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| United States Patent | 4387879 |
| Link to this page | http://www.wikipatents.com/4387879.html |
| Inventor(s) | Tauschinski; Stefan (Vienna, AT) |
| Abstract | A connector which is adapted to be connected to a plastic cannula or a vein
catheter comprises a tubular and/or conical portion that is adapted to be
tightly joined to a parenteral solution supply needle and/or to a hose
provided with a cone fitting. To ensure that a metal cannula or a vessel
catheter can be pushed through the connector without obstruction and that
the connector closes automatically as soon as the metal cannula or the
catheter or the cone fitting of a supply hose has been pulled from the
connector, the body of the latter is provided with a receptable, which is
radial with respect to the flow passage, and a disc consisting of
elastomeric material and having a central slit is held in said receptacle
and blocks the flow passage. |
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Title Information  |
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Drawing from US Patent 4387879 |
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Self-sealing connector for use with plastic cannulas and vessel catheters |
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| Publication Date |
June 14, 1983 |
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| Filing Date |
July 16, 1981 |
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| Parent Case |
This is a continuation of application Ser. No. 030,390 filed Apr. 16, 1979. |
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| Priority Data |
Apr 19, 1978[DE]2817102 |
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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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Estimate the gross annual revenues of the relevant market
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| Market Share |
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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 is:
1. A connector consisting essentially of a hollow longitudinal passage, a
hollow body portion containing a chamber, a hollow inlet portion and a
hollow outlet portion, said connector containing a longitudinally slidable
member, having a central opening, disposed within said longitudinal
passage, and slidable within limits in said longitudinal passage, said
member contacting and cooperating with a deformable elastomeric disc,
having a central slit, disposed and held in place within the chamber of
said body portion transversely across said longitudinal passage to close
off the passage, said inlet portion having a hollow conical portion
adapted to be connected to a parenteral solution supply needle or hose
having a cone fitting, said outlet portion having a hollow passage and
being adapted to be connected to a cannula, catheter or hose; said
longitudinally slidable member cooperating with said cone fitting such
that when said cone fitting is inserted into said inlet hollow conical
portion the cone fitting contacts and causes the longitudinal slidable
member to advance and protrude at least through part of the elastomeric
disc to open the slit in the disc and provide communication between the
hollow inlet portion, the chamber in the body portion and the hollow
outlet portion, the elastomeric disc providing resilient means such that
when the cone fitting is withdrawn from the inlet portion of the connector
the disc springs back to its original position closing the slit and
sealing the disc and thereby forceably urging the longitudinally slidable
member to retract to its original position.
2. The connector of claim 1 wherein the elastomeric disc is circular.
3. The connector of claim 1 wherein the disc is force-fitted across the
chamber in the body portin of the connector.
4. The connector of claim 1 wherein the elastomeric disc is disposed in the
chamber of the body portion of the connector which joins the inlet portion
to the outlet portion of the connector.
5. The connector of claim 1 wherein the slidable member has a frusto
conical shape forward end portion.
6. The connector of claim 1 wherein the chamber of the body portion when
viewed in the direction of flow is conically tapered.
7. The connector of claim 1 wherein two or more adjoining elastomeric discs
are provided and their central slits cross each other.
8. The connector of claim 1 wherein the slit in the elastomeric disc is
straight, Y-shaped or star-shaped.
9. The connector of claim 1 wherein the slidable member has a cylindrical
portion which is guided in a mating bore that is formed in the connector
body and is larger in axial length.
10. The connector of claim 1 wherein the slidable member has axially
extending splines, semicircular-sections or ribs which engage mating guide
grooves in the connector body.
11. The connector of claim 1 wherein the splines, semicircular-sections or
ribs and mating guide grooves prevent the slidable member from falling out
of the connector body. |
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Claims  |
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Description  |
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This invention relates to a connector which is adapted to be connected to a
plastic cannula or a vein catheter and comprises a tubular and/or conical
portion that is adapted to be tightly joined to a parenteral solution
supply needle and/or to a hose provided with a cone fitting.
