Manually actuated, implantable device to sequentially feed doses of a substance, in particular a therapeutant

• US 4,718,894 A
• Filed: 05/21/1986
• Issued: 01/12/1988
• Est. Priority Date: 05/21/1985
• Status: Expired due to Term

• Current Assignee: NMT NeuroSciences (International), Inc.
• Original Assignee: Applied Precision LLC (General Electric Company)
• Inventors: Lazorthes, Guy
• Primary Examiner(s): Truluck, Dalton L.
• Application Number:
  US06/865,413
• Time in Patent Office: 601 Days
• Field of Search: 604/9, 604/93, 604/153, 604/185, 604/246, 604/891
• US Class Current: 604/288.02
• CPC Class Codes: A61M 5/1428 with manual pumping action

Abstract

The invention concerns a sequential and manually actuated feed device for implantation in an accessible subcutaneous region of a patient for the purpose of sequentially dosing a liquid, in particular a therapeutant. This device comprises a reservoir consisting of a flexible pouch, a filling site (2) located at the rim of said pouch in order to inject the liquid into it, and a manual pump (3) located in the opposite zone of the pouch in order to supply the liquid dose by dose to a catheter (20). The pump has a rigid case with a recess and bearing an expulsion membrane so as to bound a volume chamber; safety means prevent any accidental injection in the event of a spurious pressure exerted on the flexible pouch.

Claims

1. A manually actuated, sequential feed device for implantation in an accessible subcutaneous region for sequentially feeding liquid doses comprising a reservoir (1) having a capacity of plural doses, a filling site (2) for the reservoir and including a filling chamber (8), a septum (7) for injecting a liquid into said chamber and communication means (9) between the filling chamber and the reservoir, and a manual pump (3) having a volume chamber (13) the capacity of which corresponds to one dose, first communication means (15) between the reservoir and said chamber for filling said chamber and second communication means (16) between said volume chamber and an external catheter (20), said reservoir comprising a flexible pouch (1) having a first external wall (1a) and a second, internal wall (1b) opposite said first wall and impermeably bonded to each other along the edges thereof, said manual pump including an integral rigid body (10) having a concave recess (11) opening toward an active side of said body in order to form said volume chamber (13), and placed between said flexible walls (1a, 1b) of said reservoir, said pump further including on its active side an expulsion membrane (12) for sealing the volume chamber and located on the side of the external flexible wall (1a), and fastened by its opposite side to the internal flexible wall, said second communication means including a one-way valve (18) with a pressure threshold designed to open the communication between the chamber and the catheter when the chamber is subjected to an excess pressure higher than a given threshold Pc, said first communication means including a check valve (21) preventing the liquid from flowing back from the chamber into the reservoir, and a safety valve (17) designed to allow gravity draining the reservoir into the volume chamber and closing off the communication if the excess pressure in the reservoir exceeds a value Fr less than or equal to Pc.

2. A feed device as in claim 1 and wherein said pump body (10) is placed between the two flexible walls (1a, 1b) near their rims, and said external flexible wall (1a) includes a window to match said expulsion membrane and is impermeably fastened on said body (10) by the edges of said window.

3. A feed device as in claim 2 and wherein said flexible pouch (1) is stiffened at the edges of the flexible walls (1a, 1b) by a peripheral frame (4) fastened to the edges of said flexible walls.

4. A feed device as in claim 3 and wherein said filling site (2) is located near the edge of the flexible walls (1a, 1b) in a zone of the flexible pouch which is opposite that of the manual pump (3), and said filling site comprises a rigid stop plate (5) fastened on the internal flexible wall (1b) and a ring (6) solidly joined to said plate and bearing the injection septum (7) in such a manner that this septum matches a window of the external flexible wall (1a) fixed impermeably around said ring.

5. A feed device as in claim 3 and wherein said flexible pouch (1) forming the reservoir has a generally triangular shape, and said manual pump (3) is located near one of the vertices and said filling site (2) near another vertex.

6. A feed device as in claim 5 and wherein each flexible wall (1a, 1b) is preformed from a flexible, biocompatible plastic so as to assume the shape of a dome at rest, said peripheral frame (4) including two elements (4a, 4b) made of a biocompatible, semi-rigid plastic fastened in mutually opposite manner respectively on the outer wall (1a) and on the inner wall (1b), and said frame (4) and the rims of the flexible walls (1a, 1b) are rounded off near the angles.

