INCREMENTAL SYRINGE

Abstract

An incremental syringe is provided and includes a syringe barrel, a finger grip disposed at the proximal end of the syringe barrel, a tab disposed inside the syringe barrel, and a plunger body having detentes, wherein the detentes are configured to interact with the tab to provide audible and tactile feedback to a user when the plunger body is pushed through the syringe barrel in a distal direction.

Claims

1. An incremental syringe comprising: a syringe barrel; a finger grip disposed at the proximal end of the syringe barrel; a tab disposed inside the syringe barrel; a plunger body having detentes, wherein the detentes are configured to interact with the tab to provide audible and tactile feedback to a user when the plunger body is pushed through the syringe barrel in a distal direction.

2. The incremental syringe of claim 1 further comprising a luer lock disposed at the distal end of the syringe barrel.

3. The incremental syringe of claim 1, wherein the finger grip comprises at least two paddles.

4. The incremental syringe of claim 1 further comprising a sealing cap attached to the distal end of the plunger body.

5. The incremental syringe of claim 1, wherein the finger grip is removably attached to the proximal end of the syringe barrel.

6. The incremental syringe of claim 1, wherein each unit of audible and tactile feedback indicates that a predetermined volume of liquid has been ejected from the syringe barrel.

7. An incremental syringe comprising: a syringe barrel; a plunger body having a first portion proximate the proximal end and a second portion proximate the distal end, wherein the first portion has a plurality of corresponding detentes on opposite sides of the first portion; a finger grip, wherein the finger grip is configured to be removably coupled to the plunger body, and wherein the finger grip is further configured to interact with the detentes to provide audible and tactile feedback to a user when the plunger body is pushed through the finger grip in a distal direction.

8. The incremental syringe of claim 7 further comprising a luer lock disposed at the distal end of the syringe barrel.

9. The incremental syringe of claim 7, wherein the finger grip comprises at least two paddles.

10. The incremental syringe of claim 7 further comprising a sealing cap attached to the distal end of the plunger body.

11. The incremental syringe of claim 7, wherein each unit of audible and tactile feedback indicates that a predetermined volume of liquid has been ejected from the syringe barrel.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0026] These and other objects, features, and characteristics will become more apparent to those skilled in the art from a study of the following Detailed Description in conjunction with the appended claims and drawings, all of which form a part of this specification. While the accompanying drawings include illustrations of various embodiments, the drawings are not intended to limit the claimed subject matter.

[0027] FIG. 1 is a side view of a medical injection assembly according to one embodiment of the present invention.

[0028] FIG. 2 is a cross-section of a sheath of an introducer according to one embodiment of the present invention.

[0029] FIG. 3 is a cut-away isometric view of a sheath of an introducer according to one embodiment of the present invention.

[0030] FIG. 4 is a cross-section of a handle of an introducer according to one embodiment of the present invention.

[0031] FIG. 5A is a side view of a cannula exiting a sheath of an introducer according to one embodiment of the present invention.

[0032] FIG. 5B is a side view of a cannula exiting a sheath of an introducer according to one embodiment of the present invention.

[0033] FIG. 5C is a side view of a cannula exiting a sheath of an introducer according to one embodiment of the present invention.

[0034] FIG. 6 is an isometric view of a plunger body according to one embodiment of the present invention.

[0035] FIG. 7 is a bird's eye view of a finger grip according to one embodiment of the present invention.

[0036] FIG. 8A is a frontal view diagram of a bladder injection pattern according to one embodiment of the present invention.

[0037] FIG. 8B is a side view diagram of a bladder injection pattern according to one embodiment of the present invention.

[0038] FIG. 9 is an isometric view of an incremental syringe according to one embodiment of the present invention.

[0039] FIG. 10 is an isometric view of an incremental syringe according to one embodiment of the present invention.

[0040] FIG. 11 is a frontal view of the distal end of a syringe barrel and finger grip according to one embodiment of the present invention.

