U.S. patent number 3,669,111 [Application Number 05/039,084] was granted by the patent office on 1972-06-13 for automatic retracting hypodermic syringe.
Invention is credited to Ben B. Dubner.
United States Patent |
3,669,111 |
Dubner |
June 13, 1972 |
AUTOMATIC RETRACTING HYPODERMIC SYRINGE
Abstract
In a hypodermic syringe, automatic retraction, achieved by
interposing resilient means between the barrel and the plunger.
Inventors: |
Dubner; Ben B. (New Hyde Park,
NY) |
Family
ID: |
21903578 |
Appl.
No.: |
05/039,084 |
Filed: |
May 20, 1970 |
Current U.S.
Class: |
604/229;
604/900 |
Current CPC
Class: |
A61M
5/3148 (20130101); A61M 5/31511 (20130101); A61M
5/31515 (20130101); A61M 5/31595 (20130101); A61M
2205/581 (20130101); A61M 5/31505 (20130101); Y10S
604/90 (20130101) |
Current International
Class: |
A61M
5/31 (20060101); A61M 5/315 (20060101); A61m
005/00 () |
Field of
Search: |
;128/218R,218P,218PA,218C,220,215,234 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
Primary Examiner: Mancene; Louis G.
Assistant Examiner: Weinhold; D. L.
Claims
As various changes might be made in the embodiments of the
invention herein disclosed, as well as other constructions
fabricated, without departing from the spirit and principles of the
invention, it is understood that all matter herein shown or
described shall be deemed illustrative, and not limiting except as
set forth in the appended claims, where what I claim as new and
desire to protect by Letters Patent is:
1. In a hypodermic syringe comprising a generally cylindrical
barrel and a plunger reciprocable in said barrel, the improvement
comprising: resilient means incorporated between said barrel and
said plunger to provide and transmit a force to move said plunger
axially in an outward direction for a limited distance; said
resilient means including a piston head of hollow configuration,
and capable of distortion in response to movement of said plunger
in an inward direction relative to an inner end of said barrel to
decrease the effective volume thereof, said piston head returning
to relatively unstressed condition upon the release of pressure
upon said plunger.
2. Structure in accordance with claim 1, including means for
attaching the plunger to the piston head; said means including a
projection from the inner heading of the plunger, which projection
gives rise to a circular collar, and, adjacently and displaced
downwardly, also gives rise to two opposing lugs, and where the
piston head is of a composite structure with components of varying
resiliency and thickness, including two headings with through
bores, the bore of the outer heading allowing its being forced over
the collar of the projection to make a liquid tight connection with
the plunger, the other heading having around its periphery sealing
rims for yielding liquid tight contact with the inner aspect of the
barrel, and same other heading having at its outer aspect a partial
slot extension of its bore, and immediately adjacent and displaced
downwardly and opening centrally into the bore, two opposing
notches, said notches receiving, when pressure upon the plunger
causes the projection to enter the bore, and upon subsequent
turning of the plunger, the lugs of the projection, to interlock
both headings of the piston head with the plungers; said headings
being connected by a circular bellows attached to the peripheral
areas of said headings.
3. A hypodermic syringe as defined in claim 2, wherein said piston
head is of a composite construction, with said components being of
different thicknesses of resilient material to vary the firmness
and resiliency of said components, and wherein the two opposing
headings are of a greater thickness than the connecting circular
bellows, and wherein said bellows is fabricated with such that
resilient force tends to maintain the opposing heads apart from
each other in relatively unstressed condition.
Description
My invention relates to a device commonly known in the medical arts
by the term "hypodermic" syringe, which is utilized either for the
introduction or withdrawal of materials to and from human and
animal bodies.
Proper and safe use of such syringes requires first, that air
within a syringe be expelled before the attached hollow needle is
inserted into a body, and second, that the position of the open end
of the needle be ascertained before material is injected.
Sometimes it is desirable that the opening be within a blood vessel
or other fluid containing areas. At other times, it is essential
that the needle point should not be within such vessels or areas,
but rather within other tissues, subcutaneously, or
intramuscularly.
Testing for the position of the needle opening merely requires a
pulling back, or retraction, of the plunger for a short distance
within the barrel of the syringe. This lowers the pressure within
the syringe, as well as providing space so that any fluids at the
needle tip will flow thru the needle and be seen within the barrel
of the syringe. In solid tissues no fluids will be visible.
Retraction should be done every time the position of the needle is
changed, whether it is for infiltration of a large area, or merely
to prevent a "pooling" when medication is deposited in one
area.
In the usual and customary syringes, retraction requires the use of
both hands, one to hold the barrel, and the other to pull back on
the plunger.
