Manufacture of tubing assembly for drainage catheter

Claim 3

The method according to claim 1, wherein said ion sputtering step includes passing a source of argon gas through an ion beam generator.

Claim 4

The method according to claim 1, wherein said ion sputtered length of tubing is a fluoropolymer tubing, and wherein said elastomeric tubing is a silicone rubber tubing.

Claim 5

The method according to claim 1, wherein said inserting step includes inserting said ion sputtered length of tubing such that the ion sputtered length of tubing is spaced from and defines a leading, distal length and a proximal length of said elastomeric tubing length.

Claim 6

The method according to claim 1, wherein said adhesive is a medical-grade adhesive and wherein said adhesive forms a seal between said ion sputtered tubing and said elastomeric length of tubing substantially at said axial edges of the ion sputtered length of tubing.

Claim 7

The method according to claim 1, further including closing the distal end of the elastomeric length of tubing by inserting an elastomeric plug thereinto.

Claim 8

The method according to claim 1, wherein said ion sputtered step forms micro orifices having a nominal opening width of between about 5 microns and up to about 60 microns and at which tissue ingrowth and blockage is substantially prevented.

Claim 9

The method according to claim 1, wherein said ion sputtered step forms micro orifices having a nominal opening width of between about 5 microns and about 60 microns.

Claim 10

A tubing assembly made by a process comprising: providing a length of elastomeric tubing having a selected outer diameter, and forming at least one radially directed opening through the elastomeric tubing; providing a length of non-elastomeric tubing having an internal diameter substantially equal to or less than said selected outer diameter of the elastomeric tubing; ion sputtering radially directed micro orifices through the length of non-elastomeric tubing, said ion sputtered length of non-elastomeric tubing being shorter than said elastomeric tubing length, and said ion sputtered radially directed orifices each being smaller than said radially directed opening through the length of elastomeric tubing; stretching said length of elastomeric tubing so as to reduce its said selected outer diameter, and inserting said ion sputtered length of tubing over said length of elastomeric tubing while same is at its reduced diameter, and simultaneously generally aligning said radially directed opening of the elastomeric tubing with said ion sputtered radially directed orifices of the non-elastomeric tubing; applying adhesive along the radially directed axial edges of the ion sputtered length of non-elastomeric at its reduced diameter; and relaxing said stretched elastomeric tubing length, whereby the elastomeric tubing substantially returns to its said selected outer diameter while the adhesive simultaneously flows between and adheres together with the ion sputtered length of non-elastomeric tubing and the elastomeric tubing in order to seal the non-elastomeric tubing over the elastomeric tubing at an orientation such that said opening through the elastomeric tubing is in substantially underlying relationship with said micro orifices of the non-elastomeric tubing.

Claim 11

A tubing assembly made by a process comprising: providing a length of elastomeric tubing having a selected outer diameter, and forming at least one radially directed opening through the elastomeric tubing; providing a length of non-elastomeric tubing having an internal diameter substantially equal to or less than said selected outer diameter of the elastomeric tubing; ion sputtering radially directed micro orifices through the length of non-elastomeric tubing, said ion sputtered length of non-elastomeric tubing being shorter than said elastomeric tubing length, and said ion sputtered radially directed orifices each being smaller than said radially directed opening through the length of elastomeric tubing; stretching said length of elastomeric tubing so as to reduce its said selected outer diameter, and inserting said ion sputtered length of tubing over said length of elastomeric tubing while same is at its reduced diameter, and simultaneously generally aligning said radially directed opening of the elastomeric tubing with said ion sputtered radially directed orifices of the non-elastomeric tubing; applying adhesive along the radially directed axial edges of the ion sputtered length of non-elastomeric at its reduced diameter; and relaxing said stretched elastomeric tubing length, whereby the elastomeric tubing substantially returns to its said selected outer diameter while the adhesive simultaneously flows between and adheres together with the ion sputtered length of non-elastomeric tubing and the elastomeric tubing in order to seal the non-elastomeric tubing over the elastomeric tubing at an orientation such that said opening through the elastomeric tubing is in substantially underlying relationship with said micro orifices of the non-elastomeric tubing.

Claim 12

The tubing assembly according to claim 9, wherein said adhered together ion sputtered length of tubing and said elastomeric tubing form a ventricular catheter.

Claim 13

The tubing assembly according to claim 10, wherein said ion sputtered length of tubing is a fluropolymer tubing and wherein said elastomeric tubing is a silicone rubber tubing.

