Cardioplegia delivery system with improved bubble trap

Claim 2

A bubble trap for removing bubbles from a liquid comprising: (a) a primary chamber having an entrance way for liquid disposed at the bottom, said primary chamber capable of providing a passageway for liquid leaving said entrance way, and said primary chamber having a greater cross-sectional area than said entrance way, such that when liquid enters said primary chamber from said entrance way the average velocity of the liquid is caused to decelerate; and (b) a secondary chamber separated from said primary chamber by a dam, the area above said dam providing a passageway for liquid flowing from said primary chamber to said secondary chamber, said secondary chamber bounded by said dam, an exterior side wall which is disposed opposite said dam, a front wall and back wall which is disposed opposite said front wall, and said secondary chamber having a shelf extending from said exterior wall into said secondary chamber in a direction towards said dam but not extending so far into said secondary chamber as to block the passage of liquids through said secondary chamber, and said secondary chamber having an outlet for liquid disposed at the bottom of said secondary chamber said shelf capable of re-directing liquid flow in said secondary chamber away from said outlet and towards the top of said secondary chamber.

Claim 3

A bubble trap for removing bubbles from cardioplegia medication or a mixture of arterial blood and medication in a cardioplegia system, said bubble trap having an infusion fluid inlet connected to the supply of cardioplegia infusion fluid and an outlet leading to the heart cannula, and said bubble trap comprising: (a) a primary chamber having an entrance way for infusion fluid disposed at the bottom, said entrance way adapted for connection with said infusion fluid inlet, said primary chamber capable of providing a passageway for infusion fluid leaving said entrance way, and said primary chamber having a greater cross-sectional area than said entrance way, such that when infusion fluid enters said primary chamber from said entrance way the average velocity of said infusion fluid is caused to decelerate; and (b) a secondary chamber separated from said primary chamber by a dam, the area above said dam provinding a passageway for infusion fluid flowing from said primary chamber to said secondary chamber, said secondary chamber bounded by said dam, an exterior side wall which is disposed opposite said dam, a front wall and a back wall which is disposed opposite said front wall, and said secondary chamber having a shelf extending from said exterior wall into said secondary chamber in a direction towards said dam but not extending so far into said secondary chamber as to block the passage of infusion fluid through said secondary chamber, and said secondary chamber having said outlet for infusion fluid disposed at the bottom of said secondary chamber said shelf capable of re-directing infusion fluid flow in said secondary chamber away from said outlet and towards the top of said secondary chamber.

Claim 4

A bubble trap for removing bubbles from cardioplegia medication or a mixture of arterial blood and medication in a cardioplegia system, said bubble trap having an infusion fluid inlet connected to the supply of cardioplegia infusion fluid and an outlet leading to the heart cannula, and said bubble trap comprising: (a) a primary chamber having an entrance way for infusion fluid disposed at the bottom, said entrance way adapted for connection with said infusion fluid inlet, said primary chamber capable of providing a passageway for infusion fluid leaving said entrance way, and said primary chamber having a greater cross-sectional area than said entrance way, such that when infusion fluid enters said primary chamber from said entrance way the average velocity of said infusion fluid is caused to decelerate; and (b) a secondary chamber separated from said primary chamber by a dam, the area above said dam provinding a passageway for infusion fluid flowing from said primary chamber to said secondary chamber, said secondary chamber bounded by said dam, an exterior side wall which is disposed opposite said dam, a front wall and a back wall which is disposed opposite said front wall, and said secondary chamber having a shelf extending from said exterior wall into said secondary chamber in a direction towards said dam but not extending so far into said secondary chamber as to block the passage of infusion fluid through said secondary chamber, and said secondary chamber having said outlet for infusion fluid disposed at the bottom of said secondary chamber said shelf capable of re-directing infusion fluid flow in said secondary chamber away from said outlet and towards the top of said secondary chamber.

Claim 5

The bubble trap of claim 2 wherein at least a portion of said bubble trap is transparent to provide a visual indication of the air removed from said infusion fluid.

Claim 6

The bubble trap of claim 2 wherein said bubble trap has a top wall with a vent means for purging accumulated air in said system.

Claim 7

The bubble trap of claim 2 wherein said shelf extends into said secondary chamber to such an extent that said shelf spans at least 50 percent of the distance between said front wall of said secondary chamber and said back wall of said secondary chamber.

Claim 8

The bubble trap of claim 5 wherein said shelf is comprised of a ledge portion which is disposed in a direction substantially perpendicular to said exterior side wall of said secondary chamber, and a support wall underlying and supporting said shelf.

Claim 9

The bubble trap of claim 6 wherein said support wall extends between said ledge and said exterior side wall of said secondary chamber, and wherein said support wall is disposed at an acute angle with respect to said ledge.

Claim 10

The bubble trap of claim 6 wherein said ledge is disposed in said secondary chamber so that it is located between the top of said dam and the bottom of said secondary chamber.

Claim 11

The bubble trap of claim 2 wherein the dimensions of said primary chamber are such that the average velocity of said infusion fluid decelerates by at least about 200 percent when the fluid enters said primary chamber from said entrance way.

Claim 12

The bubble trap of claim 2 wherein said outlet for infusion fluid in the bottom of said secondary chamber is located beneath said shelf and on the side of said secondary chamber furthest from said entrance way.

