Method and apparatus for impedance signal localizations from implanted devices
First Claim
1. A patient monitoring system comprising:
- an implantable medical device comprising;
a housing and a connector block configured to couple to a cardiac lead system having a plurality of electrodes;
means for selecting electrodes of a cardiac lead system to establish an impedance vector in tissue proximate a patient'"'"'s heart;
means coupled to the electrodes selecting means for measuring impedance of tissue proximate a patient'"'"'s heart based on an impedance vector formed between electrodes of a cardiac lead system; and
means for determining a quantifying value for a contributing physiological impedance factor among a plurality of physiological impedance factors associated with a physiological condition of a patient'"'"'s heart, wherein the means for determining a quantifying value for a contributing physiological impedance factor among a plurality of physiological impedance factors associated with a first physiological condition of a patient'"'"'s heart among a plurality of physiological conditions of a patient'"'"'s heart comprises;
a microprocessor operating to(1) cause the means for measuring impedance of tissue proximate a patient'"'"'s heart based upon an impedance vector formed between electrodes of a cardiac lead system to make first and second impedance measurements spaced apart in time along a first impedance vector and to make first and second impedance measurements spaced apart in time along a second impedance vector;
(2) calculate a value for a change in measured tissue impedance over time along each of the first and second impedance vectors as Δ
ZV1 and Δ
ZV2, respectively;
(3) insert each of the calculated values Δ
ZV1 and Δ
ZV2 into an equation
Δ
Z=α
L*QL+α
B*QBα
HM*QHM+α
SM*QSM+α
HV*KHV+α
LV*KLV,where QL is lung tissue fractional resistivity change,QB is blood fractional resistivity change,QHM is heart muscle fractional resistivity change,QSM is skeletal muscle fractional resistivity change,KHV is heart volume fractional change,KLV is lung volume fractional change, andeach of QL, QB, QHM, QSM, KHV, and KLV is a physiological impedance factor,α
L is lung tissue impedance sensitivity factor,α
B is blood impedance sensitivity factor,α
HM is heart muscle impedance sensitivity factor,α
SM is skeletal muscle impedance sensitivity factor,α
HV is heart volume impedance sensitivity factor,α
LV is lung volume impedance sensitivity factor;
(4) subtract Δ
ZV2 from Δ
ZV1 to form the equation
Δ
ZV1−
Δ
ZV2=(α
LV1−
α
LV2)*QL+(α
BV1−
α
BV2)*QB+(α
HMV1−
α
HMV2)*QHM+(α
SMV1−
α
SMV2)*QSM+(α
HVV1−
α
HVV2)*KHV+(α
LVV1−
α
LVV2)*KLV; and
(5) solve for one of the physiological impedance factors QL, QB, QHM, QSM, KHV, and KLV using the equation.
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Abstract
A patient monitoring system including an implantable medical device for monitoring a plurality of physiological factors contributing to physiological conditions of a patient'"'"'s heart by measuring a first impedance affected by the plurality of physiological factors, across one of a plurality of vectors, and a second impedance affected by the plurality of physiological factors, across a second one of the plurality of vectors subsequent to determining the first impedance. A change in impedance is determined based upon the first impedance and the second impedance measurements. Using an equation ΔZVX=αAVX*QA+αBVX*QB, where QA is a fractional resistivity change of a first contributing physiological impedance factor, QB is a fractional resistivity change of a second physiological impedance factor, αAVX is an impedance sensitivity factor for physiological impedance factor QA, and αBVX is an impedance sensitivity factor for physiological impedance factor QB, the value of one of the contributing physiological impedance factors is determined. The contributing physiological impedance factors may include lung resistivity, blood resistivity, heart muscle resistivity, skeletal muscle resistivity, heart volume and lung volume.
