelling medical device of claim 16 wherein said distal tip
prevents outward migration of the catheter and said external coupling
prevents inward migration of the catheter.
23. A gastrostomy feeding device comprising:
a distal tip with an opening therein,
a hollow catheter proximal to the distal tip connected to the distal tip
and extending rearward therefrom, a
hollow catheter lumen in direct fluid communication with the distal tip
opening, said
hollow catheter having an outside wall with a series of engagement elements
which are clearly visible outside the body,
said distal tip with outwardly extending retaining means,
a said distal tip including retaining means adapted for contact with the
inner wall of the stomach to prevent outward migration of the device after
placement, and
a separate external bolster with at least one matching engagement element
capable of interlocking with said engagement elements which are clearly
visible outside the body one the hollow catheter wall, said
separate external bolster further capable of being selectively positioned
on the hollow catheter such that the bolster can rest close to the skin
surface while still engaged with the elements clearly visible outside the
body on the hollow catheter,
a compression element applying inward compressive force on the external
bolster in the area of its said at least one matching engagement element
to securely interlock the bolster to the hollow catheter to prevent inward
migration of the catheter inside the body.
24. A gastrostomy feeding device of claim 23 wherein the distal tip
retaining means is hollow and deformable.
25. A gastrostomy feeding device of claim 23 wherein an anti-reflux valve
is positioned in the distal tip retaining means.
26. A gastrostomy feeding device of claim 23 wherein an anti-reflux valve
is positioned in the hollow catheter lumen.
27. A gastrostomy feeding device of claim 23 wherein a dilator is attached
to the proximal hollow catheter enabling placement of the device using the
percutaneous endoscopic gastrostomy procedure.
28. A gastrostomy feeding device of claim 23 wherein the lumen of the
hollow catheter can be connected to an administration set or connecting
tube to deliver feeding formula.
29. A gastrostomy feeding device of claim 23 including a closure cap for
the lumen of the hollow catheter.
30. A gastrostomy feeding device of claim 29 wherein the closure cap is
pre-attached to the external bolster. |
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Claims  |
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Description  |
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BACKGROUND OF THE INVENTION
The use of various indwelling catheters, especially feeding devices, is
well known in the medical art. Feeding tubes may be left in place within
the body for a considerable period of time, often up to a year. This is
possible due to the use of recent advancements in biocompatible materials,
especially silicone indwelling devices which permit long term placement of
a device without body rejection or tissue reaction.
Medical grade silicone devices are routinely used in gastrostomy feeding
devices as well as other types of devices such as wound drains and
infusion catheters. The silicone material has many biocompatibility
advantages including the ability to remain soft and flexible for long
periods of time within the body.
Feeding devices and catheters made from silicone are molded, extruded, and
assembled such that the silicone material is very smooth and the surface
finish has a very low coefficient of friction. The surface of the silicone
catheter becomes very slippery especially when it is in contact with body
fluids.
To prevent inward migration of the catheter, designers and manufactures
have added external retention devices to their products. Silicone
retention discs are manufactured in various sizes to stabilize catheters
and are produced by such companies as Wilson-Cook.
Gastrostomy feeding devices are also available from C. R. Bard, Ross
Laboratories, and Superior Biosystems (manufactured for Sandoz Nutrition
Inc.) with pre-loaded retention discs already on the catheter.
Low profile gastrostomy ports of fixed lengths are also produced by these
three manufacturers, and are available in various sizes and lengths with
molded in external bolsters to prevent tube migration.
The problem with the retention discs is that they easily slide on the
tubular shaft of the catheter and the catheter easily migrates inside the
body.
If the gastrostomy devices has an inner balloon then the ballon can block
internal body passageways and cause an obstruction if the retention disc
fails. This is often the case.
To prevent disc slippage, pull ties have been added to the disc. However,
the disc still often fails due to the smooth slippery outer surface of the
catheter and the smooth inner surface of the molded retention disc.
The low profile gastrostomy devices from C. R. Bard, Ross, or Superior must
be molded with fixed lengths which means extra devices to measure the
lengths of patients' stoma tracts and the added inventory and expense of
many different fixed lengths and sizes.
The low profile devices of Gauderer U.S. Pat. No. 4,863,438 and Russo U.S.
Pat. No. 4,944,732 all show fixed lengths.