Claim 13

The bubble trap of claim 2 wherein said shelf extends to such an extent that the distance between said shelf and said dam is between about 85 and 15 percent of the distance between said dam and said exterior side wall.

Claim 14

An improved cardioplegia system in which cardioplegia medication or a mixture of arterial blood and medication is delivered to the heart of a patient during open heart surgery, wherein the improvement comprises a one-piece monitoring module, said monitoring module having an inlet connected to the supply of cardioplegic infusion fluid and an outlet leading to the heart cannula, and said monitoring module comprising: (a) a pressure measuring device for measuring the internal pressure of said infusion fluid in said cardioplegia system; (b) a temperature measuring device for measuring the temperature of said infusion fluid; and (c) a bubble trap for removing bubbles from said infusion fluid before it passes through said outlet to said heart cannula, said bubble trap comprising: (1) a primary chamber having an entrance way for infusion fluid disposed at the bottom, said primary chamber capable of providing a passageway for infusion fluid leaving said entrance way, and said primary chamber having a greater cross-sectional area than said entrance way, such that when infusion fluid enters said primary chamber from entrance way the average velocity of said infusion fluid is caused to decelerate; and (2) a secondary chamber separated from said primary chamber by a dam, the area above said dam providing a passageway for infusion fluid flowing from said primary chamber to said secondary chamber bounded by said dam, an exterior side wall which is disposed opposite said dam, a front wall and a back wall which is disposed opposite said front wall, and said secondary chamber having a shelf extending from said exterior wall into said secondary chamber in a direction towards said dam but not extending so far into said secondary chamber as to block the passage of infusion fluid through said secondary chamber, and said secondary chamber having said outlet for infusion fluid disposed at the bottom of said secondary chamber said shelf capable of re-directing infusion fluid flow in said secondary chamber away from said outlet and towards the top of said secondary chamber.

Claim 15

An improved cardioplegia system in which cardioplegia medication or a mixture of arterial blood and medication is delivered to the heart of a patient during open heart surgery, wherein the improvement comprises a one-piece monitoring module, said monitoring module having an inlet connected to the supply of cardioplegic infusion fluid and an outlet leading to the heart cannula, and said monitoring module comprising: (a) a pressure measuring device for measuring the internal pressure of said infusion fluid in said cardioplegia system; (b) a temperature measuring device for measuring the temperature of said infusion fluid; and (c) a bubble trap for removing bubbles from said infusion fluid before it passes through said outlet to said heart cannula, said bubble trap comprising: (1) a primary chamber having an entrance way for infusion fluid disposed at the bottom, said primary chamber capable of providing a passageway for infusion fluid leaving said entrance way, and said primary chamber having a greater cross-sectional area than said entrance way, such that when infusion fluid enters said primary chamber from entrance way the average velocity of said infusion fluid is caused to decelerate; and (2) a secondary chamber separated from said primary chamber by a dam, the area above said dam providing a passageway for infusion fluid flowing from said primary chamber to said secondary chamber bounded by said dam, an exterior side wall which is disposed opposite said dam, a front wall and a back wall which is disposed opposite said front wall, and said secondary chamber having a shelf extending from said exterior wall into said secondary chamber in a direction towards said dam but not extending so far into said secondary chamber as to block the passage of infusion fluid through said secondary chamber, and said secondary chamber having said outlet for infusion fluid disposed at the bottom of said secondary chamber said shelf capable of re-directing infusion fluid flow in said secondary chamber away from said outlet and towards the top of said secondary chamber.

Claim 16

The improved cardioplegia system of claim 12 wherein said pressure measuring device comprises a single-leg manometer column connected with said supply of cardioplegic infusion fluid, said column being substantially transparent along at least a portion of its length to provide for viewing the level of infusion fluid in said column, and a graduated linear scale disposed adjacent said column for reading the level of infusion fluid contained within said column as a representation of internal infusion fluid pressure at any given time.

Claim 17

The improved cardioplegia system of claim 12 wherein said temperature monitoring device comprises a temperature monitoring column through which the infusion fluid passes, and a liquid crystal temperature sensing strip disposed adjacent said column and being in thermal contact with the infusion fluid passing through said column, said liquid crystal temperature sensing strip capable of providing a visual indication of the infusion fluid temperature.

Claim 18

The improved cardioplegia system of claim 12 wherein said one-piece monitoring module additionally comprises a filtering assembly capable of removing particulate matter from said infusion fluid.

Claim 19

The improved cardioplegia system of claim 12 wherein said monitoring module is constructed from a clear organic polymeric material, and said bubble trap is capable of providing a visual indication of the increase of air in said cardioplegia system.

Claim 20

The improved cardioplegia system of claim 12 wherein said system additionally comprises a cooling system which comprises: (a) a cooling medium; (b) a cooling tank to hold said cooling medium; and (c) at least one multiple-loop laminate supported in said tank, said laminate constructed from a flexible organic polymeric film so as to form a path for said infusion fluid comprising a plurality of connected substantially parallel rows, and having inlet and outlet ends for said infusion fluid.

Claim 21

The improved cardioplegia system of claim 17 wherein said cooling medium comprises at least one pouch packed with a water-based nontoxic gel having a depressed freezing point.