Because two hands are required, many physicians find this procedure
awkward and time consuming and therefore it frequently is not
performed, exposing a patient to unnecessary discomfort, and
danger.
It is known in the art for improvements to facilitate one handed
operation of syringes. One such improvement provides a grip for two
or more fingers attached to the barrel, with a grip for another
finger attached to the plunger.
Another improvement is a complete syringe like barrel and plunger
with an opening in said barrel to receive a pre packaged "carpule"
of medication, which is then punctured by a special two point ended
needle at one end, and griped by a clawlike device attached to the
plunger at the other end.
These, and other devices, have the disadvantage of being heavy and
difficult to manipulate. They also require sterilization after each
use. Further, prepackaging limits choice of medications, as well as
leading to waste of unused medication. Finally, they cannot be used
with the new, safe, and inexpensive disposable syringes.
A type of retractive aid that can be used with disposable syringes
teaches the attachment of a slide piece attached to the plunger,
and overriding the barrel. This slide piece is manipulated by the
thumb. This proves to be difficult to handle, especially on a small
syringe in the order of one to three cc., where the finger pushing
the slide runs into the fingers holding the barrel. In a large
syringe is is difficult to manipulate when the syringe is three
quarters or more full as the slide is pulled up to the end of the
syringe with the plunger. Further, a new technique using the thumb
axially must be evolved. Also, the slide becomes slippery to
manipulate when wet with body fluids.
It is therefore an object of this invention to provide a hypodermic
syringe which generally is of standard construction and use, and in
which retraction of the plunger can be achieved with the use of
only one hand.
Another object of the invention is to provide a hypodermic syringe,
the plunger of which automatically retracts when pressure on the
plunger is released.
Another object of the invention is to provide a hypodermic syringe
that will automatically retract with equal ease at any position of
the plunger within the barrel.
Another object of the invention is to provide a syringe which can
quickly and easily be adjusted to engage or disengage the automatic
retraction improvement.
Another object of the invention is to provide a syringe that
facilitates retraction, yet is light and easy to handle in the
conventional manner of applying pressure on the plunger.
Another object of the invention is to provide means of automatic
retraction simply and inexpensively enough to be used with
disposable syringes.
Another object of the invention is to provide means for one handed
automatic retraction that can be simply added to the conventional
hypodermic syringe.
Other objects and advantages together with the foregoing will be
apparent from a consideration of the following specifications and
drawings which disclose two embodiments constructed with the
principles of the present invention and in which:
FIG. 1 is a perspective view showing one embodiment of the
invention in place on a hypodermic syringe.
FIG. 2 is an enlarged perspective view of one embodiment of the
invention and the area of attachment to a hypodermic syringe.
FIG. 3 is a fragmentary cross section of one embodiment of the
invention, illustrating the extremes of motion of the
invention.
FIG. 4 is a cross section, the plane of which is indicated by the
line 4--4 in FIG. 3.
FIG. 5 is an exploded fragmentary perspective view showing a second
embodiment of the invention and a portion of the syringe
plunger.
FIG. 6 is an enlarged cross section view of the second embodiment
of the invention in a closed position.
FIG. 7 is a cross section view of the second embodiment of the
invention in an open position.
FIG. 8 is a cross section of the second embodiment, the plane of
which is indicated by the line 8--8.
In these embodiments, the syringe includes a generally circular
cylindrical barrel 10 made of any suitable material such as glass
or plastic, and which may be completely or semi transparent.
One end of the barrel 10 is provided with a connector 12 to receive
a standard hypodermic needle 14 in the usual way, while the other
end of the barrel 10 is provided with an outstanding terminal
flange 16 shaped so that it can act as a grip for fingers of the
users hand.
The barrel 10 is arranged to receive the plunger 18 which
reciprocates therein along the barrel's axis.
In one embodiment the plunger is a usual composite structure and
preferably includes a piston 20 which piston has a pair of sealing
rims 22 and 24 which make a movable liquid tight fit with the inner
aspect of the barrel. The piston 20 is joined to the plunger 18 by
means of a through bore (not shown) in the piston heading 22, which
bore is forced over a projection (not shown) of the plunger head
25.
The body of the plunger 18 is made up of radially arranged plates
26, 28, 30, and 32 which terminate in the heading 25 at one end,
and in a transverse disk heading 34 at the other end.
In accordance with the invention there is provided a shaped
resilient piece 36 to move the plunger 18 axially in an outward
direction for a short distance within the barrel 10. Said piece is
composed of a body 70, and two opposing shaped arms 38 and 40 that
arise from it. Said arms have distal edges 42 and 44 which have
sharp edges and contact with tension, edges of two of the radially
arranged plates of the plunger 18. The contacting distal edges 42
and 44 are centrally concave generally, with peripheral areas also
generally concave to facilitate easy engagement and maintenance of
the engagement of the edges 42 and 44 with plates of the plunger
18, as well their disengagement.
