US3143109A - Blood drawing device - Google Patents

Description

Aug. 4, 1964 H. R. GEWERTZ BLOOD DRAWING DEVICE 2 Sheets-Sheet 1 Filed Feb. 12. 1962 TEST II VVENTOR. HARRY GEWERTZ ATTORNEY Aug. 1964 H. R. GEWERTZ 3,143,109

BLOOD DRAWING DEVICE Filed Feb- 12, 1962 2 Sheets-Sheet 2 INVENTOR. v HARRY GEWERTZ ATTORNEY United States Patent 3,143,109 BLUGD DRAWING DEVICE Harry R. Gewertz, Sea Cliff, N.Y., assignor, by mesne assignments, to Raytheon Company, a corporation of Delaware Filed Feb. 12, 1962, Ser. No. 172,403 2 Claims. (Cl. 1282) This invention relates to blood receptacles and in particular relates to disposable hypodermic syringes in combination with a vacuum blood receptacle attached thereto for receiving blood specimens and similar fluid items under vacuum conditions.

In the field of medicine whenever blood is required to be extracted from the human body, a cannula type hypodermic needle is first injected into some portion of the anatomy, human or otherwise, where blood or fluid will flow freely and/ or is easily extracted. In general, this blood removal or aspiration is accomplished by producing a partial vacuum after injection by drawing up on a plunger type piston rod within the blood vial which, because of the compact arrangement between plunger and wall causes a vacuum effect. After sufiicient blood has been withdrawn, the needle is then also withdrawn. If insuflicient blood is at first extracted another injectable device is required and the process repeated. In such a process the flow velocity of the blood depends upon the vacuum created and where insuflicient blood is withdrawn, the patient is again subjected to the uncomfortable feeling of being injected.

In the present invention it is one of the principal objects to provide a hypodermic syringe and blood receptacle assembly which is simple, eflicient, rugged and inexpensive.

Another object of the invention is to provide a hypodermic syringe and blood receptacle assembly which requires but a single injection or penetration regardless of the number of blood samples taken or required.

A still further object of the invention is to provide a hypodermic syringe and blood receptacle having a prearranged vacuum within the receptacle to facilitate and speed up the process of blood removal from the body and a readily identifiable means for testing vacuum conditions.

A still further object of the invention is to provide a hypodermic syringe and blood receptacle assembly havlng no moving plunger or rod or manually moving parts for producing a vacuum and/or otherwise for the removal of blood or fluid.

Other objects and advantages will become apparent from a reading of the specification and a study of the accompanying drawings in which:

FIG. 1 shows an axial sectional View of the hypodermic syringe and blood receptacle assembly according to the invention;

FIG. 2 shows a perspective and partially exploded view of the hypodermic syringe and valve body assembly;

FIG. 3 shows a perspective and partially sectioned view of the valve;

FIG. 4 is a fragmentary sectional view of a portion of the valve and valve body in section with the valve in test position for testing the vacuum of the receptacle;

FIG. 5 is a view similar to FIG. 4 showing the valve in the operating position to permit the free flow of fluid or blood to the receptable;

FIG. 6 is an enlarged axial sectional view of the valve body and cannula hub assembly according to another embodiment of the invention; and

FIG. 7 is a view similar to FIG. 6 showing a variation of the cannula hub assembly.

Now referring to the drawings where similar parts will be identified with the same reference numbers, and

3,143,109 Patented Aug. 4., 1964 particularly to FIG. 1, there is shown therein a sectional view of the disposable hypodermic syringe and blood receptacle assembly according to the invention. In particular there is shown ablood receptacle 10 made preferably of glass, plastic or the like, sealed at one end 11 and having a flaredopening 12 at the other end to which is attached thevalve body 13. Thevalve body 13 is preferably made of solid rubber, plastic or some other suitable non-porous material having slightly elastic properties. The valve body is generally cylindrically shaped but is coned shaped at itslower extremity 14 with its. upper extremity having an annular recessedportion 15 encircled by an upwardly and inwardly extending spaced flangedportion 16 disposed to snugly engage and fixedly hold the flaredportion 12 ofbottle 10. Thevalve body 13 has its upper-most portion cylindrically shaped and disposed to snugly fit into the lower open end portion of the blood bottle to create an air-tight, water-tight seal between bottle and valve body.