Claim 14

The tubing assembly according to claim 9, wherein said length of elastomeric tubing extends beyond both of said axial edges of the ion sputtered length of tubing.

Claim 15

The tubing assembly according to claim 12, wherein one of said elastomeric tubing extensions beyond an axial edge of the ion sputtered length of tubing has a plug closing same.

Claim 16

The tubing assembly according to claim 9, wherein said adhesive is a medical-grade adhesive and wherein said adhesive forms a seal between said ion sputtered tubing and said elastomeric length of tubing substantially at said axial edges of the ion sputtered length of tubing.

Claim 17

The tubing assembly according to claim 9, wherein said micro orifices have a nominal opening width of between about 5 microns and about 60 microns.

Claim 18

An implantable cerebrospinal fluid pressure relief system including a hydrocephalus pressure relief valve, draining means and a ventricular catheter, wherein the improvement comprises said ventricular catheter being made by a process including: providing a length of elastomeric tubing having a selected outer diameter, and forming at least one radially directed opening through the elastomeric tubing; providing a length of non-elastomeric tubing having an internal diameter substantially equal to or less than said selected outer diameter of the elastomeric tubing; ion sputtering radially directed micro orifices through the length of non-elastomeric tubing, said ion sputtered length of non-elastomeric tubing being shorter than said elastomeric tubing length, and said ion sputtered radially directed orifices each being smaller than said radially directed opening through the length of elastomeric tubing; stretching said length of elastomeric tubing so as to reduce its said selected outer diameter, and inserting said ion sputtered length of tubing over said length of elastomeric tubing while same is at its reduced diameter, and simultaneously generally aligning said radially directed opening of the elastomeric tubing with said ion sputtered radially directed orifices of the non-elastomeric tubing; applying adhesive along the radially directed axial edges of the ion sputtered length of non-elastomeric tubing while the elastomeric tubing length is stretched and at its reduced diameter; and relaxing said stretched elastomeric tubing length, whereby the elastomeric tubing substantially returns to its said selected outer diameter while the adhesive simultaneously flows between and adheres together with the ion sputtered length of non-elastomeric tubing and the elastomeric tubing in order to seal the non-elastomeric tubing over the elastomeric tubing at an orientation such that said opening through the elastomeric tubing is in substantially underlying relationship with said micro orifices of the non-elastomeric tubing.

Claim 19

An implantable cerebrospinal fluid pressure relief system including a hydrocephalus pressure relief valve, draining means and a ventricular catheter, wherein the improvement comprises said ventricular catheter being made by a process including: providing a length of elastomeric tubing having a selected outer diameter, and forming at least one radially directed opening through the elastomeric tubing; providing a length of non-elastomeric tubing having an internal diameter substantially equal to or less than said selected outer diameter of the elastomeric tubing; ion sputtering radially directed micro orifices through the length of non-elastomeric tubing, said ion sputtered length of non-elastomeric tubing being shorter than said elastomeric tubing length, and said ion sputtered radially directed orifices each being smaller than said radially directed opening through the length of elastomeric tubing; stretching said length of elastomeric tubing so as to reduce its said selected outer diameter, and inserting said ion sputtered length of tubing over said length of elastomeric tubing while same is at its reduced diameter, and simultaneously generally aligning said radially directed opening of the elastomeric tubing with said ion sputtered radially directed orifices of the non-elastomeric tubing; applying adhesive along the radially directed axial edges of the ion sputtered length of non-elastomeric tubing while the elastomeric tubing length is stretched and at its reduced diameter; and relaxing said stretched elastomeric tubing length, whereby the elastomeric tubing substantially returns to its said selected outer diameter while the adhesive simultaneously flows between and adheres together with the ion sputtered length of non-elastomeric tubing and the elastomeric tubing in order to seal the non-elastomeric tubing over the elastomeric tubing at an orientation such that said opening through the elastomeric tubing is in substantially underlying relationship with said micro orifices of the non-elastomeric tubing.

Claim 20

The implantable system according to claim 16, wherein said ion sputtered length of tubing is a fluoropolymer tubing, and wherein said elastomeric tubing is a silicone rubber tubing.

Claim 21

The implantable system according to claim 16, wherein said inserting step includes inserting said ion sputtered length of tubing such that the ion sputtered length of tubing is spaced from and defines a leading, distal length and a proximal length of said elastomeric tubing length.

Claim 22

The implantable system according to claim 16, wherein said adhesive is a medical-grade adhesive and wherein said adhesive forms a seal between said ion sputtered tubing and said elastomeric length of tubing substantially at said axial edges of the ion sputtered length of tubing.

