The present disclosure relates in some aspects to an obturator configured to be used with a cannula having internal features, in particular during a medical procedure.
Various medical procedures require the provision of gases, typically carbon dioxide, to a patient during the medical procedure. For example, two general categories of medical procedures often require providing gases to a patient. These include closed type medical procedures and open type medical procedures.
In closed type medical procedures, an insufflator is arranged to deliver gases to a body cavity of the patient to inflate the body cavity and/or to resist collapse of the body cavity during the medical procedure. Examples of such medical procedures include laparoscopy and endoscopy, although an insufflator may be used with any other type of medical procedure as required. Endoscopic procedures enable a medical practitioner to visualize a body cavity by inserting an endoscope or the like through one or more natural openings, small puncture(s), or incision(s) to generate an image of the body cavity. In laparoscopy procedures, a medical practitioner typically inserts a medical instrument through natural openings, small puncture(s), or incision(s) to perform a medical procedure in the body cavity. In some cases, an initial endoscopic procedure may be carried out to assess the body cavity, and then a subsequent laparoscopy carried out to operate on the body cavity. Such procedures are widely used, for example, on the peritoneal cavity, or during a thoracoscopy, colonoscopy, gastroscopy or bronchoscopy.
Medical instruments, including apparatus for delivering gases and to visualize the body cavity can be inserted into the body cavity before and during these medical procedures. Devices can be used to create one or more entry ports for delivery of gases and medical instrument access. Obturators can be used to assist insertion of a cannula into a body cavity.
Various techniques are known in surgery for gaining entry to the body cavity. An open entry technique involves creating a wound by cutting through the tissue until the site of interest is reached. A blunt obturator is assembled into a cannula and this assembly is inserted into the wound. The cannula is retained in the wound, typically with an outer sliding retention device and the obturator is removed.
An optical entry technique uses an optical obturator in a cannula as a trocar assembly. The optical obturator has a lumen into which a surgical scope can be inserted, and an optical clear tip to allow the scope to view through the tip of the obturator. A small incision is made in the skin and the trocar assembly is inserted into the wound. The trocar is pushed through the tissue until the site of interest is reached. Using the scope viewing through the tip of the obturator, the depth of the trocar in the tissue can be determined, mitigating risk of inserting the trocar too far into the tissue. The obturator with the scope is then removed and the scope can be inserted into the remaining cannula while the patient is insufflated to visualize the body cavity.
A closed entry technique utilizes an obturator with a dilating or bladed tip. An incision is made in the skin then skin around the wound is lifted and the obturator and cannula are pushed through. Alternatively, the site of interest can be insufflated first using a Veress needle. Once the body cavity is inflated, the skin is held while a bladed or dilating obturator and cannula are pushed into the body cavity. The obturator is then removed from the cannula.
The obturator can be used together with the cannula for insertion into the body cavity. Some cannulas can have internal structures (such as ribs or guide elements) in the inner lumen or other internal surface of the cannula. It is desirable that the internal structures present on the inside or inner lumen of cannula are not damaged during use of the obturator, both for purposes of maintaining their function and also to avoid internal cannula components from dislodging and entering the body cavity.
The present disclosure provides examples of an obturator configured to accommodate a cannula with internal structural features or elements.
Structural elements can be added or provided inside the cannula for various reasons, such as, but not limited to, directing gas flow to the surgical cavity utilizing a directed gas flow cannula. These structural elements in the cannula, which protrude inwardly into the cannula lumen, may interfere with or impede the use of an obturator in a trocar assembly. The obturator may damage or break off such structural elements, impeding their intended function and/or causing pieces of the cannula to break off and potentially enter the body cavity. The present disclosure provides examples of an obturator and/or a trocar assembly that seeks to remedy or ameliorate the aforementioned problems and/or other problems (including, for example, preventing the cannula elements from interfering or impeding the use of the obturator for entry techniques).
In some cases, an obturator for use in a trocar assembly can comprise an obturator body, an obturator shaft extending from the body and a penetrating end at a distal end thereof. The obturator shaft can be at least partially positionable within a cannula and can comprise one or more internal structure accommodating portions, configured to locate around or adjacent to one or more internal structures located in and/or on an interior wall of a shaft of the cannula.