Thevalve body 13 is further disposed to have radially along the conicallower portion 14 thereof a pair of oppositely disposedtrack members 15 and 16 each forming equal arcs of a circle and attached to the said conical shaped member to receive in fixed relation a cannula coneshaped hub assembly 20. In particular, thecannula hub assembly 20 comprises a conicallyshaped cannula hub 21 having internally a conical recess at its upper extremity, such recess being disposed to snugly receive the lower portion of thevalve body 13. Thecannula hub 21 is further disposed to have at the upper extremity thereof a pair of oppositely disposed and upwardly extendingflange members 22 and 22a each forming segments of a circle and each having araceway 23 and 23a respectively along the inner periphery for receiving thetrack members 15 and 16 of the valve' body in fixed and locked position. Thevalve body 13 may be rotated with respect to thecannula hub 21 so as to cause thetrack members 15 and 16 to become disengaged from the raceways so that under these conditions the cannula hub can be removed and/or otherwise disengaged from the valve bod There is further shown within thevalve body 13 of FIG. 1 a tunnel orpassageway 25 which extends from the top of thevalve body 17 to thelower-most portion 17a, the said passageway communicating with thepassageway 26 extending longitudinally of thecannula hub 21 and within which is mounted acannula 26a, so that when the cannula hub andvalve body 13 are attached to each other they will form a single unitary member, known as the vacuum blood receptacle. There is further shown in thevalve body 13 anotherpassageway 30 extending from the upper-most portion thereof to apoint 30a intermediate the said upper portion and terminating in a passageway 31 extending transversely the direction of thepassageway 30.

The passageway 31 extending transversely thevalve body 13 is disposed to snugly receive avalve member 35, the valve member being free to move, when urged, along the passageway 31 according to the type of operation contemplated. The valve itself is composed of anelongated body member 36 having at one extremity an enlargedcylindrical base 37 and approximately midway a pair of spaced axially alignedannular recesses 38 and 39. The said valve body member is further disposed to have extending axially apassageway 42 extending through thesaid base 37 and terminating at the other extremity thereof in alarger passageway 43 which communicates with thepassageway 42. The upper enlargedpassageway 43 is further disposed to receive avalve cap 44 having a cylindrical stem 45 capable of fitting into thepassageway 43, and an enlargedflange 46 so as to permit closure of the valve body. Thecap 44 is thus permitted transverse movement with thevalve body 35 for operational purposes. Asmall porthole 47 extends transversely from thepassageway 42 to theannular recess 39 and communicates with both to permit the free flow of air or any other fluid media between them.

As previously mentioned in the objects herein, one of the primary purposes of the invention is to provide a blood receptacle assembly having a vacuum within the blood chamber or receptacle so as to readily permit the free flow of fluid or blood from the patient into the blood chamber without the necessity for manipulating a plunger or plunger handle which previously formed a part of blood receptacles. The vacuum herein is achieved by standard ordinary techniques and need not be shown or described in detail herein, but sulfice it to say that one does exist. Assuming now that there is available the necessary vacuum, FIGS. 4 and 5 show what procedure is required to obtain blood specimens. In particular, there is shown in FIG. 4 the valve body in the test position, this being the position whereby theannular recess 39 of the valve body, and the passageway ortest port 30 are in complete alignment. This permits the free flow of air into the tube chamber. In this situation air will traverse a path comprised of thepassageway 30 and terminate in and impinge upon adistensible diaphragm 40 which is attached over the upper extremity of thepassageway 30. Under these conditions, thediaphragm 40 will be subjected to atmospheric pressure and will become distended, but will not rupture. This is a visual check to determine if a vacuum is still present in the blood chamber. If the diaphragm does not distend, but remains constant, it would then be an indication that the vacuum was not present or was otherwise destroyed. Since it is contemplated that the blood receptacle will be stored before using, the length of storage being undetermined, there is always a possibility that the vacuum will be destroyed or otherwise become deteriorated, hence the reason for this testing procedure. FIG. 5 shows the operating position of the valve when aspiration is to take place on the patient. Essentially the needle is injected into the patient, then the valve body placed in the position as shown in FIG. 5 with thepassageway 25 aligned with theannular recess 38, so as to have both in complete alignment and communicating with each other to allow for the free flow of the fluid media such as blood. After the blood has been aspirated, the valve body may then be moved so as to block the passageway for the free flow of blood and the complete blood chamber or bottle assembly removed from the patient. However, in the alternative, if additional blood samples are required, the needle assembly is permitted to remain in the patient and the blood bottle removed by rotating the valve body with respect to the cannula hub in such a direction as to permit the tracks attached to the valve body to become disengaged from the raceways which are attached to and form a part of the cannula hub. After removal of the blood bottle, the procedure is repeated by slipping another blood bottle into the cannula hub and merely rotating same so as to permit the tracks attached thereto to again engage the raceways which form an integral part of the cannula hub. This action permits a positive locking action between the hub and receptacle so as to permit the process to take place again for the extraction of further samples of blood.

