Cardiac arrest treatment

Claim 3

The method described in claim 1 wherein: said step of using means external to the patient to cause compression of the heart includes applying pressure to the chest at least while blocking said flow.

Claim 4

The method described in claim 1 including: injecting oxygen-rich blood-compatible fluid through a conduit lying in the ascending aorta and past the location of blockage, while performing said step of blocking and substantially while performing said step of using means to cause compression, to encourage fluid flow toward the coronary arteries.

Claim 5

The method described in claim 1 including: at intervals of less than 2.5 minutes, ending said step of blocking flow, to allow flow through the ascending aorta to the brain.

Claim 6

The method described in claim 4 including: blocking the descending aorta at least some of the time after ending said step of blocking flow through the ascending aorta, to direct a high proportion of flow to the brain.

Claim 7

The method described in claim 1 wherein: said step of blocking is continued for a period of more than one second.

Claim 8

The method described in claim 1 wherein: said period during which the flow of blood through the ascending aorta is blocked, is on the order of 30 seconds.

Claim 9

The apparatus described in claim 7 wherein: said mechanism includes a conduit extending to a location between where the ascending aorta is blocked and a location along the coronary arteries, a container for holding oxygen-rich fluid, an da pumping device connected to said container and conduit; said control circuit is coupled to said pumping device to operate it to pump said oxygen-rich fluid at least some of the time when said control circuit is operating said mechanism to block the ascending aorta.

Claim 10

The apparatus described in claim 7 wherein: said mechanism is constructed to block substantially all flow of blood through the ascending aorta when operated to block, and to allow most of the flow into the ascending aorta to flow therethrough when operated to unblock; said control circuit is constructed to operate said mechanism to unblock after a period of less than 2.5 minutes after the beginning of each operation of said mechanism to block.

Claim 11

The apparatus described in claim 7 wherein: said control circuit is constructed to again operate said mechanism to again reduce the blockage of the ascending aorta after again blocking it; said mechanism has a second portion which is operable to at least partially block and unblock the descending aorta; said control circuit is constructed to operate said second portion to block the descending aorta, to allow substantial blood flow to the brain, during at least one of said periods when said control circuit operates said mechanism to unblock the ascending aorta.

Claim 12

Apparatus for use in resuscitating a person who has suffered cardiac arrest, comprising: a catheter having an inflatable balloon of a size to block the ascending aorta of the person when inflated, a blood compatible fluid-carrying conduit extending through said balloon and having an open distal end and having a proximal end for receiving liquid, and an inflation conduit extending to said balloon to pass fluid thereto that inflates said balloon with said inflation conduit having a proximal end distant from said balloon; a first source of blood compatible fluid; a second source of pressured inflation fluid; a first coupling for connecting said first source to said proximal end of said fluid-carrying conduit to cause fluid injection; a second coupling for connecting said second source to said proximal end of said inflation conduit to inflate said balloon and allow deflation of said balloon; a control circuit coupled to said first and second couplings, said circuit being constructed to operate said second coupling to repeatedly inflate said balloon, each time keeping said balloon inflated for a duration of a plurality of seconds, and to deflate said balloon after each of said durations of a plurality of seconds when said balloon has been kept inflated; said control circuit also operating said second coupling to cause fluid injection of said oxygen-carrying blood compatible fluid at times when said balloon is inflated.

Claim 13

Apparatus for use in resuscitating a person who has suffered cardiac arrest, comprising: a catheter having an inflatable balloon of a size to block the ascending aorta of the person when inflated, a blood compatible fluid-carrying conduit extending through said balloon and having an open distal end and having a proximal end for receiving liquid, and an inflation conduit extending to said balloon to pass fluid thereto that inflates said balloon with said inflation conduit having a proximal end distant from said balloon; a first source of blood compatible fluid; a second source of pressured inflation fluid; a first coupling for connecting said first source to said proximal end of said fluid-carrying conduit to cause fluid injection; a second coupling for connecting said second source to said proximal end of said inflation conduit to inflate said balloon and allow deflation of said balloon; a control circuit coupled to said first and second couplings, said circuit being constructed to operate said second coupling to repeatedly inflate said balloon, each time keeping said balloon inflated for a duration of a plurality of seconds, and to deflate said balloon after each of said durations of a plurality of seconds when said balloon has been kept inflated; said control circuit also operating said second coupling to cause fluid injection of said oxygen-carrying blood compatible fluid at times when said balloon is inflated.

Claim 16

The method described in claim 12 wherein: said step of injecting blood-compatible fluid includes injecting oxygen-rich fluid.

Claim 17

The method described in claim 12 including: repeatedly applying and relaxing pressure on the heart both when said balloon is inflated and when it is not inflated.

Claim 18

The method described in claim 12 including: defibrillating the heart immediately after deflation of said balloon.

Claim 19

The method described in claim 12 wherein: said catheter includes a second balloon, and said step of threading includes threading said second balloon through part of the descending aorta to a location downstream from the aortic arch; and including keeping said second balloon inflated during a plurality of periods when said balloon which lies in the ascending aorta is deflated.

Claim 20

Apparatus for use in resuscitating a person who has suffered cardiac arrest, comprising: a mechanism which is operable to at least partially block and then to reduce the blockage, of the ascending aorta of the person; a control circuit coupled to said mechanism, said circuit being constructed to operate said mechanism to block the ascending aorta for a period which has a duration of more than one second, to cause a larger than normal portion of blood pumped from the left ventricle to flow to the coronary arteries, to then operate said mechanism to reduce the blockage of the ascending aorta for a period of a plurality of seconds to allow some pumped blood to flow to the brain, and then to again operate said mechanism to block the ascending aorta for a period of more than one second.

Claim 21

Apparatus for use in resuscitating a person who has suffered cardiac arrest, comprising: a mechanism which is operable to at least partially block and then to reduce the blockage, of the ascending aorta of the person; a control circuit coupled to said mechanism, said circuit being constructed to operate said mechanism to block the ascending aorta for a period which has a duration of more than one second, to cause a larger than normal portion of blood pumped from the left ventricle to flow to the coronary arteries, to then operate said mechanism to reduce the blockage of the ascending aorta for a period of a plurality of seconds to allow some pumped blood to flow to the brain, and then to again operate said mechanism to block the ascending aorta for a period of more than one second.