|Publication number||WO1996001132 A1|
|Publication date||18 Jan 1996|
|Filing date||15 Jun 1995|
|Priority date||1 Jul 1994|
|Publication number||PCT/1995/7713, PCT/US/1995/007713, PCT/US/1995/07713, PCT/US/95/007713, PCT/US/95/07713, PCT/US1995/007713, PCT/US1995/07713, PCT/US1995007713, PCT/US199507713, PCT/US95/007713, PCT/US95/07713, PCT/US95007713, PCT/US9507713, WO 1996/001132 A1, WO 1996001132 A1, WO 1996001132A1, WO 9601132 A1, WO 9601132A1, WO-A1-1996001132, WO-A1-9601132, WO1996/001132A1, WO1996001132 A1, WO1996001132A1, WO9601132 A1, WO9601132A1|
|Inventors||Albert Nowosielski, Robert Mantell, Robert Baker|
|Applicant||Northgate Technologies Incorporated|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (8), Referenced by (43), Classifications (10), Legal Events (5)|
|External Links: Patentscope, Espacenet|
HIGH FLOW INSUFFLATION INSTRUMENT FOR LAPAROSCOPIC SURGERY
BACKGROUND OF THE INVENTION
The present invention relates to a laparoscopic surgical instrument for providing gas insufflation of a body cavity, and in particular, the present invention relates to a laparoscopic surgical instrument for providing more efficient gas insufflation and which also may accommodate an optical viewing instrument. Laparoscopic surgery involves the use of small incisions to insert surgical instruments of 3-10 millimeter diameter into the abdominal cavity. An initial step in laparoscopic surgery is to insert a needle or cannula of about 2 mm diameter through the abdominal wall such that the tip of the needle accesses in the abdominal cavity. About 2-4 liters of a sterilized gas, such as carbon dioxide, is insufflated through the needle and into the cavity. This procedure separates the abdominal wall from the organs and also may separate the organs from one another.
A conventional instrument for providing an insufflating gas to an internal body cavity is a Verres needle. A Verres needle includes a hollow cannula in which is located a hollow obturator. The cannula has a sharp distal tip for piercing the abdominal wall. The obturator has a closed, blunt distal tip and a lateral side port through the shaft of the obturator close to the distal tip. The obturator is slidable in the cannula and is biased by a spring mechanism so that the blunt distal tip of the obturator extends distally of the sharp distal tip of the cannula. As the physician pushes the Verres needle against the patient's abdominal wall, the obturator retracts back into the cannula against the bias of the spring mechanism. After the sharp tip of the cannula penetrates the abdominal wall, the distal end of the obturator springs back out past the sharp distal tip of the cannula into the abdominal cavity. During the insufflation procedure, it is an advantage that the blunt distal tip of the obturator is biased distally past the sharp distal tip of the cannula in order to reduce the chances that the sharp tip of the outer cannula might accidently contact an internal organ. An insufflating gas can be delivered to the abdominal cavity from a gas supply which is connected to a proximal portion of the obturator. The insufflating gas is conveyed through the hollow obturator and passes out the lateral port at the distal end.
In performing laparoscopic procedures, it is advantageous that the instruments used, such as a Verres- needle, be made with relatively small outer diameters to minimize the size of the incision necessary to access the desired surgical site. It is also preferable to make an insufflation instrument, such as a Verres needle, as efficient as possible so that an internal body cavity can be insufflated as quickly and with control. It would also be advantageous to be able to observe the distal end of a Verres needle when it is inserted into a patient's body cavity to determine whether it is in the proper location. Accordingly, it is an object of the present invention to provide an insufflation device that is more efficient and which may be able to accommodate a separate optical viewing device.
