Various aspects of the present disclosure relate generally to medical systems, devices, and related methods. More specifically, the present disclosure relates to disposable medical systems and/or devices.
The field of endoscopy covers systems and methods a user may employ to examine and/or treat a subject with, e.g., the assistance of an endoscope or other suitable introduction sheaths or devices. An endoscope (or other suitable introduction device) may provide for viewing of, for example, the interior of a hollow organ or cavity in the subject's body (e.g., the gastrointestinal (GI) tract, the urinary tract, the respiratory tract, etc.). Ureteroscopy, for example, is a subset of endoscopy. Ureteroscopy may include procedures in which an endoscope (such as, e.g., a ureteroscope, uteroscope, cystoscope, hysteroscope, etc.) may be passed through the subject's urethra and bladder, and directly into the subject's ureter. The endoscope may be further inserted into the subject's kidney for pyeloscopic procedures. These procedures may be useful in the diagnosis and the treatment of disorders of the subject's urinary tract, such as the presence of kidney stones that may block urinary tract ducts.
Sterilization of such endoscopes is imperative to avoid cross-contamination between patients. Unfortunately, insufficient sterilization of endoscopes is a persistent, and hazardous problem in the medical device industry. Not only is it difficult for hospitals and medical professionals to reprocess or sterilize a wide array of endoscopes effectively, it's also costly. Moreover, typical endoscopes are expensive to manufacture, requiring highly precise and often individual endoscope-specific components (e.g., camera, illumination features, various medical tool adaptors, etc.) resulting in devices exceeding tens of thousands, and possibly hundreds of thousands of dollars. Thus, such devices are impractical for use as a one-time-use disposable device.
The systems, devices, and methods of the current disclosure may rectify some of the deficiencies described above or address other aspects of the prior art.
Examples of the present disclosure relate to, among other things, medical devices. Each of the examples disclosed herein may include one or more of the features described in connection with any of the other disclosed examples.
In one example, an insertion device may include a hollow handle and a shaft extending distally of the hollow handle. The insertion device may also include a cap coupled to a distal end of the shaft. The cap may include a camera and an LED coupled thereto.
Examples of the insertion device may include one or more of the following features. The shaft may be a rigid shaft. The shaft may include a multi-lumen extrusion. The shaft may include a plurality of discrete lumens fixedly coupled together. The hollow handle may include a rounded ball-head and an extension depending therefrom. The shaft may extend from a location within the ball-head and through a side of the ball-head of the hollow handle. A port may extend from a side of the ball-head of the hollow handle opposite the side from which the shaft extends. The hollow handle may include a plug extending from a portion of the extension of the hollow handle opposite the ball-head. The plug may be selectively coupleable and uncouplable from an umbilicus connector. The handle may include two fluid ports proximate the plug. Each of the two fluid ports may be fluidly coupled to a tube extending through the hollow handle, through the shaft, and toward the cap. The umbilicus may be coupled to a computer. The LED may be a first LED, the insertion device may further include a second LED disposed on the cap. Each of the first and second LEDs may be disposed on opposing sides of the camera. A working channel may extend through and proximally of a proximal end of the shaft.
In a further example, an insertion device may consist essentially of a handle including a head having a port which may extend from a first side of the head and a grip which may depend from the head. The insertion device also may include a shaft extending distally of the hollow handle and a cap coupled to a distal end of the shaft. The cap may include a camera and a light sourced coupled thereto.
Examples of the insertion device may further include one or more of the following features. A proximal end of the shaft may be disposed within the rounded ball-head of the handle. A plug may extend from the grip in a direction opposite of the ball-head, and the plug may be selectively coupleable and uncouplable from an umbilicus connector. The grip may include two ports proximate the plug, and each of the two ports may be fluidly coupled to a tube extending through the handle, through the shaft, and toward the cap.
In a further example, an insertion device may include a handle. The handle may consist essentially of a rounded ball-head having a port extending from a first side of the rounded ball-head and a grip depending from the rounded ball-head, the grip including a pair of fluid ports and a plug extending from the grip in a direction opposite that of the rounded ball-head. The insertion device may further include a shaft having a proximal end disposed within the rounded ball-head and extending from a second side of the ball-head in a direction opposite the first side of the rounded ball-head. A cap may be coupled to a distal end of the shaft and the cap may include a camera and a light source coupled thereto.
