141 results about "Open surgery" patented technology

The invention includes a novel method and system to achieve leaflet coaptation in a cardiac valve percutaneously by creation of neochordae to prolapsing valve segments. This technique is especially useful in cases of ruptured chordae, but may be utilized in any segment of prolapsing leaflet. The technique described herein has the additional advantage of being adjustable in the beating heart. This allows tailoring of leaflet coaptation height under various loading conditions using image-guidance, such as echocardiography. This offers an additional distinct advantage over conventional open-surgery placement of artificial chordae. In traditional open surgical valve repair, chord length must be estimated in the arrested heart and may or may not be correct once the patient is weaned from cardiopulmonary bypass. The technique described below also allows for placement of multiple artificial chordae, as dictated by the patient's pathophysiology.

Ultrasonic forceps adapted for use in open surgical forceps. The device is provided in the form of traditional open surgery forceps or tweezers, and the transmitting rod which transmits ultrasonic vibration from a proximally located transducer to the distally mounted welding horn runs through a lumen in one of the arms of the forceps.

A wound protector and retractor device 1 comprises a sleeve 2, a distal member provided by a distal ring 3 of resilient material and a proximal member provided by a proximal ring 4. The sleeve 2 is led around the ring 3 and is free to move axially relative to the distal ring 3 somewhat in the manner of a pulley. The proximal ring 4 is fixed to the sleeve 2, in this case at the proximal inner end thereof. The sleeve 2 terminates in a handle or gripping portion which is reinforced by a gripping ring 15. The sleeve extends from the proximal ring 4 and the distal ring 3 is contained between inner and outer layers 2a, 2b of the sleeve 2. The resilient distal ring 3 is scrunched up and inserted through the incision 6. The sleeve 2 is then pulled upwardly. On pulling of the sleeve 2 upwardly the outer layer 2b is pulled up while the inner layer 2a is drawn around the proximal ring 3. This results in shortening the axial extent between the proximal ring 4 and the distal ring 3, tensioning the sleeve and applying a retraction force to the margins of the incision 6. As the incision is being retracted the margins are also protected by the sleeve. On retraction, an access port is provided, for example for a surgeon to insert his hand and/or an instrument to perform a procedure. The device may be used as a retractor in open surgery or as a base for a valve/seal to allow it to be used in hand assisted laparoscopic surgery or for instrument access or hand access generally.

Sutures can be placed in difficult to access areas of the human body with devices, and related methods, utilizing a needle carrier. The devices and methods can be used in conjunction with both endosurgical and traditional open surgery procedures.

Methods, devices and systems facilitate retention of a variety of therapeutic devices. Devices generally include an anchoring element, which has been designed to promote fibrotic ingrowth, and an anchored device, which has been designed to firmly engage the complementary region of the anchoring element. The anchoring element may be placed in a minimally invasive procedure temporally separated from the deployment of the anchored device. Once enough time has passed to ensure appropriate fixation of the anchoring element by tissue and cellular ingrowth at the site of placement, the anchored device may then be deployed during which it firmly engages the complementary region of the anchoring element. In this manner, a firm attachment to the implantation site may be made with a minimum of required hardware. Some embodiments are delivered through a delivery tube or catheter and while some embodiments may require laparoscopy or open surgery for one or more of the placement procedures. Some embodiments anchor devices within the cardiovascular tree while others may anchor devices within the gastrointestinal, peritoneal, pleural, pulmonary, urogynecologic, nasopharyngeal or dermatologic regions of the body.

This invention is in the domain of minimally invasive surgery and is a method and apparatus that transforms and displays images of internal organs and tissues taken from internally located imaging devices on external skin. The image displayed on the skin aligns with the actual physical location, orientation, and size of the internal organs and tissues in a way that viewers have the perception that the skin is transparent. This method and apparatus enables surgeons to have the same hand-eye coordination as in an open surgery during a minimally invasive surgery.