SUMMARY OF THE INVENTION According to a first aspect of the present invention, there is provided a high flow insufflation instru ent and method for laparoscopic surgery. The insufflation instrument comprises a sharp-tipped hollow cannula with an open distal end and a hollow obturator located in the hollow cannula. The hollow obturator has a blunt distal tip. The obturator is shiftable relative to the cannula between an advanced position in which the blunt distal tip of the obturator is located distally of the sharp distal tip of the cannula and a retracted position in which the blunt distal tip of the obturator is not located distally of the sharp distal tip of the cannula. A first insufflation flow passage is defined within the obturator and extends from a proximal portion of the obturator to at least one aperture located in a distal portion. A second insufflation flow passage is defined between the obturator and the inside of the hollow cannula and extends from the proximal end of the hollow cannula to the open distal end thereof.
According to another aspect of the present invention, there is provided a high flow insufflation instrument and method for laparoscopic surgery that provides for accommodation of an optical viewing scope. The instrument comprises a hollow cannula having an open distal end with a sharp distal tip. An obturator is located in the hollow cannula and has a blunt distal tip. A first insufflation flow passage is defined within the obturator and extends to a sealed aperture located in a distal portion. An optical viewing scope having an elongate shaft portion for transmission of optical image can be located in the first insufflation fluid flow passage for viewing through the sealed aperture.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a sectional side view of a laparoscopic instrument for providing insufflating gas to a body cavity according to a first embodiment of the present invention. FIG. 2 is a perspective view of a hub portion of the obturator depicted in FIG. 1.
FIG. 3 is a cross sectional view of the laparoscopic instrument of FIG. 1 taken along line A-A'. FIGS. 4A-4D represents diagrammatical views illustrating progressive steps in the procedure for using the embodiment of FIG. l.
FIG. 5 is a sectional side view of another embodiment of the present invention. FIG. 6 is side view of a tip portion of an alternative embodiment of the laparoscopic instrument of FIG. 1.
FIG. 7 is side view of a tip portion of another alternative embodiment of the laparoscopic instrument of FIG. 1.
FIG. 8 is side view of a tip portion of still another alternative embodiment of the laparoscopic instrument of FIG. 1.
FIG. 9 is side view of a tip portion of yet still another alternative embodiment of the laparoscopic instrument of FIG. 1.
FIG. 10 is side view of the tip portion of the embodiment of FIG. 9 showing a fiber optic viewing scope inserted through the instrument. FIG. 11 is sectional side view of a tip portion of still yet another alternative embodiment of the laparoscopic instrument of FIG. 1.
FIG. 12 is sectional side view of a tip portion of a further alternative embodiment of the laparoscopic instrument of FIG. 1.
FIG. 13 is side view of a tip portion of still a further alternative embodiment of the laparoscopic instrument of FIG. l.
FIG. 14 is sectional side view of the tip portion of the embodiment of FIG. 13 showing a fiber optic viewing scope inserted through the instrument. FIG. 15 is an end view of the embodiment of the laparoscopic instrument of FIG. 13.
FIG. 16 is an end view of an alternative embodiment of the laparoscopic instrument of FIG. 13.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
Referring to FIG. 1 there is shown a first preferred embodiment of the present invention. This embodiment is an insufflation device 10 used for laparoscopic procedures. This type of device is sometimes referred to as a "Verres needle" or a safety needle. This device is used to provide access through a wall of a person's body to a cavity internal of the body and then to provide for insufflation of the body cavity so that a medical procedure, such as a laparoscopic surgery, can be performed.
As shown in FIG. 1, the insufflation device 10 includes a cannula 14 and an obturator 18. The cannula 14 is formed of an elongate, relatively rigid, hollow shaft 20 with a sharp distal tip 22. A proximal end of the cannula shaft 20 connects to a handle-manifold 26.
The obturator 18 is located inside the hollow cannula shaft 20 and is slidable relative to the cannula shaft 20. The obturator 18 is formed of an elongate, relatively rigid, hollow shaft 28 with a relatively blunt distal tip 29. The obturator 18 has a range of movement relative to the cannula 14 such that when the obturator 18 is in a fully extended position, the blunt distal tip
29 extends distally of the sharp distal tip 22 of the cannula 14, and when the obturator 18 is in a fully retracted position, the blunt distal tip 29 is proximal of the sharp distal tip 22 of the cannula 14. Located at the blunt distal tip 29 of the obturator 18 is at least one opening. In a preferred embodiment, a first opening
30 is located at the end of the blunt distal tip 29 and is oriented in an axial direction relative to the obturator 18. Also, in a preferred embodiment, the obturator 18 has a second opening 31. The second opening 31 is located slightly proximally of the end of the blunt tip 29 and is oriented in a radial (side) direction relative to the axis of the obturator 18. The obturator 18 also has a proximal opening 32 located at the proximal end of the obturator shaft 28.