Examples of the insertion device may include one or more of the following features. A proximal end of a working channel may be coupled to the port and may extend distally through a proximal end of the shaft and towards the cap. The handle may include a plug extending from a portion of the extension of the handle opposite the ball-head, and wherein a cable or a bundle of cables may have a first end coupled to at least one of the camera and light source and a second end coupled to the plug.
Both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the features, as claimed. As used herein, the terms “comprises,” “comprising,” or other variations thereof, are intended to cover a non-exclusive inclusion such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements, but may include other elements not expressly listed or inherent to such a process, method, article, or apparatus. Additionally, the term “exemplary” is used herein in the sense of “example,” rather than “ideal.” As used herein, the terms “about,” “substantially,” and “approximately,” indicate a range of values within +/−5% of a stated value.
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate exemplary features of the present disclosure and together with the description, serve to explain the principles of the disclosure.
Examples of the present disclosure relate to medical systems and devices for diagnosing and/or treating internal areas of a subject's body. The medical system may include an insertion device and one or more medical devices operably coupled thereto for introduction of an end-effector or other object through the insertion device.
Reference will now be made in detail to examples of the present disclosure described above and illustrated in the accompanying drawings. Wherever possible, the same reference numbers will be used throughout the drawings to refer to the same or like parts.
The terms “proximal” and “distal” are used herein to refer to the relative positions of the components of an exemplary medical device or insertion device. When used herein, “proximal” refers to a position relatively closer to the exterior of the body or closer to an operator using the medical device or insertion device. In contrast, “distal” refers to a position relatively further away from the operator using the medical device or insertion device, or closer to the interior of the body.
Cap 16 includes a rounded circumferential edge and is angled so as to be atraumatic to tissue. Additionally, cap 16 may be coupled (e.g., removably or permanently) to shaft 14 in any appropriate manner such as, for example, snap fit, interference fit, adhesives, welding, molding, etc. Insertion device 10 includes any device configured to allow an operator to perform medical diagnoses and/or treatments on a subject. For example, insertion device 10 includes any device configured to allow a user to access and view internal areas of a subject's body. For example, insertion device 10 may be inserted into any portion of a urinary tract, such as a ureter, a gastrointestinal lumen, such as an esophagus; a vascular lumen; and/or an airway.
According to aspects of the present disclosure, insertion device 10 is a ureteroscope. In some contemplated examples, insertion device 10 is a sterile, single-use, and completely disposable ureteroscope. That is, upon completion of a medical procedure, insertion device 10, including hollow handle 12, shaft 14, and cap 16 may be disconnected from any appropriate console or power source (e.g., computer 40) and thrown away. As such, concerns of cross-contamination or insufficient sterilization of insertion device 10 may be alleviated. Other types of devices, however, may be substituted for the ureteroscope, including, as examples, a hysteroscope, a uteroscope, a bronchoscope, a cystoscope, and similar devices. Any such devices may be single-use and completely disposable.
Hollow handle 12 of insertion device 10 may have any shape suitable for gripping and controlling insertion device 10. For example, hollow handle 12 may have an ergonomic shape designed to be held comfortably in the hand, e.g., the palm of the hand of a medical professional. For example, as shown in
As shown in
As noted above, hollow handle 12 includes a plurality of ports. For example, port 18 extends from ball-head 12A parallel or aligned with longitudinal axis S and communicates with a working channel 30 extending through shaft 14 and tip 16, as shown in
As shown in
Additionally, insertion device 10 includes an illumination unit including one or more (e.g., two) light-emitting diodes (“LED”) 36. LEDs 36 may be at a distalmost tip of cap 16 and/or may be at least partially embedded within cap 16. As shown, LEDs 36 may be located on opposite sides of camera 34 and may emit light upon receipt of an appropriate power supply. LED 36 may include, for example, a high-power sub 2 mm LED with a CCT range of 5000-6500K. Any other suitable LED may be used. Further, insertion device 10 includes a pressure sensor 29 at least partially embedded within cap 16. Pressure sensor 29 may be arranged to directly measure body cavity pressure of a patient. Pressure sensor 29 may include a piezoresistive pressure die (such as, e.g., the P330 Series 1F Absolute Pressure Sensor Die from Nova Sensor).
