CA2070810A1 - Steroid eluting intramuscular lead - Google Patents
Steroid eluting intramuscular leadInfo
- Publication number
- CA2070810A1 CA2070810A1 CA002070810A CA2070810A CA2070810A1 CA 2070810 A1 CA2070810 A1 CA 2070810A1 CA 002070810 A CA002070810 A CA 002070810A CA 2070810 A CA2070810 A CA 2070810A CA 2070810 A1 CA2070810 A1 CA 2070810A1
- Authority
- CA
- Canada
- Prior art keywords
- skeletal muscle
- electrode
- suture material
- lead
- electrical conductor
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/05—Electrodes for implantation or insertion into the body, e.g. heart electrode
- A61N1/0587—Epicardial electrode systems; Endocardial electrodes piercing the pericardium
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/06—Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials
- A61B17/06166—Sutures
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/10—Location thereof with respect to the patient's body
- A61M60/122—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body
- A61M60/126—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body implantable via, into, inside, in line, branching on, or around a blood vessel
- A61M60/148—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body implantable via, into, inside, in line, branching on, or around a blood vessel in line with a blood vessel using resection or like techniques, e.g. permanent endovascular heart assist devices
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/10—Location thereof with respect to the patient's body
- A61M60/122—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body
- A61M60/165—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body implantable in, on, or around the heart
- A61M60/178—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body implantable in, on, or around the heart drawing blood from a ventricle and returning the blood to the arterial system via a cannula external to the ventricle, e.g. left or right ventricular assist devices
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/50—Details relating to control
- A61M60/508—Electronic control means, e.g. for feedback regulation
- A61M60/515—Regulation using real-time patient data
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/80—Constructional details other than related to driving
- A61M60/855—Constructional details other than related to driving of implantable pumps or pumping devices
- A61M60/861—Connections or anchorings for connecting or anchoring pumps or pumping devices to parts of the patient's body
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/80—Constructional details other than related to driving
- A61M60/855—Constructional details other than related to driving of implantable pumps or pumping devices
- A61M60/871—Energy supply devices; Converters therefor
- A61M60/878—Electrical connections within the patient's body
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/80—Constructional details other than related to driving
- A61M60/855—Constructional details other than related to driving of implantable pumps or pumping devices
- A61M60/871—Energy supply devices; Converters therefor
- A61M60/882—Devices powered by the patient, e.g. skeletal muscle powered devices
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/10—Location thereof with respect to the patient's body
- A61M60/122—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body
- A61M60/126—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body implantable via, into, inside, in line, branching on, or around a blood vessel
- A61M60/161—Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body implantable via, into, inside, in line, branching on, or around a blood vessel mechanically acting upon the outside of the patient's blood vessel structure, e.g. compressive structures placed around a vessel
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M60/00—Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
- A61M60/20—Type thereof
- A61M60/289—Devices for mechanical circulatory actuation assisting the residual heart function by means mechanically acting upon the patient's native heart or blood vessel structure, e.g. direct cardiac compression [DCC] devices
Abstract
An improved lead (100) for electrically stimulating muscle tissue particularly configured for a cardiac assist system powered by surgically modified skeletal muscle tissue. The skeletal muscle is either wrapped about the heart itself, or about an auxiliary pumping chamber attached to the aorta. Electrical stimulation is supplied via the improved lead (100) to cause contraction of the skeletal muscle in synchronism with the natural or artificially paced heart rate and timed to obtain the desired hemodynamic effect.
The improved lead (100) has an electrode (114, 124) which is embedded in the skeletal muscle. The stimulation threshold of the skeletal muscle is held relatively low by the action of a glucocorticosteroid imbedded within the suture material (120). By placing the drug material in this position, it acts as an anti-inflammatory along the entire path of the suture material (120) and treats the specific area of electrode contact from within the muscle itself. The specific area of electrode contact may also be treated from the electrode side by placing a similar drug within the electrode (124).
The improved lead (100) has an electrode (114, 124) which is embedded in the skeletal muscle. The stimulation threshold of the skeletal muscle is held relatively low by the action of a glucocorticosteroid imbedded within the suture material (120). By placing the drug material in this position, it acts as an anti-inflammatory along the entire path of the suture material (120) and treats the specific area of electrode contact from within the muscle itself. The specific area of electrode contact may also be treated from the electrode side by placing a similar drug within the electrode (124).
