Australian Patents Act 1990 - Regulation 3.2A ORIGINAL COMPLETE SPECIFICATION STANDARD PATENT Invention Title "IV Catheter" The following statement is a full description of this invention, including the best method of performing it known to me/us: P/00/00 I C:\NRPornbl\DCC\TZS\4757383_ I.DOC - 21/1 1/12 C:WRPonbl\DCCTZS757125_.DOC-2NIl/21 2 IV CATHETER The disclosure of the complete specification of Australian Patent Application No. 2009233612 as originally filed is incorporated herein by reference. The invention relates to a safety needle assembly which can form part of a safety 5 intravenous (IV) catheter device. Safety IV catheter devices comprise a needle protecting means which slides to the needle point as the needle is removed from the catheter and permanently blocks the needle point such that the needle point cannot be inserted into objects or persons. A safety intravenous catheter device is disclosed in International application WO 10 99/08 742 by the present applicant. Said catheter device comprises a tubular catheter having a catheter hub at the proximal end, a hollow needle adapted to be inserted into the catheter and provided with a needle hub at the proximal end, and a needle protecting means. The needle protecting means is located in a hollow space of the catheter hub, the hollow space being closed by the needle hub, 15 wherein the needle passes through the needle protecting means and the needle protecting means comprises a spring portion made of steel through which the needle is adapted to slide. The needle protecting means comprises an engagement element which, when the needle is retracted relatively to the catheter, engages with an irregularly configured portion of the needle in order to remove the 20 needle protecting means from the proximal end of the catheter hub. The needle protecting means comprises a bent sheet-metal portion made from spring steel which presses against the wall of the hollow space of the catheter hub, the sheet-metal portion thus being supported. Said support is no longer given when the needle protecting means is moved over the needle point when the needle is 25 retracted, the needle protecting means thus being protected. Then the needle protecting means, together with the needle, can be removed from the hollow space of the catheter hub. In the case of the known catheter device the projection, with which the needle protecting means lockingly engages, is configured as a retaining protrusion molded to the inner wall of the catheter hub, or a retaining 30 groove.
C:\NRorbl\DCOTZSW?$7125_I.DOC-22012 2 A catheter device of this type protecting means poses the problem that the needle protecting means must be fastened in the catheter hub, with a bend or an elbow of the needle protecting means having to be moved over the projection on the inner side of the catheter hub, such that a reliable support of the needle protecting 5 means in the hollow space of the catheter hub is ensured. It is an object of the present invention to provide an intravenous catheter device comprising a needle protecting means where fastening of the needle protecting means in the catheter hub is facilitated. 10 According to the invention, there is provided an IV catheter apparatus including a tubular catheter having a proximal end and a distal end, a needle having a needle shaft and a tip and wherein the needle is attached to a distal end of a needle hub, said needle being received within said tubular catheter when the needle is in a ready position, a catheter hub attached to the proximal end of said catheter, said 15 catheter hub having a hollow interior and an inner wall, said needle being movable between said ready position in which said tip is outside of said catheter hub and a retracted position in which said tip is within the interior of said catheter hub, a needle guard positioned in the interior of said catheter hub in a spaced apart relationship from the distal end of the needle hub; wherein the needle guard 20 has a resilient portion engaged by said needle shaft when said needle is in its ready position, the needle guard resilient portion is movable within the interior of said catheter hub to a blocking position distal of said needle tip when said needle is in its retracted position in which said needle shaft no longer exerts a force on said resilient portion of said needle guard; wherein an outer contact surface on 25 the needle guard is secured to a groove formed in the catheter hub hollow interior when the resilient portion is engaged by the side of the needle shaft and biased radially outwardly; and wherein the needle guard further includes a needle guard proximal end, wherein the needle guard is secured to the needle tip when the needle is in the fully retracted position by a portion of the needle guard proximal 30 end making contact with a needle crimp and the resilient portion blocking the needle tip.
