Cardio therapeutic heart sack
This invention relates to implantable heart sack that can be equipped with pacemaker leads and/or defibrillation leads for the treatment of cardiomyopathy, hypertrophic cardiomyopathy, tachycardia, bradycardia, ventricular fibrillation, atrial fibrillation etc. The hear sack was prepared from biocompatible, biostable, implantable polyetherurethane, polycarbonateurethane, silicone, polysiloxaneurethane, polyfluoroethylene, or hydrogenated poly(styrene-butadiene) copolymer. The heart sack is equipped with attached sutures to make it easier to attach onto the heart. The heart sack can be made semipermeable or perforated to have numerous holes. The heart sack can be reinforce with fiber or filament. Ordinary pacemaker leads can be attached to the inner side of the heart sack. However, the pacemaker leads of this invention were prepared from noble metal (gold, platinum, rhodium and platinum-Rhodium alloys) or stainless steel coated, deposited or plated mono-filaments, yarns, braids, cords, wires or films, or cylindrical tubes of polyamide, polyimide, polyester, and/or polypropylene that are encased in multi-lumen insulating tube or coaxial tube made of biocompatible, biostable, implantable polyetherurethane, polycarbonateurethane, silicone, polysiloxaneurethane, polyfluoroethylene, or hydrogenated poly(styrene-butadiene) copolymer. The leads can be mounted onto the inner surface of the heart sack and contoured to the heart. The heart sack can be coated with hydrophilic coating containing an antimicrobial agent that gives the heart sack a low coefficient of friction, excellent biocompatibility and antimicrobial properties.
1. A system for treating ventricular dilation, the device comprising:
(a) a device configured to surround the heart and limit dilation of the ventricle, comprised of:
material; the material being constructed of a biocompatible material and being substantially inelastic; and
plurality of electrodes operably configured to contact a surface of the heart; and
(b) an electrical impulse generator operably connected to the electrodes, whereby electrical stimulation of the heart improves cardiac contraction.
2. The device according to claim 1 , wherein the plurality of stimulation electrodes are imbedded in the material and are configured to contact a surface of the heart.
3. The device according to claim 1 wherein the stimulation electrodes are electrically isolated.
4. The device according to claim 1 wherein the electrodes are constructed from a biostable material.
5. The device according to claim 1 wherein the material is closed ended.
6. The device according to claim 1 , wherein the material defines holes.
7. The device according to claim 1 , wherein the material defines pores.
8. The device according to claim 1 wherein the material is a non-mesh material.
9. A cardiac reinforcement device, said device comprising:
a sack of biomedical material configured to surround a heart and prevent cardiac expansion, said sack comprising a open base end for applying said sack to the heart such that when applied the base end is oriented toward the base of the heart; and
a plurality of stimulation electrodes configured to contact the heart, whereby the sack is configured to limit dilation of the heart and the stimulation electrodes are capable of improving cardiac contraction.
10. A method for treating a disease of a heart, the method comprising:
attaching a cardiac reinforcement device to a surface of the heart, the device comprising a sack of inelastic material and a plurality of stimulation electrodes configured to contact the heart;
limiting dilation of the heart by surrounding the heart with the sack; and
stimulating contraction of the heart by activating the stimulation electrodes.
11. A system for treating ventricular dilation comprising:
(a) a device configured to surround the heart, comprised of a non-mesh material; and
plurality of electrodes operably configured to contact a surface of the heart; and
(b) an electrical impulse generator operably connected to the electrodes, whereby electrical stimulation of the heart improves cardiac contraction.
12. The system according to claim 11 , wherein the plurality of stimulation electrodes are embedded in the material and are configured to contact a surface of the heart.
13. The system according to claim 11 wherein the stimulation electrodes are electrically isolated.
14. The system according to claim 11 wherein the electrodes are constructed from a biostable material.
15. The system according to claim 11 wherein the material is closed ended.
16. A system for treating ventricular dilation comprising:
(a) a cuff configured to be disposed around at least a portion of a heart comprised of:
a substrate; and
a plurality of stimulation electrodes configured to be in contact with the heart,
wherein the cuff limits the dilation of the heart; and
(b) a stimulator that sends one or more electrical impulses to one or more of the stimulation electrodes.
17. The system of claim 16 wherein:
(a) the cuff is constructed of a biologically inert material and is substantially inelastic, whereby the cuff will not allow further dilation of the ventricle.
18. The system of claim 16 wherein
(a) the plurality of stimulation electrodes are embedded in the material and are configured to contact a surface of the heart.
19. The system of claim 18 wherein:
(a) the stimulation electrodes are electrically isolated.
20. The system of claim 16 wherein:
(a) the cuff is closed ended.
21. The system of claim 16 wherein:
(a) the cuff comprises an inelastic non-mesh material.