Description
W091/08~5 2 ~ 7 0 81~ PCT/US90/07~1 STEROID ELUTING INTRAMUSCULAR LEAD
~TEROID E~U~ING INTRAM~SCULAR LBAD
CROSS REFERENCES TO CO-PENDING APPLICATIONS
This application is related to Serial No.
, Filed , entitled "Muscle Fitness Detection by Colorimetry" by the same assignee; Serial No. , Filed , entitled "Muscle Output Monitor by Intramuscular Temperature Variation Measurement" by the same assignee; and Serial No. , Filed , entitled "Muscle Contraction Control by ~--Intramuscular Pressure Monitoring" by the same assignee.
BACRGRO~ND OF T~E INVEN$ION
1. Field of the Invention - The present invention generally pertains to skeletal muscle stimulation, and more particularly, pertains to improved lead systems for .
stimulating skeletal muscle powered cardiac assist systems.
~TEROID E~U~ING INTRAM~SCULAR LBAD
CROSS REFERENCES TO CO-PENDING APPLICATIONS
This application is related to Serial No.
, Filed , entitled "Muscle Fitness Detection by Colorimetry" by the same assignee; Serial No. , Filed , entitled "Muscle Output Monitor by Intramuscular Temperature Variation Measurement" by the same assignee; and Serial No. , Filed , entitled "Muscle Contraction Control by ~--Intramuscular Pressure Monitoring" by the same assignee.
BACRGRO~ND OF T~E INVEN$ION
1. Field of the Invention - The present invention generally pertains to skeletal muscle stimulation, and more particularly, pertains to improved lead systems for .
stimulating skeletal muscle powered cardiac assist systems.
2. Description of the Prior Art - The use of sXeletal muscle tissue to power chronically implantable cardiac assist systems has met with some success. See, for example, U.S. Patent No. 4,813,952, issued to Aida XhalaSalla herein incorporated by reference which describes such a system.
Using the patient's own muscle tissue overcomes the problems associated with the storage and transmission of en~rgy from artificial sources. The result is a very compact system -requiring no percutaneous energy transmission.
A problem presented by the use of skeletal muscle power is application of stimulation signals to cause muscle contraction. The earliest skeletal muscle powered cardiac assist systems used cardiac pacing leads for skeletal muscle stimulation.
A major improvement to such leads is fou~d in the use of steroid eluting pacing leads. U.S. Patent No. 4,711,251 issued to Stokes, which teaches an endocardial pacing lead WO91/0800~ 2 0 7~81 ~ PCT/~Sgo/0709l_ having steroid drug embedded in the distal tip. This embedded steroid drug treats the heart tissue immediately in contact with the pacing electrode. U.S. Patent Nos.
4,506,680; 4,577,642; and 4,606,118 teach similar endocardial leads, all of which treat the electrode contact area with a steroid. United States Statutory Invention Registration No. H356 discloses an endocardial pacing lead suitable for epicardial insertion which elutes a steroid ~;~
drug from the electrode.
All of these pacing leads are directed to stimulating the heart muscle, which is configured in a predetermined shape. The skeletal muscle used to power the cardiac assist system, on the other hand, is likely to be configured in a wide variety of shapes, any specific one of which cannot be -known until the surgical procedure is actually performed.
For that reason a flexible, specifically designed lead is ~
far more appropriate than one especially directed to cardiac - -pacing applications.
2 0 8~RY OF q~lE INVENTION
The subject invention is an adaptation of a type of cardiac pacing lead (called a heart wire) designed for-acute use. The lead has a terminal pin at the proximal end, an insulated wire body, an electrode made by not insulating the distal portion of the conductor, a strand of suture material running the entire length of the lead and extending distal to the electrode, and a curved surgical needle attached to the distal end of the strand of suture material.
In the present invention, the suture material is treated with a steroid drug, such as a glucocorticosteroid, along its entire length. Upon chronic implantation, the steroid drug is eluted from the suture material, thus treating possible tissue inflammation or damage caused by the implantation procedure or subsequent irritation. This treatment is accomplished along the entire length of the ;, '.'. , ' ~ , . , ' ' ` :
W091~08005 PCT/US90/07~1 suture/tissue contact, not just at the site of the electrode. However, because the suture material runs within the conductor coil, the site of the electrode tissue contact is also treated as in the prior art.