[0041] FIG. 12 is an isometric view of a plunger body according one embodiment of the present invention.

DETAILED DESCRIPTION

[0042] In the following description, for the purposes of explanation, numerous specific details are set forth in order to provide a thorough understanding of the embodiments of the invention. One skilled in the art will recognize that the embodiments of the invention may be practiced without these specific details or with an equivalent arrangement. In other instances, well-known structures and devices are shown in block diagram form in order to avoid unnecessarily obscuring the embodiments of the invention.

[0043] The presently disclosed subject matter is presented with sufficient details to provide an understanding of one or more particular embodiments of broader inventive subject matters. The descriptions expound upon and exemplify particular features of those particular embodiments without limiting the inventive subject matters to the explicitly described embodiments and features. Considerations in view of these descriptions will likely give rise to additional and similar embodiments and features without departing from the scope of the presently disclosed subject matter.

[0044] Referring now to FIG. 1, a medical injection assembly 1 according to an embodiment of the present invention is shown. The medical injection assembly 1 may comprise an introducer 100. The introducer may comprise a handle 101, and sheath 102, a scope lumen 103 extending from a first proximal end of the handle 101 to a distal end of the sheath 102, wherein the scope lumen 103 is configured to receive an endoscope 110 at the first proximal end of the handle 101 and hold the endoscope in a desired position, and a cannula lumen 104 extending from a second proximal end of the handle 101 to the distal end of the sheath 102, wherein the cannula lumen 104 is configured to receive a cannula 109 at the second proximal end of the handle 101 and hold the cannula 109 in a desired position. The introducer 100 may further comprise a fluid line 105, wherein the distal end is in fluid communication with the scope lumen 103.

[0045] The medical injection assembly 1 may further comprise a cannula 109 configured such that the distance between the distal tip of the cannula 109 and the axis defined by the sheath 102 of the introducer increases as the cannula 109 is moved in a distal direction. The medical injection assembly may further comprise a syringe 111 connected to the proximal end of the cannula 109.

[0046] The fluid line 105 may further comprise a second fluid connector 106. The fluid line 105 may further comprise a pinch valve 107 configured to control flow of fluid through the fluid line 105.

[0047] Referring now to FIGS. 2 and 3, the sheath 102 of an introducer 100 according to an embodiment of the present invention is shown. Scope lumen 103 may be configured to receive a variety of endo scopes 110 for illuminating and visualizing target tissue within the body. In preferred embodiments, the endoscope 110 may be a cystoscope. The diameter of the scope lumen 103 should be sufficient to fit industry standard cystoscopes known in the art. In preferable embodiments, the scope lumen 103 may have a diameter of about 4 mm to about 5 mm.

[0048] The cannula lumen 104 may be configured to receive a cannula 109 according to the present invention as further described herein. The diameter of the cannula lumen 104 should be sufficient to fit said cannulas 109. In preferred embodiments, the cannula lumen 104 may have a diameter of about 1 mm to about 2 mm. The walls of the sheath 102 are must be minimized so as to allow the introducer 100 to fit through a patient's urethra while maintaining its strength and rigidity. In preferred embodiments, the sheath walls may have a thickness of about 0.1 mm to about 0.4 mm. The sheath 102 may be comprised of polyether block amides, polyethylene, or other materials with similar rigidity characteristics.

[0049] Referring now to FIG. 4, a cross-section of the handle 101 of an introducer 100 according to an embodiment of the present invention is shown. The scope lumen 103 may extend from a proximal end of the handle 101 and may be configured to receive an endoscope 110 from a proximal end of the handle 101. A scope seal 112 may be positioned at a proximal end of the handle 101 to engage an endoscope 110. The scope seal 112 may be comprised of a material with coefficient of friction sufficient to hold an endoscope 110 in place. In preferable embodiments, the scope seal 112 may be comprised of silicone.

