MR-compatible methods and systems for cardiac monitoring and gating
First Claim
1. A method for detecting a phase in a cardiac cycle comprising the steps of:
- (a) optically detecting movements of an anatomic structure affected by cardiac activity;
(b) deriving a cardiac signal in response to said optically detected movements which is indicative of a phase in a cardiac cycle; and
(c) generating a trigger signal in response to said derived cardiac signal which is indicative of said phase of the cardiac cycle.
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Accused Products
Abstract
Noninvasive, MR-compatible methods and systems optically detect mechanical cardiac activity by anatomic (e.g., esophageal) movements. Most preferably, esophageal motion is detected optically and is indicative rhythmic cardiac activities. This esophageal motion may then be detected and used to provide a signal indicative of periods of cardiac activity and inactivity. The signal may be further processed so as to generate a trigger signal that may be input to a MR scanner. In such a manner, MR microscopy may be accomplished to acquire information at a specific phase of the cardiac cycle, for example, in synchrony with periods of cardiac inactivity. Moreover, since mechanical cardiac activity is detected and employed, instead of electrical activity as is employed in conventional techniques, the present invention is immune to electromagnetic interference during MR microscopy. As a result, robust cardiac signals may be monitored and gated during 2-dimensional and 3-dimensional in vivo microscopy. The present invention is therefore especially well suited for MR microscopy of small animals, such as laboratory mice and rats.
42 Citations
30 Claims
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1. A method for detecting a phase in a cardiac cycle comprising the steps of:
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(a) optically detecting movements of an anatomic structure affected by cardiac activity;
(b) deriving a cardiac signal in response to said optically detected movements which is indicative of a phase in a cardiac cycle; and
(c) generating a trigger signal in response to said derived cardiac signal which is indicative of said phase of the cardiac cycle. - View Dependent Claims (2, 3, 4, 5)
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6. A method of conducting magnetic resonance (MR) microscopy comprising the steps of:
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(a) optically detecting internal anatomic physical movement in response to rhythmic periods of cardiac activity and inactivity during a cardiac cycle;
(b) conducting MR microscopy during said periods of cardiac inactivity; and
(c) using the derived cardiac signal to produce cardiac images at specific phases of the cardiac cycle. - View Dependent Claims (7, 8, 9, 10, 11, 12, 13, 14, 16, 17, 19, 20)
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15. A magnetic resonance (MR) microscopy method comprising the steps of:
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(a) inserting an optical fiber probe into a vertebrate esophagus;
(b) illuminating a site of the esophagus with light emitted by said probe;
(c) detecting reflected light from the esophagus site by a photodetector coupled optically to said probe;
(d) determining movements of the esophagus at said site indicative of rhythmic periods of cardiac activity and inactivity based on said detected reflected light and generating an output signal therefrom; and
(e) providing said output signal to a MR scanner and synchronizing MR microscopy in response to said detected periods of cardiac inactivity.
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18. A gating system for coordinating cardiac activity to a magnetic resonance (MR) imaging pulse, comprising:
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(a) an optical probe assembly for optically detecting esophageal movements in response to rhythmic periods of cardiac activity and inactivity;
(b) a photodetector optically coupled to said probe assembly for deriving a cardiac signal in response to said optically detected esophageal movements which is indicative of said rhythmic periods of cardiac activity and inactivity; and
(c) a signal processor which receives said cardiac signal and generates a trigger signal in response to said derived cardiac signal which is indicative of a period of cardiac inactivity.
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21. A magnetic resonance (MR) microscopy system comprising:
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(a) an optical detection system for optically detecting physical anatomic movement in response to rhythmic periods of a cardiac cycle and generating a trigger signal during a desired phase of said cardiac cycle; and
(b) a MR scanner which conducts an MR scan pulse in response to receiving said trigger signal. - View Dependent Claims (22, 23, 24, 25, 27, 28, 29, 30)
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26. A magnetic resonance (MR) microscopy system comprising:
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(a) an optical fiber probe capable of insertion into a vertebrate esophagus;
(b) a light source coupled to said probe for illuminating a site of the esophagus with light emitted by said probe;
(c) a photodetector coupled operatively to said probe for detecting reflected light from the esophagus site, and for determining movements of the esophagus at said site based on said detected reflected light, said photodetector generating an output signal in response to said detected reflected light which is indicative of rhythmic periods of cardiac activity and inactivity; and
(d) a MR scanner which receives said output signal and which conducts MR microscopy in synchronized response to said detected periods of cardiac inactivity.
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Specification