The obturator described in any of the preceding paragraphs may further comprise one or more of the following features. The one or more internal structure accommodating portions can comprise one or more recesses, slots or openings located in a surface of the obturator shaft. The one or more internal structure accommodating portions can comprise a portion of the obturator shaft comprising a reduced diameter relative to the diameter of the remainder of the obturator shaft. The one or more internal structure accommodating portions can comprise a deformable material disposed around a portion of the obturator shaft, wherein the deformable material deforms/flexes around the internal structures on the cannula when the obturator is inserted in the cannula. The one or more internal structure accommodating portions can be located at or adjacent to the distal end of the obturator shaft. The one or more recesses or openings can provide clearance for the obturator from the internal structures on the cannula and may also facilitate ease of insertion and placement of the obturator inside the cannula. The one or more recesses or openings can extend from the distal end of the obturator shaft, extending at least partway towards the obturator body. The deformable material can be configured as a sheath around the distal end of the obturator shaft. The deformable material can be provided as a ring around the distal end of the obturator shaft. The ring can deform when the obturator slides within the cannula and spring open on exiting the open distal end of the cannula to prevent debris from entering the cannula/sticking to internal structures.
The obturator body can have one or more locating elements that can be configured to mate with one or more corresponding receiving elements in the cannula. The one or more locating elements can comprise one or more pins extending from an underside of the obturator body. The one or more locating elements can orient the obturator to the cannula before the cannula internal structures contact the obturator. The one or more locating elements can include at least one locking finger extending outwardly or distally from a lower surface of the obturator body, the at least one locking finger configured to be received in a corresponding aperture in the cannula. The locking finger can comprise a locking tab configured to engage with a corresponding engagement tab in the cannula.
The obturator can be an optical obturator, comprising a lumen configured to receive a scope. The obturator body can have one or more seal elements configured to prevent gas leaking from the obturator lumen. The one or more seal elements can comprise an upper seal configured to seal around a medical instrument when inserted into the obturator lumen and a lower seal configured to create a gas seal when there is no medical instrument in the obturator lumen. The one or more seal elements can be located about the proximal open end of the obturator body, the one or more seal elements configured to prevent gas leaking out of the obturator body. The one or more seal elements can be a flexible or deformable material which provide a seal against the medical instrument when inserted into the obturator. In this application, reference to a medical instrument may include an endoscope or camera, laparoscope or other scope device. The flexible or deformable material can fit over a top surface of the obturator body. The penetrating end of the obturator can have a blunt or dilating tip. The tip can be bladed or unbladed.
In some cases, a trocar assembly can comprise a cannula comprising a shaft with a lumen, and one or more internal structures disposed on at least a portion of the lumen; and an obturator, the obturator comprising an obturator shaft with one or more internal structure accommodating portions configured to locate around or adjacent to the one or more internal structures on the cannula lumen when the obturator shaft is located in the lumen of the cannula.
The trocar assembly described in any of the preceding paragraphs may further comprise one or more of the following features. The obturator can further comprise an obturator body, an obturator shaft extending from the obturator body and a penetrating end at a distal end thereof. The obturator shaft can comprise one or more internal structure accommodating portions, configured to locate around or adjacent to the one or more internal structures on the cannula lumen.
The one or more internal structure accommodating portions can comprise one or more recesses or openings located in a surface of the obturator shaft. The one or more internal structure accommodating portions can comprise a portion of the obturator shaft comprising a reduced diameter relative to the diameter of the remainder of the obturator shaft. The one or more internal structure accommodating portions can comprise a deformable material disposed at least partly around a portion of the obturator shaft, wherein the deformable material deforms/flexes around the one or more internal structures when the obturator is inserted in the cannula. The one or more internal structure accommodating portions can be located at or adjacent to the distal end of the obturator shaft.
The one or more recesses or openings can provide clearance for the obturator from the internal structures on the cannula. The one or more recesses or openings can extend from the distal end of the obturator shaft, extending at least partway towards the obturator body. The deformable material can be configured as a sheath around the distal end of the obturator shaft. The deformable material can be provided as a ring around the distal end of the obturator shaft. The ring can deform when the obturator slides within the cannula and springs open on exiting the open distal end of cannula to prevent debris from entering the cannula/sticking to internal structures.