A proximal portion of the obturator shaft 28 extends into a bore 34 of the handle 26. Connected around a proximal portion of the obturator shaft 28 is a hub 64. The hub 36 has a cylindrically-shaped body 38 and a conically profiled distal face 40. The hub 36 has a size and/or diameter such that a substantial gap 41 is formed between the outside surface of the hub 36 and the inside surface of the bore 34. A spring 42, or other biasing means, is also located in the bore 34 of the handle 26. The spring 42 is located between a proximal side of the hub 36 and a rear shoulder 44 located in the bore 34 of the handle 26. When mounted in the handle 26, the spring 42 is under compression thereby biasing the hub 36 (and therefore the obturator shaft 28) in a distal direction, as shown in FIG. 1. In the absence of a proximally-directed force, the spring 42 biases the distal tapered face 40 of the hub 36 against a tapered forward shoulder 48 located in the bore 34 of the handle 26. The distal face 40 of the hub 36 and the forward shoulder 48 of the handle 26 have irregular facing surfaces so that substantial spaces or gaps extend across the interface between the distal face 40 of the hub 36 and the forward shoulder 48 when the hub 36 is biased against the shoulder 48 by the spring 42. One way to provide for these gaps or spaces is to have the distal face 40 of the hub 36 formed with grooves or ridges 49, as shown in FIG. 2. These grooves or ridges 49 provide a fluid path across the surface of the distal face 40 even when the hub 36 bears against the shoulder 48.
Alternatively, the grooves may be formed on the surface of the shoulder 48 instead of the distal face of the hub 36.
The handle-manifold 26 also includes at least one port, and in a preferred embodiment the handle 26 includes a first port 50 and a second port 52. Both the ports 50 and 52 communicate with the bore 34. The first port 50 is aligned with an axis of the handle 26 and the second port 52 is oriented at an angle, e.g. 90 degrees, to the axis of the handle 26. Both ports have suitable fittings associated with them, such as luer lock-type fittings, so that a source of insufflation fluid, or other devices such as syringes, can be connected to the insufflation device. In addition, the port 50 may have a valve apparatus associated with it, such as a duck-bill type valve 56. This enables the introduction of instruments into the insufflation device 10 through the port 50 while maintaining a fluid pressure inside the insufflation device 10.
In a present embodiment, the cannula shaft 20 and the obturator shaft 28 are made of suitably durable materials, such as stainless steel. The handle-manifold 26 is composed of a suitably hard plastic material such as polycarbonate or lexan. The handle-manifold 26 is preferably transparent, at least in the portion surrounding the hub 36. The hub 36 is also made of a suitably hard plastic, such as polycarbonate or lexan, and is preferably a contrasting color to facilitate observation of the hub 36 through the transparent handle- manifold 26. The cannula shaft 20 is approximately 6 inches in length, although other lengths may be used. The end hole 30 has a diameter of .065 inches and the side hole 31 has a length of approximately .125 inches. The cannula shaft 20 has an O.D. of approximately .109 inches and an I.D. of approximately .095 inches. The obturator shaft 28 has an O.D. of approximately .083 inches and an I.D. of approximately .072 inches. The relative sizes of the shaft of the cannula and the shaft of the obturator are such that a substantial portion of the cross sectional area of the insufflation device consists of the annular area 60 between the outside surface of the obturator shaft 28 and the inside surface of the cannula shaft, as depicted in FIG. 3. For example, in the embodiment of the insufflation device of FIGS. 1-3, the annular area 60 is approximately .0095 square inches and the area 62 inside the hollow obturator shaft 28 is .0041 square inches.