The low profile devices of Gauderer and Russo have many advantages,
however, many hospitals do not use these devices because of the large
inventory of different sizes and lengths required, and the frustration of
doctors and nurses in selecting the right size. Even with all the sizes
available, some patients cannot be fit with a low profile device because
the correct length is not available.
Manufacturing and inventory costs of the low profile devices make them very
expensive for most patients and hospitals.
BRIEF SUMMARY AND OBJECTIVES OF THE INVENTION
With the foregoing in mind, the present invention offers all the advantages
of the prior art with additional features and at a lower cost.
The present invention has an infinitely adjustable external bolster to
prevent inward tube migration and can be locked in place to eliminate tube
slippage.
Accordingly, it is primary objective to provide a device which is safer,
more convenient to use, and less expensive than the devices presently
manufactured.
An objective is to provide an external bolster which can be easily
positioned by the physician.
Another objective is to provide an external bolster which can be locked in
place after being positioned by the physician.
Another objective is to have the bolster, after locking it in place, become
unitized on the catheter such that the catheter cannot move inward inside
the body.
Another objective is to have the bolster with external flanges to further
prevent tube migration after the bolster is permanently positioned on the
catheter.
Another important objective is to provide a low profile, close to the skin
surface catheter device which can be infinitely adjustable as to lengths
desired inside the body.
Another objective is to provide a low profile gastrostomy feeding port
close to the skin surface which is infinitely adjustable to fit any length
of stoma tract.
Another objective is to eliminate the need for stoma tract length measuring
devices in low profile gastrostomy feeding ports.
Another important objective is to provide a low profile, close to the skin
surface gastrostomy device which can be placed for the first time in a
patient using the percutaneous endoscopic gastrostomy technique.
Another objective is to provide a replacement low profile, close to the
skin surface gastrostomy device which can be easily inserted and adjusted
to the stoma tract length.
DESCRIPTION OF THE DRAWINGS
The following drawings illustrates the best mode presently contemplated for
carrying out the invention.
FIG. 1 is a side-view of a tubular catheter including engagement elements
on its outside diameter, a flexible tip with an anti-reflux valve shown
normally closed.
FIG. 2 is an enlarged partial sectional view of the engagement elements.
FIG. 3 is an underside view of the flexible tip with the anti-reflux valve.
FIG. 4 is a partial sectional side view of the flexible tip with the
anti-reflux valve shown opened by a rounded tip drainage catheter.
FIG. 5 is a side-view of the external bolster showing internal engagement
elements and a closure cap.
FIG. 6 is a top-view of the external bolster.
FIG. 7 is a partial sectional enlarged view of the internal engagement
elements.
FIG. 8 is a sectional view of the catheter after placement in a body cavity
showing it pre-assembled to a dilator, with the external bolster adjusted
down close to the skin surface and a compression pull tie securing the
engagement elements.
FIG. 9 is a sectional view of the catheter in a body cavity after the
dilator and compression pull tie have been trimmed away, with the closure
cap in place with the device shown in a low profile, close to the skin
surface mode.
DESCRIPTION OF THE INVENTION
FIG. 1 shows molded catheter 10 which is tubular in shape with outside wall
11 and inside lumen 12. Lumen 12 extends the full length of the catheter.
The catheter can be molded from medical grade silicone either by
compression or the liquid injection molding process.
A small percentage, about 5%, Barium can be formulated within the silicone
to make the device radiopaque.
Distal tip 13 is integrally molded as part of the tubular catheter.
The tip has outwardly extending flanges 14 and 15.
Protruding downward and moded into the tip is square shaped lug 16.
Separately silicone moded anti-reflux valve 17 is of the flapper type.
Externally molded onto the outside wall 11 is a series of saw tooth rings
18 which are molded around the entire circumference of the outside wall
11.
The saw tooth rings 18 should begin with 1/2 inch of the distal tip and
extend proximally along the catheter for a length of at least 3 inches.
FIG. 2 is an enlarged sectional view of the saw tooth rings 18.
The crest of the tooth 19 is the same dimension for all crested teeth.
The valley 20 of the tooth is also the same dimension for all valleys
portions of the tooth.
The width of the tooth at its base 21 is about 0.050 inches and the height
of each tooth 22 from valley to crest is also 0.050 inches
Inside lumen 12 is molded smooth.
FIG. 3 which shows the underside of the distal tip shows flanges 14 and 15
with rounded edges 23 and 24.
Anti-reflux flapper valve 17 is molded flat with a rounded forward edge 25
and rearward straight edge 26.