[0050] The cannula lumen 104 may extend from a proximal end of the handle 101 and may be configured to receive a cannula 109 from a proximal end of the handle 101. A cannula seal 113 may be positioned at a proximal end of the handle 101 to engage a cannula 109. The cannula seal 113 may be comprised of a material with coefficient of friction sufficient to hold a cannula 109 in place. In preferable embodiments, the cannula seal 113 may be comprised of silicone.

[0051] The handle may further comprise a fluid line 105 in fluid communication with the scope lumen 103. The distal end of the fluid line 105 may connect to the scope lumen 103 via a watertight fluid connector. In yet other embodiments, the distal end of the fluid line 105 may be integrated directly into the scope lumen 103 via known manufacturing methods such as various molding techniques, welding, 3D printing, adhesives, etc. The fluid line 105 may comprise a second fluid connector 106. In preferred embodiments, the second fluid connector 106 may be a luer lock. The fluid line 105 may further comprise a pinch valve 107. The pinch valve 107 may control the flow of fluid form a fluid source through the fluid line 105 and into the scope lumen 103.

[0052] Referring now to FIGS. 5A-5C, a cannula 109 according to an embodiment of the present invention in use is shown. The cannula 109 may comprise a needle 114 attached to a distal tip of the cannula 109. The cannula 109 may further comprise a first fluid connector 115 attached to a proximal end of the cannula 109, wherein the cannula 109 may be comprised of a biocompatible thermoplastic polymer, and wherein a distal portion of the cannula 109 may maintain a predefined curvature in the absence of a deforming force.

[0053] The needle 114 may be any commercially available hypodermic needle suitable for performing injections of OnabotulinumtoxinA. In preferred embodiments, the diameter of the needle 114 is less than the diameter of the cannula 109, and the needle 114 may be a 23 gauge needle and may extend past the cannula 109 about 1.0 mm to about 3.0 mm in length. In such configurations, the distal tip of the cannula 109 acts as a wall, preventing the needle 114 from penetrating into the target tissue past the distal tip of the cannula 109.

[0054] The biocompatible thermoplastic polymer may be any such polymer having a flexural modulus of about 595,000 psi. Importantly, such a flexural modulus allows the user of the device to insert the needle into bladder tissue without causing the cannula itself to bend or deform in a clinically significant manner. In preferred embodiments, the biocompatible thermoplastic polymer may be polyether ether-ketone (PEEK).

[0055] The cannula 109 may be configured such that the distance between the distal tip of the cannula 109 and the axis defined by the sheath 102 of the introducer 100 increases as the cannula 109 is moved in a distal direction. According to at least one embodiment of the present invention, such a configuration may be achieved by forming the cannula 109 such that a distal portion of the cannula 109 maintains a predefined curvature in the absence of a deforming force. Thus, as the distal portion of the cannula 109 exits the distal end of the introducer 100, it returns to a predefined curvature that causes the distal tip of the cannula 109 to move away from the axis defined by the sheath 102 of the introducer 100. In preferred embodiments, the predefined curvature may be defined by an inverse tangent function. But one of ordinary skill in the art will recognize that any predefined curvature that causes the distal tip of the cannula 109 to move away from the axis defined by the sheath 102 of the introducer 100 may be used in the present invention.

[0056] Referring now to FIGS. 6-7, the syringe 111 may comprise a syringe barrel. The syringe 111 may also comprise a plunger body 116 having a first portion 117 proximate the proximal end and second portion 118 proximate the distal end, wherein the first portion 117 has a plurality of corresponding detentes 119 on opposite sides of the first portion 117. The syringe 111 may also comprise a sealing cap 120 attached to the distal end of the plunger body 116 and a finger grip 121 comprising two paddles 122. The finger grip may be configured to be removably coupled to the plunger body 116 and to interact with the detentes 119 to provide audible and tactile feedback to a user when the plunger body 116 is pushed through the finger grip 121 in a distal direction.

