APPARATUS TO PROVIDE AN ADJUSTABLE MECHANISM FOR RADIAL ULTRASOUND PORT AND FLUSH PORT
20200359995 ยท 2020-11-19
Inventors
Cpc classification
A61B8/12
HUMAN NECESSITIES
A61B2017/0034
HUMAN NECESSITIES
A61B10/04
HUMAN NECESSITIES
A61B8/4461
HUMAN NECESSITIES
A61B8/4455
HUMAN NECESSITIES
A61B10/0283
HUMAN NECESSITIES
A61B8/085
HUMAN NECESSITIES
A61B17/24
HUMAN NECESSITIES
A61B8/5238
HUMAN NECESSITIES
A61B2010/0208
HUMAN NECESSITIES
A61B8/4494
HUMAN NECESSITIES
A61M25/0026
HUMAN NECESSITIES
A61B17/3415
HUMAN NECESSITIES
A61B90/39
HUMAN NECESSITIES
International classification
Abstract
The present disclosure relates generally to the field of medical devices. In particular, the present disclosure relates to an assembly with an adjustable ultrasound port and flush port for lateral and axial positioning of a radial ultrasound probe within a patient.
Claims
1. An adjustable probe assembly, comprising: a housing defining an internal chamber; an ultrasound port formed within a proximal portion of the housing, wherein the ultrasound port is coextensive with the internal chamber; a flush port disposed along a middle portion of the housing, the flush port defining a fluid channel therethrough, wherein the fluid channel is coextensive with the internal chamber; and a fitting disposed around a distal portion of the housing; wherein the housing is configured to rotate relative to the fitting to alter an axial position of the flush port relative to the fitting.
2. The adjustable probe assembly of claim 1, wherein an outer surface of the distal portion of the housing includes a surface feature configured to frictionally engage an inner surface of the fitting.
3. The adjustable probe assembly of claim 1, wherein the fitting includes a projection.
4. The adjustable probe assembly of claim 1, further comprising a first seal disposed within a distal portion of the internal chamber and a second seal disposed within a proximal portion of the internal chamber.
5. The adjustable probe assembly of claim 4, further comprising a bearing disposed within a proximal portion of the internal chamber and proximal to the second seal.
6. The adjustable probe assembly of claim 5, wherein the housing and ultrasound port are configured to receive a radial ultrasound probe therethrough.
7. The adjustable probe assembly of claim 6, wherein the bearing is configured to support rotation of the radial ultrasound probe.
8. The adjustable probe assembly of claim 7, wherein the radial ultrasound probe includes a drive cable, and wherein the drive cable extends through the ultrasound port and is supported by the bearing.
9. The adjustable probe assembly of claim 8, wherein the radial ultrasound probe includes a sheath, and wherein a proximal end of the sheath is disposed within the housing between the first and second seals.
10. The adjustable assembly of claim 9, wherein the housing is configured to rotate relative to the fitting to alter an axial position of the radial ultrasound probe, and wherein the proximal portion of the housing is configured to rotate relative to a remaining portion of the housing to alter an axial position of the radial ultrasound probe.
11. A system, comprising: a handle of a catheter; an adjustable probe assembly attached to the handle, wherein the adjustable probe assembly is configured to move laterally and axially relative to the handle; and a radial ultrasound probe extending through the adjustable probe assembly, the handle and a shaft of the catheter.
12. The system of claim 11, wherein the adjustable probe assembly includes a housing defining an internal chamber, an ultrasound port formed within a proximal portion of the housing and a flush port disposed along a middle portion of the housing.
13. The system of claim 12, wherein the radial ultrasound probe includes a drive cable, and wherein the drive cable extends through the ultrasound port.
14. The system of claim 12, wherein the flush port includes a fluid channel configured to deliver fluid into the internal chamber and through a sheath of the radial ultrasound probe.
15. The system of claim 14, further comprising a first seal disposed within a distal portion of the internal chamber and a second seal disposed within a proximal portion of the internal chamber, wherein the first and second seals prevent fluid introduced through the flush port from exiting the internal chamber.
16. A method, comprising: attaching an adjustable probe assembly to a handle of a catheter such that a radial ultrasound probe attached to the adjustable probe assembly extends through the handle and a shaft of the catheter; adjusting a lateral position of the adjustable probe assembly relative to the handle; and adjusting an axial position of the adjustable probe assembly relative to the handle.