Preferably, the annular area 60 substantially exceeds the area 62 and in the embodiment of FIG. 3, the annular area 60 is more than twice the area 62 inside the obturator 18.
Methods of Use
The insufflation device 10 may be used similarly to conventional "Verres" type needles. For example, when a physician desires to insufflate a body cavity in order to perform a laparoscopic surgery, the distal end of the insufflation device 10 is pressed against the body 63 of the patient causing the blunt tip 29 of the obturator 18 to retract rearward against the biasing of the spring 42. This allows the sharp tip 22 of the cannula 14 to pierce the outer body tissue of the patient, as shown in FIGS. 4A and 4B. The sharp tip 22 of the outer cannula 14 continues to pierce through the patient's skin 63 until the tip 22 reaches a cavity 64 inside the body, as shown in FIG. 4C. When the cavity 64 is reached, the force pushing against the blunt tip 29 of the obturator 18 is removed and the obturator 18 is biased distally of the sharp tip 22 of the cannula 14 by the spring 42. The physician can determine when the blunt tip 29 of the obturator 18 is extending distally of the sharp tip 22 of the cannula 14 by observing the relative positions of the distal end of the obturator hub 38 and the forward shoulder 48 of the handle 26. This observation is facilitated because the handle-manifold 26 is made, at least in part, of a transparent plastic. Specifically, the physician observes the position of the hub 36 (which is directly attached to the obturator 18) relative to the shoulder 48 (which is connected to the cannula shaft 20) . When the hub 38 shifts forward towards the shoulder 48, it is an indication that the blunt tip 29 of the obturator 18 is distal of the sharp tip 22 of the cannula 14, and therefore in the desired abdominal cavity 64. With the tip of the insufflation device in the desired body cavity, gas can be insufflated through the device 10 to enlarge the cavity. At this point, the physician has several alternative options.
A. Alternative Method # 1 According to one method, the physician can insufflate the body cavity without using an optical viewing device. This can be accomplished by attaching a source of insufflating gas to the manifold-handle 26. A source of insufflating gas can be attached to either port 50 or 52 of the handle-manifold 26. The insufflating gas passes into the bore 34 of the handle 26 and is conveyed to the distal end of the insufflation device 10 by means of two flow paths. The first flow path is defined by the annular area 60 between the obturator 18 and the cannula 14 and the second flow path is defined by the area 62 inside the hollow obturator 18. By utilizing both flow paths, the body cavity can be insufflated much more quickly and efficiently. Both these fluid flow paths are available because both fluid flow paths communicate with the bore 34. The second flow path communicates directly with the area of the bore 34 through an opening in the proximal end of the obturator shaft 28. The first flow path communicates with the bore 34 around the hub 36. Passage of insufflating gas across the hub 36 is facilitated by the grooves 49 and the gap 41 provided around the hub 36. After the body cavity is insufflated, the physician can proceed with the laparoscopic procedure.
B. Alternative Method # 2
After the physician has penetrated the body wall 63, it may be desirable to view the location of the distal end of the insufflation device before fully insufflating the cavity 64. As mentioned before, it may be a concern whether the distal tip of the insufflation device 10 is properly located in the abdominal cavity. It sometimes occurs that the insufflation device reaches a portion of the abdominal wall of the patient that has a gap or void in it or is relatively soft. Also, it is possible that the tip has been inserted too far and has pierced into an internal organ. When this occurs, the obturator 18 may shift forward giving the physician a false indication that the tip is in the proper body cavity. If a substantial amount of gas were to be supplied through the insufflation device when the tip is still in a portion of the patient's abdominal wall or in an organ, complications to the patient might ensue. This difficulty can be avoided through use of the present embodiment.