109 Citations
18 Claims
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1. A patient monitoring system comprising:
-
an implantable medical device comprising;
a housing and a connector block configured to couple to a cardiac lead system having a plurality of electrodes;means for selecting electrodes of a cardiac lead system to establish an impedance vector in tissue proximate a patient'"'"'s heart; means coupled to the electrodes selecting means for measuring impedance of tissue proximate a patient'"'"'s heart based on an impedance vector formed between electrodes of a cardiac lead system; and means for determining a quantifying value for a contributing physiological impedance factor among a plurality of physiological impedance factors associated with a physiological condition of a patient'"'"'s heart, wherein the means for determining a quantifying value for a contributing physiological impedance factor among a plurality of physiological impedance factors associated with a first physiological condition of a patient'"'"'s heart among a plurality of physiological conditions of a patient'"'"'s heart comprises; a microprocessor operating to (1) cause the means for measuring impedance of tissue proximate a patient'"'"'s heart based upon an impedance vector formed between electrodes of a cardiac lead system to make first and second impedance measurements spaced apart in time along a first impedance vector and to make first and second impedance measurements spaced apart in time along a second impedance vector; (2) calculate a value for a change in measured tissue impedance over time along each of the first and second impedance vectors as Δ
ZV1 and Δ
ZV2, respectively;(3) insert each of the calculated values Δ
ZV1 and Δ
ZV2 into an equation
Δ
Z=α
L*QL+α
B*QBα
HM*QHM+α
SM*QSM+α
HV*KHV+α
LV*KLV,where QL is lung tissue fractional resistivity change, QB is blood fractional resistivity change, QHM is heart muscle fractional resistivity change, QSM is skeletal muscle fractional resistivity change, KHV is heart volume fractional change, KLV is lung volume fractional change, and each of QL, QB, QHM, QSM, KHV, and KLV is a physiological impedance factor, α
L is lung tissue impedance sensitivity factor,α
B is blood impedance sensitivity factor,α
HM is heart muscle impedance sensitivity factor,α
SM is skeletal muscle impedance sensitivity factor,α
HV is heart volume impedance sensitivity factor,α
LV is lung volume impedance sensitivity factor;(4) subtract Δ
ZV2 from Δ
ZV1 to form the equation
Δ
ZV1−
Δ
ZV2=(α
LV1−
α
LV2)*QL+(α
BV1−
α
BV2)*QB+(α
HMV1−
α
HMV2)*QHM+(α
SMV1−
α
SMV2)*QSM+(α
HVV1−
α
HVV2)*KHV+(α
LVV1−
α
LVV2)*KLV; and(5) solve for one of the physiological impedance factors QL, QB, QHM, QSM, KHV, and KLV using the equation. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12)
-
-
13. A patient monitoring system comprising:
-
an implantable medical device comprising;
a housing and a connector block configured to couple to a cardiac lead system having a plurality of electrodes;means for selecting electrodes of a cardiac lead system to establish an impedance vector in tissue proximate a patient'"'"'s heart; means coupled to the electrodes selecting means for measuring impedance of tissue proximate a patient'"'"'s heart based on an impedance vector formed between electrodes of a cardiac lead system; and means for determining a quantifying value for a contributing physiological impedance factor among a plurality of physiological impedance factors associated with a physiological condition of a patient'"'"'s heart, wherein the means for determining a quantifying value for a contributing physiological impedance factor among a plurality of physiological impedance factors associated with a first physiological condition of a patient'"'"'s heart among a plurality of physiological conditions of a patient'"'"'s heart comprises; a processor operating to (1) cause the means for measuring impedance of tissue proximate a patient'"'"'s heart based upon an impedance vector formed between electrodes of a cardiac lead system to make first and second impedance measurements spaced apart in time along a first impedance vector and to make first and second impedance measurements spaced apart in time along a second impedance vector; (2) calculate a value for a change in measured tissue impedance over time along each of the first and second impedance vectors as Δ
ZV1 and Δ
ZV2, respectively;(3) insert each of the calculated values Δ
ZV1 and Δ
ZV2 into an equation
Δ
ZVX=α
AVX*QA+α
BVX*QBwhere QA is a first fractional resistivity change of a physiological impedance factor, QB is a second fractional resistivity change of a physiological impedance factor, α
AVX is an impedance sensitivity factor for physiological impedance factor QA, andα
BVX is an impedance sensitivity factor for physiological impedance factor QB;(4) subtract Δ
ZV2 from Δ
ZV1 to form the equation
Δ
ZV1−
Δ
ZV2=(α
AV1−
α
AV2)*QA+(α
BV1−
α
BV2)*QB; and(5) solve for a quantifying value for one of the physiological impedance factors QA and QB using the equation. - View Dependent Claims (14, 15, 16, 17, 18)
-
Specification