17. The method of claim 16, further comprising re-adjusting the lateral position of the adjustable probe assembly relative to the handle to alter a lateral position of the radial ultrasound probe within a lumen of the catheter shaft.
18. The method of claim 17, further comprising rotating a housing of the adjustable probe assembly relative to the handle to rotate the radial ultrasound probe within the lumen of the catheter.
19. The method of claim 16, further comprising rotating a housing of the adjustable probe assembly relative to the handle to alter an axial position of a flush port disposed along a middle portion of the housing relative to the handle.
20. The method of claim 19, further comprising introducing a fluid through the flush port and into an internal chamber of the adjustable probe assembly.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0013] Non-limiting embodiments of the present disclosure are described by way of example with reference to the accompanying figures, which are schematic and not intended to be drawn to scale. In the figures, each identical or nearly identical component illustrated is typically represented by a single numeral. For purposes of clarity, not every component is labeled in every figure, nor is every component of each embodiment shown where illustration is not necessary to allow those of ordinary skill in the art to understand the disclosure. In the figures:
[0014]
[0015]
[0016]
DETAILED DESCRIPTION
[0017] The present disclosure is not limited to the particular embodiments described herein. The terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting beyond the scope of the appended claims. Unless otherwise defined, all technical terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the disclosure belongs.
[0018] Although embodiments of the present disclosure are described with specific reference to probe assemblies, systems and methods of use thereof, and particularly leak-proof assemblies, which include an adjustable ultrasound port and/or flush port designed to maintain visual imaging of a peripheral pulmonary nodule while allowing lateral and/or axial repositioning of the radial ultrasound probe and/or flush port, it should be appreciated that such probe assemblies, systems and methods may be used to visualize and manipulate a variety of tissues within a variety of different body lumens and/or body passages.
[0019] As used herein, the singular forms a, an, and the are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms comprises and/or comprising, or includes and/or including when used herein, specify the presence of stated features, regions, steps elements and/or components, but do not preclude the presence or addition of one or more other features, regions, integers, steps, operations, elements, components and/or groups thereof.
[0020] As used herein, the term distal refers to the end farthest away from the medical professional or physician when introducing a device into a patient, while the term proximal refers to the end closest to the medical professional or physician when introducing a device into a patient.
[0021] In various embodiments, the present disclosure relates generally to an adjustable and leak-proof probe assembly configured for use with a bronchial radial ultrasound system to provide real-time imaging and targeting of difficult to access pulmonary nodules. For example, the adjustable probe assembly may include an adjustable ultrasound port and flush port configured to allow a physician to laterally (e.g., along a longitudinal axis) and/or axially (e.g., about or around a longitudinal axis) position/reposition components of the bronchial radial ultrasound system (e.g., ultrasound probe, flush port and/or probe assembly) within a peripheral region of the lung while maintaining a leak-proof seal to simultaneously flush fluid through a lumen of a radial ultrasound probe.
[0022] Referring to
[0023] In one embodiment, a first seal 122 (e.g., O-ring, etc.) may be disposed within a distal portion of the internal chamber 111 (e.g., proximal to a distal opening of the housing 110) and a second seal 124 may be disposed within a proximal portion of the internal chamber 111 (e.g., distal to a proximal opening of the housing 110). The first and second seals 122, 124 may be configured to prevent fluid introduced (e.g., flushed) through the fluid channel 115 of the flush port 114 from exiting the internal chamber 111 (e.g., flowing/leaking distally beyond the first seal 122 or proximally beyond the second seal 124). A bearing 126 may be disposed within the proximal portion of the internal chamber 111 proximal to the second seal 124. In various embodiments, the housing 110 and ultrasound port 112 may be configured to receive a proximal portion of a radial ultrasound probe 130 therethrough (
[0024] Referring to
[0025] Referring to
[0026] All of the devices and/or methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While the devices and methods of this disclosure have been described in terms of preferred embodiments, it may be apparent to those of skill in the art that variations can be applied to the devices and/or methods and in the steps or in the sequence of steps of the method described herein without departing from the concept, spirit and scope of the disclosure. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the disclosure as defined by the appended claims.