The present invention relates to a catheter insertion needle that is retractable into a safety position after use to prevent accidental sticks.
The introduction of a device through tissue of a living body typically requires the use of a sharp instrument such as a scalpel or a needle to provide access into the tissue. For example, for the insertion of a catheter into a blood vessel a needle is used to access the vessel. The needle includes a hollow bore cannula that provides a conduit for an introducer device, such as a guide wire, to be inserted through the cannula and into the blood vessel. After insertion of the guide wire, the needle is withdrawn proximally along the guide wire and discarded. The catheter is then inserted into the vessel over the guide wire, and the guide wire is then removed.
The removal of the needle exposes the sharp insertion tip of the needle to the medical personnel inserting the catheter. This sharp tip poses a danger of a needle stick to the medical personnel. Addtionally, this tip is contaminated with the patient's blood, which leads to the danger of blood-borne pathogens, such as HIV or hepatitis, to contaminate the needle and pose a further health risk for the medical personnel administering the needle.
It would be beneficial to provide a needle that can be easily and quickly placed into a safety position after removal from the patient's blood vessel in order to minimize the chance for a needle stick.
Briefly, the present invention provides a catheter insertion needle assembly. The assembly includes a generally elongated body having a proximal end and a distal end. A needle guard is disposed at the distal end of the body in a needle guard plane. A first locking member is disposed proximate to the distal end of the body. A second locking member is disposed at the proximal end of the body. A slider assembly includes a slider being slidably disposed on the body and a needle having an elongated needle body. A tip is disposed at a distal end of the elongated needle body and a cannulating portion extends through the elongated needle body. The needle extends distally of the slider and through the needle guard. A first locking tab is releasably engageable with the first locking member. A second locking portion is lockably engageable with the second locking member. The first locking tab is releasable from the first locking member to allow the slider to slide between a distal position relative to the body wherein the tip extends distally of the needle guard and a proximal position relative to the body wherein the tip is disposed within the needle guard plane. When the slider is disposed at the proximal position, the second locking portion engages the second locking member to preclude the slider from sliding distally relative to the body.
Further, the present invention provides a catheter insertion needle assembly. The assembly includes a generally elongated body having a proximal end and a distal end. A needle guard is disposed at the distal end of the body in a needle guard plane. A slider assembly comprises a slider being slidably disposed on the body and a needle having an elongated needle body. A tip is disposed at a distal end of the elongated needle body and a cannulating portion extends through the elongated needle body. The needle extends distally of the slider and through the needle guard. A first means for releasably retaining the slider in a distal position relative to the body and a second means for retaining the slider in a proximal position relative to the body are also provided.
The accompanying drawings, which are incorporated herein and constitute part of this specification, illustrate the presently preferred embodiments of the invention, and, together with the general description given above and the detailed description given below, serve to explain the features of the invention. In the drawings:
In the drawings, like numerals indicate like elements throughout. Certain terminology is used herein for convenience only and is not to be taken as a limitation on the present invention. The words “proximal” and “distal” refer to directions away from and closer to, respectively, the insertion tip of the needle in the catheter insertion needle assembly according to the present invention. The terminology includes the words above specifically mentioned, derivatives thereof, and words of similar import. The following describes preferred embodiments of the invention. However, it should be understood based on this disclosure, that the invention is not limited by the preferred embodiments described herein.
Referring to
A slider assembly 120 is slidingly disposed on the body 110 for sliding translation between the distal end 112 and the proximal end 114 of the body 110. The slider assembly 120 includes a slider body 122 that includes a first leg portion 123 and a second leg portion 124 that extends perpendicularly from the first leg portion 123. The first leg portion 123 includes a slot 125 that is sized to allow the body 110 to be slidingly disposed therethrough. The first leg portion 123 also includes a locking tab 121 that extends below slot 125. A needle assembly 126 extends through the first leg portion 123 along an axis 127 generally parallel to the longitudinal axis 116. The needle assembly 126 includes a proximal portion 128 that preferably includes a female luer fitting 129 and a distal portion 130 that includes a cannulating portion 132 with a needle tip 134. The needle tip 134 fluidly communicates with the female luer fitting 129 to allow fluid and/or a catheter guide wire (not shown) to be transmitted through the needle assembly 126.
