Patent Application
20220354742
The invention relates to needle assemblies for acupuncture and dry needling.
Conventional needle assemblies for use in acupuncture and dry needling typically comprise a guide tube and a needle located within the guide tube. The needle has a handle which is secured via adhesive to the inside of the guide tube, to thereby retain the needle (specifically, the distal tip of the needle) within the guide tube. In use, the practitioner applies the distal end of the guide tube to the patient's skin (aligned with an acupuncture point or a pressure point), and applies a force to the proximal end of the handle, eg by tapping, to disengage the needle from the guide tube, resulting in the distal tip of the needle penetrating the patient's skin.
However, the adhesive attaching the handle to the guide tube is conventionally single-use and loses its function once the handle has been separated from the guide tube. Therefore, if the needle is inadvertently dislodged from the guide tube during packing, transport or storage, it cannot be used (due to hygiene reasons) and has to be discarded.
Further, there is also a challenge during manufacturing of conventional needle assemblies of applying a consistent amount of adhesive to each needle. A consistent predetermined amount is important, since excessive adhesive affects the ease with which the practitioner dislodges the needle from the guide tube, while insufficient adhesive results in a larger number of needles being inadvertently dislodged during transit or in storage.
In this context, there is a need for improved needle assemblies.
According to an aspect of the present invention, there is provided a needle assembly comprising:
a needle having a handle at a proximal end portion thereof; and
a guide tube sized to house the needle and handle, the guide tube comprising an inwardly-extending projection adjacent a proximal end thereof,
said inwardly-extending projection being configured to engage an engagement portion of the handle for retaining the needle within the guide tube such that a distal tip of the needle is positioned within the guide tube and a proximal end portion of the handle extends from the proximal end of the guide tube;
said engagement being releasable upon a force applied to a proximal end of the handle to extend the distal tip of the needle out of the guide tube.
The handle may be secured to the proximal end portion of the needle.
The engagement portion of the handle may comprise a textured anti-slip surface.
The engagement portion of the handle may be etched to define the textured anti-slip surface.
The engagement portion of the handle may be located intermediate distal and proximal end portions of the handle.
The guide tube may be manufactured of a translucent polymer.
The needle and handle may each be manufactured of a metallic material.
The needle may be manufactured of a stainless steel and the handle may be manufactured of aluminum or an aluminum alloy.
In the engaged configuration, a distance between the inwardly-extending projection and a proximal end of the handle may be between about 5 mm and 8 mm.
A diameter of the handle may be between about 2 mm and 2.5 mm.
One or both of the proximal end portion and the distal end portion of the handle may comprise at least one indent for securing the needle to the handle.
Following release of said engagement due to said force being applied to the handle, said engagement may be reinstatable by repositioning the needle such that the inwardly-extending projection re-engages the engagement portion.
In a further aspect, the present invention provides a method of assembling a needle assembly described above, the method comprising:
inserting the proximal end portion of the needle into a central bore of the handle; and
inserting the needle and handle combination into the guide tube,
the handle being positioned such that the engagement portion of the handle engages the inwardly-extending projection of the guide tube.
A diameter of the central bore of the handle may be between about 0.5 to 1 time the diameter of the proximal end portion of the needle such that the needle is secured in the handle via interference fit.
The method may further comprise providing a plurality of bends in the proximal end portion of the needle prior to inserting the proximal end portion of the needle into the central bore of the handle.
The method may further comprise pressing the proximal and/or distal end portion(s) of the handle onto the needle to form said at least one indent for securing the needle to the handle.
The inwardly-extending projection may be pressed into the guide tube to engage said engagement portion of the handle.
The invention will now be described, by way of non-limiting example only, with reference to the accompanying drawings, in which:
The inwardly-extending projection preferably extends inwardly to such an extent that when engaged with the engagement portion 222 of the handle, the opposite face of the handle abuts the internal wall of the guide tube 1.
The engagement portion 222 of the handle 22 comprises a textured anti-slip surface. The roughness of the textured surface increases the coefficient of friction between the engagement portion 222 and the inwardly-extending projection 11, resulting in a more secure engagement of the two components in the engaged state. In a preferred embodiment, the engagement portion 222 of the handle 22 is etched to define the textured anti-slip surface. Alternatively, the textured anti-slip surface may be formed by other methods, eg by cutting grooves, corrugations, notches, etc, into the engagement portion 222 of the handle 2.
In yet other embodiments, the engagement portion 222 may comprise additional or alternative surface modifications or finishes to increase the coefficient of friction between the engagement portion 222 and the inwardly-extending projection 11, eg applying a tacky material to the engagement portion 222, adding ribs, embossing, etc.
