Pedia-cadio pump

Claim 2

An implantable electric pump for assisting blood flow in a patient in need thereof, said pump comprising: (1) a non-rotating pump housing having an inner surface, two ends, and a central axial flow path passing therethrough, with an opening at each said end of said housing for inflow and outflow of blood; and (2) an electric motor enclosed within said housing, all components of said motor being disposed within said housing in a manner that does not substantially block blood flow through the central axial flow path, wherein said motor comprises: (a) a stator fixedly mounted within said housing and containing a first set of electromagnetically interactive torque-generating components; (b) a rotor coaxially and rotatably disposed within said stator, said rotor having: (i) a rotor vane extending outwardly towards said stator, and (ii) a second set of electromagnetically interacting torque-generating components disposed on said vane for rotation therewith, said second set interacting with said first set to cause rotation of said rotor relative to said stator when electrical current is passed through said first set; the pump central axial flow path being bounded by a central longitudinal axis of said rotor and said inner surface of said stator, and said rotor vane having a configuration, height, and angled orientation which impart pumping force to blood within the central axial flow path when said rotor is rotated; said pump being surgically insertable into, or parallel with, a ventricular outflow artery to cause at least some of the blood ejected by a ventricle to flow through the central axial flow path; and (c) first engaging means adjacent an inner surface of said stator and second engaging means adjacent an outer surface of said rotor, said first and second engaging means cooperatively limiting longitudinal and radial movement of said rotor relative to said stator.

Claim 3

The pump of claim 1 wherein said first engaging means is a spaced apart pair of annular bushings and said second engaging means is a spaced apart pair of radial protrusions, one protrusion disposed adjacent each end of said rotor and each protrusion being configured and dimensioned for receipt in a respective one of said annular bushings.

Claim 4

The pump of claim 1 wherein said rotor is relatively freely rotatable by the blood flowing in the central axial flow path in the absence of any magnetic field within said stator.

Claim 5

The pump of claim 1 wherein said rotor vane extends helically about a longitudinal axis of said rotor.

Claim 6

The pump of claim 1 wherein said rotor essentially consists of said rotor vane and said second set.

Claim 7

An assembly comprising the pump of claim 1 and means for creating a rotating magnetic field within said stator, thereby causing rotation of said rotor within said stator.

Claim 8

The assembly of claim 6 wherein said field-creating means is external of the patient.

Claim 9

The assembly of claim 6 wherein said field-creating means includes a rechargeable battery disposed within said housing.

Claim 10

The pump of claim 1 wherein said rotor is hollow and consists essentially of said vane and said second set.

Claim 11

An implantable electric pump for assisting blood flow in a patient in need thereof, said pump comprising: (1) a non-rotating pump housing having an inner surface, two ends, and a central axial flow path passing therethrough, with an opening at each said end of said housing for inflow and outflow of blood; and (2) an electric motor enclosed within said housing, all components of said motor being disposed within said housing in a manner that does not substantially block blood flow through the central axial flow path, wherein said motor comprises: (a) a stator fixedly mounted within said housing and containing a first set of electromagnetically interactive torque-generating components; (b) a rotor coaxially and rotatably disposed within said stator, said rotor having: (i) a rotor vane extending outwardly towards said stator, and (ii) a second set of electromagnetically interacting torque-generating components disposed on said vane for rotation therewith, said second set interacting with said first set to cause rotation of said rotor relative to said stator when electrical current is passed through said first set, and (iii) first engaging means adjacent an inner surface of said stator and second engaging means adjacent an outer surface of said rotor; said first and second engaging means cooperatively limiting longitudinal and radial movement of said rotor relative to said stator; the pump central axial flow path being bounded by a central longitudinal axis of said rotor and said inner surface of said stator, and said rotor vane having a configuration, height, and angled orientation which impart pumping force to blood within the central axial flow path when said rotor is rotated; said rotor vane extending helically about a longitudinal axis of said rotor and said rotor being devoid of any outer cylindrical wall about said rotor vane and relatively freely rotatable by the blood flowing in the central axial flow path in the absence of any magnetic field within said stator; and said pump being surgically insertable into, or parallel with, a ventricular outflow artery to cause at least some of the blood ejected by a ventricle to flow through the central axial flow path.