The obturator body can have one or more locating elements configured to mate with one or more corresponding receiving element in the cannula. The one or more locating elements can comprise one or more pins extending from an underside of the obturator body. The one or more locating elements can orient the obturator to the cannula before the one or more internal structures protruding outwardly from a surface of the lumen of the cannula contact the obturator. The one or more locating elements can include at least one locking finger extending outwardly from lower surface of the obturator body, the at least one locking finger configured to be received in a corresponding aperture in the cannula. The at least one locking finger can comprise a locking tab configured to engage with corresponding engagement tab in the cannula.
The obturator can be an optical obturator, comprising a lumen configured to receive a scope. The obturator body can have one or more seal elements configured to prevent gas leaking from the obturator lumen. The one or more seal elements can comprise an upper seal configured to seal about a scope when inserted into the obturator lumen and a lower seal configured to create a gas seal when there is no scope in the obturator lumen. The one or more seal elements can be located about the proximal open end of the obturator body, the seal elements configured to prevent gas leaking out of the obturator body. The one or more seal elements can be a flexible or deformable material which provide a seal against the scope when inserted into the obturator. The flexible or deformable material can fit over a top surface of the obturator body.
The penetrating end of the obturator can have a blunt or dilating tip. The tip can be bladed or unbladed. The trocar assembly can be configured to be used with a humidifier and/or insufflator system to supply gases to a patient, and/or with other medical instruments, such as those typically used in laparoscopic medical procedures.
These and other features, aspects, and advantages of the present disclosure are described with reference to the drawings of certain embodiments, which are intended to schematically illustrate certain embodiments and not to limit the disclosure. In some cases, a “slice” has been shown for clarity purposes for some sectional and cross-sectional views of a three-dimensional cannula. A person reasonably skilled in the art would be able to appreciate that these figures illustrate a slice of a three-dimensional cannula. In some cases, the projection surfaces have not been shown for clarity. For example, projecting hole surfaces have not been shown in some views.
Although certain embodiments and examples are described below, those of skill in the art will appreciate that the disclosure extends beyond the specifically disclosed embodiments and/or uses and obvious modifications and equivalents thereof. Thus, it is intended that the scope of the disclosure herein disclosed should not be limited by any particular embodiments described below.
Fluids, for example, gases can be introduced to a surgical cavity, for example, the peritoneal cavity via a cannula inserted through an incision made in a patient's body (for example, the abdominal wall). A trocar can be used to create an entry point and/or to insert the cannula into the patient's body. The trocar can include an obturator and a cannula. The cannula and obturator can be used in creating and/or maintaning a medical instrument entry port. The obturator can fit down the bore or inner lumen of the cannula to create the entry port. As described herein, structures such as guide elements may be present on the inner wall of the cannula. These structures or guide elements can interfere with ordinary use of an obturator yet need to remain intact throughout the medical procedure to achieve their intended purpose.
The cannula can be coupled to an insufflator. The gases flow from the insufflator can be provided to inflate the surgical cavity (for example, to maintain a pneumoperitoneum, which is a cavity filled with gas within the abdomen). A medical instrument can be inserted through the cannula into the inflated surgical cavity. For example, an endoscope, another vision system, including but not limited to a scope, or a camera unit can be inserted into the cavity. Visibility in the cavity can be assisted by introduction of fluid (gas or liquid), which can be air, carbon dioxide, saline, or any other suitable gas or liquid. In some cases, while the term gas or gases can be used to refer to the fluid that is inserted through the cannula and/or into the cavity as described herein, it is understood that any fluid, including any gas or liquid, can be used. After initial insufflation and insertion of the instrument (for example, a laparoscope) through the cannula, additional cannulas can be placed in the surgical cavity under laparoscopic observation. A trocar can be used to create and/or maintain the entry ports. At the end of the operating procedure, all instruments and cannulas are removed from the surgical cavity, the gases are expelled, and each incision is closed. In some embodiments, the pressure within the surgical cavity is maintained to be substantially constant by the insufflator. The system can also include one or more vents to remove (e.g., vent out) smoke and gases from the cavity. The vent may in some cases include a tap that is manually activated by a medical professional. The insufflator may be controlled to compensate for reduction in pressure during venting, e.g., via controlling delivery of fresh insufflation gases into the cavity. For thoracoscopy, colonoscopy, sigmoidoscopy, gastroscopy, bronchoscopy, and/or others, the same or substantially similar procedure for introducing gases to a surgical cavity can be followed. The quantity and flow of gases can be controlled by the clinician performing the examination and/or automatically by the surgical system.