Altho the piece 36 and any of its essential parts may be integrally
part of the barrel 10 or of its flange 16, in this embodiment it is
attached by means of its grooved shaped body 70 which permits that
it be forced on to the flange 16 where it is maintained in position
by friction.
The piece 36 and its component parts are of a resilient material
which may plastic, metal, or wire.
Preferably, the edges of the radial plates 26,28,30 and 32 are
roughened for better engagement with the arms 38,40.
In use, the syringe would, preferably, be dispensed with the arms
38 and 40 disengaged from any of the radial plates of the plunger
18. Upon filling of the syringe and expelling of the trapped air,
injection is made, after which the plunger is turned to bring any
two of the radial plates 26,28,30,32 into engagement with the ends
of the arms 38 and 40. An initial manual retraction of the plunger
18 in conjunction with the turning of the plunger, will bring the
arms to positions 38A and 40A and the attached piston head to 20 A
as illustrated in FIG. 3. Then, inward pressure on the plunger 18
to expell material from the syringe will concumatly depress the
arms to positions illustrated as 38 B and 40 B, and the piston head
to 20B. In this position, because of the angle of the arms, tension
is increased so that upon cessation of the expelling pressure, the
resilient tension will move the plunger 18 axially within the
barrel in an outward direction, thus creating the necessary
lessened pressure, as well as space within the barrel 10, as the
piston head is moved to position 20 A.
When the plunger is pressed in an inward direction sufficiently to
cause the arms 38 and 40 to reach the extent of their range of
motion, or the flange 16, the resiliency of the arms will cause
them to give way to allow any further inward movement of the
plunger. The clicking of this movement caused by the action of the
edges of the arms 38 and 40 on the roughened edges of the radial
plates of the plunger will give an audial indication of the amounts
of fluids expelled into the body.
In the second embodiment, the means for providing automatic
retraction include a hypodermic syringe with customary rigid barrel
10, and plunger 18 reciprocal therein, said plunger having attached
an improved piston head 46.
The plunger 18 is a composite structure, including radially
arranged plates 26 to 32 which terminate in circular headings 25
and 34 at opposing ends. Arising from the inner heading 25 is a
circular projection 42. Disposed substantially adjacent and spaced
downwardly, is a circular collar 44 for attachment of the piston
head 46. Disposed adjacently, and spaced downwardly are two
opposing lugs 48 and 50.
The piston head 46, of a customary resilient material that can be
either rubber or plastic, is a composite structure with varying
degrees of firmness and resiliency achieved by varying the
thickness of each of the component parts. Said component parts
include the headings 52 and 54, and the connecting circular bellows
56, which is the thinnest component.
The bellows 56 are preferably fabricated in its extended position
as shown in FIG. 7 so there will always be a tension within it to
cause it to constantly seek this extended position. Other means,
not illustrated, but known in the art, may be incorporated to
augment this tension.
The piston heading 52 has a through bore 58 which is forced over
projection 42 and its circular collar 44 to achieve a liquid proof
attachment with the plunger 18.
The piston heading 54 has a through bore 60 which is aligned with
the projection 42. Centrally disposed and opening into the bore 60
are two opposing notches 66 and 68 for reception of lugs 48 and 50.
Disposed adjacently and spaced upwardly, the bore 60 is elongated
at right angles to the notches 66 and 68 to form a slot 62, 64
which easily permits the entrance of the projection 42 and its lugs
48 and 50 into the bore 60 without interference or interlocking. In
this position, turning of the plunger 18 will turn the lugs 48 and
50 into the notches 66 and 68 and thus effectively interlock the
headings 52 and 54 with the projection 42 which unites the plunger
18 and the piston 46 so that they then function as one piece.
Preferably the syringe will be dispensed with the plunger
interlocked as illustrated in FIG. 6, to facilitate withdrawing of
material into the syringe, expelling of the air, and injection of
the needle into the body.
After injection, the plunger 18 is turned to bring the lugs 48 and
50 into alignment with the slot 62,64. In this unlocked position,
cessation of pressure on the plunger will release the tension of
the bellows 56 and allow it to extend pulling the projection 42 out
of the bore 60 and permitting any liquid at the needle end to flow
back into the syringe as illustrated in FIG. 7. To further expel
material into the body, pressure is resumed on the plunger 18. As
long as there is no turning of the plunger, it will be free to
retract at any time pressure on it is relieved .
* * * * *