7. A feed device as in claim 6 and wherein said flexible pouch (1) forming the reservoir has the general shape of an approximately right triangle with one side (v) of the right angle being shorter than the other, said manual pump (3) being located in the acute angle subtended by the short side (v) and the hypotenuse near the corresponding vertex, said filling site (2) being located in the acute angle subtended by the long side (h) and the hypotenuse near the corresponding vertex, and a plurality of suture holes (23) in the rim of the flexible pouch near the right angle and near the acute angle adjacent said manual pump (3).

8. A feed device as in claim 7 for implantation in the abdominal wall of a patient in the right lateral position, and wherein said triangular pouch is geometrically designed so that its long side (h) extends to the right when the device is in a vertical plane and with its short side (v) vertical and its manual pump (3) is in the lower part and when viewed in elevation on the side of the external wall (1a).

9. A feed device as in claim 7, for implanation in the abdominal wall of a patient in the left lateral position, and wherein said triangular pouch is geometrically designed so that its long side extends to the left when the device is in a vertical plane with its short side vertical and its manual pump in the lower part and when viewed in elevation from the side of the external wall.

10. A feed device as in claim 6 and wherein said recess (11) of the pump unit is shallow oompared with the dimensions of its cross-sectional opening at the active side of said unit, said case (10) being provided around the recess with a rim on which is impermeably fixed the rim of the expulsion membrane (12), and said expulsion membrane when at rest being essentially planar.

11. A feed device as in claim 1 and wherein said recess (11) of the pump has a shape matching that of the forefinger.

12. A feed device as in claim 1 and wherein the active side of the pump body (10) and the expulsion membranes (12) supported by it slope with respect to the opposite side of the unit whereby said unit decreases in thickness toward the catheter (20).

13. A device as in claim 10 and wherein said pump case (10) and its recess (11) have an elongated shape symmetrical with respect to an axial plane.

14. A feed device as in claim 10 and wherein said pump body (10) is integrally molded from a rigid biocompatible plastic and said expulsion membrane (12) is cut to fit the rim of the recess (11) from an elastic biocompatible material.

15. A feed device as in claim 14, and wherein said expulsion membrane (12) is made of an elastic plastic material of the self-sealing type in order to provide the pump with an accessory function of a chronic-injection access site.

16. A feed devices as in claim 14 and wherein said frame element (4a) fixed to the external flexible wall (1a) is provided with an extension (4c) around the pump case (10).

17. A feed device as in claim 10 and wherein said second communication means includes a duct (16) through the case (10) and issuing into the recess (11) near its bottom and into its peripheral edge outside the pouch (1), the end of the catheter (20) being impermeably fastened into said duct, the threshold, one-way valve (18) being housed in said duct (16) and fitted to open it above a threshold pressure Pc approximately between 50 and 60 millibars said second communication means including a duct (15) through the case (10) and issuing into the recess (11) near its bottom and at its peripheral edge between the flexible walls (1a, 1b) bounding the reservoir, the safety valve (17) being housed in said duct (15) and fitted to seal the communication above a pressure Pr essentially between 20 and 30 millibars in the reservoir.

18. A feed device as in claim 10 and wherein the recess (11) has a volume roughly between 0.4 and 0.6 cm³ in order to bound together with the expulsion membrane at rest a volume chamber (13) with a capacity corresponding to one embolus, and wherein the two flexible walls (1, 1b) bound a reservoir with a capacity substantially between 30 and 50 cm³.

19. A feed device as in claim 14, and wherein said injection septum (7) of the filling site comprises two elastic membranes (7a, 7b) supported on the ring (6) so as to be separated by a vacuum.

20. A feed device as in claim 19, and wherein the stop plate (5) of the filling site is made of a rigid biocompatible material, each membrane (7a, 7b) includes a peripheral bead (7c) and comprises an elastic biocompatible material, the ring (6) includes two annular elements (6a, 6b) which form the core of peripheral membrane beads (7c) comprising a rigid biocompatible material.

21. Feed device as in claim 1, characterized by being wholly covered with a thin flexible coat (22) made of a biocompatible material.