The embodiment of the insufflation device of FIGS. 1-3 provides the physician with the capability to view the location of the distal end at various stages of use. After the hub 36 has shifted forward indicating that the blunt end 29 of the obturator 18 has shifted forward of the sharp tip 22 of the cannula 14 and before a significant amount of gas has been insufflated into the body cavity, the physician may insert an optical viewing scope 66 through the obturator 18 so that the location of the distal end of the insufflation device can be determined. Specifically, the viewing member 66 is inserted through the port 50 of the handle-manifold 26 and into the shaft 28 of the obturator 18. The optical viewing scope 66 should have a sufficient length relative to the obturator 18 so that a distal end of the optical viewing member 66 extends through the opening 30 at the distal end of the obturator and distally past the distal end 29, as shown in FIG. 4D. Since the blunt tip 29 of the obturator 18 is distal of the sharp tip 22 of the cannula 14 during insertion of the viewing member 66, the risk of injuring an internal organ of the body is reduced. The optical scope 66 should have a sufficiently small O.D. so that it passes freely through the inside of the obturator and out the distal opening 30. A suitable optical scope is commercially available from Optimed and has an O.D. of 1.48 mm.
With the optical scope 66 inserted in the insufflation device 10, the physician may observe the location of the distal end of the insufflation device through an eyepiece 67 of the viewing scope to determine whether the distal end is properly located in the peritoneum, as shown in FIG. 4D. It may be helpful at this stage to insufflate a small amount of gas through the cannula to clear the area immediately around the distal end of the insufflation device 10 to provide for at least a minimal separation of tissue from the face of the optical scope lens. The small amount of gas that would be insufflated at this stage would be less than the amount normally used to insufflate the peritoneum to perform the surgery in case the distal end of the insufflation device were not properly located. Gas may be insulated through the insufflation device 10 by connecting a supply of gas to the port 52 on the handle 26. Although the viewing device 66 occupies a portion of the insufflating channel inside the obturator 18, because the insufflating gas supplied to the port 52 can also pass both through the obturator 18 and through the annular area 60 between the obturator 18 and the cannula 14, insufflation may still proceed efficiently.
If the physician determines by observation through the viewing scope 66 that the distal end of the insufflation device 10 is in the proper position in the peritoneum, the physician can operate the gas supply to insufflate additional gas through the port 52 and the surgery can proceed in a usual manner. If during observation through the viewing member 66, the physician determines that the distal end of the insufflation device 10 is still in the skin of the patient, the physician can partially withdraw the scope and advance the insufflation device further into the patient until the cavity 64 has been properly reached. This may be done with the viewing member 66 inside the obturator 18 or fully or partially withdrawn from the obturator. If the tip is spread apart by the scope (as in FIG. 13) , the scope should be retracted first. The needle can then be advanced to the new position where the scope may then reinserted and advanced out the obturator.
If at any time during the observation through the optical scope 66, the physician observes that the distal tip of the insufflation device 10 has pierced an organ, he can immediately withdraw the device 10 and thereby avoid further injury by not supplying additional insufflation gas.
It is an advantage of the present embodiment that the position of the sharp tip 22 of the cannula 14 can be ascertained after the physician has observed the conventional "Verres needle"-type signal, i.e. the obturator 18 clicking forward, that indicates that the tip of the insufflation device is in the peritoneal cavity.
Referring to FIG. 5, there is shown an alternative embodiment of the present invention. This embodiment shows a Verres-type needle 70 used for accessing an internal body cavity of a patient and insufflating a fluid into the cavity. The needle 70 includes an cannula 72 with a sharp tip 74 and a hollow obturator 76 slidably located inside the cannula 72. The obturator 76 has a blunt tip 78. Located at the end of the blunt tip 78 is an end hole 79. A side hole 80 is located slightly proximally of the end hole 79. The obturator 76 is connected to the cannula 72 so that the blunt tip 78 is biased distally of the sharp tip 74 by a compression spring 81 located in a handle 82 which is connected to the proximal end of the cannula 72. The spring 81 is located in a bore 84 of the handle 82 and is compressed between a rear wall 86 of the handle 82 and a hub 88 connected to a shaft portion 90 of the obturator 76.