[0057] The second portion 118 may fit into commercially available syringe barrels with the sealing cap 120 forming a watertight seal within the syringe barrel. In preferred embodiments, commercially available 10 cc syringe barrels may be used. The finger grip 121 may be configured to clip on to the plunger body 116. The finger grip 121 may include tabs 123 on the interior of both paddles 122. The tabs 123 may fit into grooves between the detentes 119 on the first portion 117. When the user pushes the plunger body 116 in a distal direction into the syringe barrel, the detentes 119 provide resistance against the movement until the tabs 123 bend enough to clear a set of detentes 119 and fit into the next set of grooves. The detentes 119 may be spaced along the first portion 117 such that clearing one set of detentes 119 results in an ejection of a specific amount of fluid from the syringe. In preferred embodiments, clearing one set of detentes would result in the ejection of 1 cc of fluid from the syringe. When the user causes tabs 123 to clear a set of detentes 119 and the tabs 123 come to rest in the subsequent grooves, the user is provided with tactile and audible feedback to indicate that one such predetermined unit of fluid has been ejected from the syringe.

[0058] According to another embodiment of the present invention, a method for treating overactive bladder may comprise inserting an endoscope 110 into a scope lumen 103 of an introducer 100. The method may further comprise inserting a cannula 109 into a cannula lumen 104 of the introducer 100, the cannula 109 configured such that the distance between the distal tip of the cannula 109 and the axis defined by the sheath 102 of the introducer 100 increases as the cannula 109 is moved in a distal direction, wherein a syringe 111 filled with OnabotulinumtoxinA is coupled to the proximal end of the cannula 109. The method may further comprise guiding the introducer 100 through the urethra of a patient to the patient's bladder. The method may further include extending the distal portion of the cannula 109 past the distal end of the introducer 100 until a needle 114 attached to the distal end of the cannula 109 is placed at a desired radial distance from the axis defined by the sheath of the introducer. The method may further comprise rotating the introducer 100 to position the needle 114 at a desired position. The method may further comprise moving the introducer in a distal direction to insert the needle 114 into the bladder. The method may further include activating the syringe 111 to inject OnabotulinumtoxinA into the bladder. The method may further include moving the introducer 100 in a proximal direction to remove the needle 114 from the bladder. The method may further include repeating the extending, rotating, moving distally, activating, and moving proximally steps until a therapeutically effective amount of OnabotulinumtoxinA has been injected in a therapeutically effective pattern into the bladder.

[0059] Referring now to FIGS. 8A-8B, therapeutically effective patterns of injections according to at least one embodiment of the present invention is shown. It is beneficial to disperse the injections of OnabotulinumtoxinA across the bladder tissue. In preferred embodiments, injections patterns may comprise three concentric semi-circles in the lower half of the bladder with radii A, B, and C. Such an injection pattern may be created by moving the cannula 109 distally until the needle 114 is at a distance A from the axis defined by the sheath 102 of the introducer 100. The introducer 100 may then be rotated until the needle 114 is at injection site 200. The introducer 100 may be moved distally to inject the bladder with OnabotulinumtoxinA and then moved proximally to withdraw the needle 114 from the bladder. The introducer 100 may then be rotated counterclockwise until the needle 114 is at injection site 201, and the injection process may be repeated. Once the injection pattern for the semi-circle with radius A is complete, the cannula 109 may be moved distally until the needle 114 is at a distance B from the axis defined by the sheath 102 of the introducer 100, and the previous steps may be repeated to create the injection patterns for the semi-circles with radii B and C.

[0060] Preferably, A is approximately 0.43 inches, B is approximately 0.8 inches, and C is approximately 1.2 inches.

[0061] By rotating the introducer 100 to position the needle rather than moving the introducer 100 laterally, the patient experiences less discomfort and possible injury from lateral stretching of the urethra.

[0062] Referring now to FIGS. 9-12, according to one embodiment of the present invention, an incremental syringe 3 may comprise a syringe barrel 300, a finger grip 301 disposed at the proximal end of the syringe barrel 300, a tab 302, disposed inside the syringe barrel 300, and a plunger body 303 having detentes 304. The detentes 304 may be configured to interact with the tab 302 to provide audible and tactile feedback to a user when the plunger body 303 is pushed through the syringe barrel 300 in a distal direction.

