专利汇可以提供Handheld Devices For Dilating Tissue专利检索,专利查询,专利分析的服务。并且Embodiments of handheld devices for dilating tissue along the paranasal sinuses include a handle assembly that includes a grip portion, an inflation mechanism, and a digital actuation member configured to actuate the inflation mechanism. The handheld devices also include a rigid cannula that includes a distal end and a proximal end, where the rigid cannula is coupled to the handle assembly along the proximal end. The handheld devices further include an inflatable balloon coupled to an outside of the rigid cannula proximate to the distal end, an inflation lumen at least partially disposed along the rigid cannula and in fluid communication with the inflatable balloon and the inflation mechanism, and an aspiration lumen at least partially disposed along the rigid cannula and includes an aspiration port proximate to the distal end.,下面是Handheld Devices For Dilating Tissue专利的具体信息内容。
What is claimed is:
The present application is a continuation of International Application No. PCT/US2011/034540 filed Apr. 29, 2011, which claims the benefit of U.S. Provisional Application Ser. No. 61/329,833, titled “Manual Inflation of Balloon Using Triggers” filed Apr. 30, 2010.
The present disclosure is generally directed to balloon catheters and, more specifically, balloon catheters attached to rigid cannulae.
Inflammation of the sinus mucosa lining the sinus cavities causes sinusitis in patients. The mucosal lining includes mucosal glands and goblet cells that, together, secrete mucus. The mucus covers the mucosal lining of the sinuses and nose, and traps small particles such as dust, particulate matter, and allergens, as well as infectious agents such as bacteria, and prevents these particles from entering the respiratory system.
When the mucosal lining of the paranasal sinuses become inflamed, sinus ostia, or openings that connect sinuses to the naval cavity itself, tend to constrict or become obstructed. Constriction of the sinus ostia may lead to collection of mucus in the paranasal sinuses themselves, which may cause discomfort to the patient and lead to infection. Therapeutic treatment to relieve pressure in the paranasal sinuses may include dilation of the sinus ostia and drainage of the collected mucus. Accordingly, handheld devices that allow a medical practitioner to dilate tissue along the paranasal sinuses of a patient may be desired. Such a device may also facilitate atraumatic dissection when the need arises to surgically remove tissue and create larger openings.
In one embodiment, a handheld device for dilating tissue includes a handle assembly that includes a grip portion, an inflation mechanism, and a digital actuation member configured to actuate the inflation mechanism. The handheld device also includes a rigid cannula that includes a distal end and a proximal end, where the rigid cannula is coupled to the handle assembly along the proximal end. The handheld device further includes an inflatable balloon coupled to an outside of the rigid cannula proximate to the distal end, an inflation lumen at least partially disposed along the rigid cannula and in fluid communication with the inflatable balloon and the inflation mechanism, and an aspiration lumen at least partially disposed along the rigid cannula and includes an aspiration port proximate to the distal end.
In another embodiment, a handheld device for dilating tissue includes a handle assembly that includes a grip portion, an inflation mechanism, and a digital actuation member configured to actuate the inflation mechanism. The handheld device also includes a rigid cannula including a distal end and a proximal end, where the rigid cannula is coupled to the handle assembly along the proximal end, an inflatable balloon coupled to an outside of the rigid cannula proximate to the distal end, and an inflation lumen at least partially disposed along the rigid cannula and in fluid communication with the inflatable balloon and the inflation mechanism. The inflation mechanism includes a hydraulic system adapted to be operated by the digital actuation member, and translation of the digital actuation member displaces a working fluid from a working fluid reservoir to the inflatable balloon.
In yet another embodiment, a method of dilating tissue to facilitate atraumatic dissection within the nose and paranasal sinuses of a patient to thereby improve mucus drainage using a handheld device having a handle assembly, a rigid cannula coupled to the handle assembly, an inflatable balloon coupled to an outside of the rigid cannula, an aspiration lumen at least partially disposed along the inside of the rigid cannula, and an inflation mechanism in fluid communication with the inflatable balloon and operated by a digital actuation member including inserting the rigid cannula through a nasal opening of the patient as to place the inflatable balloon adjacent to the paranasal sinus of the patient. The method further includes depressing the digital actuation member such that the inflation mechanism causes the inflatable balloon to expand, and dilating tissue of the paranasal sinus.
The following detailed description of specific embodiments of the present disclosure can be best understood when read in conjunction with the drawings enclosed herewith.
The embodiments set forth in the drawings are illustrative in nature and not intended to be limiting of the disclosure defined by the claims. Moreover, individual features of the drawings and disclosure will be more fully apparent and understood in view of the detailed description.