Devices and methods are disclosed for achieving hemostasis in solid visceral wounds. Such devices and methods are especially useful in the emergency, trauma surgery or military setting. In such cases, the patient may have received trauma to the abdominal viscera. The devices utilize flexible, variable depth transfixing bolts that penetrate the viscera. These bolts are pulled tight to bring the tissue into apposition and hold said tissue in apposition while the wound heals. These bolts overcome the limitations of sutures that are currently used for the same purposes. The bolts come in a variety of lengths and diameters. Since the bolts are flexible, the curvature may be adjusted by the surgeon. The devices are flexible, bendable, and conformable in their wet or dry state. They can be used either straight or through a broad range of curvatures to suit the needs of various pathologies. The bolts include pressure plates that are capable of exerting compressive pressure over broad areas of visceral wounds without causing tearing of the friable parenchyma. The bolts may be placed and removed by open surgery or laparoscopic access.

A system for telesurgery having a plurality of operative end units respectively linked to remote master end units. All the master and operative end units of the system consist of a common module having a base plate to which a slender shaft is slidingly attached. A slender shaft is further rotatable about its axis as well as about a center point disposed above the distal surface of the base plate. Surgical effectors, cameras and/or LEDs can be attached to the distal end of slender shafts of operative end units which is distally disposed relative to the base plate of its respective operative end unit. Operating handles for manipulating and/or activating the respective slender shaft or attached surgical effectors, are attached to the proximal end and/or to the distal end of slender shafts of master end units. Linking a master end unit to its respective operative end unit is accomplished by mechanical, hydraulic, pneumatic and or electric transmission, such that a slender shaft of an operative end units simultaneously move in the same movement in which the slender shaft of the respective master end unit is moved. An operator is able to manipulate a slender shaft within the lumen enclosing the surgical site within a patient's body by sliding, inclining and/or rotating the slender shaft of a remote master end unit as in a common endoscopic procedure. The operator is further able to manipulate and/or activate a surgical effector either as in an endoscopic or in an open surgery by means of the operating handles of a remote master end unit.

Devices and methods are provided for percutaneously treating atherosclerotic plaques within blood vessels. Atherosclerotic plaques cause significant morbidity and mortality by narrowing the arteries, which adversely affects blood flow, and by acting as a source for thrombi and emboli thus causing acute organ ischemia. Current treatments include open surgery with its inherent drawbacks, and stenting, which is less invasive but leaves the plaque material in the artery, which promotes restenosis. The present invention combines the advantages of both approaches. In general, the invention provides tools that enable percutaneously dissecting the plaque from the arterial wall and removing it from the body.

The invention relates to a surgical tool. In particular, the invention relates to a multi-functional surgical tool that has a cutting means, and a grasping means, with a buffer region between the cutting and grasping means. The invention particularly relates to a multi-functional surgical tool that is suitable for use in endoscopic or laparoscopic surgery, but may also be used in open surgery.

A new extra-vascular wrapping (EVW) is disclosed. The EVW comprises of a (i) wrapping adapted to at least partially encircle at least a segment of an aorta, especially an aneurysmatic aorta, and (ii) anchoring means located at the distal portion of the wrapping adapted to immobilize the wrapping to the aorto-iliac bifurcation via engagement of the aorto-iliac junction, wherein the bifurcation-anchored wrapping is applied external to the aorta and further wherein the wrapping is collapse-resistant in the proximal-to-distal direction of the aorta. The EVW is presented with its various embodiments, such as gusset-like structured EVW, Sustained drug delivery EVW, supported EVW and ringed EVW. Methods for treating aneurysmatic aorta in an open-surgery procedure by utilizing the EVWs and by applying step of positioning a macroporous medical textile externally adjacent to the aorta are also disclosed.

A surgical instrument assembly (10, 11) configurable for performing a dermatotomy in a percutaneous procedure and further configurable for performing cuts in open surgery includes a pointed scalpel blade (68) and a hollow sheath body (18, 200) disposed to encapsulate the pointed scalpel blade (68) inside a longitudinal instrument cavity (32) to protect a user. The hollow sheath body (18, 200) is supported for longitudinal translation with respect to the scalpel blade (68). The hollow sheath (18) may be positioned and locked at a first position to completely encapsulate the scalpel blade (68) inside the instrument cavity (32) for safe handling. Otherwise the hollow sheath body (18, 200) is movable to second and third positions with different lengths of the surgical instrument extending out through a front face (23) of the hollow sheath body (18, 200). A compression spring biases the hollow sheath body (18) toward the first safety position. The instrument is usable to make a precise pierce cut with a consistent cut depth and cut length.

