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Description  |
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FIELD OF THE INVENTION
This invention relates to an hypodermic syringe for use in administrating
subcutaneous or intravenous injections to persons and animals. While not
limited thereto, the invention has particular application for use in
hazardous situations in which the patient may possibly or actually be
infected with a fatally lethal and incurable virus, microvirus or
bacteria.
BACKGROUND OF THE INVENTION
Hypodermic syringes are well-known in the art, including pre-sterilized
syringes having a protective cap over the cannula or needle, and which is
to be removed immediately prior to administering an injection. The cover
is intended subsequently to be replaced over the needle after use of the
syringe.
However, at this point, the cannula or needle of the syringe has been
contaminated by its use on the patient, and, the needle or cannula itself
is potentially lethal, in that it then is a carrier of the virus,
microvirus, or bacteria. Careless handling, or, in the absence of the
protective cap, can result in the user unintentially being pricked,
scratched or cut by the sharpened end of the needle, this resulting in
infection of the user.
Numerous proposals have been made to avoid this occurrence, but none has
been entirely successful.
During use, sudden retraction of the needle into the syringe by spring
force, as has been prior proposed, can cause fracturing of the needle
within the patient. It can also cause splattering of contaminants on the
needle onto the hands of the user, and possibly into the user's eyes in
the event that a visor is not worn by the user. Also, the impact of
retraction of the needle under spring force can cause an impact on the
syringe, resulting in accidental dropping of the syringe, with possible
dangerous consequences.
Other prior proposals involve a manually retractable and manually
extendable needle guard. However, such needle guards require the use of
both hands for them to be forced manually into the extended position in
order to break the holding force of a resiliently engaged retaining
member. If the user's hand should slip off the needle guard during the
extension of the needle guard, there again is the possibility of the
user's hand being impaled by the unprotected needle.
SUMMARY OF THE INVENTION
It is an object of this invention to materially reduce the hazards to the
user in using a hypodermic syringe, by providing a syringe assembly having
an axially slidable needle guard that is releasable and retractable under
manual force, and which is then lockable in a retracted position, and
which subsequently can be released and extended under manual force for it
to shroud the used needle.
According to the present invention, in order to ready the syringe for use,
the user grasps the barrel of the syringe with one hand, and then grasps
the needle guard with the other hand, subsequent to which the needle guard
is squeezed using a single hand to release a locking projection on the
needle guard from a retaining notch in the barrel. The guard can then be
slid axially of the barrel of the syringe, with the locking projection
travelling within an axial slide track in the barrel.
Having reached the fully retracted position of the needle guard, the
locking projection enters a retaining notch at the other end of the axial
slide track to lock the needle guard in its retracted position.
In order to permit the release of the locking projection from the retaining
notch, the barrel is formed of circular cross section, and the needle
guard is formed of elliptical cross section with the locking projection
positioned on the minor axis of the ellipse and extending radially
inwardly of the bore of the needle guard. Thus, squeezing of the needle
guard along its major axis will cause radially outward movement of the
locking projection to withdraw it from the retaining notch, permitting the
locking projection then to slide within an axial channel formed in the
outer surface of the syringe barrel.
When using the syringe, the user's fingers engage holding tabs on the
syringe barrel to provide the required axial force on the syringe, this
further minimizing the possibility of the user being impaled by the
needle. Also, the user's fingers are at that time positioned in engagement
with the needle guard and act to retain the locking projection firmly
seated within the retaining notch.
Having used the syringe to effect either an injection on the patient, or
withdrawal of blood, the user then again squeezes the needle guard on its
major axis using a single hand to free it for return movement
longitudinally of the barrel of the syringe, the locking projection
travelling within the axial slide track to return the locking projection
to the first retaining notch.
This forward movement of the needle guard to its extended position can be
under the assist of a spring reacting between the needle guard and the
barrel of the syringe. If such a spring assist is provided, then, movement
of the needle guard to its extended position proceeds under the manual
control of the user, in that the needle guard is at that time being
grasped by one of the user's hands, which is used to squeeze the needle
guard.
Thus, both of the user's hands are located out of proximity to the
sharpened end of the cannula or needle, and in a location of maximum
safety.
In another preferred embodiment of the invention, the syringe barrel is
provided with circumferentially extending slide tracks at the opposite
ends of the axial slide track, the circumferentially extending portions of
the slide track incorporating either indents or projections providing
retaining notches for cooperation with the locking projection formed
internally of the needle guard.
In another preferred embodiment of the invention, in which the syringe is
supplied with the needle guard retracted, co-operating formations are
provided on the syringe barrel and needle that will permit movement of the
needle guard to an extended position but which inhibit reverse movement of
the needle guard.
Optionally, the needle guard is closed by a removable cap, and is further
closed by a frangible diaphragm which is punctured by the needle upon
retraction of the needle guard. Puncturing of the diaphragm will provide a
clear indication that the syringe has been used.
DESCRIPTION OF THE DRAWINGS
Preferred embodiments of the present invention will now be described with
reference to the accompanying drawings, in which:
FIG. 1 is a front elevation of the syringe of the present invention,
showing the needle guard in cross-section, and in an extended position,
FIG. 2 is a view similar to FIG. 1, but rotated through 90.degree. and
showing the needle guard in a retracted position;
FIG. 3 is a transverse cross-section through the syringe illustrating the
cross-section of a needle guard of elliptical cross-section;
FIG. 4 is a cross-sectional view corresponding with FIG. 3 and showing the
needle guard when compressed in the direction of its major axis;
FIGS. 5 and 6 illustrate a modification of FIGS. 1 and 2; and
FIG. 7 illustrated a further modification.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The syringe of the present invention includes, as is conventional, a barrel
10 having finger engageable tabs. A plunger is axially slidable within the
barrel, the plunger having been omitted for the purpose of clarity.