In some figures described herein, a slice of the trocar, cannula, and/or obturator can be shown as opposed to a cross-section.
As shown in
The system can also optionally include a venting cannula 22, which can have substantially the same features as the cannula 15 and which can be coupled to a filtration system to filter out smoke and the like. The gases delivery conduit 13 can be connected to a humidifier, such as a humidifier with a humidifier chamber 5. The humidifier chamber 5 can be in fluid communication with a gases supply 9 via a further conduit 10. The humidifier may include a controller or control unit 21, which can include a microprocessor for controlling supply of energy to a heating element of the humidifier. A filter 6 can be connected downstream of the humidifier's outlet 11 or upstream of the humidifier inlet. The filter can also be located along the further conduit 10, or at an inlet of the cannula 15. The humidifier and components of the system can be any type suitable for use in medical procedures, such as the Fisher and Paykel Healthcare Humigard SH870 surgical humidifier and the ST320 humidified insufflation kit for laparoscopic and open surgery.
As described herein, a proximal direction with respect to an obturator or cannula generally can refer to the top end of the cannula or obturator body. A distal direction generally can refer to the bottom end of the obturator or cannula shaft configured to be the first section of the trocar assembly inserted into the surgical cavity. As described herein, a proximal direction with respect to a medical instrument generally can refer to the top end of the medical instrument body, while a distal direction with respect to a medical instrument generally can refer to the bottom end of the medical instrument body configured to be the first section of the medical instrument inserted into the cannula and/or surgical cavity. Reference numerals of the same or substantially the same features may share the same last two digits.
The cannula 400 shown in
The guide elements 420 may be configured to assist in preventing or at least reducing condensation that may form on or drip onto a viewing surface that could result in impairment of vision or a ‘fogging effect’. Similarly, non-water based particles such as smoke particles in or around the viewing surface may impair vision. The guide elements 420 can be configured to substantially direct the gases along the medical instrument 410 and/or beyond the distal end of the medical instrument such that the gases create an environment adjacent to and/or around the lens to achieve the two example effects described above. However, the guide elements 420 located in the cannula may obstruct other medical instruments from being inserted through the lumen 404 in the cannula shaft, such as an obturator for example. It would be desirable then, that the obturator be compatible with the cannula that it is used with. Similar problems may apply where there is at least one region and/or feature located on and/or within the cannula shaft and/or body for example, bumps, fins, dimples or any other structure. One advantage of such an obturator is that it provides compatibility across a range of cannula types, that is, cannulas with and without ‘guide elements’ or other similar such internal structures.
The arrangement of the medical instrument 410 within the cannula shaft 406, for example where the medical instrument 410 is positioned substantially concentrically with respect to the longitudinal axis of the cannula shaft 406, promotes or encourages maintained contact of the insufflation gases with the instrument, e.g. a lens of a scope. This contact may also allow for defogging of or clearing of smoke or other particles from the instrument, in particular the lens. In general, increasing the flow rate of the insufflation gases can reduce the required defogging/clearing time. Cold dry gas provided to the cannula while the instrument is held within the cannula shaft can also help to defog or clear the lens. The defogging/clearing can be improved with warming of gases. Warming of the gas can be achieved using a humidifier such as the SH870 humidifier from Fisher & Paykel Healthcare (Auckland, NZ) which can further humidify the gases.
More detailed examples of the cannula features or guide elements that the obturator described herein are designed to be compatible with are described in International Application No. PCT/NZ2019/050100, titled “DIRECTED GAS FLOW SURGICAL CANNULA FOR PROVIDING GASES TO A PATIENT,” filed on Aug. 16, 2019, the disclosures of which are hereby incorporated by reference in their entirety.