C:\NRPonbl\DCCTZS\4757125 .. DOC-20/1V/20i 2 3 Fig. 1 shows a longitudinal section across a first embodiment of an intravenous catheter device, Fig. 2 shows the distal end of the needle with the needle protecting means protecting the needle point when the needle has been removed from the catheter, 5 Fig. 3 shows a section along line Ill-Ill of Fig. 1, Fig. 4 shows a similar representation as Fig. 3 of a second embodiment having an essentially annular projection with a small interruption, Fig. 5 shows a section across a third embodiment with a bipartite annular projection whose segments are separated from each other by two interruptions, 10 Fig. 6 shows a schematic side view of the distal area of the needle shown in Fig. 1, Fig. 7 shows a view of the needle shown in Fig. 6 as seen from the direction indicated by arrow VII, Fig. 8 shows a perspective representation of a tool for fastening the needle 15 protecting means, Fig. 9 shows a schematic cross-section of another embodiment of the catheter with the needle protecting means being oriented such that it can be inserted into the hollow space of the catheter hub, and Fig. 10 shows by way of the same representation as Fig. 9 the condition of the 20 needle protecting means after a rotation by approximately 450 with the needle protecting means gripping behind the segments of the projection and being in engagement with the projection. The embodiment of the present invention shown in Fig. 1 comprises an elongate hollow tubular catheter 24 concentrically connected at its proximal end (remote 25 from the patient) with the distal end of a catheter hub 26. The catheter hub 26 has C.WRPo1l\CC\TZSW757125. .DOC-2Wil1/20124 a hollow space 27 communicating with the volume of the catheter 24 and being open at the proximal end. The needle 16 passes through the catheter 24. The needle 16 is an elongate hollow needle made of steel and comprising a needle point 18 at the distal end. At 5 a certain distance from the distal end 18 an irregularly configured portion 138 is provided. In the present embodiment said irregularly configured portion 138 is a flattened section of the needle which increases the width of the needle in one direction and decreases it in the direction perpendicular thereto. Said irregularly configured portion 138 can alternatively be a local projection. 10 At the proximal end of the needle 16 a needle hub 12 is attached which has a hollow space 13 communicating with the volume of the needle. The distal step in said needle hub 12 abuts the proximal end of said catheter hub 26. In this position of the needle hub 12 relative to the catheter hub 26 the distal end of the needle 16 and the needle point 18 project from the distal end of the catheter 24. 15 On the needle point 18 a needle protecting means 120 is provided which is configured generally in the same way as the needle protecting means shown and described in Figs. 10A, 10B and 11 of WO 99/08 742. However, the needle protecting means may also be of different configuration and numerous configurations are suggested by the prior art. In particular the needle protecting 20 means needs not comprise any clamping means for clamping the needle in the locked position. The needle protecting means 120 which is shown in the ready condition in Fig. 1 and in the protecting condition in Fig. 2 is an integral part made of spring steel. It comprises a rear wall 126 extending transversely to the needle 16 and containing 25 an opening. Said opening forms the engagement element 127 engaging with the irregularly configured portion 138 of the needle 16. Said opening or engagement element 127 is dimensioned such that it can be freely shifted on the needle 16 but cannot pass the irregularly configured portion 138. Consequently, the rear wall is C:WRPorbl\DCC\TZSX457125_-DOC.2fVI 112n[2 5 shiftable in the area between the irregularly configured portion 138 and the needle hub 12. From the ends of the rear wall 126 of the needle protecting means 120 arms 122 and 124 project which are generally oriented in distal direction and cross each 5 other, with each arm 122,124 being located on a different side of the needle 16. At the end of each arm 122,124 an end wall 129,130 is arranged orthogonally to the arm. At the transition between the arm and the end wall a bend 128 or elbow oriented towards the outside is located. At the free end of the front wall 129 and 130, respectively, a lip 132 bent by more than 900 is provided. The arm 122 is 10 shorter than the other arm 124 such that the front walls 129,130 do not collide with each other in the protected condition of the needle protecting means. The front walls 129 and 130 are wider than the arms 122,124 such that, in said protecting condition, they can cover the needle point 18 and protect it against contact with other parts or bodies. 