The embodiment of FIG. 5 differs from the embodiment of FIGS. 1-3 in that the obturator shaft 90 extends proximally from a proximal end of the handle 82. In one embodiment, the proximal end of the obturator shaft 90 extends approximately 1 inch from the handle 82. Located at a proximal end of the obturator shaft 90 is a manifold 92. The manifold 92 has at least one port and in a preferred embodiment has a first port 94 and a second port 96. The manifold 92 also has a cock 98 associated with it to open either the first port 94 or the second port 96 or to close both ports. Similar to the first embodiment, the embodiment of FIG. 5 provides for high flow through the Verres needle by utilizing both the area inside the obturator 76 as well as the annular area between the obturator 76 and the cannula 72. In the embodiment of FIG. 5, fluid communication between the inside and the outside of the obturator 76 is provided by one or more openings or apertures 100 located through the obturator shaft 90 along a portion located adjacent a proximal portion 102 of the cannula 72. Each of these openings 100 may be approximately 1/8 inches in length. In a present embodiment, there are 2 openings. These openings 100 permit the fluid insufflated into the Verres needle 70 through either the ports 94 or 96 to be conveyed to the distal end of the device through both the area inside the obturator shaft 90 as well as between the obturator shaft 90 and the cannula 72.
The insufflation device of FIG. 5 may also have another proximal insufflation port 101 located in the handle portion 82. If an insufflation port is located on the handle 82, fluid communication from the bore 84 may be provided across the hub 88 by means of grooves or a gap as described in the previous embodiment, or through additional apertures through the obturator shaft located in the area of the bore 84.
The embodiment of the Verres needle of FIG. 5 may have similar dimensions as the embodiment of FIGS. 1- 3. Also, the embodiment of the Verres needle 70 in FIG. 5 may be used in a manner similar to that of FIGS. 1-3 for accessing an internal body cavity and may be used with a separate optical viewing scope in a similar manner.
FIGS. 6-16 show alternative embodiments for the tip portion of an insufflation device. The proximal portions of each of the embodiments in FIGS. 6-16 may be similar to either the embodiment of FIGS. 1-3 or the embodiment of FIG. 5.
In FIG. 6, a blunt tipped obturator 110 extends distally of a sharp tipped cannula 112. In this embodiment, the blunt tipped obturator 110 does not have an end hole. Instead, the blunt end of the obturator 110 is closed. The obturator 110 of this embodiment is provided with a side hole 114. This embodiment may provide for high flow insufflation but may not be suitable for accommodating a separate optical viewing device since there is no opening through which the viewing device can exit.
FIG. 7 shows another embodiment of a high flow Verres-needle. In this embodiment, a blunt tipped obturator 116 extends past a sharp tipped cannula 118. This embodiment, like the embodiment of FIG. 6, does not include an end hole and therefore is not especially suitable for use with an optical viewing member. The embodiment of FIG. 7 differs from the embodiment of FIG. 6 with the provision of multiple insufflation openings 120 and 122 located through the obturator 116 near the tip. These multiple openings provide for fluid efficiency for insufflation through the device. In a present embodiment, the openings 120 and 122 are located on opposite sides of the obturator shaft. If more than two openings are provided, the openings may be staggered around the circumference of the obturator shaft.
FIG. 8 shows another embodiment of a high flow Verres-needle. In this embodiment, a blunt tipped obturator 124 extends past a sharp tipped cannula 126. A side hole 128 is located through the wall of the obturator 124 near the distal tip. This embodiment has an end hole 130 to accommodate an optical viewing device, however the end hole is covered with a transparent lens
132. The transparent lens 132 shields the viewing device when it is placed in the obturator 124 and helps prevent it from becoming occluded with tissue or blood.