An obturator with features compatible with cannula having internal structural elements or features (for example, the cannulas described with reference to
The cannulas described herein have internal structures, such as guide elements, which, as discussed, can interfere with the obturator. Therefore, the obturator described herein can be designed to be compatible with these types of cannula.
When the obturator is used with the cannula the obturator can be designed to prevent gas from leaking out or around the obturator. The obturator can be removably coupled with the cannula. In some cases, a medical instrument, e.g. a scope, can be inserted and retained in an obturator that allows optical instrumentation or visualization. In some cases, the medical instrument can visualize through the tip of an obturator that has an optically clear or transparent material. As used herein, an optical version of the obturator or an optical obturator can refer to an obturator that has an optically clear or transparent material at its tip to allow visualization through the tip, for example to contribute to optical clarity and clear vision for the medical instrument at the surgical cavity. The obturator-cannula assembly can be fit for the purpose of inserting the cannula into the patient. The obturator-cannula assembly can be used to gain entry into the patient's body and/or for re-entry, for example, to gain access again after removal of a tissue sample.
The obturator can have features configured to be compatible with the cannula with structural features disposed on and/or within an inner surface of the cannula shaft and/or body to avoid interference with or damage of the internal structures. The obturator shaft and/or tip can have a region or feature that accommodates the internal structures without compromising their function. In some cases, as used herein, the internal structures can be guide elements as described herein or other internal structures within the cannula.
In some cases, the obturator can have features to accommodate other features on the inner surface of the cannula, for example features that create turbulence as well as instrument retaining elements e.g. dimples, outwardly extending walls or other protrusions.
Tip of Obturator
The obturator can have a variety of tips on the penetrating distal end of the shaft. The tip of the obturator can be designed to be received by the cannula without causing damage to the internal structures located in the cannula or the tip itself. This can allow the obturator to be compatible with a cannula with internal structures. In some cases, the obturator can be compatible with a range of different cannula types. For example, the obturator can be compatible with cannulas with and without internal structures, such as guide elements.
The obturator tip can have a penetrating end at the distal end. The variations of the tip shown in
In some cases, the obturator can have one or more internal structure accommodating portions 563 on the obturator shaft at or adjacent to the obturator tip 562. The position of the one or more internal structure accommodating portions 563 may substantially coincide with the location of the one or more internal structures on the cannula inner wall. In some cases, the region of the obturator shaft which has the internal structure accommodating portions can be removably attached to the obturator shaft. In some cases, different designs of the internal structure accommodating portions could be removably attached to the obturator shaft to be suitable for differently shaped and/or differently positioned cannula internal structures. For example, the cannula may have internal structures at the proximal end of the cannula and/or at the distal end of the cannula or at any position along its length. Accordingly, the internal structure accommodating portions may include one or more recesses, openings or slots at any point along the obturator shaft as well as, or instead of, at or adjacent to the obturator tip 562. The one or more recesses, openings or slots can include multiple discrete internal structure accommodating portions 563 or can include elongate recesses, openings or slots that extend substantially the length of the obturator shaft and/or the distal tip 562
The or each internal structure accommodating portion 563 can provide clearance for the obturator from the internal structures so the obturator can be inserted into the cannula and the obturator shaft received in the cannula lumen.
As shown in
In some cases, for example in the hollow body obturator, the obturator can have a lumen that runs substantially through the length of the obturator. The lumen in the obturator can be defined by a sidewall, such as an inner sidewall of the obturator shaft. The lumen can extend substantially the length of the obturator shaft. The obturator with a lumen running through can be an optical obturator. The lumen can act as a pathway to allow access for a medical instrument, such as a vision accessory, and/or surgical scope. The lumen can create a pathway that can allow access for a viewing instrument such as a scope or camera element to provide visualization.
The obturator 760 has openings 763 at or adjacent the tip 762. The openings 763 may be configured to coincide with the location of internal structures 720 on the cannula 700. This means that the openings 763 provide clearance for the obturator 760 from the internal structures 720 so the obturator 760 can be inserted into the cannula 700. The openings 763 can provide an opening or recess on the surface of the shaft of the obturator 760. In some cases, the openings 763 can be positioned anywhere in or on the obturator shaft 761, such as at a distance from the tip 762, for example. The openings 763 can also be located at or near the proximal end, distal end or at a mid-point of the obturator shaft 761 or may extend along substantially the entire length thereof.