Claim 12

An implantable electric pump for assisting blood flow in a patient in need thereof, said pump comprising: (1) a non-rotating pump housing having an inner surface, two ends, and a central axial flow path passing therethrough, with an opening at each said end of said housing for inflow and outflow of blood; and (2) an electric motor enclosed within said housing, all components of said motor being disposed within said housing in a manner that does not substantially block blood flow through the central axial flow path, wherein said motor comprises: (a) a stator fixedly mounted within said housing and containing a first set of electromagnetically interactive torque-generating components; (b) a rotor coaxially and rotatably disposed within said stator, said rotor having: (i) a rotor vane extending outwardly towards said stator, and (ii) a second set of electromagnetically interacting torque-generating components disposed on said vane for rotation therewith, said second set interacting with said first set to cause rotation of said rotor relative to said stator when electrical current is passed through said first set, and (iii) first engaging means adjacent an inner surface of said stator and second engaging means adjacent an outer surface of said rotor; said first and second engaging means cooperatively limiting longitudinal and radial movement of said rotor relative to said stator; the pump central axial flow path being bounded by a central longitudinal axis of said rotor and said inner surface of said stator, and said rotor vane having a configuration, height, and angled orientation which impart pumping force to blood within the central axial flow path when said rotor is rotated; said rotor vane extending helically about a longitudinal axis of said rotor and said rotor being devoid of any outer cylindrical wall about said rotor vane and relatively freely rotatable by the blood flowing in the central axial flow path in the absence of any magnetic field within said stator; and said pump being surgically insertable into, or parallel with, a ventricular outflow artery to cause at least some of the blood ejected by a ventricle to flow through the central axial flow path.

Claim 13

The pump of claim 10 wherein said first engaging means is a spaced apart pair of annular bushings and said second engaging means is a spaced apart pair of radial protrusions, one protrusion disposed adjacent each end of said rotor and each protrusion being configured and dimensioned for receipt in a respective one of said annular bushings.

Claim 14

An assembly comprising the pump of claim 10 and means for creating a rotating magnetic field within said stator, thereby causing rotation of said rotor within said stator.

Claim 15

An implantable electric pump for assisting blood flow in a patient in need thereof, said pump comprising: (1) a non-rotating pump housing having an inner surface, two ends, and a central axial flow path passing therethrough, with an opening at each said end of said housing for inflow and outflow of blood; and (2) an electric motor enclosed within said housing, all components of said motor being disposed within said housing in a manner that does not substantially block blood flow through the central axial flow path, wherein said motor comprises: (a) a stator fixedly mounted within said housing and containing a first set of electromagnetically interactive torque-generating components; (b) a hollow rotor coaxially and rotatably disposed within said stator, said rotor consisting essentially of: (i) a rotor vane extending outwardly towards said stator, and (ii) a second set of electromagnetically interacting torque-generating components disposed on said vane for rotation therewith, said second set interacting with said first set to cause rotation of said rotor relative to said stator when electrical current is passed through said first set; the pump central axial flow path being bounded by a central longitudinal axis of said rotor and said inner surface of said stator, and said rotor vane having a configuration, height, and angled orientation which impart pumping force to blood within the central axial flow path when said rotor is rotated; said pump being surgically insertable into, or parallel with, a ventricular outflow artery to cause at least some of the blood ejected by a ventricle to flow through the central axial flow path.

Claim 16

An implantable electric pump for assisting blood flow in a patient in need thereof, said pump comprising: (1) a non-rotating pump housing having an inner surface, two ends, and a central axial flow path passing therethrough, with an opening at each said end of said housing for inflow and outflow of blood; and (2) an electric motor enclosed within said housing, all components of said motor being disposed within said housing in a manner that does not substantially block blood flow through the central axial flow path, wherein said motor comprises: (a) a stator fixedly mounted within said housing and containing a first set of electromagnetically interactive torque-generating components; (b) a hollow rotor coaxially and rotatably disposed within said stator, said rotor consisting essentially of: (i) a rotor vane extending outwardly towards said stator, and (ii) a second set of electromagnetically interacting torque-generating components disposed on said vane for rotation therewith, said second set interacting with said first set to cause rotation of said rotor relative to said stator when electrical current is passed through said first set; the pump central axial flow path being bounded by a central longitudinal axis of said rotor and said inner surface of said stator, and said rotor vane having a configuration, height, and angled orientation which impart pumping force to blood within the central axial flow path when said rotor is rotated; said pump being surgically insertable into, or parallel with, a ventricular outflow artery to cause at least some of the blood ejected by a ventricle to flow through the central axial flow path.