BRIEF DE8CRIPTION OP T~B DRAWINGS
Other objects of the present invention and many of the attendant advantages of the present invention will be readily appreciated as the same become better understood by reference to the following detailed description when considered in connection with the accompanying drawings, in which like reference numerals desi~nate like parts throughout the figures thereof and wherein:
FIG. l is an overall view of one configuration of the lS cardiac assist system;
FIG. 2 is a plan view of a chronically implantable stimulation lead of the present invention;
PIG. 3 is a plan view of an alternative embodiment of a chronically implantable stimulation lead of the present invention;
FIG. ~ is a view of the electrode and concentric strand of suture material of the present invention;
FIG. 5 is a cross-sectional view of the chronically implantable lead; and, 2S FIG. 6 is a view of the chronically implantable lead as positioned in the skeletal muscle.
DETAI~ED DESCRIPTION OF T~E PREPERRED EMBODIMENTS
Cardiac assist systems do not replace the patient's natural heart, but merely supplement it in performing blood circulation. This assistance takes two (2) basic forms.
The first of these directly assist the natural heart by increasing aortic pressure at the same time as the heart.
This may be implemented by wrapping the skeletal muscle about the heart, about the aorta, or about a compressible : :,, : ,.. .. , : : -: ., : - ~:: ~, ,. ;.
'~, . ,,, , :. ~, ~
.i.~: , ,, : :
WO91~0800j PCT/US~/07091 20~08~ ~
chamber in series with or parallel to a portion of the aorta.
The second form increases circulatory system pressure during relaxation of the heart. The resulting increase in coronary perfusion provides the desired assistance to the heart by alleviating excess cellular fatigue. With either form of cardiac assist, the heart is electrically sensed to ensure that the skeletal muscle is stimulated in the proper timing relationship to heart contractions.
FIG. 1 shows a typical cardiac assist system. This - particular mode performs counter pulsation for enhanced perfusion as an indirect cardiac assist. A single ~ode is shown for the purpose of illustration only and not by way of limiting the scope of the present invention. Other modes of cardiac assist may be found in U.S. Patent No. 4,813,952.
Human heart 10 is assisted by counter pulse contraction of skeletal muscle 22 by the enhanced perfusion of cardiac tissue. Pulse generator 36 senses contractions of human heart 10 by tranvenous lead 34. After a delay, phase generator sends stimulating pulses to skeletal muscle 22 via lead 100, thereby inducing contraction. As skeletal muscle 22 contrzcts, it reduces the diameter of chamber 20 which is - coupled to aorta 12 via stub 16. This contraction increases aortic pressure, thereby improving perfusion through the coronary vascular system.
Skeletal muscle 22 must be conditioned to respond in the desired manner without fatigue. U.S. Patent No.
4,411,268 issued to James Cox, incorporated herein by reference, teaches such a method of conditioning.
FIG. 2 is a plan view of a chronically implantable lead 100 for stimulation of skeletal muscle which powers the cardiac assist system of FIG. 1. The proximal e~d of the lead contains a connector 102 which couples to implantable pulse generator 36. Connector 102 has sealing rings 10 which seal the connection with the implantable pulse :
-~'' . - .
W09l/0800~ 2 0 7 0 8 1~ PCT/US~/07091 generator 36 against the ingress of bodily fluids. Terminal pin 106 electrically couples the lead to implantabl~ pulse generator 36.
Insulating sheath 108 insulates lead 100 fro~ unwanted electrical contact with body tissue. Slidable suture sleeve 110 slides along the length of insulating sheath 108.
Sutures used to tie down lead 100 are imbedded in groove 112 of slidable suture sleeve 110. Coaxial sheath 116 further helps insulate and strengthen the body of lead 100.
Electrode 114 comprises an uninsulated portion of a space wound wire conducting coil internal to insulating sheaths 108 and 116 and coaxial therewith. Electrode 114 is electrically coupled to terminal pin 106.
