1. Field of the Invention
The present invention relates to an improved safety needle for use with a syringe and accessories therefor.
2. Description of the Related Art
In the medical industry, injection devices such as syringes and needles are used everyday. Safety precautions should be taken to prevent the user, phlebotomist, nurse, doctor, or medical technician from being stuck with a used needle and potentially transferring blood-related diseases. Further, precautions must be taken to eliminate use of the same needle more than one time.
The prior art has provided safety needles which include a slidable sleeve positioned in surrounding relationship of the needle such as those described in U.S. Pat. Nos. 4,813,940 and 5,104,384, assigned to the assignee of the present invention. A sleeve covers the shaft of the needle, with the sharp needle tip exposed prior to use. As the needle is inserted into the patient, the sleeve makes contact with the patient and retracts into the safety needle casing against the bias of a spring. As the needle is removed from the patient, the sleeve remains in contact with the patient until the needle is completely removed and then the sleeve returns to its fully extended position, covering the used tip of the needle. The end of the sleeve is generally tapered toward an opening having a diameter small enough to prevent a person from contacting with the needle with a finger for example. Once the sleeve is in the fully extended position after use of the syringe, the safety needle is provided with means for locking the sleeve in that position.
One particular prior art means for locking the sleeve position after use of the safety needle includes a collar mounted in the safety needle casing. The sleeve is provided with a projection that engages a track formed in the collar. As the sleeve moves into the casing, the projection follows the pathway defined by the track such that, as the sleeve returns to its extended position, the projection is directed into a locking mechanism. Once the projection is received in the locking mechanism, the sleeve is prevented from retracting and exposing the used needle.
A problem with this method of locking the extended position of the sleeve is that, after use of the device, the track and the locking mechanism formed in the collar are fragile and may easily be damaged to allow the sleeve to retract and to again expose the needle. Further, due to the small size of the safety needle, there are difficulties molding the collar. The safety needle may also be difficult to assemble due to the small and fragile nature of the parts.
It is desired to provide a safety needle having a more robust design with an improved method of locking the slidable sleeve in an extended position.
The present invention provides a safety needle for use with a syringe having a sleeve for preventing use of or being stuck with a used needle.
The present invention includes a casing in which a needle for use, for instance, with a hypodermic syringe or phlebotomy device is mounted. A sleeve is slidably mounted in the casing. The sleeve is biased by a spring into a partially extended position in which the sharp end of the needle is exposed, but the main shaft of the needle is encased by the sleeve. As the needle is inserted into a patient, the end of the sleeve makes contact with the patient. The sleeve retracts against the bias of the spring into the casing and remains in contact with the patient while the needle is being inserted, thus preventing exposure of the needle. When the needle is removed, the sleeve returns to a fully extended position, covering the contaminated needle tip, and, by operation of a locking mechanism, locks into place, thus preventing contact with the used needle and reuse of the needle.
The sleeve is provided with a plurality of fingers, at least one of which has a projection formed thereon. The projection engages a track system integrally formed in the inner wall of the safety needle casing. The projection is received in a recessed cavity formed in the casing wall in the initial position of the sleeve. As the sleeve retracts, the projection travels into a longitudinal passageway formed in the wall. When the needle is removed from the patient, the sleeve extends with the projection passing through the passageway. The projection is directed by a cam profile formed in the track system into a second passage portion. The projection exits the passageway and the fingers engage an annular ledge formed in the casing to lock the sleeve in an extended position and to prevent contact with the needle.
An advantage of the present invention is that the safety needle is easy to assemble, including fewer parts with less fragile components than prior art devices.
A further advantage of the present invention is that the safety needle includes an improved and simplified locking mechanism without fragile components.
An additional advantage of the present invention is that the safety needle has a more robust design which reduces the difficulty of assembly and reduces the possibility of the locking mechanism breaking which would allow the sleeve to again retract after the needle has been used.
The above mentioned and other features and objects of this invention, and the manner of attaining them, will become more apparent and the invention itself will be better understood by reference to the following description of embodiments of the invention taken in conjunction with the accompanying drawings, wherein:
Corresponding reference characters indicate corresponding parts throughout the several views. Although the exemplification set out herein illustrates several embodiments of the invention, in one form, the embodiments disclosed below are not intended to be exhaustive or to be construed as limiting the scope of the invention to the precise forms disclosed.
Referring to
For particular applications where the patient may have to self-inject, or where the patient is needle-phobic, the design can be adapted to permit the needle sleeve in its initial position to entirely cover and hide the needle. The needle sleeve can also be manufactured from an opaque material.
