The present invention relates in general to surgical devices and procedures, and more particularly to minimally invasive surgery.
Surgical procedures are often used to treat and cure a wide range of diseases, conditions, and injuries. Surgery often requires access to internal tissue through open surgical procedures or minimally invasive surgical procedures. Minimally invasive surgery often involves using an endoscope, such as laparoscopes, arthroscopes, and flexible endoscopes, to visualize internal tissue of a patient, which sometimes referred to as “endoscopic surgery”. Endoscopes and instruments are typically introduced into a patient through percuateous punctures or incisions, or through a patient's natural orifices to access intraluminal anatomy or for transluminal procedures.
Minimally invasive surgery has numerous advantages compared to traditional open surgical procedures, including reduced trauma, faster recovery, reduced risk of infection, and reduced scarring. Minimally invasive surgery is often performed with an insufflatory fluid present within the body cavity, such as carbon dioxide or saline, to provide adequate space to perform the intended surgical procedures. The insufflated cavity is generally under pressure and is sometimes referred to as being in a state of pneumoperitoneum. Surgical access devices are often used to facilitate surgical manipulation of internal tissue while maintaining pneumoperitoneum. For example, trocars may be used to provide a port through which endoscopes and surgical tools are passed. Trocars generally have an instrument seal, which prevents the insufflatory fluid from escaping while an endoscope or surgical instrument is positioned in the trocar.
Minimally invasive surgery may also be performed using magnetic anchors that enable positioning and manipulation of surgical tools that are introduced into a patient's abdominal cavity through percutaneous punctures or incisions. Using magnetic anchors may reduce the number of trocars needed in a particular procedure and in turn reduce the number of incisions to the patient's body.
While the specification concludes with claims which particularly point out and distinctly claim the invention, it is believed the invention will be better understood from the following description taken in conjunction with the accompanying drawings illustrating some non-limiting examples of the invention. Unless otherwise indicated, like-numbered references refer to the same elements in the various figures. Unless otherwise indicated, the figures are not necessarily drawn to scale, but rather to illustrate the principles of the invention.
In one embodiment, a surgical device comprises a first and a second ex vivo magnets adapted for manipulation of in vivo instruments. A separator has a first end, a second end, and an elongate body extending between the first and second ends. A first connector at the first end releasably engages the first ex vivo magnet, and a second connector at the second end of the elongated body releasably engages the second ex vivo magnet. The elongated body may be fully rigid. Alternatively it may comprise a locking flexible section with alternating rigid and flexible segments.
The first connector may comprise a ball and a socket joint to facilitate the movement of the connector relative to the elongated body. The first connector may also comprise a pivot pin. The first connector may comprise a track for operably receiving a mating element at the first end of the elongated body. The first connector may be in the shape of a ring that circumscribes the first ex vivo magnet, and may allow the ex vivo magnet to rotate relative to it.
In another embodiment, a surgical device comprises an ex vivo magnet and an in vivo magnet attracted to the ex vivo magnet, whereby the in vivo magnet can be positioned and anchored within a patient by moving the ex vivo magnet. A non-magnetic housing substantially encloses the ex vivo magnet and has a wall thickness sufficient to minimize attraction between the ex vivo magnet and other ex vivo magnets. The ex vivo magnet may be fully enclosed in the non-magnetic housing.
In yet another embodiment, a surgical device comprises an ex vivo magnet, an in vivo magnet attracted to the ex vivo magnet, whereby the in vivo magnet can be positioned and anchored within a patient by moving the ex vivo magnet A sensor detects the relative distance between the ex vivo magnet and another ex vivo magnet. An an indicator warns an operator that further movement of the ex vivo magnet in the direction of the other ex vivo magnet may cause clumping. In one embodiment, the sensor is an ultrasonic sensor. The indicator may be a light indicator. It may also be a sound indicator.
The embodiment shown in
The anchor (10) includes a magnet (12). The magnet (12) is contained within a casing (16) that forms an ergonomic handle. The anchor (11) includes a magnet (14) contained within a casing (17). The magnets (12, 14) can take a variety of forms such as permanent magnets, rare earth magnets, electromagnets, and the like.
In the present embodiment, a non-clumping unit (40) is used to prevent the anchors (10, 11) from clumping together during a surgical procedure. The attractive forces between the anchors (10, 11) increase as the distance separating them decreases. The term clumping describes two or more magnetic anchors being magnetically coupled to one another. Clumping may occur during a surgical procedure if the surgeon positions the anchors (10, 11) in close proximity to each causing the attractive forces between the anchors (10, 11) to overcome the forces keeping them stationary. Sometimes clumping can occur through a rapid clashing of the magnets to one another. Once clumped together, the attractive forces between anchors (10, 11) are at their highest and separating the anchors (10, 11) may prove difficult.
In the present embodiment, the non-clumping unit (40) comprises two ring shaped connectors (41, 42) where the connectors (41, 42) are fixed at opposite ends of an elongated bar (43). The anchors (10, 11) are releasably coupled to connectors (41, 42). Anchors (10, 11) may be freely rotated each around its central axis while coupled to the connectors (41, 42). The connectors (41, 42) may be rigid or flexible.
Elongated bar (43) is of sufficient length to ensure that anchors (10, 11) remain a suitable distance apart from each other such that a surgeon can operate each freely without any significant interference caused by the attractive forces between the anchors (10, 11). For example, two identical anchors comprising 2 inch cube neodymium magnets should be kept a minimum distance of 4-6 cm apart at all times during a surgical procedure to reduce the risk of clumping. Preferably the anchors should be kept 6 cm apart. In this example, a non-clumping unit with an elongated bar having a length of about 6 cm may be used to allow the surgeon to operate the anchors freely without constantly worrying about clumping.
Use of multiple anchors may be preferable in a surgical procedure as it permits the surgeon to utilize multiple sled bases. The sled bases (30, 31) are sized to pass through a standard trocar, such as a 12 mm, 18 mm, or 20 mm trocar. A slid base may comprise a camera, a light source, or a surgical end effector. A variety of end effectors could be used, including graspers, scissors, ultrasonic blades, bi-polar clamps, surgical staplers, ultrasonic sensors, cameras, suturing devices, and the like. In this embodiment, the sled base (31) comprises a wireless camera (33) and LEDs (34). The sled base (30) comprises a surgical cautery end effector (35). A wire (36) is operatively connected to the surgical caurtery end effector (35) and extends from the sled base (30) to deliver electrical energy.
In yet another embodiment, magnetic anchors in a surgical procedure can be equipped with sensors to measure the relative distance between them. A controller may be used to process the information and signal an indicator when the magnetic anchors are too close to each other. A light or a sound indicator can be used to warn an operator that the anchors are too close to each other which protects against clumping.
Having shown and described various embodiments and examples of the present invention, further adaptations of the methods and devices described herein can be accomplished by appropriate modifications by one of ordinary skill in the art without departing from the scope of the present invention. Several of such potential modifications have been mentioned, and others will be apparent to those skilled in the art. For instance, the specific materials, dimensions, and the scale of drawings will be understood to be non-limiting examples. Accordingly, the scope of the present invention should be considered in terms of the following claims and is understood not to be limited to the details of structure, materials, or acts shown and described in the specification and drawings.