Strand 120 of suture material of polypropoline or other polymer is mechanically attached to the proximal end of the lead, runs the length of lead 100, and is coaxial with insulating sheathes 108 and 116 and with the conducting coil. A curved surgical needle 118 is mechanically attached to the distal end of strand 120 of suture material. Not easily seen is the steroid drug, preferably a glucocorticosteroid. This drug is releasably imbedded within the polymer of strand 120. During the life of lead 100, this drug leaches out into the surrounding tissue at a predetermined rate.
Preformed helix 122 is deformably molded into strand 120 to aid in attachment. A detailed explanation of preformed helix 122 is found in U.S. Patent No. 4,341,226 issued to Peters, incorporated herein by reference.
FSG. 3 is an alternative embodiment of the lead of FIG.
2. It is identical in all respects except that electrode 124 replaces electrode 114. Electrode 124 exposes a great deal more of the coiled conductor, thereby creating a much larger surface area for stimulation. The optimal surface area for stimulation varies with the specific application, and will normally be selected by the physician in charge O r '"'. :: ' -.' ' .,'" ' :
. . . . .
,"~,:, , , . ,. , ' , :' ~ ' ' ~:: . . : , .
'~x,~ '` ,' ' .
WO9l/0800~ 8 1 ~ PCT/USgo/07091 the surgery.
FIG. 4 is a close up view of electrode 114 (or electrode 124 in the alternative embodiment) as located concentrically about strand 120 of suture material. As explained above, strand 120 is a polymer imbedded with a glucocorticosteroid.
.
. . .
.. . . . .
.. , ,.. , ~ .. .
'""' " "' ' ' . ' . ' ' ' ' , ' ' ' ,' ':. ' , ' ~; ' .
WO91/08005 2 0 7 ~ 8 1~ PCT/US90/07091 FIG. 5 is a cross-sectional view of lead 100. Strand 120 comprises the inner diameter. It is surrounded by electrode 114 and insulating sheaths 108 and 116.
FIG. 6 shows the implantation of lead 100. Curved surgical needle 118 enters skeletal muscle 22 at puncture 128. It proceeds along path 132 and exits skeletal muscle 22 at exit point 130. Preformed helix 122 sustains electrode 114 in contact with skeletal muscle 22 at puncture 128. The glucocorticosteroid leaches out from strand 120 all along path 132 including puncture 128 and exit point 130 to minimize acute and chronic irritation.
Having thus described the preferred embodiments, those of skill in the art will be readily able to apply the present invention without departing from the scope of the claims which are hereto attached.
~r-:',~'`i:,`' ', - , :
:: - ' ' . ' - , ~
. : .
. .. . . .
Using the patient's own muscle tissue overcomes the problems associated with the storage and transmission of en~rgy from artificial sources. The result is a very compact system -requiring no percutaneous energy transmission.
A problem presented by the use of skeletal muscle power is application of stimulation signals to cause muscle contraction. The earliest skeletal muscle powered cardiac assist systems used cardiac pacing leads for skeletal muscle stimulation.
A major improvement to such leads is fou~d in the use of steroid eluting pacing leads. U.S. Patent No. 4,711,251 issued to Stokes, which teaches an endocardial pacing lead WO91/0800~ 2 0 7~81 ~ PCT/~Sgo/0709l_ having steroid drug embedded in the distal tip. This embedded steroid drug treats the heart tissue immediately in contact with the pacing electrode. U.S. Patent Nos.
4,506,680; 4,577,642; and 4,606,118 teach similar endocardial leads, all of which treat the electrode contact area with a steroid. United States Statutory Invention Registration No. H356 discloses an endocardial pacing lead suitable for epicardial insertion which elutes a steroid ~;~
drug from the electrode.
All of these pacing leads are directed to stimulating the heart muscle, which is configured in a predetermined shape. The skeletal muscle used to power the cardiac assist system, on the other hand, is likely to be configured in a wide variety of shapes, any specific one of which cannot be -known until the surgical procedure is actually performed.
For that reason a flexible, specifically designed lead is ~
far more appropriate than one especially directed to cardiac - -pacing applications.
2 0 8~RY OF q~lE INVENTION
The subject invention is an adaptation of a type of cardiac pacing lead (called a heart wire) designed for-acute use. The lead has a terminal pin at the proximal end, an insulated wire body, an electrode made by not insulating the distal portion of the conductor, a strand of suture material running the entire length of the lead and extending distal to the electrode, and a curved surgical needle attached to the distal end of the strand of suture material.
