Claims Analysis
Total Claims: 12
Claim 1
Independent Claim
348 words
A prosthetic sphincter for surgical implantation to achieve coaptive continence, said sphincter including an occlusion cuff to surround at least some of a patient's lumen for applying variable occlusive pressures for occluding and relaxing the lumen and thereby controlling the movement of material therethrough, said occlusion cuff having first and second expandable chambers positioned opposite one another for engaging the patient's lumen and being adapted to receive a fluid medium to apply diametric occlusive pressures to the lumen for achieving coaptive continence when such chambers are expanded by the receipt therein of such fluid, there being no fluid communication between said first and second chambers, and said sphincter comprising first and second occlusive pressure adjustment means to be operated independently of one another and respectively interconnected with said first and second expandable chambers for supplying a selected one or the other of said chambers with fluid medium for expanding said chambers to vary the occlusive pressures being applied to the patient's lumen, said first occlusive presure adjustment means including a compressible reservoir containing a supply of said fluid medium, a first delivery tube extending between said reservoir and said first expandable chamber for delivering fluid medium to said chamber, a normally closed flow control valve to permit the movement of said fluid medium between said reservoir and said first chamber to expand said first chamber when said reservoir is compressed and said flow control valve is thereby temporarily opened, and pressure relief means location at the periphery of said flow control valve and surgically implanted so as to be manually activated to temporarily open said flow control valve to permit the movement of said fluid medium from said first chamber to said reservoir to shrink said fluid chamber, said second occlusive pressure adjustment means including a subcantaneously disposed entry port for receiving the tip of a fluid medium supplying syringe and a second delivery tube extending between said entry port and said second expandable chamber for delivering fluid medium to said second chamber to expand said second chamber when said fluid medium is injected into said entry port.
Claim 2
Dependent Claim
348 words
A prosthetic sphincter for surgical implantation to achieve coaptive continence, said sphincter including an occlusion cuff to surround at least some of a patient's lumen for applying variable occlusive pressures for occluding and relaxing the lumen and thereby controlling the movement of material therethrough, said occlusion cuff having first and second expandable chambers positioned opposite one another for engaging the patient's lumen and being adapted to receive a fluid medium to apply diametric occlusive pressures to the lumen for achieving coaptive continence when such chambers are expanded by the receipt therein of such fluid, there being no fluid communication between said first and second chambers, and said sphincter comprising first and second occlusive pressure adjustment means to be operated independently of one another and respectively interconnected with said first and second expandable chambers for supplying a selected one or the other of said chambers with fluid medium for expanding said chambers to vary the occlusive pressures being applied to the patient's lumen, said first occlusive presure adjustment means including a compressible reservoir containing a supply of said fluid medium, a first delivery tube extending between said reservoir and said first expandable chamber for delivering fluid medium to said chamber, a normally closed flow control valve to permit the movement of said fluid medium between said reservoir and said first chamber to expand said first chamber when said reservoir is compressed and said flow control valve is thereby temporarily opened, and pressure relief means location at the periphery of said flow control valve and surgically implanted so as to be manually activated to temporarily open said flow control valve to permit the movement of said fluid medium from said first chamber to said reservoir to shrink said fluid chamber, said second occlusive pressure adjustment means including a subcantaneously disposed entry port for receiving the tip of a fluid medium supplying syringe and a second delivery tube extending between said entry port and said second expandable chamber for delivering fluid medium to said second chamber to expand said second chamber when said fluid medium is injected into said entry port.
Claim 3
Dependent Claim
53 words
The prosthetic sphincter recited in claim 1, wherein each of said first and second expandable chambers includes respective expansion limiting means for causing the chambers to have substantially flat opposing contact surfaces for engaging the patient's lumens when in an expanded condition, said opposing contact surfaces applying diametric occlusive pressures to the lumen.
Claim 4
Dependent Claim
62 words
The prosthetic sphincter recited in claim 1, wherein said entry port comprises an insert having a path extending therethrough to permit the passage of fluid medium to said second delivery tube, said insert having a conical end for receiving the tip of a medium supplying syringe to be inserted through said sphincter and a tubular end for interconnection with said delivery tube.
Claim 5
Dependent Claim
47 words
The prosthetic sphincter recited in claim 3, wherein the tubular end of said insert is particularly dimensioned to stop the movement therepast of a syringe tip in order to prevent damage to said delivery tube when said tip is inserted into the conical end of said insert.
Claim 6
Dependent Claim
36 words
The prosthetic sphincter recited in claim 3, wherein a sealing gel is located within the conical end of said insert for healing a puncture formed in said sphincter when the syringe is withdrawn from said insert.
Claim 7
Dependent Claim
46 words
The prosthetic sphincter recited in claim 1, wherein said occlusion cuff includes first and second ends and fastening means for releasably connecting said first and second ends together for varying the circumference of said cuff depending upon the circumference of the patient's lumen to be surrounded.
Claim 8
Dependent Claim
59 words
The prosthetic sphincter recited in claim 6, wherein said fastening means includes a series of locking ridges at the first occlusion cuff end and a locking clip at the second occlusion cuff end, said occlusion cuff ends being releasably connected together around a patient's lumen when said locking clip is received between a pair of adjacently disposed locking ridges.
Claim 9
Dependent Claim
61 words
The prosthetic sphincter recited in claim 1, wherein said occlusion cuff includes a matrix of pressure transmitting protuberances extending in a direction for engaging the patient's lumen and transmitting occlusive pressures from said cuff to the lumen, the area of said cuff surrounding said protuberances providing regions of relatively lower occlusive pressure for maximizing blood flow and minimizing possible tissue damage.
Claim 10
Dependent Claim
52 words
The prosthetic sphincter recited in claim 1, further comprising a connecting channel enclosing the first and second delivery tubes of said first and second occlusive pressure adjustment means such that said first and second delivery tubes extend through said connecting channel for delivering fluid medium to said first and second expandable chambers.
Claim 11
Dependent Claim
55 words
The prosthetic sphincter recited in claim 9, wherein said connecting channel is helically wound and has a compression resistant cross-section for resisting kinking and a possible occlusion of said first or second delivery tubes which extend therethrough, said helically wound connecting channel having an extensible length for accommodating movement by the patient after sphincter implantation.
Claim 12
Dependent Claim
28 words
The prosthetic sphincter recited in claim 1, wherein said entry port is located at the interior of said reservoir for receipt thereat of said fluid medium supplying syringe.