Method and apparatus for treatment of cardiac disorders
The present invention is directed to systems and methods for delivering therapy for a cardiac disorder, wherein the system comprises a source for supplying a protein formulation containing a protein that is otherwise deficient in cardiac cells in a patient with a cardiac disorder, and a catheter having a proximal end and a distal end for delivering the protein formulation to the pericardial sac region of a human heart.
1. A method comprising:
diagnosing a patient as having a cardiac disorder caused by a protein deficiency due to a gene mutation, the disorder being selected from the group consisting of glycogen storage disease Type II and Fabry disease;
injecting a therapeutic protein formulation into an implantable source, the therapeutic protein formulation comprising a protein in a form that is deficient in cardiac cells in the patient with the cardiac disorder, the protein being selected from lysosomal acid α-glucosidase and α-galactosidase;
determining a rate for delivering the therapeutic protein formulation based on the genetic sequence of the patient's gene encoding the deficient protein; and
delivering the therapeutic protein formulation from the source through an implantable catheter directly to a pericardial sac region of a heart of a patient,
wherein the source is an implantable pump that provides for a programmable delivery rate of the protein formulation, and wherein the protein formulation is delivered at the determined delivery rate.
2. The method of claim 1 , wherein integrity and activity of the protein formulation is maintained by adding to the protein formulation, at least one species operable for maintaining a desired pH.
3. The method of claim 1 , wherein the pump includes a refillable reservoir to store the protein formulation prior to delivery to the pericardial sac.
4. The method of claim 1 , wherein the disorder is glycogen storage disease Type II and the protein is lysosomal acid α-glucosidase.
5. The method of claim 1 , wherein the disease is Fabry disease and the protein is α-galactosidase.