Subcutaneous device for monitoring and/or providing therapies
A subcutaneously implantable device includes a housing, a clip attached to a top side of the housing, a first prong with a proximal end attached to the housing and a distal end extending away from the housing, and a first electrode on the first prong. The clip is configured to anchor the device to a muscle, a bone, and/or a tissue. The first prong is configured to contact a heart. The first electrode is configured to contact the heart. Sensing circuitry in the housing that is configured to sense an electrical signal from the heart, and therapeutic circuitry in the housing is in electrical communication with the first electrode and is configured to deliver electrical stimulation to the heart through the first electrode.
1. A subcutaneously implantable device comprising:
a housing;
a clip attached to a top side of the housing that is configured to anchor the device to a muscle, a bone, and/or a first tissue;
a first prong with a proximal end attached to the housing and a distal end extending away from the housing that is configured to be positioned inferior to a heart;
a first defibrillator coil on the distal end of the first prong;
a first electrode on the device;
a drug pump having a drug reservoir in the housing;
a second prong with a lumen extending through the second prong and having a proximal end attached to the housing and fluidly connected to the drug pump, and a distal end extending away from the housing that is configured to extend to an organ, a nerve, and/or a second tissue; and
circuitry in the housing in electrical communication with the first defibrillator coil and the first electrode that is configured to deliver a shock to the heart through the first defibrillator coil, and in electrical communication with the drug pump that is configured to deliver a signal to the drug pump to provide a targeted or systemic therapeutic drug to the organ, the nerve, and/or the second tissue through the lumen extending through the second prong.
2. The device of claim 1 , wherein the clip is configured to attach the device to a xiphoid process and/or a sternum of a patient.
3. The device of claim 1 , wherein the clip further comprises:
a top portion;
a bottom portion; and
a spring portion extending between and connecting the top portion to the bottom portion, wherein the spring portion is configured to act as a spring for the clip to push the top portion of the clip onto the bone, the muscle, and/or the first tissue to which it is anchored.
4. The device of claim 1 , wherein the first electrode is positioned on the housing, the clip, the first prong, and/or the second prong and is configured to sense an electrical signal from the organ, the nerve, the first tissue and/or the second tissue.
5. The device of claim 1 , wherein the first electrode is positioned on the housing, the first prong, and/or the second prong and is configured to deliver electrical stimulation to the organ, the nerve, the first tissue and/or the second tissue.
6. The device of claim 1 , wherein the therapeutic drug in the drug reservoir is configured to be pumped into the lumen of the second prong using the drug pump.
7. The device of claim 1 , wherein the housing further comprises:
a first port on a back side of the housing, wherein the proximal end of the second prong is positioned in the first port.
8. The device of claim 1 , and further comprising:
a third prong with a lumen extending through the third prong and having a proximal end attached to the housing and fluidly connected to the drug reservoir, and a distal end extending away from the housing.
9. The device of claim 8 , wherein the housing further comprises:
a second port on a back side of the housing, wherein the proximal end of the third prong is positioned in the second port.
10. The device of claim 8 , wherein the third prong is configured to receive replenishment of the drug reservoir through an opening at the distal end of the third prong.
11. The device of claim 1 , wherein the circuitry is configured to sense an electrical signal from the heart through the first electrode and/or the first defibrillator coil.
12. The device of claim 1 , wherein the first electrode is on a front end of the housing, wherein the first defibrillator coil creates a first vector with the first electrode, and wherein the first vector passes through the heart.
13. The device of claim 1 , and further comprising:
a second defibrillator coil on the distal end of the second prong.
14. The device of claim 1 , and further comprising:
a third prong with a proximal end attached to the housing and a distal end extending away from the housing that is configured to contact a heart.
15. The device of claim 14 , wherein the first electrode is positioned on the third prong and is configured to sense an electrical signal from the heart and/or deliver electrical stimulation to the heart.
16. The device of claim 14 , and further comprising:
a second electrode on the third prong that is in electrical communication with the circuitry and is configured to sense an electrical signal from the heart and/or deliver electrical stimulation to the heart.
17. The device of claim 14 , wherein the third prong is configured to contact a right ventricle of the heart, a left ventricle of the heart, a right atrium of the heart, or a left atrium of the heart.
18. The device of claim 1 , and further comprising:
a third prong with a proximal end attached to the housing and a distal end extending away from the housing that is configured to be positioned on a first side of the housing; and
a second defibrillator coil on the distal end of the third prong.
19. The device of claim 18 , wherein the first defibrillator coil creates a first vector with the second defibrillator coil, and wherein the first vector passes through the heart.
20. The device of claim 18 , wherein the first defibrillator coil creates a first vector with the first electrode and a second vector with the second defibrillator coil, and wherein the first vector and the second vector pass through the heart.