15 The needle protecting means 120 is retained in the catheter hub 26. For this purpose an annular projection 136a extending about the inner wall of the catheter hub 26 is provided. While the lips 132 press against the outer wall of the needle 16 from opposite sides (Fig. 1), the bends 128 grip behind the projection 136a. When the needle 16 is removed from the catheter 24 the needle protecting means 120 is 20 retained in the catheter hub 26 such that the needle 16 slides through the catheter hub. When the needle point passes the lips 132 the arms 122,124 resiliently move into the position shown in Fig. 2 in which the front walls 129,130 cover the needle point. In this condition the engagement element 127 abuts the irregularly configured portion 138 such that the needle protecting means 120 is prevented 25 from sliding beyond the distal end of the needle 16. In the embodiment shown in Fig. 1 the projection 136a is of completely round and continuous configuration. The annular projection 136a retains the needle protecting means 120 in the catheter hub 26 when the needle 16 is removed from the catheter hub 26 until the arms 122,124 of the needle protecting means 120 are no longer supported by the 30 needle 16 and resiliently move towards the inside. Here, the projection 136 is integrally molded to the catheter hub 26, e. g. by injection molding.
C\NRPonbl\DCCTZSM1571 251 DOC-21VI 112012 6 In the embodiment shown in Fig. 4 the projection 136b oriented towards the inside is of generally C-shaped configuration. Said C-shaped projection 136b can be made from a metal snap ring partially seated in an annular groove on the inside of the catheter hub. In this way it is possible to produce the projection 136b by 5 inserting the snap ring into the catheter hub 26 until it lockingly engages the corresponding groove. Fig. 5 shows another alternative where the projection 136c is divided into two segments with intermediate interruptions 137. Each segment has a larger circumferential extension than the intermediate interruptions 137. Further, the 10 circumferential extension is considerably larger than the width of the distal front walls 129,130 of the needle protecting means. Preferably, the generally annular projection projecting towards the inside does not have any interruptions 137 whose width is larger than the width of the distal front walls 129 and 130, respectively, of the needle protecting means. The interruptions 137 being 15 dimensioned such that they are smaller than the width of the front walls prevents the needle protecting means 120 from unintentionally passing the interruptions 137 thus sliding out of the catheter hub without covering the needle point. According to the present invention any number of separate segments forming a generally annular projection may be provided as long as the needle protecting 20 means 120 is securely retained in the catheter hub when the needle 16 is removed from the catheter 24. As shown in Figs. 6 and 7 the irregularly configured portion 138 of the needle 16 is preferably produced by deformation, with two bulges 138a oriented in opposite directions and at right angles thereto two dents 138b also located opposite each 25 other being produced. The bulges 138a have a width W which is small enough to allow the needle 16 to move in the catheter 24 as shown in Fig. 1, but which is too large to pass the opening forming the engagement element 127 in the basis wall 126 of the needle protecting means 120. The catheter device according to Fig. 1 is assembled by pushing the needle 30 protecting means 120 over the point 18 of the needle 16 before the irregularly C:\NRPonbl\DCCTZSM4757123_.DOC-2IVI l2012 7 configured portion 138 is produced on the needle. The needle 16 then passes the engagement element 134 which is an opening in the basis wall 126 of the needle protecting means 120. The distal arms 132 are pressed apart and the needle 16 passes between them. Then the irregularly configured portion 138 is produced on 5 the needle 16 such that the needle protecting means 120 is captured between the irregularly configured portion 138 and the needle hub. Then the needle 16 and the needle protecting means 120 located thereupon are inserted into the catheter hub 26 such that the acute needle point 18 enters the catheter 24. The needle 16 is inserted into the catheter 24 to such an 5 extent that 10 the bends 128 of the needle protecting means abut the projection 136a. When the bends 128 abut the annular projection 136a the advance movement of the needle