There is now shown in FIG. 6 another embodiment of the invention and in particular there is shown a needle and receptacle assembly comprising a valve body 5% having avalve 51 attached thereto and forming a part thereof and acannula hub 53 disposed to combine with the valve body so as to form a single complete unitary structure therewith. Thevalve body 50 in particular is a generally cylindrically shaped body having its lower extremity partially recessed, the saidrecess 51a being defined by a downwardly extending circumferential flange 52 and an inner concentrically located tapered hub 53a extending axially downward beyond the termination of the said errcumferential flange, the said hub having anaxial bore 54 extending from itslower mostportion 55 and terminating in acylindrical bore 56 extending tranversely completely across the valve body member. Thetransverse bore 56 has one extremity thereof 56a countersunk and is further disposed to receive thevalve 55, the said valve being freely movable within the said bore when used by some external force. In particular, the valve consists of a cylindrical member 57 having peripheral rings 57a and 58, the said rings defining a series of annular shapedpassageways 62 and 60. Thevalve bore 56 is so arranged as to receive a pair of valve caps or stems at opposing ends to permit the free movement of the valve by manual means. Theupper portion 61a of the valve body is cylindrical in shape and is provided with a partially tapered outer wall 61b having spacedcorrugated type ridges 61c for engaging internally any receptacles, bottles, containers or otherwise (not shown) where placed thereover and to fixedly retain same to keep them from freely moving and to also provide a seal-tight arrangement therewith. There is further provided in the upper portion of the valve body member a pair of longitudinally extending ports orpassageways 59 and 63, thefirst passageway 59 being relatively short to permit the access or free flow of fluid, whereas theother port 63 is relatively longer and has attached thereto at its upper extremity a small elastic type water and airproof bag for permitting passage of air therein under vacuum conditions as previously described. In testing for vacuum conditions, the valve is displaced in a direction so as to permitpassageway 60 to communicate withport 63, air then being available so as to permit its access via the countersunk portion 56a of thebore 56,passageway 60, andport 63, thus allowing the bag to become inflated. For the reception of blood, thevalve 55 is displaced in the opposite direction to that for test purposes, so as toallow the blood to flow through thebore 54 of thehub 53, thepassageway 62, and theblood port 59 as heretofore described.

Thecannula hub 53 is generally conical in shape and is provided with a lower dependingcylindrical stem 65 having anaxial bore 66 terminating at one extremity in and communicating with an upper tapered bore 67 which extends axially the length of acylindrical hub 68 forming an integral part of thecannula hub 53. The tapered bore 67 is so arranged as to engage the tapered hub 53a of the valve body to form a snug immovable unitary structure. Acannula member 68 is mounted within the cannula hub structure along thebore portions 66 and 67 thereof, and extends upwardly and beyond and into the bore of the tapered hub forming a part of the valve body.

FIG. 7 shows a needle and bottle assembly which is similar in construction and design to the assembly shown in FIG. 6 but differs therefrom in that thestem 65 is now placed within thebore 67 to provide sturdier support means for the cannula. The cannula is pressed or force fit within the stem orferrule 65 so that the cannula will be firmly fixed therein.

