Anastomotic marking device and related method

Claim 1

A sutureless, anastomotic marking device for the fluoroscopic localization of coronary grafts, said device comprising: a sheet of flexible, hemostatic microfibrillar collagen, said hemostatic microfibrillar collagen being of the general type that dissolves after being in contact with body fluids for a period of time, said sheet having a first and second surface; said sheet having an inner edge and defining a centrally located opening through the sheet for accommodating a coronary artery bypass graft passing therethrough, said opening having a diameter substantially equal to the diameter of said coronary artery bypass graft, said sheet further having an outer edge concentric with said central opening and defining an annular surface on said sheet first and second surface between said opening and said outer edge, said sheet having a plurality of means defining a slit extending radially outward for some distance from said opening in said sheet, said sheet having a number of said radial slits to facilitate the encirclement of said sheet around said bypass graft, and wherein one of said slits extends fully from said opening in said sheet to the outer edge of said sheet so that said sheet may be separated at said fully extended slit to allow the sheet to be placed about the bypass graft, a number of radiopaque indicators circumferentially arranged on one of said first and second surfaces, each of said indicators having a surface area substantially less than the annular surface area of said sheet, and means for attaching said radiopaque indicators to said one surface of said hemostatic sheet.

Claim 7

A method of mounting an anastomotic marking device around a coronary bypass graft artery comprising the steps of: providing a sheet of flexible, hemostatic material of the general type that dissolves after contact with body fluids for a period of time, said sheet further defining a centrally located opening therethrough; arranging circumferentially around the opening a number of radiopaque indicators; attaching the indicators to one surface of the hemostatic sheet; cutting the hemostatic sheet from an edge of the central opening to the outer edge of the sheet so that the hemostatic sheet is separated completely along the cut part; folding the sheet in on itself so that said indicators are generally facing one another and along a line extending along the cut part so as to form two half sections, each of said half sections being in a plane substantially parallel to one another; spreading portions of the folded sheet along the cut part; moving the bypass graft artery and the sheet relative to one another so that the graft artery moves between the spread portions of the sheet and the sheet moves into enveloping relationship with the graft artery and the graft artery is situated between the half sections and extends through the central opening; unfolding the sheet so that the two half sections lie generally in a common plane and surround the graft artery extending through the central opening, said indicators being on the one surface away from the anastomosis and the other surface being in contact with the anastomotic graft area, and dissolving the hemostatic material during the anastomosis healing period so that the radiopaque indicators carried by the hemostatic material come into contact with the proximal anastomotic area of the coronary graft whereby the radiopaque indicators are held in contact with the anastomotic area by the fibrous body tissues surrounding the anastomosis.

Claim 8

A method of mounting an anastomotic marking device around a coronary bypass graft artery comprising the steps of: providing a sheet of flexible, hemostatic material of the general type that dissolves after contact with body fluids for a period of time, said sheet further defining a centrally located opening therethrough; arranging circumferentially around the opening a number of radiopaque indicators; attaching the indicators to one surface of the hemostatic sheet; cutting the hemostatic sheet from an edge of the central opening to the outer edge of the sheet so that the hemostatic sheet is separated completely along the cut part; folding the sheet in on itself so that said indicators are generally facing one another and along a line extending along the cut part so as to form two half sections, each of said half sections being in a plane substantially parallel to one another; spreading portions of the folded sheet along the cut part; moving the bypass graft artery and the sheet relative to one another so that the graft artery moves between the spread portions of the sheet and the sheet moves into enveloping relationship with the graft artery and the graft artery is situated between the half sections and extends through the central opening; unfolding the sheet so that the two half sections lie generally in a common plane and surround the graft artery extending through the central opening, said indicators being on the one surface away from the anastomosis and the other surface being in contact with the anastomotic graft area, and dissolving the hemostatic material during the anastomosis healing period so that the radiopaque indicators carried by the hemostatic material come into contact with the proximal anastomotic area of the coronary graft whereby the radiopaque indicators are held in contact with the anastomotic area by the fibrous body tissues surrounding the anastomosis.

Claim 9

A method of mounting an anastomotic marking device around a coronary bypass graft artery comprising the steps of: providing a sheet of flexible, hemostatic material of the general type that dissolves after contact with body fluids for a period of time, said sheet further defining a centrally located opening therethrough; arranging circumferentially around the opening a number of radiopaque indicators; attaching the indicators to one surface of the hemostatic sheet; cutting the hemostatic sheet from an edge of the central opening to the outer edge of the sheet so that the hemostatic sheet is separated completely along the cut part; folding the sheet in on itself so that said indicators are generally facing one another and along a line extending along the cut part so as to form two half sections, each of said half sections being in a plane substantially parallel to one another; spreading portions of the folded sheet along the cut part; moving the bypass graft artery and the sheet relative to one another so that graft artery moves between the spread portions of the sheet and the sheet moves into enveloping relationship with the graft artery and the graft artery is situated between the half sections and extends through the central opening; unfolding the sheet so that the two half sections lie generally in a common plane and in surrounding relationship to the graft artery extending through the central opening, said indicators being on the one surface away from the anastomosis and the other surface being in contact with the anastomotic graft area, and leaving the hemostatic sheet in surrounding relationship to the graft artery extending through the central opening to permit the hemostatic sheet to be dissolved by contact with body fluids during the anastomotic healing period so that the radiopaque indicators carried by the hemostatic material come into contact with the proximal anastomotic area of the coronary graft whereby the radiopaque indicators are held in contact with the anastomotic area by the fibrous body tissues surrounding the anastomosis.

Claim 10

A method of mounting an anastomotic marking device around a coronary bypass graft artery comprising the steps of: providing a sheet of flexible, hemostatic material of the general type that dissolves after contact with body fluids for a period of time, said sheet further defining a centrally located opening therethrough; arranging circumferentially around the opening a number of radiopaque indicators; attaching the indicators to one surface of the hemostatic sheet; cutting the hemostatic sheet from an edge of the central opening to the outer edge of the sheet so that the hemostatic sheet is separated completely along the cut part; folding the sheet in on itself so that said indicators are generally facing one another and along a line extending along the cut part so as to form two half sections, each of said half sections being in a plane substantially parallel to one another; spreading portions of the folded sheet along the cut part; moving the bypass graft artery and the sheet relative to one another so that graft artery moves between the spread portions of the sheet and the sheet moves into enveloping relationship with the graft artery and the graft artery is situated between the half sections and extends through the central opening; unfolding the sheet so that the two half sections lie generally in a common plane and in surrounding relationship to the graft artery extending through the central opening, said indicators being on the one surface away from the anastomosis and the other surface being in contact with the anastomotic graft area, and leaving the hemostatic sheet in surrounding relationship to the graft artery extending through the central opening to permit the hemostatic sheet to be dissolved by contact with body fluids during the anastomotic healing period so that the radiopaque indicators carried by the hemostatic material come into contact with the proximal anastomotic area of the coronary graft whereby the radiopaque indicators are held in contact with the anastomotic area by the fibrous body tissues surrounding the anastomosis.