The obturator 760 can have various internal structure accommodating portions that allow the obturator shaft 761 to be inserted into the cannula 700 and allow compatibility of the obturator 760 with a cannula 700 with internal structures. For example, the obturator 760 can include recesses, slots or openings as described in
As used herein, the reduced diameter portion 863 at the distal end of the obturator and/or the obturator tip 862 of the obturator 860 in the embodiment of
In some cases, the obturator can have a flexible or deformable material in or on the obturator shaft and/or tip to accommodate the cannula internal structures. The flexible or deformable material may allow for improved sealing of the cannula during insufflation and/or may help prevent blockage or occlusion of the cannula by unwanted media.
The obturator 960 can have a deformable material 963 at the tip 962 to allow the obturator 960 to flex, compress or otherwise deform so as to yield to the internal structures 920 in the cannula 900. The deformable material 963 can allow the obturator 960 to be received by the cannula 900 without interfering with or damaging the internal structures 920 in the cannula 900 and/or the obturator itself. In some cases, as shown in
In some cases, such as the embodiment shown in
The obturator tip 1062 can include a flexible structure 1063 disposed about the obturator shaft and/or tip. The flexible material 1063 can prevent the internal structures 1020 in the cannula 1000 from interfering with the obturator 1060.
The flexible structure 1063 at the tip 1062 of the obturator 1060 can flex, compress or otherwise deform as it passes over the internal structures 1020 of the cannula 1000 as the obturator shaft 1061 is inserted into the cannula 1000. Once the obturator 1060 is positioned in the cannula shaft to form the trocar assembly, the flexible structure 1063 can spring open or otherwise return to its pre-flexed, pre-compressed or pre-deformed state to cover the tip of the cannula 1000. For example, an outer edge 1065 of the flexible ring may lie adjacent to an outer edge 1067 of the distal end of the cannula 1000. Once the flexible structure 1063 passes over the internal structures 1020, the flexible structure 1063 can be located at the distal end of the cannula 1000 with its outer edge 1065 lying adjacent the outer edge 1067 of the cannula distal end. Since the diameter of the obturator 1060 is smaller than the diameter of the inner lumen of the cannula 1000, a gap created between the obturator 1060 and the inner sidewall of the cannula lumen can allow for debris to enter the cannula lumen. The flexible structure 1063 can be located at the distal end of the cannula 1000 and can create a seal, covering the distal end of the cannula 1000. This can help to prevent fluid, tissue, and debris from entering the cannula 1000 as the obturator and cannula are inserted into the surgical cavity. Preventing fluid, tissue and debris from entering the cannula 1000 can be advantageous in some cases to prevent this fluid, tissue, and debris from sticking or otherwise attaching to the cannula internal structures 1020 and potentially reducing their function. In some cases, the flexible structure 1063 can provide for smoother insertion of the obturator 1060 and can reduce the likelihood of tissues, organs, or other substances getting stuck in the gaps between the obturator and inner wall of cannula. The obturator 1060 can be removed from the cannula 1000 by pulling it back up through the cannula 1000. The flexible structure 1063 can flex out of the way of the internal structures 1020. The obturator 1060 thus can have a flexible structure 1063 at or adjacent the tip 1062 which can deform on contacting the internal structures 1020 during insertion into the cannula shaft and/or removal from the cannula 1000. The flexible structure 1063 can physically contact the internal structures 1020 as the obturator 1060 is passed through the lumen of the cannula 1000.
Locating Elements of Obturator
The obturator may need to be in a certain orientation before it is attached to the cannula. The obturator may have one or more locating elements to locate the obturator onto the cannula and ensure that it is orientated correctly. Proper orientation of the obturator can prevent the obturator from damaging internal structures in the cannula or itself during engagement with the cannula.
In some cases, such as shown in
As shown in
As illustrated in
In some cases, the obturator can include a locating element 1271 on the obturator body 1267 at a proximal end of the obturator. The locating element can clip into or otherwise engage the cannula to properly orient the obturator 1260 axially within the cannula 1200, to assist with aligning the internal structure accommodating portions 1263 of the obturator with the internal structures of the cannula 1200 before it is fully inserted into the cannula. In some cases, one or more locating elements can be used that clips the obturator into the cannula.