[0063] The incremental syringe 3 may further comprise a luer lock 305 disposed at the distal end of the syringe barrel 300. The luer lock 305 may be connected to a corresponding luer lock on a cannula to form a water-tight connection between the incremental syringe 3 and cannula. Liquids ejected from the incremental syringe 3 may travel through the cannula to a target tissue.

[0064] The finger grip 301 may comprise at least two paddles 306, 307. The finger grip 301 allows for one-handed operation of the incremental syringe 3 when the user places at least one finger on each of the two paddles 306, 307 and uses the thumb to move the plunger body 303 in a distal direction.

[0065] The incremental syringe 3 may further comprise a sealing cap 308 attached to the distal end of the plunger body 303. The circumference of the sealing cap 308 forms a water-tight seal against the interior circumference of the syringe barrel 300. The sealing cap 308 may be comprised of rubbers, silicones, other high-friction deformable plastics known in the art, or combinations thereof.

[0066] The tab 302 in a first position is parallel to the plane defined by the cross-section of the syringe barrel 300 when it is aligned with one of the grooves adjacent to the detentes 304. However, when tab 302 is in a second position not aligned with one of the grooves adjacent to the detentes 304, the detentes 304 displace tab 302 such that it is not parallel to the plane defined by the cross-section of the syringe barrel 300. In operation, when the plunger body 303 is moved in a distal direction such that tab 302 moves from a second position to a first position, an audible and tactile click can be heard and felt by the user. Each unit of audible and tactile feedback indicates that a predetermined volume of liquid has been ejected from the syringe barrel 300. The spacing of the detentes 304 or the diameter of the syringe 3 may be adjusted to dispense varying amounts of liquid from the syringe 3.

[0067] The above description and drawings are illustrative and are not to be construed as limiting the invention to the precise forms disclosed. Persons skilled in the relevant art can appreciate that many modifications and variations are possible in light of the above disclosure. Numerous specific details are described to provide a thorough understanding of the disclosure. However, in certain instances, well-known or conventional details are not described in order to avoid obscuring the description.

[0068] Reference in this specification to one embodiment or an embodiment means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment of the disclosure. The appearances of the phrase in one embodiment in various places in the specification are not necessarily all referring to the same embodiment, nor are separate or alternative embodiments mutually exclusive of other embodiments. Moreover, various features are described which may be exhibited by some embodiments and not by others. Similarly, various requirements are described which may be requirements for some embodiments but not other embodiments.

[0069] Unless the context clearly requires otherwise, throughout the description and the claims, the words comprise, comprising, and the like are to be construed in an inclusive sense, as opposed to an exclusive or exhaustive sense; that is to say, in the sense of including, but not limited to. As used herein, the terms connected, coupled, or any variant thereof, means any connection or coupling, either direct or indirect, between two or more elements; the coupling of connection between the elements can be physical, logical, or any combination thereof. Additionally, the words herein, above, below, and words of similar import, when used in this application, shall refer to this application as a whole and not to any particular portions of this application. Where the context permits, words in the above Detailed Description using the singular or plural number may also include the plural or singular number respectively. The word or, in reference to a list of two or more items, covers all of the following interpretations of the word: any of the items in the list, all of the items in the list, and any combination of the items in the list.

[0070] The teachings of the disclosure provided herein can be applied to other systems, not necessarily the system described above. The elements and acts of the various embodiments described above can be combined to provide further embodiments.