Referring to
Sleeve 22 has central main body portion 44 positioned primarily within casing 30 and tapered end portion 46 extending outwardly from the main body portion. Tapered end portion 46 passes through collar 36 when safety needle 20 is assembled to cover all but the sharp tip 26 of the needle 28 as shown in
Collar 36 further includes flanged portion 50 which engages end 32 of casing 30, and threads 52 which engage threads 54 formed in casing inner wall 56. Any other suitable means of attachment between collar 36 and casing 30 may be utilized. Opening 58 is defined in end 60 of tapered end portion 46 through which end 26 of needle 28 passes when safety needle 20 is used. Tapered end opening 58 is large enough to allow passage of needle 28, but small enough to prevent a person from sticking a finger into tapered end portion 46 and contacting needle 28.
The opposite end of sleeve main body portion 44 is provided with a plurality of resilient fingers 62. Fingers 62 are integrally formed about the upper end of main body portion 44. Fingers 62 extend outwardly from main body portion 44 at an angle relative to the central longitudinal axis of body portion 44 and engage inner wall 56 of casing 30 as will be described further hereinbelow. Fingers 62 are resilient and can be flexed inwardly toward the central longitudinal axis of sleeve 22. At least one of fingers 62 is provided with projection 64 which follows track system 66 integrally formed on casing inner wall 56 to facilitate locking of sleeve 22 in its extended position after use of safety needle 20. Fingers 62 further define cup-shaped cavity 68 in which end 70 of spring 42 is received for applying a biasing force against bottom 72 of cavity 68. Edge 74 of collar opening 48 may be engaged by ledge 76 defined by fingers 62 if sleeve 22 moves out of casing 30 beyond its locked position of
Needle mount 38 is threadedly secured to end 34 of casing 30 by means of flanged portion 78 which engages casing end 34 and threads 80 which engage threads 82 formed in casing inner wall 56. Any other suitable means of attachment between needle mount 38 and casing 30 may be utilized. Needle mount 38 includes central portion 84 through which needle 28 extends and is fixedly mounted by any suitable method. Positioned in surrounding relationship of central portion 84 is annular wall 86 which together with central portion 84 defines cavity 88 in which end 90 of spring 42 is received. Central portion 84 extends into the center of spring 42 when safety needle 20 is assembled. Needle mount 38 is also provided with receiving end 40 which is extends outwardly from engagement with casing 30. Receiving end 40 includes annular wall 92 which defines cavity 94 to which end 96 of needle 28 extends. A syringe is secured to receiving end 40 of safety needle 20 such that needle 28 is in fluid communication with the syringe.
The components of safety needle 20 are constructed from any suitable medical grade materials able to withstand sterilization and use. Sleeve 22, casing 30, collar 36 and needle mount 38 may be constructed from plastic materials, for example, by any suitable method including injection molding, or the like. Needle 28 is a conventional needle formed from medical grade stainless steel or other suitable material. Spring 42 is a conventional spring which may be formed from plastic or metal materials able to withstand the biasing forces exerted during use of safety needle 20.
Referring to
During assembly of safety needle 20, sleeve 22 is assembled with casing 30, and resilient fingers 62 with projections 64 are aligned with installation ramps 102, by the use of an assembly tool which guides the fingers with projections onto the ramps in the casing and also deflects the remaining fingers inwardly towards the main axis such that they may bypass the locking feature. Projections 64 slide across plateau 104 and are received in recessed cavities 106 (
During operation of safety needle 20, projections 64 travel along track system 66 to guide sleeve 22 into a locked position. The safety needle 20 is placed against the skin of the patient with needle 28 penetrating the skin of the patient. Tapered end portion 46 of sleeve 22 then makes contact with the patient. End 60 of sleeve 22 remains in contact with the patient during the injection such that needle 28 is not exposed. At this point, sleeve 22 is in a retracted position shown in
It should be noted that, while the fingers 62 have been shown as formed integrally with sleeve 22, and the track system 66 with casing 30, it is also possible that the fingers could be formed as part of casing 30 and the track could be part of sleeve 22.
While this invention has been described as having exemplary designs, the present invention may be further modified within the spirit and scope of this disclosure. This application is therefore intended to cover any variations, uses, or adaptations of the invention using its general principles. Further, this application is intended to cover such departures from the present disclosure as come within known or customary practice in the art to which this invention pertains.
Number | Date | Country | Kind |
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GB 0327136.8 | Nov 2003 | GB | national |