One or more locating elements 1271 may extend from a cannula contacting surface 1273 of the obturator body 1267 or may extend from other parts of the obturator body 1267, for example its outer surface 1269. In the embodiment shown in
A portion of the locking finger locating elements 1271 that extends downwardly from the cannula contacting surface 1273 can have a length L. The length L can be long enough to ensure that the obturator 1260 does not interfere with the internal structures in the cannula 1200 before it is properly orientated. The proximal end of the cannula 1200 can include corresponding apertures 1275 that are a size and shape that can receive the locking finger locating elements 1271 when the obturator is engaged with the cannula as shown in
As shown in
The obturator 1260 can have a locking finger locating element 1271 that clips into the proximal end of the cannula to help retain the obturator 1260 inside the cannula. The locking finger locating element 1271 can ensure that the obturator 1260 and cannula will not come apart during use. Once the cannula has been inserted as required for the surgical procedure, the release structures 1274 on the side can be pressed which allows the obturator 1260 to be removed from the cannula.
The obturator 1260 can have locking finger locating elements 1271 that are long enough to ensure that the clips orient the obturator 1260 to the cannula correctly before the internal structures in the cannula contact the obturator 1260. This may prevent the obturator being inserted in the wrong orientation. The locking finger locating elements 1271 can clip or otherwise engage into the proximal end of the cannula which may help retain the obturator 1260 inside the cannula.
Examples of Optical Obturator that Prevents Gas Leaking around the Medical Instrument
As described previously, an optical obturator can include a lumen that runs longitudinally through the obturator from an opening in the proximal body towards a distal end of the shaft or the tip. In such embodiments, gas may leak out of the obturator. For example, gas can leak out of an opening in the body of the obturator, where the medical instrument, e.g. surgical scope, enters the lumen of the obturator. The obturator can include one or more seal elements to prevent or mitigate such gas leak, such as the example embodiments shown in
The one or more seal elements 1380 can include an upper seal 1381 and a lower seal 1382. The upper seal 1381 can seal around a medical instrument, for example a scope, when the medical instrument is inserted into the obturator 1360. The lower seal 1382 can create a gas seal for example when there is no medical instrument inserted in the obturator 1360.
The obturator 1360 can have a seal element 1380 with one or more seals in the proximal end of the obturator. The seal element 1380 can be located in the obturator body 1367. The seal element 1380 can be located in or on the inner sidewall of the lumen 1365 in the obturator body 1367. The seal elements 1380 can extend inwardly into the lumen 1365 of the obturator 1360. The seal elements 1380 can create an annular sealing ring (as shown in
The one or more proximal seals 1480 can be positioned on the proximal end of the obturator body 1467 to prevent gas escaping through the lumen 1465 of the obturator 1460. The proximal seal 1480 can be an annular seal or ring or any other suitable seal that is positioned on the proximal most surface of the obturator body 1467. The proximal seal 1480 can be an annular seal or ring around the proximal opening of the lumen 1467 in the obturator 1460. In some cases, the proximal seal 1480 can have an inner diameter that is smaller than the inner diameter of the lumen 1465 of the obturator 1460. Gas has the potential to enter the lumen 1465 if the obturator 1460 has slots, recesses or other similar openings in the obturator shaft. The one or more seals 1480 can be a flexible or deformable material which can be removably attached to the proximal end of the obturator 1460. The one or more seals 1480 can provide a seal around a medical instrument, for example a scope, when the medical instrument is inserted into the obturator 1460. In some cases, the flexible or deformable material can fit over a top or proximal surface of the obturator body 1467.
In some cases, the one or more seals 1480 at the proximal end of the obturator prevents gas leaking out of the proximal opening of the lumen 1465.