An implantable shunt device for draining cerebrospinal fluid from a patient's subarachnoid space. The device includes a shunt having opposed first and second ends. A one-way valve is located at the first end of the shunt. A helical tip is disposed at the second end. The helical tip is constructed to penetrate a sinus wall of the patient. Upon implantation, a hollow passageway extends between the helical tip and one-way valve such that fluid can be drained through the helical tip and out through the valve. The endovascular cerebrospinal fluid shunt of the present invention can be placed into a patient percutaneously via a catheter inserted into the venous system of the body through a needle hole, without the need for open surgery and the skin incisions required with current shunt devices. The device also allows for more physiologic drainage of cerebrospinal fluid since the device is shunting cerebrospinal fluid into the same cerebral venous system that occurs naturally in normal people.

Methods, devices and systems facilitate retention of a variety of therapeutic devices. Devices generally include an anchoring element, which has been designed to promote fibrotic ingrowth, and an anchored device, which has been designed to firmly engage the complementary region of the anchoring element. The anchoring element may be placed in a minimally invasive procedure temporally separated from the deployment of the anchored device. Once enough time has passed to ensure appropriate fixation of the anchoring element by tissue and cellular ingrowth at the site of placement, the anchored device may then be deployed during which it firmly engages the complementary region of the anchoring element. In this manner, a firm attachment to the implantation site may be made with a minimum of required hardware. Some embodiments are delivered through a delivery tube or catheter and while some embodiments may require laparoscopy or open surgery for one or more of the placement procedures. Some embodiments anchor devices within the cardiovascular tree while others may anchor devices within the gastrointestinal, peritoneal, pleural, pulmonary, urogynecologic, nasopharyngeal or dermatologic regions of the body. An alternative embodiment provides for the placement of the anchoring element and anchored device simultaneously, but allows for their removal separately. This embodiment allows the device, which may be placed only temporarily and be designed to be removed, to experience significant fibrotic ingrowth, but then to be easily detached from the ingrowth-anchored region to allow for simple and quick device removal.

An apparatus is provided for correcting spinal abnormalities, and particularly for providing compression and/or distraction of vertebrae without additional tools or instrumentation. A plate member is provided with a plurality of slots, one of which has a sloped internal edge or surface. The plate is anchored to one vertebra by a first anchor, and a second anchor is then placed through the slot with the sloped internal edge or surface and tightened. Such tightening causes the plate to move with respect to the tightened anchor, and thus to transmit compression or distraction to the vertebrae. The apparatus is particularly useful in minimally-invasive surgeries but can also be used in more traditional open surgeries.

A coaxial tube assembly, a bag, a bag-translating assembly, a de-bulking tool, and a drive assembly. The bag is delivered into a cavity in a patient's body either manually for open surgery or through the coaxial tube assembly by operation of the drive assembly for minimally invasive surgery. After a mass of tissue is placed in the bag, which is now secured to the bag-translating assembly, the drive assembly is operated to activate the bag-translation assembly to retract the bag into the annular space of the coaxial tube assembly. As the bag is being retracted, the mass in the bag is pulled into engagement with the de-bulking tool, which extends through the lumen of the coaxial tube assembly. The drive assembly activates the de-bulking tool to morcellate the mass in the bag and convey the morcellated bits of the mass through the lumen of the coaxial tube assembly.

The invention is directed to a system and method for releasably holding a surgical instrument (14), such as an endoscopic instrument configured for delivery through a small percutaneous penetration in a patient. The instrument comprises an elongate shaft (100) with a pair of mounting pins (116) laterally extending from the shaft between its proximal and distal ends. An instrument holder comprises a support having a central bore (202) and an axially extending slot (204) for receiving the instrument shaft and the mounting pins. A pair of locking slots (206) are cut into the support transversely to and in communication with the axial slot so that the mounting pins can be rotated within the locking slots. The instrument support further includes a latch assembly for automatically locking the mounting pins within the locking slots to releasably couple the instrument to the instrument holder. With this twist-lock motion, the surgeon can rapidly engage and disengage various instruments from the holder during a surgical procedure, such as open surgery, laparoscopy or thoracoscopy.