Plastic cannulas and vein catheters are used in medicine to supply blood or
parenteral solution into the vessel system of patients. The plastic
cannula or a short catheter contains a sharp metal cannula and by means of
the latter is pierced through the skin and the tissue and introduced into
a blood vessel. Through a plastic cannula which has been applied, a long
catheter can be introduced into the vessel system. If a peripheral vein is
to be punctured the same is squeezed off on its distal side and is thus
caused to swell to a larger volume. When the vein has been punctured the
metal needle is removed from the plastic cannula. In that operation it has
hardly been possible before to prevent an emergence of blood from the cone
fitting which was connected to the cannula. When a short catheter is
introduced by means of an internally disposed needle into a large vena
cava and is subsequently advanced as far as to the vena cava superior, an
emergence of blood from the cone fitting cannot be prevented even when the
patient is properly placed. If the patient is improperly placed or when he
makes spontaneous movements or coughs, there is an additional danger that
a vacuum may occur in the punctured vena cava so that air is sucked
through the catheter. This may result in air embolism.
In another method of vein catheterizing, the bore of the catheter is sealed
by a core and the catheter is introduced through a plastic cannula, which
has previously been introduced into the vein. In that method an emergence
of blood from the cannula and from the catheter when the sealing core has
been removed can hardly be avoided.
A special danger resides in that the supply hose for the parenteral
solution may inadvertently detach from the cone fitting of the vein
catheter. When a subclavian catheter is applied to a seated patient, for
instance, this may result in air embolism. On the other hand, blood would
continually emerge from a peripheral catheter or the latter would be
clogged by coagulation.
The emergence of blood from the cone fitting of cannulas and catheters had
previously to be put up with although it may have most serious
consequences particularly in long-term treatments. For instance, mass
examinations of vessel catheters have shown that a high percentage of the
catheters was infected with bacteria.
In that finding it was most remarkable that in most cases the infection had
been effected at the tip of the catheter rather than at the point where
the catheter emerged from the skin. This suggests that the bacteria had
grown through the catheter, which was contaminated with blood, and had
thus entered the interior of the catheter and accumulated at its tip.
It has been attempted to prevent an emergence of blood and a risk of an
entrance of air into the vein by the provision of a two-way of three-way
cock between the cannula or catheter, on the one hand, and the cone
fitting, on the other hand. But because the physician must use both hands
in handling the plastic cannula or the catheter, a helper is required for
turning the cock to its closed position. Besides, the cock must be closed
very promptly because blood will otherwise enter the fitting. And even
such cock cannot prevent an inadvertent detaching of the hose from the
catheter.
For this reason it is an object of the present invention to provide a
connector which is of the kind mentioned first hereinbefore and through
which a metal cannula or a vessel catheter can be pushed without
obstruction but which will close automatically as soon as the metal
cannula or the catheter or the cone fitting of a supply hose has been
pulled from such connector. The connector is intended to close as the
metal cannula, the vessel catheter or the cone fitting of the supply hose
are pulled out of the fitting or inadvertently fall from the same, and the
closed connector is intended to prevent an emergence of blood or an
ingress of air through the fitting.
This object is accomplished according to the invention in that the body of
the connector is provided with a receptacle, which is radial with respect
to the flow passage, and a disc consisting of electromeric material and
having a central slit is held in said receptacle and blocks the flow
passage. The slit may be straight or Y-shaped or star-shaped. A metal
cannula or a catheter hose can be inserted through the central slit of the
rubber-elastic, plane disc of the connector according to the invention,
and when the cannula or hose has been pulled out the slit is tightly
closed to seal the passage, owing to the elasticity of the disc. In
consideration of the diameter, the thickness and the material of the disc,
the length of the slit is selected so that metal cannulas and catheter
hoses can properly be pushed through the slit and that a tight seal is
ensured when such cannula or hose has been removed.