The obturator 1760 has at least one internal structure accommodating portion located thereon. In
The obturator body 1767 includes a cannula contacting surface 1773. The obturator 1760 can include at least one locating element 1771 that extends downwardly from the cannula contacting surface 1773. The locating element 1771 can clip into or otherwise engage the cannula or interact with the cannula features to properly orient the obturator 1760 within the cannula. In some embodiments, a plurality of locating elements can be used that clip the obturator into, or otherwise engage with, the cannula. In other embodiments, the locating elements may be dimensioned to fit in e.g. slots on the cannula but may not touch the cannula directly. However if the obturator is twisted, then the location of the locating elements within the slots may prevent it from twisting further. The locating elements 1771 of the embodiment of
In some cases, any of the obturators described herein can include a handle or grip portion to assist with using the obturator and/or removing the obturator from the cannula.
Examples of obturators and obturator-cannula assembly systems and associated components and methods have been described with reference to the figures. The figures show various systems and modules and connections between them. The various modules and systems can be combined in various configurations and connections between the various modules and systems can represent physical or logical links. The representations in the figures have been presented to clearly illustrate the principles and details regarding divisions of modules or systems have been provided for ease of description rather than attempting to delineate separate physical embodiments. The examples and figures are intended to illustrate and not to limit the scope of the inventions described herein. It will be apparent to the skilled person that one or more features of the various described embodiments may be readily used in combination with one or more features of other described embodiments where appropriate.
Examples described herein illustrate a cannula and/or obturator used in combination with and supporting a scope. However, in some cases, the cannula can be used to hold other medical instruments. Additionally, as referred to herein the terms “concentric”, “concentrically”, and/or “substantially concentric” or any variations of these terms can also refer to minor axis offsets between the cannula and medical instrument. In some case, for example, the axis offsets can include 0-30 degrees offset.
Although certain embodiments and examples are disclosed herein, inventive subject matter extends beyond the specifically disclosed embodiments to other alternative embodiments and/or uses, and to modifications and equivalents thereof. Thus, the scope of the claims or embodiments appended hereto is not limited by any of the particular embodiments described herein. For example, in any method or process disclosed herein, the acts or operations of the method or process can be performed in any suitable sequence and are not necessarily limited to any particular disclosed sequence. Various operations can be described as multiple discrete operations in turn, in a manner that can be helpful in understanding certain embodiments; however, the order of description should not be construed to imply that these operations are order dependent. Additionally, the structures described herein can be embodied as integrated components or as separate components. For purposes of comparing various embodiments, certain aspects and advantages of these embodiments are described. Not necessarily all such aspects or advantages are achieved by any particular embodiment. Thus, for example, various embodiments can be carried out in a manner that achieves or optimizes one advantage or group of advantages as taught herein without necessarily achieving other aspects or advantages as can also be taught or suggested herein.
Conditional language used herein, such as, among others, “can,” “could,” “might,” “may,” “e.g.,” and the like, unless specifically stated otherwise, or otherwise understood within the context as used, is generally intended to convey that certain embodiments include, while other embodiments do not include, certain features, elements and/or states. Thus, such conditional language is not generally intended to imply that features, elements and/or states are in any way required for one or more embodiments. As used herein, the terms “comprises,” “comprising,” “includes,” “including,” “has,” “having” or any other variation thereof, are intended to cover a non-exclusive inclusion. For example, a process, method, article, or apparatus that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Also, the term “or” is used in its inclusive sense (and not in its exclusive sense) so that when used, for example, to connect a list of elements, the term “or” means one, some, or all of the elements in the list. Conjunctive language such as the phrase “at least one of X, Y and Z,” unless specifically stated otherwise, is otherwise understood with the context as used in general to convey that an item, term, etc. may be either X, Y or Z. Thus, such conjunctive language is not generally intended to imply that certain embodiments require at least one of X, at least one of Y and at least one of Z each to be present. As used herein, the words “about” or “approximately” can mean a value is within ±10%, within ±5%, or within ±1% of the stated value.
It should be emphasized that many variations and modifications may be made to the embodiments described herein, the elements of which are to be understood as being among other acceptable examples. All such modifications and variations are intended to be included herein within the scope of this disclosure and protected by the following claims. Further, nothing in the foregoing disclosure is intended to imply that any particular component, characteristic or process step is necessary or essential.
Filing Document | Filing Date | Country | Kind |
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PCT/IB2021/051151 | 2/12/2021 | WO |
Number | Date | Country | |
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62976991 | Feb 2020 | US |