In contrast with prior art needle assemblies, the engagement between guide tube 1 and the needle 22 is not via adhesive. As discussed above, a problem with the prior art adhesive engagement is that once disengaged, the needle cannot be securely repositioned in the engaged configuration. In comparison with such prior art assemblies, the needle assembly according to embodiments of the present invention is repositionable. That is, following release of engagement between the inwardly-extending projection 11 and the engagement portion 222, the engagement is reinstatable by repositioning the needle such that the inwardly-extending projection 11 re-engages the engagement portion 222. Therefore, if the needle 21 is inadvertently dislodged from its engaged position during packing, transit or storage, it may be repositioned within the guide tube 1 into the engaged/ready-to-use configuration, provided there has been no contamination of the distal tip of the needle.
In the engaged configuration, the distance between the inwardly-extending projection 11 and the proximal end 30 of the handle (ie the distance L1 plus L2) is between about 5 mm and 8 mm. In the released configuration, the extension of the distal tip of the needle from the distal end of the guide tube (ie the distance L0) is between about 5 mm and 8 mm.
The handle 22 may be circular in cross-section, with a diameter of the handle 22 between about 2 mm and 2.5 mm. It is envisaged that such a diameter facilitates handling of the needle.
As illustrated most clearly in
Additionally or alternatively, the needle is secured within the handle via interference fit. With reference to
Additionally or alternatively, the proximal end portion of the needle may be provided with a plurality of kinks or bends 50 such that the proximal end portion diverges from linear. When the needle is forced into the linear bore 40 of the handle, the bent portion of the needle is forced into a linear configuration that is resisted by the elasticity of the needle, which helps to secure the needle in the handle.
The guide tube 1 is preferably manufactured of a transparent or translucent polymer. In a preferred embodiment, the guide tube is formed by injection molding. Alternative processing methods may also be suitable, such as plastics extrusion. The proximal and distal ends of the guide tube 1 preferably comprise smooth surfaces to prevent scratching of the skin in use.
The needle 21 is preferably manufactured of a metallic material, for flexibility of the needle and ease of sterilisation. For example, the needle may be manufactured of a stainless steel.
The handle 22 is preferably manufactured of a metallic material, for example, aluminum or an aluminum alloy.
The present invention also relates to methods of making and assembling needle assembly 10.
In one embodiment, the assembly method comprises inserting the proximal end portion of the needle 21 into the central bore 40 of the handle 22, inserting the needle and handle combination 2 into the guide tube 1, the handle being positioned such that the engagement portion 222 of the handle engages the inwardly-extending projection 11 of the guide tube.
In one example, prior to insertion of the needle 21 into the handle 22, the proximal end portion of the needle is crimped or otherwise shaped to form the plurality of kinks/bends 50. The needle 21 is then pulled through the bore 40 of the handle 22 such that the kinks/bends 50 are positioned within the handle 22. In some embodiments, the diameter of the bore 40 is less than the diameter of the proximal end portion of the needle, so that the needle is secured within the handle via interference fit. The distal end of the needle may then be sharpened to a suitable tip. In other examples, the sharp distal tip of the needle is formed prior to insertion of the needle into the handle.
In some embodiments, once the needle 21 has been inserted into the handle 22, the proximal end portion 221 and/or the distal end portion 223 is/are pressed to form the projection(s) 224 and/or indent(s) 225 that help to secure the needle to the handle.
The engagement portion 222 of the handle is preferably formed, eg via etching as discussed above, before the needle 21 is inserted into the handle, to reduce the risk of contaminating the distal tip of the needle during such processing. However, the engagement portion 222 could conceivably alternatively be formed on the handle portion during or after insertion of the needle into the handle.
In one embodiment, the inwardly-extending projection 11 is formed after the needle and handle combination 2 has been inserted into the guide tube 1. For example, the proximal end portion of the guide tube 1 may be crimped, pressed or stamped to form the inwardly-extending projection 11.
The needle assembly 10 may be packaged for distribution, eg in sterile blister packs 70 as illustrated in
To use the needle, the practitioner removes the needle assembly 10 from the packaging, applies the distal end of the guide tube 1 to the patient's skin, and applies a force on the proximal end of the handle 22 (eg by tapping) to insert the needle into the patient's skin. Once the engagement between the inwardly-extending projection 11 and the engagement portion 222 has been released (by the force applied to the proximal end of the handle 22), the needle slides smoothly along the guide tube to extend out of the distal end thereof (ie there are no further disruptions to the movement of the needle within the guide tube).
While various embodiments of the present invention have been described above, it should be understood that they have been presented by way of example only, and not by way of limitation. It will be apparent to a person skilled in the relevant art that various changes in form and detail can be made therein without departing from the spirit and scope of the invention. Thus, the present invention should not be limited by any of the above described exemplary embodiments.
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 knowledge in the field of endeavor to which this specification relates.
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 group of integers or steps.
This application is a Continuation of U.S. patent application Ser. No. 16/993,932 filed on Aug. 14, 2020, which claims priority to and all the benefits of U.S. Provisional Application No. 62/886,693 filed on Aug. 14, 2019, the disclosures of which are expressly incorporated by reference in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| 62886693 | Aug 2019 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16993932 | Aug 2020 | US |
| Child | 17872695 | US |