The disc may be circular and is suitably larger than its receptacle so that
the disc is force-fitted in the receptacle and applies to the periphery of
the receptacle a pressure which improves the seal at the slit.
According to a preferred further feature of the invention, a member having
a central through hole is guided in the conical entrance passage of the
connector body and is longitudinally slidable within limits to such an
extent that when the member is retracted its forward end face is clear of
the flat disc and when the member is advanced it protrudes at least
through part of the disc to open the slit. If the connector body has a
hollow-conical extension and a cone fitting, e.g., of a supply hose, is
pushed into said extension, the cone fitting will advance the
longitudinally slidable member toward the disc to open the slit and to
lock said member in position. When the cone fitting of the supply hose is
pulled out or falls off inadvertently, the elastically deformed disc will
urge the member back so that the slit closes tightly.
Further desirable embodiments of the invention will be defined more in
detail in the sub-claims.
All illustrative embodiment of the invention will now be explained more
fully with reference to the accompanying drawing, in which
FIG. 1 is a longitudinal sectional view showing on an enlarged scale a
connector provided with a slit sealing disc,
FIG. 2 is a view similar to FIG. 1 and shows a connector having an axially
slidable, central member, and
FIG. 3 shows the connector of FIG. 2 with the member advanced to open the
slit in the disc.
FIG. 4 shows the connector of FIG. 1 with two adjoining elastomeric discs
having their central slits cross each other.
A plastic connector body shown in FIG. 1 has at its entrance and a
hollow-conical portion 2, which can be tightly connected to an inserted
fitting cone of a hose for supplying a parenteral solution. The connector
body 1 is provided at its exit end with a cylindrical passage 4, which has
a diameter that has been selected in view of the diameter of a cannula or
catheter which can be inserted. That portion of the connector body which
surrounds the passage 4 is conically tapered and provided with peripheral
annular ribs and serves to retain a hose, which leads to the vessel
system. A chamber 6 connects the interior of the hollow-conical portion 2
to the passage 4 and is provided with a peripheral annular radial groove
7, in which a disc 3 of elastic material is held. The disc 3 is provided
with a central slit 8, which terminates short of the edge of the disc.
The embodiment shown in FIGS. 2 and 3 differs from the embodiment shown in
FIG. 1 in that the inside surface of the hollow-conical portion 2 is
formed with two or more axial guide grooves 9, which are engaged by mating
splines of a member 10, which is axially slidable between limits.
Alternatively, the cylindrical portion of the member 10 may be guided in a
mating cylindrical bore. The member 10 has a central through bore and has
a square rear end face whereas its forward end portion is frustoconical.
In the position shown in FIG. 2 the forward end of the member 10 just
contacts the disc 3, which has sprung back to its plane position, so that
the slit 8 of the disc 3 is tightly closed.
In FIG. 3 the member 10 is shown in a position to which it has been
advanced by a oval fitting, not shown, of a supply hose. In that position
the slit 8 is open because it has been expanded.
Instead of one slit disc of elastomeric material, two or more adjoining
discs may be provided, which have central slits crossing each other. When
two discs are provided, the crossing slits may extend at an angle of
90.degree. to each other. When three discs are provided, adjacent slits
include an angle of 60.degree..
In FIG. 4 there is shown peripheral annular radial groove 7 in which 3' is
provided with a central slit 8', which terminates a short distance short
of the edge of the disc.
The slidable member 10 need not be guided in grooves but may have a
cylindrical outside surface, provided that suitable means are provided to
prevent the member 10 from falling out of the connector 1.
To ensure that the member 10 is easily slidable, ribs which are preferably
semicircular in cross-section may be provided on the inside surface of the
hollow-conical portion 2 or on the peripheral surface of the slidable
member 10. The member 10 does not only open the slit 8 in the disc 3 but
reduces also the friction between the disc 3 and the inserted element,
which may consist of a cannula, a catheter, or a core for a catheter.
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Description  |
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