Partial aortic occlusion devices and methods for cerebral perfusion augmentation
First Claim
1. A method for increasing cerebral blood flow, comprising the steps of:
- providing an elongate tubular member having a proximal end, a distal end, a lumen therebetween, and an elongate non-spherical balloon approximately 3-6 cm in length mounted on the distal end of the elongate tubular member and communicating with the lumen, the balloon having a compliance of approximately 0.3-1.25 mm per psi and configured such that it has an initial wrinkle-free diameter of approximately 10-15 mm, and thereafter expands upon inflation, and the elongated tubular member and the balloon being configured for placement in the descending aorta downstream from the takeoff of the brachiocephalic artery;
inserting the elongate tubular member into the descending aorta;
locating the balloon downstream from the takeoff of the brachiocephalic artery in the descending aorta; and
expanding the balloon to at least partially obstruct blood flow in the descending aorta.
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Accused Products
Abstract
Methods are provided for partial aortic obstruction for cerebral perfusion augmentation in patients suffering from global or focal cerebral ischemia. Alternatively, the methods can be used to partially obstruct aortic blood flow to condition the spinal cord to secrete neuroprotective agents prior to abdominal aortic aneurysm repair. Partial obstruction of a vessel can be accomplished by a device comprising an elongate catheter and a distally mounted expandable member. The expandable member may comprise one or two balloons. Other medical devices, such as an angioplasty, stent, or atherectomy catheter, can be inserted distal the expandable member to provide therapeutic intervention.
80 Citations
4 Claims
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1. A method for increasing cerebral blood flow, comprising the steps of:
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providing an elongate tubular member having a proximal end, a distal end, a lumen therebetween, and an elongate non-spherical balloon approximately 3-6 cm in length mounted on the distal end of the elongate tubular member and communicating with the lumen, the balloon having a compliance of approximately 0.3-1.25 mm per psi and configured such that it has an initial wrinkle-free diameter of approximately 10-15 mm, and thereafter expands upon inflation, and the elongated tubular member and the balloon being configured for placement in the descending aorta downstream from the takeoff of the brachiocephalic artery; inserting the elongate tubular member into the descending aorta; locating the balloon downstream from the takeoff of the brachiocephalic artery in the descending aorta; and expanding the balloon to at least partially obstruct blood flow in the descending aorta. - View Dependent Claims (2, 3, 4)
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Specification