Implantable catheter with electrical pulse nerve stimulators and drug delivery system

Claim 1

A method of pain treatment carried out in the epidural spaces of a patient comprising: (a) implanting an apparatus for pain relief into a patient, said apparatus comprising three discrete interconnected elements; (i) a catheter implanted in the epidural spaces of said patient, (hi) a battery operated drug pump having a drug reservoir comprising a membrane whereby a liquid pain-relieving agent may be injected through the patient's skin into said reservoir to replenish a supply of a pain-relieving agent in said reservoir, said drug pump further comprising means for delivering said liquid pain-relieving agent to a lumen in said catheter, and (iii) a battery operated electrical pulse generating means operatively connected to a plurality of ring electrodes on said catheter; said catheter comprising means for administering said liquid pain-relieving agent to said patient further comprising an elongated hollow body having a distal end and a proximal end, said lumen therebetween, said body further comprising a first opening at said proximal end and a second opening at said distal end whereby said liquid pain-relieving agent is introduced through said first opening by said delivering means of said drug pump, flows through said lumen and out of said second opening into the patient, at least two ring electrodes spaced downwardly from said distal end on the exterior surface of said lumen and electrically insulated from one another, a separate wire connected to each said ring electrode, each said wire being embedded in the wall of said elongated hollow body from each said electrode to said proximal end of said elongated hollow body and terminating in a separate terminal external to said lumen, and operatively connected to said electrical pulse generating means for administering electrical pulses to said ring electrodes for pain relief in the patient; (b) pulsing electricity through at least two said ring electrodes of said catheter in a manner consistent with relieving pain; (c) continually and gradually delivering said liquid pain-relieving agent from said drug pump through said lumen into the epidural spaces of said patient through said drug delivery means of said drug pump; (d) leaving said catheter in place in the epidural spaces of the patient for an indefinite lengthy period of at least three days, thereby providing steady and continuous pain relief to the patient.

Claim 2

A method of pain treatment carried out in the epidural spaces of a patient comprising: (a) implanting an apparatus for pain relief into a patient, said apparatus comprising three discrete interconnected elements; (i) a catheter implanted in the epidural spaces of said patient, (hi) a battery operated drug pump having a drug reservoir comprising a membrane whereby a liquid pain-relieving agent may be injected through the patient's skin into said reservoir to replenish a supply of a pain-relieving agent in said reservoir, said drug pump further comprising means for delivering said liquid pain-relieving agent to a lumen in said catheter, and (iii) a battery operated electrical pulse generating means operatively connected to a plurality of ring electrodes on said catheter; said catheter comprising means for administering said liquid pain-relieving agent to said patient further comprising an elongated hollow body having a distal end and a proximal end, said lumen therebetween, said body further comprising a first opening at said proximal end and a second opening at said distal end whereby said liquid pain-relieving agent is introduced through said first opening by said delivering means of said drug pump, flows through said lumen and out of said second opening into the patient, at least two ring electrodes spaced downwardly from said distal end on the exterior surface of said lumen and electrically insulated from one another, a separate wire connected to each said ring electrode, each said wire being embedded in the wall of said elongated hollow body from each said electrode to said proximal end of said elongated hollow body and terminating in a separate terminal external to said lumen, and operatively connected to said electrical pulse generating means for administering electrical pulses to said ring electrodes for pain relief in the patient; (b) pulsing electricity through at least two said ring electrodes of said catheter in a manner consistent with relieving pain; (c) continually and gradually delivering said liquid pain-relieving agent from said drug pump through said lumen into the epidural spaces of said patient through said drug delivery means of said drug pump; (d) leaving said catheter in place in the epidural spaces of the patient for an indefinite lengthy period of at least three days, thereby providing steady and continuous pain relief to the patient.