Extending axially from the barrel 10 is a hollow needle or cannula 12,
which is secured in the end of the barrel 10 in any convenient manner,
such as the barrel 10 having been molded in-situ about one end of the
needle 12.
Positioned externally of the syringe barrel 10 is a needle guard 14, the
needle guard 14 being formed of any suitable resilient and compliant
plastics material such as polyvinyl chloride, the needle barrel 10 being
formed from andy suitable material, such as a substantially rigid plastics
material such as polymethacrylate.
Extending axially of the syringe barrel 10 is a slide track indicated
generally at 16, the slide track comprising an axially linear groove 18.
Located internally within the needle guard 14 is a radially inwardly
extending projection 24 of a shape complimentary to the transverse
cross-section of slide track 18, the projection 24 being moveable along
the slide track 18 in order to permit retraction of the needle guard 14
from the extended position shown in FIG. 1 to the retracted position shown
in FIG. 2. As will be appreciated, the track and the projection could be
reversed, the track being provided within the needle guard, and the
projection being provided on the needle barrel.
Optionally, a compression spring 26 is positioned internally of the needle
guard 12 and reacts against one end of the needle guard and the juxtaposed
end of the syringe barrel. The purpose of this spring 26 is to ensure that
the needle guard 14 is moved to an extended positioned at all times other
than when it is intentionally latched in the retracted position.
Conveniently also, the needle guard is provided with a removable closure
cap 28, and, is provided with a frangible diaphragm 30 underlying the cap
28, the diaphragm 30 being puncturable by the needle 12 upon retraction of
the needle guard 14.
As more clearly illustrated in FIGS. 3 and 4, the needle guard 14 is formed
for it to be other than circular. As illustrated in FIG. 3, the needle
guard is formed elliptical in transverse cross-section, with the
projection 24 lying on the minor axis of the ellipse, and the major axis
extending perpendicularly thereto. The projection 24 can be received
within one of two retaining notches 20, 22 located at opposite axial ends.
of the slide track 18.
In an initial condition, the projection 24 extends radially inwardly into
locking engagement with the retaining notch 20, to hold the needle guard
immoveable relative to the syringe barrel.
As is illustrated in FIG. 4, the application of manual pressure along the
major axis of the needle guard 14 in the direction of the arrows P-P in
FIGS. 3 and 4 will cause movement of the projection 24 in a direction
radially outwardly of the axis of the syringe barrel 10, and out of
engagement within the retaining notch 20 in the needle barrel 10.
The needle guard 14 is at that time freed for movement axially of the
syringe barrel 10, this movement being guided by the projection 24 riding
within the axially extending groove 18.
Having reached the end of its permissible travel, the projection 24 snaps
into and then becomes engaged within the retaining notch 22 at the
opposite axial end of the slide track 18, to lock needle guard 14 in the
retracted position shown in FIG. 2.
This retraction is effected against the bias of the spring 26, in the event
that such a spring is provided. In the event that the user should release
the needle guard 14 prior to its being latched in a fully retracted
position, or, the user releases the projection 24 by again squeezing the
needle guard, then, the needle guard 14 will be returned to its initial
position as shown in FIG. 1.
The locking will proceed automatically due to the resilience of the needle
guard 14, which inherently will attempt to return to its elliptical
formation as illustrated in FIG. 3.
After use of the syringe, the needle guard 14 is unlocked in exactly the
same manner as that previously described. This unlocking, requires that
the syringe assembly be grasped by at least one of the users hands, and
effectively maintains the user's hands isolated from the needle 12, which
at that time is possibly contaminated.
An even more positive lock can be provided by providing circumferential
extensions of the slide track 18 at the opposite axial ends thereof, as
illustrated in FIGS. 5 and 6, in which the same reference numbers have
been used to identify parts in common with FIGS. 1 and 2. In FIGS. 5 and
6, a user is required to use both hands to retract or extend the needle
guard, this requiring relative rotational movements of the needle guard
and barrel prior to axial relative movement between those members.
As will be appreciated, various modifications in the structure illustrated
can be effected without departing from the scope of the invention as
defined in the appended claims. For example, if the needle 12 is a short
needle, then, the slide track 18 can be arranged as a scroll cam with
indentations at its respective opposite ends, such that rotation of the
needle guard relative to the barrel 10 after release of the projection 24
from the indentation 20 will automatically cause retraction of the needle
guard 14 against the bias of the spring 26, the spring 26 being available
to return the needle guard 14 to its extended position at any time prior
to locking of the needle guard in its retracted position. Further, as will
be readily appreciated, instead of being arranged such that a reverse
rotational movement of the needle-barrel is required to lock it, as in
FIGS. 5 and 6, the circumferentially extending portions at opposite ends
of the slide track 18 could be oppositely extending such that a first turn
is required to move the projection 24 into the groove 18, and, second turn
in the same direction is required to re-lock the needle guard when in its
retracted position, and vice versa.
The syringe could be supplied with the needle guard in a retracted position
and ready for use. After use, the needle guard can then be extended and
locked to provide safety to the user, in which event, and as illustrated
in FIG. 7, the projection 24 and the bottom wall of the axial groove 18
can be formed as ratchet teeth 50, which will permit movement of the
needle guard to an extended position, but, which will inhibit return
movement of the needle guard. This can readily be accomplished by making
the distance on major axis at the inner face of the needle guard just
sufficient to cause release of the projection 24 from the retaining notch
22, subsequent to which the projection 24 can be ratcheted over the rigid
teeth 52 of the syringe barrel, this being permitted by the resilience of
the material from which the needle guard is formed, and its ability to
stretch to a limited extent.
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