A bundle of cables 38 (or alternatively, a single cable 38 adapted for conveyance of both power and data) may be coupled to one or more of camera 34, LEDs 36, and pressure sensor 29 and extend proximally along shaft 14 between an outer wall of working channel 30 and an inner wall of shaft 14, and connect to plug 20. Plug 20 includes an electrical connector to connect hollow handle 12, including cable/bundle 38, to an umbilicus 50 for facilitating electrical connections and functions, such as transferring data to/from camera 34, pressure sensor 29, and/or powering LEDs 36. As shown in
To facilitate secure connection or mating between adaptors 54 and 56, adaptors 54 and 56 may be magnetically attracted toward one another, or threadably connected to maintain contact therebetween, or use a method of interfering parts (snap or lever release connection) to hold the mating halves together. Additionally or alternatively, at least one of adaptors 54 and 56 may include one or more leads (not shown) arranged to mate or otherwise connect with one or more receptacles 59 on the other of adaptors 54 and 56 so as to convey signals (e.g., power and/or data) from/to cable/bundle 38 to or from umbilicus 50, which is in turn coupled to a computer 40.
Computer 40 may include a smartphone, tablet computer, laptop computer, desktop computer, and/or any other suitable computing device. Computer 40 may include a display 42, as well as other electronic components (not shown), such as a central processing unit, memory, video and graphics cards, wireless and wired networking devices, audio devices, one or more input/output ports, a power supply, and/or any other suitable computer features. Display 42 may include a touch screen for displaying image data, and for receiving inputs or commands from a user. User interaction may be directed toward aspects of image capture, video capture, brightness control, mode controls, narrow band imaging toggle, and/or any other controls that may be part of a typical ureteroscopy procedure. Computer 40 may include imaging electronics configured to process and/or transfer the image data, display the image data on display 42 for viewing by a user, and send signals to camera 34 and LEDs 36.
Each of ports 22 and 24 may include a luer (or other mating configuration) fluidly coupled with one of first and second channels, passages, or tubes 44 extending through shaft 14 and tip 16, as shown in
In any such arrangement, ports 22 and 24 are located on a proximal end thereof of extension 12B opposite the position of the ball-head 12A. As shown in
Shaft 14 of
In use, a medical professional may grasp hollow handle 12 (e.g., either via ball-head 12A or extension 12B) and direct shaft 14 to enter one or more body passages of a patient. If desired or necessary, the medical professional may deliver one or more medical tools or devices (e.g., baskets, forceps, etc.) through port 18 and working channel 30 so as to perform a medical procedure. Additionally, if it is determined desirable or necessary, the medical professional may cause one or more of an irrigation fluid, aspiration fluid, or medicament infusion to be delivered through tubes 44 and distally of shaft 14. Once a medical procedure has been completed, the medical professional may retract shaft 14 from the patient, uncouple umbilicus 50 from plug 20, and discard or throw away the entirety of hollow handle 12, including plug 20 and shaft 14. In such a manner, cross-contamination and insufficient sterilization concerns are alleviated.
While principles of the present disclosure are described herein with reference to illustrative examples for particular applications, it should be understood that the disclosure is not limited thereto. Those having ordinary skill in the art and access to the teachings provided herein will recognize additional modifications, applications, embodiments, and substitution of equivalents all fall within the scope of the features described herein. Accordingly, the claimed features are not to be considered as limited by the foregoing description.
This patent application claims the benefit of priority under 35 U.S.C. § 119 to U.S. Provisional Patent Application No. 62/420,938, filed Nov. 11, 2016, which is herein incorporated by reference in its entirety.
Number | Date | Country | |
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62420938 | Nov 2016 | US |