FIGS. 9 and 10 show another embodiment of the high flow insufflation device. In this embodiment, a blunt tipped obturator 134 having a side hole 135 extends past a sharp tipped cannula 136. An end hole 138 located through the tip of the obturator 134 accommodates a viewing device 140 which may be similar to the viewing device 66, noted above. In this embodiment, a closure valve 142 is located in the end hole 138. The closure valve 142 includes resilient flaps 144 that part to accommodate the viewing device 140 and reseal again when the viewing device 140 is removed. FIG. 11 shows still another embodiment of the high flow insufflation device with a sealed end hole to accommodate an optical fiber scope. In this embodiment, a hollow obturator 146 is located inside a hollow cannula 147. The hollow obturator 146 has an end hole 148."««rThe end hole 148 is occupied by an inner obturator 150. The inner obturator 150 is in place in the hollow obturator 146 but can be removed and replaced with an optical scope if viewing through the insufflation device is required. If viewing is not required, the inner obturator 150 can remain in place and serves to seal the end hole 148. The inner obturator 150 may be made of a suitable metal or plastic material.
FIG. 12 shows another embodiment of the insufflation device with a sealed end hole. In this embodiment, an obturator 154 located inside a cannula 156 has an end hole 158. The end hole 158 is covered by a membrane 160 located across it. The high flow insufflation device in this embodiment can be used without a viewing scope, however, if the physician determines that viewing would be helpful, a scope can be inserted through the obturator 154. The scope punctures the membrane 160 thereby allowing the scope to extend distally of the tip of the obturator 154 to permit viewing of the distal end of the insufflation device.
FIGS 13-16 show another embodiment of the high flow Verres needle. In this embodiment, an obturator 162 is located inside a cannula 164. The blunt tip of the obturator 162 has at least one slit 166 located across it. The obturator 162 is formed of a resilient material. The slit 166 allows the distal end of the obturator to open when an optical scope 167 is inserted through it, as shown in FIG. 14. The resilient obturator 162 recovers its initial closed configuration when the optical scope is removed, as shown in FIG. 13. The blunt end of the obturator 162 can have one slit 166 as shown in FIG. "15 or can have multiple slits as shown in FIG. 16.
As noted above, the above-described embodiments of the present invention are particularly advantageous for laparoscopy. However, embodiments of the present invention could also be used for other types of medical procedures, such as arthroscopy, with appropriate dimensional modifications. It is intended that the foregoing detailed description be regarded as illustrative rather than limiting and that it is understood that the following claims including all equivalents are intended to define the scope of the invention.
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|US8961493||1 Apr 2011||24 Feb 2015||Applied Medical Resources Corporation||Surgical access apparatus and method|
|US9155558||23 Jan 2012||13 Oct 2015||Applied Medical Resources Corporation||Insufflating optical surgical instrument|
|US9254125||23 Dec 2013||9 Feb 2016||Applied Medical Resources Corporation||Bladeless obturator|
|US9254148||2 May 2012||9 Feb 2016||Applied Medical Resources Corporation||Low-profile surgical universal access port|
|US9265899||26 Jan 2009||23 Feb 2016||Applied Medical Resources Corporation||Insufflating access system|
|US9314266||8 Aug 2013||19 Apr 2016||Applied Medical Resources Corporation||First-entry trocar system|
|US9358040||12 Jul 2013||7 Jun 2016||Applied Medical Resources Corporation||First-entry trocar system|
|US9492062||12 Aug 2013||15 Nov 2016||Applied Medical Resources Corporation||Visual insufflation port|
|US9545248||18 Nov 2013||17 Jan 2017||Applied Medical Resources Corporation||Blunt tip obturator|
|US9597112||8 Oct 2010||21 Mar 2017||Surgiquest, Inc.||Low-profile surgical access devices with anchoring|
|US9655643||16 Dec 2014||23 May 2017||Applied Medical Resources Corporation||Bladeless optical obturator|
|International Classification||A61B19/00, A61M13/00, A61B17/34|
|Cooperative Classification||A61M13/003, A61B17/3496, A61B17/3498, A61B17/3474, A61B2090/3614|
|European Classification||A61M13/00G, A61B17/34S2|
|18 Jan 1996||AK||Designated states|
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|14 Mar 1996||DFPE||Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)|
|24 Apr 1996||121||Ep: the epo has been informed by wipo that ep was designated in this application|
|22 Oct 1997||122||Ep: pct application non-entry in european phase|