SWITCHED SAFETY PROTECTION CIRCUIT FOR AN AIMD SYSTEM DURING EXPOSURE TO HIGH POWER ELECTROMAGNETIC FIELDS
First Claim
1. An implantable medical device, comprising:
- a) a thermally or electrically conductive housing for the implantable medical device containing tissue-stimulating or biological-sensing circuits;
b) a feedthrough terminal disposed in the conductive housing;
c) a first conductive path electrically coupled between the feedthrough terminal and the tissue-stimulating or biological-sensing circuits;
d) a switch electrically coupled in series along the first conductive path, the switch comprising a first throw end, a second throw end and a pole end, wherein the pole end is permanently electrically coupled to the tissue-stimulating or biological-sensing circuit and the first throw end is permanently connected to the feedthrough terminal; and
e) a second conductive path permanently electrically coupled between the second throw end of the switch and the conductive housing;
f) wherein the switch is configured to be selectively actuatable in response to a programmable telemetry signal to either connect the pole to the first throw end or to connect the pole to the second throw end.
5 Assignments
0 Petitions
Accused Products
Abstract
An energy management system that facilitates the transfer of high frequency energy induced on an implanted lead or a leadwire includes an energy dissipating surface associated with the implanted lead or the leadwire, a diversion or diverter circuit associated with the energy dissipating surface, and at least one switch disposed between the diversion circuit and the AIMD electronics for diverting energy in the implanted lead or the leadwire through the diversion circuit to the energy dissipating surface. The switch may comprise a single or multi-pole double or single throw switch. The diversion circuit may be either a high pass filter or a low pass filter.
8 Citations
17 Claims
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1. An implantable medical device, comprising:
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a) a thermally or electrically conductive housing for the implantable medical device containing tissue-stimulating or biological-sensing circuits; b) a feedthrough terminal disposed in the conductive housing; c) a first conductive path electrically coupled between the feedthrough terminal and the tissue-stimulating or biological-sensing circuits; d) a switch electrically coupled in series along the first conductive path, the switch comprising a first throw end, a second throw end and a pole end, wherein the pole end is permanently electrically coupled to the tissue-stimulating or biological-sensing circuit and the first throw end is permanently connected to the feedthrough terminal; and e) a second conductive path permanently electrically coupled between the second throw end of the switch and the conductive housing; f) wherein the switch is configured to be selectively actuatable in response to a programmable telemetry signal to either connect the pole to the first throw end or to connect the pole to the second throw end. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15)
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16. An implantable medical device, comprising:
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a) a thermally or electrically conductive housing for the implantable medical device containing tissue-stimulating or biological-sensing circuits; b) a feedthrough terminal disposed in the conductive housing; a first conductive path electrically coupled between the feedthrough terminal and the tissue-stimulating or biological-sensing circuits; d) a switch electrically coupled in series along the first conductive path, the switch comprising a first throw end, a second throw end and a pole end, wherein the pole end is permanently electrically coupled to the tissue-stimulating or biological-sensing circuit and the first throw end is permanently connected to the feedthrough terminal; and e) a second conductive path permanently electrically coupled between the second throw end of the switch and the conductive housing; f) wherein the switch is configured to be selectively actuatable in response to a programmable telemetry signal to either connect the pole to the first throw end in a normal operating mode or to connect the pole to the second throw end in an MRI mode; and g) a third conductive path coupled at a first end anywhere along the first conductive path between the feedthrough terminal and the first throw end of the switch, and coupled at a second end to the conductive housing, wherein a frequency variable diverter element is coupled in series along the third conductive path.
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17. An implantable medical device, comprising:
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a) a thermally or electrically conductive housing for the implantable medical device containing tissue stimulating or biological-sensing circuits; b) a feedthrough terminal disposed in the conductive housing; c) a first conductive path electrically coupled between the feedthrough terminal and the tissue-stimulating or biological-sensing circuits; d) a switch electrically coupled in series along the first conductive path, the switch comprising a first throw end, a second throw end and a pole end, wherein the pole end is permanently electrically coupled to the tissue-stimulating or biological-sensing circuit and the first throw end is permanently connected to the feedthrough terminal; and e) a second conductive path permanently electrically coupled between the second throw end of the switch and the conductive housing; f) wherein the switch is configured to be actuatable in response to a magnetic resonance B0 field sensor that, in the absence of a static magnetic field, electrically connects the pole to the first throw end, and in the presence of a static magnetic field, electrically connects the pole to the second throw end.
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Specification