Anti-embolic device and method

A device, comprising:

• a central axis;
• a longitudinal carotid expandable member that expands from a non-expanded configuration to an expanded configuration, wherein when in the expanded configuration the longitudinal carotid expandable member is configured to compress a first carotid artery of a patient, wherein the longitudinal carotid expandable member is configured to overlay the first carotid artery, wherein the longitudinal carotid expandable member in the expanded configuration is configured to cause blood flow with emboli to be diverted away from the first carotid artery;
• wherein a non-expandable portion of the longitudinal carotid expandable member faces away from the central axis in a radial direction and is not expandable;
• a pressure source that supplies pressure to the longitudinal carotid expandable member to cause the longitudinal carotid expandable member to move from the non-expanded configuration to the expanded configuration, wherein the expandable member is configured to move from the non-expanded configuration to the expanded configuration during an emboligenic intervention, wherein in the expanded configuration the pressure source applies an amount of pressure to the longitudinal carotid expandable member so that the longitudinal carotid expandable member has a pressure that exceeds a systemic pressure of the patient by at least 10 mm Hg;
• a monitoring system that is configured for measuring the systemic pressure of the patient;
• wherein the longitudinal carotid expandable member is a first longitudinal expandable member;
• a second longitudinal expandable member that is configured to overlay a second carotid artery of the patient, wherein the second longitudinal carotid expandable member expands from a non-expanded configuration to an expanded configuration in which the second longitudinal carotid expandable member is configured to compress the second carotid artery of the patient;
• and
• a connecting tube that places the first longitudinal carotid expandable member into fluid communication with the second longitudinal carotid expandable member wherein pressure that expands the first longitudinal carotid expandable member is fluid from the pressure source that enters the first longitudinal carotid expandable member via pressure tubing and is then transferred from the first longitudinal carotid expandable member through the connecting tube and to the second longitudinal carotid expandable member to cause the second longitudinal expandable member to expand from the non-expanded configuration to the expanded configuration, wherein the connecting tube extends between and is open into only the first longitudinal carotid expandable member and the second longitudinal carotid expandable member and is not in direct fluid communication with the pressure source but is instead in indirect fluid communication with the pressure source through the first longitudinal carotid expandable member and the pressure tubing, wherein the second longitudinal carotid expandable member is completely sealed except for an opening that leads to the connecting tube such that fluid in the second longitudinal carotid expandable member escapes therefrom only though the opening that leads to the connecting tube, and wherein the connecting tube is open such that the fluid is configured to flow from the second longitudinal carotid expandable member through the connecting tube and into the first longitudinal carotid expandable member;
• at least one strap configured for holding the device to a neck of the patient, wherein a vertical direction extends in the same direction as the central axis, wherein the longitudinal carotid expandable member extends a greater length in the vertical direction in the non-expanded configuration than does the extension of the at least one strap in the vertical direction;
• and
• an alarm system that provides an alarm, wherein the alarm system is triggered when the first and second longitudinal carotid expandable members are in their respective expanded configurations for a lengthy amount of time.

A device for use in preventing stroke, comprising:

• a central axis;
• an expandable member that expands from a non-expanded configuration to an expanded configuration, wherein the expandable member is configured to be located at a neck of a patient, wherein the expandable member when in the expanded configuration is configured to create an area of compression of a carotid artery of the patient and restrict blood flow through the carotid artery, wherein the area of compression created by the expandable member in the expanded configuration is configured to cause blood flow with emboli to be diverted away from the carotid artery, wherein the expandable member is configured to expand from the non-expanded configuration to the expanded configuration during an emboligenic intervention;
• wherein a non-expandable portion of the expandable member faces away from the central axis in a radial direction and is not expandable, wherein the expandable member has an expandable portion such that the expandable portion and the non-expandable portion of the expandable member define an interior of the expandable member such that fluid that enters the expandable member when inside of the expandable member engages both the expandable portion and the non-expandable portion, wherein an outward section of the device that carries the expandable member engages the non-expandable portion and is configured for being located farther from the carotid artery than the expandable member such that the expandable member is configured for being located between the outward section of the device and the carotid artery;
• two straps configured for holding the device to the neck of the patient, wherein a vertical direction extends in the same direction as the central axis, wherein the expandable member extends a greater length in the vertical direction in the non-expanded configuration than does the extension of the two straps in the vertical direction;
• a monitoring system that is configured for measuring a systemic pressure of the patient, wherein the monitoring system is configured for measuring a time of expansion of the expandable member and for measuring a magnitude of pressure of the expandable member when expanded;
• a pressure source that applies pressure to the expandable member to move the expandable member from the non-expanded configuration to the expanded configuration, wherein in the expanded configuration the pressure source applies an amount of pressure to the expandable member so that the expandable member has a pressure that exceeds the systemic pressure of the patient by at least 10 mm Hg for 30-90 seconds;
• and
• an alarm system that is configured for triggering an alarm if the time of expansion of the expandable member is too lengthy, and wherein the alarm system is configured for triggering the alarm if the magnitude of pressure of the expandable member when expanded is excessive.

A device for use in preventing stroke, comprising:

• a central axis;
• an expandable member that expands from a non-expanded configuration to an expanded configuration, wherein the expandable member is configured to be located at a neck of a patient, wherein the expandable member when in the expanded configuration is configured to create an area of compression of a carotid artery of the patient and restrict blood flow through the carotid artery, wherein the area of compression created by the expandable member in the expanded configuration is configured to cause blood flow with emboli to be diverted away from the carotid artery, wherein the expandable member is configured to expand from the non-expanded configuration to the expanded configuration during an emboligenic intervention;
• wherein a non-expandable portion of the expandable member faces away from the central axis in a radial direction and is not expandable, wherein the expandable member has an expandable portion such that the expandable portion and the non-expandable portion of the expandable member define an interior of the expandable member such that fluid that enters the expandable member when inside of the expandable member engages both the expandable portion and the non-expandable portion, wherein an outward section of the device that carries the expandable member engages the non-expandable portion and is configured for being located farther from the carotid artery than the expandable member such that the expandable member is configured for being located between the outward section of the device and the carotid artery;
• a monitoring system that is configured for measuring a systemic pressure of the patient, wherein the monitoring system is configured for measuring a time of expansion of the expandable member;
• a pressure source that applies pressure to the expandable member to move the expandable member from the non-expanded configuration to the expanded configuration, wherein in the expanded configuration the pressure source applies an amount of pressure to the expandable member so that the expandable member has a pressure that exceeds the systemic pressure of the patient by at least 10 mm Hg for 30-90 seconds;
• a manometer that measures the pressure applied by the pressure source;
• wherein the monitoring system monitors interruption of blood flow through one or more carotid arteries of the patient;
• and
• an alarm system that provides an alarm, wherein the alarm system is triggered by lengthy compression of the first and second carotid arteries.