[0071] These and other changes can be made to the disclosure in light of the above Detailed Description. While the above description describes certain embodiments of the disclosure, and describes the best mode contemplated, no matter how detailed the above appears in text, the teachings can be practiced in many ways. Details of the system may vary considerably in its implementation details, while still being encompassed by the subject matter disclosed herein. As noted above, particular terminology used when describing certain features or aspects of the disclosure should not be taken to imply that the terminology is being redefined herein to be restricted to any specific characteristics, features, or aspects of the disclosure with which that terminology is associated. In general, the terms used in the following claims should not be construed to limit the disclosure to the specific embodiments disclosed in the specification, unless the above Detailed Description section explicitly defines such terms. Accordingly, the actual scope of the disclosure encompasses not only the disclosed embodiments, but also all equivalent ways of practicing or implementing the disclosure under the claims.

[0072] The terms used in this specification generally have their ordinary meanings in the art, within the context of the disclosure, and in the specific context where each term is used. Certain terms that are used to describe the disclosure are discussed above, or elsewhere in the specification, to provide additional guidance to the practitioner regarding the description of the disclosure. For convenience, certain terms may be highlighted, for example using capitalization, italics and/or quotation marks. The use of highlighting has no influence on the scope and meaning of a term; the scope and meaning of a term is the same, in the same context, whether or not it is highlighted. It will be appreciated that same element can be described in more than one way.

[0073] Consequently, alternative language and synonyms may be used for any one or more of the terms discussed herein, nor is any special significance to be placed upon whether or not a term is elaborated or discussed herein. Synonyms for certain terms are provided. A recital of one or more synonyms does not exclude the use of other synonyms. The use of examples anywhere in this specification including examples of any terms discussed herein is illustrative only, and is not intended to further limit the scope and meaning of the disclosure or of any exemplified term. Likewise, the disclosure is not limited to various embodiments given in this specification.

[0074] Without intent to further limit the scope of the disclosure, examples of instruments, apparatus, methods and their related results according to the embodiments of the present disclosure are given below. Note that titles or subtitles may be used in the examples for convenience of a reader, which in no way should limit the scope of the disclosure. Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure pertains. In the case of conflict, the present document, including definitions will control.

[0075] Some portions of this description describe the embodiments of the invention in terms of algorithms and symbolic representations of operations on information. These algorithmic descriptions and representations are commonly used by those skilled in the data processing arts to convey the substance of their work effectively to others skilled in the art. These operations, while described functionally, computationally, or logically, are understood to be implemented by computer programs or equivalent electrical circuits, microcode, or the like. Furthermore, it has also proven convenient at times, to refer to these arrangements of operations as modules, without loss of generality. The described operations and their associated modules may be embodied in software, firmware, hardware, or any combinations thereof.

[0076] Finally, the language used in the specification has been principally selected for readability and instructional purposes, and it may not have been selected to delineate or circumscribe the inventive subject matter. It is therefore intended that the scope of the invention be limited not by this detailed description, but rather by any claims that issue on an application based hereon. Accordingly, the disclosure of the embodiments of the invention is intended to be illustrative, but not limiting, of the scope of the invention, which is set forth in the following claims.

[0077] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood to one of ordinary skill in the art to which the presently disclosed subject matter pertains. Although any methods, devices, and materials similar or equivalent to those described herein can be used in the practice or testing of the presently disclosed subject matter, representative methods, devices, and materials are now described.

[0078] Following long-standing patent law convention, the terms a, an, and the refer to one or more when used in the subject specification, including the claims. Thus, for example reference to an additive can include a plurality of such additives, and so forth.

[0079] Unless otherwise indicated, all numbers expressing quantities of components, conditions, and so forth used in the specification and claims are to be understood as being modified in all instances by the term about. Accordingly, unless indicated to the contrary, the numerical parameters set forth in the instant specification and attached claims are approximations that can vary depending upon the desired properties sought to be obtained by the presently disclosed subject matter.

[0080] As used herein, the term about, when referring to a value or to an amount of mass, weight, time, volume, concentration, and/or percentage can encompass variations of, in some embodiments +/?20%, in some embodiments, +/?10%, in some embodiments +/?5%, in some embodiments +/?1%, in some embodiments +/?0.5%, and in some embodiments, +/?0.1%, from the specified amount, as such variations are appropriate in the disclosed products and methods.