Pressure-controlled continuous coronary sinus occlusion device and methods of use
First Claim
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1. A method of providing retrograde transvenous myocardial perfusion, the comprising:
- providing a device comprising a tubular member having a distal portion adapted to be disposed in a patient'"'"'s venous system, a proximal end having means for sealing the proximal end, a first valve which opens when pressure distal to the first valve exceeds a predetermined maximum pressure and an occlusion element located on said distal portion;
delivering the device into a portion of a patient'"'"'s venous vasculature;
using the occlusion element to substantially block blood flow at a selected location within the patient'"'"'s venous vasculature; and
opening the first valve when the venous blood pressure distal to the valve exceeds the predetermined maximum pressure, thereby allowing blood to flow through the first valve in the direction of normal venous blood flow so long as the pressure distal to the first valve is in excess of the predetermined maximum pressure.
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Abstract
Apparatus and methods for perfusing ischemic myocardium are provided using a tubular member having an end region adapted to be disposed in a portion of a patient'"'"'s venous vasculature. The end region includes a lumen and a valve in communication with the lumen that controls pressure within an occluded portion of the vasculature by venting excess blood at a location proximal of a point of occlusion of the vasculature via the valve. An occlusion element optionally may be provided in the end region that retains the tubular member within the patient'"'"'s venous vasculature and occludes the flow of blow around the lumen.
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5 Claims
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1. A method of providing retrograde transvenous myocardial perfusion, the comprising:
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providing a device comprising a tubular member having a distal portion adapted to be disposed in a patient'"'"'s venous system, a proximal end having means for sealing the proximal end, a first valve which opens when pressure distal to the first valve exceeds a predetermined maximum pressure and an occlusion element located on said distal portion;
delivering the device into a portion of a patient'"'"'s venous vasculature;
using the occlusion element to substantially block blood flow at a selected location within the patient'"'"'s venous vasculature; and
opening the first valve when the venous blood pressure distal to the valve exceeds the predetermined maximum pressure, thereby allowing blood to flow through the first valve in the direction of normal venous blood flow so long as the pressure distal to the first valve is in excess of the predetermined maximum pressure. - View Dependent Claims (2, 3, 4, 5)
moving the sheath relative to the one or more additional valves to adjust a value of a pressure related parameter.
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5. The method of claim 4 wherein the tubular member comprises an elongated catheter, the method further comprising:
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coupling the proximal end to a monitoring device to measure a pressure in the lumen; and
moving the sheath relative to the one or more additional valves to adjust the value of the pressure measured by the monitoring device.
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Specification