In the present invention, the suture material is treated with a steroid drug, such as a glucocorticosteroid, along its entire length. Upon chronic implantation, the steroid drug is eluted from the suture material, thus treating possible tissue inflammation or damage caused by the implantation procedure or subsequent irritation. This treatment is accomplished along the entire length of the ;, '.'. , ' ~ , . , ' ' ` :
W091~08005 PCT/US90/07~1 suture/tissue contact, not just at the site of the electrode. However, because the suture material runs within the conductor coil, the site of the electrode tissue contact is also treated as in the prior art.
BRIEF DE8CRIPTION OP T~B DRAWINGS
Other objects of the present invention and many of the attendant advantages of the present invention will be readily appreciated as the same become better understood by reference to the following detailed description when considered in connection with the accompanying drawings, in which like reference numerals desi~nate like parts throughout the figures thereof and wherein:
FIG. l is an overall view of one configuration of the lS cardiac assist system;
FIG. 2 is a plan view of a chronically implantable stimulation lead of the present invention;
PIG. 3 is a plan view of an alternative embodiment of a chronically implantable stimulation lead of the present invention;
FIG. ~ is a view of the electrode and concentric strand of suture material of the present invention;
FIG. 5 is a cross-sectional view of the chronically implantable lead; and, 2S FIG. 6 is a view of the chronically implantable lead as positioned in the skeletal muscle.
DETAI~ED DESCRIPTION OF T~E PREPERRED EMBODIMENTS
Cardiac assist systems do not replace the patient's natural heart, but merely supplement it in performing blood circulation. This assistance takes two (2) basic forms.
The first of these directly assist the natural heart by increasing aortic pressure at the same time as the heart.
This may be implemented by wrapping the skeletal muscle about the heart, about the aorta, or about a compressible : :,, : ,.. .. , : : -: ., : - ~:: ~, ,. ;.
'~, . ,,, , :. ~, ~
.i.~: , ,, : :
WO91~0800j PCT/US~/07091 20~08~ ~
chamber in series with or parallel to a portion of the aorta.
The second form increases circulatory system pressure during relaxation of the heart. The resulting increase in coronary perfusion provides the desired assistance to the heart by alleviating excess cellular fatigue. With either form of cardiac assist, the heart is electrically sensed to ensure that the skeletal muscle is stimulated in the proper timing relationship to heart contractions.
FIG. 1 shows a typical cardiac assist system. This - particular mode performs counter pulsation for enhanced perfusion as an indirect cardiac assist. A single ~ode is shown for the purpose of illustration only and not by way of limiting the scope of the present invention. Other modes of cardiac assist may be found in U.S. Patent No. 4,813,952.
Human heart 10 is assisted by counter pulse contraction of skeletal muscle 22 by the enhanced perfusion of cardiac tissue. Pulse generator 36 senses contractions of human heart 10 by tranvenous lead 34. After a delay, phase generator sends stimulating pulses to skeletal muscle 22 via lead 100, thereby inducing contraction. As skeletal muscle 22 contrzcts, it reduces the diameter of chamber 20 which is - coupled to aorta 12 via stub 16. This contraction increases aortic pressure, thereby improving perfusion through the coronary vascular system.
Skeletal muscle 22 must be conditioned to respond in the desired manner without fatigue. U.S. Patent No.
4,411,268 issued to James Cox, incorporated herein by reference, teaches such a method of conditioning.
FIG. 2 is a plan view of a chronically implantable lead 100 for stimulation of skeletal muscle which powers the cardiac assist system of FIG. 1. The proximal e~d of the lead contains a connector 102 which couples to implantable pulse generator 36. Connector 102 has sealing rings 10 which seal the connection with the implantable pulse :
-~'' . - .
W09l/0800~ 2 0 7 0 8 1~ PCT/US~/07091 generator 36 against the ingress of bodily fluids. Terminal pin 106 electrically couples the lead to implantabl~ pulse generator 36.
Insulating sheath 108 insulates lead 100 fro~ unwanted electrical contact with body tissue. Slidable suture sleeve 110 slides along the length of insulating sheath 108.