protecting means is stopped. This advance movement may also 10 be stopped earlier since the inner wall of the catheter hub 26 tapers such that the needle protecting means 120 is compressed during its advance movement. If the 15 needle protecting means 120 cannot be advanced, a tool is used for advancing the needle protecting means 120 further into the catheter hub 26 until the bends 128 of the needle protecting means 120 lockingly engage with the projection 136a. For this purpose an adequate force must be exerted by the tool on the needle protecting means 120 such that the bends 128 resiliently move towards each other 20 to move over the projection 136a. Then they move towards the outside again and press against the inner wall of the catheter hub 26. The needle protecting means 120 is now in the ready position as 20 shown in Fig. 1. The tool for inserting the needle protecting means may have any suitable form. Preferably, the tool shown in Fig. 8 is used which comprises a simple pin 200 25 having a longitudinal slot 202 extending over the overall length. The tool 200 can accommodate the needle 16 in said slot 202 while advancing the needle protecting means 120. The annular projection 136a retains the needle protecting means 120 when the needle is retracted until the lips 132 of the needle protecting means 120 lockingly C NRPonbI\DCC\TZS\47571251 DOC-2WVl 1/2012 8 engage with the needle point such that the bends 128 work free from the annular projection 136a and the needle protecting means, together with the needle 16, can be removed from the catheter hub 26. An alternative method of assembling the intravenous catheter comprising a spring 5 clip according to the present invention is realized by employing the embodiment shown in Fig. 4 where the projection 136b is an open snap ring. In this case the open snap ring can be slipped onto the needle protecting means such that it is positioned between the proximal end and the distal end of the needle protecting means. Prior to this the needle protecting means 120 has been slipped onto the 10 needle 16 which is then deformed to produce the irregularly configured portion 138. Thereafter the needle protecting means 120 and the open ring 136b are simultaneously inserted into the catheter hub 26 by means of the same tool. Said tool preferably comprises two fingers each of which extends along one side of the needle protecting means 120. Using these fingers the open ring 136b is 15 pushed further into the catheter hub than the proximal end of the needle protecting means 120. Thus it is not necessary to push the needle protecting means 120 over the annular projection 136b. On the contrary, the needle protecting means 120 and the annular projection 136b are inserted together. Thus the annular projection 136b is inserted into the catheter hub 26 such that the needle protecting 20 means 120 lockingly engages with said lockingly annular projection 136b and remains in that condition until the needle 16 is retracted. Figs. 9 and 10 show another embodiment of the device, which allows a different fastening method. Here, the annular projection 136d is configured such that it comprises at least 4 interruptions 137 between the segments, with the corners 250 25 of the needle protecting means 120a being adapted to be pushed through the interruptions 137 at a low force or no force at all. When the needle protecting means 120a has been inserted into the catheter hub 26 until it is positioned behind the projection 136d, the needle protecting means 120a is rotated such that the four corners 250 are positioned behind the segments of the projection 136d as shown C:NRPonblWCC\TZS\4757 1251 DOC-2111/20 12 9 in Fig. 10. Thus the needle protecting means 120a is retained in the catheter hub 26 until the needle 16 is retracted. It may be appropriate to configure the needle protecting means 120 such that it has a generally square profile, as shown in Figs. 9 and 10, but other rectangular or 5 polygonal contours of the needle protecting means 120a are also suitable. It is merely necessary to arrange the interruptions 137 of the projection 136d such that the needle protecting means 120 can be easily pushed through said interruptions 137 and then lockingly engages with the projection 136d when the needle protecting means 120a has been rotated such that the corners 250 abut the 10 segments of the projection 136d. Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or 15 group of integers or steps. The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as an acknowledgment or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general 20 knowledge in the field of endeavour to which this specification relates.