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Advanced Interventional Technologies, Inc.

Advanced International Technologies, Inc.

Frederick Gotha

Jeffrey S Kadan

James Clayton Peacock, Iii

Ronald L Coleman

Gregory M Miles

Brendan J Carroll

James C Peacock

Ronald Coleman

A medical device system and method allows an arterial bypass graft to be proximally anastomosed to an aorta during a beating heart procedure without substantial loss of blood by use of an endolumenal aorta isolation assembly provided along the distal end portion of an elongate catheter body. The aorta isolation assembly includes proximal and distal portions that are separated by an isolation region and that are adjustable to first and second extended positions, respectively, which are adapted to circumferentially engage the aortic wall and isolate upstream and downstream aspects of an exterior space between the elongate body and the aortic wall. The intermediate region is adapted to be positioned along the proximal anastomosis site such that the distal and proximal portions when adjusted to the first and second extended positions circumferentially engage the aortic wall on upstream and downstream sides of the proximal anastomosis site. Blood flowing within the aorta is thereby isolated from the proximal anastomosis site along the intermediate region and is shunted from an upstream region of the aorta, through the distal port into the flow lumen, proximally along the flow lumen, out from the flow lumen though the proximal port.

Endolumenal aortic isolation assembly and method

A medical device assembly is adapted to isolate the heart from systemic circulation while perfusing oxygenated blood to the systemic arterial circulation during a minimally invasive bypasss procedure. An arterial catheter with an external shunt valve forms a funnel which shunts antegrade aortic blood flow from the aortic root, into a distal flow port and through an internal flow lumen in the catheter, out an intermediate flow port along the catheter proximally of the anchor, and into the systemic arterial circulation. A distal internal valve selectively occludes the shunted antegrade aortic blood flow between the distal flow port and the intermediate flow port and isolates the left heart chambers from the systemic arterial circulation. Oxygenated blood may then flow from a cardiopulmonary bypass pump, distally through the internal flow lumen, out the intermediate port. The assembly also includes a venous catheter which aspirates venous blood from the vena cavae and into the cardiopulmonary bypass pump while substantially isolating the right heart chambers from the vena cavae and without circumferentially engaging the internal walls of the vena cavae. Distal and intermediate external valves are positioned along the venous catheter within the superior and inferior vena cava, respectively, and between the sinus venarum into the right atrium and either a distal or intermediate flow port, also respectively. The flow ports communicate with a cardiopulmonary bypass pump through at least one flow lumen through the catheter. Each external valve is adjustable to have an outer diameter which is slightly less than the inner diameter of the respective vena cava so that venous blood is substantially occluded from flowing into the sinus venarum and is instead aspirated into the adjacent flow port.

Cardiac bypass catheter system and method of use

A laparascopic incision closure device comprised of an ejector housing having a handpiece trigger that is activated by compression and is biased to return to an initial position. The handpiece is so carried by the ejector housing that compression and retraction of the handpiece sequentially advances a flexible wire push-rod to eject a T-bar suture and retracts the flexible wire push-rod to index a ratchet which feeds the T-bar portion of a T-bar suture into the longitudinal bore of a needle carried by the ejector housing. The strand portion of the T-bar suture trails the T-bar portion through the longitudinal bore. Multiple T-bar sutures are axially spaced and detachably carried on a suture spline by spline mount tabs connected to the T-bar portion of the T-bar sutures and are stored in the interior of the ejector housing for quick and easy placement through fascia on opposite sides of a wound. In the preferred embodiment the device is constructed of a disposable plastic material with sutures being formed of an absorbable material.

Laparascopic incision closure device

A laparascopic incision closure device comprised of an ejector housing having finger holding rings and a thumb ring attached to a plunger shaft and plunger for sequentially ejecting T-bar sutures into a trocar site incision through a needle. T-bar sutures are ejected by operation of a trigger mounted in the ejector housing for quick and easy operation to eject a T-bar through fascia adjacent to a trocar site incision. Multiple T-bar sutures are stored in the interior of the ejector housing and needle for quick and easy placement through fascia on opposite sides of a wound. In the preferred embodiment the device is constructed of a disposable plastic material with sutures being formed of an absorbable material.

A medical device assembly is adapted to isolate the heart from systemic circulation while perfusing oxygenated blood to the systemic arterial circulation during a minimally invasive bypass procedure. The assembly includes an arterial catheter with an external shunt valve which forms an anchor to secure the distal end portion within the aortic arch and which also forms a funnel which shunts antegrade aortic blood flow from the aortic root, into a distal flow port and through an internal flow lumen in the catheter, out an intermediate flow port along the catheter proximally of the anchor, and into the systemic arterial circulation. A distal internal valve is further provided within the internal flow lumen between the distal and intermediate flow ports. The distal internal valve selectively occludes the shunted antegrade aortic blood flow between the distal flow port and the intermediate flow port and isolates the left heart chambers from the systemic arterial circulation. Oxygenated blood may then flow from a cardiopulmonary bypass pump, distally through the internal flow lumen, out the intermediate port. The assembly also includes a venous catheter which aspirates venous blood from the vena cavae and into the cardiopulmonary bypass pump while substantially isolating the right heart chambers from the vena cavae and without circumferentially engaging the internal walls of the vena cavae. Distal and intermediate external valves are positioned along the venous catheter within the superior and inferior vena cava, respectively, and between the sinus venarum into the right atrium and either a distal or intermediate flow port, also respectively. The flow ports communicate with a cardiopulmonary bypass pump through at least one flow lumen through the catheter. Each external valve is adjustable to have an outer diameter which is slightly less than the inner diameter of the respective vena cava so that venous blood is substantially occluded from flowing into the sinus venarum and is instead aspirated into the adjacent flow port. A leakage port may also be provided between the distal and intermediate flow ports. The venous catheter may alternatively include an external valve with a valve member which is adjustable from a first radial position at a discrete location around the catheter's circumference to a radially displaced position within the right atrium.

Growing community of inventors

Arcadia, CA, United States of America

Frederick Gotha