Referring now to
Referring back to
A first locking member 150 is disposed proximate to the distal end 112 of the body 110. The first locking member 150 includes a fixed portion 152 that extends away from the body 110 preferably generally perpendicularly to the longitudinal axis 116 of the body 110. A free portion 154 of the first locking member 150 extends from the fixed portion 152 generally parallel to the longitudinal axis 116 of the body 110 and toward the proximal end 114 of the body 110. The free portion 154 of the first locking member 150 preferably includes a first tapered portion 156 that tapers from a larger distal end 156a to a narrower proximal end 156b. An open space 158 is formed between the fixed portion 152 and the distal end 156a of the first tapered portion 156 that is sized to retain the locking tab 121 of the slider assembly 120. A second tapered portion 157 extends proximally from the first tapered portion 156. A detent 159 is formed between the first tapered portion 156 and the second tapered portion 157. The detent 159 allows the slider assembly 120 to be partially drawn distally so that the needle tip 134 is drawn into the needle sheath 160 prior to insertion of the needle 130 into the patient.
The free portion 154 of the first locking member 150 is able to be biased away from the body 110 to disengage the locking tab 121 of the slider assembly 120 from the free portion 154 of the first locking member 150 in order to enable the slider assembly 120 to be disposed proximally along the body 110.
Preferably, both the body 110 and the slider assembly 120 are constructed from as suitable polymer, such as polystyrene or ISOPLAST®, although those skilled in the art will recognize that the body 110 and the slider 120 may be constructed from other materials instead.
Initially, the slider assembly 120 is disposed toward the distal end of the body 110, such that the locking tab 121 is disposed within the open space 158, such as is shown in
When the medical personnel is ready to administer the needle assembly 126, the medical personnel biases the free portion 154 of the first locking member 150 away from the longitudinal axis 116 of the body 110 until the distal end 156b of the first tapered portion 156 of the first locking member 150 clears the locking tab 121 of the slider assembly 120. The slider assembly 120 is then disposed proximally along the body 110 to the position shown in
The tubular safety sheath 162 is then removed from the needle assembly 126 and the sheath 160 by sliding the tubular safety sheath 162 distally along the length of the needle assembly 126 until the tubular safety sheath 162 is removed from the needle assembly 126. The tubular safety sheath 162 is no longer needed and may be discarded. The needle assembly 126 is slid distally until the locking tab 121 locks into the open space 158, allowing the needle tip 134 to extend distally of the sheath 160. The cannulating portion 132 of the needle assembly 126 is then inserted into the desired location in a patient according to methods well known in the art.
When it is desired to withdraw the needle assembly 126 from the patient, the free portion 154 of the first locking member 150 is biased away from the longitudinal axis 116 of the body 110 until the distal end 156b of the free portion 154 of the first locking member 150 clears the locking tab 121 of the slider assembly 120. The slider assembly 120 is then disposed proximally along the body 110 to the position shown in
As the slider assembly 120 is disposed toward the proximal end 114 of the body 110, the slider assembly 120 engages the proximal locking member 118, depressing the proximal end 118b toward the longitudinal axis 116. As the proximal locking member 118 clears the slot 125, the proximal end 118b of the proximal locking member 118 biases back to its original position, preventing the slider assembly 120 from being disposed distally beyond the proximal locking member 118. Preferably generally simultaneously, the distal tip 134 of the needle assembly 126 is disposed proximally through the sheath 160 and into the needle guard 140, where the needle guard 140 prevents a user from being accidentally stuck. If the optional seal 144 is used, the distal tip 134 of the needle assembly 126 is disposed within the seal 134 as a further safety precaution. To prevent the slider assembly 120 from being pulled off of the body 110, the stop 115 engages the locking tab 121 if the locking tab 121 is slid too far proximally along the body 110.
At this point, the distal tip 134 of the needle assembly 126 is fully retracted from the sheath 160, and the sheath 160 may be slidingly removed from the sheath retainer 146, by sliding the sheath 160 in a direction toward either the top or bottom of the page of
An alternate embodiment of a catheter needle insertion assembly 200, shown in
It will be appreciated by those skilled in the art that changes could be made to the embodiments described above without departing from the broad inventive concept thereof. It is understood, therefore, that this invention is not limited to the particular embodiments disclosed, but it is intended to cover modifications within the spirit and scope of the present invention as defined by the appended claims.
The present application claims the benefit of U.S. Provisional Patent Application Ser. No. 60/548,427, filed on 26 Feb. 2004.
Number | Date | Country | |
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60548427 | Feb 2004 | US |