High-frequency transvalvular axisymmetric blood pump
AssigneeNimbus Medical, Inc.
InventorRichard K. Wampler
Life of this patent
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Abstract
A high-frequency transvalvular blood pump for temporary cardiac assist provides suction to decompress the ventricular cavity during both systole and diastole. The intake end of the pump is connected to a cannula which is inserted into the ventricular cavity through the aortic valve, and which has an intake opening at its distal end. The intake and outflow ends of the pump are closed, respectively, by one-way valves which allow blood flow only in the direction of body perfusion. The pump itself consists of a stiff barrel whose interior volume can be alternately reduced and expanded by a flexible membrane controlled by pneumatic or hydraulic pressure from an extracorporeal location through a percutaneously inserted lumen.
Claims7
A high-frequency transvalvular blood pump, comprising:
- (a) a substantially cylindrical, stiff barrel dimensioned to be inserted into a blood vessel of a patient and having an outer diameter substantially less than that of said blood vessel, said barrel having an intake end and an outflow end;
- (b) a cannula for insertion into a ventricular cavity through a heart valve, said cannula having a distal and a proximal end and being sealingly joined at said proximal end to said intake end in fluid communication with the interior of said barrel, and said cannula having an intake opening at said distal end for intake of blood from said ventricular cavity when inserted therein;
- (c) fluid-operated pumping means in said barrel for alternately drawing blood into the interior of said barrel and expelling it therefrom, the frequency of alternation of said pumping means being substantially 600 to 1000 cycles per minute;
- and
- (d) valving means at each end of said barrel for allowing blood flow into and out of said barrel only in the direction from said cannula to said outflow end.
A method of providing to a patient cardiac assist with good myocardial preservation, comprising the steps of:
- (a) introducing into a major blood vessel adjacent the patient's heart a pulsatile pumping device having an intake end and an outflow end;
- (b) positioning said device so that its intake and outflow ends are located on opposite sides of a heart valve;
- and
- (c) operating said device so as to produce a pulsatile blood flow having a frequency of substantially 600-1000 cycles per minute through said device across said heart valve during both systole and diastole;
- (d) said device being non-occluding and being of a size sufficiently small to allow substantial blood flow through said blood vessel exteriorly of said device.
Dependencies are inferred from the claim text.