The following text sets forth a broad description of numerous different embodiments of the present disclosure. The description is to be construed as exemplary only and does not describe every possible embodiment since describing every possible embodiment would be impractical, if not impossible, and it will be understood that any feature, characteristic, component, composition, ingredient, product, step or methodology described herein can be deleted, combined with or substituted for, in whole or part, any other feature, characteristic, component, composition, ingredient, product, step or methodology described herein. Numerous alternative embodiments could be implemented, using either current technology or technology developed after the filing date of this patent, which would still fall within the scope of the claims.
Embodiments of the present disclosure are directed to handheld devices that allow a medical practitioner to insert an inflatable balloon into an ostium along the paranasal sinuses of a patient, or along tissue planes leading to that ostium, and then to atraumatically dilate that ostium, or those tissue planes. Dilation of ostia may allow for evacuation of the paranasal sinuses from any mucus that has accumulated due to inflammation of the mucosal lining of the paranasal sinuses. Mucus retained in the paranasal sinuses of a patient may be evacuated using a suction device that is integrated into the handheld device, such that the medical practitioner using the handheld device can place the inflatable balloon in the ostia, dilate the ostia, and evacuate the paranasal sinus.
One embodiment of the handheld device 100 for dilating tissue is depicted in
Referring now to
The handheld device 100 includes an inflation lumen 104 that is at least partially disposed along the rigid cannula 140. The inflation lumen 104 is in fluid communication with the inflatable balloon 150 and the inflation mechanism 120, such that when the inflation mechanism 120 pressurizes a working fluid, the working fluid travels along the inflation lumen 104 and into the inflatable balloon 150, placing the inflatable balloon 150 into an inflated state.
The digital actuation member 114 may include a trigger 115 that pivots about a fulcrum pin 113. As depicted in
The handle assembly 110 may further include a return mechanism 118 that returns the digital actuation member 114 to its non-actuated position. As the digital actuation member 114 is coupled to the inflation mechanism 120, returning the digital actuation member 114 to its non-actuated position causes the inflation mechanism 120 to draw working fluid back into the working fluid reservoir 124, which displaces working fluid away from the inflatable balloon 150. In the embodiment depicted in
Referring again to
Still referring to
Referring now to
Cross sections of multiple embodiments of the rigid cannula 140 are shown in
Referring again to
When the medical practitioner is satisfied that the inflatable balloon 150 is accurately placed within the ostium 94, the medical practitioner may actuate the digital actuation member 114. As a medical practitioner applies a force that rotates the digital actuation member 114, the digital actuation member 114 causes the hydraulic system 122 to transfer a working fluid from a working fluid reservoir 124 along the inflation lumen 104 and into the inflatable balloon 150. Introduction of this working fluid places the inflatable balloon 150 in an inflated state. Because the digital actuation member 114 is configured to actuate the inflation mechanism 120, as the medical practitioner continues to depress the digital actuation member 114, the inflation mechanism 120 continues to inflate the inflatable balloon 150 located within the ostium 94 or tissue plane. The medical practitioner may continue to inflate the inflatable balloon 150 until such point that the desired inflation of the inflatable balloon 150, and corresponding dilation of the ostium 94, or tissue plane, has been achieved, or until the maximum inflation of the inflatable balloon 150 has been reached.
The rigid cannula 140 and the inflatable balloon 150 may be of a diameter that allows insertion of the inflatable balloon 150 within the ostium 94. The diameter of the rigid cannula 140 may be from about 2 mm to about 4 mm, and may be made from a material that is non-reactive with the tissue of a patient 90 and have a modulus of elasticity, or characteristic stiffness of the material, that is great enough such that the rigid cannula 140 does not perceptively flex while in operation. Materials satisfying these requirements include, but are not limited to, stainless steels, titanium, nickel, and alloys thereof. The rigidity of the rigid cannula 140 allows the medical practitioner to accurately and reliably place the distal end 142 of the rigid cannula 140 in a position relative to the ostium 94. Further, the rigidity of the rigid cannula 140 may allow the medical practitioner to apply a slight force to the tissues of the paranasal sinus 96 as to overcome any resistance encountered when inserting the inflatable balloon 150 into the ostium 94.