Claim 23

The implantable system according to claim 16, wherein said ion sputtered step forms micro orifices having a nominal opening width of between about 5 microns and up to about 60 microns and at which tissue ingrowth and blockage is substantially prevented.

Claim 24

An intracranial pressure monitoring and cerebrospinal fluid drainage system including a ventricular catheter, a tubing assembly for joining the ventricular catheter to fluid measurement means and to pressure monitoring means, wherein the improvement comprises said ventricular catheter being made by a process including: providing a length of elastomeric tubing having a selected outer diameter, and forming at least one radially directed opening through the elastomeric tubing; providing a length of non-elastomeric tubing having an internal diameter substantially equal to or less than said selected outer diameter of the elastomeric tubing; ion sputtering radially directed micro orifices through the length of non-elastomeric tubing, said ion sputtered length of non-elastomeric tubing being shorter than said elastomeric tubing length, and said ion sputtered radially directed orifices each being smaller than said radially directed opening through the length of elastomeric tubing; stretching said length of elastomeric tubing so as to reduce its said selected outer diameter, and inserting said ion sputtered length of tubing over said length of elastomeric tubing while same is at its reduced diameter, and simultaneously generally aligning said radially directed opening of the elastomeric tubing with said ion sputtered radially directed orifices of the non-elastomeric tubing; applying adhesive along the radially directed axial edges of the ion sputtered length of non-elastomeric tubing while the elastomeric tubing length is stretched and at its reduced diameter; and relaxing said stretched elastomeric tubing length, whereby the elastomeric tubing substantially returns to its said selected outer diameter while the adhesive simultaneously flows between and adheres together with the ion sputtered length of non-elastomeric tubing and the elastomeric tubing in order to seal the non-elastomeric tubing over the elastomeric tubing at an orientation such that said opening through the elastomeric tubing is in substantially underlying relationship with said micro orifices of the non-elastomeric tubing.

Claim 25

An intracranial pressure monitoring and cerebrospinal fluid drainage system including a ventricular catheter, a tubing assembly for joining the ventricular catheter to fluid measurement means and to pressure monitoring means, wherein the improvement comprises said ventricular catheter being made by a process including: providing a length of elastomeric tubing having a selected outer diameter, and forming at least one radially directed opening through the elastomeric tubing; providing a length of non-elastomeric tubing having an internal diameter substantially equal to or less than said selected outer diameter of the elastomeric tubing; ion sputtering radially directed micro orifices through the length of non-elastomeric tubing, said ion sputtered length of non-elastomeric tubing being shorter than said elastomeric tubing length, and said ion sputtered radially directed orifices each being smaller than said radially directed opening through the length of elastomeric tubing; stretching said length of elastomeric tubing so as to reduce its said selected outer diameter, and inserting said ion sputtered length of tubing over said length of elastomeric tubing while same is at its reduced diameter, and simultaneously generally aligning said radially directed opening of the elastomeric tubing with said ion sputtered radially directed orifices of the non-elastomeric tubing; applying adhesive along the radially directed axial edges of the ion sputtered length of non-elastomeric tubing while the elastomeric tubing length is stretched and at its reduced diameter; and relaxing said stretched elastomeric tubing length, whereby the elastomeric tubing substantially returns to its said selected outer diameter while the adhesive simultaneously flows between and adheres together with the ion sputtered length of non-elastomeric tubing and the elastomeric tubing in order to seal the non-elastomeric tubing over the elastomeric tubing at an orientation such that said opening through the elastomeric tubing is in substantially underlying relationship with said micro orifices of the non-elastomeric tubing.

Claim 26

The system according to claim 21, wherein said ion sputtered length of tubing is a fluoropolymer tubing, and wherein said elastomeric tubing is a silicone rubber tubing.

Claim 27

The system according to claim 21, wherein said inserting step includes inserting said ion sputtered length of tubing such that the ion sputtered length of tubing is spaced from and defines a leading, distal length and a proximal length of said elastomeric tubing length.

Claim 28

The system according to claim 21, wherein said adhesive is a medical-grade adhesive and wherein said adhesive forms a seal between said ion sputtered tubing and said elastomeric length of tubing substantially at said axial edges of the ion sputtered length of tubing.

Claim 29

The system according to claim 21, wherein said ion sputtered step forms micro orifices having a nominal opening width of between about 5 microns and up to about 60 microns and at which tissue ingrowth and blockage is substantially prevented.