Body cavity access device containing a hormone source

Claim 2

An implantable device for providing safe access to a patient's body cavity comprising: (a) a housing constituted by a sack and a hollow stem; the sack having at least one access opening and being constructed of a semipermeable membrane compatible with body tissue and permeable to peritoneal fluid but substantially impermeable to bacteria; the hollow stem having a distal end defining an extracorporeal segment and a proximal end defining a subcutaneous segment, the stem being compatible with body tissue and impermeable to body fluids; the sack access opening being sealingly coupled with the proximal end of the stem and together with the stem defining an access passageway to the sack, the housing being adapted to be implanted in the patient with the extracorporeal segment extending outside the body of the patient; (b) a plug to seal the distal end of the stem; and (c) a sensor to measure properties of body fluid located within the sack, the sensor having a transmission line extending outside the housing, and including a cannula extending into the housing to deliver medication into the sack.

Claim 3

The implantable device of claim 1 including at least one porous cuff surrounding a portion of the subcutaneous segment of the hollow stem.

Claim 4

The implantable device of claim 1 wherein the extracorporeal segment includes a flexible zone comprising a plurality of circumferential grooves.

Claim 5

The implantable device of claim 1 wherein the sack has a membrane with an effective pore size less than about 0.5 microns.

Claim 6

The implantable device of claim 4, wherein the pore size is sufficient to substantially prevent the passage of molecules having a molecular weight greater than about 50,000 daltons.

Claim 7

The implantable device of claim 1 including a hormone source situated within the sack.

Claim 8

The implantable device of claim 1 including live hormone producing cells removably placed within the housing.

Claim 9

The implantable device of claim 7 wherein the hormone producing cells are pancreatic islet cells.

Claim 10

The implantable device of claim 1 wherein the sack has a generally tubular shape having two ends, one end closed and the other end defining the access opening.

Claim 11

The implantable device of claim 1 including a second stem having a distal end defining an extracorporeal segment and a proximal end defining a subcutaneous segment, the second stem being compatible with body tissue and impermeable to body fluids, and wherein the sack has a generally tubular shape having two access openings sealingly coupled with the proximal end of each stem to form a hose with each stem defining an access passageway to the sack.

Claim 12

An implantable device for providing safe access to a patient's body cavity comprising: (a) a housing constituted by a sack and a hollow stem; the sack having a generally disc-like shape defining a chamber in fluid communication with the stem, at least one access opening, and being constructed of a semipermeable membrane compatible with body tissue and permeable to peritoneal fluid but substantially impermeable to bacteria; the hollow stem having a distal end defining an extracorporeal segment and a proximal end defining a subcutaneous segment, the stem being compatible with body tissue and impermeable to body fluids; the sack access opening being sealingly coupled with the proximal end of the stem and togehter with the stem defining an access passageway to the sack, the housing being adapted to be implanted in the patient with the extracorporeal segment extending outside the body of the patient; (b) a plug to seal the distal end of the stem; and (c) a separating wall plate dividing the chamber into a first chamber section and a second chamber section, the chamber sections being in fluid communication about the periphery of the plate and wherein the stem is constituted by an extermal stem member attached to the sack and in fluid communication with the second chamber section and an internal stem member located within the external stem member and in fluid communication with the first chamber section.

Claim 13

An implantable device for providing safe access to a patient's body cavity comprising: (a) a housing constituted by a sack and a hollow stem; the sack having a generally disc-like shape defining a chamber in fluid communication with the stem, at least one access opening, and being constructed of a semipermeable membrane compatible with body tissue and permeable to peritoneal fluid but substantially impermeable to bacteria; the hollow stem having a distal end defining an extracorporeal segment and a proximal end defining a subcutaneous segment, the stem being compatible with body tissue and impermeable to body fluids; the sack access opening being sealingly coupled with the proximal end of the stem and togehter with the stem defining an access passageway to the sack, the housing being adapted to be implanted in the patient with the extracorporeal segment extending outside the body of the patient; (b) a plug to seal the distal end of the stem; and (c) a separating wall plate dividing the chamber into a first chamber section and a second chamber section, the chamber sections being in fluid communication about the periphery of the plate and wherein the stem is constituted by an extermal stem member attached to the sack and in fluid communication with the second chamber section and an internal stem member located within the external stem member and in fluid communication with the first chamber section.

Claim 14

The implantable device of claim 11 wherein the chamber sections have a height between the plate and the sack of about 0.5 millimeters to about 5 millimeters.

Claim 15

An implantable device for supplying hormones to a patient comprising: (a) a housing constituted by a plurality of tubes and two hollow stems and including a flow dividing unit to place the tubes in sealed fluid communication with the stems; each of the tubes having two open ends and being constructed of a membrane compatible with body tissue and permeable to body fluids but substantially impermeable to bacteria; each stem having a distal end defining an extracorporeal segment and a proximal end defining a subcutaneous segment, each stem being compatible with body tissue and impermeable to body fluids; each end of each tube sealingly coupled with the proximal end of each stem such that each stem defines an access passageway to the tubes; (b) live hormone producing cells within the housing; and (c) plugs to seal the distal end of each stem.

Claim 16

An implantable device for supplying hormones to a patient comprising: (a) a housing constituted by a plurality of tubes and two hollow stems and including a flow dividing unit to place the tubes in sealed fluid communication with the stems; each of the tubes having two open ends and being constructed of a membrane compatible with body tissue and permeable to body fluids but substantially impermeable to bacteria; each stem having a distal end defining an extracorporeal segment and a proximal end defining a subcutaneous segment, each stem being compatible with body tissue and impermeable to body fluids; each end of each tube sealingly coupled with the proximal end of each stem such that each stem defines an access passageway to the tubes; (b) live hormone producing cells within the housing; and (c) plugs to seal the distal end of each stem.

Claim 17

The implantable device of claim 13 including at least one porous cuff surrounding a portion of the subcutaneous segment of each hollow stem.

Claim 18

The implantable device of claim 13 wherein the hormone producing cells are pancreatic islet cells.

Claim 19

The implantable device of claim 13 including spacer means on at least some of the tubes for maintaining a space between tubes.

Claim 20

The implantable device of claim 13 wherein the tubes have an inside diameter of about 200 microns to about 1000 microns.

Claim 21

The implantable device of claim 13 wherein each tube has a broad flattened construction.

Claim 22

The implantable device of claim 13 wherein the tubes have a membrane with an effective pore size of less than about 0.5 microns.

Claim 23

The implantable device of claim 13 wherein the pore size is sufficient to substantially prevent the passage of molecules having a molecular weight greater than about 50,000 daltons.