Sutures used to tie down lead 100 are imbedded in groove 112 of slidable suture sleeve 110. Coaxial sheath 116 further helps insulate and strengthen the body of lead 100.
Electrode 114 comprises an uninsulated portion of a space wound wire conducting coil internal to insulating sheaths 108 and 116 and coaxial therewith. Electrode 114 is electrically coupled to terminal pin 106.
Strand 120 of suture material of polypropoline or other polymer is mechanically attached to the proximal end of the lead, runs the length of lead 100, and is coaxial with insulating sheathes 108 and 116 and with the conducting coil. A curved surgical needle 118 is mechanically attached to the distal end of strand 120 of suture material. Not easily seen is the steroid drug, preferably a glucocorticosteroid. This drug is releasably imbedded within the polymer of strand 120. During the life of lead 100, this drug leaches out into the surrounding tissue at a predetermined rate.
Preformed helix 122 is deformably molded into strand 120 to aid in attachment. A detailed explanation of preformed helix 122 is found in U.S. Patent No. 4,341,226 issued to Peters, incorporated herein by reference.
FSG. 3 is an alternative embodiment of the lead of FIG.
2. It is identical in all respects except that electrode 124 replaces electrode 114. Electrode 124 exposes a great deal more of the coiled conductor, thereby creating a much larger surface area for stimulation. The optimal surface area for stimulation varies with the specific application, and will normally be selected by the physician in charge O r '"'. :: ' -.' ' .,'" ' :
. . . . .
,"~,:, , , . ,. , ' , :' ~ ' ' ~:: . . : , .
'~x,~ '` ,' ' .
WO9l/0800~ 8 1 ~ PCT/USgo/07091 the surgery.
FIG. 4 is a close up view of electrode 114 (or electrode 124 in the alternative embodiment) as located concentrically about strand 120 of suture material. As explained above, strand 120 is a polymer imbedded with a glucocorticosteroid.
.
. . .
.. . . . .
.. , ,.. , ~ .. .
'""' " "' ' ' . ' . ' ' ' ' , ' ' ' ,' ':. ' , ' ~; ' .
WO91/08005 2 0 7 ~ 8 1~ PCT/US90/07091 FIG. 5 is a cross-sectional view of lead 100. Strand 120 comprises the inner diameter. It is surrounded by electrode 114 and insulating sheaths 108 and 116.
FIG. 6 shows the implantation of lead 100. Curved surgical needle 118 enters skeletal muscle 22 at puncture 128. It proceeds along path 132 and exits skeletal muscle 22 at exit point 130. Preformed helix 122 sustains electrode 114 in contact with skeletal muscle 22 at puncture 128. The glucocorticosteroid leaches out from strand 120 all along path 132 including puncture 128 and exit point 130 to minimize acute and chronic irritation.
Having thus described the preferred embodiments, those of skill in the art will be readily able to apply the present invention without departing from the scope of the claims which are hereto attached.
~r-:',~'`i:,`' ', - , :
:: - ' ' . ' - , ~
. : .
. .. . . .
Claims (8)
1. In an implantable lead for stimulation of skeletal muscle having a proximal end with a terminal connector, having an electrical conductor electrically coupled to said terminal connector wherein said electrical conductor is electrically insulated, having an electrode electrically coupled to said electrical conductor for transmitting electrical energy to body tissue, having suture material mechanically coupled to said electrical conductor, and having a surgical needle mechanically coupled to said suture material, the improvement comprising anti-inflammatory drug removably embedded in said suture material.
2. The improvement according to claim 1 wherein said anti-inflammatory drug leaches out into said skeletal muscle at an essentially predetermined rate.
3. The improvement according to claim 2 wherein said anti-inflammatory drug is a steroid.
4. The improvement according to claim 3 wherein said steroid is a glucocorticosteroid.
5. In an implantable lead for stimulation of skeletal muscle comprising:
a. a proximal end with a terminal connector;
b. an electrical conductor electrically coupled to said terminal connector wherein said electrical conductor is electrically insulated c. an electrode electrically coupled to said electrical conductor for transmitting electrical energy to body tissue;
d. suture material mechanically coupled to said electrical conductor;
e. a surgical needle mechanically coupled to said suture material; and, f. an anti-inflammatory drug removably embedded in said suture material.
a. a proximal end with a terminal connector;
b. an electrical conductor electrically coupled to said terminal connector wherein said electrical conductor is electrically insulated c. an electrode electrically coupled to said electrical conductor for transmitting electrical energy to body tissue;
d. suture material mechanically coupled to said electrical conductor;
e. a surgical needle mechanically coupled to said suture material; and, f. an anti-inflammatory drug removably embedded in said suture material.