Having described the invention, what is claimed is:

l. A blood drawing device comprising a receptacle having an open end,

a valve body sealed at one end to the open end of the receptacle and extending outwardly therefrom,

means at the other end of the valve body for receiving and supporting a hollow needle,

a first passageway extending longitudinally of the valve body, said passageway communicating with said means at one end and with the receptacle at the other end,

valve means in said valve body comprising a trans Versely movable cylinder having a body portion intercepting said first passageway when the valve is located in a first position, said body portion having a port therein which provides continuation of the passageway when the valve is located in a second position for permitting uninterrupted flow of blood from the needle into the receptacle,

a second passageway extending longitudinally of the valve body in spaced relation to the first passageway and communicating at opposite ends with the valve cylinder and receptacle,

a second port in said body portion of the valve located in spaced relation to said first port and in communication with said second passageway when the valve is in said first position,

a distensible member covering the receptacle end of the second passageway, and a bore in the valve connecting said second port with atmosphere external of the device. 2. A blood drawing device comprising a receptacle having an open end,

a valve body sealed at one end to the open end of the receptacle and extending outwardly therefrom,

means at the other end of the valve body for receiving and supporting a hollow needle,

a first passageway extending longitudinally of the valve body, said passageway communicating with said means at one end and with the receptacle at the other end,

a second passageway extending longitudinally of the valve body in spaced relation to the first passageway,

valve. means in said valve body for selectively permitting flow of blood through said first passageway or external gas through said second passageway, said through the body intercepting said first passageway and terminating one end of the second passageway, and a cylinder located within and slidable longitudinally of the bore, said cylinder having a pair of spaced ports therein and being movable to a first position wherein said second passageway is blocked and one of said ports provides continuation of the first passageway for uninterrupted flow of blood from said first means to the receptacle, said cylinder further having an opening therein connecting said second port with gas external of the device and being movable to a second position wherein said first passageway is blocked and the second of said ports provides communication between the second passageway and the opening in the cylinder, and a distensible member covering the receptacle end of the second passageway.

Reterenees Cited in the file of this patent UNITED STATES PATENTS

Claims (1)

1. A BLOOD DRAWING DEVICE COMPRISING A RECEPTACLE HAVING AN OPEN END, A VALVE BODY SEALED AT ONE END TO THE OPEN END OF THE RECEPTACLE AND EXTENDING OUTWARDLY THEREFROM, MEANS AT THE OTHER END OF THE VALVE BODY FOR RECEIVING AND SUPPORTING A HOLLOW NEEDLE, A FIRST PASSAGEWAY EXTENDING LONGITUDINALLY OF THE VALVE BODY, SAID PASSAGEWAY COMMUNICATING WITH SAID MEANS AT ONE END AND WITH THE RECEPTACLE AT THE OTHER END, VALVE MEANS IN SAID VALVE BODY COMPRISING A TRANSVERSELY MOVABLE CYLINDER HAVING A BODY PORTION INTERCEPTING SAID FIRST PASSAGEWAY WHEN THE VALVE IS LOCATED IN A FIRST POSITION, SAID BODY PORTION HAVING A PORT THEREIN WHICH PROVIDES CONTINUATION OF THE PASSAGEWAY WHEN THE VALVE IS LOCATED IN A SECOND POSITION FOR PERMITTING UNINTERRUPTED FLOW OF BLOOD FROM THE NEEDLE INTO THE RECEPTACLE, A SECOND PASSAGEWAY EXTENDING LONGITUDINALLY OF THE VALVE BODY IN SPACED RELATION TO THE FIRST PASSAGEWAY AND COMMUNICATING AT OPPOSITE ENDS WITH THE VALVE CYLINDER AND RECEPTACLE, A SECOND PORT IN SAID BODY PORTION OF THE VALVE LOCATED IN SPACED RELATION TO SAID FIRST PORT AND IN COMMUNICATION WITH SAID SECOND PASSAGEWAY WHEN THE VALVE IS IN SAID FIRST POSITION, A DISTENSIBLE MEMBER COVERING THE RECEPTACLE END OF THE SECOND PASSAGEWAY, AND A BORE IN THE VALVE CONNECTING SAID SECOND PORT WITH ATMOSPHERE EXTERNAL OF THE DEVICE.

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