A square shaped hole 27 is molded into the valve to mate with square shaped
lug 16 on the distal tip.
FIG. 4 shows lug 16 extending slightly beyond the valve surface so that
liquid silicone adhesive 28 can adhesive bond that lug to valve.
Square lug 16 both positions and correctly aligns the valve in place and
acts as an adhesive lug.
Rounded edge 25 is free to flap open as in 29.
A hollow drainage obturator which is semi-rigid extruded and molded of PVC
plastic can easily open flap valve 17 to drain or decompress a body
cavity. Side drainage holes 31 can be positioned at the obturator tip.
FIG. 5 shows a side view of external bolster 32 which is also molded of
silicone rubber.
The bolster has a molded in opening with internal saw teeth rings 34 which
match external saw teeth rings 18 on the tubular shaft of catheter 10.
Extending off to one side of bolster 33 is a molded in strap 35 with a male
closure plug 36.
FIG. 6 is a top view of the bolster which shows outward flanges 37 and 38.
FIG. 7 is an enlarged partial sectional view of the bolster in the saw
teeth area.
The internally molded saw teeth have corresponding crests 39 and valleys 40
to crests 19 and valleys 20 as shown in FIG. 2.
The body of the bolster has a recessed groove 41 which runs around the
entire outside surface of the bolster.
Above groove 41 is a projected annular ring 42.
FIG. 8 shows the catheter after placement within the body.
If the catheter were to be used as a gastrostomy feeding device it can be
placed using the standard percutaneous endoscopic technique using either
the "push" method or the "pull" method.
Attached to the proximal end of the catheter can be a long tapered dilator
43 which facilitates placement using the endoscopic technique.
The catheter is placed through the stomach wall 44.
Bolster 32 is slid over dilator 43 and ratchets down over saw teeth 18 on
the catheter shaft.
Matching internal saw teeth 34 engage with saw teeth 18.
In practice, the external bolster can ratchet down 0.050 inches at a time
for an infinitely precise fit down to skin surface 44.
Flanges 37 and 38 on the bolster can rest gently on the skin surface 44.
If the bolster is too tight down on the skin surface, it can be retracted
upward by grabbing projected ring 42.
The bolster can be adjustable in either upward or downward movement on the
tubular shaft in precise 0.050 inch increments.
Once in position, nylon pull tie 45 can be compressed securely into
recessed ring 41 on the bolster.
The pull tie compresses the internal saw teeth on the bolster to
permanently lock the matching teeth in place.
Once compressed, the crests and valleys of the teeth cannot move out of
position and the bolster is securely locked onto the catheter shaft.
Pull tie 45 is of the one-way compression engagement nylon molded type.
Once pulled tight it cannot be retracted.
After securing the pull tie the catheter is carefully trimmed at surface 46
to remove excess tube 47 and dilator 43.
FIG. 9 shows a cross sectional view of the device in its final form after
placement and in its low profile, close to the skin surface look.
After trimming the catheter at surface 46 the pull tie is also trimmed back
to point 47 for a neat appearance.
The catheter lumen is fully open at point 48 and extends the full length to
outward opening 49 at the distal tip.
Closure plug 36 will fit directly into lumen 46 at point 48.
The device now becomes a complete easy to place, low profile, close to the
skin surface portal device.
The cap can be opened by pulling on tab 50 on the strap 35.
The catheter can be attached to any desired administration set for the
delivery of feeding formula or medications.
The anti-reflux valve 17 permits one-way infusion into the device, but
prevents body fluids from escaping.
The valve can be opened at anytime to drain the device by opening cap 36
and inserting drainage tube 30.
Some physicians prefer other style distal tips such as pezzer type, conical
type, mushroom type, or malecot type. These are all hollow bulbous types
of tips which are deformable to be inserted or placed inside a body
cavity, particularly the stomach.
Rigid obturators are used to stretch out these tips during insertion.
Anti-reflux valves can be incorporated in any one of these alternate style
tips, and the device can readily be designed with any of these tips in
mind.
As can be seen from FIG. 9 the device in its final form is a very low
profile, close to the skin surface device. It also meets all of the
objectives. Ease of placement, patient comfort, low cost, and the ability
for the patient to lead a normal active life, are all advantages of this
device.
While there is shown and described herein specific structures of the
device, it will be apparent to anyone skilled in the art to make various
modifications to the device without departing from the spirit and scope of
the invention.
The invention, therefore, is not limited to particular forms or elements
herein shown and described.
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Description  |
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