6. An implantable lead according to claim 5 wherein said anti-inflammatory drug leaches out into said skeletal muscle at an essentially predetermined rate.
7. An implantable lead according to claim 6 wherein said anti-inflammatory drug is a steroid.
8. An implantable lead according to claim 7 wherein said steroid is a glucocorticosteroid.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US446,594 | 1989-12-06 | ||
| US07/446,594 US5009229A (en) | 1989-12-06 | 1989-12-06 | Steroid eluting intramuscular lead |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2070810A1 true CA2070810A1 (en) | 1991-06-07 |
Family
ID=23773171
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002070810A Abandoned CA2070810A1 (en) | 1989-12-06 | 1990-12-04 | Steroid eluting intramuscular lead |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US5009229A (en) |
| EP (1) | EP0504297B1 (en) |
| JP (1) | JPH05504700A (en) |
| AU (1) | AU646423B2 (en) |
| CA (1) | CA2070810A1 (en) |
| DE (1) | DE69009193T2 (en) |
| WO (1) | WO1991008005A1 (en) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5358519A (en) * | 1989-12-06 | 1994-10-25 | Medtronic, Inc. | Muscle control and monitoring system |
| AU3058092A (en) * | 1991-10-31 | 1993-06-07 | Medtronic, Inc. | Muscle control and monitoring system |
| US5241957A (en) * | 1991-11-18 | 1993-09-07 | Medtronic, Inc. | Bipolar temporary pacing lead and connector and permanent bipolar nerve wire |
| US5251621A (en) * | 1991-12-18 | 1993-10-12 | Telectronics Pacing Systems, Inc. | Arrhythmia control pacer using skeletal muscle cardiac graft stimulation |
| DE4219083C1 (en) * | 1992-06-11 | 1993-10-07 | Vasco Med Inst Fuer Katheterte | Fluid dispensing electrode for cardiology, neurology or gynaecology - has anchoring element provided by hollow helix allowing storage of dispensed medicament |
| US5324323A (en) * | 1992-09-09 | 1994-06-28 | Telectronics Pacing Systems, Inc. | Multiple channel cardiosynchronous myoplasty apparatus |
| US5425751A (en) * | 1993-07-30 | 1995-06-20 | Medtronic, Inc. | Method and apparatus for optimum positioning of a muscle stimulating implant |
| US5489294A (en) * | 1994-02-01 | 1996-02-06 | Medtronic, Inc. | Steroid eluting stitch-in chronic cardiac lead |
| US5716392A (en) * | 1996-01-05 | 1998-02-10 | Medtronic, Inc. | Minimally invasive medical electrical lead |
| US7658727B1 (en) | 1998-04-20 | 2010-02-09 | Medtronic, Inc | Implantable medical device with enhanced biocompatibility and biostability |
| US6304786B1 (en) * | 1999-03-29 | 2001-10-16 | Cardiac Pacemakers, Inc. | Implantable lead with dissolvable coating for improved fixation and extraction |
| US20030199962A1 (en) * | 2002-04-22 | 2003-10-23 | Chester Struble | Anti-slip leads for placement within tissue |
| AU2003261252A1 (en) * | 2002-07-26 | 2004-02-16 | Myomend, Inc. | Cardiac rhythm management system with intramural myocardial pacing leads and electrodes |
| DE10316177B4 (en) * | 2003-04-10 | 2007-05-31 | Cardiac Pacemakers, Inc., St. Paul | Pacemaker electrode arrangement |
| US7953499B2 (en) * | 2003-09-30 | 2011-05-31 | Cardiac Pacemakers, Inc. | Drug-eluting electrode |
| US7499759B2 (en) * | 2003-10-24 | 2009-03-03 | Cardiac Pacemakers, Inc. | Distal or proximal fixation of over-the-tether myocardial leads |