The inflatable balloon 150 may be made from a variety of materials that are resilient and are non-reactive with the tissue of a patient 90. In one embodiment, the inflatable balloon 150 may be made from polyethylene terephthalate (PET). The PET may be formed into a thin membrane-like surface that allows the inflatable balloon 150 to collapse onto the rigid cannula 140 when deflated. In the embodiment of the handheld device 100 depicted in
The working fluid that is displaced by the inflation mechanism 120 along the inflation lumen 104 and into the inflatable balloon 150 may be an incompressible fluid. Because the fluid is incompressible, the force that a medical practitioner applies to the digital actuation member 114 will generally correspond to the pressure of the fluid in the inflatable balloon 150. In the embodiment depicted in
The pressure of the working fluid inside the inflatable balloon 150, the inflation lumen 104, and the inflation mechanism 120 may provide a haptic feedback to the medical practitioner who is using the handheld device 100. The inflatable balloon 150 is inserted into the ostium 94 or appropriate tissue plane of the patient 90 in a deflated state. The medical practitioner applies a force to the digital actuation member 114 that causes the inflation mechanism 120 to displace working fluid along the inflation lumen 104 and into the inflatable balloon 150. As the inflatable balloon 150 contacts the tissue along the paranasal sinus 96, the ostium 94 or tissue plane may resist dilation and apply a resistive force to the inflatable balloon 150. The resistive force increases the pressure of the working fluid in the inflatable balloon 150. The medical practitioner may feel this increased pressure from contact with the digital actuation member 114. As the ostium 94 continues to dilate, an increased force is applied to the inflatable balloon 150 by the ostium 94 and the surrounding tissue of the paranasal sinus 96. The increased force increases the pressure of the working fluid within the inflatable balloon 150. The medical practitioner using the handheld device 100 may feel this increased pressure from contact with the digital actuation member 114. Thus, the digital actuation member 114 provides a haptic feedback to the medical practitioner that relates a pressure of the working fluid.
If the medical practitioner chooses to continue to fill the inflatable balloon 150 until it reaches its maximum inflation state, the inflation-limiting stop 127 will intervene to limit the amount of working fluid the inflation mechanism 120 may introduce to the inflatable balloon 150. The inflation-limiting stop 127 may mechanically prevent the medical practitioner from further introducing working fluid to the inflatable balloon 150. The medical practitioner using the handheld device 100 may feel the mechanical stop from contact with the digital actuation member 114. Thus, the digital actuation member 114 provides a haptic feedback to the medical practitioner that relates maximum inflation of the inflatable balloon 150. Further, in some embodiments, the inflation-limiting stop 127 may make an audible sound that the medical practitioner may perceive aurally.
With the ostium 94 dilated, the medical practitioner may aspirate the paranasal sinus 96 to remove accumulated mucus from the sinus cavity. With the inflatable balloon 150 still in an inflated state, the medical practitioner may apply suction to the aspiration lumen 102 by applying suction at the aspiration connector 105. As depicted in
With the ostium 94 dilated to the desire of the medical practitioner, the pressure of the working fluid within the inflatable balloon 150 may be relieved by the medical practitioner releasing force on the digital actuation member 114. The return mechanism 118 draws the working fluid away from the inflatable balloon 150 and towards the working fluid reservoir 124. When the inflatable balloon 150 is fully deflated, the medical practitioner may remove the handheld device 100 from the nasal cavity of the patient 90, and free from the nasal opening 92.
It should now be understood that handheld devices for dilating tissues along the paranasal sinuses include a rigid cannula that allows a medical practitioner to accurately and reliably place an inflatable balloon within a constricted ostium or tissue plane. The handheld devices allow the medical practitioner to dilate the tissue, and receive direct feedback from the handheld device that relates the pressure inside the inflatable balloon and the stiffness of the tissue itself. The handheld device may further include an aspiration lumen that allows the medical practitioner to remove mucus from the paranasal sinus volume to provide relief to the patient.
It is further noted that terms like “preferably,” “generally,” “commonly,” and “typically” are not utilized herein to limit the scope of the claimed disclosure or to imply that certain features are critical, essential, or even important to the structure or function of the claimed disclosure. Rather, these terms are merely intended to highlight alternative or additional features that may or may not be utilized in a particular embodiment of the present disclosure.
For the purposes of describing and defining the present disclosure it is additionally noted that the term “substantially” is utilized herein to represent the inherent degree of uncertainty that may be attributed to any quantitative comparison, value, measurement, or other representation. The term “substantially” is also utilized herein to represent the degree by which a quantitative representation may vary from a stated reference without resulting in a change in the basic function of the subject matter at issue.
Having described the disclosure in detail and by reference to specific embodiments thereof, it will be apparent that modifications and variations are possible without departing from the scope of the disclosure defined in the appended claims. More specifically, although some aspects of the present disclosure are identified herein as preferred or particularly advantageous, it is contemplated that the present disclosure is not necessarily limited to these preferred aspects of the disclosure.
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