Claim 14

A method of pain treatment for chronic pain carried out in the epidural spaces of a patient comprising the sequential steps of: (a) implanting an apparatus for pain relief into said patient, said apparatus comprising three interconnected elements; (i) said catheter implanted in the epidural spaces of a patient, (ii) a battery operated drug pump having a drug reservoir comprising a membrane whereby a liquid pain-relieving agent may be injected through the skin of said patient into said reservoir to replenish a supply of said pain-relieving agent in said reservoir, said drug pump further comprising drug delivery means for delivering said pain-relieving agent to a lumen in said catheter, and (iii) a battery operated electrical pulse generating means operatively connected to a plurality of ring electrodes on said catheter; said catheter comprising means for administering said liquid pain-relieving agent to said patient further comprising an elongated hollow body having a distal end and a proximal end, said lumen therebetween, said body further comprising a first opening at said proximal end and a second opening at said distal end whereby said liquid pain-relieving agent is introduced through said first opening by said drug delivery means of said drug pump, flows through said lumen and out of said second opening into said patient, at least two ring electrodes spaced downwardly from said distal end on an exterior surface of said lumen and electrically insulated from one another, a separate wire connected to each said ring electrode, each said wire being embedded in a side wall of said elongated hollow body from each said electrode to said proximal end of said elongated hollow body and terminating in a separate terminal external to said lumen, and operatively connected to said electrical pulse generating means for administering electrical pulses to said ring electrodes for pain relief in said patient; (b) continually and gradually delivering a narcotic through said lumen into said epidural spaces of said patient through a delivery means connected to said proximal end of said lumen until toxic doses of said narcotic no longer controls pain effectively and a state of tolerance develops in said patient; (c) terminating delivery of said narcotic through said lumen when said state of tolerance has developed; (d) continually and gradually administering a local anesthetic through said lumen into said epidural spaces of said patient through said drug delivery means connected to said proximal end of said lumen until said tolerance for said narcotic disappears; (e) pulsing electricity through at least two said terminals in a manner consistent with relieving pain simultaneously with step (d), until said tolerance of said narcotic disappears; and (f) resuming delivery of said narcotic, terminating said step of pulsing of electricity through said electrodes, and terminating said step of administering a local anesthetic; thereby providing steady and continuous pain relief to said patient.

Claim 15

A method of pain treatment for chronic pain carried out in the epidural spaces of a patient comprising the sequential steps of: (a) implanting an apparatus for pain relief into said patient, said apparatus comprising three interconnected elements; (i) said catheter implanted in the epidural spaces of a patient, (ii) a battery operated drug pump having a drug reservoir comprising a membrane whereby a liquid pain-relieving agent may be injected through the skin of said patient into said reservoir to replenish a supply of said pain-relieving agent in said reservoir, said drug pump further comprising drug delivery means for delivering said pain-relieving agent to a lumen in said catheter, and (iii) a battery operated electrical pulse generating means operatively connected to a plurality of ring electrodes on said catheter; said catheter comprising means for administering said liquid pain-relieving agent to said patient further comprising an elongated hollow body having a distal end and a proximal end, said lumen therebetween, said body further comprising a first opening at said proximal end and a second opening at said distal end whereby said liquid pain-relieving agent is introduced through said first opening by said drug delivery means of said drug pump, flows through said lumen and out of said second opening into said patient, at least two ring electrodes spaced downwardly from said distal end on an exterior surface of said lumen and electrically insulated from one another, a separate wire connected to each said ring electrode, each said wire being embedded in a side wall of said elongated hollow body from each said electrode to said proximal end of said elongated hollow body and terminating in a separate terminal external to said lumen, and operatively connected to said electrical pulse generating means for administering electrical pulses to said ring electrodes for pain relief in said patient; (b) continually and gradually delivering a narcotic through said lumen into said epidural spaces of said patient through a delivery means connected to said proximal end of said lumen until toxic doses of said narcotic no longer controls pain effectively and a state of tolerance develops in said patient; (c) terminating delivery of said narcotic through said lumen when said state of tolerance has developed; (d) continually and gradually administering a local anesthetic through said lumen into said epidural spaces of said patient through said drug delivery means connected to said proximal end of said lumen until said tolerance for said narcotic disappears; (e) pulsing electricity through at least two said terminals in a manner consistent with relieving pain simultaneously with step (d), until said tolerance of said narcotic disappears; and (f) resuming delivery of said narcotic, terminating said step of pulsing of electricity through said electrodes, and terminating said step of administering a local anesthetic; thereby providing steady and continuous pain relief to said patient.