| US7418298B2 (en) * | 2003-10-24 | 2008-08-26 | Cardiac Pacemakers, Inc. | Myocardial lead with fixation mechanism |
| US8019438B2 (en) * | 2005-06-28 | 2011-09-13 | Cardiac Pacemakers, Inc. | Anchor for electrode delivery system |
| US20080103572A1 (en) | 2006-10-31 | 2008-05-01 | Medtronic, Inc. | Implantable medical lead with threaded fixation |
| EP2139491A1 (en) * | 2007-03-16 | 2010-01-06 | Durect Corporation | Use of glucocorticoids for treatment of congestive heart failure |
| DE102008043452A1 (en) * | 2008-11-04 | 2010-05-06 | Biotronik Crm Patent Ag | Device for introducing medical implants |
| US20110106230A1 (en) * | 2009-11-04 | 2011-05-05 | Erhard Flach | Placement device for inserting medical implants such as electrode lines |
| CN102500056B (en) * | 2011-10-25 | 2013-12-25 | 上海交通大学 | Auxiliary-implanted flexible microelectrode for absorbable suture and preparation method thereof |
| WO2016100948A1 (en) | 2014-12-19 | 2016-06-23 | Cardiac Pacemakers, Inc. | Medical lead anchoring |
| US20180020944A1 (en) * | 2015-01-20 | 2018-01-25 | Med-El Elektromedizinische Geraete Gmbh | Stapedius Muscle Reflex Recording Electrode with a Sacrificial Part |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3896813A (en) * | 1967-06-23 | 1975-07-29 | Sutures Inc | Sutures having long-lasting biocidal properties |
| US3698853A (en) * | 1969-10-31 | 1972-10-17 | American Cyanamid Co | Fray resistant catgut sutures |
| US3991766A (en) * | 1973-05-31 | 1976-11-16 | American Cyanamid Company | Controlled release of medicaments using polymers from glycolic acid |
| US3918455A (en) * | 1974-04-29 | 1975-11-11 | Albany Int Corp | Combined surgical suture and needle |
| CA1174284A (en) * | 1980-09-02 | 1984-09-11 | Medtronic, Inc. | Body implantable lead |
| US4341226A (en) * | 1980-09-22 | 1982-07-27 | Medtronic, Inc. | Temporary lead with insertion tool |
| US4338947A (en) * | 1980-11-03 | 1982-07-13 | Medtronic, Inc. | Positive fixation heart wire |
| US4444207A (en) * | 1981-10-19 | 1984-04-24 | Cordis Corporation | Method of anchoring a temporary cardiac pacing lead |
| US4506680A (en) * | 1983-03-17 | 1985-03-26 | Medtronic, Inc. | Drug dispensing body implantable lead |
| US4712553A (en) * | 1985-05-30 | 1987-12-15 | Cordis Corporation | Sutures having a porous surface |
| US4813952A (en) * | 1985-08-01 | 1989-03-21 | Medtronic, Inc. | Cardiac assist device |
-
1989
- 1989-12-06 US US07/446,594 patent/US5009229A/en not_active Expired - Fee Related
-
1990
- 1990-12-04 WO PCT/US1990/007091 patent/WO1991008005A1/en not_active Application Discontinuation
- 1990-12-04 AU AU69796/91A patent/AU646423B2/en not_active Ceased
- 1990-12-04 DE DE69009193T patent/DE69009193T2/en not_active Revoked
- 1990-12-04 CA CA002070810A patent/CA2070810A1/en not_active Abandoned
- 1990-12-04 JP JP3501954A patent/JPH05504700A/en active Pending
- 1990-12-04 EP EP91901526A patent/EP0504297B1/en not_active Revoked
Also Published As
| Publication number | Publication date |
|---|---|
| EP0504297B1 (en) | 1994-05-25 |
| WO1991008005A1 (en) | 1991-06-13 |
| AU646423B2 (en) | 1994-02-24 |
| EP0504297A1 (en) | 1992-09-23 |
| DE69009193D1 (en) | 1994-06-30 |
| JPH05504700A (en) | 1993-07-22 |
| US5009229A (en) | 1991-04-23 |
| AU6979691A (en) | 1991-06-26 |
| DE69009193T2 (en) | 1994-09-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |